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
125880181	12588018	1	I	20160702	20160713	20160725	20160725	EXP	IT-MINISAL02-367001	IT-TEVA-678511ACC	TEVA		44.91	YR		F	Y	0.00000		20160725		MD	IT	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
125880181	12588018	1	PS	CITALOPRAM	CITALOPRAM HYDROBROMIDE	1	Oral	10 ML TOTAL			Y				77232	10	ML
125880181	12588018	2	SS	EFFERALGAN	ACETAMINOPHEN	1	Oral	2 G TOTAL			Y				0	2	G

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125880181	12588018	1	Intentional self-injury
125880181	12588018	2	Intentional self-injury

Outcome of event

Event ID	CASEID	OUTC COD
125880181	12588018	HO

Reactions reported

Event ID	CASEID	PT
125880181	12588018	Drug abuse
125880181	12588018	Hypokinesia
125880181	12588018	Intentional self-injury
125880181	12588018	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
125880181	12588018	1	20160702	20160702	0
125880181	12588018	2	20160702	20160702	0