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
115255722	11525572	2	F	2007	20160629	20150918	20160705	EXP		US-TAKEDA-TPA2012A02612	TAKEDA		0.00				Y	0.00000		20160705		LW	US	US

Drug(s) used by person

Event ID	CASEID	DRUG SEQ	ROLE COD	DRUGNAME	PROD AI	VAL VBM	ROUTE	DOSE VBM	RECHAL	NDA NUM	DOSE AMT	DOSE UNIT	DOSE FORM
115255722	11525572	1	PS	ACTOS	PIOGLITAZONE HYDROCHLORIDE	1	Oral	30 MG, UNK		21073	30	MG	TABLET
115255722	11525572	2	SS	ACTOS	PIOGLITAZONE HYDROCHLORIDE	1	Oral	45 MG, UNK		21073	45	MG	TABLET
115255722	11525572	3	C	METFORMIN	METFORMIN HYDROCHLORIDE	1		500 MG, UNK	U	0	500	MG

Indications of drugs used

Event ID	CASEID	INDI DRUG SEQ	INDI PT
115255722	11525572	1	Type 2 diabetes mellitus

Outcome of event

Event ID	CASEID	OUTC COD
115255722	11525572	DE
115255722	11525572	OT

Reactions reported

Event ID	CASEID	PT
115255722	11525572	Bladder cancer
115255722	11525572	Death
115255722	11525572	Urinary incontinence
115255722	11525572	Urine flow decreased

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
115255722	11525572	1	20050414	20071113
115255722	11525572	2	20080227	20120426
115255722	11525572	3	2005