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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5205207 | 6175869 | F | 1 | 5205207-1 | 20060601 | 20061227 | 20070108 | EXP | 231912 | GENENTECH, INC. | 72 | YR | F | N | 20070105 | MD | JAPAN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5205207 | 1008030165 | PS | RITUXAN | 1 | INTRAVENOUS | 500 MG, INTRAVENOUS | D | D | |||
5205207 | 1008064924 | C | CYCLOPHOSPHAMIDE | 1 | |||||||
5205207 | 1008064926 | C | ADIRACIN (DOXORUBICIN HYDROCHOLORIDE) | 2 | |||||||
5205207 | 1008064928 | C | ONCOVIN | 1 | |||||||
5205207 | 1008064930 | C | PREDNISOLONE | 1 | |||||||
5205207 | 1008064932 | C | VEPESID | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5205207 | 1008030165 | NON-HODGKIN'S LYMPHOMA |
Outcome of event
Event ID | OUTC COD |
---|---|
5205207 | DS |
Reactions reported
Event ID | PT |
---|---|
5205207 | ARTHRALGIA |
5205207 | GAIT DISTURBANCE |
5205207 | JOINT SWELLING |
5205207 | OSTEONECROSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5205207 | FGN |
5205207 | HP |
5205207 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5205207 | 1008030165 | 20030507 | 20060908 |