Marcie,
My husband is the CML patient and he has occasional night sweats. Oddly, being
extremely hot and sweating a lot were the symptoms that sent him to the doctor
before he was dx'd with CML. So he had this symptom before starting any TKI's.
He was first on Gleevec and the sweating pretty much disappeared. He was
allergic to Gleevec and put on Sprycel. Had a few night sweats, but not often.
Now he has had PE with Sprycel and has been off of it since Aug, 2014. He is
still having occasional night sweats. I guess we never associated it with the
TKI's because they started for him before he was on them. Interested in
anything anyone else has to say about hotness and sweating. All the best to
you in this new year.
Joyce in IL
On Jan 5, 2015, at 7:36 AM, 'Marcie Goodman' via CMLHope wrote:
> Happy New Year, dear friends. I'm wondering if any of you suffer with night
> sweats as a side effect of your TKI. I do, and have, over the years of my
> treatment. I don't know that it is happening more frequently but the sweats
> seem to be more intense. Is there anything that you know of that will help?
>
> Many thanks for always being there to offer encouragement and assistance.
>
> Marcie
>
> Sent from my iPad
>
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