Anyone had adverse effects from Jakafi (ruxolitinib) for PV?
I am 74 years old, female. Three years ago diagnosed with PV After five phlebotomies I was told my platelets were too high to continue. Hematologist offered hydroxy…..I read about it and determined to self manage for as long as I oils keep numbers down.
I have fatigue and tiredness so have begun nappping on a daily basis. Makes me feel much better. Occasional headaches for which I take aspirin. I am now being pursued to take JakaFi for the high red and white cells. Again, upon exploring the side effects, I’m a bit hesitant in trying it. HAS ANYONE WITH PV TAKEN JAKAFI? Any side effects, comments to share. Thank you.
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I have been on Jakafi for 3 years for GVHD (I had AML and a stem cell transplant). I have tolerated the medication very well. In the beginning my red blood cell count dropped quite a bit, so I had to be monitored and had regular blood draws. That has stabilized and I see a lot of good progress in controlling my GVHD. I understand that each person reacts differently to Jakafi. I know that some patients have to stop Jakafi because their blood cell count dropped too much. I definitely recommend to give it a try and see if it works for you.
Thank you for your comments. My RBC, WBC, and platelets are at the top of the range, so my understanding it will take a few months to get them down to an acceptable range. I have digestive issues that may be related to the enlarged spleen….I was informed that .the medication should help that also. I will have one additional CBC to confirm the blood levels and then determine weather to pursue the JakaFi.
I appreciate any comments. They are helpful and calm my heart!
M
I have been taking 5ml Jakafi twice a day for three years. It has been a life changer for PV side effects such as fatigue and optical migraines.
Thank you for the info on side effects. Did you have either prior to taking the med? I have fatigue and occasional ocular migraines.
10 mg twice a day suggested for me. Good to know I could get 5mg.
Thsnk you again! I’m beginning to feel better about taking it! God bless you all!!
@mcvorbs, you might also be interested in these related discussions:
- What's the latest Jakafi (ruxolitinib) for polycythemia vera (PV)?
https://connect.mayoclinic.org/discussion/polycemia-vera/
- Has anyone had experience with Jakafi?
https://connect.mayoclinic.org/discussion/has-anyone-had-experience-with-jakafi/
Did you decide to start treatment with Jakafi (ruxolitinib)?