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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126116601 | 12611660 | 1 | I | 20140424 | 20160801 | 20160801 | EXP | US-TAKEDA-2014TUS000428 | TAKEDA | 0.00 | Y | 0.00000 | 20160801 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126116601 | 12611660 | 1 | PS | ACTOS | PIOGLITAZONE HYDROCHLORIDE | 1 | Oral | UNK | U | 21073 | TABLET | ||||||||
| 126116601 | 12611660 | 2 | C | LEVEMIR | INSULIN DETEMIR | 1 | UNK | U | 0 | ||||||||||
| 126116601 | 12611660 | 3 | C | NOVOLOG | INSULIN ASPART | 1 | 100 IU, UNK | U | 0 | 100 | IU |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126116601 | 12611660 | 1 | Type 2 diabetes mellitus |
| 126116601 | 12611660 | 3 | Diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126116601 | 12611660 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126116601 | 12611660 | Bladder cancer | |
| 126116601 | 12611660 | Bladder disorder | |
| 126116601 | 12611660 | Bladder irritation | |
| 126116601 | 12611660 | Urinary incontinence |
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 |
|---|---|---|---|---|---|---|
| 126116601 | 12611660 | 1 | 2003 | 2009 | 0 |