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
123894474	12389447	4	F	20160506	20160802	20160520	20160812	EXP		PL-CELGENEUS-POL-2016051843	CELGENE		69.34	YR		F	Y	95.00000	KG	20160812		OT	PL	PL

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
123894474	12389447	1	PS	REVLIMID	LENALIDOMIDE	1	Oral	18.75 MILLIGRAM				U	11F0223		21880	25	MG	CAPSULES
123894474	12389447	2	SS	DEXAMETHASONE.	DEXAMETHASONE	1	Oral	3 MILLIGRAM				U	103058		0	40	MG	UNKNOWN	/wk

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
123894474	12389447	1	Plasma cell myeloma
123894474	12389447	2	Plasma cell myeloma

Outcome of event

Reactions reported

Event ID	CASEID	PT
123894474	12389447	Candida pneumonia
123894474	12389447	Circulatory collapse
123894474	12389447	Respiratory failure

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
123894474	12389447	1	20130924	20160412	0
123894474	12389447	2	20130924	20160413	0