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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6713471 | 7382930 | F | 6713471-2 | 20100419 | 20100504 | EXP | TPG2010A00255 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | YR | F | N | 20100503 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6713471 | 1013637858 | PS | ACTOS | 1 | ORAL | PER ORAL | U | U | 21073 | ||
| 6713471 | 1013659966 | SS | CANDESARTAN CILEXETIL | 1 | ORAL | PER ORAL | |||||
| 6713471 | 1013659967 | C | SIMVASTATIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6713471 | 1013637858 | DRUG USE FOR UNKNOWN INDICATION |
| 6713471 | 1013659966 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6713471 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6713471 | BLOOD PRESSURE INCREASED |
| 6713471 | CHILLS |
| 6713471 | DIZZINESS |
| 6713471 | MUSCULAR WEAKNESS |
| 6713471 | MYOCARDIAL INFARCTION |
| 6713471 | TACHYCARDIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6713471 | FGN |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6713471 | 1013637858 | 4 | WK | ||
| 6713471 | 1013659966 | 3 | WK |