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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6794729 | 7440476 | I | 6794729-8 | 20100624 | DIR | YR | F | N | 20100529 | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6794729 | 1013953561 | PS | ACTOS | 1 | ORAL | 45MG 1 X DAILY ORALLY | Y | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6794729 | 1013953561 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6794729 | OT |
| 6794729 | RI |
Reactions reported
| Event ID | PT |
|---|---|
| 6794729 | ANAEMIA |
| 6794729 | COUGH |
| 6794729 | FATIGUE |
| 6794729 | FLUID RETENTION |
| 6794729 | OROPHARYNGEAL PAIN |
| 6794729 | WEIGHT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6794729 | 1013953561 | 20090401 | 20100501 |