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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6661216 | 7339071 | I | 6661216-7 | 20100321 | 20100323 | 20100331 | EXP | US-ROCHE-693831 | ROCHE | 66 | F | Y | 20100331 | CN | 20100321 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6661216 | 1013420004 | PS | XELODA | 1 | UNKNOWN | 020896 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6661216 | 1013420004 | COLON CANCER |
Outcome of event
Event ID | OUTC COD |
---|---|
6661216 | DE |
Reactions reported
Event ID | PT |
---|---|
6661216 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |