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
126047972	12604797	2	F	20160502	20160807	20160728	20160812	EXP		DE-ACTELION-A-US2016-140017	ACTELION		51.00	YR	A	F	Y	0.00000		20160812		OT	DE	CO

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
126047972	12604797	1	PS	VENTAVIS	ILOPROST	1	Respiratory (inhalation)	1 DF, Q4HRS							21779	1	DF	INHALATION VAPOUR, SOLUTION	Q4H
126047972	12604797	2	SS	RIOCIGUAT	RIOCIGUAT	1	Oral	1 MG, Q8HR							0	1	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126047972	12604797	1	Pulmonary arterial hypertension
126047972	12604797	2	Pulmonary hypertension

Outcome of event

Event ID	CASEID	OUTC COD
126047972	12604797	HO

Reactions reported

Event ID	CASEID	PT
126047972	12604797	Bacteraemia
126047972	12604797	Chest pain
126047972	12604797	Lung operation
126047972	12604797	Postoperative wound infection

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
126047972	12604797	1	20150622		0
126047972	12604797	2	20160608		0