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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127016491 | 12701649 | 1 | I | 20160817 | 20160831 | 20160831 | EXP | CA-ORION CORPORATION ORION PHARMA-TREX2016-1485 | ORION | 53.00 | YR | F | Y | 0.00000 | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127016491 | 12701649 | 1 | PS | METHOTREXATE (TRADE NAME UNKNOWN) | METHOTREXATE | 1 | Unknown | N | 0 | 20 | MG | ||||||||
| 127016491 | 12701649 | 2 | SS | METHOTREXATE (TRADE NAME UNKNOWN) | METHOTREXATE | 1 | Unknown | N | 0 | 15 | MG | ||||||||
| 127016491 | 12701649 | 3 | SS | ENBREL | ETANERCEPT | 1 | Unknown | N | 0 | ||||||||||
| 127016491 | 12701649 | 4 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | N | 0 | ||||||||||
| 127016491 | 12701649 | 5 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | N | 0 | ||||||||||
| 127016491 | 12701649 | 6 | SS | SIMPONI | GOLIMUMAB | 1 | Unknown | N | 0 | ||||||||||
| 127016491 | 12701649 | 7 | SS | ORENCIA | ABATACEPT | 1 | Unknown | N | 0 | ||||||||||
| 127016491 | 12701649 | 8 | SS | ORENCIA | ABATACEPT | 1 | Unknown | N | 0 | 1 | DF | ||||||||
| 127016491 | 12701649 | 9 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | 0 | 400 | MG | QD | ||||||||
| 127016491 | 12701649 | 10 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | N | 0 | 10 | MG | TABLET | |||||||
| 127016491 | 12701649 | 11 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127016491 | 12701649 | 1 | Rheumatoid arthritis |
| 127016491 | 12701649 | 3 | Rheumatoid arthritis |
| 127016491 | 12701649 | 4 | Rheumatoid arthritis |
| 127016491 | 12701649 | 5 | Rheumatoid arthritis |
| 127016491 | 12701649 | 6 | Rheumatoid arthritis |
| 127016491 | 12701649 | 7 | Rheumatoid arthritis |
| 127016491 | 12701649 | 9 | Rheumatoid arthritis |
| 127016491 | 12701649 | 10 | Rheumatoid arthritis |
| 127016491 | 12701649 | 11 | Polyarthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127016491 | 12701649 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127016491 | 12701649 | Alopecia | |
| 127016491 | 12701649 | Carpal tunnel syndrome | |
| 127016491 | 12701649 | Drug ineffective | |
| 127016491 | 12701649 | Drug intolerance | |
| 127016491 | 12701649 | Hip fracture | |
| 127016491 | 12701649 | Intervertebral disc disorder | |
| 127016491 | 12701649 | Nausea | |
| 127016491 | 12701649 | Rheumatoid arthritis |
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 |
|---|---|---|---|---|---|---|
| 127016491 | 12701649 | 7 | 20150122 | 0 | ||
| 127016491 | 12701649 | 8 | 20160129 | 0 | ||
| 127016491 | 12701649 | 10 | 201306 | 201309 | 0 |