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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6025685 | 6871271 | I | 6025685-8 | 20081217 | 20081231 | EXP | GB-GENENTECH-274706 | GNEFDAAERSPRD | 53 | YR | F | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6025685 | 1010944288 | PS | RITUXIMAB | 2 | NOT REPORTED | ||||||
| 6025685 | 1010944289 | SS | MITOXANTRONE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6025685 | 1010944288 | NEUROMYELITIS OPTICA |
| 6025685 | 1010944289 | IMMUNOSUPPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6025685 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6025685 | UROSEPSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |