Switching from adalimumab to tofacitinib in the treatment of patients with rheumatoid arthritis
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![Table 1 Baseline characteristics for patients randomized to double-blind adalimumab (ADA) 40 mg every 2 weeks or tofacitinib 10mg twice daily (BID) in the phase 3 study [10] and for the subgroup who then received open-label tofacitinib 10 mg BID in theextension study [13]](https://thumb-us.123doks.com/thumbv2/123dok_us/8821714.922808/3.595.58.539.327.692/baseline-characteristics-patients-randomized-adalimumab-tofacitinib-tofacitinib-theextension.webp)
![Table 2 Incidence of treatment-emergent adverse events (TEAEs), and the most commonly reported TEAEs (occurring in ≥2 % ofpatients in any group) during the last 3 months of the double-blind phase 3 study [10] and the first 3 months of the open-labelextension [13]](https://thumb-us.123doks.com/thumbv2/123dok_us/8821714.922808/4.595.59.538.315.698/incidence-treatment-emergent-commonly-reported-occurring-ofpatients-labelextension.webp)
![Table 3 Adverse events and change from baseline in selected laboratory variables during the phase 3 double-blind study [10] and the open-label extension study [13]](https://thumb-us.123doks.com/thumbv2/123dok_us/8821714.922808/5.791.56.698.66.495/table-adverse-events-baseline-selected-laboratory-variables-extension.webp)
![Table 3 Adverse events and change from baseline in selected laboratory variables during the phase 3 double-blind study [10] and the open-label extension study [13](Continued)](https://thumb-us.123doks.com/thumbv2/123dok_us/8821714.922808/6.791.54.713.81.258/table-adverse-baseline-selected-laboratory-variables-extension-continued.webp)
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