The Safety Rates Drug Report

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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
125548851 12554885 1 I 20070103 20120615 20160713 20160713 EXP US-TAKEDA-TPA2012A03852 TAKEDA 0.00 Y 0.00000 20160713 LW 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
125548851 12554885 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral UNK 21073 TABLET
125548851 12554885 2 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 45 MG, UNK 21073 45 MG TABLET
125548851 12554885 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 500 MG, UNK U 0 500 MG
125548851 12554885 4 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 UNK U 0
125548851 12554885 5 C JANUVIA SITAGLIPTIN PHOSPHATE 1 100 MG, UNK U 0 100 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125548851 12554885 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125548851 12554885 OT
125548851 12554885 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125548851 12554885 Bladder cancer
125548851 12554885 Bladder cancer recurrent
125548851 12554885 Death

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125548851 12554885 1 2001 200707 0