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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6316799 | 7086791 | I | 6316799-3 | 20090114 | 20090820 | EXP | PHHY2009AU32017 | NOVARTIS PHARMACEUTICALS CORP. | M | Y | 20090820 | CN | AUSTRALIA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6316799 | 1012079500 | PS | GLEEVEC | 1 | 600 MG, UNK | 021588 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6316799 | 1012079500 | CHRONIC MYELOID LEUKAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6316799 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6316799 | ALOPECIA |
| 6316799 | POST PROCEDURAL HAEMORRHAGE |
| 6316799 | TRANSURETHRAL PROSTATECTOMY |
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 |
|---|---|---|---|---|---|
| 6316799 | 1012079500 | 20080101 |