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REZUROCK® (belumosudil) Accessibility Statement

 

1. Commitment

Sanofi is committed to providing digital solutions that are accessible to the widest possible audience, regardless of ability, disability, race, cultural background, gender, or technological requirements.
This accessibility statement applies to www.rezurock.com.
 

2. Conformance status

The Web Content Accessibility Guidelines (WCAG) defines requirements for designers and developers to improve accessibility for people with disabilities. It defines three levels of conformance: Level A, Level AA, and Level AAA. This website is partially conformant with WCAG 2.2 Level AA, due to the limitations described below.
 

3. Known limitations

Despite our best efforts to ensure the accessibility of this website, there may be some limitations. Below is a description of known limitations and potential solutions. Please contact us if you observe an issue not listed below.

  • Images: Some images may lack descriptive alternative text.
  • Color contrast: Some text and link elements do not meet minimum color contrast requirements.
  • Error messaging: Error messages may not consistently provide sufficient guidance for resolution.
  • Keyboard accessibility: Some interactive elements may not be fully operable using a keyboard alone.
  • Keyboard focus: Keyboard focus indicators may not always be visible or clearly distinguishable.
  • Context-dependent links: Certain links may rely on surrounding context to be understood.
  • Non-color indicators: Links may not consistently include visual indicators beyond color alone.
     

4. Feedback and contact

Please contact us if you encounter accessibility barriers on this website. If you are unable to access any content or service, we will provide an accessible alternative or offer the content in another form.
 

5. Preparation of this accessibility statement

This statement was prepared on May 15, 2026.
To evaluate the current level of accessibility, the website was assessed using manual testing and automated testing in Axe DevTools, based on WCAG 2.2 Level AA, with Google Chrome and Microsoft Edge.

 

6. Formal complaints

If you are not satisfied with our response to you, you are entitled to escalate a complaint to the national authority.
To file an Americans with Disabilities Act (ADA) complaint, submit a report with the US Department of Justice, Civil Rights Division, online or by mail. Learn how to file a complaint on the Civil Rights Division website.

 

GVHD, graft-versus-host disease

USE AND IMPORTANT SAFETY INFORMATION

REZUROCK® (belumosudil) is a prescription medicine used to treat adults and children 12 years of age and older with chronic graft-versus-host disease (chronic GVHD) after you have received at least 2 prior treatments (systemic therapy) and they did not work. It is not known if REZUROCK is safe and effective in children less than 12 years old.

Before taking REZUROCK, tell your healthcare provider about all of your medical conditions, including if you:

  • have kidney or liver problems.

  • are pregnant or plan to become pregnant. REZUROCK can harm your unborn baby. If you are able to become pregnant, your healthcare provider will do a pregnancy test before starting treatment with REZUROCK. Tell your healthcare provider if you become pregnant or think you may be pregnant during treatment with REZUROCK. 

    • Females who can become pregnant should use effective birth control during treatment with REZUROCK and for 1 week after the last dose.

    • Males with female partners who can become pregnant should use effective birth control during treatment with REZUROCK and for 1 week after the last dose.

  • are breastfeeding or plan to breastfeed. It is not known if REZUROCK passes into breast milk. Do not breastfeed during treatment with REZUROCK and for 1 week after the last dose.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. REZUROCK may affect the way other medicines work, and other medicines may affect the way REZUROCK works.

Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.

How should I take REZUROCK?

  • Take REZUROCK exactly as your healthcare provider tells you to take it.

  • Do not change your dose or stop taking REZUROCK without first talking to your healthcare provider.

  • Take REZUROCK 1 time a day with a meal.

  • Take REZUROCK at about the same time each day.

  • Swallow REZUROCK tablets whole with a glass of water.

  • Do not cut, crush, or chew REZUROCK tablets.

  • Your healthcare provider will do blood tests to check your liver at least 1 time a month during treatment with REZUROCK.

  • If you miss a dose of REZUROCK, take it as soon as you remember on the same day. Take your next dose of REZUROCK at your regular time on the next day. Do not take extra doses of REZUROCK to make up for a missed dose.

  • If you take too much REZUROCK, call your healthcare provider or go to the nearest hospital emergency room right away.

What are the possible side effects of REZUROCK?

The most common side effects of REZUROCK include:

  • infections

  • tiredness or weakness

  • nausea

  • diarrhea

  • shortness of breath

  • cough

  • swelling

  • bleeding

  • stomach (abdominal) pain

  • muscle or bone pain

  • headache

  • high blood pressure

Your healthcare provider may change your dose of REZUROCK, temporarily stop, or permanently stop treatment with REZUROCK if you have certain side effects.

REZUROCK may affect fertility in males and females. Talk to your healthcare provider if this is a concern for you.

These are not all the possible side effects of REZUROCK. Call your doctor for medical advice about side effects.

Please see full Prescribing Information.

You are encouraged to report side effects of prescription drugs to the FDA. Visit www.FDA.gov/medwatch or call 1-800-FDA-1088. You may also contact Kadmon Pharmaceuticals, LLC, a Sanofi Company, at 1-800-633-1610 to report side effects.