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
127300992	12730099	2	F	20160825	20160913	20160909	20160927	EXP		MX-EMD SERONO-8105436	EMD SERONO INC		34.58	YR		M	Y	65.00000	KG	20160927		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
127300992	12730099	1	PS	REBIF	INTERFERON BETA-1A	1	Subcutaneous					Y	AU015449		103780	22	UG	INJECTION
127300992	12730099	2	SS	REBIF	INTERFERON BETA-1A	1	Subcutaneous	RESTARTED				Y	AU015449		103780			INJECTION

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127300992	12730099	1	Relapsing-remitting multiple sclerosis

Outcome of event

Event ID	CASEID	OUTC COD
127300992	12730099	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
127300992	12730099		Asphyxia
127300992	12730099	Discomfort	Discomfort
127300992	12730099	Headache	Headache
127300992	12730099		Inappropriate schedule of drug administration

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
127300992	12730099	1	20160824	20160831	0
127300992	12730099	2	20160912		0