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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6025684 | 6860848 | F | 6025684-6 | 20081118 | 20081218 | 20081231 | EXP | FR-GENENTECH-273341 | GNEFDAAERSPRD | 61 | M | Y | 20081231 | PH | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6025684 | 1010944287 | PS | MABTHERA | 2 | INTRAVENOUS | 375 MG/M2, UNK | B6024 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6025684 | 1010944287 | B-CELL LYMPHOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
6025684 | HO |
Reactions reported
Event ID | PT |
---|---|
6025684 | INFUSION RELATED REACTION |
6025684 | RESPIRATORY FAILURE |
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 |
---|---|---|---|---|---|
6025684 | 1010944287 | 20081118 | 20081118 | 1 | DAY |