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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117129222 | 11712922 | 2 | F | 20160714 | 20151108 | 20160721 | EXP | CA-AMGEN-CANSP2015117077 | AMGEN | 44.00 | YR | A | F | Y | 0.00000 | 20160721 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117129222 | 11712922 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 117129222 | 11712922 | 2 | SS | PLAQUENIL /00072602/ | HYDROXYCHLOROQUINE DIPHOSPHATE | 1 | Unknown | 400 MG, QD | 0 | 400 | MG | TABLET | QD | ||||||
| 117129222 | 11712922 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 20 UNK, QWK | 0 | /wk | |||||||||
| 117129222 | 11712922 | 4 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | 20 UNK, QD | 0 | TABLET | QD | ||||||||
| 117129222 | 11712922 | 5 | SS | CELEBREX | CELECOXIB | 1 | Unknown | UNK | 0 | ||||||||||
| 117129222 | 11712922 | 6 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 117129222 | 11712922 | 7 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | 0 | ||||||||||
| 117129222 | 11712922 | 8 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | 20 UNK, QWK | 0 | /wk |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117129222 | 11712922 | 1 | Rheumatoid arthritis |
| 117129222 | 11712922 | 2 | Rheumatoid arthritis |
| 117129222 | 11712922 | 3 | Product used for unknown indication |
| 117129222 | 11712922 | 4 | Rheumatoid arthritis |
| 117129222 | 11712922 | 5 | Product used for unknown indication |
| 117129222 | 11712922 | 6 | Rheumatoid arthritis |
| 117129222 | 11712922 | 7 | Rheumatoid arthritis |
| 117129222 | 11712922 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117129222 | 11712922 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117129222 | 11712922 | Activities of daily living impaired | |
| 117129222 | 11712922 | Arthralgia | |
| 117129222 | 11712922 | Drug hypersensitivity | |
| 117129222 | 11712922 | Drug ineffective | |
| 117129222 | 11712922 | Drug intolerance | |
| 117129222 | 11712922 | Gastric ulcer | |
| 117129222 | 11712922 | Rheumatoid arthritis | |
| 117129222 | 11712922 | Rheumatoid factor positive | |
| 117129222 | 11712922 | Therapeutic response decreased | |
| 117129222 | 11712922 | Treatment failure |
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 |
|---|---|---|---|---|---|---|
| 117129222 | 11712922 | 7 | 201508 | 0 |