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
74621334	7462133	4	F	20100609	20160822	20100709	20160822	EXP		PT-BRISTOL-MYERS SQUIBB COMPANY-14837330	BRISTOL MYERS SQUIBB		27.37	YR		F	Y	49.00000	KG	20160822		MD	PT	PT

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
74621334	7462133	1	PS	ATAZANAVIR SULFATE	ATAZANAVIR SULFATE	1	Oral	300 MG, QD	21567	300	MG	QD
74621334	7462133	2	SS	RITONAVIR.	RITONAVIR	1	Oral	100 MG, QD	0	100	MG	QD
74621334	7462133	3	SS	EMTRICITABINE W/TENOFOVIR DISOPROXIL FUMARATE	EMTRICITABINETENOFOVIR DISOPROXIL	1	Oral	1 UNK, UNK	0	1	DF	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
74621334	7462133	1	HIV infection
74621334	7462133	2	HIV infection
74621334	7462133	3	HIV infection

Outcome of event

Event ID	CASEID	OUTC COD
74621334	7462133	OT

Reactions reported

Event ID	CASEID	PT
74621334	7462133	Caesarean section
74621334	7462133	Live birth
74621334	7462133	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
74621334	7462133	1	20090120
74621334	7462133	2	20090120
74621334	7462133	3	20090120