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
125506781	12550678	1	I	20160519	20160606	20160712	20160712	EXP		DE-TAKEDA-2016MPI005469	TAKEDA		75.00	YR		M	Y	76.00000	KG	20160712		MD	DE	DE

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
125506781	12550678	1	PS	VELCADE	BORTEZOMIB	1	Subcutaneous	3.575 MG, UNK			Y		FJZSB01		21602	3.575	MG	INJECTION
125506781	12550678	2	SS	VELCADE	BORTEZOMIB	1	Subcutaneous	UNK			Y		FJZSB01		21602			INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125506781	12550678	1	Plasma cell myeloma

Outcome of event

Event ID	CASEID	OUTC COD
125506781	12550678	LT

Reactions reported

Event ID	CASEID	PT
125506781	12550678	Drug prescribing error
125506781	12550678	Incorrect route of drug administration
125506781	12550678	Overdose
125506781	12550678	Product preparation error
125506781	12550678	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
125506781	12550678	1	20160510		0
125506781	12550678	2	20160629		0