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Evoxac for Saliva

meinken's picture
meinken
Posts: 38
Joined: Jan 2010

I've been using Evoxac now for about 4 weeks.  I'm about 4 months out from my 2nd rad/chemo treatment for nasalpharengeal/maxillary sinus and eye orbit cancer.   I have to say, that, my saliva generation seems much better than it has since my first rads in 2010.  

Could just be my time to feel better.  But I would like to hear from anyone else that has used Evoxac (Cevimeline).  Has it helped you?

 

 

longtermsurvivor's picture
longtermsurvivor
Posts: 1845
Joined: Mar 2010

after my first rads. For me it didn't work, and I got a significant tacchycardia, which was an unpleasant side-effect.  Later, my saliva came back anyway<*** src="/sites/all/libraries/tinymce/jscripts/tiny_mce/plugins/emotions/***/smiley-laughing****" alt="Laughing" title="Laughing" border="0" />  For others it helps quite a bit, so if you think you've noticed a change, you probably have.  Good for you.

 

Pat

ljoy's picture
ljoy
Posts: 94
Joined: Dec 2007

Been on it for seven years after tonsil cancer. I can definitley tell if I don't take it. I agree with the above if it works great.

Hope you continue to have a long and successful recovery.

 

Greg53's picture
Greg53
Posts: 848
Joined: Apr 2010

...........everybody's different.  Used it for 6 months - nada.  But glad it worked for someone.  Just goes to show you, only way to know for sure  - try it.

 

Positive thoughts!

Greg

luv4lacrosse's picture
luv4lacrosse
Posts: 1412
Joined: Jul 2010

The drug did not work for me, and was told if you do not see a good result in two weeks, it will not work.

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