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
125636091 12563609 1 I 20110122 20130201 20160715 20160715 EXP US-TAKEDA-TPA2013A01247 TAKEDA 0.00 Y 0.00000 20160715 CN 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
125636091 12563609 1 PS ACTOS PIOGLITAZONE HYDROCHLORIDE 1 Oral 15 MG, UNK 21073 15 MG TABLET
125636091 12563609 2 C AVANDIA ROSIGLITAZONE MALEATE 1 4 MG, UNK U 0 4 MG
125636091 12563609 3 C GLUCOTROL GLIPIZIDE 1 5 MG, UNK U 0 5 MG
125636091 12563609 4 C JANUVIA SITAGLIPTIN PHOSPHATE 1 50 MG, UNK U 0 50 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125636091 12563609 1 Type 2 diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
125636091 12563609 DE
125636091 12563609 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125636091 12563609 Bladder cancer recurrent
125636091 12563609 Bladder transitional cell carcinoma
125636091 12563609 Death
125636091 12563609 Haematuria

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
125636091 12563609 1 20080609 20111010 0
125636091 12563609 2 20041018 20080512 0
125636091 12563609 3 20120531 0
125636091 12563609 4 20120206 0