A	FDA	C54596	Type of Reporter ICSR Terminology	C16960	PATIENT		LAY USER/PATIENT
A	FDA	C54596	Type of Reporter ICSR Terminology	C17649	OTHER		Other
A	FDA	C88088	Observation ICSR Terminology	C17649	OTHER		Other
A	FDA	C88088	Observation ICSR Terminology	C17998	UNKNOWN		Unknown
A	FDA	C54447	Individual Case Safety Report Terminology	C102430	Vaccine Provider		
A	FDA	C54447	Individual Case Safety Report Terminology	C102431	Funding Source for Product		
A	FDA	C54447	Individual Case Safety Report Terminology	C102432	Private Funds		
A	FDA	C54447	Individual Case Safety Report Terminology	C102433	Military Funds		
A	FDA	C54447	Individual Case Safety Report Terminology	C102434	Public Funds		
A	FDA	C54447	Individual Case Safety Report Terminology	C102436	Required emergency room/doctor visit		
A	FDA	C54447	Individual Case Safety Report Terminology	C102443	Number of Hospitalization Days		
A	FDA	C54447	Individual Case Safety Report Terminology	C102450	Resulted in prolongation of hospitalization		
A	FDA	C54447	Individual Case Safety Report Terminology	C102451	Resulted in permanent disability		
A	FDA	C54447	Individual Case Safety Report Terminology	C102467	Other vaccinations given within 4 weeks		
A	FDA	C54447	Individual Case Safety Report Terminology	C102468	Illness at time of vaccination		
A	FDA	C54447	Individual Case Safety Report Terminology	C102469	Number of Siblings		
A	FDA	C54447	Individual Case Safety Report Terminology	C102470	Adverse event following prior vaccination		
A	FDA	C54447	Individual Case Safety Report Terminology	C42709	Parent		
A	FDA	C54447	Individual Case Safety Report Terminology	C49498	Patient recovered		
A	FDA	C54447	Individual Case Safety Report Terminology	C84266	Life-threatening adverse experience		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C102436	Required emergency room/doctor visit		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C102443	Number of Hospitalization Days		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C102450	Resulted in prolongation of hospitalization		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C102451	Resulted in permanent disability		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C49498	Patient recovered		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C50414	Required hospitalization		
A	FDA	C54583	Adverse Event Outcome ICSR Terminology	C84266	Life-threatening adverse experience		
A	FDA	C54596	Type of Reporter ICSR Terminology	C102430	Vaccine Provider		
A	FDA	C54596	Type of Reporter ICSR Terminology	C42709	Parent		
A	FDA	C88088	Observation ICSR Terminology	C102431	Funding Source for Product		
A	FDA	C88088	Observation ICSR Terminology	C102432	Private Funds		
A	FDA	C88088	Observation ICSR Terminology	C102433	Military Funds		
A	FDA	C88088	Observation ICSR Terminology	C102434	Public Funds		
A	FDA	C88088	Observation ICSR Terminology	C102467	Other vaccinations given within 4 weeks		
A	FDA	C88088	Observation ICSR Terminology	C102468	Illness at time of vaccination		
A	FDA	C88088	Observation ICSR Terminology	C102469	Number of Siblings		
A	FDA	C88088	Observation ICSR Terminology	C102470	Adverse event following prior vaccination		
A	FDA	C88088	Observation ICSR Terminology	C16576	F		
A	FDA	C88088	Observation ICSR Terminology	C20197	M		
A	FDA	C88088	Observation ICSR Terminology	C28421	SEX		
C	FDA	C54447	Individual Case Safety Report Terminology	C25392	MANUFACTURER		
C	FDA	C54447	Individual Case Safety Report Terminology	C53567	USER FACILITY		
C	FDA	C54447	Individual Case Safety Report Terminology	C53609	RECALL		
C	FDA	C54447	Individual Case Safety Report Terminology	C53617	IMPORTER		
C	FDA	C54447	Individual Case Safety Report Terminology	C54068	Over-the-Counter Product		
C	FDA	C54447	Individual Case Safety Report Terminology	C54696	Combination Product		
C	FDA	C54447	Individual Case Safety Report Terminology	C93539	Reporter Confidentiality Disclosure Indicator		
C	FDA	C54447	Individual Case Safety Report Terminology	C95017	FEMALE PHYSIOLOGICAL STATUS		
C	FDA	C54447	Individual Case Safety Report Terminology	C99176	Pre-1938 Product		
C	FDA	C54587	Report Source ICSR Terminology	C53567	USER FACILITY		
C	FDA	C54594	Type of Remedial Action ICSR Terminology	C53609	RECALL		
C	FDA	C54596	Type of Reporter ICSR Terminology	C25392	MANUFACTURER		
C	FDA	C54596	Type of Reporter ICSR Terminology	C53567	USER FACILITY		
C	FDA	C54596	Type of Reporter ICSR Terminology	C53617	IMPORTER		
C	FDA	C88088	Observation ICSR Terminology	C93539	Reporter Confidentiality Disclosure Indicator		
C	FDA	C88088	Observation ICSR Terminology	C95017	FEMALE PHYSIOLOGICAL STATUS		
C	FDA	C99174	Product Characteristic ICSR Terminology	C54068	Over-the-Counter Product		
C	FDA	C99174	Product Characteristic ICSR Terminology	C54696	Combination Product		
C	FDA	C99174	Product Characteristic ICSR Terminology	C99176	Pre-1938 Product		
C	FDA	C54447	Individual Case Safety Report Terminology	C16576	F		
C	FDA	C54447	Individual Case Safety Report Terminology	C20197	M		
C	FDA	C54447	Individual Case Safety Report Terminology	C50414	Required hospitalization