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
123692123	12369212	3	F	2013	20160722	20160513	20160728	EXP		PHHY2016AR063963	NOVARTIS		0.00			F	Y	0.00000		20160728		CN	COUNTRY NOT SPECIFIED	AR

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
123692123	12369212	1	PS	DIOVAN	VALSARTAN	1	Unknown	2 DF, QD							21283	2	DF	TABLET	QD
123692123	12369212	2	SS	DIOVAN	VALSARTAN	1	Unknown	0.5 DF (80 MG), BID (HALF IN THE MORNING AND HALF AT NIGHT)							21283	.5	DF	TABLET	BID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
123692123	12369212	1	Hypertension
123692123	12369212	2	Stress

Outcome of event

Event ID	CASEID	OUTC COD
123692123	12369212	OT

Reactions reported

Event ID	CASEID	PT
123692123	12369212	Blood pressure increased
123692123	12369212	Cardiac valve disease
123692123	12369212	Drug prescribing error
123692123	12369212	Hypotension
123692123	12369212	Underdose
123692123	12369212	Wrong technique in product usage process

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
123692123	12369212	2	201507		0