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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6669722 | 7141795 | F | 6669722-6 | 20090707 | 20100322 | 20100402 | EXP | TUK2009A00153 | TAKEDA PHARMACEUTICALS NORTH AMERICA | YR | M | N | 20100401 | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6669722 | 1013454465 | PS | ACTOS | 1 | 60 MG | U | U | 21073 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6669722 | 1013454465 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6669722 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6669722 | ACCIDENTAL OVERDOSE |
| 6669722 | FALL |
| 6669722 | SYNCOPE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6669722 | FGN |
| 6669722 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6669722 | 1013454465 | 20090707 |