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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040497 | 6026598 | F | 5040497-X | 20060328 | 20060407 | 20060630 | EXP | US-ROCHE-443965 | ROCHE | 51 | YR | F | Y | 79.9 | KG | 20060630 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5040497 | 1007431419 | PS | XELODA | 1 | ORAL | FOUR PILLS IN THE MORNING AND THREE PILLS IN THE EVENING. | 20896 | ||||
| 5040497 | 1007431420 | SS | XELODA | 1 | ORAL | 020896 | |||||
| 5040497 | 1007431421 | SS | XELODA | 1 | ORAL | 020896 | |||||
| 5040497 | 1007431422 | I | DILANTIN | 1 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5040497 | 1007431419 | BREAST CANCER METASTATIC |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5040497 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5040497 | CONVULSION |
| 5040497 | DRUG LEVEL 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 |
|---|---|---|---|---|---|
| 5040497 | 1007431419 | 20060310 | 20060328 | 19 | DAY |
| 5040497 | 1007431421 | 20060415 | |||
| 5040497 | 1007431422 | 20050915 | 20060328 | 195 | DAY |