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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4389696 | 4167618 | I | 4389696-0 | 20040614 | 20040630 | EXP | 8244 | MAYNE PHARMA PTY LTD. | N | 20040624 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4389696 | 1004987152 | PS | FLUOROURACIL | 1 | INTRAHEPATIC | 1000 MG/MW PER_CYCLE IV | 88929 | ||||
| 4389696 | 1005002533 | SS | LEUCOVORIN CALCIUM | 1 | INTRAVENOUS | 200 MG/M2 PER_CYCLE IV | |||||
| 4389696 | 1005002534 | SS | ELOXATIN | 1 | INTRAVENOUS | 85 MG/M2 PER_CYCLE IV |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4389696 | 1004987152 | COLON CANCER |
| 4389696 | 1005002533 | COLON CANCER |
| 4389696 | 1005002534 | COLON CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4389696 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 4389696 | HAEMORRHAGE INTRACRANIAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4389696 | FGN |
| 4389696 | HP |
| 4389696 | LIT |
| 4389696 | OTH |
Therapies reported
| no results found |