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
126811821	12681182	1	I	201606	20160815	20160824	20160824	EXP		CN-SA-2016SA149804	AVENTIS		75.00	YR	E	M	Y	0.00000		20160824		CN	CN	CN

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
126811821	12681182	1	PS	PLAVIX	CLOPIDOGREL BISULFATE	1	Oral	5A572	20839	1	DF	FILM-COATED TABLET	QD
126811821	12681182	2	SS	PLAVIX	CLOPIDOGREL BISULFATE	1	Oral	5A708	20839	1	DF	FILM-COATED TABLET	QD
126811821	12681182	3	SS	PLAVIX	CLOPIDOGREL BISULFATE	1	Oral	5A674	20839	1	DF	FILM-COATED TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126811821	12681182	1	Stent placement
126811821	12681182	2	Stent placement
126811821	12681182	3	Stent placement

Outcome of event

Event ID	CASEID	OUTC COD
126811821	12681182	HO
126811821	12681182	DE

Reactions reported

Event ID	CASEID	PT
126811821	12681182	Angina pectoris
126811821	12681182	Death
126811821	12681182	Suspected counterfeit product

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
126811821	12681182	1	2016	20160630
126811821	12681182	2	2016	20160630
126811821	12681182	3	2016	20160630