User Reviews for Jakafi

For Polycythemia Vera "A lot of people have experienced weight gain on Jakafi and I have too. For me, I only lost weight on this med by eating low carb with some form of moderate exercise when able. I also found I slept better and generally felt better on a low carb diet while taking Jakafi. Hope this helps someone else struggling with weight gain after starting this"

For Polycythemia Vera "This is the third Rx I've had over 10 years to treat polycythemia rubes very. Started for drug trial for 87 weeks. Now on an Rx. I've had 0 Phlebotomy since on Jakafi. Itching is nearly nonexistent. I can sleep well. Mood has improved. Generally, Jakafi has given me a life back!"

For Polycythemia Vera "I have been on Jakafi for 10 months for Polycythemia Vera. It has reduced my itching, bone and joint pain, fatigue and my counts are actually normal for the first time in decades! I have gained about 5 lbs on it but no other significant side effects. I am taking a very low amount ( 5mg 2x day) and maybe that's why I haven't gained a lot of weight. This medication has literally given me my life back."

For Polycythemia Vera "I started on a higher dose and my counts came down and itching stopped, but I had weight gain! Yuck!, migraines, loud constant ringing ears, joint aches and swelling, dizziness. Then, tried a lower dose 5mg 2 x day, and side effects lessened greatly, but my counts increased. I’m off of it and on Hydrea, and trying to lose the weight now (10lbs). To add, the price of Jakafi, ruxolitinib is RIDICULOUS."

For Polycythemia Vera "I am 57 yrs., I have had PV for well over 20 years. I have had phlebotomies and then Hydrea and now have been on Jakafi for a year and a half. My overall experience with Jakafi is that it gave me my energy and life back. My joint pain disappeared immediately and my energy level was amazing! I was on 5 mg 1x day to start and then went up to 5mg 2x day, which I am on now. I have gained about 10 lbs, even on this low dose.Then about 6 months ago I got Shingles, I believe, from the Shingrix vaccine I had just gotten, and since then, I have not felt well. I get sick a lot and in the past 6 months, my joint and bone pain is so much worse, almost like pre-Jakafi. The meds are working well for all blood counts right now so I am on the fence about stopping the med."

For Polycythemia Vera "Been taking Jakafi for 9 months .... 10mg 2x daily. Just now counts slightly increasing so my Dr is adding another 5mg daily to my dose. This med has improved my life significantly .... my over functioning has improved 100% but still with some issues. It's scary to change medications, I hope my comment will give others courage and hope ... if their Dr thinks it's worth giving it a try."

For Polycythemia Vera "I am 74 yrs old and have polycythemia vera (PV) since I was 62. Was on Hydrea and phlobotomy every 3 mos. Was seriously very depressed and low energies. On Jakavi since May-2016 and no more phlobotomy. Now taking Jakavi 25mg twice a day. My life is back and feels like not having PV. Med is expensive at 25mg because I need 20+5 mg. Cost is doubled because they don't make 25mg pills!"

For Myelofibrosis "I have post essential thrombocythemia myelofibrosis. Jakafi has my platelet count and white cell count normal again. However, it caused my red cell count to go way too low and so am on Procrit shots to avoid transfusions. I am very fatigued after the slightest physical activity. I gained about 10 pounds and get pimples from it. Jakafi instantly got rid of my joint aches and pains."

For Polycythemia Vera "Took Jakafi for approximately 10 months. My itching was completely cleared up. During this entire time my bowel movements were intense. I had cramping in my stomach most mornings. Initially my dosage had to be adjusted because all of my blood levels were very low. I had developed cytopenia. Was taken off Med for 6 weeks and resumed. The last straw for me was the aching I experienced in all of my joints. Medication states a side effect can be arthralgia. Well, I got it. Had to get cortisone injections in both thumb joints, both knees, right hip and shoulder. I refuse to go back on this medication. Wish anyone able to take this Med good luck"

For Polycythemia Vera "I have been on Jakafi now for 7 months. I have had major weight gain (25lbs) and migraine headaches every day. Before I started my counts were over a million and they are only down to 800,000. So for me this isn't working. The side effects and losing days to headaches are not worth taking it."

For Polycythemia Vera "I have been taking this medication, Jakafi for 10 months. Once correct dosage was figured out, I have experienced no itching and there has been no need for phlebotomy treatments. Downside to taking this medication is that for days at a time I have trouble with my bowel movements and pain and cramping in my stomach. This happens when I eat healthy, broccoli, kale, multi grain bread. Also when I eat fried foods."

For Polycythemia Vera "I was diagnosed with polycythmia vera in 2007. Itching, terrible itching, has been my main complaint and hydroxyurea didn't help. I was taking Atarax four+ times a day plus getting light therapy 2-3 times a week. With Jakafi, I take Atarax 1-4 x day, and don't need light therapy. However, when it's really warm or allergens are in the air, I take Emend off-label. Side effects of Jakafi: more susceptible to infection, possibly anemia, possibly higher erythropoietin levels."

For Polycythemia Vera "I just don't understand, I've been on this med about 2 yrs and my Dr just increased my dose to 20 mg b.i.d. My platelet count is still thru the roof ! I changed my diet and swallowing these pills just as directed! All I get is bad reports and disappointing agitated comments from my Dr ! I give up !"

For Myelofibrosis "I am on Jakafi and all was going well until my Doc decided to prescribe 5 mg tablets. Well the price jumped exponentially to well over double for the same 15 days and same mg dose This he thought was needed for small adjustments. I was shocked to see my benefits eaten up almost instantly for one month of medication. I am furious and this medicine does not offer that kind of money relief. I am looking into transplant and warning others ..NEVER GET THE 5 mg Tablets!! over 34, 000 for one month prescription. No wonder my insurance is over 1,000 per month just for me..SMH"

For Polycythemia Vera "I've been enjoying not feeling awful all the time. With Jakafi I have had no problems with skin blisters when I am in sunlight, as I did with the previous medication. It is hard to say which med gives me vertigo issues the most. I suppose the dizziness is mild with Jakafi. In general, I have more energy and less stress over shortness of breath - until recently, again. I don't know if the current fatigue I have suddenly again, is due to the medication dose or if I am experiencing another drug side effect or my body is simply old and wearing out. I know that Jakafi has given me my life back again. But, currently, my body is not in balance - I'm not sure why: chest pain, increased heart rate, higher BP, shortness of breath, fluid retention, weight gain, fluid gain, headache, and low kidney function. My cholesterol went up - and not sure why. I am currently being worked up, again for a cardiac issue. For a year however, I felt so much better than I did without Jakafi."

For Graft-versus-host disease "So far it seems to be working. If I forget to take it I get a definite onset of itchy skin with a very marked response and regular and multiple bowel movements in the mornings. I am not sure if it is Jakavi related, but I had a stroke. I have found that my blood levels definitely stabilized and GvHD skin flares reduced quickly too. I do have regular and severe cramps in the calf in the mornings."

For Polycythemia Vera "I have benefited from Jakafi maintaining my platelet count. I have experienced UTI and not sure Jakafi caused it. I also experience gas and diarrhea."

For Graft-versus-host disease "I’ve been on Jakafi for 7 months to get rid of my GVHD rash which helped. My dose was 5 mg twice a day. Gained 30 lbs of weight and fluid. Getting weaned off now. Hoping I can lose the lbs."

For Polycythemia Vera "It’s either have to get a phlebotomy every month and become anemic or take Jakafi and be fat!"

For Myelofibrosis "Been on Jakafi for over a year. Twice a day varied from 5 to 20 Mg Frankly it has done little or none for me."

For Polycythemia Vera "It works, feel fine!"

For Polycythemia Vera "Gained weight especially in the waist. And dieting does not help."

For Graft-versus-host disease "My platelets were affected but so far my liver GVHD has improved."