This multicenter, retrospective observational study will evaluate compliance an reasons for withdrawal in patients with moderate to severe active rheumatoid arthritis on treatment with intravenous RoActemra/Actemra (tocilizumab) in daily clinical practice. Data will be collected from each eligible patient over a period of 6 months.
Study Type
OBSERVATIONAL
Enrollment
183
Unnamed facility
Agios Dimitrios, Greece
Unnamed facility
Agía Paraskeví, Greece
Unnamed facility
Argiroupoli, Greece
Percentage of patients on RoActemra/Actemra at 6 months after initiating treatment
Time frame: 12 months
Frequency of withdrawal (according to reasons)
Time frame: 12 months
Frequency of dose modifications
Time frame: 12 months
Change in disease activity (DAS28)
Time frame: from baseline to Month 6 or withdrawal, whichever comes first
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Unnamed facility
Athens, Greece
Unnamed facility
Athens, Greece
Unnamed facility
Athens, Greece
Unnamed facility
Athens, Greece
Unnamed facility
Chalandri, Greece
Unnamed facility
Chania, Greece
Unnamed facility
Corinth, Greece
...and 14 more locations