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
5002792	6032791	F	2	5002792-X	20060201	20060503	20060512	EXP	2006-03-2011	SCHERING-PLOUGH CORPORATION	81	YR	M	N			20060503	MD				FRANCE

Drug(s) used by person

Event ID	DRUG SEQ	ROLE COD	DRUGNAME	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM
5002792	1007288740	PS	CLARITIN	1	ORAL	10 MG QD ORAL	Y	D	19658
5002792	1007323283	SS	PRAVASTATIN	1	ORAL	40 MG QD ORAL	D	D
5002792	1007323284	C	VENOFER (FERRIC HYDROXIDE SACCHAROSE)	2
5002792	1007323285	C	NEORECORMON (EPOETINE BETA)	2
5002792	1007323288	SS	CALCIUM CARBONATE ORAL SUSPENSION	2	ORAL	1.54 G QD ORAL	D	D
5002792	1007323289	SS	SPECIAFOLDINE TABLETS	2	ORAL	5 MG QD ORAL	Y	D
5002792	1007323290	C	1-ALPHA-HYDROXYCHOLECALCIFEROL BIW	2
5002792	1007323291	C	SERESTA	2
5002792	1007323292	SS	LASIX	1	ORAL	500MG BID ORAL	D	D
5002792	1007323294	SS	OMEPRAZOLE	1	ORAL	10 MG QD ORAL	Y	D

Indications of drugs used

no results found

no results found

Outcome of event

Event ID	OUTC COD
5002792	HO

Reactions reported

Event ID	PT
5002792	THROMBOCYTOPENIA

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

Therapies reported

Event ID	DRUG SEQ	END DT
5002792	1007288740	20060201
5002792	1007323289	20060208
5002792	1007323294	20060201