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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6025682 | 6831409 | F | 6025682-2 | 20080524 | 20081219 | 20081231 | EXP | IT-GENENTECH-272468 | GNEFDAAERSPRD | 65 | M | Y | 20081231 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6025682 | 1010944281 | PS | RITUXIMAB | 2 | INTRAVENOUS | 630 MG, 1/WEEK | B2109, B2033 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6025682 | 1010944281 | B-CELL LYMPHOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6025682 | HO |
| 6025682 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6025682 | ANGINA PECTORIS |
| 6025682 | THROMBOSIS |
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 |
|---|---|---|---|---|---|
| 6025682 | 1010944281 | 20060427 | 20061009 | 166 | DAY |