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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6682033 | 7362452 | I | 6682033-8 | 20100414 | DIR | 73 | YR | M | N | 195 | LBS | 20100413 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6682033 | 1013505350 | PS | ACTOS | 1 | ORAL | 1 DAILY PO | Y | D | C15867 | 20120229 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6682033 | 1013505350 | TYPE 2 DIABETES MELLITUS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6682033 | ARTHRALGIA |
| 6682033 | FATIGUE |
| 6682033 | QUALITY OF LIFE DECREASED |
| 6682033 | TOOTHACHE |
| 6682033 | 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 |
|---|---|---|---|---|---|
| 6682033 | 1013505350 | 20091219 | 20100405 | 4 | MON |