Posted 4/22/2013 12:53 AM (GMT 0)
Thanks! That's what I thought but just wanted to make sure.
Before I started taking it I was having a pretty bad flare. Lots of blood, mucus, urgency, and tired all of the time. I was originally put on entocort by my doctor but then requested to be switched to Uceris. I had some improvements when I first started taking the Uceris, maybe for about two weeks. I just had less blood and mucus, but still the D and urgency. After that my symptoms returned to the same and my new GI put me on cortisone enemas and upped my lialda dosage, which still isn't working.
I really think that it just depends on how bad your flare is and probably where your UC is located to if the Uceris will help.
Hopefully it helps you! because the side effects are nothing like Prednisone. I had barely any adverse effects, not like pred at all :)