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Last Updated: 12/27/2024

Tofacitinib

Drug Name(s): Xeljanz, Xeljanz XR

Class: DMARDs

Type: Janus Kinase (JAK) inhibitors

Used to treat rheumatoid arthritis (RA), psoriatic arthritis (PsA), ankylosing spondylitis (AS), and polyarticular course juvenile idiopathic arthritis (JIA).

Dosage

Form(s): tablet, extended-release tablet 

Xeljanz: 5 mg twice daily; 5 mg once daily for patients with reduced kidney or liver function.

Xeljanz XR: 11 mg once daily.

Special Instructions

May be taken with or without food.

Do not chew tablets; do not crush enteric-coated or time-release pills or mix with water.

Potential Side Effects

The most common potential side effects are a decrease in blood counts; diarrhea; headache; hypertension; increased lipid levels; upper respiratory tract infection; skin rash.

Be Aware

The FDA has determined this and other JAK inhibitors have an increased risk of serious cardiovascular-related events, including heart attack and stroke; cancer, including lymphoma and lung cancer; thrombosis and death.

Your doctor should order periodic blood and urine tests to check for unwanted effects. Before taking any DMARD, tell your doctor if you are planning to become pregnant.

Tofacitinib suppresses the immune system and increases the risk of infections and certain cancers. Your doctor will test you for tuberculosis (TB) before starting this drug. Tell your doctor if you have a history of TB. Live vaccines should not be given with tofacitinib.

The Arthritis Foundation’s Drug Guide is meant for education — not self-medicating. The Arthritis Foundation does not endorse any products mentioned in this guide. While we endeavor to keep the information up to date, we make no representations or warranties about the completeness of the information provided.