Safety Rates Drug Report: adverse events in 2004 Q2 - FDA prescription drugs adverse events in an open, searchable, online, public database

Drug Injury Quarter

Person who experienced the adverse event (patient)

Event ID	CASE	I F COD	FOLL SEQ	IMAGE	EVENT DT	MFR DT	FDA DT	REPT COD	MFR NUM	MFR SNDR	AGE	AGE COD	GNDR COD	E SUB	WT	WT COD	REPT DT	OCCP COD	DEATH DT	TO MFR	CONFID	REPORTER COUNTRY
4415389	4196471	I		4415389-7	20030101	20031014	20040630	PER	2003037009	WWS PFIZER INC	14	YR	F	N	45.9	KG	20040617	PH

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
4415389	1005076680	PS	ZOLOFT	1	ORAL	150 MG (DAILY), ORAL	N	D	19839
4415389	1005144370	C	EFAVIRENZ (EFAVIRENZ)	2	ORAL	600 MG (DAILY), ORAL	Y	D
4415389	1005144371	C	TOCOPHEROL CONCENTRATE CAP	1
4415389	1005144372	C	STAVUDINE (STAVUDINE)	2
4415389	1005144373	C	ZALCITABINE (ZALCITABINE)	2
4415389	1005144375	C	AMPRENAVIR (AMPRENAVIR)	2
4415389	1005144376	C	TENOFOVIR DISOPROXIL FUMARATE (TENOFOVIR DISOPROXIL FUMARATE)	2
4415389	1005144377	C	LAMIVUDINE (LAMIVUDINE)	2
4415389	1005144378	C	ABACAVIR SULFATE (ABACAVIR SULFATE)	2
4415389	1005144380	C	MULTIVITAMIN	1

Indications of drugs used

Outcome of event

Event ID	OUTC COD
4415389	OT

Reactions reported

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID	RPSR COD
4415389	HP

Therapies reported

Event ID	DRUG SEQ	START DT	END DT	DUR	DUR COD
4415389	1005076680		20030830
4415389	1005144370	20030701	20030902