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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542790 | 5653256 | F | 4542790-3 | 20040101 | 20041020 | 20041231 | EXP | PHBS2004JP14102 | NOVARTIS PHARMACEUTICALS CORP. | 61 | YR | F | Y | 20041231 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542790 | 1005547055 | PS | GLEEVEC | 1 | ORAL | ||||||
| 4542790 | 1005547056 | SS | NSAID'S | 2 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542790 | 1005547055 | CHRONIC MYELOID LEUKAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542790 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4542790 | BLISTER |
| 4542790 | PSEUDOPORPHYRIA |
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 |
|---|---|---|---|---|---|
| 4542790 | 1005547055 | 20011101 |