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
125937881	12593788	1	I	20160702	20160712	20160726	20160726	EXP	IT-MINISAL02-367001	IT-FRI-1000086320	FOREST		44.91	YR		F	Y	0.00000		20160726		OT	DK	IT

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
125937881	12593788	1	PS	CITALOPRAM	CITALOPRAM HYDROBROMIDE	1	Oral	OVERDOSE: 10 ML CITALOPRAM DROPS			Y				21046			ORAL DROPS
125937881	12593788	2	SS	EFFERALGAN	ACETAMINOPHEN	1	Oral	2 TABLETS EFFERALGAN 1000MG			Y				0			EFFERVESCENT TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125937881	12593788	1	Intentional self-injury
125937881	12593788	2	Intentional self-injury

Outcome of event

Event ID	CASEID	OUTC COD
125937881	12593788	HO

Reactions reported

Event ID	CASEID	PT
125937881	12593788	Hypokinesia
125937881	12593788	Intentional self-injury
125937881	12593788	Vomiting

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
125937881	12593788	1	20160702	20160702	0
125937881	12593788	2	20160702	20160702	0