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
127303271	12730327	1	I	2009	20160902	20160909	20160909	EXP		FR-ELI_LILLY_AND_COMPANY-US201609000945	ELI LILLY AND CO		0.00			F	Y	95.00000	KG	20160909		CN	US	FR

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	DECHAL	RECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM	DOSE FREQ
127303271	12730327	1	PS	ZYPREXA	OLANZAPINE	1	Oral	5 MG, QD	U	U	20592	5	MG	TABLET	QD
127303271	12730327	2	SS	ABILIFY	ARIPIPRAZOLE	1	Oral	5 MG, QD	U	U	0	5	MG		QD
127303271	12730327	3	SS	ZOLOFT	SERTRALINE HYDROCHLORIDE	1	Oral	50 MG, UNKNOWN	U	U	0	50	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
127303271	12730327	1	Mood swings
127303271	12730327	2	Depression
127303271	12730327	3	Depression

Outcome of event

Event ID	CASEID	OUTC COD
127303271	12730327	OT

Reactions reported

Event ID	CASEID	PT
127303271	12730327	Gestational diabetes
127303271	12730327	Maternal exposure during pregnancy
127303271	12730327	Off label use
127303271	12730327	Post procedural haemorrhage

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
127303271	12730327	1	2009	20101218
127303271	12730327	2	20101218	20110301
127303271	12730327	3	2006	20100918