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
114588192 11458819 2 F 20090216 20160628 20150904 20160704 EXP US-TAKEDA-2014TUS005498 TAKEDA 0.00 Y 0.00000 20160704 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
114588192 11458819 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral UNK 21073 TABLET
114588192 11458819 2 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 15 MG, UNK 21073 15 MG TABLET
114588192 11458819 3 SS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 45 MG, UNK 21073 45 MG TABLET
114588192 11458819 4 C NOVOLOG INSULIN ASPART 1 30/70, UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114588192 11458819 1 Type 2 diabetes mellitus
114588192 11458819 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
114588192 11458819 OT
114588192 11458819 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
114588192 11458819 Bladder transitional cell carcinoma
114588192 11458819 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
114588192 11458819 1 2000 2004 0
114588192 11458819 2 200409 200610 0
114588192 11458819 3 200409 200610 0
114588192 11458819 4 2006 0