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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138280 | 6476593 | F | 6138280-7 | 20070203 | 20090316 | 20090331 | EXP | NL-GENENTECH-251614 | GNEFDAAERSPRD | 69 | M | Y | 77.5 | KG | 20090331 | MD | NETHERLANDS |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6138280 | 1011356987 | PS | RITUXIMAB | 2 | INTRAVENOUS | 375 MG/M2, Q8W | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6138280 | 1011356987 | B-CELL LYMPHOMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6138280 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6138280 | VIRAL INFECTION |
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 |
|---|---|---|---|---|---|
| 6138280 | 1011356987 | 20060619 |