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
125532342	12553234	2	F	20160704	20160919	20160713	20160921	PER		PHEH2016US017201	NOVARTIS		87.30	YR		F	Y	53.30000	KG	20160921		CN	COUNTRY NOT SPECIFIED	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	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
125532342	12553234	1	PS	PROMACTA	ELTROMBOPAG OLAMINE	1	Oral	50 MG, QD	43250	MG	D	22291	50	MG	QD
125532342	12553234	2	SS	PROMACTA	ELTROMBOPAG OLAMINE	1	Oral	100 MG, QD	43250	MG	D	22291	100	MG	QD
125532342	12553234	3	SS	PROMACTA	ELTROMBOPAG OLAMINE	1	Oral	150 MG, QD	43250	MG	D	22291	150	MG	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125532342	12553234	1	Thrombocytopenia

Outcome of event

Event ID	CASEID	OUTC COD
125532342	12553234	HO
125532342	12553234	DE

Reactions reported

Event ID	CASEID	PT
125532342	12553234	Colitis
125532342	12553234	Neutropenic colitis
125532342	12553234	Sepsis

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
125532342	12553234	1	20150127	20151228
125532342	12553234	2	20151229	20160201
125532342	12553234	3	20160202	20160703