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
127699701	12769970	1	I	20160222	20160915	20160922	20160922	EXP	HR-HALMED-2016-02468	HR-UCBSA-2016035585	UCB		0.00			F	Y	0.00000		20160922		MD	HR	HR

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
127699701	12769970	1	PS	KEPPRA	LEVETIRACETAM	1	Oral	60 G, TOTAL			U	U			21035	60	G		1X
127699701	12769970	2	SS	PHEMITON	MEPHOBARBITAL	1	Oral	6 G, TOTAL			U	U			0	6	G	TABLET	1X

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127699701	12769970	1	Product used for unknown indication
127699701	12769970	2	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
127699701	12769970	HO
127699701	12769970	OT

Reactions reported

Event ID	CASEID	PT
127699701	12769970	Intentional overdose
127699701	12769970	Somnolence
127699701	12769970	Suicide attempt

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
127699701	12769970	1	20160222	20160222	0
127699701	12769970	2	20160222	20160222	0