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
124324762	12432476	2	F	20160125	20160706	20160603	20160713	EXP		MX-BAYER-2016-106102	BAYER		52.00	YR	A	M	Y	0.00000		20160713		CN	MX	MX

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
124324762	12432476	1	PS	NEXAVAR	SORAFENIB	1		400 MG, BID	107200	MG					21923	400	MG	FILM-COATED TABLET	BID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
124324762	12432476	1	Renal cancer

Outcome of event

Reactions reported

Event ID	CASEID	PT
124324762	12432476	Adverse event
124324762	12432476	Cardiac arrest
124324762	12432476	Dehydration
124324762	12432476	Gait disturbance
124324762	12432476	Hyperkeratosis
124324762	12432476	Pain in extremity
124324762	12432476	Palmar-plantar erythrodysaesthesia syndrome
124324762	12432476	Platelet disorder
124324762	12432476	Thermohyperaesthesia

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
124324762	12432476	1	20160125	20160606	0