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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113871948 | 11387194 | 8 | F | 20160712 | 20150817 | 20160718 | EXP | CA-AMGEN-CANSP2014106179 | AMGEN | 47.00 | YR | A | F | Y | 0.00000 | 20160718 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113871948 | 11387194 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 113871948 | 11387194 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Subcutaneous | 25 MG, UNK | 0 | 25 | MG | ||||||||
| 113871948 | 11387194 | 3 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | 0 | ||||||||||
| 113871948 | 11387194 | 4 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | UNK | 0 | POWDER AND SOLVENT FOR SOLUTION FOR INFUSION | |||||||||
| 113871948 | 11387194 | 5 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 10 MG, 2 EVERY DAY | 0 | 10 | MG | TABLET | BID | ||||||
| 113871948 | 11387194 | 6 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | 5 MG, 1 EVERY 2 DAYS | 0 | 5 | MG | TABLET | BID | ||||||
| 113871948 | 11387194 | 7 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, UNK | 0 | 25 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 113871948 | 11387194 | 1 | Rheumatoid arthritis |
| 113871948 | 11387194 | 2 | Rheumatoid arthritis |
| 113871948 | 11387194 | 3 | Rheumatoid arthritis |
| 113871948 | 11387194 | 4 | Rheumatoid arthritis |
| 113871948 | 11387194 | 5 | Rheumatoid arthritis |
| 113871948 | 11387194 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 113871948 | 11387194 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 113871948 | 11387194 | Condition aggravated | |
| 113871948 | 11387194 | Drug ineffective | |
| 113871948 | 11387194 | Hand deformity | |
| 113871948 | 11387194 | Pain | |
| 113871948 | 11387194 | Rheumatoid arthritis | |
| 113871948 | 11387194 | Stress | |
| 113871948 | 11387194 | Swelling |
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 |
|---|---|---|---|---|---|---|
| 113871948 | 11387194 | 6 | 20141023 | 0 |