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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1174845410 | 11748454 | 10 | F | 20150616 | 20160815 | 20151117 | 20160830 | EXP | CA-CONCORDIA PHARMACEUTICALS INC.-CO-PL-CA-2015-365 | CONCORDIA | 54.00 | YR | M | Y | 0.00000 | 20160830 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 1174845410 | 11748454 | 1 | PS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | Y | 9768 | 200 | MG | QD | |||||||
| 1174845410 | 11748454 | 2 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Oral | 0 | 20 | MG | /wk | ||||||||
| 1174845410 | 11748454 | 3 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | Y | 0 | 5 | MG | BID | |||||||
| 1174845410 | 11748454 | 4 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Oral | Y | 0 | ||||||||||
| 1174845410 | 11748454 | 5 | SS | CELEBREX | CELECOXIB | 1 | Oral | 0 | 200 | MG | BID | ||||||||
| 1174845410 | 11748454 | 6 | SS | CELEBREX | CELECOXIB | 1 | Oral | 0 | |||||||||||
| 1174845410 | 11748454 | 7 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 | 2.5 | MG | QD | ||||||||
| 1174845410 | 11748454 | 8 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | 0 | 2.5 | MG | QOD | ||||||||
| 1174845410 | 11748454 | 9 | C | ADVIL | IBUPROFEN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 1174845410 | 11748454 | 1 | Rheumatoid arthritis |
| 1174845410 | 11748454 | 2 | Rheumatoid arthritis |
| 1174845410 | 11748454 | 3 | Rheumatoid arthritis |
| 1174845410 | 11748454 | 5 | Rheumatoid arthritis |
| 1174845410 | 11748454 | 6 | Pain |
| 1174845410 | 11748454 | 7 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 1174845410 | 11748454 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 1174845410 | 11748454 | Abasia | |
| 1174845410 | 11748454 | Abdominal pain | |
| 1174845410 | 11748454 | Abdominal pain upper | |
| 1174845410 | 11748454 | Arthralgia | |
| 1174845410 | 11748454 | Constipation | |
| 1174845410 | 11748454 | Cough | |
| 1174845410 | 11748454 | Depressed mood | |
| 1174845410 | 11748454 | Fatigue | |
| 1174845410 | 11748454 | Inflammation | |
| 1174845410 | 11748454 | Irritability | |
| 1174845410 | 11748454 | Musculoskeletal stiffness | |
| 1174845410 | 11748454 | Nasal congestion | |
| 1174845410 | 11748454 | Nasopharyngitis | |
| 1174845410 | 11748454 | Pain | |
| 1174845410 | 11748454 | Pain in extremity | |
| 1174845410 | 11748454 | Peripheral swelling | |
| 1174845410 | 11748454 | Rheumatoid arthritis | |
| 1174845410 | 11748454 | Synovitis |
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 |
|---|---|---|---|---|---|---|
| 1174845410 | 11748454 | 1 | 20150220 | 20151016 | 0 | |
| 1174845410 | 11748454 | 2 | 20150220 | 0 | ||
| 1174845410 | 11748454 | 3 | 20150716 | 201601 | 0 | |
| 1174845410 | 11748454 | 5 | 20151015 | 0 | ||
| 1174845410 | 11748454 | 8 | 20150904 | 0 |