Anyone had an allergic reaction to Asacol?

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Jan 3, 2013
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Asacol seems to work very well in controlling Crohn's symptoms but in the 2 months I've been on it I have developed increasingly intense rashes on my face, lips, throat, and around my eyes that burn and swell like crazy, swollen finger joints, and I bleed like crazy if I so much as scrape myself a tiny bit.

Anyone else had symptoms like these, or symptoms that could be interpreted as allergic reactions to Asacol?

Thanks!
 
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I took Asacol for years with no problems. Then I developed intense joint pain all over my body...worse in the evenings...a little better during the day. It seemed to start in my fingers and wrists, but eventually it affected almost all of my joints. The joint pain went away after stopping the Asacol, and returned when I started taking it again. I did not experience any rashes though.
 
I went for a Sigmoidoscopy in November '12 and the Dr. thought I had colitis and put me on asacol. 5 pills per day (I think they were the 800mg ones). They worked AMAZING for about a month until 1 day at work I started to get a stomach ache. This turned into the most intense pain during my 4 days off. I went to a walk in clinic who said it was from excess stomach acid. He gave me prevacid. I literally threw them in the garbage after 3 days of even more intense pain.

I stopped taking everything until my colonoscopy in January. Turned out I actually have Crohns, but very mild, so the Asacol didn't work properly for me. I take Mezavant now, which works pretty well, but sometimes I poop like 5 or 6 times in a day. The majority of it is in the mornings, and after that I am good.

I am not sure what the Asacol was actually doing to me. I wouldnt call it an allergic reaction, but intense stomach pain, and I actually had a headache from it too.
 
I have relatively mild Crohn's just in the terminal ileum. I didn't have an allergic reaction to Asacol HD 800, but my none of the mesalamines seemed to work on me. Asacol worked on me for awhile last year, we just tried it again but this time started with 1 pill 2 x a day, and after 2 weeks increased to 2 pills 2 x a day. 2 hours after I increased the dose, I got really watery projectile diarrhea. Thought it was something I ate, stayed on the meds next day. Following morning, felt queasy, very gassy, extreme abdominal pain. Ate just a bowl of rice for lunch. 2 hours later, still queasy. Sipped some ginger ale (with real ginger, from the health food store). 1/2 hour later started vomiting and did not stop for 6 hours. Also projectile watery diarrhea for 9 hours, which finally stopped after 3rd dose of 2 Immodium capsules - which is another story, I am allergic to the yellow dye #10 in regular Immodium. I am now afraid to try any other mesalamines at any dosage (Lialda and Pentasa never worked for me anyway, and Lialda made me nauseous.)

Only thing that ever worked on me was steroids. When I was on Entocort last year I had horrible horrible foot & leg cramps and tingling in my fingers. However just recently I was diagnosed with psoriatic arthritis and while I was on prednisone for that, I had awful side effects - insomnia, short-term memory loss, mood changes, gained 7 pounds I don't need - but NO Crohn's symptoms. Also thinking the foot & leg cramps may be more related to psoriatic arthritis tendinitis more than muscle cramping. I'm not on anything now, and guess what, still getting occasional foot & leg cramps, and also in my index finger which is the one most affected by the psoriatic arthritis. So I just told the GI doc I am afraid to try any more mesalamines but would like to try Entocort again....

Does anyone know if bad reaction to one mesalamine is a predictor of bad reaction to another mesalamine???
 
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