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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126824451 | 12682445 | 1 | I | 20050425 | 20051110 | 20160825 | 20160825 | EXP | CA-AMGEN-KDL157634 | AMGEN | 65.00 | YR | E | M | Y | 0.00000 | 20160824 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126824451 | 12682445 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 25 MG, 2 TIMES/WK | U | 103795 | 25 | MG | UNKNOWN FORMULATION | BIW | |||||
| 126824451 | 12682445 | 2 | SS | CELEBREX | CELECOXIB | 1 | Unknown | UNK | 0 | CAPSULE | |||||||||
| 126824451 | 12682445 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 126824451 | 12682445 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
| 126824451 | 12682445 | 5 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | 0 | ||||||||||
| 126824451 | 12682445 | 6 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
| 126824451 | 12682445 | 7 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126824451 | 12682445 | 1 | Psoriatic arthropathy |
| 126824451 | 12682445 | 2 | Rheumatoid arthritis |
| 126824451 | 12682445 | 3 | Rheumatoid arthritis |
| 126824451 | 12682445 | 4 | Rheumatoid arthritis |
| 126824451 | 12682445 | 5 | Rheumatoid arthritis |
| 126824451 | 12682445 | 6 | Rheumatoid arthritis |
| 126824451 | 12682445 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126824451 | 12682445 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126824451 | 12682445 | Condition aggravated | |
| 126824451 | 12682445 | Hypoaesthesia | |
| 126824451 | 12682445 | Multiple sclerosis | |
| 126824451 | 12682445 | Paraesthesia | |
| 126824451 | 12682445 | 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 |
|---|---|---|---|---|---|---|
| 126824451 | 12682445 | 1 | 20050425 | 0 |