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
114984822 11498482 2 F 2004 20160720 20150911 20160727 EXP US-TAKEDA-TPA2011A07375 TAKEDA 0.00 Y 0.00000 20160727 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
114984822 11498482 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 30 MG, QD 21073 30 MG TABLET QD
114984822 11498482 2 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 30 MG, UNK 21073 30 MG TABLET
114984822 11498482 3 C LANTUS INSULIN GLARGINE 1 5 IU, UNK U 0 5 IU
114984822 11498482 4 C HUMULIN 70/30 INSULIN HUMAN 1 50 IU, UNK U 0 50 IU

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114984822 11498482 1 Type 2 diabetes mellitus
114984822 11498482 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
114984822 11498482 DE
114984822 11498482 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114984822 11498482 Bladder cancer
114984822 11498482 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
114984822 11498482 1 200212 200708 0
114984822 11498482 2 2008 0
114984822 11498482 3 2013 0
114984822 11498482 4 2003 0