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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6785161 | 7330264 | F | 6785161-1 | 20040101 | 20100617 | 20100618 | EXP | TPG2010A00081 | TAKEDA PHARMACEUTICALS NORTH AMERICA | YR | F | N | 20100617 | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6785161 | 1013918263 | PS | ACTOS | 1 | ORAL | PER ORAL | Y | 21073 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6785161 | 1013918263 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6785161 | DS |
| 6785161 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6785161 | DRY SKIN |
| 6785161 | GAIT DISTURBANCE |
| 6785161 | OEDEMA |
| 6785161 | SKIN FISSURES |
| 6785161 | SKIN HAEMORRHAGE |
| 6785161 | SKIN ULCER |
| 6785161 | WEIGHT DECREASED |
| 6785161 | WEIGHT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6785161 | HP |
Therapies reported
| no results found |