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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127019881 | 12701988 | 1 | I | 20160818 | 20160831 | 20160831 | EXP | CA-ORION CORPORATION ORION PHARMA-TREX2016-1484 | ORION | 44.00 | YR | M | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127019881 | 12701988 | 1 | PS | METHOTREXATE (TRADE NAME UNKNOWN) | METHOTREXATE | 1 | Oral | 0 | 20 | MG | /wk | ||||||||
| 127019881 | 12701988 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 0 | INJECTION | ||||||||||
| 127019881 | 12701988 | 3 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | 0 | 50 | MG | |||||||||
| 127019881 | 12701988 | 4 | SS | CELEBREX | CELECOXIB | 1 | Oral | 0 | CAPSULE, HARD | ||||||||||
| 127019881 | 12701988 | 5 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Oral | 0 | 1 | G | BID | ||||||||
| 127019881 | 12701988 | 6 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | 0 | 3 | MG/KG | |||||||||
| 127019881 | 12701988 | 7 | SS | ORENCIA | ABATACEPT | 1 | Intravenous (not otherwise specified) | 0 | |||||||||||
| 127019881 | 12701988 | 8 | SS | ORENCIA | ABATACEPT | 1 | Subcutaneous | 0 | |||||||||||
| 127019881 | 12701988 | 9 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | 0 | 400 | MG | TABLET | QD | |||||||
| 127019881 | 12701988 | 10 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127019881 | 12701988 | 1 | Rheumatoid arthritis |
| 127019881 | 12701988 | 2 | Rheumatoid arthritis |
| 127019881 | 12701988 | 4 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127019881 | 12701988 | HO |
| 127019881 | 12701988 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127019881 | 12701988 | Abdominal discomfort | |
| 127019881 | 12701988 | Drug intolerance | |
| 127019881 | 12701988 | Internal haemorrhage | |
| 127019881 | 12701988 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |