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
125720081	12572008	1	I		20160713	20160719	20160719	EXP		US-BIOGEN-2016BI00265607	BIOGEN		0.00			F	Y	0.00000		20160719		CN	US	US

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
125720081	12572008	1	PS	AVONEX	INTERFERON BETA-1A	1	Intramuscular				U				103628	30	UG	UNKNOWN	/wk
125720081	12572008	2	SS	AVONEX	INTERFERON BETA-1A	1	Intramuscular				U				103628	30	UG	UNKNOWN	/wk

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125720081	12572008	1	Multiple sclerosis

Outcome of event

Event ID	CASEID	OUTC COD
125720081	12572008	HO

Reactions reported

Event ID	CASEID	PT
125720081	12572008	Dehydration
125720081	12572008	Diaphragmalgia
125720081	12572008	Gastroenteritis
125720081	12572008	Headache
125720081	12572008	Multiple sclerosis relapse
125720081	12572008	White blood cell count decreased

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
125720081	12572008	1	20160118		0
125720081	12572008	2	20160217		0