Asacol side effects mesalamine
Common Questions and Answers about Asacol side effects mesalamine
asacol
hi there,
i have UC (diagnosed in 2001) and have been on asacol most of the time. however, i had about a year of experience with pentasa... the doctor at the time told me that it was the same thing as asacol, however, i found it to be less effective. another doctor later told me that they have the same active ingredient mesalamine, but pentasa reaches a different part of your track... i think asacol stays intact longer, so it gets released lower down in your system.
Hi there,
I was diagnosed with sigmoidal colitis in 2005, but I reckon that it went unchecked for about 4 years prior to that. I was initially treated with mesalamine (Asacol) but it had no effect. My GI guy then hit me with prednisone and that knocked it down. I have been on Asacol in a prophylactic capacity since (800mg tid). Does it keep me in remission. Maybe, but maybe it is the tremendous quantities of fentanyl, diacetylmorphine and morphine I abused as well for all I know :P.
My recent result of biopsy after the colonoscopy indicates epithelial dysplasia. My doctor just advice me to continue taking the mesalamine (Asacol) Do i need an another urgent medication/treatment for dysplasia? What should be my next move?
I have been hospitalized four times in last two years. Finally I met a doctor in UK who prescribed Asacol Foam Enema. I was unable to get into remission for last so many years with all drugs, however, with this foam enema, I got in full remission in just few weeks. I was surprised to find that drug industry that makes Enemas for UC has been dominated by company that makes Rowasa Enema (Israeli Company). I am shocked to find that Rowasa has complete monopoly over this industry.
i was prescribed asacol 2x 400mg, 3 times a day for two weeks. after this time i was also diagnosed with CKD at stage 3a with a GFR of 53 and a creatinine clearance of 87.14ml/min.
i took asacol again for one month at a reduced rate of 1x 400mg, 3 times a day (3-4 tablets recommended for prevention of relapse).
then i stopped taking it for 2 months.
i took asacol again at 1x400mg, 2 times a day for 2 months.
i have had crohns for 8 years and i have been on just about everything. i have taken 6mp and i actually didnt have any side effects from it. it didnt work for me but no side effects. make sure she is seeing a gastro who specializes in cd. not all gastros are that great at treating cd/uc. tell her that all the meds they give us say they have all these terrible side effects but it doesnt necessarily mean she will get them.
Told my doc, he said it was probably in my head and wrote a new script for a different form of Mesalamine (which is what Asacol is). I decided to pursue all other options before trying this medication.
I have been on Asacol since my dx in 2005. I haven't had any side effects and it really helps to keep my c.d. under control. Good luck and I sure hope it has helped you.
Hello ,
i have uc and my GP as just prescribed prednisolene 30 mg a day reducing weekly and omeprazole 20mg a day( plus calcium supplements.) Worried about all the side effects i've read about . Anyone had a positive outcome usi
these please????
Mesalamine or Canasa suppositories works by preventing the production of substances that cause the inflammation of the colon. The usual side effects include diarrhea; dizziness; gas; hair loss; headache; mild stomach discomfort or pain; and nausea. The sour taste could be indirectly related especially if you have other gastrointestinal issues like acid peptic disease or gerd. If this symptom persists, it is best that you have this checked by your doctor for proper evaluation.
I have read about a study in which Boswellia was used in conjunction with Mesalamine. My gastroenterologist knows notheing about herbs, but is open to information that I can give her. What is available? Are there any interactions with boswellia and mesalamine that I should be cautious about? Are there any precastions about its use?
I have been on it for the last year straight and am not totally sure how much it really works. I had some side effects from it such as nausea and hair loss to a certain extent. The nausea was fixed by taking it at night which seemed to really help.
Being on it did not eliminate me from other meds as I am currently back on prednisone 40mg for a month due to a flareup. Pentasa and Asacol never worked for me either.
I guess in short every medication works for different people in different ways.
During moderate/sever flare-ups I took prednisone orally, in foam suppository as well as mesalamine orally and through suppository. In moderate flare-ups mesalamine orally w/ mesalamine suppositories.
My question is - beyond the general risk that HSV presents - how additionally risky is this for me? It is a possibility that at some point I will have a flare-up that will require immonusuppressive therapy. If I was to contract HSV could my UC symptoms become more severe?
Immuran. Now there's a whole different balancing act. Having hep C is challenge enough, but then to have to take an immunosuppressive while you're fighting a virus....a whole new level of challenge. And NSAIDS of course, just the ticket for the liver. . But as my GI put it, "the side effects of not taking this stuff are worse than the side effects of taking it."
True enough, yet it's cold comfort somehow.
I was diagnosed with Crohn's 9 years ago. I have been taking Asacol (5-ASA) and Imuran (Azathioprine). Last february I was hospitalized for the first time and was put on prednisone. I am still on prednisone and my body won't let me get off of it. My doctor wants me to start Humira, but I am scared. I don't like reading about the side effects and things that can happen when on that drug. Does anyone have any experience with this drug (Humira)? I would really appreciate it.
She is now 16-week pregnency. We are worried about the effects on Kids. Does anyone have similar experience and give us some suggestion? Thanks a lot.
Prednisone can cause acne. I had UC for ten years until I perforated and had my colon removed and a J-pouch built 16 years ago. My son has UC and moved onto the Imuran last year. He did have some acne with the prednisone too. He has been in a wonderful remission this past year and is so enjoying feeling healthy. The only change he continues to make is to leave dairy alone as he realizes he is lacto intolerant. I hope you will get the same success.
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