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
126116721 12611672 1 I 20121108 20160801 20160801 EXP US-TAKEDA-TPA2012A09047 TAKEDA 0.00 Y 0.00000 20160801 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
126116721 12611672 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 15 MG, QD U 21073 15 MG TABLET QD
126116721 12611672 2 C AVANDIA ROSIGLITAZONE MALEATE 1 UNK U 0
126116721 12611672 3 C REZULIN TROGLITAZONE 1 UNK U 0
126116721 12611672 4 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 UNK U 0
126116721 12611672 5 C GLUCOTROL GLIPIZIDE 1 UNK U 0
126116721 12611672 6 C JANUVIA SITAGLIPTIN PHOSPHATE 1 UNK U 0
126116721 12611672 7 C BYETTA EXENATIDE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126116721 12611672 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
126116721 12611672 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126116721 12611672 Bladder cancer
126116721 12611672 Myocardial infarction

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
126116721 12611672 1 2006 0
126116721 12611672 6 2011 0