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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126305811 | 12630581 | 1 | I | 20160726 | 20160801 | 20160808 | 20160808 | EXP | IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-063542 | BRISTOL MYERS SQUIBB | 69.57 | YR | M | Y | 0.00000 | 20160808 | OT | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126305811 | 12630581 | 1 | PS | ORENCIA | ABATACEPT | 1 | Unknown | 1 DF, QWK | Y | AAH1723 | 125118 | 1 | DF | SOLUTION FOR INJECTION | /wk | ||||
| 126305811 | 12630581 | 2 | C | METHOTREXATE (METHOTREXATE SODIUM) | METHOTREXATE SODIUM | 1 | Unknown | 1 DF, QWK | U | 0 | 1 | DF | INJECTION | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126305811 | 12630581 | 1 | Rheumatoid arthritis |
| 126305811 | 12630581 | 2 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126305811 | 12630581 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126305811 | 12630581 | Abdominal pain | |
| 126305811 | 12630581 | Malaise | |
| 126305811 | 12630581 | Nausea | |
| 126305811 | 12630581 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |