Safety Rates Drug Report: adverse events in 2006 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
5002271	6032375	F	1	5002271-X	20000227	20060502	20060512	EXP	GXKR2006DE01734	SANDOZ INC., BROOMFIELD SITE	85	YR	F	N	77	KG	20060510	MD				GERMANY

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
5002271	1007286233	PS	MONO-EMBOLEX 8000 IE (CERTOPARIN SODIUIM)8000IU	2	SUBCUTANEOUS	8000 IU, BID, SUBCUTANEOUS	Y	D	40118
5002271	1007318824	SS	ACETYLSALICYLIC ACID (NGX) (ACETYLSALICYLIC ACID) 100 MG	2		1 DF, QD	D	D
5002271	1007318825	C	AMLOCARD 10 (AMLODIPINE BESILATE)	2
5002271	1007318826	C	COAPROVEL 300/12.5 (HYDROCHLOROTHIAZIDE, IRBESARTAN)	2
5002271	1007318827	C	PENTALONG 50 (PENTAERITHRITYL TETRANITRATE)	2
5002271	1007318828	C	TORACARD 10 (TORASEMIDE)	2
5002271	1007318829	C	BISOPROLOL 10 (BISOPROLOL)	2

Indications of drugs used

Event ID	DRUG SEQ	INDI PT
5002271	1007286233	THROMBOSIS

Outcome of event

Event ID	OUTC COD
5002271	HO

Reactions reported

Event ID	PT
5002271	COMPARTMENT SYNDROME
5002271	HAEMATOMA

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
5002271	1007286233	20060220	20060228
5002271	1007318824		20060221