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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116953832 | 11695383 | 2 | F | 20160714 | 20151104 | 20160719 | EXP | CA-AMGEN-CANSP2015115178 | AMGEN | 39.00 | YR | A | F | Y | 0.00000 | 20160719 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116953832 | 11695383 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 116953832 | 11695383 | 2 | SS | CELEBREX | CELECOXIB | 1 | Oral | 200 MG, AS REQUIRED | 0 | 200 | MG | CAPSULE | |||||||
| 116953832 | 11695383 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 116953832 | 11695383 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | 0 | ||||||||||||
| 116953832 | 11695383 | 5 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 25 MG, QWK | 0 | 25 | MG | /wk | |||||||
| 116953832 | 11695383 | 6 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 116953832 | 11695383 | 7 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | UNK | 0 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116953832 | 11695383 | 1 | Rheumatoid arthritis |
| 116953832 | 11695383 | 2 | Rheumatoid arthritis |
| 116953832 | 11695383 | 3 | Product used for unknown indication |
| 116953832 | 11695383 | 4 | Rheumatoid arthritis |
| 116953832 | 11695383 | 5 | Rheumatoid arthritis |
| 116953832 | 11695383 | 6 | Rheumatoid arthritis |
| 116953832 | 11695383 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 116953832 | 11695383 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116953832 | 11695383 | Activities of daily living impaired | |
| 116953832 | 11695383 | Drug ineffective | |
| 116953832 | 11695383 | Hypersensitivity | |
| 116953832 | 11695383 | Impaired work ability | |
| 116953832 | 11695383 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |