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
126961002	12696100	2	F	20160820	20160915	20160829	20160919	EXP		IR-TAKEDA-2016MPI007507	TAKEDA		63.00	YR		F	Y	0.00000		20160919		MD	IR	IR

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
126961002	12696100	1	PS	VELCADE	BORTEZOMIB	1	Intravenous (not otherwise specified)	UNK			Y		EIZUZ01		21602			INJECTION
126961002	12696100	2	SS	THALIDOMIDE	THALIDOMIDE	1	Unknown	100 MG, QD			U				0	100	MG	TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126961002	12696100	1	Plasma cell myeloma
126961002	12696100	2	Plasma cell myeloma

Outcome of event

Reactions reported

Event ID	CASEID	PT
126961002	12696100	Chest pain
126961002	12696100	Chills
126961002	12696100	Cyanosis
126961002	12696100	Dyspnoea
126961002	12696100	Pyrexia

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
126961002	12696100	1	20160813	20160820	0
126961002	12696100	2	201605		0