Where Can Jakafi Be Bought? (Page 3)
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Does anybody have an idea how can Jakafi be bought outside the united states? what is the price?
Lizzy, I am a New Zealand citizen living and working in Indonesia and I have jsut been to see a doctor in Bangkok as I also have Myelofibrosis and they are arranging Jakavi for me.
Please call company Incyte. They can do something called compassionate drug treatment. This means they can send you or your doctor the drug even though it may not be approved in your country. 855 4462983 is the phone number for the company. Ask for Dr Larry Robinson. You can call me at 909 {edited for privacy}
We are dr. Hilliard,s patient too. We have been taking jakafi also. We would love to talk to you. This is such a rare condition and medicine, we would like to have someone to talk to. Please call me at 909 {edited for privacy}
My husband Ray is now bed ridden with myelofibrosis and urgently needs Jakafi.
The hospital has to date not had a reply from their wholesalers in the USA. We live in New Zealand (just below Australia)
Was your local Dr able to order Fakafi or did you need to bring it to where ever you are via a hospital pharmacy?
Hope you are doing well on the treatment.
All the very best,
Kind Regards,
Raye
Thank you guys for all the info.
I am in Indonesia at the moment. I was about to take my dad to US, but with his condition, I don't think he can travel to US, he gets tired very easy. And I asked one of my relatives in Florida to get JAKAFI from Walgreen, but they did not let her buy without prescription.
Can anyone help me to get this medicine? Please email me
I am in southern Calif. I drug is now approved for sale. My Dr. is DR. Hillard. He works out of Beaver medical Center in Highland City in Riverside County, Ca. He is running a clinical trail for myelofibrosis. The medicine is working great for me. I hope this helps.
Its is now available at the drugs stores in U.S.. I have been trying o find out the cost. As i am on the cilinical trial right now. Walgreens sell it for $4.400.00 a month without insurance. Still checking with other drug stores.
I am in Indonesia at the moment, and my dad's doctor recommended him to try JAKAFI. But it is only still available in US. My dad is feeling horrible at the moment from his enlarged spleen. So I'm planning to take him to US.
Can anyone recommend me a good specialist or doctor for his myelofibrosis in US?
And how can we get JAKAFI in US?
Thanks
That is correct, it is currently still in the investigational stage, so it hasn't actually been approved and isn't publicly available anywhere, which also means that there is no price to give anyone.
You can learn more about it here:
https://rxchat.com/wiki/Jakafi/
Are there any other questions or comments?
I got Jakafi through my doctor for the treatment of myelofibrosis. We had to fill out an application for it from the pharmacuetical company, "Incyte". It has not been made available to local pharmacies, only through the way I just described.
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