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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6698450 | 7367474 | I | 6698450-6 | 20100407 | 20100419 | 20100427 | EXP | CA-ROCHE-698706 | ROCHE | 45 | YR | M | Y | 20100427 | MD | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6698450 | 1013576532 | PS | MYCOPHENOLATE MOFETIL | 1 | ORAL | 50722 | |||||
6698450 | 1013576533 | SS | BLINDED ABATACEPT | 2 | INTRAVENOUS | DOSE BLINDED | |||||
6698450 | 1013576534 | SS | PREDNISONE | 2 | ORAL | BACKGROUND THERAPY | |||||
6698450 | 1013576535 | SS | ABATACEPT | 2 | INTRAVENOUS | ||||||
6698450 | 1013576536 | C | BENAZEPRIL HYDROCHLORIDE | 1 | |||||||
6698450 | 1013576537 | C | CALTRATE + D | 2 | |||||||
6698450 | 1013576538 | C | NORVASC | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6698450 | 1013576532 | SYSTEMIC LUPUS ERYTHEMATOSUS |
6698450 | 1013576533 | SYSTEMIC LUPUS ERYTHEMATOSUS |
6698450 | 1013576534 | SYSTEMIC LUPUS ERYTHEMATOSUS |
6698450 | 1013576535 | SYSTEMIC LUPUS ERYTHEMATOSUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6698450 | HO |
Reactions reported
Event ID | PT |
---|---|
6698450 | VENTRICULAR EXTRASYSTOLES |
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 |
---|---|---|---|---|---|
6698450 | 1013576532 | 20090407 | |||
6698450 | 1013576534 | 20090213 | |||
6698450 | 1013576535 | 20090407 | |||
6698450 | 1013576536 | 20090220 | |||
6698450 | 1013576537 | 20090226 | |||
6698450 | 1013576538 | 20100112 |