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
124878332	12487833	2	F	201302	20160725	20160622	20160729	EXP		PHHY2013CA072675	NOVARTIS		73.28	YR		M	Y	0.00000		20160729		CN	CA	CA

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
124878332	12487833	1	PS	GLEEVEC	IMATINIB MESYLATE	1	Oral	500 MG, QD	21588	500	MG	QD
124878332	12487833	2	SS	GLEEVEC	IMATINIB MESYLATE	1	Oral	600 MG, QD	21588	600	MG	QD
124878332	12487833	3	SS	GLEEVEC	IMATINIB MESYLATE	1	Oral	600 MG, UNK	21588	600	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124878332	12487833	1	Chronic myeloid leukaemia

Outcome of event

Event ID	CASEID	OUTC COD
124878332	12487833	HO

Reactions reported

Event ID	CASEID	PT
124878332	12487833	Arthralgia
124878332	12487833	Arthritis
124878332	12487833	Atrial fibrillation
124878332	12487833	Drug ineffective
124878332	12487833	Gait disturbance
124878332	12487833	Vomiting

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
124878332	12487833	1	20020621	2004
124878332	12487833	2	2004
124878332	12487833	3	201107