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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6759419 | 7418029 | I | 6759419-6 | 20100526 | 20100603 | EXP | TPA2010A03238 | TAKEDA PHARMACEUTICALS NORTH AMERICA | YR | F | N | 20100602 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6759419 | 1013822455 | PS | ACTOS | 1 | Y | D | 21073 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6759419 | LT |
Reactions reported
| Event ID | PT |
|---|---|
| 6759419 | APPARENT DEATH |
| 6759419 | PERICARDIAL EFFUSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6759419 | CSM |
Therapies reported
| no results found |