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
126929821	12692982	1	I	20160721	20160726	20160829	20160829	PER		BR-BAYER-2016-145271	BAYER		74.00	YR	E	F	Y	0.00000		20160829		CN	BR	BR

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
126929821	12692982	1	PS	NEXAVAR	SORAFENIB	1	Oral	400 MG, QD					NOT REPORTED		21923	400	MG	FILM-COATED TABLET	QD
126929821	12692982	2	SS	NEXAVAR	SORAFENIB	1	Oral	800 MG, QD							21923	800	MG	FILM-COATED TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126929821	12692982	1	Renal cancer
126929821	12692982	2	Renal cancer

Outcome of event

Event ID	CASEID	OUTC COD
126929821	12692982	DE
126929821	12692982	HO

Reactions reported

Event ID	CASEID	PT
126929821	12692982	Asthenia
126929821	12692982	Lung infection
126929821	12692982	Malaise
126929821	12692982	Nausea
126929821	12692982	Pharyngitis
126929821	12692982	Pyrexia

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
126929821	12692982	1	20160720	2016	0
126929821	12692982	2	2016	20160815	0