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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126590811 | 12659081 | 1 | I | 20160815 | 20160817 | 20160817 | EXP | CA-ROCHE-1814713 | ROCHE | 0.00 | A | F | Y | 0.00000 | 20160817 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126590811 | 12659081 | 1 | PS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | WORKED THE BEST | U | 125276 | |||||||||
| 126590811 | 12659081 | 2 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | THE PT TRIED THIS MEDICATION LAST | U | 103705 | |||||||||
| 126590811 | 12659081 | 3 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | USED MEDICATION FOR 7 YEARS | U | 0 | |||||||||
| 126590811 | 12659081 | 4 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | TRIED 6 YEARS AGO (2010) | U | 0 | |||||||||
| 126590811 | 12659081 | 5 | SS | ENBREL | ETANERCEPT | 1 | Unknown | TRIED 1ST | U | 0 | |||||||||
| 126590811 | 12659081 | 6 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | TRIED SECOND | U | 0 | |||||||||
| 126590811 | 12659081 | 7 | SS | ORENCIA | ABATACEPT | 1 | Unknown | TRIED | U | 0 | |||||||||
| 126590811 | 12659081 | 8 | SS | CELEBREX | CELECOXIB | 1 | Oral | U | 0 | 200 | MG | BID | |||||||
| 126590811 | 12659081 | 9 | C | TRAMADOL. | TRAMADOL | 1 | Unknown | SLOW RELEASE AS NEEDED | 0 | 100 | MG | ||||||||
| 126590811 | 12659081 | 10 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | 7-10MG SLIDING SCALE AS PERHEUMATOLOGIST | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126590811 | 12659081 | 1 | Rheumatoid arthritis |
| 126590811 | 12659081 | 2 | Product used for unknown indication |
| 126590811 | 12659081 | 3 | Product used for unknown indication |
| 126590811 | 12659081 | 4 | Product used for unknown indication |
| 126590811 | 12659081 | 5 | Rheumatoid arthritis |
| 126590811 | 12659081 | 6 | Product used for unknown indication |
| 126590811 | 12659081 | 7 | Product used for unknown indication |
| 126590811 | 12659081 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126590811 | 12659081 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126590811 | 12659081 | Arthropathy | |
| 126590811 | 12659081 | Drug ineffective | |
| 126590811 | 12659081 | Lung disorder | |
| 126590811 | 12659081 | Lupus-like syndrome | |
| 126590811 | 12659081 | Musculoskeletal stiffness | |
| 126590811 | 12659081 | Pain | |
| 126590811 | 12659081 | Quality of life decreased | |
| 126590811 | 12659081 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |