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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523393 | 7234931 | I | 6523393-8 | 20091215 | 20091222 | 20091231 | EXP | US-ROCHE-676536 | ROCHE | 60 | F | Y | 49.9 | KG | 20091231 | CN | 20091215 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523393 | 1012885622 | PS | CAPECITABINE | 1 | ORAL | 020896 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523393 | 1012885622 | BREAST CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523393 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6523393 | DEATH |
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 |
|---|---|---|---|---|---|
| 6523393 | 1012885622 | 20080726 | 20091014 |