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
60487292	6048729	2	F	20060504	20160721	20060519	20160728	EXP		KR-BRISTOL-MYERS SQUIBB COMPANY-13377957	BRISTOL MYERS SQUIBB		24.00	YR		F	Y	0.00000		20160728		CN	KR	KR

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	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
60487292	6048729	1	PS	ARIPIPRAZOLE.	ARIPIPRAZOLE	1	Oral	30 MG, QD	1050	MG	U	21436	30	MG	TABLET	QD
60487292	6048729	2	SS	ARIPIPRAZOLE.	ARIPIPRAZOLE	1	Oral	2 MG, UNK	1050	MG	U	21436	2	MG	TABLET
60487292	6048729	3	C	RISPERIDONE.	RISPERIDONE	1	Unknown	2 MG, UNK			U	0	2	MG
60487292	6048729	4	C	LORAZEPAM.	LORAZEPAM	1	Oral	2 MG, UNK			U	0	2	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
60487292	6048729	1	Schizophrenia
60487292	6048729	3	Schizophrenia
60487292	6048729	4	Anxiety

Outcome of event

Event ID	CASEID	OUTC COD
60487292	6048729	DE
60487292	6048729	OT

Reactions reported

Event ID	CASEID	DRUG REC ACT	PT
60487292	6048729		Completed suicide
60487292	6048729		Prescribed overdose

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
60487292	6048729	1	20060330	20060503
60487292	6048729	3	20060503	20060503
60487292	6048729	4	20060424	20060503