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Mezavant ( mesalamine)
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Ulcerative Colitis
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skidder
New Member
Joined : Jun 2011
Posts : 19
Posted 8/17/2011 1:59 PM (GMT 0)
Just wondering if anyone out there takes Mezavant? My GI switched me from Pentasa to Mezavant yesterday.
Experienced any side effects?
Did it work as well as the pentasa?
Any input would be appreciated
quincy
Elite Member
Joined : May 2003
Posts : 33769
Posted 8/17/2011 8:40 PM (GMT 0)
Did you ask the doc about
rectal mesalamine?
What's the dosage of mezavant you're now on?
q
skidder
New Member
Joined : Jun 2011
Posts : 19
Posted 8/18/2011 12:19 AM (GMT 0)
No didn't ask about
the rectal mesalamine....personally I would prefer to swallow a pill :)
The dosage is 4 x 1.2 g once a day.
quincy
Elite Member
Joined : May 2003
Posts : 33769
Posted 8/18/2011 8:13 AM (GMT 0)
That's unfortunate.
q
Anthonyv
Regular Member
Joined : Jul 2011
Posts : 153
Posted 8/18/2011 8:19 AM (GMT 0)
i'd rather not be sick :) rectal mesalazine works heeeeeeeaaaps better in my opinion you should get on it
fruitgirl
Veteran Member
Joined : Feb 2009
Posts : 7164
Posted 8/18/2011 12:04 PM (GMT 0)
I'd rather stick meds up my butt than flare -- studies show that people who use rectal meds in addition to oral meds reach remission more quickly (and stay in remission longer, when they're used for maintenance) than those who only use oral meds. The oral meds don't do a good job at treating the distal parts of the colon.
Easy choice, IMO.
skidder
New Member
Joined : Jun 2011
Posts : 19
Posted 8/18/2011 12:09 PM (GMT 0)
hmmm interesting, thanks everyone that responded. Funny that my GI didn't even mention rectal meds???
I don't see him again till November, hopefully I do well until then.
Will definetly ask him about
them when I see him.
Didn't realize that they worked so well.
When I was originally diagnosed with Proctitis I was on the rectal Pentasa.
fruitgirl
Veteran Member
Joined : Feb 2009
Posts : 7164
Posted 8/18/2011 12:12 PM (GMT 0)
A lot of them don't, for some reason. Probably b/c they think too many people won't want to use them. I'd go ahead and call and request them now rather than waiting until November. And don't let him tell you they're only for people with left sided UC or proctitis. They made a huge difference for me when I was flaring, and I had pancolitis. And I've been in remision for over two years now and credit a lot of that to using enemas twice a week (plus never skipping my oral meds).
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