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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6740708 | 7402682 | I | 6740708-6 | 20100512 | 20100521 | EXP | TUK2010A00171 | TAKEDA PHARMACEUTICALS NORTH AMERICA | YR | F | N | 20100520 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6740708 | 1013749359 | PS | ACTOS | 1 | 45 MG, 30 MG, 60 MG | 21073 | |||||
| 6740708 | 1013768166 | C | METFORMIN | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6740708 | 1013749359 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6740708 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 6740708 | ARTHRALGIA |
| 6740708 | ASTHENIA |
| 6740708 | DEPRESSION |
| 6740708 | DYSPNOEA |
| 6740708 | INSOMNIA |
| 6740708 | VISION BLURRED |
| 6740708 | WEIGHT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6740708 | FGN |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6740708 | 1013749359 | 20091201 | 20100420 | ||
| 6740708 | 1013749359 | 20100501 | 6 | MON | |
| 6740708 | 1013749359 | 20100401 |