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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4872504 | 5956151 | I | 4872504-9 | 20051202 | 20051230 | DIR | F | N | 55 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4872504 | 1006787616 | PS | TEMOZOLOMIDE | 2 | SEE IMAGE |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4872504 | 1006787616 | NON-SMALL CELL LUNG CANCER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4872504 | HO |
| 4872504 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4872504 | HEART RATE INCREASED |
| 4872504 | OXYGEN SATURATION DECREASED |
| 4872504 | PNEUMONIA |
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 |
|---|---|---|---|---|---|
| 4872504 | 1006787616 | 20051129 | 20051201 |