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/
hydroxyurea or interferon? My dr wants hydroxyurea because of the side affects of anxiety creation
Treatments for ET with hypothyroidism and EBV reactivated
How bad are the side effects for Besremi? I have ET jak2, am 68, not tolerating HU, and my platelets are hovering 640,000.