Baricitinib is a Janus kinase (JAK) inhibitor indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more TNF antagonist therapies.
The recommended dose of Baricitinib is 2 mg once daily. It may be used as monotherapy or in combination with methotrexate or other DMARDs.
Baricitinib is not recommended in patients taking strong Organic Anion Transporter 3 (OAT3) inhibitors (e.g., probenecid).
Serious Infections: Avoid use of Baricitinib in patients with active, serious infection, including localized infections. If a serious infection develops, interrupt Baricitinib therapy until the infection is controlled. Do not give Baricitinib to patients with active tuberculosis. Thrombosis: Use with caution in patients who may be at increased risk. Gastrointestinal Perforations: Use with caution in patients who may be at increased risk. Laboratory Assessment: Recommended due to potential changes in lymphocytes, neutrophils, hemoglobin, liver enzymes, and lipids. Vaccinations: Avoid use of Baricitinib with live vaccines.
upper respiratory tract infections, nausea, herpes simplex, and herpes zoster.
Data in pregnant women are insufficient to inform pregnancy category.
