This multi-center, observational study will evaluate the clinical practice patterns, efficacy and safety of RoActemra/Actemra (tocilizumab) in participants with moderate to severe rheumatoid arthritis. Data will be collected from each eligible participant initiated on RoActemra/Actemra treatment by their treating physician according to local label for 6 months from start of treatment.
Participants received tocilizumab according to individualized physician-prescribed regimens.
Buenos Aires, Argentina
Buenos Aires, Argentina
Ciudad Autonoma de, Argentina
La Plata, Argentina
San Juan, Argentina
San Juan Bautista, Argentina
San Miguel de Tucumán, Argentina