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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5120035 | 6050021 | F | 1 | 5120035-3 | 20060423 | 20060918 | 20060929 | EXP | 2006056073 | PFIZER INC | 74 | YR | M | N | 20060928 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5120035 | 1007726856 | PS | SUTENT | 1 | ORAL | 50 MG (50 MG, 1 IN 1 D), ORAL | D | D | 21968 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5120035 | 1007726856 | RENAL CELL CARCINOMA STAGE UNSPECIFIED |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5120035 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5120035 | FACE OEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5120035 | FGN |
| 5120035 | HP |
| 5120035 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5120035 | 1007726856 | 20060322 | 20060418 |