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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472349 | 6431114 | I | 5472349-5 | 20050101 | 20070917 | 20070930 | EXP | US-SHR-US-2007-035102 | BERLEX | 49 | YR | F | Y | 20070928 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5472349 | 1008989638 | PS | FLUDARABINE FOR INJECTION | 2 | 48.25 MG/D | 20038 | |||||
| 5472349 | 1008989639 | SS | RITUXIMAB | 2 | 724 MG |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5472349 | 1008989638 | LYMPHOMA |
| 5472349 | 1008989639 | LYMPHOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5472349 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5472349 | ACUTE MYELOID LEUKAEMIA |
| 5472349 | ADENOCARCINOMA |
| 5472349 | BREAST CANCER FEMALE |
| 5472349 | CHROMOSOME ANALYSIS ABNORMAL |
| 5472349 | PANCYTOPENIA |
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 |
|---|---|---|---|---|---|
| 5472349 | 1008989638 | 19980518 | 19981016 | 151 | DAY |
| 5472349 | 1008989639 | 19980511 | 19981009 | 151 | DAY |