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
56902346	5690234	6	F	20040430	20160823	20041207	20160823	EXP		US-BRISTOL-MYERS SQUIBB COMPANY-12784559	BRISTOL MYERS SQUIBB		0.00	DY		M	Y	1.70000	KG	20160823		CN	US	US

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
56902346	5690234	1	PS	ABILIFY	ARIPIPRAZOLE	1	Transplacental	15 MG, QD	3255	MG	U				21436	15	MG	TABLET	QD
56902346	5690234	2	SS	ABILIFY	ARIPIPRAZOLE	1	Transplacental	22.5 MG, QD	3255	MG	U				21436	22.5	MG	TABLET	QD

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
56902346	5690234	1	Product used for unknown indication

Outcome of event

Event ID	CASEID	OUTC COD
56902346	5690234	DE
56902346	5690234	OT

Reactions reported

Event ID	CASEID	PT
56902346	5690234	Foetal exposure during pregnancy
56902346	5690234	Neonatal respiratory distress syndrome
56902346	5690234	Premature baby

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
56902346	5690234	1	20030128	20030213	0
56902346	5690234	2	20030213		0