Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117827832 | 11782783 | 2 | F | 20151015 | 20160829 | 20151127 | 20160902 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-079938 | BRISTOL MYERS SQUIBB | 61.01 | YR | F | Y | 0.00000 | 20160902 | CN | FR | FR |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117827832 | 11782783 | 1 | PS | ORENCIA | ABATACEPT | 1 | Subcutaneous | 125 MG, QWK | Y | 125118 | 125 | MG | SOLUTION FOR INJECTION | /wk | |||||
117827832 | 11782783 | 2 | SS | ORENCIA | ABATACEPT | 1 | Intravenous (not otherwise specified) | 500 MG, UNK | Y | 125118 | 500 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
117827832 | 11782783 | 1 | Rheumatoid arthritis |
117827832 | 11782783 | 2 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
117827832 | 11782783 | OT |
117827832 | 11782783 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
117827832 | 11782783 | Paradoxical drug reaction | |
117827832 | 11782783 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
117827832 | 11782783 | 1 | 20150323 | 201507 | 0 | |
117827832 | 11782783 | 2 | 20151013 | 0 |