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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542791 | 5699058 | F | 4542791-5 | 20041214 | 20041231 | EXP | PHBS2004JP16773 | NOVARTIS PHARMACEUTICALS CORP. | 65 | YR | M | Y | 53 | KG | 20041231 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4542791 | 1005547057 | PS | GLEEVEC | 1 | ORAL | 400 MG/D | |||||
| 4542791 | 1005547058 | SS | GLEEVEC | 1 | ORAL | 300 MG/DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4542791 | 1005547057 | CHRONIC MYELOID LEUKAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4542791 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4542791 | C-REACTIVE PROTEIN INCREASED |
| 4542791 | INDURATION |
| 4542791 | PAIN |
| 4542791 | PSEUDOMONAS INFECTION |
| 4542791 | SEPTAL PANNICULITIS |
| 4542791 | STAPHYLOCOCCAL INFECTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |