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
127386161	12738616	1	I	20160407	0	20160912	20160912	DIR	US-FDA-350401		FDA-CTU		31.00	YR		M	N	66.15000	KG	20160912	N	PH	US	US

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
127386161	12738616	1	PS	TRIUMEQ	ABACAVIR SULFATEDOLUTEGRAVIR SODIUMLAMIVUDINE	1	Oral				N	D			0	1	DF		QD
127386161	12738616	2	SS	BACTRIM	SULFAMETHOXAZOLETRIMETHOPRIM	1	Oral				N	D			0	1	DF		QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127386161	12738616	1	Acquired immunodeficiency syndrome
127386161	12738616	2	Antifungal prophylaxis

Outcome of event

no results found

no results found

Reactions reported

Event ID	CASEID	PT
127386161	12738616	Nausea
127386161	12738616	Paraesthesia
127386161	12738616	Rash
127386161	12738616	Tachycardia
127386161	12738616	Vomiting

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID	CASEID	RPSR COD
127386161	12738616	HP

Therapies reported

Event ID	CASEID	DSG DRUG SEQ	START DT	END DT	DUR	DUR COD
127386161	12738616	1	20160407	20160407	0
127386161	12738616	2	20160407	20160407	0