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
125326001	12532600	1	I	20160327	20160413	20160706	20160706	EXP		DE-ACTELION-A-US2016-134956	ACTELION		61.00	YR	A	F	Y	0.00000		20160706		OT	DE	NL

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
125326001	12532600	1	PS	VENTAVIS	ILOPROST	1	Respiratory (inhalation)	2.5 MCG/ML, 6X A DAY							21779			INHALATION VAPOUR, SOLUTION
125326001	12532600	2	SS	VENTAVIS	ILOPROST	1	Respiratory (inhalation)	2.5 MCG, 6X A DAY							21779	2.5	UG	INHALATION VAPOUR, SOLUTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125326001	12532600	1	Pulmonary arterial hypertension

Outcome of event

Event ID	CASEID	OUTC COD
125326001	12532600	DE
125326001	12532600	HO

Reactions reported

Event ID	CASEID	PT
125326001	12532600	Cerebral haemorrhage
125326001	12532600	Complications of transplanted lung
125326001	12532600	Mydriasis
125326001	12532600	Oedema peripheral

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
125326001	12532600	1	20141201		0
125326001	12532600	2	20141202	20160512	0