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
125548361 12554836 1 I 200811 20130614 20160713 20160713 EXP US-TAKEDA-TPA2013A05319 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
125548361 12554836 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 15 MG, UNK 21073 15 MG TABLET
125548361 12554836 2 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 30 MG, UNK 21073 30 MG TABLET
125548361 12554836 3 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral UNK 21073 TABLET
125548361 12554836 4 C HUMALOG INSULIN LISPRO 1 UNK U 0
125548361 12554836 5 C DIABETA GLYBURIDE 1 5 MG, UNK U 0 5 MG
125548361 12554836 6 C LANTUS INSULIN GLARGINE 1 10 MG, UNK U 0 10 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125548361 12554836 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125548361 12554836 OT
125548361 12554836 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125548361 12554836 Bladder cancer recurrent
125548361 12554836 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
125548361 12554836 1 2005 200603 0
125548361 12554836 2 2006 2011 0
125548361 12554836 3 2012 0