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
104677012	10467701	2	F	20140822	20160908	20140922	20160921	EXP	FR-AFSSAPS-RE20140790	FR-FRI-1000070838	FOREST		42.20	YR		M	Y	0.00000		20160921		OT	DK	FR

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
104677012	10467701	1	PS	ESCITALOPRAM	ESCITALOPRAM OXALATE	1		OVERDOSE OF 20 DF ONCE			Y				21323	20	DF	COATED TABLET	1X
104677012	10467701	2	SS	BACLOFENE	BACLOFEN	1	Oral	OVERDOSE OF 140 DF ONCE			Y				0	140	DF	TABLET	1X

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
104677012	10467701	1	Product used for unknown indication
104677012	10467701	2	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
104677012	10467701	LT

Reactions reported

Event ID	CASEID	PT
104677012	10467701	Confusional state
104677012	10467701	Hallucination
104677012	10467701	Intentional overdose
104677012	10467701	Neuroleptic malignant syndrome

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
104677012	10467701	1		20140822	0
104677012	10467701	2		20140822	0