Mom On Jakafi
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My mom was recently (two weeks ago) put on Jakafi, 10 mg twice daily. Her red blood cells went from 10.5 to 9.9...something like that. I am concerned it's the jakafi as i know that was something we were told to possibly expect. Just wondering if anyone has been on this long term (from the study) or even short term and how they are feeling?

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32

In Feb. 2015, I started Jakafi at 10 mg. twice a day. when my platelet count dropped to 70, the Jakafi was reduced to 5mg. twice a day, and I have remained on this doseage for over a year with monthly CBC's. My biggest concern is my extremely elevated white count, but my oncologist is not that concerned since I'm doing very well overall. I have had none of the other documented side effects such as extreme fatigue or need for blood transfusions. I think myelofibrosis may have different side effects for different people. Hopefully your mother will be able to tolerate the Jakafi.

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31

I just started first 5 mg Jakafi today. scared- my counts starting out are lower.

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30

Amit, I have been on Jakafi, same mg. as your father, since Mar. 2015. I have not experienced fevers, but, according to the site, many have, so it must not be uncommon.

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29

I have been on Jakafi since Feb. 2015 for treatment of symptoms associated with myelofibrosis. Initially, I was placed on the same mg. doseage as your mother, but my platelets dropped to 70, and my Hem/Onc decreased me to 5 mg twice a day. I have remained relatively stable with a decrease in my RBC. My Hgb also dropped to 10.5. Yesterday I had an ultrasound of my abdomen to check the size of my spleen and other other surrounding organs. I return to my Hem/Onc. for another CBC and results of the ultrasound. Please let me know if you have specific concerns or questions. Since this drug has only been FDA approved and on the market for a few years, there are no longitudinal studies available. Guess that means your mother and I and some others are paving the way.

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28

Nick, I don't think there are any longitudinal studies on this drug yet. It has only been FDA approved in the US since 2012, I think. I started taking Jakafi in Feb. 2015 at 10 mg twice a day, however, that was quickly decreased to 5mg due to drop in platelets. I am on this site to inquire about side effects other than those documented by Incyte. I have terrible calf and foot spasms and contractions at night, which wakes me up. Any feedback is appreciated.

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27

Hi,

I have myelofibrosis and was on Jakafi. It did not help much. I think it did mitigate the night sweats but killed my red blood cell count and I became transfusion dependent.

I underwent a stem cell transplant at Seattle Cancer Care Alliance on April 23 2014. My youngest sister was a perfect match. I am now recovering from the stem cell transplant waiting for engraftment. Seattle Cancer Care Alliance does seem to have some success in this area.

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26

I have been on jakafi for years now. it helps me. I was itching so bad until the dr. put me on jakafiyes it does help

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25

My father age 65 is suffering from primary myelofibrosis and doctor has recommeded him jakavi 5 mg. my question : do patient with myelofibrosis have high fever. If yes, do jakavi helps in lowering the fever

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24

Dr Patrik Tan is a great guy with a wonderful manner and very experienced specialist in this field. I can personally recommend him. Jakavi in Singapore is a bit more expensive than the price we were quoted in Bangkok, but then ended being refused from Bangkok Hospital anyway. DONT GO TO BANGKOK HOSPITAL FOR THIS.

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23

Hi. I was on Jakafi for about a month. My red blood cells went down as low as 18. We have stopped the Jakafi and after transfusions we got my red blood cell count back up to around 27. It has slid back down to 23 and the doc is thinking of getting me another 2 units of blood. I will go visit the doc on Wednesday, but am reluctant to go back on the Jakafi. I was on 15 mg twice daily.

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22

Hi:
My dad started Jakafi 6 weeks ago. He gets severe Hematoma in his legs and swollen foot. Is this a side effect of the med? Where can I find the info

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21

Hello all. My dad has mylofibrosis and we are waiting for the jakafi drug. We were told it has to be approved by Medicare and Humana and it'd be about 3 weeks- we are still waiting. He's in hospital right now with no appetite at all. Can anyone please tell me what the normal wait time was to receive the jakafi? We are beside ourselves with worry as he continues to get worse with each passing day. Please, any information or hope would help us greatly.

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20

Hi Guys. I am my third day of taking 15mg of Jakafi twice daily to mitigate myleofibrosis spleen swelling and night sweats. It seems to be working. I hope to regain my flight physical in about 30 days. Jakafi just mitigates symptoms. The cure of myleofibrosis will take a bone marrow transplant.

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19

Doctor Ellen Richie. New York Presbyterian hosp. See google. 212-746-2098

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18

Hi Lizzy, try at Mount Elizabeth hos w/ dr Patrick Tan. Lead time for the drug almost 1 month, cause hos doesn't stock the drug yet.

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17

hi where in singapore hospital did you exactly get Jakafi? I've been trying for my dad.
Thanks

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16

Hi, my mom in law is diagnosed myelofibrosis and she has taken lelonidomite and thalidomite, but she is not seem better (spleen still growing and more frequent blood tranfussio). This happened until 2 weeks ago, after she took Jakafi, her spleen size decrease and red blood cell seem ok and she is the first patient in singapore hospital whose taken this drug, i guess. I've just wondering what is the side effect on long term or short term after taking this drug.

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15

Hi, my mum needed transfusion every month before she change her oral medicine from thalidomide to lenolidomide (revlimid), and now after taking it, it has improved a lot that she does not required tranfusion anymore for past 7 months and her spleen has reduced from 7cm to 3cm and is still reducing. Her RBC has also increasing every month. I would suggest you or your love one to try it if you haven't.

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14

thanks all for the info!! I'm trying to get my dad on trial in Taiwan now.. but the doctor said that my dad has heart problem that has to be cured first, so they still put him on hold and still the application takes long as well here. Hopefully we can get it soon.

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13

Dr Mesa mayo clinic inArizona.The MPN .support group and LLS website has alot of info.How does one afford this med.Mine is on hold trying to get on incyte program,But my husbands pension puts us in a higher than 30 k a year that is reguired by many

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