This observational study will evaluate the safety, tolerability and efficacy of RoActemra/Actemra (tocilizumab) in combination with methotrexate in patients with moderate to severe rheumatoid arthritis. Data will be collected for 12 months from patients initiated on treatment with RoActemra/Actemra (8 mg/kg intravenously every 4 weeks) and methotrexate (weekly dose at the discretion of the physician).
Study Type
OBSERVATIONAL
Enrollment
251
Unnamed facility
Budapest, Hungary
Unnamed facility
Budapest, Hungary
Unnamed facility
Budapest, Hungary
Safety: Incidence of adverse events
Time frame: 12 months
Efficacy: Disease Activity Score (DAS 28)
Time frame: 12 months
Pain: Visual Analogue Scale (VAS) pain scale
Time frame: 12 months
Physical Function: Health Assessments Questionnaire (HAQ)
Time frame: 12 months
Incidence of patients with all-cause discontinuation of tocilizumab
Time frame: 12 months
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Unnamed facility
Debrecen, Hungary
Unnamed facility
Debrecen, Hungary
Unnamed facility
Eger, Hungary
Unnamed facility
Esztergom, Hungary
Unnamed facility
Győr, Hungary
Unnamed facility
Gyula, Hungary
Unnamed facility
Hévíz, Hungary
...and 10 more locations