Safety Rates Drug Report: adverse events in 2004 Q4 - 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
4542785	4124245	F		4542785-X	20030901	20040405	20041231	EXP	PHHO2004JP05140	NOVARTIS PHARMACEUTICALS CORP.	77	YR	M	Y			20041230	MD

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM
4542785	1005547035	PS	DIOVAN	1	ORAL
4542785	1005547036	C	MEVALOTIN	2	ORAL	10 MG,
4542785	1005547037	C	ASPIRIN	1	ORAL	100 MG,
4542785	1005547038	C	DORNER	2	ORAL	60 UG,
4542785	1005547039	C	RENIVACE	2	ORAL	10 MG,
4542785	1005547040	C	FAMOTIDINE	1	ORAL	10 MG,

Indications of drugs used

Event ID	DRUG SEQ	INDI PT
4542785	1005547035	HYPERTENSION
4542785	1005547036	HYPERCHOLESTEROLAEMIA
4542785	1005547037	ATHEROSCLEROSIS OBLITERANS
4542785	1005547038	ATHEROSCLEROSIS OBLITERANS
4542785	1005547039	HYPERTENSION
4542785	1005547040	GASTRITIS

Outcome of event

Event ID	OUTC COD
4542785	HO

Reactions reported

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

Event ID	RPSR COD
4542785	HP

Therapies reported

Event ID	DRUG SEQ	START DT	END DT	DUR	DUR COD
4542785	1005547035	20021111	20030901	295	DAY
4542785	1005547036	20020422	20031209	597	DAY
4542785	1005547037	20020422	20031209	597	DAY
4542785	1005547038	20020422	20030901	498	DAY
4542785	1005547039	20020422	20030901	498	DAY
4542785	1005547040	20020422	20031209	597	DAY