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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523652 | 7235082 | I | 6523652-9 | 20091229 | 20091231 | EXP | PHHY2009CA59468 | NOVARTIS PHARMACEUTICAL CORPORATION | M | Y | 20091231 | CN | CANADA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6523652 | 1012886615 | PS | TASIGNA | 1 | ORAL | UNK | 022068 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6523652 | 1012886615 | GASTROINTESTINAL STROMAL TUMOUR |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6523652 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6523652 | DEATH |
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 |
|---|---|---|---|---|---|
| 6523652 | 1012886615 | 20091101 |