Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6734595 | 7398531 | I | 6734595-X | 20100505 | 20100519 | EXP | TPA2010A02651 | TAKEDA PHARMACEUTICALS NORTH AMERICA | YR | M | N | 20100518 | MD | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6734595 | 1013724836 | PS | ACTOS | 1 | ORAL | PER ORAL | 21073 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6734595 | 1013724836 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6734595 | HO |
| 6734595 | OT |
| 6734595 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 6734595 | MYOCARDIAL INFARCTION |
| 6734595 | VASCULAR GRAFT |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6734595 | CR |
| 6734595 | HP |
Therapies reported
| no results found |