Video Resources

Patient Stories

Hear from real patients taking Jakafi® (ruxolitinib) and their loved ones. If you have intermediate- or high-risk myelofibrosis, you’re not alone.

Nick’s Story

Nick was diagnosed with high-risk MF after a routine medical check. Hear Nick discuss his experience with MF symptoms, as well as some of the challenges he faces living with MF.

Sue’s Story

A devoted wife and mother, Sue was surprised when a diagnosis of intermediate-risk MF made her miss out on plans to see her oldest son play college baseball. Watch Sue's story and learn about her journey with intermediate-risk MF.

Dan’s Story

Hear Dan talk about fatigue, itching, and other symptoms of his myelofibrosis (MF) before and after he started taking Jakafi.

IncyteCARES Patient Experiences

Hear how the patient support program, IncyteCARES, has helped eligible patients with information and support for the treatment journey with Jakafi.

Sue’s IncyteCARES Story

Hear Sue share how IncyteCARES—a patient support program for eligible adults taking Jakafi—connected her with information regarding coverage and educational support to help her throughout her journey with Jakafi.

Rob’s IncyteCARES Story

IncyteCARES gave Rob additional support to help move his treatment journey forward. Learn more about this patient support program for eligible adults taking Jakafi.

Dan’s IncyteCARES Story

IncyteCARES helped support Dan through his treatment journey with Jakafi. Find out how this patient support program for adults taking Jakafi has provided ongoing support when he needed it.

Professional Perspectives

Hear from a medical professional who specializes in myeloproliferative neoplasms including myelofibrosis. When it comes to learning about your condition, it can be helpful to listen to real myeloproliferative neoplasm (MPN) experts who treat these rare, chronic blood cancers every day. The following videos have been developed to help you learn more about your myelofibrosis and discover what may be possible with Jakafi.

Jakafi: a Targeted Therapy

Discover how Jakafi works to reduce overactive JAK signaling.

What Effects Has Jakafi Shown in Clinical Trials?

Learn about the results of two clinical studies that explored whether Jakafi® (ruxolitinib) reduced enlarged spleens in certain patients.

What Long-Term Data Are Available for Jakafi?

Learn more about the results of two clinical studies for Jakafi that researched spleen size and analyzed overall survival in certain types of MF.

How Can Certain Risk Factors Help Me Understand My Myelofibrosis?

Explore 8 risk factors that Healthcare Professionals use to determine the severity of myelofibrosis (MF) in patients.

How Do I Take Jakafi?

Find out how patients can work with their Healthcare Professional to ensure they are prescribed the dose of Jakafi that is appropriate for their particular circumstances.

Is Jakafi Long-Term Treatment?

Learn about the patients and conditions Jakafi is used to treat.

What Are the Common Side Effects of Jakafi?

Explore the most common side effects of Jakafi and learn what patients should report to their Healthcare Professional.

Educational Videos

Learn more about myelofibrosis with an educational video designed to support your treatment journey with Jakafi.

Myelofibrosis, Spleen Size & You

Learn why spleen size is an important health focus in MF and how patients can partner with their Healthcare Professionals to help identify and monitor the signs and symptoms of spleen enlargement in MF.


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Jakafi is a prescription medicine used to treat adults with polycythemia vera who have already taken a medicine called hydroxyurea and it did not work well enough or they could not tolerate it.

Jakafi is used to treat adults with certain types of myelofibrosis.

Jakafi is also used to treat adults and children 12 years of age and older with acute graft-versus-host disease (GVHD) who have taken corticosteroids and they did not work well enough.

Important Safety Information

Jakafi can cause serious side effects, including:

Low blood counts: Jakafi® (ruxolitinib) may cause your platelet, red blood cell, or white blood cell counts to be lowered. If you develop bleeding, stop taking Jakafi and call your healthcare provider. Your healthcare provider will perform blood tests to check your blood counts before you start Jakafi and regularly during your treatment. Your healthcare provider may change your dose of Jakafi or stop your treatment based on the results of your blood tests. Tell your healthcare provider right away if you develop or have worsening symptoms such as unusual bleeding, bruising, tiredness, shortness of breath, or a fever.

Infection: You may be at risk for developing a serious infection during treatment with Jakafi. Tell your healthcare provider if you develop any of the following symptoms of infection: chills, nausea, vomiting, aches, weakness, fever, painful skin rash or blisters.

Skin cancers: Some people who take Jakafi have developed certain types of non-melanoma skin cancers. Tell your healthcare provider if you develop any new or changing skin lesions.

Increases in cholesterol: You may have changes in your blood cholesterol levels. Your healthcare provider will do blood tests to check your cholesterol levels during your treatment with Jakafi.

The most common side effects of Jakafi include: for certain types of MF and PV – low platelet or red blood cell counts, bruising, dizziness, headache, and diarrhea; and for acute GVHD – low platelet, red or white blood cell counts, infections, and fluid retention.

These are not all the possible side effects of Jakafi. Ask your pharmacist or healthcare provider for more information. Tell your healthcare provider about any side effect that bothers you or that does not go away.

Before taking Jakafi, tell your healthcare provider about: all the medications, vitamins, and herbal supplements you are taking and all your medical conditions, including if you have an infection, have or had tuberculosis (TB) or have been in close contact with someone who has TB, have or had hepatitis B, have or had liver or kidney problems, are on dialysis, have high cholesterol or triglycerides, had skin cancer, or have any other medical condition. Take Jakafi exactly as your healthcare provider tells you. Do not change your dose or stop taking Jakafi without first talking to your healthcare provider.

Women should not take Jakafi while pregnant or planning to become pregnant. Do not breastfeed during treatment with Jakafi and for 2 weeks after the final dose.

Please see the Full Prescribing Information, which includes a more complete discussion of the risks associated with Jakafi.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit, or call 1-800-FDA-1088.

You may also report side effects to Incyte Medical Information at 1-855-463-3463.