Welcome to Medications.com

Large bowel symptoms and conditions

Here are side effects posted by other members, that mention large bowel.
Click on a listing to see the full text of the user's posting, and any replies.
50 Side Effects posted for large bowel

September 25th
2008
5:11 PM

I have been put through the wringer with Crohn's. 15 surgeries, all of my terminal ileum removed, 1/3 of my large bowel removed, etc., etc,- Those with sever Crohn's know.

I spent years on high doses of Prednisone, Imuran, Sulfasizine and other drugs and nothing worked.

I was even retired from the US Air Force due to its severity.

Remicade has help tremendously. However, some of the side effects listed above, I have also been through. Some of them, have been explained through other factors and those attributed to the Remicade I take other meds to offset them.

For example, Head aches. I figured the head aches were from allergies that I have had for some time. I attributed some of the headaches to the Remicade. The head aches are very sever after my infusions and decrease to a dull roar after that. I take four aspirin and Sudifed PE and this leaves me with a dull roar shortly after the infusions and does away with them till the next infusion - perhaps this will help some of you.

The muscle soreness is horrible and I take aspirin or Tylenol, but that barely takes the edge off.

I started get those little red dots. Then the dots turn to blisters. I get these on my hands, feet and scalp. My GI Doctor said it wasn't the Remicade, but a Dermatologist showed me a recent article that should Remicade could cause Psoriasis. I take Clobetasol Propionate for these and it has cleared them up.

I took the Remicade years ago and then it was stopped - it was the way it was done then - not constant, just three doses spread out over three months.

I got the tingling fingers during those. A neurologist attributed it to the Steroids I had been on. The nerve damage is permanent.

A few years later, they started the infusions again and I experienced no muscle soreness, headaches, etc. and it did not help the Crohn's as it had before. When I talked to my GI doctor he showed me a study that people build anti-bodies to the Remicade over time. They doubled the dose and it started working again. For those who are experiencing the Remicade not working - perhaps this is what has happened to you.

I get the mood swings, but had never considered it might be the Remicade. I will talk to my doctor about this one.

I have the blood pressure decrease during my infusions, but it has not been sever.

More recently, my joints have begun to ache and initially the Remicade had helped to stop the minor joint pains I already had. Come to find out, I have had bone thinning due to the Crohn's.

The one symptom I have started getting this week is random, sever pain in odd locations - not joints.. They have been deep and feel like they are in the bone. One midway up on my shine, one midway down on my foreman and one in my right thumb. Has anyone experienced this. The pain has been horrible and it does scare me.

I also suffer from depression, but have had it for years prior to the Remicade treatments.

-- By ben1961 | Reply | Private Message me

September 25th
2007
5:19 PM

I've took a very high dosage of prednisone for 6 years, from the age of ten years old. 17 years later, i still have an extreme moon face. The only thing that has ever helped me was a facial exerciser (a microcurrent devise), but those results can be hard an expensive to maintain. As anyone else ever had a moon face that wouldnt go away even after stopping their prednisone usage after a long period of time? Does anyone have any advice for me, on how i can finally get rid of this horrible extreme moonface? my face and all my facial features are swollen, including my eyelids, this has been goin on for years. I also have suffered for years from severe chronic diarrhea from an illeostomy reversal. Please help me.

-- By ezabbellla | Reply | (2) replies | Private Message me

April 20th
2006
11:58 AM

Hi! Have taken aciphex twice daily for almost a year now. I have to say I never felt better. I was really suffering with such symptoms.
The only side effect I have is dry mouth and I sometimes have large bowel movements every day or so. But this is a small price to pay for the relief I now have. I am so thankful for aciphex. I tried protonix and it did nothing for me. My husband takes protonix and it has been like a miracle for him.

-- By mikeb77095 | Reply | Private Message me

April 24th
2005
5:00 AM

Soreness in muscles, especially upper body, and very large bowel movements (solid but in a big hurry to leave). Also dry mouth.
Used it for two weeks for prostate infection. Always took it with food. Infection came back after a few days of being off it. Long-haul trucker.

-- By tsionbenjudah | Reply | Private Message me


 

© 2002-2007, Skylabs Inc.  |  About Us  |  Disclaimer/Terms of Use  |  Advertise  |  Contact Us  |  Site Map  |  Developed by: W3matter.com | Sleep Apnea