MPN10 Tracker
Help patients monitor symptoms with the MPN10 tracker.
This page is intended for UK healthcare professionals and other relevant decision makers only. If you are a member of the public, please click here.
This portal is funded and owned by Novartis Pharmaceuticals UK Ltd and includes content approved by Novartis.
Adverse events reporting information can be found in the footer of this page.
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JAKAVI® (ruxolitinib) is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. JAKAVI® is also indicated for adult patients with polycythaemia vera who are resistant to or intolerant of hydroxyurea.1
This website is intended for healthcare professionals. Please do not direct patients to this page.
It is important patients living with MPNs (such as myelofibrosis, polycythaemia and essential thrombocythaemia) know how to track their symptoms, as this will help them manage their disease. Validated tools such as MPN 10 can help them record and identify any changes in their health and guide conversations you have with them in the clinic.
Click play to watch two patients discuss their symptoms with a consultant nurse specialist and the advantages of using the validated tool, MPN 10, to monitor them.
MPN, myeloproliferative neoplasm.
Reference
JAKAVI® (ruxolitinib) Summary of Product Characteristics.
UK | November 2025 | FA-11531983
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should also be reported to Novartis online through the pharmacovigilance intake (PVI) tool at www.novartis.com/report, or alternatively email [email protected] or call 01276 698370.