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
126869452	12686945	2	F	20160322	20160830	20160826	20160901	EXP		TW-ROCHE-1817427	ROCHE		50.10	YR			Y	0.00000		20160901		MD	TW	TW

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
126869452	12686945	1	PS	PEGASYS	PEGINTERFERON ALFA-2A	1	Unknown				U				103964
126869452	12686945	2	SS	Robatrol	RIBAVIRIN	1	Unknown				U				21511	1000	MG	CAPSULE	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126869452	12686945	1	Hepatitis C
126869452	12686945	2	Hepatitis C

Outcome of event

Event ID	CASEID	OUTC COD
126869452	12686945	OT

Reactions reported

Event ID	CASEID	PT
126869452	12686945	Brain oedema
126869452	12686945	Cold sweat
126869452	12686945	Dizziness
126869452	12686945	Poor quality sleep
126869452	12686945	Sjogren's syndrome
126869452	12686945	Speech disorder

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
126869452	12686945	1	20160315	2016	0
126869452	12686945	2	20160315		0