Safety Rates Drug Report: adverse events in 2005 Q1 - 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
4627344	5774412	I		4627344-2		20050315	20050331	EXP	S05-SWE-01177-01	FOREST LABORATORIES INC.	60	YR	M	N			20050329		20041216

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
4627344	1005848164	PS	CITALOPRAM HYDROBROMIDE	1	ORAL	20 MG QD; PO	D	D	20822
4627344	1005871351	SS	VOLTAREN	1	ORAL	50 MG TID; PO	D	D
4627344	1005871353	SS	ASPIRIN	1	ORAL	75 MG QD; PO	D	D
4627344	1005871354	C	NEURONTIN	1
4627344	1005871355	C	SELOKEN ZOC (METOPROLOL SUCCINATE)	2
4627344	1005871356	C	RAMIPRIL	1
4627344	1005871357	C	SALURES-K	2
4627344	1005871358	C	SUSCARD (GLYCERYL TRINITRATE)	2
4627344	1005871359	C	ZOCORD (SIMVASTATIN)	2
4627344	1005871360	C	NORVASC	1
4627344	1005871362	C	IMDUR	1

Indications of drugs used

Outcome of event

Event ID	OUTC COD
4627344	DE

Reactions reported

Event ID	PT
4627344	ARTERIOSCLEROSIS
4627344	CEREBRAL HAEMORRHAGE
4627344	CHEST PAIN
4627344	DRUG INTERACTION
4627344	DUODENAL ULCER PERFORATION
4627344	GASTROINTESTINAL HAEMORRHAGE
4627344	POOR PERIPHERAL CIRCULATION

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

Therapies reported

Event ID	DRUG SEQ	START DT	END DT	DUR	DUR COD
4627344	1005871351	20040501	20041215
4627344	1005871353	19900101	20041215