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
117037222	11703722	2	F	20080920	20160131	20151106	20160701	EXP		UG-BRISTOL-MYERS SQUIBB COMPANY-14902597	BRISTOL MYERS SQUIBB		35.00	YR		F	Y	0.00000		20160701		OT	UG	UG

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	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
117037222	11703722	1	PS	EFAVIRENZ	EFAVIRENZ	1	Oral	600 MG, QD	267600	MG	Y	20972	600	MG	QD
117037222	11703722	2	SS	VIDEX	DIDANOSINE	1	Oral	250 MG, QD				0	250	MG	QD
117037222	11703722	3	SS	VIRAMUNE	NEVIRAPINE	1	Oral	200 MG, QD	3000	MG		0	200	MG	QD
117037222	11703722	4	SS	VIRAMUNE	NEVIRAPINE	1	Oral	400 MG, QD	3000	MG		0	400	MG	QD
117037222	11703722	5	SS	ALUVIA	LOPINAVIRRITONAVIR	1	Oral	1500 MG, QD				0	1500	MG	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
117037222	11703722	1	Antiretroviral therapy
117037222	11703722	2	Antiretroviral therapy
117037222	11703722	3	Antiretroviral therapy
117037222	11703722	5	Antiretroviral therapy

Outcome of event

Event ID	CASEID	OUTC COD
117037222	11703722	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
117037222	11703722		Abortion induced
117037222	11703722		Maternal exposure during pregnancy

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
117037222	11703722	1	20070503	20080721
117037222	11703722	2	20070503
117037222	11703722	3	20080721	20080804
117037222	11703722	4	20080804
117037222	11703722	5	20070503