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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4466786 | 4214966 | F | 1 | 4466786-5 | 20040629 | 20040917 | 20040930 | EXP | HQWYE971010SEP04 | WYETH LABS (RA) | 34 | YR | F | N | 53.57 | KG | 20040929 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4466786 | 1005268333 | PS | MYLOTARG | 1 | INTRAVENOUS | 6.6 1X PER 1 DAY, INTRAVENOUS | D | D | 21174 | ||
| 4466786 | 1005288041 | SS | CYTARABINE | 1 | D | D | |||||
| 4466786 | 1005288046 | SS | FLUDARABINE PHOSPHATE | 1 | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4466786 | 1005268333 | ACUTE MYELOID LEUKAEMIA |
| 4466786 | 1005288041 | ACUTE MYELOID LEUKAEMIA |
| 4466786 | 1005288046 | ACUTE MYELOID LEUKAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4466786 | HO |
| 4466786 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4466786 | NEUTROPENIA |
| 4466786 | PYREXIA |
| 4466786 | RED BLOOD CELL COUNT DECREASED |
| 4466786 | THROMBOCYTOPENIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4466786 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4466786 | 1005268333 | 20040624 | 20040624 | ||
| 4466786 | 1005288041 | 20040601 | 20040601 | ||
| 4466786 | 1005288046 | 20040601 | 20040601 |