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
122705014	12270501	4	F	20150604	20160719	20160415	20160801	EXP		BE-CELGENEUS-BEL-2015075361	CELGENE		62.00	YR		M	Y	78.00000	KG	20160801		OT	BE	BE

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
122705014	12270501	1	PS	POMALIDOMIDE	POMALIDOMIDE	1	Oral					U			204026	4	MG	CAPSULES
122705014	12270501	2	SS	DEXAMETHASONE.	DEXAMETHASONE	1	Unknown					U			0	20	MG	UNKNOWN	/wk

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
122705014	12270501	1	Plasma cell myeloma
122705014	12270501	2	Plasma cell myeloma

Outcome of event

Reactions reported

Event ID	CASEID	PT
122705014	12270501	Acute respiratory distress syndrome
122705014	12270501	Epistaxis
122705014	12270501	Neutropenia
122705014	12270501	Thrombocytopenia

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
122705014	12270501	1	20150522	20150611	0
122705014	12270501	2	20150522	20150612	0