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?
Has anyone tried Lialda? Does it perform any better than Asacol? How much more is your co-pay for Lialda than Asacol. I want to ask my doc to make a switch.
He was switched from Asacol to Pentasa when his liver enzymes were slightly elevated. He was on a steroid for the first 2 years after he was diagnosed. He hasn't been on a steroid since 2006, when he was diagnosed with Diabetes. The Steroids are more for the flares, the Pentasa is used more as a maintenance drug. He is also on Purinethol, which is chemotherapy agent, to help decrease abnormal growths. Good luck.
Had coloscopy in August-showed some mild inflammation in ilieum and rectal area-was put on Asacol. Asacol helped the rectal pain but RLQ pain continued. Went back to ED in Nov for severe RLQ pain. CT and bloodwork normal. 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.
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.
A related discussion, <a href="/posts/Gastroenterology/Asacol-800/show/1876778">Asacol 800</a> was started.
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?
Is there a program where my son can get help with his Rx for asacol? He does not have insurance.
I do still take Asacol because I look at controlling the inflammation as being very important. Her symptoms may have subsided, but you don't want the disease to do further damage to her digestive system...so that would be my only fear of not taking a medical treatment.
It sounds like you have a good combination of supplements going.
The idea is to get off the steroids asap but make sure the bleeding is stopped. The other thing is to increase the Asacol right away to get the UC under control and adjust her dosage to manage it. If she is still having trouble then she needs to treat it from both ends, so get her GI to prescribe an enema nightly with her regular Asacol orally but it's very important to get her off the prednezone. It's bad taking it continuously.
I'm sure your Oncologist would not recommend any treatment that would be contradicted by any other ailment you might have. He/She should have your complete medical history unless you have withheld some information. You should discuss this in detail with him/her if you have any questions regarding your treatment. Regards ....
Try to stay away from dairy, alcohol, grains (have rice instead). If you can figure out what triggered the flare, that would be helpful so you know to avoid it in the future.
I hate Asacol and I find it does nothing but cause joint pain especially in my fingers to the point that I can't pick up a glass. I have never felt any benefit from it and I know there are alternative meds out there, but my doctor refuses to give me anything else. My crohns is in the rectum and large intestine.
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.
after being diagnosed with uc he was placed on asacol 1200mg. 3 times a day, prednisone a couple of times last year, entocort most recently, and asacol enemas at night at times. Just recently he started getting muscle cramps, flu like symptoms with bronchitis and had a glucose level of 169, and a cholesterol level in the high 160s as well. He had had an alkaline phosphate level up to almost 600 for years and stays very fatigued and in pain. i am so worried about him. he is overweight.
However, he also still has many symptoms that are unrelated to the Crohn’s Disease and they are now testing him for other diseases which may be Lupus, MS and or Rheumatoid Arthritis. We are wondering if there are any recommended treatment for Crohn’s other than Prednisone and Align and if there is any other disease that it may be and how to get tested for it. We have tried so many things and nothing seems to be working at this point. We would appreciate any advice.
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