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Sensitive to mesalamine! What now?

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Ulcerative Colitis
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 6:36 AM (GMT -7)
My GI and I thought we'd finally found a mesalamine formulation that would work to control my symptoms - Lialda - but it turns out I have a sensitivity! So far, I've tried Asacol, Lialda, Canasa and Rowasa. At first, things always start out great. However, as time goes on, I start to develop urgency, then bleeding, then even greater urgency and frequency until symptoms are as bad as the disease itself. We tried reducing the dose of Lialda from 4 a day to 2 a day - which did not help. We then tried splitting up the doses throughout the day - which didn't help, either. Finally, we tried discontinuing the medication altogether, which resolved most of my symptoms within 3 days. However, I still have rectal bleeding.

My colonoscopy in January revealed active inflammation in only the last inch of my rectum. Everything else looks great. (I have pancolitis, so this is great news!) However, I'm at my wits' end trying to resolve this stubborn proctitis. Right now, I have a two week supply of cortifoam, which we hope will help resolve this. However, my GI is not a fan of long-term steroid use, even in topical form.

Does anyone have any ideas for resolving this? I strictly follow the SCD, which helps greatly for the rest of my colon, but has not been able to resolve my issues with proctitis. Stupid proctitis! Auggg!

Thank you for reading this! I appreciate any ideas you might have!
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Andrina
Veteran Member
Joined : Aug 2011
Posts : 3690
Posted 4/4/2013 6:40 AM (GMT -7)
Have you tried balsalazide (colazal) or sulfasalazine yet?

What else have you tried? Prednisone? Azathioprine? MTX? Remicade/Humira?
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 6:45 AM (GMT -7)
I have tried sulfasalazine - had a reaction similar to mesalamine. Helped at first, then developed increasing sensitivity the longer I took it. I have also tried prednisone and Remicade. I haven't explored Humira or Colazal. Thank you for the suggestions! :)
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 6:46 AM (GMT -7)
I have more information about my diagnosis and treatments in my signature. For some reason, I can't get it to show up in my posts. :(
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kazbern
Veteran Member
Joined : May 2010
Posts : 8384
Posted 4/4/2013 6:58 AM (GMT -7)
Writergirl, that is a tough situation. I understand your DR's concern about topical steroids - with long term use they thin the tissue and that may be as much of a problem as the inflammation.

I'm stumped, personally. I wonder if you would be intolerant of the salicylates in a more natural form, like willow bark? Just grabbing at straws here. There are some folks on the forum who are really well-versed in herbal remedies.
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 7:02 AM (GMT -7)
Awesome! I'm going to research Humira, colazal and willow bark today. I love it that we have a community that can help each other out with ideas! Thank you!!!
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colitis91895
Regular Member
Joined : Feb 2013
Posts : 275
Posted 4/4/2013 10:33 AM (GMT -7)
Did you try apriso? Its mesalamine also
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 11:57 AM (GMT -7)
I think we have decided, at this point, that I will probably react badly to any 5-ASA. But thank you so much for the suggestion!
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GidHike
Regular Member
Joined : Jun 2011
Posts : 128
Posted 4/4/2013 3:51 PM (GMT -7)
Humira should definitely not be your next step. It's a very serious medication (in case you didn't know it's in fact an injection, not a pill).

After 5-ASAs you should think about immune suppressants (6MP/Imuran).

But are you positive you don't tolerate mesalamines? Sulfa is not a mesalamine so you shouldn't have the same side effects. Maybe it's just UC and you just think it's the meds
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 4:43 PM (GMT -7)
We aren't sure it's the mesalamines, but the trend has been the same throughout the Asacol, Lialda, Canasa and Rowasa. We're leaning toward thinking it is a medication sensitivity because each time the 5-ASA was discontinued, most of the symptoms disappeared within a few days to a week.

I'm not sure why I had a bad reaction to the sulfa. But, the longer I was on it (6 months at one point), the bleeding and urgency increased. When we discontinued it, most of the bleeding and urgency stopped.

Now, it's just this stubborn proctitis that has refused to go into remission! We tried the rectal mesalamines, but had the same issue.

You all have given me several medications to research and talk with my G.I. about. Thank you!!!
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IamCurious
Veteran Member
Joined : Jan 2010
Posts : 3542
Posted 4/4/2013 5:10 PM (GMT -7)
There are some folks on the forum who are really well-versed in herbal remedies

I cannot tolerate mesalamines either. But in my case it is almost a blessing in disguise because my IBD can be controlled with natural supplements without the side effects from meds. Government sponsored research shows that it can indeed work for some people.

I take a variety of supplements but my mainstay is powdered psyllium seed and prescription VSL#3DS probiotics. But supplements aren't very effective for me unless I also monitor my diet, not with the standard SCD but a food diary that told me that I must restrict food triggers like gluten and certain vegetables.

Below is a link to some government research. Besides supplements another drug many have found to help with IBD is LDN. I don't know what to tell you if LDN and natural supplements with diet modification are ineffective for you. I guess you would have to graduate to the "big gun" meds?

www.healingwell.com/community/default.aspx?f=38&m=2204683

www.ncbi.nlm.nih.gov/pubmed/10022641
CONCLUSIONS:
Plantago ovata seeds (dietary fiber from psyllium seed) might be as effective as mesalamine to maintain remission in ulcerative colitis.
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46&crashing
Veteran Member
Joined : Sep 2011
Posts : 500
Posted 4/4/2013 5:48 PM (GMT -7)
I am allergic to sulfa drugs, but when all this started for me the GI told me that drugs like Pentasa and Lialda were not regular sulfa drugs. Pentasa did not do much for me so new GI switched me to Lialda and put me on Pred to get me out of flare. When I started tapering the Pred, that is when the itching and rash started. We realized I was reacting to the Lialda. Doc then put me on Imuran. Some days now I feel like maybe I'm in remission, but some days I still have blood and other issues.
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Writergirl
Regular Member
Joined : Mar 2013
Posts : 43
Posted 4/4/2013 6:15 PM (GMT -7)
You guys are awesome! Thank you!
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