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
125994671	12599467	1	I	20160531	20160719	20160727	20160727	EXP		DE-ACTELION-A-US2016-139968	ACTELION		55.00	YR	A	F	Y	0.00000		20160727		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
125994671	12599467	1	PS	VENTAVIS	ILOPROST	1	Respiratory (inhalation)	6 DF, QD							21779	6	DF	INHALATION VAPOUR, SOLUTION	QD
125994671	12599467	2	SS	RIOCIGUAT	RIOCIGUAT	1	Oral	2 MG, Q8HR							0	2	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125994671	12599467	1	Pulmonary hypertension
125994671	12599467	2	Pulmonary hypertension

Outcome of event

Event ID	CASEID	OUTC COD
125994671	12599467	HO

Reactions reported

Event ID	CASEID	PT
125994671	12599467	Choking sensation
125994671	12599467	Cough
125994671	12599467	Dysphonia
125994671	12599467	Dyspnoea
125994671	12599467	Influenza

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
125994671	12599467	1	20140506		0
125994671	12599467	2	20160331		0