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
118948182	11894818	2	F		20160826	20160107	20160826	EXP		GB-BRISTOL-MYERS SQUIBB COMPANY-BMS-2004-000012	BRISTOL MYERS SQUIBB		33.00	YR		F	Y	82.00000	KG	20160826		OT	GB	GB

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
118948182	11894818	1	PS	VIDEX	DIDANOSINE	1	Oral	400 MG, QD	20156	400	MG	QD
118948182	11894818	2	SS	NEVIRAPINE.	NEVIRAPINE	1	Oral	400 MG, QD	0	400	MG	QD
118948182	11894818	3	SS	RETROVIR	ZIDOVUDINE	1	Oral	500 MG, QD	0	500	MG	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
118948182	11894818	1	HIV infection
118948182	11894818	2	HIV infection
118948182	11894818	3	HIV infection

Outcome of event

Event ID	CASEID	OUTC COD
118948182	11894818	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
118948182	11894818		Pregnancy
118948182	11894818		Stillbirth

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
118948182	11894818	1	20040122
118948182	11894818	2	20000122
118948182	11894818	3	200001