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
126129931	12612993	1	I	20160704	20160726	20160802	20160802	EXP		IT-ROCHE-1802887	ROCHE		50.23	YR		M	Y	0.00000		20160802		OT	IT	IT

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FREQ
126129931	12612993	1	PS	RIVOTRIL	CLONAZEPAM	1	Oral	2.5 MG/ML 10 ML BOTTLE	Y	17533	60	GTT	QD
126129931	12612993	2	SS	PARACETAMOL	ACETAMINOPHEN	1	Oral		Y	0	20	G	/month
126129931	12612993	3	SS	ELETRIPTAN	ELETRIPTAN	1	Oral		Y	0	400	MG	/month

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
126129931	12612993	1	Product used for unknown indication
126129931	12612993	2	Headache
126129931	12612993	3	Headache

Outcome of event

Event ID	CASEID	OUTC COD
126129931	12612993	HO

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
126129931	12612993		Blood creatine phosphokinase increased
126129931	12612993		Drug abuse

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
126129931	12612993	1	20151201	20160704
126129931	12612993	2	20151201	20160704
126129931	12612993	3	20151201	20160704