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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127055901 | 12705590 | 1 | I | 20160830 | 20160901 | 20160901 | EXP | CA-ROCHE-1822907 | ROCHE | 61.00 | YR | F | Y | 0.00000 | 20160901 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127055901 | 12705590 | 1 | PS | Tocilizumab | TOCILIZUMAB | 1 | Unknown | U | 125276 | ||||||||||
| 127055901 | 12705590 | 2 | SS | ALEVE | NAPROXEN SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 127055901 | 12705590 | 3 | SS | ENBREL | ETANERCEPT | 1 | Unknown | U | 0 | ||||||||||
| 127055901 | 12705590 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | U | 0 | ||||||||||
| 127055901 | 12705590 | 5 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | U | 0 | ||||||||||
| 127055901 | 12705590 | 6 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | U | 0 | TABLET | |||||||||
| 127055901 | 12705590 | 7 | SS | ORENCIA | ABATACEPT | 1 | Intravenous (not otherwise specified) | U | 0 | ||||||||||
| 127055901 | 12705590 | 8 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | U | 0 | ||||||||||
| 127055901 | 12705590 | 9 | C | HYDROXYCHLOROQUINE SULFATE. | HYDROXYCHLOROQUINE SULFATE | 1 | 0 | ||||||||||||
| 127055901 | 12705590 | 10 | C | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | 0 | ||||||||||||
| 127055901 | 12705590 | 11 | C | FOLIC ACID. | FOLIC ACID | 1 | 0 | ||||||||||||
| 127055901 | 12705590 | 12 | C | METHOTREXATE. | METHOTREXATE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127055901 | 12705590 | 1 | Product used for unknown indication |
| 127055901 | 12705590 | 2 | Rheumatoid arthritis |
| 127055901 | 12705590 | 3 | Rheumatoid arthritis |
| 127055901 | 12705590 | 4 | Rheumatoid arthritis |
| 127055901 | 12705590 | 5 | Rheumatoid arthritis |
| 127055901 | 12705590 | 6 | Product used for unknown indication |
| 127055901 | 12705590 | 7 | Rheumatoid arthritis |
| 127055901 | 12705590 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127055901 | 12705590 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127055901 | 12705590 | Arthropathy | |
| 127055901 | 12705590 | C-reactive protein abnormal | |
| 127055901 | 12705590 | Fatigue | |
| 127055901 | 12705590 | Femur fracture | |
| 127055901 | 12705590 | Osteoporosis | |
| 127055901 | 12705590 | Pain | |
| 127055901 | 12705590 | Rash | |
| 127055901 | 12705590 | Red blood cell sedimentation rate abnormal | |
| 127055901 | 12705590 | Synovitis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |