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.
I have a NEW G.I. doc who keeps referring me to a colonoscopy and an MRCP before she decides to do anything but I've had a flare-up of UC for a month and need some relief. Today I saw a whole Asacol HD tablet excreted and the G.I.doc said "that's ok--it's still absorbed." Ok--so now I must be reasonable and ask a question as how is it absorbed when NONE OF IT--repeat, NONE OF IT---is degraded at all? This woman doesn't get it. Anyway, what should I do now?
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 believe that pentasa is more for management of colitis once it's under control from steroids like once the steroids bring down your flare up u will continue to take pentasa to maintain your colitis control so you could be on it for quite sometime i have never taken pentasa myself thought they have me on salofalk which i believe is for the same thing, just to keep uc under control. not sure if that helped at all but anyways good luck wishing you the best.
A related discussion, <a href="/posts/Gastroenterology/Asacol-800/show/1876778">Asacol 800</a> was started.
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 have noticed that my asacol is not breaking down and is being passed in my stool! Is their a reason for this? What can/should I do?
I have chrons and I'm 18 I totally understand how she feels they told me the same thing I didn't listen I continued to take 10 mg there are so many other ways around 6mp look for a specialist in your area .. trust I found a good one and she switch up my medss and now I'm doing great ..
Keep in mind the hospital floor that I worked on was full of patients with cdiff. I have never had any problems before and have no family history of IBD.
I noticed blood in my stool and saw a GI who did a stool study which came back neg for c diff, he then did a scope which showed pancolitis and upon biopsy showed crypt cell abscesses. That day he started me on Asacol which I had no response to for months.
He also did a IBD serology 7 which he says showed that I had ulcerative colitis.
I had changed from Asacol to Pentasa the week before and the rectal pain had come back-significant burning pain. Went to another doctor and had more bloodwork-borderline IBD tests. Went off Pentasa for a few days in Dec and had severe RLQ pain and right hand pain. Got better after a week back on Pentasa. Had another colonoscopy-essentially negative in late Jan. I continue to have burning pain in my rectum and RLQ and right hand, general fatigue. Stress makes it worse.
Diagnosed w/ Ulcerated colitus -Asacol prescribed. Have had disease since I was 16 -- I'm now 61. The days and weeks of diahrrea limit my life and activities. Outside of Colostomy, I know there is no cure, but can taking over the counter drugs like acidolphus bring any relief. Taking Immodium Ad only adds to the problem with severe stomach cramps. I know steroid treatment is out there, but not looking forward to side effect.
The Gastro doc wants to treat me with Asacol, but I am suffering from CKD GFRaround 45%.......I told doc and he said ok entercort would be the alternative. that is also an issue as i am a diabetic I have read that just taking imodium and fiber works quiet often also pepto bismol is this correct, Immodium is what i have been using for the last four years any where from 1/2 a pill per day to 1 pill depending if I have not had a movement for day then i back off until I do.
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