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Welcome to MAVENCLAD™

Mavenclad welcome

Click here for additional safety information and for a link to the product monograph discussing:

  • Contraindications in patients with increased risk for opportunistic infections, latent or active infections, a history of progressive multifocal leukoencephalopathy (PML), active malignancy, moderate or severe renal impairment and patients who are pregnant or breastfeeding.
  • Relevant warnings and precautions regarding malignancy; patients who require blood transfusion; increased risk of infection; elderly patients; patients with moderate or severe hepatic impairment; patients with fructose intolerance; additive hematological adverse reactions with concomitant medications; decreases in lymphocyte count, neutrophil count, red blood cell count, hematocrit, hemoglobin or platelet count; activation of latent infections; risk of active vaccine infection; evaluating for complete blood count, active and inactive tuberculosis infection, hepatitis B and C viruses, varicella-zoster antibody status, pregnancy, lymphocyte counts; vaccination; risk of PML; use of contraception; serious risk to the fetus.
  • Conditions of clinical use, adverse reactions, drug interactions, and dosing instructions.

Discover MAVENCLAD

 

Demonstrated efficacy

Dosing and administration

MOA

 

 

Explore MAVENCLAD’s efficacy.

Learn more

View MAVENCLAD’s weight-based
dosing regimen.1    

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Understand MAVENCLAD’s MOA.

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  MONITORING PATIENT EXPERIENCE SAFETY AND TOLERABILITY PROFILE  
 

Discover MAVENCLAD’s monitoring.

Learn more

Read about MAVENCLAD’s patient
experience, which is supported by 4
years of clinical trial experience and
up to 8 years of follow-up
experience with over 10,000 patient-years.2

Learn more

Learn about MAVENCLAD’s safety and tolerability profile.

Learn more

 
References

  1. MAVENCLAD™ Product Monograph. EMD Serono. November 2017.
  2. Letter on file. EMD Serono. December 2017.

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