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
123996612	12399661	2	F	20151101	20160623	20160524	20160701	EXP		ES-GILEAD-2016-0214120	GILEAD		0.00			F	Y	0.00000		20160701		OT	ES	ES

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
123996612	12399661	1	PS	EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE	EMTRICITABINETENOFOVIR DISOPROXIL	1	Oral	100 MG, QD	U	21752	100	MG	TABLET	QD
123996612	12399661	2	SS	DARUNAVIR	DARUNAVIR	1	Oral	800 MG, QD	U	0	800	MG		QD
123996612	12399661	3	SS	RITONAVIR.	RITONAVIR	1	Oral	100 MG, QD	U	0	100	MG		QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
123996612	12399661	1	HIV infection
123996612	12399661	2	HIV infection
123996612	12399661	3	HIV infection

Outcome of event

Event ID	CASEID	OUTC COD
123996612	12399661	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
123996612	12399661		Abortion spontaneous

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
123996612	12399661	1	20130830	20130830
123996612	12399661	2	20130830	20130830
123996612	12399661	3	20130830	20130830