What other symptoms are present? 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.
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?
Her gastroenterologist started her on Mesalamine (4 capsules daily) and later added prednisone 100 mg enemas to try and get the flare-up under control. Things are getting better and she has some of her strength back. There is one puzzling thing that the doctors are not able to pinpoint. This is an intermittent fever that starts in the afternoon and lasts to the night. In the morning the temperature is back to a low 97 degrees fahrenheit and stays stable until afternoon below 98 degrees.
Most recent episode experienced diarrhea, bleeding, fever, severe cramping, weight loss, and anorexia. Initial stool cultures were negative. Colonoscopy revealed mild proctitis and grade I hemorrhoids. Cultures done at this time came back positive for campylobacter, greater than two weeks after initial onset. Histology report diagnosis--Fragments of colon mucosa with moderate nonspecific inflammation, random colon biopsies.
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?
Last November I had a total colectomy with an ileoanal pull through for ulcerative colitis. The pouch was created during the first surgery but I had a colostomy for a few months while it all healed. In February then I had the colostomy reversed. Since then, I have had multiple complications. At first there was a great deal of pain with bowel movements. That has finally subsided however, I currently have 12 -20 bowel movements a day with several occuring at night.
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'm losing hair too. Not in clumps but I clog the drain once a week from my hair loss. And all my friends said their hair was so full and healthy during pregnancy and after lost some. I get a ball of hair during evey wash and its not normal for me also my scalp itches like crazy and I don't have bugs lol o had my husband check lol!
I lost a ton my first pregnancy. I was taking OTC prenatals. This time around my doc recommended prescription prenatals and I haven't had any hair loss or breakage this time. And bonus, the prescription prenatals are free with Affordable Healthcare Act!
I'm very early in my pregnancy and I've noticed some mild hair loss. I have a lot of hair so it's normal for me to shed but this is a lot more than usual. Anyone experience this during pregnancy? Or maybe its due to something else?
I actually posted about this a month or so ago. I have hair loss that really started post Tx. My hair didn't grow hardly at all during Tx, than about 6 weeks post Tx it really started falling out, probably lost 50%. Everyone says it should grow back fine after 6 months post Tx. I figure it is the least of my worries. Looking for my SVR12 in 3 weeks. Hang in there.
But, every few years my thyroid just burns out, and I go hypo. When I do I experience extreme hair loss and brittle nails. For me, the animal based thyroid substitutes work much better when I'm in a hypo phase. Additionally, sometimes when I am not hypo, the medication I take for my Graves' just knocks down my T4/T3 levels so low that once again I start to lose a lot of hair.
How that I am on thyroid medication, since Sept.2007, I continue to have hair loss and have lost 1/2 my hair. 1/8 off my hair in the last 3 months. Is there any way I can stop the hair loss. I am using Levothyroxin 25 and one possible side effect is hair loss, my interist is sending me to a skin doctor in over a month. Do you know what might be the reason for the loss and would a skin doctor be able to help? I had blood tests done this week and my internist found nothing wrong.
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