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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
4542794 | 5701958 | F | 4542794-0 | 20041201 | 20041216 | 20041231 | EXP | PHNU2004DE04220 | NOVARTIS PHARMACEUTICALS CORP. | 70 | YR | M | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
4542794 | 1005547066 | PS | GLEEVEC | 1 | ORAL | 400MG/DAY |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
4542794 | 1005547066 | CHRONIC MYELOID LEUKAEMIA |
Outcome of event
Event ID | OUTC COD |
---|---|
4542794 | OT |
Reactions reported
Event ID | PT |
---|---|
4542794 | BLADDER CATHETERISATION |
4542794 | DYSURIA |
4542794 | HYPERTONIC BLADDER |
4542794 | URINARY RETENTION |
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 |
---|---|---|---|---|---|
4542794 | 1005547066 | 20040901 |