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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114978732 | 11497873 | 2 | F | 20160704 | 20150911 | 20160719 | EXP | CA-CONCORDIA PHARMACEUTICALS INC.-CO-PL-CA-2015-210 | CONCORDIA | 81.00 | YR | F | Y | 0.00000 | 20160719 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
114978732 | 11497873 | 1 | PS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNKNOWN | 9768 | 400 | MG | QD | |||||||
114978732 | 11497873 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNKNOWN | 0 | 25 | MG | /wk | |||||||
114978732 | 11497873 | 3 | SS | CELEBREX | CELECOXIB | 1 | Unknown | U | UNKNOWN | 0 | |||||||||
114978732 | 11497873 | 4 | SS | FOLIC ACID. | FOLIC ACID | 1 | Unknown | UNKNOWN | 0 | ||||||||||
114978732 | 11497873 | 5 | SS | LEFLUNOMIDE. | LEFLUNOMIDE | 1 | Unknown | U | 0 | 20 | MG | ||||||||
114978732 | 11497873 | 6 | C | PREDNISONE. | PREDNISONE | 1 | 0 | ||||||||||||
114978732 | 11497873 | 7 | C | XELJANZ | TOFACITINIB CITRATE | 1 | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
114978732 | 11497873 | 1 | Rheumatoid arthritis |
114978732 | 11497873 | 2 | Rheumatoid arthritis |
114978732 | 11497873 | 3 | Rheumatoid arthritis |
114978732 | 11497873 | 4 | Rheumatoid arthritis |
114978732 | 11497873 | 5 | Product used for unknown indication |
114978732 | 11497873 | 6 | Rheumatoid arthritis |
114978732 | 11497873 | 7 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
114978732 | 11497873 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
114978732 | 11497873 | Arthralgia | |
114978732 | 11497873 | Condition aggravated | |
114978732 | 11497873 | Drug ineffective | |
114978732 | 11497873 | Pain | |
114978732 | 11497873 | 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 |
---|---|---|---|---|---|---|
114978732 | 11497873 | 1 | 201310 | 0 | ||
114978732 | 11497873 | 2 | 200904 | 0 | ||
114978732 | 11497873 | 5 | 200907 | 2013 | 0 | |
114978732 | 11497873 | 6 | 201402 | 201411 | 0 |