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
118093512	11809351	2	F	20060116	20160824	20151207	20160824	EXP		BW-BRISTOL-MYERS SQUIBB COMPANY-13604434	BRISTOL MYERS SQUIBB		33.00	YR		F	Y	0.00000		20160824		CN	BW	BW

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
118093512	11809351	1	PS	EFAVIRENZ	EFAVIRENZ	1	Oral	600 MG, QD	148200	MG	Y	20972	600	MG	QD
118093512	11809351	2	C	VIDEX	DIDANOSINE	1	Oral	300 MG, QD				0	300	MG	QD
118093512	11809351	3	C	VIRACEPT	NELFINAVIR MESYLATE	1	Oral	2500 MG, QD				0	2500	MG	QD
118093512	11809351	4	C	RETROVIR	ZIDOVUDINE	1	Oral	600 MG, QD				0	600	MG	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
118093512	11809351	1	Product used for unknown indication
118093512	11809351	2	Product used for unknown indication
118093512	11809351	3	Product used for unknown indication
118093512	11809351	4	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
118093512	11809351	OT

Reactions reported

Event ID	CASEID	PT
118093512	11809351	Caesarean section
118093512	11809351	Pregnancy
118093512	11809351	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	END DT
118093512	11809351	1	20041007	20050610
118093512	11809351	2	20040901
118093512	11809351	3	20050610
118093512	11809351	4	20040901