Powered By
ET And Interferon
Anyone that has been on hydroxyures that had to switch to interferon have any bad side effects?
I have been told I may have to switch for my ET treatment and am wondering what side effects should I expect?
Thanks
I have been on HU and Pegasys. Later switched to Besremi. The IFNs have been much for effective and much easier to tolerate for me. Note that I have PV with both erythrocytosis and thrombocytosis. Pegasys is well recognized as a viable option to treat ET. Some docs prefer is for all patients.
https://www.legeforeningen.no/contentassets/dc7...
https://mpnjournal.org/how-i-treat-mpns-2/
Anyone With ET Taking A Glp1 ? I Saw Some Research That It Can Help Lower Inflammation And Platelet Count. Only Negative I Saw Iron Levels.
Pros And Cons Of Doing The IV Thing That Removes Platelets. How Does This Work? How Often? How Long Does It Take Each Time? Does It Hurt?
Continue with Facebook
Continue with your email
Join
