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
126890074	12689007	4	F	20160502	20160921	20160826	20160927	EXP		PHHY2016TW115034	NOVARTIS		50.20	YR		F	Y	67.00000	KG	20160927		MD	TW	TW

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
126890074	12689007	1	PS	TASIGNA	NILOTINIB	1	Oral	600 MG, UNK							22068	600	MG	CAPSULE
126890074	12689007	2	SS	TASIGNA	NILOTINIB	1	Oral	UNK							22068			CAPSULE

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126890074	12689007	1	Chronic myeloid leukaemia

Outcome of event

Event ID	CASEID	OUTC COD
126890074	12689007	OT
126890074	12689007	HO

Reactions reported

Event ID	CASEID	PT
126890074	12689007	Arrhythmia
126890074	12689007	Back pain
126890074	12689007	Cardiac valve disease
126890074	12689007	Chest discomfort
126890074	12689007	Coronary artery disease
126890074	12689007	Palpitations

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
126890074	12689007	1	20150930		0
126890074	12689007	2	20160711		0