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
116295663	11629566	3	F	20150217	20160905	20151014	20160908	EXP		ZA-009507513-1510ZAF006032	MERCK		66.00	YR		M	Y	60.10000	KG	20160908		MD	ZA	ZA

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	RECHAL	LOT NUM	EXP DT	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
116295663	11629566	1	SS	EFAVIRENZ (+) EMTRICITABINE (+) TENOFOVIR DISOPROXIL FUMARATE	EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE	1	Oral	1 DF, QD 600 MG/200 MG/300 MG							0	1	DF	TABLET	QD
116295663	11629566	2	PS	FUROSEMIDE.	FUROSEMIDE	1	Oral	40 MG, BID							70017	40	MG	TABLET	BID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
116295663	11629566	1	HIV infection
116295663	11629566	2	Diuretic therapy

Outcome of event

Event ID	CASEID	OUTC COD
116295663	11629566	HO
116295663	11629566	DE

Reactions reported

Event ID	CASEID	PT
116295663	11629566	Acute kidney injury
116295663	11629566	Cardiac failure congestive
116295663	11629566	Hypernatraemia

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	DUR	DUR COD
116295663	11629566	1	20150211		0
116295663	11629566	2	201502	20150224	0