Release Date	Request Code	Change Type	NCI Code	CDISC Term Type	CDISC Codelist (Short Name)	CDISC Codelist (Long Name)	Change Summary	Original	New	Change Implementation Instructions
2022-09-30	CDISC-5503	Add	C165460	Term	ACCPARTY	Accountable Party	Add new term to new codelist	- - -	COURIER	
2022-09-30	CDISC-5503	Add	C189265	CDISC Codelist	ACCPARTY	Accountable Party	Addition of new codelist	- - -	ACCPARTY	
2022-09-30	CDISC-5503	Add	C189365	Term	ACCPARTY	Accountable Party	Add new term to new codelist	- - -	STORAGE FACILITY	
2022-09-30	CDISC-5503	Add	C25392	Term	ACCPARTY	Accountable Party	Add new term to new codelist	- - -	MANUFACTURER	
2022-09-30	CDISC-5503	Add	C37984	Term	ACCPARTY	Accountable Party	Add new term to new codelist	- - -	LABORATORY	
2022-09-30	CDISC-5503	Add	C41189	Term	ACCPARTY	Accountable Party	Add new term to new codelist	- - -	SUBJECT	
2022-09-30	CDISC-5503	Add	C70793	Term	ACCPARTY	Accountable Party	Add new term to new codelist	- - -	SPONSOR	
2022-09-30	CDISC-5706	Add	C189693	CDISC Codelist	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Addition of new codelist	- - -	BPRSA118OR	
2022-09-30	CDISC-5706	Add	C189733	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Not observed	
2022-09-30	CDISC-5706	Add	C189734	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Very Mild	
2022-09-30	CDISC-5706	Add	C189735	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Mild	
2022-09-30	CDISC-5706	Add	C189736	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Moderate	
2022-09-30	CDISC-5706	Add	C189737	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Moderately Severe	
2022-09-30	CDISC-5706	Add	C189738	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Severe	
2022-09-30	CDISC-5706	Add	C189739	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Very Severe	
2022-09-30	CDISC-5706	Add	C189740	Term	BPRSA118OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES for BPRSA118 TN/TC	Add new term to new codelist	- - -	Cannot be assessed adequately because of severe formal thought disorder, uncooperativeness, or marked evasiveness/guardedness; or Not assessed	
2022-09-30	CDISC-5706	Add	C189694	CDISC Codelist	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Addition of new codelist	- - -	BPRSA118STR	
2022-09-30	CDISC-5706	Add	C189741	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	1	
2022-09-30	CDISC-5706	Add	C189742	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	2	
2022-09-30	CDISC-5706	Add	C189743	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	3	
2022-09-30	CDISC-5706	Add	C189744	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	4	
2022-09-30	CDISC-5706	Add	C189745	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	5	
2022-09-30	CDISC-5706	Add	C189746	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	6	
2022-09-30	CDISC-5706	Add	C189747	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	7	
2022-09-30	CDISC-5706	Add	C189748	Term	BPRSA118STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC for BPRSA118 TN/TC	Add new term to new codelist	- - -	9	
2022-09-30	CDISC-5706	Add	C189689	CDISC Codelist	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Addition of new codelist	- - -	BPRSA1SET1OR	
2022-09-30	CDISC-5706	Add	C189703	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Not reported	
2022-09-30	CDISC-5706	Add	C189704	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Very Mild	
2022-09-30	CDISC-5706	Add	C189705	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Mild	
2022-09-30	CDISC-5706	Add	C189706	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Moderate	
2022-09-30	CDISC-5706	Add	C189707	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Moderately Severe	
2022-09-30	CDISC-5706	Add	C189708	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Severe	
2022-09-30	CDISC-5706	Add	C189709	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Very Severe	
2022-09-30	CDISC-5706	Add	C189710	Term	BPRSA1SET1OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	Cannot be assessed adequately because of severe formal thought disorder, uncooperativeness, or marked evasiveness/guardedness; or Not assessed	
2022-09-30	CDISC-5706	Add	C189690	CDISC Codelist	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Addition of new codelist	- - -	BPRSA1SET1STR	
2022-09-30	CDISC-5706	Add	C189711	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	1	
2022-09-30	CDISC-5706	Add	C189712	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	2	
2022-09-30	CDISC-5706	Add	C189713	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	3	
2022-09-30	CDISC-5706	Add	C189714	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	4	
2022-09-30	CDISC-5706	Add	C189715	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	5	
2022-09-30	CDISC-5706	Add	C189716	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	6	
2022-09-30	CDISC-5706	Add	C189717	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	7	
2022-09-30	CDISC-5706	Add	C189718	Term	BPRSA1SET1STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA101 TN/TC	Add new term to new codelist	- - -	9	
2022-09-30	CDISC-5706	Add	C189691	CDISC Codelist	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Addition of new codelist	- - -	BPRSA1SET2OR	
2022-09-30	CDISC-5706	Add	C189719	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Not observed	
2022-09-30	CDISC-5706	Add	C189720	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Very Mild	
2022-09-30	CDISC-5706	Add	C189721	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Mild	
2022-09-30	CDISC-5706	Add	C189722	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Moderate	
2022-09-30	CDISC-5706	Add	C189723	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Moderately Severe	
2022-09-30	CDISC-5706	Add	C189724	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Severe	
2022-09-30	CDISC-5706	Add	C189725	Term	BPRSA1SET2OR	Brief Psychiatric Rating Scale-Anchored Clinical Classification ORRES the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	Very Severe	
2022-09-30	CDISC-5706	Add	C189692	CDISC Codelist	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Addition of new codelist	- - -	BPRSA1SET2STR	
2022-09-30	CDISC-5706	Add	C189726	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	1	
2022-09-30	CDISC-5706	Add	C189727	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	2	
2022-09-30	CDISC-5706	Add	C189728	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	3	
2022-09-30	CDISC-5706	Add	C189729	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	4	
2022-09-30	CDISC-5706	Add	C189730	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	5	
2022-09-30	CDISC-5706	Add	C189731	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	6	
2022-09-30	CDISC-5706	Add	C189732	Term	BPRSA1SET2STR	Brief Psychiatric Rating Scale-Anchored Clinical Classification STRESC the Same as BPRSA103 TN/TC	Add new term to new codelist	- - -	7	
2022-09-30	CDISC-5753	Add	C123556	Term	BSTEST	Biospecimen Characteristics Test Name	Add new term to existing codelist	- - -	Tumor Cells/Total Cells	C127771 being merged into C123556.
2022-09-30	CDISC-5753	Add	C123556	Term	BSTESTCD	Biospecimen Characteristics Test Code	Add new term to existing codelist	- - -	TUMCECE	C127771 being merged into C123556.
2022-09-30	CDISC-4724	Add	C189701	Term	CCCAT	Category of Clinical Classification	Add new term to existing codelist	- - -	CIRS-G	
2022-09-30	CDISC-5140	Add	C189366	Term	CLMETH	Specimen Collection Method	Add new term to existing codelist	- - -	CLEAN CATCH MID-STREAM	
2022-09-30	CDISC-5753	Add	C189297	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Sub/MDSC	
2022-09-30	CDISC-5753	Add	C189298	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC/Leuk	
2022-09-30	CDISC-5753	Add	C189299	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Intermed/Leuk	
2022-09-30	CDISC-5753	Add	C189300	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189301	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Dbl Neg	
2022-09-30	CDISC-5494	Add	C189302	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym GD/Lym	
2022-09-30	CDISC-5753	Add	C189303	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat Sub/NK	
2022-09-30	CDISC-5753	Add	C189304	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Immat/Lym	
2022-09-30	CDISC-5753	Add	C189305	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed/Lym	
2022-09-30	CDISC-5753	Add	C189306	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat/Lym	
2022-09-30	CDISC-5753	Add	C189307	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK TLym/Lym	
2022-09-30	CDISC-5753	Add	C189308	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Immat	
2022-09-30	CDISC-5753	Add	C189309	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed	
2022-09-30	CDISC-5753	Add	C189310	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat	
2022-09-30	CDISC-5753	Add	C189324	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Dbl Neg Sub/MDSC	
2022-09-30	CDISC-5753	Add	C189325	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Gran Sub/MDSC	
2022-09-30	CDISC-5753	Add	C189326	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Mono Sub/MDSC	
2022-09-30	CDISC-5753	Add	C189327	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Mono/Leuk	
2022-09-30	CDISC-5753	Add	C189343	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Gran/Lym Sub	
2022-09-30	CDISC-5753	Add	C189344	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Gran/Gran	
2022-09-30	CDISC-5753	Add	C189367	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Dbl Neg Sub/MDSC Dbl Neg	
2022-09-30	CDISC-5753	Add	C189368	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Gran Sub/MDSC Gran	
2022-09-30	CDISC-5753	Add	C189369	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Mono Sub/MDSC Mono	
2022-09-30	CDISC-5753	Add	C189370	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Sub/MDSC Sub	
2022-09-30	CDISC-5753	Add	C189371	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Classic Sub/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189372	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Intermed Sub/Mono Intermed	
2022-09-30	CDISC-5753	Add	C189373	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Intermed Sub/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189374	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono NonClassic Sub/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189375	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Dbl Neg/MDSC	
2022-09-30	CDISC-5753	Add	C189376	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Gran/Leuk	
2022-09-30	CDISC-5753	Add	C189377	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Gran/MDSC	
2022-09-30	CDISC-5753	Add	C189378	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Mono/MDSC	
2022-09-30	CDISC-5753	Add	C189379	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Mono/Mono	
2022-09-30	CDISC-5753	Add	C189380	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC/Non-Gran Leuk	
2022-09-30	CDISC-5753	Add	C189381	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189382	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Classic/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189383	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Intermed/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189384	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono NonClassic/Non-TBNK Leuk	
2022-09-30	CDISC-5753	Add	C189385	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Non-TBNK Leuk/Leuk	
2022-09-30	CDISC-5753	Add	C189386	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	MDSC Dbl Neg Sub	
2022-09-30	CDISC-5753	Add	C189387	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Non-TBNK Leuk	
2022-09-30	CDISC-5439	Add	C189388	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	CD16 Expression	
2022-09-30	CDISC-5440	Add	C189389	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	CD86 Expression	
2022-09-30	CDISC-5441	Add	C189390	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	HLADR Expression	
2022-09-30	CDISC-5446	Add	C189391	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono NonClassic Sub	
2022-09-30	CDISC-5446	Add	C189392	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Classic Sub	
2022-09-30	CDISC-5753	Add	C189393	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono NonClassic Sub/Mono NonClassic	
2022-09-30	CDISC-5753	Add	C189394	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Classic Sub/Mono Classic	
2022-09-30	CDISC-5753	Add	C189395	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	Mono Intermed Sub	
2022-09-30	CDISC-5497	Add	C189396	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Help Reg/Lym	
2022-09-30	CDISC-5753	Add	C189397	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Immat Sub/NK Immat	
2022-09-30	CDISC-5753	Add	C189398	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed Sub/Leuk	
2022-09-30	CDISC-5753	Add	C189399	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed Sub/Lym	
2022-09-30	CDISC-5753	Add	C189400	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed Sub/NK Intermed	
2022-09-30	CDISC-5753	Add	C189401	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat Sub/Leuk	
2022-09-30	CDISC-5753	Add	C189402	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat Sub/Lym	
2022-09-30	CDISC-5753	Add	C189403	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat Sub/NK Mat	
2022-09-30	CDISC-5753	Add	C189404	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK TLym Sub/NKT	
2022-09-30	CDISC-5753	Add	C189405	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK TLym Sub/TLym	
2022-09-30	CDISC-5753	Add	C189406	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym AB Sub/TLym AB	
2022-09-30	CDISC-5753	Add	C189407	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Cen Mem Sub/TLymC	
2022-09-30	CDISC-5753	Add	C189408	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Cen Mem Sub/TLymCCM	
2022-09-30	CDISC-5753	Add	C189409	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Eff Mem Sub/TLymC	
2022-09-30	CDISC-5753	Add	C189410	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Eff Mem Sub/TLymCEM	
2022-09-30	CDISC-5753	Add	C189411	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Mem Sub/TLymC	
2022-09-30	CDISC-5753	Add	C189412	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Naive Sub/TLymC	
2022-09-30	CDISC-5753	Add	C189413	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Naive Sub/TLymCN	
2022-09-30	CDISC-5753	Add	C189414	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym GD Sub/TLym GD	
2022-09-30	CDISC-5753	Add	C189415	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Immat/Leuk	
2022-09-30	CDISC-5753	Add	C189416	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Immat/NK	
2022-09-30	CDISC-5753	Add	C189417	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed/Leuk	
2022-09-30	CDISC-5753	Add	C189418	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed/NK	
2022-09-30	CDISC-5753	Add	C189419	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat/Leuk	
2022-09-30	CDISC-5753	Add	C189420	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat/NK	
2022-09-30	CDISC-5753	Add	C189421	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK TLym/TLym	
2022-09-30	CDISC-5753	Add	C189422	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Immat Sub	
2022-09-30	CDISC-5753	Add	C189423	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Intermed Sub	
2022-09-30	CDISC-5753	Add	C189424	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	NK Cells Mat Sub	
2022-09-30	CDISC-5753	Add	C189425	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym AB/TLym	
2022-09-30	CDISC-5753	Add	C189426	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym GD/TLym	
2022-09-30	CDISC-5492	Add	C189427	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Help Sub/TLym Help	
2022-09-30	CDISC-5753	Add	C189428	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Term Mem Sub/TLymCTM	
2022-09-30	CDISC-5753	Add	C189429	Term	CPTEST	Cell Phenotyping Test Name	Add new term to existing codelist	- - -	TLym Cytx Term Mem/TLymC	
2022-09-30	CDISC-5753	Add	C189297	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSSP	
2022-09-30	CDISC-5753	Add	C189298	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSLE	
2022-09-30	CDISC-5753	Add	C189299	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNINLE	
2022-09-30	CDISC-5753	Add	C189300	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189300	
2022-09-30	CDISC-5753	Add	C189301	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSDN	
2022-09-30	CDISC-5494	Add	C189302	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLGDLY	
2022-09-30	CDISC-5753	Add	C189303	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMASNK	
2022-09-30	CDISC-5753	Add	C189304	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIMLY	
2022-09-30	CDISC-5753	Add	C189305	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINLY	
2022-09-30	CDISC-5753	Add	C189306	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMALY	
2022-09-30	CDISC-5753	Add	C189307	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKTLY	
2022-09-30	CDISC-5753	Add	C189308	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIM	
2022-09-30	CDISC-5753	Add	C189309	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIN	
2022-09-30	CDISC-5753	Add	C189310	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMA	
2022-09-30	CDISC-5753	Add	C189324	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSDNSMS	
2022-09-30	CDISC-5753	Add	C189325	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSGSMS	
2022-09-30	CDISC-5753	Add	C189326	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSMSMS	
2022-09-30	CDISC-5753	Add	C189327	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSMLE	
2022-09-30	CDISC-5753	Add	C189343	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSGLYS	
2022-09-30	CDISC-5753	Add	C189344	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSGG	
2022-09-30	CDISC-5753	Add	C189367	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSDNSP	
2022-09-30	CDISC-5753	Add	C189368	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSGSP	
2022-09-30	CDISC-5753	Add	C189369	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSMSP	
2022-09-30	CDISC-5753	Add	C189370	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSSMDSS	
2022-09-30	CDISC-5753	Add	C189371	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189371	
2022-09-30	CDISC-5753	Add	C189372	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNINSP	
2022-09-30	CDISC-5753	Add	C189373	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189373	
2022-09-30	CDISC-5753	Add	C189374	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189374	
2022-09-30	CDISC-5753	Add	C189375	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSDNMS	
2022-09-30	CDISC-5753	Add	C189376	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSGLE	
2022-09-30	CDISC-5753	Add	C189377	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSGMS	
2022-09-30	CDISC-5753	Add	C189378	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSMMS	
2022-09-30	CDISC-5753	Add	C189379	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSMM	
2022-09-30	CDISC-5753	Add	C189380	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSNGLE	
2022-09-30	CDISC-5753	Add	C189381	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189381	
2022-09-30	CDISC-5753	Add	C189382	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189382	
2022-09-30	CDISC-5753	Add	C189383	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189383	
2022-09-30	CDISC-5753	Add	C189384	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	C189384	
2022-09-30	CDISC-5753	Add	C189385	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NTBNKLLE	
2022-09-30	CDISC-5753	Add	C189386	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MDSDNS	
2022-09-30	CDISC-5753	Add	C189387	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NTBNKL	
2022-09-30	CDISC-5439	Add	C189388	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	CD16X	
2022-09-30	CDISC-5440	Add	C189389	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	CD86X	
2022-09-30	CDISC-5441	Add	C189390	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	HLADRX	
2022-09-30	CDISC-5446	Add	C189391	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNCLS	
2022-09-30	CDISC-5446	Add	C189392	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNNCLS	
2022-09-30	CDISC-5753	Add	C189393	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNCLSP	
2022-09-30	CDISC-5753	Add	C189394	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNNCLSP	
2022-09-30	CDISC-5753	Add	C189395	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	MNINS	
2022-09-30	CDISC-5497	Add	C189396	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLYHRLY	
2022-09-30	CDISC-5753	Add	C189397	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIMSP	
2022-09-30	CDISC-5753	Add	C189398	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINSLE	
2022-09-30	CDISC-5753	Add	C189399	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINSLY	
2022-09-30	CDISC-5753	Add	C189400	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINSP	
2022-09-30	CDISC-5753	Add	C189401	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMASLE	
2022-09-30	CDISC-5753	Add	C189402	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMASLY	
2022-09-30	CDISC-5753	Add	C189403	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMASP	
2022-09-30	CDISC-5753	Add	C189404	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKTSP	
2022-09-30	CDISC-5753	Add	C189405	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKTSTLY	
2022-09-30	CDISC-5753	Add	C189406	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLABSP	
2022-09-30	CDISC-5753	Add	C189407	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCCMSTC	
2022-09-30	CDISC-5753	Add	C189408	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCCMSP	
2022-09-30	CDISC-5753	Add	C189409	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCEMSTC	
2022-09-30	CDISC-5753	Add	C189410	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCEMSP	
2022-09-30	CDISC-5753	Add	C189411	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCMSTC	
2022-09-30	CDISC-5753	Add	C189412	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCNSTC	
2022-09-30	CDISC-5753	Add	C189413	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCNSP	
2022-09-30	CDISC-5753	Add	C189414	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLGDSP	
2022-09-30	CDISC-5753	Add	C189415	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIMLE	
2022-09-30	CDISC-5753	Add	C189416	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIMNK	
2022-09-30	CDISC-5753	Add	C189417	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINLE	
2022-09-30	CDISC-5753	Add	C189418	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINNK	
2022-09-30	CDISC-5753	Add	C189419	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMALE	
2022-09-30	CDISC-5753	Add	C189420	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMANK	
2022-09-30	CDISC-5753	Add	C189421	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKTTLY	
2022-09-30	CDISC-5753	Add	C189422	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKIMS	
2022-09-30	CDISC-5753	Add	C189423	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKINS	
2022-09-30	CDISC-5753	Add	C189424	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	NKMAS	
2022-09-30	CDISC-5753	Add	C189425	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLABTLY	
2022-09-30	CDISC-5753	Add	C189426	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLGDTLY	
2022-09-30	CDISC-5492	Add	C189427	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLHSP	
2022-09-30	CDISC-5753	Add	C189428	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCTMSP	
2022-09-30	CDISC-5753	Add	C189429	Term	CPTESTCD	Cell Phenotyping Test Code	Add new term to existing codelist	- - -	TLCTMTLC	
2022-09-30	CDISC-5159	Add	C189430	Term	DATEST	Drug Accountability Test Name	Add new term to existing codelist	- - -	Lost Amount	
2022-09-30	CDISC-5159	Add	C189430	Term	DATESTCD	Drug Accountability Test Code	Add new term to existing codelist	- - -	LOSTAMT	
2022-09-30	CDISC-5457	Add	C37978	Term	DICTNAM	Dictionary Name	Add new term to existing codelist	- - -	ICD-O	
2022-09-30	CDISC-5246	Add	C189311	Term	EVAL	Evaluator	Add new term to existing codelist	- - -	CERTIFIED ASSESSOR	
2022-09-30	CDISC-5068	Add	C189312	Term	EVAL	Evaluator	Add new term to existing codelist	- - -	NUCLEAR MEDICINE PHYSICIAN	
2022-09-30	CDISC-5080	Add	C189313	Term	EVAL	Evaluator	Add new term to existing codelist	- - -	PHARMACOKINETICIST	
2022-09-30	CDISC-5068	Add	C93061	Term	EVAL	Evaluator	Add new term to existing codelist	- - -	NEUROONCOLOGIST	
2022-09-30	CDISC-5298	Add	C176277	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Number of Devices Present	
2022-09-30	CDISC-5298	Add	C176278	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Maximum Dose Amount	
2022-09-30	CDISC-5298	Add	C176279	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Frequency of Maximum Dose Amount	
2022-09-30	CDISC-5298	Add	C176280	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Final Dose Amount	
2022-09-30	CDISC-5298	Add	C176281	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Frequency of Final Dose Amount	
2022-09-30	CDISC-5298	Add	C176282	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Unable to Taper Dependent Indicator	
2022-09-30	CDISC-5298	Add	C176283	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Relapse after Discon Dependent Indicator	
2022-09-30	CDISC-5298	Add	C176284	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Unable to Discon Dependent Indicator	
2022-09-30	CDISC-5298	Add	C176285	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Substance Dependence Indicator	
2022-09-30	CDISC-4819	Add	C189431	Term	FATEST	Findings About Test Name	Add new term to existing codelist	- - -	Event Related to Incr Phys Activity Ind	
2022-09-30	CDISC-5298	Add	C176277	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	DEVPNUM	
2022-09-30	CDISC-5298	Add	C176278	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	MXDOSAMT	
2022-09-30	CDISC-5298	Add	C176279	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	MXDOSFRQ	
2022-09-30	CDISC-5298	Add	C176280	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	FNDOSAMT	
2022-09-30	CDISC-5298	Add	C176281	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	FNDOSFRQ	
2022-09-30	CDISC-5298	Add	C176282	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	TPDEPIND	
2022-09-30	CDISC-5298	Add	C176283	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	RLDEPIND	
2022-09-30	CDISC-5298	Add	C176284	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	DCDEPIND	
2022-09-30	CDISC-5298	Add	C176285	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	SBDEPIND	
2022-09-30	CDISC-4819	Add	C189431	Term	FATESTCD	Findings About Test Code	Add new term to existing codelist	- - -	EVRIPIND	
2022-09-30	CDISC-5246	Add	C189432	Term	FREQ	Frequency	Add new term to existing codelist	- - -	EVERY 4 YEARS	
2022-09-30	CDISC-5246	Add	C189433	Term	FREQ	Frequency	Add new term to existing codelist	- - -	EVERY 10 WEEKS	
2022-09-30	CDISC-5246	Add	C189434	Term	FREQ	Frequency	Add new term to existing codelist	- - -	EVERY 13 WEEKS	
2022-09-30	CDISC-5246	Add	C189435	Term	FREQ	Frequency	Add new term to existing codelist	- - -	EVERY 10 YEARS	
2022-09-30	CDISC-5246	Add	C189436	Term	FREQ	Frequency	Add new term to existing codelist	- - -	Q96H	
2022-09-30	CDISC-5079	Add	C189437	Term	GASTRO	Gastrointestinal Test Name	Add new term to existing codelist	- - -	Proton Density Fat Fraction	
2022-09-30	CDISC-5079	Add	C189437	Term	GASTROCD	Gastrointestinal Test Code	Add new term to existing codelist	- - -	PDFF	
2022-09-30	CDISC-5753	Add	C189438	Term	GFANMET	Genomic Findings Analytical Method Calculation Formula	Add new term to existing codelist	- - -	ADME VARIANT PROFILE	
2022-09-30	CDISC-5753	Add	C189439	Term	GFTEST	Genomic Findings Test Name	Add new term to existing codelist	- - -	Sequence Rearrangement	
2022-09-30	CDISC-5753	Add	C189440	Term	GFTEST	Genomic Findings Test Name	Add new term to existing codelist	- - -	Variable Number Tandem Repeats	
2022-09-30	CDISC-5753	Add	C189441	Term	GFTEST	Genomic Findings Test Name	Add new term to existing codelist	- - -	Variant Profile	
2022-09-30	CDISC-5753	Add	C189439	Term	GFTESTCD	Genomic Findings Test Code	Add new term to existing codelist	- - -	SEQREAR	
2022-09-30	CDISC-5753	Add	C189440	Term	GFTESTCD	Genomic Findings Test Code	Add new term to existing codelist	- - -	VNTR	
2022-09-30	CDISC-5753	Add	C189441	Term	GFTESTCD	Genomic Findings Test Code	Add new term to existing codelist	- - -	VARPROF	
2022-09-30	CDISC-5753	Add	C189314	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	NUMBER OF CAG REPEATS	
2022-09-30	CDISC-5753	Add	C189443	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	REARRANGEMENT GENE 1	
2022-09-30	CDISC-5753	Add	C189444	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	REARRANGEMENT GENE 2	
2022-09-30	CDISC-5753	Add	C189445	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	REARRANGEMENT TYPE	
2022-09-30	CDISC-5753	Add	C189446	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	PREDICTED IN-FRAME INDICATOR	
2022-09-30	CDISC-5753	Add	C189447	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	ALLELE SEQUENCE	
2022-09-30	CDISC-5753	Add	C189448	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	NORMALIZED NUMBER OF SEQUENCE VARIANTS	
2022-09-30	CDISC-5753	Add	C189449	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	PREDICTED DIPLOTYPE	
2022-09-30	CDISC-5753	Add	C189450	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	PREDICTED PHENOTYPE	
2022-09-30	CDISC-5753	Add	C189451	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	PREDICTED NUMBER OF CAG REPEATS	
2022-09-30	CDISC-5753	Add	C189657	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	REARRANGEMENT IMPACT CLASSIFICATION	
2022-09-30	CDISC-5753	Add	C45374	Term	GFTSDTL	Genomic Findings Test Detail	Add new term to existing codelist	- - -	NUCLEOTIDE SEQUENCE	
2022-09-30	CDISC-5753	Add	C74580	Term	INTEGU	Integumentary System Test Name	Add new term to existing codelist	- - -	Skin Type	C74580 removed from SCTEST-CD codelist and added into INTEGU-CD codelist.
2022-09-30	CDISC-5753	Add	C74580	Term	INTEGUCD	Integumentary System Test Code	Add new term to existing codelist	- - -	SKINTYP	C74580 removed from SCTEST-CD codelist and added into INTEGU-CD codelist.
2022-09-30	CDISC-5753	Add	C189452	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	AMERICAN COCKROACH ANTIGEN	
2022-09-30	CDISC-5753	Add	C189453	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	PEANUT ANTIGEN	
2022-09-30	CDISC-5753	Add	C189454	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	BEE MIX VENOM ANTIGENS	
2022-09-30	CDISC-5753	Add	C189455	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	BOX ELDER POLLEN	
2022-09-30	CDISC-5753	Add	C189456	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	COMMON RAGWEED POLLEN	
2022-09-30	CDISC-5753	Add	C189457	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	COW MILK ANTIGEN	
2022-09-30	CDISC-5753	Add	C189458	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	AMERICAN HOUSE DUST MITE ANTIGEN	
2022-09-30	CDISC-5753	Add	C189459	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	EUROPEAN HOUSE DUST MITE ANTIGEN	
2022-09-30	CDISC-5753	Add	C189460	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	DAIRY MIX ANTIGENS	
2022-09-30	CDISC-5753	Add	C189461	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	EGG WHITE ANTIGEN	
2022-09-30	CDISC-5753	Add	C189462	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	GERMAN COCKROACH ANTIGEN	
2022-09-30	CDISC-5753	Add	C189463	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	GLIADIN ANTIGEN	
2022-09-30	CDISC-5753	Add	C189464	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	SOYBEAN ANTIGEN	
2022-09-30	CDISC-5753	Add	C189465	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	GRASS MIX POLLENS	
2022-09-30	CDISC-5753	Add	C189466	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	CHEMICAL MIX ANTIGENS	
2022-09-30	CDISC-5753	Add	C189467	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	KEYHOLE LIMPET HEMOCYANIN	
2022-09-30	CDISC-5753	Add	C189468	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	MOLD MIX ANTIGENS	
2022-09-30	CDISC-5753	Add	C189469	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	NUT MIX ANTIGENS	
2022-09-30	CDISC-5753	Add	C189470	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	SHELLFISH MIX ANTIGENS	
2022-09-30	CDISC-5753	Add	C189471	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	TREE MIX POLLENS	
2022-09-30	CDISC-5753	Add	C189472	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	TRITICUM AESTIVUM ANTIGEN	
2022-09-30	CDISC-5753	Add	C189473	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	WEED MIX POLLENS	
2022-09-30	CDISC-5753	Add	C189474	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	WHITE ELM POLLEN	
2022-09-30	CDISC-5753	Add	C189475	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	WHITE OAK POLLEN	
2022-09-30	CDISC-5753	Add	C189476	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	CORN ANTIGEN	
2022-09-30	CDISC-5753	Add	C189477	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	BERMUDA GRASS POLLEN	
2022-09-30	CDISC-5753	Add	C189478	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	CASHEW NUT ANTIGEN	
2022-09-30	CDISC-5753	Add	C189479	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	ENGLISH PLANTAIN POLLEN	
2022-09-30	CDISC-5753	Add	C189480	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	CORYLUS AVELLANA NUT ANTIGEN	
2022-09-30	CDISC-5753	Add	C189481	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	JOHNSON GRASS POLLEN	
2022-09-30	CDISC-5753	Add	C189482	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	MIXED ANTIGENS	
2022-09-30	CDISC-5753	Add	C189483	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	OLIVE TREE POLLEN	
2022-09-30	CDISC-5753	Add	C189484	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	ORCHARD GRASS POLLEN	
2022-09-30	CDISC-5753	Add	C189485	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	RUSSIAN THISTLE POLLEN	
2022-09-30	CDISC-5753	Add	C189486	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	SILVER BIRCH POLLEN	
2022-09-30	CDISC-5753	Add	C189487	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	TIMOTHY GRASS POLLEN	
2022-09-30	CDISC-5753	Add	C189488	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	TRITICUM SPECIES ANTIGEN	
2022-09-30	CDISC-5753	Add	C189489	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	WESTERN RAGWEED POLLEN	
2022-09-30	CDISC-5753	Add	C189490	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	WILD RYE GRASS POLLEN	
2022-09-30	CDISC-5753	Add	C189491	Term	ISBDAGT	Binding Agent for Immunogenicity Tests	Add new term to existing codelist	- - -	WALNUT ANTIGEN	
2022-09-30	CDISC-5753	Add	C189267	CDISC Codelist	ISFTSDTL	Immunogenicity Specimen Test Details	Addition of new codelist	- - -	ISFTSDTL	
2022-09-30	CDISC-5753	Add	C189492	Term	ISFTSDTL	Immunogenicity Specimen Test Details	Add new term to new codelist	- - -	STAINING PATTERN	
2022-09-30	CDISC-5753	Add	C189493	Term	ISFTSDTL	Immunogenicity Specimen Test Details	Add new term to new codelist	- - -	RAST SCORE	
2022-09-30	CDISC-5753	Add	C189315	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Para Aminohippurate	C127631 removed from codelist and replaced with C189315/Para Aminohippurate/PAHPP
2022-09-30	CDISC-5434	Add	C189346	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Pyknotic Cells	
2022-09-30	CDISC-5222	Add	C189494	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Desmethylcitalopram	
2022-09-30	CDISC-5288	Add	C189495	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Soluble Mesothelin Related Peptides	
2022-09-30	CDISC-5291	Add	C189496	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	TATA Box Binding Protein	
2022-09-30	CDISC-5300	Add	C189497	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Alk Phos, Liver + Bone/Total Alk Phos	
2022-09-30	CDISC-5300	Add	C189498	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Fibrin Monomer	
2022-09-30	CDISC-5300	Add	C189499	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Total Plasma Cells/Lymphocytes	
2022-09-30	CDISC-5300	Add	C189500	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Citrulline/Creatinine	
2022-09-30	CDISC-5300	Add	C189501	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Normoblasts	
2022-09-30	CDISC-5300	Add	C189502	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Acid Alpha-Glucosidase	
2022-09-30	CDISC-5753	Add	C189503	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Lymphoblasts/Lymphocytes	
2022-09-30	CDISC-5332	Add	C189504	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Connective Tissue Growth Factor	
2022-09-30	CDISC-5339	Add	C189505	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Lithium	
2022-09-30	CDISC-5353	Add	C189506	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	LDL Triglyceride	
2022-09-30	CDISC-5354	Add	C189507	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	IDL Triglyceride	
2022-09-30	CDISC-5355	Add	C189508	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	LDL Apolipoprotein B	
2022-09-30	CDISC-5361	Add	C189509	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Neutrophilic Metamyelocytes/Total Cells	
2022-09-30	CDISC-5363	Add	C189510	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	HLA-DR51 Antigen Type	
2022-09-30	CDISC-5364	Add	C189511	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	HLA-DR52 Antigen Type	
2022-09-30	CDISC-5365	Add	C189512	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	HLA-DR53 Antigen Type	
2022-09-30	CDISC-5374	Add	C189513	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Prothrombin Fragment 2	
2022-09-30	CDISC-5753	Add	C189514	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Prothrombin Fragment 1	
2022-09-30	CDISC-5375	Add	C189515	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Prostaglandin D2 Receptor 2	
2022-09-30	CDISC-5376	Add	C189516	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Leukotriene C4 Synthase	
2022-09-30	CDISC-5377	Add	C189517	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Cysteinyl Leukotriene Receptor 1	
2022-09-30	CDISC-5386	Add	C189518	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Pigment Casts	
2022-09-30	CDISC-5398	Add	C189519	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Ketone Bodies Excretion Rate	
2022-09-30	CDISC-5399	Add	C189520	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Beta-Hydroxybutyrate Excretion Rate	
2022-09-30	CDISC-5400	Add	C189521	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Acetoacetic Acid Excretion Rate	
2022-09-30	CDISC-5420	Add	C189522	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Acid Sphingomyelinase	
2022-09-30	CDISC-5420	Add	C189523	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Retinol Binding Protein 4	
2022-09-30	CDISC-5753	Add	C189524	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Retinol Binding Protein 3	
2022-09-30	CDISC-5753	Add	C189525	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Retinol Binding Protein 2	
2022-09-30	CDISC-5753	Add	C189526	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Retinol Binding Protein 1	
2022-09-30	CDISC-5473	Add	C189527	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Alpha-1 Antitrypsin Z-Polymer	
2022-09-30	CDISC-5492	Add	C189528	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Glial Fibrillary Acidic Protein	
2022-09-30	CDISC-5492	Add	C189529	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Ubiquitin C-Terminal Hydrolase L1	
2022-09-30	CDISC-5753	Add	C189530	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Para Aminohippurate Clearance	
2022-09-30	CDISC-5753	Add	C189655	Term	LBTEST	Laboratory Test Name	Add new term to existing codelist	- - -	Di-Desmethylcitalopram	
2022-09-30	CDISC-5753	Add	C189315	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PAHPP	C127631 removed from codelist and replaced with C189315/Para Aminohippurate/PAHPP
2022-09-30	CDISC-5434	Add	C189346	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PYKCE	
2022-09-30	CDISC-5222	Add	C189494	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	CTLPRMD	
2022-09-30	CDISC-5288	Add	C189495	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	SMRP	
2022-09-30	CDISC-5291	Add	C189496	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	TBP	
2022-09-30	CDISC-5300	Add	C189497	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	ALPLBALP	
2022-09-30	CDISC-5300	Add	C189498	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	FIBMONO	
2022-09-30	CDISC-5300	Add	C189499	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PLSTCELY	
2022-09-30	CDISC-5300	Add	C189500	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	CTLCREAT	
2022-09-30	CDISC-5300	Add	C189501	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	BLSTNM	
2022-09-30	CDISC-5300	Add	C189502	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	GAA	
2022-09-30	CDISC-5753	Add	C189503	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	BLSTLYLY	
2022-09-30	CDISC-5332	Add	C189504	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	CTGF	
2022-09-30	CDISC-5339	Add	C189505	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	LITHIUM	
2022-09-30	CDISC-5353	Add	C189506	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	LDLT	
2022-09-30	CDISC-5354	Add	C189507	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	IDLT	
2022-09-30	CDISC-5355	Add	C189508	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	LAPOB	
2022-09-30	CDISC-5361	Add	C189509	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	NEUTMMCE	
2022-09-30	CDISC-5363	Add	C189510	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	HDR51AGT	
2022-09-30	CDISC-5364	Add	C189511	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	HDR52AGT	
2022-09-30	CDISC-5365	Add	C189512	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	HDR53AGT	
2022-09-30	CDISC-5374	Add	C189513	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PTF2	
2022-09-30	CDISC-5753	Add	C189514	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PTF1	
2022-09-30	CDISC-5375	Add	C189515	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PGD2R2	
2022-09-30	CDISC-5376	Add	C189516	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	LTC4SN	
2022-09-30	CDISC-5377	Add	C189517	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	CYSLTR1	
2022-09-30	CDISC-5386	Add	C189518	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	CSPIG	
2022-09-30	CDISC-5398	Add	C189519	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	KTBDEXR	
2022-09-30	CDISC-5399	Add	C189520	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	BHBEXR	
2022-09-30	CDISC-5400	Add	C189521	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	ACTACEXR	
2022-09-30	CDISC-5420	Add	C189522	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	ACSPGM	
2022-09-30	CDISC-5420	Add	C189523	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	RBP4	
2022-09-30	CDISC-5753	Add	C189524	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	RBP3	
2022-09-30	CDISC-5753	Add	C189525	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	RBP2	
2022-09-30	CDISC-5753	Add	C189526	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	RBP1	
2022-09-30	CDISC-5473	Add	C189527	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	AATZPL	
2022-09-30	CDISC-5492	Add	C189528	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	GFAP	
2022-09-30	CDISC-5492	Add	C189529	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	UCHL1	
2022-09-30	CDISC-5753	Add	C189530	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	PAHPPCLR	
2022-09-30	CDISC-5753	Add	C189655	Term	LBTESTCD	Laboratory Test Code	Add new term to existing codelist	- - -	CTLPRMDD	
2022-09-30	CDISC-5034	Add	C12776	Term	LOC	Anatomical Location	Add new term to existing codelist	- - -	PULMONARY VEIN	
2022-09-30	CDISC-5061	Add	C189531	Term	LOC	Anatomical Location	Add new term to existing codelist	- - -	PELVIC SIDEWALL	
2022-09-30	CDISC-5060	Add	C189532	Term	LOC	Anatomical Location	Add new term to existing codelist	- - -	SUBDURAL SPACE	
2022-09-30	CDISC-5034	Add	C26463	Term	LOC	Anatomical Location	Add new term to existing codelist	- - -	FOVEA	
2022-09-30	CDISC-5034	Add	C52809	Term	LOC	Anatomical Location	Add new term to existing codelist	- - -	TIBIAL NERVE	
2022-09-30	CDISC-5036	Add	C52814	Term	LOC	Anatomical Location	Add new term to existing codelist	- - -	PERONEAL NERVE	
2022-09-30	CDISC-5301	Add	C189316	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Herpes Virus 8	
2022-09-30	CDISC-5301	Add	C189533	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Nontuberculous Mycobacteria Nucleic Acid	
2022-09-30	CDISC-5301	Add	C189534	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Listeria monocytogenes	
2022-09-30	CDISC-5301	Add	C189535	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Chlamydophila psittaci DNA	
2022-09-30	CDISC-5301	Add	C189536	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Helicobacter pylori	
2022-09-30	CDISC-5301	Add	C189537	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Ureaplasma urealyticum	
2022-09-30	CDISC-5301	Add	C189538	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Enterococcus faecium	
2022-09-30	CDISC-5301	Add	C189539	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Fusobacterium nucleatum	
2022-09-30	CDISC-5301	Add	C189540	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Aspergillus Antigen	
2022-09-30	CDISC-5301	Add	C189541	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Candida Antigen	
2022-09-30	CDISC-5301	Add	C189542	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Giardia lamblia/Cryptosporidium Antigen	
2022-09-30	CDISC-5301	Add	C189543	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Entamoeba dispar	
2022-09-30	CDISC-5301	Add	C189544	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Entamoeba dispar DNA	
2022-09-30	CDISC-5301	Add	C189545	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Enterococcus faecalis DNA	
2022-09-30	CDISC-5038	Add	C189546	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Bacterial Lipopolysaccharide Antigen	
2022-09-30	CDISC-5356	Add	C189547	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	SARS-CoV-2 Nucleocapsid Protein Antigen	
2022-09-30	CDISC-5360	Add	C189548	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Mumps Virus RNA	
2022-09-30	CDISC-5360	Add	C189549	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Herpesvirus 7 DNA	
2022-09-30	CDISC-5369	Add	C189550	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Firmicutes/Bacteroidetes Ratio	
2022-09-30	CDISC-5421	Add	C189551	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Candida dubliniensis	
2022-09-30	CDISC-5460	Add	C189552	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Herpesvirus 8 DNA	
2022-09-30	CDISC-5461	Add	C189553	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Hepatitis B Virus	
2022-09-30	CDISC-5462	Add	C189554	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Hepatitis C Virus	
2022-09-30	CDISC-5464	Add	C189555	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Varicella Zoster Virus	
2022-09-30	CDISC-5465	Add	C189556	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 34	
2022-09-30	CDISC-5465	Add	C189557	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 40	
2022-09-30	CDISC-5465	Add	C189558	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 42	
2022-09-30	CDISC-5465	Add	C189559	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 43	
2022-09-30	CDISC-5465	Add	C189560	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 44	
2022-09-30	CDISC-5465	Add	C189561	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 53	
2022-09-30	CDISC-5465	Add	C189562	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 54	
2022-09-30	CDISC-5465	Add	C189563	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 66	
2022-09-30	CDISC-5465	Add	C189564	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 70	
2022-09-30	CDISC-5465	Add	C189565	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 74	
2022-09-30	CDISC-5465	Add	C189566	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 31	
2022-09-30	CDISC-5465	Add	C189567	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 33	
2022-09-30	CDISC-5465	Add	C189568	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 35	
2022-09-30	CDISC-5465	Add	C189569	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 39	
2022-09-30	CDISC-5465	Add	C189570	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 45	
2022-09-30	CDISC-5465	Add	C189571	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 51	
2022-09-30	CDISC-5465	Add	C189572	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 52	
2022-09-30	CDISC-5465	Add	C189573	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 56	
2022-09-30	CDISC-5465	Add	C189574	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 58	
2022-09-30	CDISC-5465	Add	C189575	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 59	
2022-09-30	CDISC-5465	Add	C189576	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 68	
2022-09-30	CDISC-5465	Add	C189577	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Human Papillomavirus Type 69	
2022-09-30	CDISC-5469	Add	C189578	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Campylobacter	
2022-09-30	CDISC-5470	Add	C189579	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Norovirus	
2022-09-30	CDISC-5505	Add	C189580	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Staphylococcus, Coagulase Positive	
2022-09-30	CDISC-5505	Add	C189581	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Staphylococcus, Coagulase Negative	
2022-09-30	CDISC-5505	Add	C189582	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Streptococcus Group A	
2022-09-30	CDISC-5505	Add	C189583	Term	MBTEST	Microbiology Test Name	Add new term to existing codelist	- - -	Streptococcus Group B	
2022-09-30	CDISC-5301	Add	C189316	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HHV8	
2022-09-30	CDISC-5301	Add	C189533	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	NTMNUAC	
2022-09-30	CDISC-5301	Add	C189534	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	LMO	
2022-09-30	CDISC-5301	Add	C189535	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	CPSDNA	
2022-09-30	CDISC-5301	Add	C189536	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPY	
2022-09-30	CDISC-5301	Add	C189537	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	UUR	
2022-09-30	CDISC-5301	Add	C189538	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	EFAM	
2022-09-30	CDISC-5301	Add	C189539	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	FNU	
2022-09-30	CDISC-5301	Add	C189540	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	ASPAG	
2022-09-30	CDISC-5301	Add	C189541	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	CANAG	
2022-09-30	CDISC-5301	Add	C189542	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	GLACRAG	
2022-09-30	CDISC-5301	Add	C189543	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	EDI	
2022-09-30	CDISC-5301	Add	C189544	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	EDIDNA	
2022-09-30	CDISC-5301	Add	C189545	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	EFADNA	
2022-09-30	CDISC-5038	Add	C189546	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	BACLPSAG	
2022-09-30	CDISC-5356	Add	C189547	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	SAR2NPAG	
2022-09-30	CDISC-5360	Add	C189548	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	MMPRNA	
2022-09-30	CDISC-5360	Add	C189549	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HHV7DNA	
2022-09-30	CDISC-5369	Add	C189550	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	FIRMBCRA	
2022-09-30	CDISC-5421	Add	C189551	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	CDU	
2022-09-30	CDISC-5460	Add	C189552	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HHV8DNA	
2022-09-30	CDISC-5461	Add	C189553	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HBV	
2022-09-30	CDISC-5462	Add	C189554	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HCV	
2022-09-30	CDISC-5464	Add	C189555	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	VZV	
2022-09-30	CDISC-5465	Add	C189556	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV34	
2022-09-30	CDISC-5465	Add	C189557	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV40	
2022-09-30	CDISC-5465	Add	C189558	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV42	
2022-09-30	CDISC-5465	Add	C189559	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV43	
2022-09-30	CDISC-5465	Add	C189560	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV44	
2022-09-30	CDISC-5465	Add	C189561	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV53	
2022-09-30	CDISC-5465	Add	C189562	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV54	
2022-09-30	CDISC-5465	Add	C189563	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV66	
2022-09-30	CDISC-5465	Add	C189564	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV70	
2022-09-30	CDISC-5465	Add	C189565	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV74	
2022-09-30	CDISC-5465	Add	C189566	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV31	
2022-09-30	CDISC-5465	Add	C189567	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV33	
2022-09-30	CDISC-5465	Add	C189568	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV35	
2022-09-30	CDISC-5465	Add	C189569	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV39	
2022-09-30	CDISC-5465	Add	C189570	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV45	
2022-09-30	CDISC-5465	Add	C189571	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV51	
2022-09-30	CDISC-5465	Add	C189572	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV52	
2022-09-30	CDISC-5465	Add	C189573	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV56	
2022-09-30	CDISC-5465	Add	C189574	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV58	
2022-09-30	CDISC-5465	Add	C189575	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV59	
2022-09-30	CDISC-5465	Add	C189576	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV68	
2022-09-30	CDISC-5465	Add	C189577	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	HPV69	
2022-09-30	CDISC-5469	Add	C189578	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	CAMPYLOB	
2022-09-30	CDISC-5470	Add	C189579	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	NOROVIRU	
2022-09-30	CDISC-5505	Add	C189580	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	STAPHCGP	
2022-09-30	CDISC-5505	Add	C189581	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	STAPHCGN	
2022-09-30	CDISC-5505	Add	C189582	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	GAS	
2022-09-30	CDISC-5505	Add	C189583	Term	MBTESTCD	Microbiology Test Code	Add new term to existing codelist	- - -	GBS	
2022-09-30	CDISC-5068	Add	C189584	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	NEUROONCOLOGIST 1	
2022-09-30	CDISC-5068	Add	C189585	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	NUCLEAR MEDICINE PHYSICIAN 1	
2022-09-30	CDISC-5080	Add	C189586	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	PHARMACOKINETICIST 1	
2022-09-30	CDISC-5753	Add	C189587	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	CERTIFIED ASSESSOR 1	
2022-09-30	CDISC-5753	Add	C189588	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	CARDIOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189589	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	CLINICAL PATHOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189590	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	DERMATOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189591	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	DEVELOPMENTAL BEHAVIORAL PEDIATRICIAN 2	
2022-09-30	CDISC-5753	Add	C189592	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	DEVELOPMENTAL PSYCHOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189593	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	ENDOCRINOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189594	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	FORENSIC PATHOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189595	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	HEMATOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189596	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	INTERNIST 2	
2022-09-30	CDISC-5753	Add	C189597	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	OPHTHALMOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189598	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	OPTOMETRIST 2	
2022-09-30	CDISC-5753	Add	C189599	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	OTOLARYNGOLOGIST 2	
2022-09-30	CDISC-5753	Add	C189600	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	PEDIATRIC NEUROLOGIST 2	
2022-09-30	CDISC-5753	Add	C189601	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	PHYSIOTHERAPIST 2	
2022-09-30	CDISC-5753	Add	C189602	Term	MEDEVAL	Medical Evaluator Identifier	Add new term to existing codelist	- - -	UROLOGIST 2	
2022-09-30	CDISC-5228	Add	C189603	Term	METHOD	Method	Add new term to existing codelist	- - -	CO-OXIMETRY	
2022-09-30	CDISC-5315	Add	C189604	Term	METHOD	Method	Add new term to existing codelist	- - -	MICROFLUIDIC ELISA	
2022-09-30	CDISC-5465	Add	C102904	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 31	
2022-09-30	CDISC-5465	Add	C102996	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 33	
2022-09-30	CDISC-5465	Add	C102997	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 35	
2022-09-30	CDISC-5465	Add	C102998	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 39	
2022-09-30	CDISC-5465	Add	C102999	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 45	
2022-09-30	CDISC-5465	Add	C103000	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 51	
2022-09-30	CDISC-5465	Add	C103001	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 52	
2022-09-30	CDISC-5465	Add	C103002	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 53	
2022-09-30	CDISC-5465	Add	C103003	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 56	
2022-09-30	CDISC-5465	Add	C103004	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 58	
2022-09-30	CDISC-5465	Add	C103005	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 59	
2022-09-30	CDISC-5465	Add	C103006	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 66	
2022-09-30	CDISC-5465	Add	C103007	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 68	
2022-09-30	CDISC-5465	Add	C156055	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 70	
2022-09-30	CDISC-5465	Add	C186749	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 34	
2022-09-30	CDISC-5465	Add	C186750	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 40	
2022-09-30	CDISC-5465	Add	C186751	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 42	
2022-09-30	CDISC-5465	Add	C186752	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 43	
2022-09-30	CDISC-5465	Add	C186753	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 44	
2022-09-30	CDISC-5465	Add	C186754	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 54	
2022-09-30	CDISC-5465	Add	C186755	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 69	
2022-09-30	CDISC-5465	Add	C186780	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN PAPILLOMAVIRUS TYPE 74	
2022-09-30	CDISC-5319	Add	C189605	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN IMMUNODEFICIENCY VIRUS 1 SUBTYPE A	
2022-09-30	CDISC-5319	Add	C189606	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN IMMUNODEFICIENCY VIRUS 1 SUBTYPE B	
2022-09-30	CDISC-5319	Add	C189607	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN IMMUNODEFICIENCY VIRUS 1 SUBTYPE C	
2022-09-30	CDISC-5319	Add	C189608	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN IMMUNODEFICIENCY VIRUS 1 SUBTYPE D	
2022-09-30	CDISC-5319	Add	C189609	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN IMMUNODEFICIENCY VIRUS 1 SUBTYPE F	
2022-09-30	CDISC-5319	Add	C189610	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	HUMAN IMMUNODEFICIENCY VIRUS 1 SUBTYPE G	
2022-09-30	CDISC-5405	Add	C189611	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	LACTICASEIBACILLUS PARACASEI SUBSP. PARACASEI	
2022-09-30	CDISC-5301	Add	C189612	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	NEISSERIA MENINGITIDIS SEROGROUP B	
2022-09-30	CDISC-5520	Add	C189613	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	STENOTROPHOMONAS ACIDAMINIPHILA	
2022-09-30	CDISC-5505	Add	C189614	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	BETA STREPTOCOCCUS, GROUP A	
2022-09-30	CDISC-5505	Add	C189615	Term	MICROORG	Microorganism	Add new term to existing codelist	- - -	BETA STREPTOCOCCUS, GROUP B	
2022-09-30	CDISC-5311	Add	C189616	Term	MIFTSDTL	Microscopic Findings Test Details	Add new term to existing codelist	- - -	WHO CLASSIFICATION OF TUMORS OF THE DIGESTIVE SYSTEM 2010	
2022-09-30	CDISC-5311	Add	C189617	Term	MIFTSDTL	Microscopic Findings Test Details	Add new term to existing codelist	- - -	WHO CLASSIFICATION OF TUMORS OF ENDOCRINE ORGANS 2017	
2022-09-30	CDISC-5311	Add	C189618	Term	MIFTSDTL	Microscopic Findings Test Details	Add new term to existing codelist	- - -	WHO CLASSIFICATION OF TUMORS OF THE DIGESTIVE SYSTEM 2019	
2022-09-30	CDISC-5311	Add	C189619	Term	MIFTSDTL	Microscopic Findings Test Details	Add new term to existing codelist	- - -	IARC AND WHO CLASSIFICATION OF NEUROENDOCRINE NEOPLASMS 2018	
2022-09-30	CDISC-5753	Add	C189346	Term	MITS	SDTM Microscopic Findings Test Name	Add new term to existing codelist	- - -	Pyknotic Cells	
2022-09-30	CDISC-5412	Add	C189620	Term	MITS	SDTM Microscopic Findings Test Name	Add new term to existing codelist	- - -	Number of Lymph Nodes Involved	
2022-09-30	CDISC-5495	Add	C189621	Term	MITS	SDTM Microscopic Findings Test Name	Add new term to existing codelist	- - -	Goblet Cells	
2022-09-30	CDISC-5496	Add	C189622	Term	MITS	SDTM Microscopic Findings Test Name	Add new term to existing codelist	- - -	Goblet Cells/Epithelial Cells	
2022-09-30	CDISC-5753	Add	C189346	Term	MITSCD	SDTM Microscopic Findings Test Code	Add new term to existing codelist	- - -	PYKCE	
2022-09-30	CDISC-5412	Add	C189620	Term	MITSCD	SDTM Microscopic Findings Test Code	Add new term to existing codelist	- - -	LNINNUM	
2022-09-30	CDISC-5495	Add	C189621	Term	MITSCD	SDTM Microscopic Findings Test Code	Add new term to existing codelist	- - -	GOBCE	
2022-09-30	CDISC-5496	Add	C189622	Term	MITSCD	SDTM Microscopic Findings Test Code	Add new term to existing codelist	- - -	GOBCEPIC	
2022-09-30	CDISC-5007	Add	C189623	Term	OETEST	Ophthalmic Exam Test Name	Add new term to existing codelist	- - -	Opacity	
2022-09-30	CDISC-5008	Add	C189624	Term	OETEST	Ophthalmic Exam Test Name	Add new term to existing codelist	- - -	Margin Reflex Distance 1	
2022-09-30	CDISC-5009	Add	C189625	Term	OETEST	Ophthalmic Exam Test Name	Add new term to existing codelist	- - -	Margin Reflex Distance 2	
2022-09-30	CDISC-5010	Add	C189626	Term	OETEST	Ophthalmic Exam Test Name	Add new term to existing codelist	- - -	Margin Limbal Distance	
2022-09-30	CDISC-5007	Add	C189623	Term	OETESTCD	Ophthalmic Exam Test Code	Add new term to existing codelist	- - -	OPACITY	
2022-09-30	CDISC-5008	Add	C189624	Term	OETESTCD	Ophthalmic Exam Test Code	Add new term to existing codelist	- - -	MRD1	
2022-09-30	CDISC-5009	Add	C189625	Term	OETESTCD	Ophthalmic Exam Test Code	Add new term to existing codelist	- - -	MRD2	
2022-09-30	CDISC-5010	Add	C189626	Term	OETESTCD	Ophthalmic Exam Test Code	Add new term to existing codelist	- - -	MLD	
2022-09-30	N/A	Add	C124039	Term	PROCEDUR	Procedure	Add new term to existing codelist	- - -	BILEVEL POSITIVE AIRWAY PRESSURE VENTILATION	C171500 being merged into C124039
2022-09-30	CDISC-4597; CDISC-4621; CDISC-4923; CDISC-4938	Add	C17649	Term	RACE	Race	Add new term to existing codelist	- - -	OTHER	
2022-09-30	CDISC-5753	Add	C17649	Term	RACEC	Race As Collected	Add new term to existing codelist	- - -	OTHER	
2022-09-30	CDISC-5753	Add	C43853	Term	RACEC	Race As Collected	Add new term to existing codelist	- - -	ENGLISH	
2022-09-30	CDISC-5753	Add	C43856	Term	RACEC	Race As Collected	Add new term to existing codelist	- - -	IRISH	
2022-09-30	CDISC-5327	Add	C189627	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	MASS DECIMAL FRACTION	
2022-09-30	CDISC-5327	Add	C189628	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	CATALYTIC DECIMAL FRACTION	
2022-09-30	CDISC-5327	Add	C189629	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	VOLUME DECIMAL FRACTION	
2022-09-30	CDISC-5327	Add	C189630	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	SATURATION FRACTION	
2022-09-30	CDISC-5327	Add	C189631	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	QUINTILE	
2022-09-30	CDISC-5327	Add	C48919	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	PERCENTILE	
2022-09-30	CDISC-5327	Add	C68741	Term	RESTYPRS	Result Type Response	Add new term to existing codelist	- - -	Z SCORE	
2022-09-30	CDISC-5244	Add	C189632	Term	RETEST	Respiratory Test Name	Add new term to existing codelist	- - -	Dominant Lung Pattern	
2022-09-30	CDISC-5244	Add	C189633	Term	RETEST	Respiratory Test Name	Add new term to existing codelist	- - -	Dominant Lung Pattern Distribution	
2022-09-30	CDISC-5244	Add	C189634	Term	RETEST	Respiratory Test Name	Add new term to existing codelist	- - -	Additional Disease-Related Findings	
2022-09-30	CDISC-5474; CDISC-5326	Add	C189635	Term	RETEST	Respiratory Test Name	Add new term to existing codelist	- - -	Oxygenation Index	
2022-09-30	CDISC-5244	Add	C189632	Term	RETESTCD	Respiratory Test Code	Add new term to existing codelist	- - -	DOMLGPT	
2022-09-30	CDISC-5244	Add	C189633	Term	RETESTCD	Respiratory Test Code	Add new term to existing codelist	- - -	DOMLGPTD	
2022-09-30	CDISC-5244	Add	C189634	Term	RETESTCD	Respiratory Test Code	Add new term to existing codelist	- - -	ADDRELF	
2022-09-30	CDISC-5474; CDISC-5326	Add	C189635	Term	RETESTCD	Respiratory Test Code	Add new term to existing codelist	- - -	OI	
2022-09-30	CDISC-5011	Add	C189352	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Bleed/Spot Between Menstrual Periods Ind	
2022-09-30	CDISC-5011	Add	C189353	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Irregular Menstrual Periods Indicator	
2022-09-30	CDISC-5011	Add	C189354	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Average Menstrual Cycle Duration	
2022-09-30	CDISC-5011	Add	C189355	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Surgically Sterile Indicator	
2022-09-30	CDISC-5011	Add	C189356	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Infertility Indicator	
2022-09-30	CDISC-5011	Add	C189357	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Duration of Sexual Abstinence	
2022-09-30	CDISC-5011	Add	C189358	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Number of Cesarean Sections	
2022-09-30	CDISC-5011	Add	C189359	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Number of Vaginal Deliveries	
2022-09-30	CDISC-5011	Add	C189360	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Subj Currently Breastfeeding a Child Ind	
2022-09-30	CDISC-5072	Add	C189361	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Thelarche Age	
2022-09-30	CDISC-5072	Add	C189362	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Adrenarche Age	
2022-09-30	CDISC-5121	Add	C189363	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Breastfeeding Start Date	
2022-09-30	CDISC-5122; CDISC-5225	Add	C189364	Term	RPTEST	Reproductive System Findings Test Name	Add new term to existing codelist	- - -	Breastfeeding End Date	
2022-09-30	CDISC-5011	Add	C189352	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	BSBMPIND	
2022-09-30	CDISC-5011	Add	C189353	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	IRRMPIND	
2022-09-30	CDISC-5011	Add	C189354	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	MENSDURA	
2022-09-30	CDISC-5011	Add	C189355	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	SRGSTIND	
2022-09-30	CDISC-5011	Add	C189356	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	INFRTIND	
2022-09-30	CDISC-5011	Add	C189357	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	SEXABDUR	
2022-09-30	CDISC-5011	Add	C189358	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	CSRSCTN	
2022-09-30	CDISC-5011	Add	C189359	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	VAGDLVN	
2022-09-30	CDISC-5011	Add	C189360	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	SCBFCIND	
2022-09-30	CDISC-5072	Add	C189361	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	THLARAGE	
2022-09-30	CDISC-5072	Add	C189362	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	ADRNRAGE	
2022-09-30	CDISC-5121	Add	C189363	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	BRFSTDTC	
2022-09-30	CDISC-5122; CDISC-5225	Add	C189364	Term	RPTESTCD	Reproductive System Findings Test Code	Add new term to existing codelist	- - -	BRFENDTC	
2022-09-30	CDISC-5753	Add	C189266	CDISC Codelist	SDTMDVRS	SDTMIG Medical Device Version Response	Addition of new codelist	- - -	SDTMDVRS	
2022-09-30	CDISC-5753	Add	C189636	Term	SDTMDVRS	SDTMIG Medical Device Version Response	Add new term to new codelist	- - -	1	
2022-09-30	CDISC-5753	Add	C189637	Term	SDTMDVRS	SDTMIG Medical Device Version Response	Add new term to new codelist	- - -	1.1	
2022-09-30	CDISC-5753	Add	C189638	Term	SDTMIGRS	SDTMIG Version Response	Add new term to existing codelist	- - -	3.4	
2022-09-30	CDISC-5753	Add	C189639	Term	SDTMVRS	SDTM Version Response	Add new term to existing codelist	- - -	2	
2022-09-30	CDISC-5352	Add	C189640	Term	SPECTYPE	Specimen Type	Add new term to existing codelist	- - -	SUPERNATANT, LAVAGE FLUID	
2022-09-30	CDISC-5513	Add	C189641	Term	SPECTYPE	Specimen Type	Add new term to existing codelist	- - -	CORD PLASMA	
2022-09-30	CDISC-5059	Add	C189317	Term	TSPARM	Trial Summary Parameter Test Name	Add new term to existing codelist	- - -	SDTMIG Medical Device Version	
2022-09-30	CDISC-5059	Add	C189317	Term	TSPARMCD	Trial Summary Parameter Test Code	Add new term to existing codelist	- - -	SDTMDVER	
2022-09-30	CDISC-5234	Add	C158699	Term	UNIT	Unit	Add new term to existing codelist	- - -	/10 HPFs	
2022-09-30	CDISC-5154	Add	C189642	Term	UNIT	Unit	Add new term to existing codelist	- - -	ARMOUR UNIT	
2022-09-30	CDISC-5216	Add	C189643	Term	UNIT	Unit	Add new term to existing codelist	- - -	mkat/L	
2022-09-30	CDISC-5217; CDISC-5246	Add	C189644	Term	UNIT	Unit	Add new term to existing codelist	- - -	mmol/L/h	
2022-09-30	CDISC-5217; CDISC-5304	Add	C189645	Term	UNIT	Unit	Add new term to existing codelist	- - -	nmol/L/s	
2022-09-30	CDISC-5234	Add	C189646	Term	UNIT	Unit	Add new term to existing codelist	- - -	/2 mm2	
2022-09-30	CDISC-5235	Add	C189647	Term	UNIT	Unit	Add new term to existing codelist	- - -	Binding Ab Unit/mL	
2022-09-30	CDISC-5246	Add	C189648	Term	UNIT	Unit	Add new term to existing codelist	- - -	mmol/L/day	
2022-09-30	CDISC-5322	Add	C189649	Term	UNIT	Unit	Add new term to existing codelist	- - -	mm2/us	
2022-09-30	CDISC-5406	Add	C189650	Term	UNIT	Unit	Add new term to existing codelist	- - -	FFU/mL	
2022-09-30	CDISC-5419	Add	C189651	Term	UNIT	Unit	Add new term to existing codelist	- - -	ukat/g Hb	
2022-09-30	CDISC-5246	Add	C66970	Term	UNIT	Unit	Add new term to existing codelist	- - -	U/h	
2022-09-30	CDISC-5246	Add	C85720	Term	UNIT	Unit	Add new term to existing codelist	- - -	mmol/h	
2022-09-30	CDISC-5753	Add	C139219	Term	VSTEST	Vital Signs Test Name	Add new term to existing codelist	- - -	Lean Body Mass to Total Body Mass Ratio	C139219 removed from MUSCTS-CD codelist and added into VSTEST-CD codelist.
2022-09-30	CDISC-5753	Add	C139219	Term	VSTESTCD	Vital Signs Test Code	Add new term to existing codelist	- - -	LBMTBMR	C139219 removed from MUSCTS-CD codelist and added into VSTEST-CD codelist.
2022-09-30	CDISC-5753	Remove	C127771	Term	BSTEST	Biospecimen Characteristics Test Name	Remove term entirely from codelist	Tumor Cells/Total Cells	- - -	C127771 being merged into C123556.
2022-09-30	CDISC-5753	Remove	C127771	Term	BSTESTCD	Biospecimen Characteristics Test Code	Remove term entirely from codelist	TUMCECE	- - -	C127771 being merged into C123556.
2022-09-30	CDISC-5753	Remove	C111282	Term	DOMAIN	SDTM Domain Abbreviation	Remove term entirely from codelist	AX	- - -	This is an ADaM dataset naming convention, not an SDTM domain. This convention in described in both the SDTMIG and ADaMIG and therefore is unnecessary to include in this codelist.
2022-09-30	CDISC-5753	Remove	C49563	Term	DOMAIN	SDTM Domain Abbreviation	Remove term entirely from codelist	AD	- - -	This is an ADaM dataset naming convention, not an SDTM domain. This convention in described in both the SDTMIG and ADaMIG and therefore is unnecessary to include in this codelist.
2022-09-30	CDISC-5753	Remove	C127631	Term	LBTEST	Laboratory Test Name	Remove term entirely from codelist	P-Aminohippurate Sodium	- - -	C127631 removed from codelist and replaced with C189315/Para Aminohippurate/PAHPP
2022-09-30	CDISC-5753	Remove	C181138	Term	LBTEST	Laboratory Test Name	Remove term entirely from codelist	Soluble CD40	- - -	C181138 removed from codelist and merged into C174312, which is already in the codelist..
2022-09-30	CDISC-5753	Remove	C181139	Term	LBTEST	Laboratory Test Name	Remove term entirely from codelist	Soluble CD40 Ligand	- - -	C181139 removed from codelist and merged into C174308, which is already in the codelist..
2022-09-30	CDISC-5753	Remove	C127631	Term	LBTESTCD	Laboratory Test Code	Remove term entirely from codelist	PAH	- - -	C127631 removed from codelist and replaced with C189315/Para Aminohippurate/PAHPP
2022-09-30	CDISC-5753	Remove	C181138	Term	LBTESTCD	Laboratory Test Code	Remove term entirely from codelist	CD40S	- - -	C181138 removed from codelist and merged into C174312, which is already in the codelist..
2022-09-30	CDISC-5753	Remove	C181139	Term	LBTESTCD	Laboratory Test Code	Remove term entirely from codelist	CD40LS	- - -	C181139 removed from codelist and merged into C174308, which is already in the codelist..
2022-09-30	CDISC-5753	Remove	C125951	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	CARDIOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C132303	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	MICROSCOPIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C132304	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	RATER	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C132424	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	OPTOMETRIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C142332	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	CLINICAL PATHOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C142333	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	FORENSIC PATHOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C147461	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	DEVELOPMENTAL BEHAVIORAL PEDIATRICIAN	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C147462	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	DEVELOPMENTAL PSYCHOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C147463	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	PEDIATRIC NEUROLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17721	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	NEUROLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17723	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	PATHOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17816	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	DERMATOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17817	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	ENDOCRINOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17821	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	ONCOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17822	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	OPHTHALMOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17823	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	OTOLARYNGOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17824	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	RADIOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17826	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	UROLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17831	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	HEMATOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C17832	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	INTERNIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C28747	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	READER	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C53422	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	PHYSIOTHERAPIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C93058	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	NEURORADIOLOGIST	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C96561	Term	MEDEVAL	Medical Evaluator	Remove term entirely from codelist	ADJUDICATOR	- - -	Remove from codelist. Please use the new terms in the EVAL codelist (and EVAL variable) if there is only one assessor, and the numbered terms in the MEDEVAL codelist (and the EVALID variable) if more than one assessor.
2022-09-30	CDISC-5753	Remove	C127771	Term	MITS	SDTM Microscopic Findings Test Name	Remove term entirely from codelist	Tumor Cells/Total Cells	- - -	C127771 being merged into C123556.
2022-09-30	CDISC-5753	Remove	C127771	Term	MITSCD	SDTM Microscopic Findings Test Code	Remove term entirely from codelist	TUMCECE	- - -	C127771 being merged into C123556.
2022-09-30	CDISC-5753	Remove	C139219	Term	MUSCTS	Musculoskeletal System Finding Test Name	Remove term entirely from codelist	Lean Body Mass to Total Body Mass Ratio	- - -	C139219 removed from MUSCTS-CD codelist and added into VSTEST-CD codelist.
2022-09-30	CDISC-5753	Remove	C139219	Term	MUSCTSCD	Musculoskeletal System Finding Test Code	Remove term entirely from codelist	LBMTBMR	- - -	C139219 removed from MUSCTS-CD codelist and added into VSTEST-CD codelist.
2022-09-30	N/A	Remove	C171500	Term	PROCEDUR	Procedure	Remove term entirely from codelist	BILEVEL POSITIVE AIRWAY PRESSURE VENTILATION	- - -	C171500 being merged into C124039
2022-09-30	CDISC-5205	Remove	C74580	Term	SCTEST	Subject Characteristic Test Name	Remove term entirely from codelist	Skin Type	- - -	C74580 removed from SCTEST-CD codelist and added into INTEGU-CD codelist.
2022-09-30	CDISC-5205	Remove	C74580	Term	SCTESTCD	Subject Characteristic Test Code	Remove term entirely from codelist	SKINTYP	- - -	C74580 removed from SCTEST-CD codelist and added into INTEGU-CD codelist.
2022-09-30	CDISC-5706	Update	C100134	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100134	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	The Brief Psychiatric Rating Scale-A test code.	The Brief Psychiatric Rating Scale-Anchored test code.	
2022-09-30	CDISC-5706	Update	C100134	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	CDISC Clinical Classification BPRS-A Test Code Terminology	CDISC Clinical Classification BPRS-Anchored Test Code Terminology	
2022-09-30	CDISC-5706	Update	C100134	CDISC Synonym	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Add new CDISC Synonym	- - -	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100134	CDISC Synonym	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Remove CDISC Synonym	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	- - -	
2022-09-30	CDISC-5706	Update	C100372	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100372	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Somatic Concern.	Brief Psychiatric Rating Scale-Anchored - Somatic Concern.	
2022-09-30	CDISC-5706	Update	C100372	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Somatic Concern	BPRS-Anchored - Somatic Concern	
2022-09-30	CDISC-5706	Update	C100373	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100373	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Anxiety.	Brief Psychiatric Rating Scale-Anchored - Anxiety.	
2022-09-30	CDISC-5706	Update	C100373	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Anxiety	BPRS-Anchored - Anxiety	
2022-09-30	CDISC-5706	Update	C100374	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100374	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Emotional Withdrawal.	Brief Psychiatric Rating Scale-Anchored - Emotional Withdrawal.	
2022-09-30	CDISC-5706	Update	C100374	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Emotional Withdrawal	BPRS-Anchored - Emotional Withdrawal	
2022-09-30	CDISC-5706	Update	C100375	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100375	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Conceptual Disorganization.	Brief Psychiatric Rating Scale-Anchored - Conceptual Disorganization.	
2022-09-30	CDISC-5706	Update	C100375	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Conceptual Disorganization	BPRS-Anchored - Conceptual Disorganization	
2022-09-30	CDISC-5706	Update	C100376	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100376	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Guilt Feelings.	Brief Psychiatric Rating Scale-Anchored - Guilt Feelings.	
2022-09-30	CDISC-5706	Update	C100376	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Guilt Feelings	BPRS-Anchored - Guilt Feelings	
2022-09-30	CDISC-5706	Update	C100377	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100377	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Tension.	Brief Psychiatric Rating Scale-Anchored - Tension.	
2022-09-30	CDISC-5706	Update	C100377	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Tension	BPRS-Anchored - Tension	
2022-09-30	CDISC-5706	Update	C100378	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100378	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Mannerisms and Posturing.	Brief Psychiatric Rating Scale-Anchored - Mannerisms and Posturing.	
2022-09-30	CDISC-5706	Update	C100378	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Mannerisms and Posturing	BPRS-Anchored - Mannerisms and Posturing	
2022-09-30	CDISC-5706	Update	C100379	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100379	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Grandiosity.	Brief Psychiatric Rating Scale-Anchored - Grandiosity.	
2022-09-30	CDISC-5706	Update	C100379	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Grandiosity	BPRS-Anchored - Grandiosity	
2022-09-30	CDISC-5706	Update	C100380	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100380	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Depressive Mood.	Brief Psychiatric Rating Scale-Anchored - Depressive Mood.	
2022-09-30	CDISC-5706	Update	C100380	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Depressive Mood	BPRS-Anchored - Depressive Mood	
2022-09-30	CDISC-5706	Update	C100381	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100381	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Hostility.	Brief Psychiatric Rating Scale-Anchored - Hostility.	
2022-09-30	CDISC-5706	Update	C100381	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Hostility	BPRS-Anchored - Hostility	
2022-09-30	CDISC-5706	Update	C100382	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100382	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Suspiciousness.	Brief Psychiatric Rating Scale-Anchored - Suspiciousness.	
2022-09-30	CDISC-5706	Update	C100382	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Suspiciousness	BPRS-Anchored - Suspiciousness	
2022-09-30	CDISC-5706	Update	C100383	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100383	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Hallucinatory Behavior.	Brief Psychiatric Rating Scale-Anchored - Hallucinatory Behavior.	
2022-09-30	CDISC-5706	Update	C100383	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Hallucinatory Behavior	BPRS-Anchored - Hallucinatory Behavior	
2022-09-30	CDISC-5706	Update	C100384	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100384	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Motor Retardation.	Brief Psychiatric Rating Scale-Anchored - Motor Retardation.	
2022-09-30	CDISC-5706	Update	C100384	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Motor Retardation	BPRS-Anchored - Motor Retardation	
2022-09-30	CDISC-5706	Update	C100385	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100385	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Uncooperativeness.	Brief Psychiatric Rating Scale-Anchored - Uncooperativeness.	
2022-09-30	CDISC-5706	Update	C100385	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Uncooperativeness	BPRS-Anchored - Uncooperativeness	
2022-09-30	CDISC-5706	Update	C100386	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100386	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Unusual Thought Content.	Brief Psychiatric Rating Scale-Anchored - Unusual Thought Content.	
2022-09-30	CDISC-5706	Update	C100386	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Unusual Thought Content	BPRS-Anchored - Unusual Thought Content	
2022-09-30	CDISC-5706	Update	C100387	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100387	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Blunted Affect.	Brief Psychiatric Rating Scale-Anchored - Blunted Affect.	
2022-09-30	CDISC-5706	Update	C100387	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Blunted Affect	BPRS-Anchored - Blunted Affect	
2022-09-30	CDISC-5706	Update	C100388	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100388	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Excitement.	Brief Psychiatric Rating Scale-Anchored - Excitement.	
2022-09-30	CDISC-5706	Update	C100388	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Excitement	BPRS-Anchored - Excitement	
2022-09-30	CDISC-5706	Update	C100389	CDISC Codelist Name	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Code	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	
2022-09-30	CDISC-5706	Update	C100389	CDISC Definition	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Disorientation.	Brief Psychiatric Rating Scale-Anchored - Disorientation.	
2022-09-30	CDISC-5706	Update	C100389	NCI Preferred Term	BPRSA1TC	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Code	Update NCI Preferred Term	BPRS-A - Disorientation	BPRS-Anchored - Disorientation	
2022-09-30	CDISC-5706	Update	C100133	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100133	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	The Brief Psychiatric Rating Scale-A test name.	The Brief Psychiatric Rating Scale-Anchored test name.	
2022-09-30	CDISC-5706	Update	C100133	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	CDISC Clinical Classification BPRS-A Test Name Terminology	CDISC Clinical Classification BPRS-Anchored Test Name Terminology	
2022-09-30	CDISC-5706	Update	C100133	CDISC Synonym	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Add new CDISC Synonym	- - -	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100133	CDISC Synonym	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Remove CDISC Synonym	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	- - -	
2022-09-30	CDISC-5706	Update	C100372	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100372	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Somatic Concern.	Brief Psychiatric Rating Scale-Anchored - Somatic Concern.	
2022-09-30	CDISC-5706	Update	C100372	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Somatic Concern	BPRS-Anchored - Somatic Concern	
2022-09-30	CDISC-5706	Update	C100373	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100373	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Anxiety.	Brief Psychiatric Rating Scale-Anchored - Anxiety.	
2022-09-30	CDISC-5706	Update	C100373	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Anxiety	BPRS-Anchored - Anxiety	
2022-09-30	CDISC-5706	Update	C100374	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100374	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Emotional Withdrawal.	Brief Psychiatric Rating Scale-Anchored - Emotional Withdrawal.	
2022-09-30	CDISC-5706	Update	C100374	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Emotional Withdrawal	BPRS-Anchored - Emotional Withdrawal	
2022-09-30	CDISC-5706	Update	C100375	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100375	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Conceptual Disorganization.	Brief Psychiatric Rating Scale-Anchored - Conceptual Disorganization.	
2022-09-30	CDISC-5706	Update	C100375	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Conceptual Disorganization	BPRS-Anchored - Conceptual Disorganization	
2022-09-30	CDISC-5706	Update	C100376	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100376	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Guilt Feelings.	Brief Psychiatric Rating Scale-Anchored - Guilt Feelings.	
2022-09-30	CDISC-5706	Update	C100376	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Guilt Feelings	BPRS-Anchored - Guilt Feelings	
2022-09-30	CDISC-5706	Update	C100377	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100377	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Tension.	Brief Psychiatric Rating Scale-Anchored - Tension.	
2022-09-30	CDISC-5706	Update	C100377	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Tension	BPRS-Anchored - Tension	
2022-09-30	CDISC-5706	Update	C100378	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100378	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Mannerisms and Posturing.	Brief Psychiatric Rating Scale-Anchored - Mannerisms and Posturing.	
2022-09-30	CDISC-5706	Update	C100378	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Mannerisms and Posturing	BPRS-Anchored - Mannerisms and Posturing	
2022-09-30	CDISC-5706	Update	C100379	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100379	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Grandiosity.	Brief Psychiatric Rating Scale-Anchored - Grandiosity.	
2022-09-30	CDISC-5706	Update	C100379	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Grandiosity	BPRS-Anchored - Grandiosity	
2022-09-30	CDISC-5706	Update	C100380	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100380	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Depressive Mood.	Brief Psychiatric Rating Scale-Anchored - Depressive Mood.	
2022-09-30	CDISC-5706	Update	C100380	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Depressive Mood	BPRS-Anchored - Depressive Mood	
2022-09-30	CDISC-5706	Update	C100381	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100381	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Hostility.	Brief Psychiatric Rating Scale-Anchored - Hostility.	
2022-09-30	CDISC-5706	Update	C100381	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Hostility	BPRS-Anchored - Hostility	
2022-09-30	CDISC-5706	Update	C100382	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100382	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Suspiciousness.	Brief Psychiatric Rating Scale-Anchored - Suspiciousness.	
2022-09-30	CDISC-5706	Update	C100382	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Suspiciousness	BPRS-Anchored - Suspiciousness	
2022-09-30	CDISC-5706	Update	C100383	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100383	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Hallucinatory Behavior.	Brief Psychiatric Rating Scale-Anchored - Hallucinatory Behavior.	
2022-09-30	CDISC-5706	Update	C100383	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Hallucinatory Behavior	BPRS-Anchored - Hallucinatory Behavior	
2022-09-30	CDISC-5706	Update	C100384	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100384	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Motor Retardation.	Brief Psychiatric Rating Scale-Anchored - Motor Retardation.	
2022-09-30	CDISC-5706	Update	C100384	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Motor Retardation	BPRS-Anchored - Motor Retardation	
2022-09-30	CDISC-5706	Update	C100385	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100385	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Uncooperativeness.	Brief Psychiatric Rating Scale-Anchored - Uncooperativeness.	
2022-09-30	CDISC-5706	Update	C100385	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Uncooperativeness	BPRS-Anchored - Uncooperativeness	
2022-09-30	CDISC-5706	Update	C100386	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100386	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Unusual Thought Content.	Brief Psychiatric Rating Scale-Anchored - Unusual Thought Content.	
2022-09-30	CDISC-5706	Update	C100386	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Unusual Thought Content	BPRS-Anchored - Unusual Thought Content	
2022-09-30	CDISC-5706	Update	C100387	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100387	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Blunted Affect.	Brief Psychiatric Rating Scale-Anchored - Blunted Affect.	
2022-09-30	CDISC-5706	Update	C100387	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Blunted Affect	BPRS-Anchored - Blunted Affect	
2022-09-30	CDISC-5706	Update	C100388	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100388	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Excitement.	Brief Psychiatric Rating Scale-Anchored - Excitement.	
2022-09-30	CDISC-5706	Update	C100388	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Excitement	BPRS-Anchored - Excitement	
2022-09-30	CDISC-5706	Update	C100389	CDISC Codelist Name	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Codelist Name	Brief Psychiatric Rating Scale-A Clinical Classification Test Name	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	
2022-09-30	CDISC-5706	Update	C100389	CDISC Definition	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update CDISC Definition	Brief Psychiatric Rating Scale-A - Disorientation.	Brief Psychiatric Rating Scale-Anchored - Disorientation.	
2022-09-30	CDISC-5706	Update	C100389	NCI Preferred Term	BPRSA1TN	Brief Psychiatric Rating Scale-Anchored Clinical Classification Test Name	Update NCI Preferred Term	BPRS-A - Disorientation	BPRS-Anchored - Disorientation	
2022-09-30	N/A	Update	C95802	NCI Preferred Term	CVFARS	Cardiovascular Findings About Results	Update NCI Preferred Term	Ischemic Cerebrovascular Accident	Ischemic Stroke	
2022-09-30	N/A	Update	C95803	NCI Preferred Term	CVFARS	Cardiovascular Findings About Results	Update NCI Preferred Term	Hemorrhagic Cerebrovascular Accident	Hemorrhagic Stroke	
2022-09-30	CDISC-5753	Update	C181357	CDISC Submission Value	ISBDAGT	Binding Agent for Immunogenicity Tests	Update CDISC Submission Value	ANIMAL MIX ANTIGENS, MULTIPLE	ANIMAL MIX ANTIGENS	
2022-09-30	CDISC-5753	Update	C181357	CDISC Definition	ISBDAGT	Binding Agent for Immunogenicity Tests	Update CDISC Definition	A mixture of allergens obtained from animals.	Antigen(s) from a mix of animals that are considered as animal allergen(s).	
2022-09-30	CDISC-5753	Update	C181358	CDISC Definition	ISBDAGT	Binding Agent for Immunogenicity Tests	Update CDISC Definition	An animal allergen in the form of dander (skin flakes) produced by the species Canis lupus familiaris (dog).	Antigen(s) in the dander (skin flakes) of the species Canis lupus familiaris (dog) that are considered as animal allergen(s).	
2022-09-30	CDISC-5753	Update	C181359	CDISC Definition	ISBDAGT	Binding Agent for Immunogenicity Tests	Update CDISC Definition	An animal allergen in the form of dander (skin flakes) produced by the species Felis catus (domestic cat).	Antigen(s) in the dander (skin flakes) of the species Felis catus (domestic cat) that are considered as animal allergen(s).	
2022-09-30	CDISC-5753	Update	C181360	CDISC Definition	ISBDAGT	Binding Agent for Immunogenicity Tests	Update CDISC Definition	An animal allergen in the form of dander (skin flakes) produced by the species Equus caballus (domestic horse).	Antigen(s) in the dander (skin flakes) of the species Equus caballus (domestic horse) that are considered as animal allergen(s).	
2022-09-30	CDISC-5753	Update	C181361	CDISC Definition	ISBDAGT	Binding Agent for Immunogenicity Tests	Update CDISC Definition	An animal allergen in the form of dander (skin flakes) produced by the species Bos taurus (cow).	Antigen(s) in the dander (skin flakes) of the species Bos taurus (cow) that are considered as animal allergen(s).	
2022-09-30	CDISC-5613	Update	C182477	CDISC Codelist Name	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update CDISC Codelist Name	Kurtzke Functional System Scores Clinical Classification ORRES for KFSS102A and KFSS106A TN/TC	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182477	CDISC Submission Value	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update CDISC Submission Value	KFSS102A_6AOR	KFSS1SET1OR	
2022-09-30	CDISC-5613	Update	C182477	NCI Preferred Term	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update NCI Preferred Term	CDISC Clinical Classification Kurtzke Functional System Scores KFSS102A and KFSS106A Original Response Terminology	CDISC Clinical Classification Kurtzke Functional System Scores KFSS1SET1 Original Response Terminology	
2022-09-30	CDISC-5613	Update	C182477	CDISC Synonym	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Add new CDISC Synonym	- - -	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182477	CDISC Synonym	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Remove CDISC Synonym	Kurtzke Functional System Scores Clinical Classification ORRES for KFSS102A and KFSS106A TN/TC	- - -	
2022-09-30	CDISC-5613	Update	C182796	CDISC Codelist Name	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update CDISC Codelist Name	Kurtzke Functional System Scores Clinical Classification ORRES for KFSS102A and KFSS106A TN/TC	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182796	NCI Preferred Term	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update NCI Preferred Term	Kurtzke Functional System Scores KFSS102 and KFSS106A Original Result - CHECKED	Kurtzke Functional System Scores KFSS1SET1 Original Result - Checked	
2022-09-30	CDISC-5613	Update	C182796	CDISC Synonym	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Add new CDISC Synonym	- - -	KFSS1SET1-CHECKED	
2022-09-30	CDISC-5613	Update	C182796	CDISC Synonym	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Remove CDISC Synonym	KFSS102 and KFSS106A-CHECKED	- - -	
2022-09-30	CDISC-5613	Update	C182797	CDISC Codelist Name	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update CDISC Codelist Name	Kurtzke Functional System Scores Clinical Classification ORRES for KFSS102A and KFSS106A TN/TC	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182797	NCI Preferred Term	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Update NCI Preferred Term	Kurtzke Functional System Scores KFSS102 and KFSS106A Original Result - NOT CHECKED	Kurtzke Functional System Scores KFSS1SET1 Original Result - Not Checked	
2022-09-30	CDISC-5613	Update	C182797	CDISC Synonym	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Add new CDISC Synonym	- - -	KFSS1SET1-NOT CHECKED	
2022-09-30	CDISC-5613	Update	C182797	CDISC Synonym	KFSS1SET1OR	Kurtzke Functional System Scores Clinical Classification ORRES the Same as KFSS102A TN/TC	Remove CDISC Synonym	KFSS102 and KFSS106A-NOT CHECKED	- - -	
2022-09-30	CDISC-5613	Update	C182515	CDISC Codelist Name	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update CDISC Codelist Name	Kurtzke Functional System Scores Clinical Classification STRESC for KFSS102A and KFSS106A TN/TC	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182515	CDISC Submission Value	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update CDISC Submission Value	KFSS102A_6ASTR	KFSS1SET1STR	
2022-09-30	CDISC-5613	Update	C182515	NCI Preferred Term	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update NCI Preferred Term	CDISC Clinical Classification Kurtzke Functional System Scores KFSS102A and KFSS106A Standardized Character Response Terminology	CDISC Clinical Classification Kurtzke Functional System Scores KFSS1SET1 Standardized Character Response Terminology	
2022-09-30	CDISC-5613	Update	C182515	CDISC Synonym	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Add new CDISC Synonym	- - -	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182515	CDISC Synonym	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Remove CDISC Synonym	Kurtzke Functional System Scores Clinical Classification STRESC for KFSS102A and KFSS106A TN/TC	- - -	
2022-09-30	CDISC-5613	Update	C182798	CDISC Codelist Name	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update CDISC Codelist Name	Kurtzke Functional System Scores Clinical Classification STRESC for KFSS102A and KFSS106A TN/TC	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182798	NCI Preferred Term	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update NCI Preferred Term	Kurtzke Functional System Scores KFSS102A and KFSS106A Standardized Character Result Checked - Checked	Kurtzke Functional System Scores KFSS1SET1 Standardized Character Result Checked - Checked	
2022-09-30	CDISC-5613	Update	C182798	CDISC Synonym	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Add new CDISC Synonym	- - -	KFSS1SET1-CHECKED	
2022-09-30	CDISC-5613	Update	C182798	CDISC Synonym	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Remove CDISC Synonym	KFSS102A and KFSS106A-CHECKED	- - -	
2022-09-30	CDISC-5613	Update	C182799	CDISC Codelist Name	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update CDISC Codelist Name	Kurtzke Functional System Scores Clinical Classification STRESC for KFSS102A and KFSS106A TN/TC	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	
2022-09-30	CDISC-5613	Update	C182799	NCI Preferred Term	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Update NCI Preferred Term	Kurtzke Functional System Scores KFSS102A and KFSS106A Standardized Character Result Not Checked - Not Checked	Kurtzke Functional System Scores KFSS1SET1 Standardized Character Result Not Checked - Not Checked	
2022-09-30	CDISC-5613	Update	C182799	CDISC Synonym	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Add new CDISC Synonym	- - -	KFSS1SET1-NOT CHECKED	
2022-09-30	CDISC-5613	Update	C182799	CDISC Synonym	KFSS1SET1STR	Kurtzke Functional System Scores Clinical Classification STRESC the Same as KFSS102A TN/TC	Remove CDISC Synonym	KFSS102A and KFSS106A-NOT CHECKED	- - -	
2022-09-30	CDISC-5361	Update	C142282	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	CD25	
2022-09-30	CDISC-5481	Update	C142285	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	NEFL	
2022-09-30	CDISC-5481	Update	C142285	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	NF-L	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble CD25	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble IL-2Ra	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble Interleukin 2 Receptor Subunit Alpha	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	sCD25	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble CD40 Ligand	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble CD40LG	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble T-BAM	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble TRAP	
2022-09-30	CDISC-5753	Update	C174312	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble Tumor Necrosis Factor Receptor Superfamily, Member 5	
2022-09-30	CDISC-5753	Update	C174312	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Soluble p50	
2022-09-30	N/A	Update	C64470	NCI Preferred Term	LBTEST	Laboratory Test Name	Update NCI Preferred Term	Total Basophil Count	Absolute Basophil Count	
2022-09-30	CDISC-5434	Update	C74773	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Squamous Cells	
2022-09-30	CDISC-5420	Update	C96568	CDISC Synonym	LBTEST	Laboratory Test Name	Add new CDISC Synonym	- - -	Beta-Hydroxybutyric Acid	
2022-09-30	CDISC-5361	Update	C142282	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	CD25	
2022-09-30	CDISC-5481	Update	C142285	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	NEFL	
2022-09-30	CDISC-5481	Update	C142285	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	NF-L	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble CD25	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble IL-2Ra	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble Interleukin 2 Receptor Subunit Alpha	
2022-09-30	CDISC-5361	Update	C158220	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	sCD25	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble CD40 Ligand	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble CD40LG	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble T-BAM	
2022-09-30	CDISC-5753	Update	C174308	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble TRAP	
2022-09-30	CDISC-5753	Update	C174312	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble Tumor Necrosis Factor Receptor Superfamily, Member 5	
2022-09-30	CDISC-5753	Update	C174312	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Soluble p50	
2022-09-30	CDISC-5753	Update	C186068	CDISC Submission Value	LBTESTCD	Laboratory Test Code	Update CDISC Submission Value	HXDX 18	HXDX18	
2022-09-30	N/A	Update	C64470	NCI Preferred Term	LBTESTCD	Laboratory Test Code	Update NCI Preferred Term	Total Basophil Count	Absolute Basophil Count	
2022-09-30	CDISC-5434	Update	C74773	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Squamous Cells	
2022-09-30	CDISC-5420	Update	C96568	CDISC Synonym	LBTESTCD	Laboratory Test Code	Add new CDISC Synonym	- - -	Beta-Hydroxybutyric Acid	
2022-09-30	CDISC-5753	Update	C132421	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C132422	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C132423	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C132425	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C132426	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C139209	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C150867	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C150868	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C150869	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C154836	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C154837	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C184676	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C184677	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187876	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187877	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187878	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187879	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187880	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187881	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187882	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187883	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187884	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187885	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187886	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187887	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187888	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187889	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187890	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C187891	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C94530	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C94531	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C94532	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C94533	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96606	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96611	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96612	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96692	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96777	CDISC Codelist Name	MEDEVAL	Medical Evaluator Identifier	Update CDISC Codelist Name	Medical Evaluator	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96777	CDISC Definition	MEDEVAL	Medical Evaluator Identifier	Update CDISC Definition	The individual responsible for the medical assessment.	A terminology codelist containing identifiers used to uniquely distinguish multiple evaluators with the same role.	
2022-09-30	CDISC-5753	Update	C96777	NCI Preferred Term	MEDEVAL	Medical Evaluator Identifier	Update NCI Preferred Term	CDISC SDTM Medical Evaluator Terminology	CDISC SDTM Medical Evaluator Identifier Terminology	
2022-09-30	CDISC-5753	Update	C96777	CDISC Synonym	MEDEVAL	Medical Evaluator Identifier	Add new CDISC Synonym	- - -	Medical Evaluator Identifier	
2022-09-30	CDISC-5753	Update	C96777	CDISC Synonym	MEDEVAL	Medical Evaluator Identifier	Remove CDISC Synonym	Medical Evaluator	- - -	
2022-09-30	N/A	Update	C111235	NCI Preferred Term	METHOD	Method	Update NCI Preferred Term	Immunochemiluminometric Assay	Chemiluminescent Immunoassay	
2022-09-30	N/A	Update	C120695	NCI Preferred Term	METHOD	Method	Update NCI Preferred Term	Microneutralization Assay	Virus Neutralization Assay	
2022-09-30	N/A	Update	C17230	NCI Preferred Term	METHOD	Method	Update NCI Preferred Term	Ultrasonography	Ultrasound Imaging	
2022-09-30	CDISC-5478	Update	C18136	CDISC Definition	METHOD	Method	Update CDISC Definition	A molecular biology technique used to recreate and amplify complimentary DNA (cDNA) from total RNA or messenger RNA (mRNA), using reverse transcriptase and DNA polymerase.	A molecular biology technique used to recreate and amplify complementary DNA (cDNA) from total RNA or messenger RNA (mRNA), using reverse transcriptase and DNA polymerase.	
2022-09-30	N/A	Update	C38073	NCI Preferred Term	METHOD	Method	Update NCI Preferred Term	Radionuclide Ventriculogram Scan	Multigated Acquisition Scan	
2022-09-30	CDISC-5480; CDISC-5488; CDISC-5519	Update	C156813	CDISC Submission Value	MHEDTTYP	Medical History Event Date Type	Update CDISC Submission Value	INTIAL DIAGNOSIS	INITIAL DIAGNOSIS	
2022-09-30	CDISC-5753	Update	C86191	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	GCS	
2022-09-30	CDISC-5753	Update	C86191	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	Streptococcus Group C	
2022-09-30	CDISC-5753	Update	C86192	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	GFS	
2022-09-30	CDISC-5753	Update	C86192	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	Streptococcus Group F	
2022-09-30	CDISC-5753	Update	C86193	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	GGS	
2022-09-30	CDISC-5753	Update	C86193	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	Streptococcus Group G	
2022-09-30	CDISC-5479	Update	C86356	CDISC Synonym	MICROORG	Microorganism	Add new CDISC Synonym	- - -	Klebsiella aerogenes	
2022-09-30	CDISC-5753	Update	C123556	CDISC Synonym	MITS	SDTM Microscopic Findings Test Name	Add new CDISC Synonym	- - -	Tumor Cells/Total Cells	
2022-09-30	CDISC-5753	Update	C154801	CDISC Submission Value	MITS	SDTM Microscopic Findings Test Name	Update CDISC Submission Value	Tumor Cells	Neoplastic Cells	
2022-09-30	CDISC-5753	Update	C154801	CDISC Definition	MITS	SDTM Microscopic Findings Test Name	Update CDISC Definition	A measurement of the tumor cells in a biological specimen.	A measurement of the neoplastic cells in a biological specimen.	
2022-09-30	CDISC-5753	Update	C154801	CDISC Synonym	MITS	SDTM Microscopic Findings Test Name	Add new CDISC Synonym	- - -	Neoplastic Cells	
2022-09-30	CDISC-5753	Update	C154801	CDISC Synonym	MITS	SDTM Microscopic Findings Test Name	Remove CDISC Synonym	Tumor Cells	- - -	
2022-09-30	CDISC-5753	Update	C18000	CDISC Synonym	MITS	SDTM Microscopic Findings Test Name	Add new CDISC Synonym	- - -	Histologic Grade	
2022-09-30	CDISC-5753	Update	C123556	CDISC Synonym	MITSCD	SDTM Microscopic Findings Test Code	Add new CDISC Synonym	- - -	Tumor Cells/Total Cells	
2022-09-30	CDISC-5753	Update	C154801	CDISC Submission Value	MITSCD	SDTM Microscopic Findings Test Code	Update CDISC Submission Value	TMCE	NEOCE	
2022-09-30	CDISC-5753	Update	C154801	CDISC Definition	MITSCD	SDTM Microscopic Findings Test Code	Update CDISC Definition	A measurement of the tumor cells in a biological specimen.	A measurement of the neoplastic cells in a biological specimen.	
2022-09-30	CDISC-5753	Update	C154801	CDISC Synonym	MITSCD	SDTM Microscopic Findings Test Code	Add new CDISC Synonym	- - -	Neoplastic Cells	
2022-09-30	CDISC-5753	Update	C154801	CDISC Synonym	MITSCD	SDTM Microscopic Findings Test Code	Remove CDISC Synonym	Tumor Cells	- - -	
2022-09-30	CDISC-5753	Update	C18000	CDISC Synonym	MITSCD	SDTM Microscopic Findings Test Code	Add new CDISC Synonym	- - -	Histologic Grade	
2022-09-30	CDISC-5150	Update	C147472	CDISC Synonym	MUSCTS	Musculoskeletal System Finding Test Name	Add new CDISC Synonym	- - -	Bone Mass	
2022-09-30	CDISC-5150	Update	C147472	CDISC Synonym	MUSCTS	Musculoskeletal System Finding Test Name	Add new CDISC Synonym	- - -	Bone Mineral Mass	
2022-09-30	CDISC-5150	Update	C147472	CDISC Synonym	MUSCTSCD	Musculoskeletal System Finding Test Code	Add new CDISC Synonym	- - -	Bone Mass	
2022-09-30	CDISC-5150	Update	C147472	CDISC Synonym	MUSCTSCD	Musculoskeletal System Finding Test Code	Add new CDISC Synonym	- - -	Bone Mineral Mass	
2022-09-30	CDISC-5753	Update	C123575	CDISC Synonym	ONCRSR	Oncology Response Assessment Result	Add new CDISC Synonym	- - -	Complete Hematologic Remission	
2022-09-30	N/A	Update	C124427	NCI Preferred Term	ONCRSR	Oncology Response Assessment Result	Update NCI Preferred Term	Complete Minimal Residual Disease Response	Complete Measurable Residual Disease Response	
2022-09-30	N/A	Update	C124428	NCI Preferred Term	ONCRSR	Oncology Response Assessment Result	Update NCI Preferred Term	Minimal Residual Disease Negativity	Measurable Residual Disease Negativity	
2022-09-30	N/A	Update	C124429	NCI Preferred Term	ONCRSR	Oncology Response Assessment Result	Update NCI Preferred Term	Minimal Residual Disease Persistence	Measurable Residual Disease Persistence	
2022-09-30	N/A	Update	C124430	NCI Preferred Term	ONCRSR	Oncology Response Assessment Result	Update NCI Preferred Term	Minimal Residual Disease Relapse	Measurable Residual Disease Relapse	
2022-09-30	N/A	Update	C124431	NCI Preferred Term	ONCRSR	Oncology Response Assessment Result	Update NCI Preferred Term	Non-Quantifiable Minimal Residual Disease Positivity	Non-Quantifiable Measurable Residual Disease Positivity	
2022-09-30	N/A	Update	C124432	NCI Preferred Term	ONCRSR	Oncology Response Assessment Result	Update NCI Preferred Term	Quantifiable Minimal Residual Disease Positivity	Quantifiable Measurable Residual Disease Positivity	
2022-09-30	N/A	Update	C124433	NCI Preferred Term	ONCRTS	Oncology Response Assessment Test Name	Update NCI Preferred Term	Minimal Residual Disease Response	Measurable Residual Disease Response	
2022-09-30	N/A	Update	C172578	NCI Preferred Term	ONCRTS	Oncology Response Assessment Test Name	Update NCI Preferred Term	Minimal Residual Disease Indicator	Measurable Residual Disease Indicator	
2022-09-30	N/A	Update	C124433	NCI Preferred Term	ONCRTSCD	Oncology Response Assessment Test Code	Update NCI Preferred Term	Minimal Residual Disease Response	Measurable Residual Disease Response	
2022-09-30	N/A	Update	C172578	NCI Preferred Term	ONCRTSCD	Oncology Response Assessment Test Code	Update NCI Preferred Term	Minimal Residual Disease Indicator	Measurable Residual Disease Indicator	
2022-09-30	N/A	Update	C38073	NCI Preferred Term	PROCEDUR	Procedure	Update NCI Preferred Term	Radionuclide Ventriculogram Scan	Multigated Acquisition Scan	
2022-09-30	CDISC-5518	Update	C179942	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C179942	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 test code.	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 test code.	
2022-09-30	CDISC-5518	Update	C179942	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	CDISC Questionnaire PRO-CTCAE V1.0 Version Date 4/26/2020 Test Code Terminology	CDISC Questionnaire PRO-CTCAE Version 1.0 Test Code Terminology	
2022-09-30	CDISC-5518	Update	C179942	CDISC Synonym	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Add new CDISC Synonym	- - -	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C179942	CDISC Synonym	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Remove CDISC Synonym	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	- - -	
2022-09-30	CDISC-5518	Update	C180044	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180044	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your dry mouth at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your dry mouth at its worst?	
2022-09-30	CDISC-5518	Update	C180044	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Dry Mouth Severity	PRO-CTCAE V1.0 - Dry Mouth Severity	
2022-09-30	CDISC-5518	Update	C180045	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180045	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your difficulty swallowing at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your difficulty swallowing at its worst?	
2022-09-30	CDISC-5518	Update	C180045	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Difficulty Swallowing Severity	PRO-CTCAE V1.0 - Difficulty Swallowing Severity	
2022-09-30	CDISC-5518	Update	C180046	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180046	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your mouth or throat sores at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your mouth or throat sores at their worst?	
2022-09-30	CDISC-5518	Update	C180046	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Mouth/Throat Sores Severity	PRO-CTCAE V1.0 - Mouth/Throat Sores Severity	
2022-09-30	CDISC-5518	Update	C180047	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180047	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did mouth or throat sores interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did mouth or throat sores interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180047	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Mouth/Throat Sores Interference	PRO-CTCAE V1.0 - Mouth/Throat Sores Interference	
2022-09-30	CDISC-5518	Update	C180048	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180048	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of skin cracking at the corners of your mouth at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of skin cracking at the corners of your mouth at its worst?	
2022-09-30	CDISC-5518	Update	C180048	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Cracking Corners of Mouth Severity	PRO-CTCAE V1.0 - Cracking Corners of Mouth Severity	
2022-09-30	CDISC-5518	Update	C180049	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180049	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any voice changes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any voice changes?	
2022-09-30	CDISC-5518	Update	C180049	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Voice Quality Changes Presence	PRO-CTCAE V1.0 - Voice Quality Changes Presence	
2022-09-30	CDISC-5518	Update	C180050	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180050	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hoarse voice at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hoarse voice at its worst?	
2022-09-30	CDISC-5518	Update	C180050	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hoarseness Severity	PRO-CTCAE V1.0 - Hoarseness Severity	
2022-09-30	CDISC-5518	Update	C180051	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180051	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your problems with tasting food or drink at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your problems with tasting food or drink at their worst?	
2022-09-30	CDISC-5518	Update	C180051	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Taste Changes Severity	PRO-CTCAE V1.0 - Taste Changes Severity	
2022-09-30	CDISC-5518	Update	C180052	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180052	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your decreased appetite at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your decreased appetite at its worst?	
2022-09-30	CDISC-5518	Update	C180052	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Appetite Severity	PRO-CTCAE V1.0 - Decreased Appetite Severity	
2022-09-30	CDISC-5518	Update	C180053	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180053	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did decreased appetite interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did decreased appetite interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180053	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Appetite Interference	PRO-CTCAE V1.0 - Decreased Appetite Interference	
2022-09-30	CDISC-5518	Update	C180054	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180054	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have nausea?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have nausea?	
2022-09-30	CDISC-5518	Update	C180054	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nausea Frequency	PRO-CTCAE V1.0 - Nausea Frequency	
2022-09-30	CDISC-5518	Update	C180055	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180055	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your nausea at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your nausea at its worst?	
2022-09-30	CDISC-5518	Update	C180055	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nausea Severity	PRO-CTCAE V1.0 - Nausea Severity	
2022-09-30	CDISC-5518	Update	C180056	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180056	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have vomiting?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have vomiting?	
2022-09-30	CDISC-5518	Update	C180056	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vomiting Frequency	PRO-CTCAE V1.0 - Vomiting Frequency	
2022-09-30	CDISC-5518	Update	C180057	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180057	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your vomiting at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your vomiting at its worst?	
2022-09-30	CDISC-5518	Update	C180057	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vomiting Severity	PRO-CTCAE V1.0 - Vomiting Severity	
2022-09-30	CDISC-5518	Update	C180058	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180058	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have heartburn?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have heartburn?	
2022-09-30	CDISC-5518	Update	C180058	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heartburn Frequency	PRO-CTCAE V1.0 - Heartburn Frequency	
2022-09-30	CDISC-5518	Update	C180059	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180059	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your heartburn at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your heartburn at its worst?	
2022-09-30	CDISC-5518	Update	C180059	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heartburn Severity	PRO-CTCAE V1.0 - Heartburn Severity	
2022-09-30	CDISC-5518	Update	C180060	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180060	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any increased passing of gas (flatulence)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any increased passing of gas (flatulence)?	
2022-09-30	CDISC-5518	Update	C180060	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Gas Presence	PRO-CTCAE V1.0 - Gas Presence	
2022-09-30	CDISC-5518	Update	C180061	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180061	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have bloating of the abdomen (belly)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have bloating of the abdomen (belly)?	
2022-09-30	CDISC-5518	Update	C180061	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bloating Frequency	PRO-CTCAE V1.0 - Bloating Frequency	
2022-09-30	CDISC-5518	Update	C180062	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180062	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your bloating of the abdomen (belly) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your bloating of the abdomen (belly) at its worst?	
2022-09-30	CDISC-5518	Update	C180062	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bloating Severity	PRO-CTCAE V1.0 - Bloating Severity	
2022-09-30	CDISC-5518	Update	C180063	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180063	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have hiccups?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have hiccups?	
2022-09-30	CDISC-5518	Update	C180063	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hiccups Frequency	PRO-CTCAE V1.0 - Hiccups Frequency	
2022-09-30	CDISC-5518	Update	C180064	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180064	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hiccups at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hiccups at their worst?	
2022-09-30	CDISC-5518	Update	C180064	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hiccups Severity	PRO-CTCAE V1.0 - Hiccups Severity	
2022-09-30	CDISC-5518	Update	C180065	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180065	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your constipation at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your constipation at its worst?	
2022-09-30	CDISC-5518	Update	C180065	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Constipation Severity	PRO-CTCAE V1.0 - Constipation Severity	
2022-09-30	CDISC-5518	Update	C180066	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180066	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have loose or watery stools (diarrhea/diarrhoea)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have loose or watery stools (diarrhea/diarrhoea)?	
2022-09-30	CDISC-5518	Update	C180066	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Diarrhea Frequency	PRO-CTCAE V1.0 - Diarrhea Frequency	
2022-09-30	CDISC-5518	Update	C180067	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180067	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have pain in the abdomen (belly area)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have pain in the abdomen (belly area)?	
2022-09-30	CDISC-5518	Update	C180067	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Abdominal Pain Frequency	PRO-CTCAE V1.0 - Abdominal Pain Frequency	
2022-09-30	CDISC-5518	Update	C180068	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180068	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain in the abdomen (belly area) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain in the abdomen (belly area) at its worst?	
2022-09-30	CDISC-5518	Update	C180068	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Abdominal Pain Severity	PRO-CTCAE V1.0 - Abdominal Pain Severity	
2022-09-30	CDISC-5518	Update	C180069	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180069	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did pain in the abdomen (belly area) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did pain in the abdomen (belly area) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180069	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Abdominal Pain Interference	PRO-CTCAE V1.0 - Abdominal Pain Interference	
2022-09-30	CDISC-5518	Update	C180070	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180070	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you lose control of bowel movements?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you lose control of bowel movements?	
2022-09-30	CDISC-5518	Update	C180070	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fecal Incontinence Frequency	PRO-CTCAE V1.0 - Fecal Incontinence Frequency	
2022-09-30	CDISC-5518	Update	C180071	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180071	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did loss of control of bowel movements interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did loss of control of bowel movements interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180071	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fecal Incontinence Interference	PRO-CTCAE V1.0 - Fecal Incontinence Interference	
2022-09-30	CDISC-5518	Update	C180072	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180072	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your shortness of breath at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your shortness of breath at its worst?	
2022-09-30	CDISC-5518	Update	C180072	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Shortness of Breath Severity	PRO-CTCAE V1.0 - Shortness of Breath Severity	
2022-09-30	CDISC-5518	Update	C180073	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180073	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did your shortness of breath interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did your shortness of breath interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180073	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Shortness of Breath Interference	PRO-CTCAE V1.0 - Shortness of Breath Interference	
2022-09-30	CDISC-5518	Update	C180074	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180074	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your cough at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your cough at its worst?	
2022-09-30	CDISC-5518	Update	C180074	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Cough Severity	PRO-CTCAE V1.0 - Cough Severity	
2022-09-30	CDISC-5518	Update	C180075	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180075	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did cough interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did cough interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180075	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Cough Interference	PRO-CTCAE V1.0 - Cough Interference	
2022-09-30	CDISC-5518	Update	C180076	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180076	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your wheezing (whistling noise in the chest with breathing) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your wheezing (whistling noise in the chest with breathing) at its worst?	
2022-09-30	CDISC-5518	Update	C180076	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Wheezing Severity	PRO-CTCAE V1.0 - Wheezing Severity	
2022-09-30	CDISC-5518	Update	C180077	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180077	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have arm or leg swelling?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have arm or leg swelling?	
2022-09-30	CDISC-5518	Update	C180077	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Swelling Frequency	PRO-CTCAE V1.0 - Swelling Frequency	
2022-09-30	CDISC-5518	Update	C180078	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180078	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your arm or leg swelling at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your arm or leg swelling at its worst?	
2022-09-30	CDISC-5518	Update	C180078	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Swelling Severity	PRO-CTCAE V1.0 - Swelling Severity	
2022-09-30	CDISC-5518	Update	C180079	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180079	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did arm or leg swelling interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did arm or leg swelling interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180079	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Swelling Interference	PRO-CTCAE V1.0 - Swelling Interference	
2022-09-30	CDISC-5518	Update	C180080	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180080	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel a pounding or racing heartbeat (palpitations)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel a pounding or racing heartbeat (palpitations)?	
2022-09-30	CDISC-5518	Update	C180080	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heart Palpitations Frequency	PRO-CTCAE V1.0 - Heart Palpitations Frequency	
2022-09-30	CDISC-5518	Update	C180081	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180081	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pounding or racing heartbeat (palpitations) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pounding or racing heartbeat (palpitations) at its worst?	
2022-09-30	CDISC-5518	Update	C180081	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heart Palpitations Severity	PRO-CTCAE V1.0 - Heart Palpitations Severity	
2022-09-30	CDISC-5518	Update	C180082	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180082	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any rash?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any rash?	
2022-09-30	CDISC-5518	Update	C180082	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Rash Presence	PRO-CTCAE V1.0 - Rash Presence	
2022-09-30	CDISC-5518	Update	C180083	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180083	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your dry skin at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your dry skin at its worst?	
2022-09-30	CDISC-5518	Update	C180083	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Skin Dryness Severity	PRO-CTCAE V1.0 - Skin Dryness Severity	
2022-09-30	CDISC-5518	Update	C180084	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180084	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your acne or pimples on the face or chest at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your acne or pimples on the face or chest at its worst?	
2022-09-30	CDISC-5518	Update	C180084	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Acne Severity	PRO-CTCAE V1.0 - Acne Severity	
2022-09-30	CDISC-5518	Update	C180085	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180085	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any hair loss?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any hair loss?	
2022-09-30	CDISC-5518	Update	C180085	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hair Loss Amount	PRO-CTCAE V1.0 - Hair Loss Amount	
2022-09-30	CDISC-5518	Update	C180086	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180086	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your itchy skin at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your itchy skin at its worst?	
2022-09-30	CDISC-5518	Update	C180086	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Itching Severity	PRO-CTCAE V1.0 - Itching Severity	
2022-09-30	CDISC-5518	Update	C180087	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180087	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any hives (itchy red bumps on the skin)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any hives (itchy red bumps on the skin)?	
2022-09-30	CDISC-5518	Update	C180087	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hives Presence	PRO-CTCAE V1.0 - Hives Presence	
2022-09-30	CDISC-5518	Update	C180088	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180088	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hand-foot syndrome (a rash of the hands or feet that can cause cracking, peeling, redness or pain) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hand-foot syndrome (a rash of the hands or feet that can cause cracking, peeling, redness or pain) at its worst?	
2022-09-30	CDISC-5518	Update	C180088	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hand-Foot Syndrome Severity	PRO-CTCAE V1.0 - Hand-Foot Syndrome Severity	
2022-09-30	CDISC-5518	Update	C180089	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180089	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you lose any fingernails or toenails?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you lose any fingernails or toenails?	
2022-09-30	CDISC-5518	Update	C180089	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nail Loss Presence	PRO-CTCAE V1.0 - Nail Loss Presence	
2022-09-30	CDISC-5518	Update	C180090	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180090	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any ridges or bumps on your fingernails or toenails?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any ridges or bumps on your fingernails or toenails?	
2022-09-30	CDISC-5518	Update	C180090	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nail Ridging Presence	PRO-CTCAE V1.0 - Nail Ridging Presence	
2022-09-30	CDISC-5518	Update	C180091	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180091	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any change in the color of your fingernails or toenails?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any change in the color of your fingernails or toenails?	
2022-09-30	CDISC-5518	Update	C180091	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nail Discoloration Presence	PRO-CTCAE V1.0 - Nail Discoloration Presence	
2022-09-30	CDISC-5518	Update	C180092	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180092	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any increased skin sensitivity to sunlight?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any increased skin sensitivity to sunlight?	
2022-09-30	CDISC-5518	Update	C180092	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sensitivity to Sunlight Presence	PRO-CTCAE V1.0 - Sensitivity to Sunlight Presence	
2022-09-30	CDISC-5518	Update	C180093	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180093	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any bed sores?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any bed sores?	
2022-09-30	CDISC-5518	Update	C180093	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bed/Pressure Sores Presence	PRO-CTCAE V1.0 - Bed/Pressure Sores Presence	
2022-09-30	CDISC-5518	Update	C180094	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180094	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your skin burns from radiation at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your skin burns from radiation at their worst?	
2022-09-30	CDISC-5518	Update	C180094	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Radiation Skin Reaction Severity	PRO-CTCAE V1.0 - Radiation Skin Reaction Severity	
2022-09-30	CDISC-5518	Update	C180095	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180095	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any unusual darkening of the skin?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any unusual darkening of the skin?	
2022-09-30	CDISC-5518	Update	C180095	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Skin Darkening Presence	PRO-CTCAE V1.0 - Skin Darkening Presence	
2022-09-30	CDISC-5518	Update	C180096	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180096	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any stretch marks?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any stretch marks?	
2022-09-30	CDISC-5518	Update	C180096	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Stretch Marks Presence	PRO-CTCAE V1.0 - Stretch Marks Presence	
2022-09-30	CDISC-5518	Update	C180097	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180097	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your numbness or tingling in your hands or feet at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your numbness or tingling in your hands or feet at its worst?	
2022-09-30	CDISC-5518	Update	C180097	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Numbness & Tingling Severity	PRO-CTCAE V1.0 - Numbness & Tingling Severity	
2022-09-30	CDISC-5518	Update	C180098	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180098	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did numbness or tingling in your hands or feet interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did numbness or tingling in your hands or feet interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180098	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Numbness & Tingling Interference	PRO-CTCAE V1.0 - Numbness & Tingling Interference	
2022-09-30	CDISC-5518	Update	C180099	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180099	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your dizziness at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your dizziness at its worst?	
2022-09-30	CDISC-5518	Update	C180099	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Dizziness Severity	PRO-CTCAE V1.0 - Dizziness Severity	
2022-09-30	CDISC-5518	Update	C180100	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180100	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did dizziness interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did dizziness interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180100	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Dizziness Interference	PRO-CTCAE V1.0 - Dizziness Interference	
2022-09-30	CDISC-5518	Update	C180101	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180101	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your blurry vision at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your blurry vision at its worst?	
2022-09-30	CDISC-5518	Update	C180101	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Blurred Vision Severity	PRO-CTCAE V1.0 - Blurred Vision Severity	
2022-09-30	CDISC-5518	Update	C180102	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180102	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did blurry vision interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did blurry vision interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180102	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Blurred Vision Interference	PRO-CTCAE V1.0 - Blurred Vision Interference	
2022-09-30	CDISC-5518	Update	C180103	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180103	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any flashing lights in front of your eyes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any flashing lights in front of your eyes?	
2022-09-30	CDISC-5518	Update	C180103	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Flashing Lights in Eyes Presence	PRO-CTCAE V1.0 - Flashing Lights in Eyes Presence	
2022-09-30	CDISC-5518	Update	C180104	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180104	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any spots or lines (floaters) that drift in front of your eyes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any spots or lines (floaters) that drift in front of your eyes?	
2022-09-30	CDISC-5518	Update	C180104	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Visual Floaters Presence	PRO-CTCAE V1.0 - Visual Floaters Presence	
2022-09-30	CDISC-5518	Update	C180105	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180105	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your watery eyes (tearing) at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your watery eyes (tearing) at their worst?	
2022-09-30	CDISC-5518	Update	C180105	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Watery Eyes Severity	PRO-CTCAE V1.0 - Watery Eyes Severity	
2022-09-30	CDISC-5518	Update	C180106	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180106	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did watery eyes (tearing) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did watery eyes (tearing) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180106	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Watery Eyes Interference	PRO-CTCAE V1.0 - Watery Eyes Interference	
2022-09-30	CDISC-5518	Update	C180107	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180107	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of ringing in your ears at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of ringing in your ears at its worst?	
2022-09-30	CDISC-5518	Update	C180107	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Ringing in Ears Severity	PRO-CTCAE V1.0 - Ringing in Ears Severity	
2022-09-30	CDISC-5518	Update	C180108	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180108	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your problems with concentration at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your problems with concentration at their worst?	
2022-09-30	CDISC-5518	Update	C180108	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Concentration Problems Severity	PRO-CTCAE V1.0 - Concentration Problems Severity	
2022-09-30	CDISC-5518	Update	C180109	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180109	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did problems with concentration interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did problems with concentration interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180109	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Concentration Problems Interference	PRO-CTCAE V1.0 - Concentration Problems Interference	
2022-09-30	CDISC-5518	Update	C180110	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180110	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your problems with memory at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your problems with memory at their worst?	
2022-09-30	CDISC-5518	Update	C180110	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Memory Problems Severity	PRO-CTCAE V1.0 - Memory Problems Severity	
2022-09-30	CDISC-5518	Update	C180111	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180111	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did problems with memory interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did problems with memory interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180111	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Memory Problems Interference	PRO-CTCAE V1.0 - Memory Problems Interference	
2022-09-30	CDISC-5518	Update	C180112	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180112	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have pain?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have pain?	
2022-09-30	CDISC-5518	Update	C180112	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - General Pain Frequency	PRO-CTCAE V1.0 - General Pain Frequency	
2022-09-30	CDISC-5518	Update	C180113	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180113	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain at its worst?	
2022-09-30	CDISC-5518	Update	C180113	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - General Pain Severity	PRO-CTCAE V1.0 - General Pain Severity	
2022-09-30	CDISC-5518	Update	C180114	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180114	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did pain interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did pain interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180114	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - General Pain Interference	PRO-CTCAE V1.0 - General Pain Interference	
2022-09-30	CDISC-5518	Update	C180115	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180115	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have a headache?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have a headache?	
2022-09-30	CDISC-5518	Update	C180115	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Headache Frequency	PRO-CTCAE V1.0 - Headache Frequency	
2022-09-30	CDISC-5518	Update	C180116	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180116	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your headache at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your headache at its worst?	
2022-09-30	CDISC-5518	Update	C180116	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Headache Severity	PRO-CTCAE V1.0 - Headache Severity	
2022-09-30	CDISC-5518	Update	C180117	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180117	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did your headache interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did your headache interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180117	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Headache Interference	PRO-CTCAE V1.0 - Headache Interference	
2022-09-30	CDISC-5518	Update	C180118	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180118	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have aching muscles?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have aching muscles?	
2022-09-30	CDISC-5518	Update	C180118	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Muscle Pain Frequency	PRO-CTCAE V1.0 - Muscle Pain Frequency	
2022-09-30	CDISC-5518	Update	C180119	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180119	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your aching muscles at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your aching muscles at their worst?	
2022-09-30	CDISC-5518	Update	C180119	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Muscle Pain Severity	PRO-CTCAE V1.0 - Muscle Pain Severity	
2022-09-30	CDISC-5518	Update	C180120	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180120	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did aching muscles interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did aching muscles interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180120	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Muscle Pain Interference	PRO-CTCAE V1.0 - Muscle Pain Interference	
2022-09-30	CDISC-5518	Update	C180121	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180121	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have aching joints (such as elbows, knees, shoulders)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have aching joints (such as elbows, knees, shoulders)?	
2022-09-30	CDISC-5518	Update	C180121	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Joint Pain Frequency	PRO-CTCAE V1.0 - Joint Pain Frequency	
2022-09-30	CDISC-5518	Update	C180122	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180122	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your aching joints (such as elbows, knees, shoulders) at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your aching joints (such as elbows, knees, shoulders) at their worst?	
2022-09-30	CDISC-5518	Update	C180122	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Joint Pain Severity	PRO-CTCAE V1.0 - Joint Pain Severity	
2022-09-30	CDISC-5518	Update	C180123	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180123	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did aching joints (such as elbows, knees, shoulders) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did aching joints (such as elbows, knees, shoulders) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180123	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Joint Pain Interference	PRO-CTCAE V1.0 - Joint Pain Interference	
2022-09-30	CDISC-5518	Update	C180124	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180124	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your insomnia (including difficulty falling asleep, staying asleep, or waking up early) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your insomnia (including difficulty falling asleep, staying asleep, or waking up early) at its worst?	
2022-09-30	CDISC-5518	Update	C180124	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Insomnia Severity	PRO-CTCAE V1.0 - Insomnia Severity	
2022-09-30	CDISC-5518	Update	C180125	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180125	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did insomnia (including difficulty falling asleep, staying asleep, or waking up early) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did insomnia (including difficulty falling asleep, staying asleep, or waking up early) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180125	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Insomnia Interference	PRO-CTCAE V1.0 - Insomnia Interference	
2022-09-30	CDISC-5518	Update	C180126	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180126	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your fatigue, tiredness, or lack of energy at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your fatigue, tiredness, or lack of energy at its worst?	
2022-09-30	CDISC-5518	Update	C180126	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fatigue Severity	PRO-CTCAE V1.0 - Fatigue Severity	
2022-09-30	CDISC-5518	Update	C180127	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180127	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did fatigue, tiredness, or lack of energy interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did fatigue, tiredness, or lack of energy interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180127	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fatigue Interference	PRO-CTCAE V1.0 - Fatigue Interference	
2022-09-30	CDISC-5518	Update	C180128	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180128	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel anxiety?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel anxiety?	
2022-09-30	CDISC-5518	Update	C180128	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Anxious Frequency	PRO-CTCAE V1.0 - Anxious Frequency	
2022-09-30	CDISC-5518	Update	C180129	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180129	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your anxiety at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your anxiety at its worst?	
2022-09-30	CDISC-5518	Update	C180129	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Anxious Severity	PRO-CTCAE V1.0 - Anxious Severity	
2022-09-30	CDISC-5518	Update	C180130	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180130	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did anxiety interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did anxiety interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180130	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Anxious Interference	PRO-CTCAE V1.0 - Anxious Interference	
2022-09-30	CDISC-5518	Update	C180131	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180131	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel that nothing could cheer you up?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel that nothing could cheer you up?	
2022-09-30	CDISC-5518	Update	C180131	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Discouraged Frequency	PRO-CTCAE V1.0 - Discouraged Frequency	
2022-09-30	CDISC-5518	Update	C180132	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180132	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your feelings that nothing could cheer you up at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your feelings that nothing could cheer you up at their worst?	
2022-09-30	CDISC-5518	Update	C180132	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Discouraged Severity	PRO-CTCAE V1.0 - Discouraged Severity	
2022-09-30	CDISC-5518	Update	C180133	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180133	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did feeling that nothing could cheer you up interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did feeling that nothing could cheer you up interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180133	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Discouraged Interference	PRO-CTCAE V1.0 - Discouraged Interference	
2022-09-30	CDISC-5518	Update	C180134	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180134	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have sad or unhappy feelings?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have sad or unhappy feelings?	
2022-09-30	CDISC-5518	Update	C180134	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sad Frequency	PRO-CTCAE V1.0 - Sad Frequency	
2022-09-30	CDISC-5518	Update	C180135	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180135	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your sad or unhappy feelings at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your sad or unhappy feelings at their worst?	
2022-09-30	CDISC-5518	Update	C180135	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sad Severity	PRO-CTCAE V1.0 - Sad Severity	
2022-09-30	CDISC-5518	Update	C180136	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180136	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did sad or unhappy feelings interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did sad or unhappy feelings interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180136	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sad Interference	PRO-CTCAE V1.0 - Sad Interference	
2022-09-30	CDISC-5518	Update	C180137	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180137	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any irregular menstrual periods?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any irregular menstrual periods?	
2022-09-30	CDISC-5518	Update	C180137	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Irregular Menstrual Period Presence	PRO-CTCAE V1.0 - Irregular Menstrual Period Presence	
2022-09-30	CDISC-5518	Update	C180138	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180138	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you miss an expected menstrual period?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you miss an expected menstrual period?	
2022-09-30	CDISC-5518	Update	C180138	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Missed Menstrual Period Presence	PRO-CTCAE V1.0 - Missed Menstrual Period Presence	
2022-09-30	CDISC-5518	Update	C180139	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180139	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any unusual vaginal discharge?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any unusual vaginal discharge?	
2022-09-30	CDISC-5518	Update	C180139	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vaginal Discharge Amount	PRO-CTCAE V1.0 - Vaginal Discharge Amount	
2022-09-30	CDISC-5518	Update	C180140	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180140	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your vaginal dryness at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your vaginal dryness at its worst?	
2022-09-30	CDISC-5518	Update	C180140	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vaginal Dryness Severity	PRO-CTCAE V1.0 - Vaginal Dryness Severity	
2022-09-30	CDISC-5518	Update	C180141	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180141	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain or burning with urination at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain or burning with urination at its worst?	
2022-09-30	CDISC-5518	Update	C180141	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Painful Urination Severity	PRO-CTCAE V1.0 - Painful Urination Severity	
2022-09-30	CDISC-5518	Update	C180142	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180142	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel an urge to urinate all of a sudden?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel an urge to urinate all of a sudden?	
2022-09-30	CDISC-5518	Update	C180142	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Urgency Frequency	PRO-CTCAE V1.0 - Urinary Urgency Frequency	
2022-09-30	CDISC-5518	Update	C180143	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180143	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did sudden urges to urinate interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did sudden urges to urinate interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180143	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Urgency Interference	PRO-CTCAE V1.0 - Urinary Urgency Interference	
2022-09-30	CDISC-5518	Update	C180144	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180144	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, were there times when you had to urinate frequently?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, were there times when you had to urinate frequently?	
2022-09-30	CDISC-5518	Update	C180144	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Frequency Frequency	PRO-CTCAE V1.0 - Urinary Frequency Frequency	
2022-09-30	CDISC-5518	Update	C180145	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180145	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did frequent urination interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did frequent urination interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180145	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Frequency Interference	PRO-CTCAE V1.0 - Urinary Frequency Interference	
2022-09-30	CDISC-5518	Update	C180146	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180146	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any urine color change?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any urine color change?	
2022-09-30	CDISC-5518	Update	C180146	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urine Color Change Presence	PRO-CTCAE V1.0 - Urine Color Change Presence	
2022-09-30	CDISC-5518	Update	C180147	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180147	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have loss of control of urine (leakage)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have loss of control of urine (leakage)?	
2022-09-30	CDISC-5518	Update	C180147	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Incontinence Frequency	PRO-CTCAE V1.0 - Urinary Incontinence Frequency	
2022-09-30	CDISC-5518	Update	C180148	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180148	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did loss of control of urine (leakage) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did loss of control of urine (leakage) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180148	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Incontinence Interference	PRO-CTCAE V1.0 - Urinary Incontinence Interference	
2022-09-30	CDISC-5518	Update	C180149	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180149	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your difficulty getting or keeping an erection at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your difficulty getting or keeping an erection at its worst?	
2022-09-30	CDISC-5518	Update	C180149	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Achieve&Maintain Erection Severity	PRO-CTCAE V1.0 - Achieve&Maintain Erection Severity	
2022-09-30	CDISC-5518	Update	C180150	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180150	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have ejaculation problems?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have ejaculation problems?	
2022-09-30	CDISC-5518	Update	C180150	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Ejaculation Frequency	PRO-CTCAE V1.0 - Ejaculation Frequency	
2022-09-30	CDISC-5518	Update	C180151	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180151	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your decreased sexual interest at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your decreased sexual interest at its worst?	
2022-09-30	CDISC-5518	Update	C180151	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Libido Severity	PRO-CTCAE V1.0 - Decreased Libido Severity	
2022-09-30	CDISC-5518	Update	C180152	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180152	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you feel that it took too long to have an orgasm or climax?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you feel that it took too long to have an orgasm or climax?	
2022-09-30	CDISC-5518	Update	C180152	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Delayed Orgasm Presence	PRO-CTCAE V1.0 - Delayed Orgasm Presence	
2022-09-30	CDISC-5518	Update	C180153	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180153	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, were you unable to have an orgasm or climax?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, were you unable to have an orgasm or climax?	
2022-09-30	CDISC-5518	Update	C180153	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Unable to Have Orgasm Presence	PRO-CTCAE V1.0 - Unable to Have Orgasm Presence	
2022-09-30	CDISC-5518	Update	C180154	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180154	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain during vaginal sex at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain during vaginal sex at its worst?	
2022-09-30	CDISC-5518	Update	C180154	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Pain w/Sexual Intercourse Severity	PRO-CTCAE V1.0 - Pain w/Sexual Intercourse Severity	
2022-09-30	CDISC-5518	Update	C180155	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180155	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your breast area enlargement or tenderness at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your breast area enlargement or tenderness at its worst?	
2022-09-30	CDISC-5518	Update	C180155	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Breast Swelling&Tenderness Severity	PRO-CTCAE V1.0 - Breast Swelling&Tenderness Severity	
2022-09-30	CDISC-5518	Update	C180156	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180156	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you bruise easily (black and blue marks)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you bruise easily (black and blue marks)?	
2022-09-30	CDISC-5518	Update	C180156	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bruising Presence	PRO-CTCAE V1.0 - Bruising Presence	
2022-09-30	CDISC-5518	Update	C180157	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180157	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have shivering or shaking chills?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have shivering or shaking chills?	
2022-09-30	CDISC-5518	Update	C180157	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Chills Frequency	PRO-CTCAE V1.0 - Chills Frequency	
2022-09-30	CDISC-5518	Update	C180158	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180158	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your shivering or shaking chills at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your shivering or shaking chills at their worst?	
2022-09-30	CDISC-5518	Update	C180158	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Chills Severity	PRO-CTCAE V1.0 - Chills Severity	
2022-09-30	CDISC-5518	Update	C180159	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180159	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes)?	
2022-09-30	CDISC-5518	Update	C180159	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Increased Sweating Frequency	PRO-CTCAE V1.0 - Increased Sweating Frequency	
2022-09-30	CDISC-5518	Update	C180160	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180160	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes) at its worst?	
2022-09-30	CDISC-5518	Update	C180160	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Increased Sweating Severity	PRO-CTCAE V1.0 - Increased Sweating Severity	
2022-09-30	CDISC-5518	Update	C180161	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180161	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have an unexpected decrease in sweating?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have an unexpected decrease in sweating?	
2022-09-30	CDISC-5518	Update	C180161	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Sweating Presence	PRO-CTCAE V1.0 - Decreased Sweating Presence	
2022-09-30	CDISC-5518	Update	C180162	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180162	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have hot flashes/flushes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have hot flashes/flushes?	
2022-09-30	CDISC-5518	Update	C180162	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hot Flashes Frequency	PRO-CTCAE V1.0 - Hot Flashes Frequency	
2022-09-30	CDISC-5518	Update	C180163	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180163	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hot flashes/flushes at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hot flashes/flushes at their worst?	
2022-09-30	CDISC-5518	Update	C180163	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hot Flashes Severity	PRO-CTCAE V1.0 - Hot Flashes Severity	
2022-09-30	CDISC-5518	Update	C180164	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180164	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have nosebleeds?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have nosebleeds?	
2022-09-30	CDISC-5518	Update	C180164	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nosebleed Frequency	PRO-CTCAE V1.0 - Nosebleed Frequency	
2022-09-30	CDISC-5518	Update	C180165	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180165	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your nosebleeds at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your nosebleeds at their worst?	
2022-09-30	CDISC-5518	Update	C180165	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nosebleed Severity	PRO-CTCAE V1.0 - Nosebleed Severity	
2022-09-30	CDISC-5518	Update	C180166	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180166	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any pain, swelling, or redness at a site of drug injection or IV?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any pain, swelling, or redness at a site of drug injection or IV?	
2022-09-30	CDISC-5518	Update	C180166	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Pain&Swelling at Inj Site Presence	PRO-CTCAE V1.0 - Pain&Swelling at Inj Site Presence	
2022-09-30	CDISC-5518	Update	C180167	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180167	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your body odor at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your body odor at its worst?	
2022-09-30	CDISC-5518	Update	C180167	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Body Odor Severity	PRO-CTCAE V1.0 - Body Odor Severity	
2022-09-30	CDISC-5518	Update	C180168	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180168	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Do you have any other symptoms that you wish to report?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Do you have any other symptoms that you wish to report?	
2022-09-30	CDISC-5518	Update	C180168	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Any Other Symptoms Reported	PRO-CTCAE V1.0 - Any Other Symptoms Reported	
2022-09-30	CDISC-5518	Update	C180169	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180169	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 1?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 1?	
2022-09-30	CDISC-5518	Update	C180169	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 1	PRO-CTCAE V1.0 - Other Symptom 1	
2022-09-30	CDISC-5518	Update	C180170	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180170	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 1 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 1 at its worst?	
2022-09-30	CDISC-5518	Update	C180170	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 1 Severity	PRO-CTCAE V1.0 - Other Symptom 1 Severity	
2022-09-30	CDISC-5518	Update	C180171	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180171	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 2?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 2?	
2022-09-30	CDISC-5518	Update	C180171	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 2	PRO-CTCAE V1.0 - Other Symptom 2	
2022-09-30	CDISC-5518	Update	C180172	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180172	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 2 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 2 at its worst?	
2022-09-30	CDISC-5518	Update	C180172	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 2 Severity	PRO-CTCAE V1.0 - Other Symptom 2 Severity	
2022-09-30	CDISC-5518	Update	C180173	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180173	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 3?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 3?	
2022-09-30	CDISC-5518	Update	C180173	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 3	PRO-CTCAE V1.0 - Other Symptom 3	
2022-09-30	CDISC-5518	Update	C180174	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180174	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 3 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 3 at its worst?	
2022-09-30	CDISC-5518	Update	C180174	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 3 Severity	PRO-CTCAE V1.0 - Other Symptom 3 Severity	
2022-09-30	CDISC-5518	Update	C180175	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180175	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 4?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 4?	
2022-09-30	CDISC-5518	Update	C180175	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 4	PRO-CTCAE V1.0 - Other Symptom 4	
2022-09-30	CDISC-5518	Update	C180176	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180176	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 4 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 4 at its worst?	
2022-09-30	CDISC-5518	Update	C180176	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 4 Severity	PRO-CTCAE V1.0 - Other Symptom 4 Severity	
2022-09-30	CDISC-5518	Update	C180177	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180177	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 5?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 5?	
2022-09-30	CDISC-5518	Update	C180177	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 5	PRO-CTCAE V1.0 - Other Symptom 5	
2022-09-30	CDISC-5518	Update	C180178	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180178	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 5 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 5 at its worst?	
2022-09-30	CDISC-5518	Update	C180178	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 5 Severity	PRO-CTCAE V1.0 - Other Symptom 5 Severity	
2022-09-30	CDISC-5518	Update	C180179	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180179	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 6?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 6?	
2022-09-30	CDISC-5518	Update	C180179	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 6	PRO-CTCAE V1.0 - Other Symptom 6	
2022-09-30	CDISC-5518	Update	C180180	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180180	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 6 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 6 at its worst?	
2022-09-30	CDISC-5518	Update	C180180	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 6 Severity	PRO-CTCAE V1.0 - Other Symptom 6 Severity	
2022-09-30	CDISC-5518	Update	C180181	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180181	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 7?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 7?	
2022-09-30	CDISC-5518	Update	C180181	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 7	PRO-CTCAE V1.0 - Other Symptom 7	
2022-09-30	CDISC-5518	Update	C180182	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180182	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 7 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 7 at its worst?	
2022-09-30	CDISC-5518	Update	C180182	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 7 Severity	PRO-CTCAE V1.0 - Other Symptom 7 Severity	
2022-09-30	CDISC-5518	Update	C180183	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180183	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 8?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 8?	
2022-09-30	CDISC-5518	Update	C180183	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 8	PRO-CTCAE V1.0 - Other Symptom 8	
2022-09-30	CDISC-5518	Update	C180184	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180184	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 8 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 8 at its worst?	
2022-09-30	CDISC-5518	Update	C180184	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 8 Severity	PRO-CTCAE V1.0 - Other Symptom 8 Severity	
2022-09-30	CDISC-5518	Update	C180185	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180185	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 9?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 9?	
2022-09-30	CDISC-5518	Update	C180185	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 9	PRO-CTCAE V1.0 - Other Symptom 9	
2022-09-30	CDISC-5518	Update	C180186	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180186	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 9 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 9 at its worst?	
2022-09-30	CDISC-5518	Update	C180186	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 9 Severity	PRO-CTCAE V1.0 - Other Symptom 9 Severity	
2022-09-30	CDISC-5518	Update	C180187	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180187	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 10?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 10?	
2022-09-30	CDISC-5518	Update	C180187	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 10	PRO-CTCAE V1.0 - Other Symptom 10	
2022-09-30	CDISC-5518	Update	C180188	CDISC Codelist Name	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Code	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	
2022-09-30	CDISC-5518	Update	C180188	CDISC Definition	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 10 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 10 at its worst?	
2022-09-30	CDISC-5518	Update	C180188	NCI Preferred Term	PT01TC	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Code	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 10 Severity	PRO-CTCAE V1.0 - Other Symptom 10 Severity	
2022-09-30	CDISC-5518	Update	C179941	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C179941	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 test name.	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 test name.	
2022-09-30	CDISC-5518	Update	C179941	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	CDISC Questionnaire PRO-CTCAE V1.0 Version Date 4/26/2020 Test Name Terminology	CDISC Questionnaire PRO-CTCAE Version 1.0 Test Name Terminology	
2022-09-30	CDISC-5518	Update	C179941	CDISC Synonym	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Add new CDISC Synonym	- - -	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C179941	CDISC Synonym	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Remove CDISC Synonym	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	- - -	
2022-09-30	CDISC-5518	Update	C180044	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180044	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your dry mouth at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your dry mouth at its worst?	
2022-09-30	CDISC-5518	Update	C180044	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Dry Mouth Severity	PRO-CTCAE V1.0 - Dry Mouth Severity	
2022-09-30	CDISC-5518	Update	C180045	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180045	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your difficulty swallowing at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your difficulty swallowing at its worst?	
2022-09-30	CDISC-5518	Update	C180045	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Difficulty Swallowing Severity	PRO-CTCAE V1.0 - Difficulty Swallowing Severity	
2022-09-30	CDISC-5518	Update	C180046	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180046	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your mouth or throat sores at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your mouth or throat sores at their worst?	
2022-09-30	CDISC-5518	Update	C180046	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Mouth/Throat Sores Severity	PRO-CTCAE V1.0 - Mouth/Throat Sores Severity	
2022-09-30	CDISC-5518	Update	C180047	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180047	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did mouth or throat sores interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did mouth or throat sores interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180047	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Mouth/Throat Sores Interference	PRO-CTCAE V1.0 - Mouth/Throat Sores Interference	
2022-09-30	CDISC-5518	Update	C180048	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180048	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of skin cracking at the corners of your mouth at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of skin cracking at the corners of your mouth at its worst?	
2022-09-30	CDISC-5518	Update	C180048	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Cracking Corners of Mouth Severity	PRO-CTCAE V1.0 - Cracking Corners of Mouth Severity	
2022-09-30	CDISC-5518	Update	C180049	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180049	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any voice changes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any voice changes?	
2022-09-30	CDISC-5518	Update	C180049	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Voice Quality Changes Presence	PRO-CTCAE V1.0 - Voice Quality Changes Presence	
2022-09-30	CDISC-5518	Update	C180050	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180050	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hoarse voice at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hoarse voice at its worst?	
2022-09-30	CDISC-5518	Update	C180050	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hoarseness Severity	PRO-CTCAE V1.0 - Hoarseness Severity	
2022-09-30	CDISC-5518	Update	C180051	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180051	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your problems with tasting food or drink at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your problems with tasting food or drink at their worst?	
2022-09-30	CDISC-5518	Update	C180051	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Taste Changes Severity	PRO-CTCAE V1.0 - Taste Changes Severity	
2022-09-30	CDISC-5518	Update	C180052	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180052	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your decreased appetite at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your decreased appetite at its worst?	
2022-09-30	CDISC-5518	Update	C180052	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Appetite Severity	PRO-CTCAE V1.0 - Decreased Appetite Severity	
2022-09-30	CDISC-5518	Update	C180053	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180053	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did decreased appetite interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did decreased appetite interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180053	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Appetite Interference	PRO-CTCAE V1.0 - Decreased Appetite Interference	
2022-09-30	CDISC-5518	Update	C180054	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180054	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have nausea?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have nausea?	
2022-09-30	CDISC-5518	Update	C180054	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nausea Frequency	PRO-CTCAE V1.0 - Nausea Frequency	
2022-09-30	CDISC-5518	Update	C180055	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180055	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your nausea at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your nausea at its worst?	
2022-09-30	CDISC-5518	Update	C180055	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nausea Severity	PRO-CTCAE V1.0 - Nausea Severity	
2022-09-30	CDISC-5518	Update	C180056	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180056	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have vomiting?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have vomiting?	
2022-09-30	CDISC-5518	Update	C180056	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vomiting Frequency	PRO-CTCAE V1.0 - Vomiting Frequency	
2022-09-30	CDISC-5518	Update	C180057	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180057	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your vomiting at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your vomiting at its worst?	
2022-09-30	CDISC-5518	Update	C180057	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vomiting Severity	PRO-CTCAE V1.0 - Vomiting Severity	
2022-09-30	CDISC-5518	Update	C180058	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180058	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have heartburn?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have heartburn?	
2022-09-30	CDISC-5518	Update	C180058	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heartburn Frequency	PRO-CTCAE V1.0 - Heartburn Frequency	
2022-09-30	CDISC-5518	Update	C180059	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180059	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your heartburn at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your heartburn at its worst?	
2022-09-30	CDISC-5518	Update	C180059	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heartburn Severity	PRO-CTCAE V1.0 - Heartburn Severity	
2022-09-30	CDISC-5518	Update	C180060	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180060	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any increased passing of gas (flatulence)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any increased passing of gas (flatulence)?	
2022-09-30	CDISC-5518	Update	C180060	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Gas Presence	PRO-CTCAE V1.0 - Gas Presence	
2022-09-30	CDISC-5518	Update	C180061	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180061	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have bloating of the abdomen (belly)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have bloating of the abdomen (belly)?	
2022-09-30	CDISC-5518	Update	C180061	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bloating Frequency	PRO-CTCAE V1.0 - Bloating Frequency	
2022-09-30	CDISC-5518	Update	C180062	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180062	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your bloating of the abdomen (belly) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your bloating of the abdomen (belly) at its worst?	
2022-09-30	CDISC-5518	Update	C180062	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bloating Severity	PRO-CTCAE V1.0 - Bloating Severity	
2022-09-30	CDISC-5518	Update	C180063	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180063	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have hiccups?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have hiccups?	
2022-09-30	CDISC-5518	Update	C180063	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hiccups Frequency	PRO-CTCAE V1.0 - Hiccups Frequency	
2022-09-30	CDISC-5518	Update	C180064	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180064	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hiccups at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hiccups at their worst?	
2022-09-30	CDISC-5518	Update	C180064	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hiccups Severity	PRO-CTCAE V1.0 - Hiccups Severity	
2022-09-30	CDISC-5518	Update	C180065	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180065	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your constipation at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your constipation at its worst?	
2022-09-30	CDISC-5518	Update	C180065	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Constipation Severity	PRO-CTCAE V1.0 - Constipation Severity	
2022-09-30	CDISC-5518	Update	C180066	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180066	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have loose or watery stools (diarrhea/diarrhoea)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have loose or watery stools (diarrhea/diarrhoea)?	
2022-09-30	CDISC-5518	Update	C180066	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Diarrhea Frequency	PRO-CTCAE V1.0 - Diarrhea Frequency	
2022-09-30	CDISC-5518	Update	C180067	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180067	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have pain in the abdomen (belly area)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have pain in the abdomen (belly area)?	
2022-09-30	CDISC-5518	Update	C180067	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Abdominal Pain Frequency	PRO-CTCAE V1.0 - Abdominal Pain Frequency	
2022-09-30	CDISC-5518	Update	C180068	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180068	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain in the abdomen (belly area) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain in the abdomen (belly area) at its worst?	
2022-09-30	CDISC-5518	Update	C180068	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Abdominal Pain Severity	PRO-CTCAE V1.0 - Abdominal Pain Severity	
2022-09-30	CDISC-5518	Update	C180069	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180069	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did pain in the abdomen (belly area) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did pain in the abdomen (belly area) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180069	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Abdominal Pain Interference	PRO-CTCAE V1.0 - Abdominal Pain Interference	
2022-09-30	CDISC-5518	Update	C180070	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180070	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you lose control of bowel movements?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you lose control of bowel movements?	
2022-09-30	CDISC-5518	Update	C180070	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fecal Incontinence Frequency	PRO-CTCAE V1.0 - Fecal Incontinence Frequency	
2022-09-30	CDISC-5518	Update	C180071	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180071	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did loss of control of bowel movements interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did loss of control of bowel movements interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180071	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fecal Incontinence Interference	PRO-CTCAE V1.0 - Fecal Incontinence Interference	
2022-09-30	CDISC-5518	Update	C180072	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180072	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your shortness of breath at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your shortness of breath at its worst?	
2022-09-30	CDISC-5518	Update	C180072	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Shortness of Breath Severity	PRO-CTCAE V1.0 - Shortness of Breath Severity	
2022-09-30	CDISC-5518	Update	C180073	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180073	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did your shortness of breath interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did your shortness of breath interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180073	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Shortness of Breath Interference	PRO-CTCAE V1.0 - Shortness of Breath Interference	
2022-09-30	CDISC-5518	Update	C180074	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180074	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your cough at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your cough at its worst?	
2022-09-30	CDISC-5518	Update	C180074	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Cough Severity	PRO-CTCAE V1.0 - Cough Severity	
2022-09-30	CDISC-5518	Update	C180075	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180075	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did cough interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did cough interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180075	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Cough Interference	PRO-CTCAE V1.0 - Cough Interference	
2022-09-30	CDISC-5518	Update	C180076	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180076	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your wheezing (whistling noise in the chest with breathing) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your wheezing (whistling noise in the chest with breathing) at its worst?	
2022-09-30	CDISC-5518	Update	C180076	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Wheezing Severity	PRO-CTCAE V1.0 - Wheezing Severity	
2022-09-30	CDISC-5518	Update	C180077	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180077	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have arm or leg swelling?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have arm or leg swelling?	
2022-09-30	CDISC-5518	Update	C180077	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Swelling Frequency	PRO-CTCAE V1.0 - Swelling Frequency	
2022-09-30	CDISC-5518	Update	C180078	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180078	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your arm or leg swelling at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your arm or leg swelling at its worst?	
2022-09-30	CDISC-5518	Update	C180078	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Swelling Severity	PRO-CTCAE V1.0 - Swelling Severity	
2022-09-30	CDISC-5518	Update	C180079	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180079	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did arm or leg swelling interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did arm or leg swelling interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180079	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Swelling Interference	PRO-CTCAE V1.0 - Swelling Interference	
2022-09-30	CDISC-5518	Update	C180080	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180080	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel a pounding or racing heartbeat (palpitations)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel a pounding or racing heartbeat (palpitations)?	
2022-09-30	CDISC-5518	Update	C180080	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heart Palpitations Frequency	PRO-CTCAE V1.0 - Heart Palpitations Frequency	
2022-09-30	CDISC-5518	Update	C180081	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180081	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pounding or racing heartbeat (palpitations) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pounding or racing heartbeat (palpitations) at its worst?	
2022-09-30	CDISC-5518	Update	C180081	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Heart Palpitations Severity	PRO-CTCAE V1.0 - Heart Palpitations Severity	
2022-09-30	CDISC-5518	Update	C180082	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180082	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any rash?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any rash?	
2022-09-30	CDISC-5518	Update	C180082	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Rash Presence	PRO-CTCAE V1.0 - Rash Presence	
2022-09-30	CDISC-5518	Update	C180083	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180083	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your dry skin at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your dry skin at its worst?	
2022-09-30	CDISC-5518	Update	C180083	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Skin Dryness Severity	PRO-CTCAE V1.0 - Skin Dryness Severity	
2022-09-30	CDISC-5518	Update	C180084	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180084	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your acne or pimples on the face or chest at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your acne or pimples on the face or chest at its worst?	
2022-09-30	CDISC-5518	Update	C180084	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Acne Severity	PRO-CTCAE V1.0 - Acne Severity	
2022-09-30	CDISC-5518	Update	C180085	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180085	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any hair loss?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any hair loss?	
2022-09-30	CDISC-5518	Update	C180085	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hair Loss Amount	PRO-CTCAE V1.0 - Hair Loss Amount	
2022-09-30	CDISC-5518	Update	C180086	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180086	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your itchy skin at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your itchy skin at its worst?	
2022-09-30	CDISC-5518	Update	C180086	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Itching Severity	PRO-CTCAE V1.0 - Itching Severity	
2022-09-30	CDISC-5518	Update	C180087	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180087	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any hives (itchy red bumps on the skin)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any hives (itchy red bumps on the skin)?	
2022-09-30	CDISC-5518	Update	C180087	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hives Presence	PRO-CTCAE V1.0 - Hives Presence	
2022-09-30	CDISC-5518	Update	C180088	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180088	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hand-foot syndrome (a rash of the hands or feet that can cause cracking, peeling, redness or pain) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hand-foot syndrome (a rash of the hands or feet that can cause cracking, peeling, redness or pain) at its worst?	
2022-09-30	CDISC-5518	Update	C180088	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hand-Foot Syndrome Severity	PRO-CTCAE V1.0 - Hand-Foot Syndrome Severity	
2022-09-30	CDISC-5518	Update	C180089	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180089	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you lose any fingernails or toenails?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you lose any fingernails or toenails?	
2022-09-30	CDISC-5518	Update	C180089	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nail Loss Presence	PRO-CTCAE V1.0 - Nail Loss Presence	
2022-09-30	CDISC-5518	Update	C180090	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180090	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any ridges or bumps on your fingernails or toenails?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any ridges or bumps on your fingernails or toenails?	
2022-09-30	CDISC-5518	Update	C180090	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nail Ridging Presence	PRO-CTCAE V1.0 - Nail Ridging Presence	
2022-09-30	CDISC-5518	Update	C180091	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180091	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any change in the color of your fingernails or toenails?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any change in the color of your fingernails or toenails?	
2022-09-30	CDISC-5518	Update	C180091	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nail Discoloration Presence	PRO-CTCAE V1.0 - Nail Discoloration Presence	
2022-09-30	CDISC-5518	Update	C180092	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180092	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any increased skin sensitivity to sunlight?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any increased skin sensitivity to sunlight?	
2022-09-30	CDISC-5518	Update	C180092	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sensitivity to Sunlight Presence	PRO-CTCAE V1.0 - Sensitivity to Sunlight Presence	
2022-09-30	CDISC-5518	Update	C180093	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180093	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any bed sores?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any bed sores?	
2022-09-30	CDISC-5518	Update	C180093	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bed/Pressure Sores Presence	PRO-CTCAE V1.0 - Bed/Pressure Sores Presence	
2022-09-30	CDISC-5518	Update	C180094	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180094	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your skin burns from radiation at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your skin burns from radiation at their worst?	
2022-09-30	CDISC-5518	Update	C180094	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Radiation Skin Reaction Severity	PRO-CTCAE V1.0 - Radiation Skin Reaction Severity	
2022-09-30	CDISC-5518	Update	C180095	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180095	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any unusual darkening of the skin?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any unusual darkening of the skin?	
2022-09-30	CDISC-5518	Update	C180095	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Skin Darkening Presence	PRO-CTCAE V1.0 - Skin Darkening Presence	
2022-09-30	CDISC-5518	Update	C180096	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180096	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any stretch marks?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any stretch marks?	
2022-09-30	CDISC-5518	Update	C180096	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Stretch Marks Presence	PRO-CTCAE V1.0 - Stretch Marks Presence	
2022-09-30	CDISC-5518	Update	C180097	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180097	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your numbness or tingling in your hands or feet at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your numbness or tingling in your hands or feet at its worst?	
2022-09-30	CDISC-5518	Update	C180097	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Numbness & Tingling Severity	PRO-CTCAE V1.0 - Numbness & Tingling Severity	
2022-09-30	CDISC-5518	Update	C180098	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180098	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did numbness or tingling in your hands or feet interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did numbness or tingling in your hands or feet interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180098	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Numbness & Tingling Interference	PRO-CTCAE V1.0 - Numbness & Tingling Interference	
2022-09-30	CDISC-5518	Update	C180099	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180099	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your dizziness at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your dizziness at its worst?	
2022-09-30	CDISC-5518	Update	C180099	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Dizziness Severity	PRO-CTCAE V1.0 - Dizziness Severity	
2022-09-30	CDISC-5518	Update	C180100	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180100	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did dizziness interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did dizziness interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180100	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Dizziness Interference	PRO-CTCAE V1.0 - Dizziness Interference	
2022-09-30	CDISC-5518	Update	C180101	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180101	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your blurry vision at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your blurry vision at its worst?	
2022-09-30	CDISC-5518	Update	C180101	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Blurred Vision Severity	PRO-CTCAE V1.0 - Blurred Vision Severity	
2022-09-30	CDISC-5518	Update	C180102	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180102	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did blurry vision interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did blurry vision interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180102	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Blurred Vision Interference	PRO-CTCAE V1.0 - Blurred Vision Interference	
2022-09-30	CDISC-5518	Update	C180103	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180103	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any flashing lights in front of your eyes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any flashing lights in front of your eyes?	
2022-09-30	CDISC-5518	Update	C180103	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Flashing Lights in Eyes Presence	PRO-CTCAE V1.0 - Flashing Lights in Eyes Presence	
2022-09-30	CDISC-5518	Update	C180104	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180104	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any spots or lines (floaters) that drift in front of your eyes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any spots or lines (floaters) that drift in front of your eyes?	
2022-09-30	CDISC-5518	Update	C180104	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Visual Floaters Presence	PRO-CTCAE V1.0 - Visual Floaters Presence	
2022-09-30	CDISC-5518	Update	C180105	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180105	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your watery eyes (tearing) at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your watery eyes (tearing) at their worst?	
2022-09-30	CDISC-5518	Update	C180105	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Watery Eyes Severity	PRO-CTCAE V1.0 - Watery Eyes Severity	
2022-09-30	CDISC-5518	Update	C180106	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180106	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did watery eyes (tearing) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did watery eyes (tearing) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180106	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Watery Eyes Interference	PRO-CTCAE V1.0 - Watery Eyes Interference	
2022-09-30	CDISC-5518	Update	C180107	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180107	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of ringing in your ears at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of ringing in your ears at its worst?	
2022-09-30	CDISC-5518	Update	C180107	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Ringing in Ears Severity	PRO-CTCAE V1.0 - Ringing in Ears Severity	
2022-09-30	CDISC-5518	Update	C180108	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180108	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your problems with concentration at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your problems with concentration at their worst?	
2022-09-30	CDISC-5518	Update	C180108	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Concentration Problems Severity	PRO-CTCAE V1.0 - Concentration Problems Severity	
2022-09-30	CDISC-5518	Update	C180109	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180109	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did problems with concentration interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did problems with concentration interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180109	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Concentration Problems Interference	PRO-CTCAE V1.0 - Concentration Problems Interference	
2022-09-30	CDISC-5518	Update	C180110	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180110	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your problems with memory at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your problems with memory at their worst?	
2022-09-30	CDISC-5518	Update	C180110	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Memory Problems Severity	PRO-CTCAE V1.0 - Memory Problems Severity	
2022-09-30	CDISC-5518	Update	C180111	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180111	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did problems with memory interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did problems with memory interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180111	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Memory Problems Interference	PRO-CTCAE V1.0 - Memory Problems Interference	
2022-09-30	CDISC-5518	Update	C180112	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180112	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have pain?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have pain?	
2022-09-30	CDISC-5518	Update	C180112	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - General Pain Frequency	PRO-CTCAE V1.0 - General Pain Frequency	
2022-09-30	CDISC-5518	Update	C180113	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180113	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain at its worst?	
2022-09-30	CDISC-5518	Update	C180113	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - General Pain Severity	PRO-CTCAE V1.0 - General Pain Severity	
2022-09-30	CDISC-5518	Update	C180114	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180114	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did pain interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did pain interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180114	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - General Pain Interference	PRO-CTCAE V1.0 - General Pain Interference	
2022-09-30	CDISC-5518	Update	C180115	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180115	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have a headache?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have a headache?	
2022-09-30	CDISC-5518	Update	C180115	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Headache Frequency	PRO-CTCAE V1.0 - Headache Frequency	
2022-09-30	CDISC-5518	Update	C180116	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180116	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your headache at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your headache at its worst?	
2022-09-30	CDISC-5518	Update	C180116	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Headache Severity	PRO-CTCAE V1.0 - Headache Severity	
2022-09-30	CDISC-5518	Update	C180117	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180117	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did your headache interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did your headache interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180117	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Headache Interference	PRO-CTCAE V1.0 - Headache Interference	
2022-09-30	CDISC-5518	Update	C180118	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180118	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have aching muscles?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have aching muscles?	
2022-09-30	CDISC-5518	Update	C180118	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Muscle Pain Frequency	PRO-CTCAE V1.0 - Muscle Pain Frequency	
2022-09-30	CDISC-5518	Update	C180119	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180119	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your aching muscles at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your aching muscles at their worst?	
2022-09-30	CDISC-5518	Update	C180119	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Muscle Pain Severity	PRO-CTCAE V1.0 - Muscle Pain Severity	
2022-09-30	CDISC-5518	Update	C180120	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180120	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did aching muscles interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did aching muscles interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180120	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Muscle Pain Interference	PRO-CTCAE V1.0 - Muscle Pain Interference	
2022-09-30	CDISC-5518	Update	C180121	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180121	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have aching joints (such as elbows, knees, shoulders)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have aching joints (such as elbows, knees, shoulders)?	
2022-09-30	CDISC-5518	Update	C180121	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Joint Pain Frequency	PRO-CTCAE V1.0 - Joint Pain Frequency	
2022-09-30	CDISC-5518	Update	C180122	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180122	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your aching joints (such as elbows, knees, shoulders) at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your aching joints (such as elbows, knees, shoulders) at their worst?	
2022-09-30	CDISC-5518	Update	C180122	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Joint Pain Severity	PRO-CTCAE V1.0 - Joint Pain Severity	
2022-09-30	CDISC-5518	Update	C180123	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180123	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did aching joints (such as elbows, knees, shoulders) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did aching joints (such as elbows, knees, shoulders) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180123	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Joint Pain Interference	PRO-CTCAE V1.0 - Joint Pain Interference	
2022-09-30	CDISC-5518	Update	C180124	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180124	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your insomnia (including difficulty falling asleep, staying asleep, or waking up early) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your insomnia (including difficulty falling asleep, staying asleep, or waking up early) at its worst?	
2022-09-30	CDISC-5518	Update	C180124	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Insomnia Severity	PRO-CTCAE V1.0 - Insomnia Severity	
2022-09-30	CDISC-5518	Update	C180125	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180125	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did insomnia (including difficulty falling asleep, staying asleep, or waking up early) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did insomnia (including difficulty falling asleep, staying asleep, or waking up early) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180125	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Insomnia Interference	PRO-CTCAE V1.0 - Insomnia Interference	
2022-09-30	CDISC-5518	Update	C180126	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180126	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your fatigue, tiredness, or lack of energy at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your fatigue, tiredness, or lack of energy at its worst?	
2022-09-30	CDISC-5518	Update	C180126	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fatigue Severity	PRO-CTCAE V1.0 - Fatigue Severity	
2022-09-30	CDISC-5518	Update	C180127	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180127	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did fatigue, tiredness, or lack of energy interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did fatigue, tiredness, or lack of energy interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180127	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Fatigue Interference	PRO-CTCAE V1.0 - Fatigue Interference	
2022-09-30	CDISC-5518	Update	C180128	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180128	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel anxiety?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel anxiety?	
2022-09-30	CDISC-5518	Update	C180128	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Anxious Frequency	PRO-CTCAE V1.0 - Anxious Frequency	
2022-09-30	CDISC-5518	Update	C180129	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180129	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your anxiety at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your anxiety at its worst?	
2022-09-30	CDISC-5518	Update	C180129	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Anxious Severity	PRO-CTCAE V1.0 - Anxious Severity	
2022-09-30	CDISC-5518	Update	C180130	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180130	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did anxiety interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did anxiety interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180130	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Anxious Interference	PRO-CTCAE V1.0 - Anxious Interference	
2022-09-30	CDISC-5518	Update	C180131	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180131	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel that nothing could cheer you up?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel that nothing could cheer you up?	
2022-09-30	CDISC-5518	Update	C180131	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Discouraged Frequency	PRO-CTCAE V1.0 - Discouraged Frequency	
2022-09-30	CDISC-5518	Update	C180132	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180132	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your feelings that nothing could cheer you up at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your feelings that nothing could cheer you up at their worst?	
2022-09-30	CDISC-5518	Update	C180132	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Discouraged Severity	PRO-CTCAE V1.0 - Discouraged Severity	
2022-09-30	CDISC-5518	Update	C180133	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180133	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did feeling that nothing could cheer you up interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did feeling that nothing could cheer you up interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180133	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Discouraged Interference	PRO-CTCAE V1.0 - Discouraged Interference	
2022-09-30	CDISC-5518	Update	C180134	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180134	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have sad or unhappy feelings?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have sad or unhappy feelings?	
2022-09-30	CDISC-5518	Update	C180134	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sad Frequency	PRO-CTCAE V1.0 - Sad Frequency	
2022-09-30	CDISC-5518	Update	C180135	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180135	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your sad or unhappy feelings at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your sad or unhappy feelings at their worst?	
2022-09-30	CDISC-5518	Update	C180135	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sad Severity	PRO-CTCAE V1.0 - Sad Severity	
2022-09-30	CDISC-5518	Update	C180136	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180136	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did sad or unhappy feelings interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did sad or unhappy feelings interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180136	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Sad Interference	PRO-CTCAE V1.0 - Sad Interference	
2022-09-30	CDISC-5518	Update	C180137	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180137	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any irregular menstrual periods?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any irregular menstrual periods?	
2022-09-30	CDISC-5518	Update	C180137	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Irregular Menstrual Period Presence	PRO-CTCAE V1.0 - Irregular Menstrual Period Presence	
2022-09-30	CDISC-5518	Update	C180138	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180138	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you miss an expected menstrual period?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you miss an expected menstrual period?	
2022-09-30	CDISC-5518	Update	C180138	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Missed Menstrual Period Presence	PRO-CTCAE V1.0 - Missed Menstrual Period Presence	
2022-09-30	CDISC-5518	Update	C180139	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180139	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any unusual vaginal discharge?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any unusual vaginal discharge?	
2022-09-30	CDISC-5518	Update	C180139	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vaginal Discharge Amount	PRO-CTCAE V1.0 - Vaginal Discharge Amount	
2022-09-30	CDISC-5518	Update	C180140	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180140	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your vaginal dryness at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your vaginal dryness at its worst?	
2022-09-30	CDISC-5518	Update	C180140	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Vaginal Dryness Severity	PRO-CTCAE V1.0 - Vaginal Dryness Severity	
2022-09-30	CDISC-5518	Update	C180141	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180141	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain or burning with urination at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain or burning with urination at its worst?	
2022-09-30	CDISC-5518	Update	C180141	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Painful Urination Severity	PRO-CTCAE V1.0 - Painful Urination Severity	
2022-09-30	CDISC-5518	Update	C180142	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180142	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you feel an urge to urinate all of a sudden?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you feel an urge to urinate all of a sudden?	
2022-09-30	CDISC-5518	Update	C180142	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Urgency Frequency	PRO-CTCAE V1.0 - Urinary Urgency Frequency	
2022-09-30	CDISC-5518	Update	C180143	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180143	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did sudden urges to urinate interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did sudden urges to urinate interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180143	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Urgency Interference	PRO-CTCAE V1.0 - Urinary Urgency Interference	
2022-09-30	CDISC-5518	Update	C180144	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180144	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, were there times when you had to urinate frequently?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, were there times when you had to urinate frequently?	
2022-09-30	CDISC-5518	Update	C180144	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Frequency Frequency	PRO-CTCAE V1.0 - Urinary Frequency Frequency	
2022-09-30	CDISC-5518	Update	C180145	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180145	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did frequent urination interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did frequent urination interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180145	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Frequency Interference	PRO-CTCAE V1.0 - Urinary Frequency Interference	
2022-09-30	CDISC-5518	Update	C180146	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180146	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any urine color change?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any urine color change?	
2022-09-30	CDISC-5518	Update	C180146	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urine Color Change Presence	PRO-CTCAE V1.0 - Urine Color Change Presence	
2022-09-30	CDISC-5518	Update	C180147	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180147	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have loss of control of urine (leakage)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have loss of control of urine (leakage)?	
2022-09-30	CDISC-5518	Update	C180147	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Incontinence Frequency	PRO-CTCAE V1.0 - Urinary Incontinence Frequency	
2022-09-30	CDISC-5518	Update	C180148	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180148	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how much did loss of control of urine (leakage) interfere with your usual or daily activities?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how much did loss of control of urine (leakage) interfere with your usual or daily activities?	
2022-09-30	CDISC-5518	Update	C180148	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Urinary Incontinence Interference	PRO-CTCAE V1.0 - Urinary Incontinence Interference	
2022-09-30	CDISC-5518	Update	C180149	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180149	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your difficulty getting or keeping an erection at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your difficulty getting or keeping an erection at its worst?	
2022-09-30	CDISC-5518	Update	C180149	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Achieve&Maintain Erection Severity	PRO-CTCAE V1.0 - Achieve&Maintain Erection Severity	
2022-09-30	CDISC-5518	Update	C180150	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180150	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have ejaculation problems?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have ejaculation problems?	
2022-09-30	CDISC-5518	Update	C180150	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Ejaculation Frequency	PRO-CTCAE V1.0 - Ejaculation Frequency	
2022-09-30	CDISC-5518	Update	C180151	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180151	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your decreased sexual interest at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your decreased sexual interest at its worst?	
2022-09-30	CDISC-5518	Update	C180151	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Libido Severity	PRO-CTCAE V1.0 - Decreased Libido Severity	
2022-09-30	CDISC-5518	Update	C180152	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180152	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you feel that it took too long to have an orgasm or climax?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you feel that it took too long to have an orgasm or climax?	
2022-09-30	CDISC-5518	Update	C180152	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Delayed Orgasm Presence	PRO-CTCAE V1.0 - Delayed Orgasm Presence	
2022-09-30	CDISC-5518	Update	C180153	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180153	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, were you unable to have an orgasm or climax?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, were you unable to have an orgasm or climax?	
2022-09-30	CDISC-5518	Update	C180153	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Unable to Have Orgasm Presence	PRO-CTCAE V1.0 - Unable to Have Orgasm Presence	
2022-09-30	CDISC-5518	Update	C180154	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180154	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your pain during vaginal sex at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your pain during vaginal sex at its worst?	
2022-09-30	CDISC-5518	Update	C180154	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Pain w/Sexual Intercourse Severity	PRO-CTCAE V1.0 - Pain w/Sexual Intercourse Severity	
2022-09-30	CDISC-5518	Update	C180155	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180155	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your breast area enlargement or tenderness at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your breast area enlargement or tenderness at its worst?	
2022-09-30	CDISC-5518	Update	C180155	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Breast Swelling&Tenderness Severity	PRO-CTCAE V1.0 - Breast Swelling&Tenderness Severity	
2022-09-30	CDISC-5518	Update	C180156	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180156	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you bruise easily (black and blue marks)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you bruise easily (black and blue marks)?	
2022-09-30	CDISC-5518	Update	C180156	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Bruising Presence	PRO-CTCAE V1.0 - Bruising Presence	
2022-09-30	CDISC-5518	Update	C180157	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180157	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have shivering or shaking chills?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have shivering or shaking chills?	
2022-09-30	CDISC-5518	Update	C180157	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Chills Frequency	PRO-CTCAE V1.0 - Chills Frequency	
2022-09-30	CDISC-5518	Update	C180158	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180158	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your shivering or shaking chills at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your shivering or shaking chills at their worst?	
2022-09-30	CDISC-5518	Update	C180158	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Chills Severity	PRO-CTCAE V1.0 - Chills Severity	
2022-09-30	CDISC-5518	Update	C180159	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180159	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes)?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes)?	
2022-09-30	CDISC-5518	Update	C180159	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Increased Sweating Frequency	PRO-CTCAE V1.0 - Increased Sweating Frequency	
2022-09-30	CDISC-5518	Update	C180160	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180160	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes) at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your unexpected or excessive sweating during the day or nighttime (not related to hot flashes/flushes) at its worst?	
2022-09-30	CDISC-5518	Update	C180160	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Increased Sweating Severity	PRO-CTCAE V1.0 - Increased Sweating Severity	
2022-09-30	CDISC-5518	Update	C180161	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180161	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have an unexpected decrease in sweating?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have an unexpected decrease in sweating?	
2022-09-30	CDISC-5518	Update	C180161	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Decreased Sweating Presence	PRO-CTCAE V1.0 - Decreased Sweating Presence	
2022-09-30	CDISC-5518	Update	C180162	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180162	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have hot flashes/flushes?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have hot flashes/flushes?	
2022-09-30	CDISC-5518	Update	C180162	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hot Flashes Frequency	PRO-CTCAE V1.0 - Hot Flashes Frequency	
2022-09-30	CDISC-5518	Update	C180163	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180163	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your hot flashes/flushes at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your hot flashes/flushes at their worst?	
2022-09-30	CDISC-5518	Update	C180163	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Hot Flashes Severity	PRO-CTCAE V1.0 - Hot Flashes Severity	
2022-09-30	CDISC-5518	Update	C180164	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180164	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, how often did you have nosebleeds?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, how often did you have nosebleeds?	
2022-09-30	CDISC-5518	Update	C180164	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nosebleed Frequency	PRO-CTCAE V1.0 - Nosebleed Frequency	
2022-09-30	CDISC-5518	Update	C180165	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180165	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your nosebleeds at their worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your nosebleeds at their worst?	
2022-09-30	CDISC-5518	Update	C180165	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Nosebleed Severity	PRO-CTCAE V1.0 - Nosebleed Severity	
2022-09-30	CDISC-5518	Update	C180166	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180166	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, did you have any pain, swelling, or redness at a site of drug injection or IV?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, did you have any pain, swelling, or redness at a site of drug injection or IV?	
2022-09-30	CDISC-5518	Update	C180166	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Pain&Swelling at Inj Site Presence	PRO-CTCAE V1.0 - Pain&Swelling at Inj Site Presence	
2022-09-30	CDISC-5518	Update	C180167	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180167	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of your body odor at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of your body odor at its worst?	
2022-09-30	CDISC-5518	Update	C180167	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Body Odor Severity	PRO-CTCAE V1.0 - Body Odor Severity	
2022-09-30	CDISC-5518	Update	C180168	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180168	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Do you have any other symptoms that you wish to report?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Do you have any other symptoms that you wish to report?	
2022-09-30	CDISC-5518	Update	C180168	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Any Other Symptoms Reported	PRO-CTCAE V1.0 - Any Other Symptoms Reported	
2022-09-30	CDISC-5518	Update	C180169	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180169	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 1?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 1?	
2022-09-30	CDISC-5518	Update	C180169	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 1	PRO-CTCAE V1.0 - Other Symptom 1	
2022-09-30	CDISC-5518	Update	C180170	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180170	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 1 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 1 at its worst?	
2022-09-30	CDISC-5518	Update	C180170	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 1 Severity	PRO-CTCAE V1.0 - Other Symptom 1 Severity	
2022-09-30	CDISC-5518	Update	C180171	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180171	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 2?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 2?	
2022-09-30	CDISC-5518	Update	C180171	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 2	PRO-CTCAE V1.0 - Other Symptom 2	
2022-09-30	CDISC-5518	Update	C180172	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180172	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 2 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 2 at its worst?	
2022-09-30	CDISC-5518	Update	C180172	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 2 Severity	PRO-CTCAE V1.0 - Other Symptom 2 Severity	
2022-09-30	CDISC-5518	Update	C180173	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180173	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 3?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 3?	
2022-09-30	CDISC-5518	Update	C180173	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 3	PRO-CTCAE V1.0 - Other Symptom 3	
2022-09-30	CDISC-5518	Update	C180174	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180174	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 3 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 3 at its worst?	
2022-09-30	CDISC-5518	Update	C180174	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 3 Severity	PRO-CTCAE V1.0 - Other Symptom 3 Severity	
2022-09-30	CDISC-5518	Update	C180175	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180175	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 4?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 4?	
2022-09-30	CDISC-5518	Update	C180175	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 4	PRO-CTCAE V1.0 - Other Symptom 4	
2022-09-30	CDISC-5518	Update	C180176	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180176	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 4 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 4 at its worst?	
2022-09-30	CDISC-5518	Update	C180176	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 4 Severity	PRO-CTCAE V1.0 - Other Symptom 4 Severity	
2022-09-30	CDISC-5518	Update	C180177	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180177	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 5?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 5?	
2022-09-30	CDISC-5518	Update	C180177	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 5	PRO-CTCAE V1.0 - Other Symptom 5	
2022-09-30	CDISC-5518	Update	C180178	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180178	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 5 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 5 at its worst?	
2022-09-30	CDISC-5518	Update	C180178	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 5 Severity	PRO-CTCAE V1.0 - Other Symptom 5 Severity	
2022-09-30	CDISC-5518	Update	C180179	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180179	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 6?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 6?	
2022-09-30	CDISC-5518	Update	C180179	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 6	PRO-CTCAE V1.0 - Other Symptom 6	
2022-09-30	CDISC-5518	Update	C180180	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180180	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 6 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 6 at its worst?	
2022-09-30	CDISC-5518	Update	C180180	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 6 Severity	PRO-CTCAE V1.0 - Other Symptom 6 Severity	
2022-09-30	CDISC-5518	Update	C180181	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180181	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 7?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 7?	
2022-09-30	CDISC-5518	Update	C180181	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 7	PRO-CTCAE V1.0 - Other Symptom 7	
2022-09-30	CDISC-5518	Update	C180182	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180182	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 7 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 7 at its worst?	
2022-09-30	CDISC-5518	Update	C180182	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 7 Severity	PRO-CTCAE V1.0 - Other Symptom 7 Severity	
2022-09-30	CDISC-5518	Update	C180183	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180183	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 8?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 8?	
2022-09-30	CDISC-5518	Update	C180183	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 8	PRO-CTCAE V1.0 - Other Symptom 8	
2022-09-30	CDISC-5518	Update	C180184	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180184	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 8 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 8 at its worst?	
2022-09-30	CDISC-5518	Update	C180184	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 8 Severity	PRO-CTCAE V1.0 - Other Symptom 8 Severity	
2022-09-30	CDISC-5518	Update	C180185	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180185	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 9?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 9?	
2022-09-30	CDISC-5518	Update	C180185	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 9	PRO-CTCAE V1.0 - Other Symptom 9	
2022-09-30	CDISC-5518	Update	C180186	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180186	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 9 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 9 at its worst?	
2022-09-30	CDISC-5518	Update	C180186	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 9 Severity	PRO-CTCAE V1.0 - Other Symptom 9 Severity	
2022-09-30	CDISC-5518	Update	C180187	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180187	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - Other symptom term 10?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - Other symptom term 10?	
2022-09-30	CDISC-5518	Update	C180187	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 10	PRO-CTCAE V1.0 - Other Symptom 10	
2022-09-30	CDISC-5518	Update	C180188	CDISC Codelist Name	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Codelist Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire Test Name	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	
2022-09-30	CDISC-5518	Update	C180188	CDISC Definition	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update CDISC Definition	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 - In the last 7 days, what was the severity of this symptom 10 at its worst?	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 - In the last 7 days, what was the severity of this symptom 10 at its worst?	
2022-09-30	CDISC-5518	Update	C180188	NCI Preferred Term	PT01TN	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire Test Name	Update NCI Preferred Term	PRO-CTCAE V1.0 Version Date 4/26/2020 - Other Symptom 10 Severity	PRO-CTCAE V1.0 - Other Symptom 10 Severity	
2022-09-30	CDISC-5652	Update	C105167	CDISC Definition	QSCAT	Category of Questionnaire	Update CDISC Definition	The Pain Intensity (PI) questions were created by STANDARDS (Standardized Analgesic Database for Research, Discovery, and Submissions) and sponsored by ACTTION (Analgesic Clinical Trial Translations, Innovations, Opportunities, and Networks) www.acttion.org; 2012-08-07 v1.	Pain Intensity (PI) (STANDARDS, Standardized Analgesic Database for Research, Discovery, and Submissions, and sponsored by ACTTION, Analgesic Clinical Trial Translations, Innovations, Opportunities, and Networks. www.acttion.org; 2012-08-07 v1. Handbook of Pain Assessment, Third Edition [Hardcover] Chapter 2 - Self-Report Scales and Procedures for Assessing Pain in Adults: Dennis C. Turk PhD (Editor), Ronald Melzack PhD (Editor)). CDISC believes this instrument to be in the public domain, but you should perform your own assessment.	
2022-09-30	CDISC-5652	Update	C105168	CDISC Definition	QSCAT	Category of Questionnaire	Update CDISC Definition	The Pain Relief (PR) questions were created by STANDARDS (Standardized Analgesic Database for Research, Discovery, and Submissions) and sponsored by ACTTION (Analgesic Clinical Trial Translations, Innovations, Opportunities, and Networks) www.acttion.org; 2012-08-07 v1.	Pain Relief (PR) (STANDARDS, Standardized Analgesic Database for Research, Discovery, and Submissions, and sponsored by ACTTION, Analgesic Clinical Trial Translations, Innovations, Opportunities, and Networks. www.acttion.org; 2012-08-07 v1. Handbook of Pain Assessment, Third Edition [Hardcover] Chapter 2 - Self-Report Scales and Procedures for Assessing Pain in Adults: Dennis C. Turk PhD (Editor), Ronald Melzack PhD (Editor)). CDISC believes this instrument to be in the public domain, but you should perform your own assessment.	
2022-09-30	CDISC-5600	Update	C122373	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM01	
2022-09-30	CDISC-5600	Update	C122373	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM01	- - -	
2022-09-30	CDISC-5600	Update	C122374	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM02	
2022-09-30	CDISC-5600	Update	C122374	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM02	- - -	
2022-09-30	CDISC-5600	Update	C122375	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM03	
2022-09-30	CDISC-5600	Update	C122375	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM03	- - -	
2022-09-30	CDISC-5600	Update	C122376	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM04	
2022-09-30	CDISC-5600	Update	C122376	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM04	- - -	
2022-09-30	CDISC-5600	Update	C122377	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM05	
2022-09-30	CDISC-5600	Update	C122377	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM05	- - -	
2022-09-30	CDISC-5600	Update	C122378	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM06	
2022-09-30	CDISC-5600	Update	C122378	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM06	- - -	
2022-09-30	CDISC-5600	Update	C122379	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM07	
2022-09-30	CDISC-5600	Update	C122379	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM07	- - -	
2022-09-30	CDISC-5600	Update	C122380	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM08	
2022-09-30	CDISC-5600	Update	C122380	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM08	- - -	
2022-09-30	CDISC-5600	Update	C122381	CDISC Synonym	QSCAT	Category of Questionnaire	Add new CDISC Synonym	- - -	HM09	
2022-09-30	CDISC-5600	Update	C122381	CDISC Synonym	QSCAT	Category of Questionnaire	Remove CDISC Synonym	HAEM09	- - -	
2022-09-30	CDISC-5518	Update	C179975	CDISC Submission Value	QSCAT	Category of Questionnaire	Update CDISC Submission Value	PRO-CTCAE V1.0 VERSION DATE 4/26/2020	PRO-CTCAE V1.0	
2022-09-30	CDISC-5518	Update	C179975	NCI Preferred Term	QSCAT	Category of Questionnaire	Update NCI Preferred Term	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Version Date 4/26/2020 Questionnaire	Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events Item Library Version 1.0 Questionnaire	
2022-09-30	CDISC-5615	Update	C111526	NCI Preferred Term	SDS01TC	Sheehan Disability Scale Questionnaire Test Code	Update NCI Preferred Term	SDS01-Days Underproductive	SDS - Days Underproductive	
2022-09-30	CDISC-5615	Update	C111526	NCI Preferred Term	SDS01TN	Sheehan Disability Scale Questionnaire Test Name	Update NCI Preferred Term	SDS01-Days Underproductive	SDS - Days Underproductive	
2022-09-30	CDISC-5753	Update	C160924	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C160924	CDISC Synonym	SDTMIGRS	SDTMIG Version Response	Add new CDISC Synonym	- - -	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C160924	CDISC Synonym	SDTMIGRS	SDTMIG Version Response	Remove CDISC Synonym	SDTM IG Version Response	- - -	
2022-09-30	CDISC-5753	Update	C161432	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C161433	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C161434	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C161435	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C161436	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C161437	CDISC Codelist Name	SDTMIGRS	SDTMIG Version Response	Update CDISC Codelist Name	SDTM IG Version Response	SDTMIG Version Response	
2022-09-30	CDISC-5753	Update	C119550	CDISC Synonym	SPECTYPE	Specimen Type	Add new CDISC Synonym	- - -	Umbilical Cord Serum	
2022-09-30	CDISC-5753	Update	C112038	CDISC Definition	TSPARM	Trial Summary Parameter Test Name	Update CDISC Definition	The condition, disease or disorder that the clinical trial is intended to investigate or address.	The textual representation of the condition, disease or disorder that the clinical trial is intended to investigate or address.	
2022-09-30	CDISC-5753	Update	C112038	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Trial Disease/Condition Indication Description	
2022-09-30	N/A	Update	C127797	NCI Preferred Term	TSPARM	Trial Summary Parameter Test Name	Update NCI Preferred Term	PubMed Identifier for Citation Used in Study	PubMed Unique Identifier	
2022-09-30	CDISC-5753	Update	C142175	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Study Type Classification	
2022-09-30	CDISC-5753	Update	C156604	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	SDTMIG Version	
2022-09-30	CDISC-5753	Update	C48281	CDISC Definition	TSPARM	Trial Summary Parameter Test Name	Update CDISC Definition	Any defined stage in the lifecycle of a clinical trial.	A step in the clinical research and development of a therapy from initial clinical trials to post-approval studies. NOTE: Clinical trials are generally categorized into four (sometimes five) phases. A therapeutic intervention may be evaluated in two or more phases simultaneously in different trials, and some trials may overlap two different phases. [21 CFR section 312.21; After ICH Topic E8 NOTE FOR GUIDANCE ON GENERAL CONSIDERATIONS FOR CLINICAL TRIALS, CPMP/ICH/291/95 March 1998]	
2022-09-30	CDISC-5753	Update	C48281	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Trial Phase	
2022-09-30	CDISC-5753	Update	C49802	CDISC Definition	TSPARM	Trial Summary Parameter Test Name	Update CDISC Definition	The name of a clinical trial. (NCI)	The sponsor-defined name of the clinical study.	
2022-09-30	CDISC-5753	Update	C49802	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Official Study Title	
2022-09-30	CDISC-5753	Update	C49802	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Study Title	
2022-09-30	CDISC-5753	Update	C85826	CDISC Definition	TSPARM	Trial Summary Parameter Test Name	Update CDISC Definition	The principal purpose of the trial.	A principle objective of the study.	
2022-09-30	CDISC-5753	Update	C85826	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Study Primary Objective	
2022-09-30	CDISC-5753	Update	C85827	CDISC Definition	TSPARM	Trial Summary Parameter Test Name	Update CDISC Definition	The auxiliary purpose of the trial.	An auxiliary objective of the study.	
2022-09-30	CDISC-5753	Update	C85827	CDISC Synonym	TSPARM	Trial Summary Parameter Test Name	Add new CDISC Synonym	- - -	Study Secondary Objective	
2022-09-30	CDISC-5753	Update	C112038	CDISC Definition	TSPARMCD	Trial Summary Parameter Test Code	Update CDISC Definition	The condition, disease or disorder that the clinical trial is intended to investigate or address.	The textual representation of the condition, disease or disorder that the clinical trial is intended to investigate or address.	
2022-09-30	CDISC-5753	Update	C112038	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Trial Disease/Condition Indication Description	
2022-09-30	N/A	Update	C127797	NCI Preferred Term	TSPARMCD	Trial Summary Parameter Test Code	Update NCI Preferred Term	PubMed Identifier for Citation Used in Study	PubMed Unique Identifier	
2022-09-30	CDISC-5753	Update	C142175	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Study Type Classification	
2022-09-30	CDISC-5753	Update	C156604	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	SDTMIG Version	
2022-09-30	CDISC-5753	Update	C48281	CDISC Definition	TSPARMCD	Trial Summary Parameter Test Code	Update CDISC Definition	Any defined stage in the lifecycle of a clinical trial.	A step in the clinical research and development of a therapy from initial clinical trials to post-approval studies. NOTE: Clinical trials are generally categorized into four (sometimes five) phases. A therapeutic intervention may be evaluated in two or more phases simultaneously in different trials, and some trials may overlap two different phases. [21 CFR section 312.21; After ICH Topic E8 NOTE FOR GUIDANCE ON GENERAL CONSIDERATIONS FOR CLINICAL TRIALS, CPMP/ICH/291/95 March 1998]	
2022-09-30	CDISC-5753	Update	C48281	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Trial Phase	
2022-09-30	CDISC-5753	Update	C49802	CDISC Definition	TSPARMCD	Trial Summary Parameter Test Code	Update CDISC Definition	The name of a clinical trial. (NCI)	The sponsor-defined name of the clinical study.	
2022-09-30	CDISC-5753	Update	C49802	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Official Study Title	
2022-09-30	CDISC-5753	Update	C49802	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Study Title	
2022-09-30	CDISC-5753	Update	C85826	CDISC Definition	TSPARMCD	Trial Summary Parameter Test Code	Update CDISC Definition	The principal purpose of the trial.	A principle objective of the study.	
2022-09-30	CDISC-5753	Update	C85826	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Study Primary Objective	
2022-09-30	CDISC-5753	Update	C85827	CDISC Definition	TSPARMCD	Trial Summary Parameter Test Code	Update CDISC Definition	The auxiliary purpose of the trial.	An auxiliary objective of the study.	
2022-09-30	CDISC-5753	Update	C85827	CDISC Synonym	TSPARMCD	Trial Summary Parameter Test Code	Add new CDISC Synonym	- - -	Study Secondary Objective	
2022-09-30	CDISC-5217	Update	C105498	CDISC Synonym	UNIT	Unit	Add new CDISC Synonym	- - -	umol/(L*s)	
2022-09-30	CDISC-5217	Update	C105498	CDISC Synonym	UNIT	Unit	Add new CDISC Synonym	- - -	umol/(s*L)	
2022-09-30	CDISC-5217	Update	C105498	CDISC Synonym	UNIT	Unit	Add new CDISC Synonym	- - -	umol/s/L	
2022-09-30	CDISC-5753	Update	C132472	CDISC Synonym	UNIT	Unit	Add new CDISC Synonym	- - -	Per 200 High Powered Fields	
2022-09-30	CDISC-5753	Update	C132475	CDISC Synonym	UNIT	Unit	Add new CDISC Synonym	- - -	Per 40 High Powered Fields