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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116177474 | 11617747 | 4 | F | 20160627 | 20160815 | 20151009 | 20160830 | EXP | CA-CONCORDIA PHARMACEUTICALS INC.-CO-PL-CA-2015-034 | CONCORDIA | 0.00 | F | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116177474 | 11617747 | 1 | PS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | 9768 | |||||||||||
| 116177474 | 11617747 | 2 | C | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 0 | |||||||||||
| 116177474 | 11617747 | 3 | C | CELEBREX | CELECOXIB | 1 | Unknown | 0 | |||||||||||
| 116177474 | 11617747 | 4 | C | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | 0 | |||||||||||
| 116177474 | 11617747 | 5 | C | SIMPONI | GOLIMUMAB | 1 | Unknown | 0 | |||||||||||
| 116177474 | 11617747 | 6 | C | TENS therapy | 2 | 0 | |||||||||||||
| 116177474 | 11617747 | 7 | C | CORTISONE | CORTISONEHYDROCORTISONE | 1 | Topical | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116177474 | 11617747 | 1 | Rheumatoid arthritis |
| 116177474 | 11617747 | 2 | Product used for unknown indication |
| 116177474 | 11617747 | 3 | Product used for unknown indication |
| 116177474 | 11617747 | 4 | Rheumatoid arthritis |
| 116177474 | 11617747 | 5 | Product used for unknown indication |
| 116177474 | 11617747 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 116177474 | 11617747 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116177474 | 11617747 | Arthralgia | |
| 116177474 | 11617747 | Bone erosion | |
| 116177474 | 11617747 | Cough | |
| 116177474 | 11617747 | Dysphonia | |
| 116177474 | 11617747 | Fatigue | |
| 116177474 | 11617747 | Limb discomfort | |
| 116177474 | 11617747 | Lower respiratory tract infection | |
| 116177474 | 11617747 | Pain in extremity | |
| 116177474 | 11617747 | Peripheral swelling | |
| 116177474 | 11617747 | Plantar fasciitis | |
| 116177474 | 11617747 | Rheumatoid arthritis | |
| 116177474 | 11617747 | Sciatica | |
| 116177474 | 11617747 | Sputum discoloured | |
| 116177474 | 11617747 | Tendon injury | |
| 116177474 | 11617747 | Tendon pain |
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 |
|---|---|---|---|---|---|---|
| 116177474 | 11617747 | 4 | 20141001 | 0 | ||
| 116177474 | 11617747 | 5 | 20140911 | 0 |