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
125924981	12592498	1	I	20160702	20160712	20160726	20160726	EXP		IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120790	RANBAXY		44.91	YR		F	Y	0.00000		20160726		OT	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
125924981	12592498	1	PS	CITALOPRAM	CITALOPRAM HYDROBROMIDE	1	Oral	10 ML TOTAL			Y	U			77032	10	ML
125924981	12592498	2	SS	EFFERALGAN	ACETAMINOPHEN	1	Oral	2 G TOTAL			Y	U			0	2	G

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
125924981	12592498	1	Intentional self-injury
125924981	12592498	2	Intentional self-injury

Outcome of event

Event ID	CASEID	OUTC COD
125924981	12592498	HO
125924981	12592498	OT

Reactions reported

Event ID	CASEID	PT
125924981	12592498	Hypokinesia
125924981	12592498	Intentional self-injury
125924981	12592498	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
125924981	12592498	1	20160702	20160702	0
125924981	12592498	2	20160702	20160702	0