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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6025683 | 6871270 | F | 6025683-4 | 20081001 | 20081219 | 20081231 | EXP | IE-GENENTECH-271668 | GNEFDAAERSPRD | 66 | M | Y | 20081231 | CN | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6025683 | 1010944282 | PS | MABTHERA | 2 | INTRAVENOUS | 375 MG/M2, UNK | NOT REPORTED | ||||
| 6025683 | 1010944283 | C | CYCLOPHOSPHAMIDE | 1 | UNK | ||||||
| 6025683 | 1010944284 | C | DOXORUBICIN HCL | 1 | UNK | ||||||
| 6025683 | 1010944285 | C | VINCRISTINE | 1 | UNK | ||||||
| 6025683 | 1010944286 | C | PREDNISOLONE | 1 | UNK |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6025683 | 1010944282 | NON-HODGKIN'S LYMPHOMA |
| 6025683 | 1010944283 | B-CELL LYMPHOMA |
| 6025683 | 1010944284 | B-CELL LYMPHOMA |
| 6025683 | 1010944285 | B-CELL LYMPHOMA |
| 6025683 | 1010944286 | NON-HODGKIN'S LYMPHOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6025683 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6025683 | ATRIAL FLUTTER |
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 |
|---|---|---|---|---|---|
| 6025683 | 1010944282 | 20080728 | 20081110 | 106 | DAY |
| 6025683 | 1010944283 | 20080728 | 20081110 | 106 | DAY |
| 6025683 | 1010944284 | 20080728 | 20081110 | 106 | DAY |
| 6025683 | 1010944285 | 20080728 | 20081110 | 106 | DAY |
| 6025683 | 1010944286 | 20080728 |