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
125284053	12528405	3	F	20160624	20160726	20160705	20160729	EXP		MX-BAYER-2016-128373	BAYER		58.00	YR	A	M	Y	57.00000	KG	20160729		CN	MX	MX

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 FORM	DOSE FREQ
125284053	12528405	1	PS	NEXAVAR	SORAFENIB	1	Oral	400 MG, BID	21923	400	MG	FILM-COATED TABLET	BID
125284053	12528405	2	C	PARACETAMOL	ACETAMINOPHEN	1		2 DF, Q8HR	0	2	DF		Q8H
125284053	12528405	3	C	CIPROFLOXACINO	CIPROFLOXACIN HYDROCHLORIDE	1		1 DF, BID	0	1	DF		BID

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125284053	12528405	1	Renal cancer

Outcome of event

Event ID	CASEID	OUTC COD
125284053	12528405	DE
125284053	12528405	HO

Reactions reported

Event ID	CASEID	PT
125284053	12528405	Chills
125284053	12528405	Death
125284053	12528405	Decreased appetite
125284053	12528405	Diarrhoea
125284053	12528405	Feeling abnormal
125284053	12528405	Hyperhidrosis
125284053	12528405	Hypoaesthesia
125284053	12528405	Hypotension
125284053	12528405	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
125284053	12528405	1	20160620		0