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
127690101	12769010	1	I	20160901	20160914	20160921	20160921	EXP		IT-ABBVIE-16P-083-1732692-00	ABBVIE		23.00	YR		M	Y	0.00000		20160921		OT	IT	IT

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DECHAL	LOT NUM	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM
127690101	12769010	1	PS	DEPAKINE	VALPROATE SODIUM	1	Oral		UNKNOWN	18081	10	DF	MODIFIED-RELEASE GRANULES
127690101	12769010	2	SS	RISPERIDONE.	RISPERIDONE	1	Oral		UNKNOWN	0	10	DF	FILM-COATED TABLET
127690101	12769010	3	SS	CLONAZEPAM.	CLONAZEPAM	1	Oral	U	UNKNOWN	0	10	DF	FILM-COATED TABLET

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127690101	12769010	1	Product used for unknown indication
127690101	12769010	2	Product used for unknown indication
127690101	12769010	3	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
127690101	12769010	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
127690101	12769010		Intentional overdose
127690101	12769010		Intentional self-injury

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
127690101	12769010	1	20160901	20160901	0
127690101	12769010	2	20160901	20160901	0