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
125571032	12557103	2	F	201606	20160714	20160714	20160721	EXP		CO-009507513-1607COL005277	MERCK		41.00	YR		M	Y	0.00000		20160721		OT	CO	CO

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
125571032	12557103	1	PS	ISENTRESS	RALTEGRAVIR POTASSIUM	1	Oral	400 MG, BID	N		22145	400	MG	TABLET	BID
125571032	12557103	2	C	DARUNAVIR	DARUNAVIR	1	Oral	800 MG, QD	N	U	0	800	MG	TABLET	QD
125571032	12557103	3	C	RITONAVIR.	RITONAVIR	1	Oral	100 MG, QD	N	U	0	100	MG	TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125571032	12557103	1	HIV infection
125571032	12557103	2	HIV infection
125571032	12557103	3	HIV infection

Outcome of event

Event ID	CASEID	OUTC COD
125571032	12557103	DE
125571032	12557103	OT

Reactions reported

Event ID	CASEID	PT
125571032	12557103	Cognitive disorder
125571032	12557103	Death
125571032	12557103	Renal impairment
125571032	12557103	Treatment noncompliance

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
125571032	12557103	1	2013	201606	0