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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5526323 | 6413485 | F | 5526323-0 | 20071119 | 20071127 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-13907407 | BRISTOL-MYERS SQUIBB COMPANY | M | Y | 23 | KG | 20071127 | MD | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5526323 | 1009195810 | PS | SPRYCEL | 1 | ORAL | 021986 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5526323 | 1009195810 | ACUTE MYELOID LEUKAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5526323 | HO |
| 5526323 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5526323 | DERMATITIS BULLOUS |
| 5526323 | TOXIC SKIN ERUPTION |
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 |
|---|---|---|---|---|---|
| 5526323 | 1009195810 | 4 | DAY |