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
118861812	11886181	2	F	20151002	20160726	20160104	20160729	PER		US-CELGENEUS-USA-2015126871	CELGENE		73.30	YR		M	Y	77.18000	KG	20160729		OT	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	RECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
118861812	11886181	1	PS	POMALYST	POMALIDOMIDE	1	Oral	4 MILLIGRAM	U	UNKNOWN	204026	4	MG	CAPSULES	/wk
118861812	11886181	2	SS	DEXAMETHASONE.	DEXAMETHASONE	1	Oral		U	UNKNOWN	0	40	MG	UNKNOWN	/wk
118861812	11886181	3	C	FENTANYL.	FENTANYL	1	Topical	40 MILLIGRAM			0			POULTICE OR PATCH

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
118861812	11886181	1	Plasma cell myeloma
118861812	11886181	2	Plasma cell myeloma
118861812	11886181	3	Pain

Outcome of event

Event ID	CASEID	OUTC COD
118861812	11886181	DE
118861812	11886181	HO

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
118861812	11886181		Fall
118861812	11886181		Plasma cell myeloma

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
118861812	11886181	1	20150318	20151021	0
118861812	11886181	2	20150318	20151021	0