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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6383134 | 7135601 | I | 6383134-4 | 20080306 | 20090917 | 20090930 | EXP | RU-GENENTECH-290937 | GNEFDAAERSPRD | F | Y | 20090930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6383134 | 1012357325 | PS | RITUXIMAB | 2 | INTRAVENOUS | 1000 MG, Q2W | NOT REPORTED |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6383134 | 1012357325 | RHEUMATOID ARTHRITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
6383134 | OT |
Reactions reported
Event ID | PT |
---|---|
6383134 | ANGIOEDEMA |
6383134 | ORAL HERPES |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |