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
114981982 11498198 2 F 20100121 20160720 20150911 20160726 EXP US-TAKEDA-TPA2011A07346 TAKEDA 0.00 Y 0.00000 20160726 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
114981982 11498198 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 10 MG, UNK 21073 10 MG TABLET
114981982 11498198 2 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 45 MG, UNK 21073 45 MG TABLET
114981982 11498198 3 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK U 0
114981982 11498198 4 C GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 UNK U 0
114981982 11498198 5 C LANTUS INSULIN GLARGINE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114981982 11498198 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
114981982 11498198 OT
114981982 11498198 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
114981982 11498198 Bladder cancer
114981982 11498198 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
114981982 11498198 1 20011227 20100927 0
114981982 11498198 2 20011227 20100927 0
114981982 11498198 3 1990 2013 0
114981982 11498198 4 1990 2005 0
114981982 11498198 5 1990 2013 0