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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5080777 | 6114799 | F | 1 | 5080777-5 | 20060628 | 20060809 | EXP | PHBS2006JP09425 | SANDOZ INC | 65 | YR | F | N | 20060715 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5080777 | 1007581244 | PS | CYCLOSPORINE | 1 | U | U | 80339 | ||||
5080777 | 1007598303 | SS | PREDNISOLONE | 1 | ORAL | ORAL | U | U |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5080777 | 1007581244 | SYSTEMIC LUPUS ERYTHEMATOSUS |
5080777 | 1007598303 | SYSTEMIC LUPUS ERYTHEMATOSUS |
Outcome of event
Event ID | OUTC COD |
---|---|
5080777 | OT |
Reactions reported
Event ID | PT |
---|---|
5080777 | NEOPLASM |
5080777 | SYNOVIAL CYST |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5080777 | FGN |
5080777 | HP |
5080777 | LIT |
5080777 | OTH |
Therapies reported
no results found |