Safety Rates Drug Report: adverse events in 2016 Q3 - FDA prescription drugs adverse events in an open, searchable, online, public database

Drug Injury Quarter

Person who experienced the adverse event (patient)

Event ID	CASEID	CASEVERSION	I F COD	EVENT DT	MFR DT	INIT FDA DT	FDA DT	REPT COD	AUTH NUM	MFR NUM	MFR SNDR	LIT REF	AGE	AGE COD	AGE GRP	GNDR COD	E SUB	WT	WT COD	REPT DT	TO MFR	OCCP COD	REPORTER COUNTRY	OCCR COUNTRY
116854722	11685472	2	F	20150730	20160705	20151030	20160718	EXP		FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-072506	BRISTOL MYERS SQUIBB		89.83	YR		M	Y	0.00000		20160718		CN	FR	FR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	CUM DOSE CHR	CUM DOSE UNIT	DECHAL	RECHAL	LOT NUM	EXP DT	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
116854722	11685472	1	PS	COUMADINE	WARFARIN SODIUM	1	Oral	2.5 MG, UNK			U				9218	2.5	MG	TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
116854722	11685472	1	Product used for unknown indication

Outcome of event

Reactions reported

Event ID	CASEID	PT
116854722	11685472	Anaemia
116854722	11685472	Hypotension
116854722	11685472	International normalised ratio increased
116854722	11685472	Overdose
116854722	11685472	Pneumonia aspiration
116854722	11685472	Renal failure
116854722	11685472	Transfusion

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

no results found

no results found

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
116854722	11685472	1	20140217	20150811	0