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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4872505 | 5956154 | I | 4872505-0 | 20051220 | 20051230 | DIR | F | N | 68 | KG | 20051229 | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4872505 | 1006787618 | PS | TEMOZOLOMIDE | 2 | ORAL | SEE IMAGE | |||||
| 4872505 | 1006793283 | SS | IRINOTECAN HCL | 1 | SEE IMAGE | ||||||
| 4872505 | 1006793284 | SS | RADIATION THERAPY | 2 | SEE IMAGE |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4872505 | 1006787618 | GLIOBLASTOMA MULTIFORME |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4872505 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4872505 | ABASIA |
| 4872505 | ACTIVITIES OF DAILY LIVING IMPAIRED |
| 4872505 | ARTHRALGIA |
| 4872505 | ASTHENIA |
| 4872505 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 4872505 | HEMIPARESIS |
| 4872505 | NEOPLASM |
| 4872505 | PAIN |
| 4872505 | WHEELCHAIR USER |
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 |
|---|---|---|---|---|---|
| 4872505 | 1006787618 | 20051123 | 20051127 | ||
| 4872505 | 1006793283 | 20051123 | 20051207 | ||
| 4872505 | 1006793284 | 20051123 |