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treatment of ulcerative proctitis and colitis colitis foundation of america crohn's-and colitis foundation of america dealing with ulcerative colitis treatment of colitis ulcerosa compositions and method -fo -treatment of ulcerative colitis detection and treatment of ulcerative colitis method of treating ulcerative colitis method of treating ulcerative colitis with a monoclonal antibody methods for the treatment of ulcerative colitis methods of treating established colitis using antibodies therapeutic agent for ulcerative colitis therapeutic-and-diagnostic-methods for ulcerative colitis and associated disorders treating a patient with ulcerative colitis methods of treatment for ulcerative colitis using aminosalicylate therapeutic agent for ulcerative colitis therapeutic-and-diagnostic-methods for ulcerative colitis and associated disorders treating a patient with ulcerative colitis .
fish oils benefit patients with ulcerative colitis crohn's disease and ulcerative colitis !!!!
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Ulcerative colitis (UC) is a condition that causes inflammation and sores in the form of ulcers, in the lining of the rectum and colon. The inflammation may kill the cells that line the colon, causing ulcers which may then bleed and produce pus. Inflammation in the colon may also cause the colon to empty frequently, causing diarrhea. When the inflammation occurs in the rectum and lower part of the colon it is called ulcerative proctitis. If the entire colon is affected it is called pancolitis. If only the left side of the colon is affected it is called left-sided or distal colitis. UC is a type of inflammatory bowel disease (IBD). IBD is the general name for diseases that cause inflammation in the small intestine and colon. UC is oftentimes difficult to diagnose as it shares symptoms common to other intestinal disorders and to Crohn's disease, another type of IBD. Crohn's disease differs because it causes inflammation deeper within the intestinal wall and can occur in other parts of the digestive system including the small intestine, mouth, esophagus, and stomach. One known method of drug therapy to treat UC is administration
of aminosalicylates. Aminosalicylates include 5-aminosalicylic acid (5-ASA),
salts thereof, and pro-drugs that release 5-aminosalicyclic acid, or salts
thereof, in vivo. Pro-drugs that release 5-aminosalicylic acid, or salts
thereof, in vivo include, but are not limited to: olsalazine, balsalazide,
and sulfasalazine. Aminosalicylates may be administered orally, through
an enema, or in a suppository. Most people with mild or moderate ulcerative
colitis are treated with aminosalicylates drugs first. The aminosalicylates
also used in cases of relapse and to maintain remission. ASACOL® is a product
comprising the aminosalicylate, 5-aminosalicylic acid or mesalamine. ASACOL®
is effective in treating patients with mild to moderate ulcerative colitis.
Its effectiveness also extends to the maintenance of remission for prolonged
periods. The current recommended dose of orally delivered ASACOL® for active
disease is two 400-mg tablets three times daily for a total of 2.4 g/day
(grams per day) for the treatment of mild to moderate UC. If the patient
does not respond to ASACOL®, then alternatives, such as corticosteroids,
are considered.
In one aspect of the present invention there is method of treating moderate ulcerative colitis in a mammalian male subject comprising the step of orally administering to the mammalian male subject an aminosalicylate in an amount to deliver greater than about 2.4 g/day of 5-aminosalicylic acid to the subject. In some embodiments, the step of orally administering an aminosalicylate comprises orally administering an aminosalicylate in an amount to deliver about 4.8 g/day of 5-aminosalicylic acid to said subject. In some embodiments wherein about 4.8 g/day of 5-aminosalicylic acid is delivered to the subject, the aminosalicylate comprises mesalamine or a salt thereof. In some embodiments wherein about 4.8 g/day of 5-aminosalicylic acid is delivered to the subject, the step of orally administering comprises orally administering once per day, twice per day, three times per day, or four times per day. In some embodiments, the aminosalicylate comprises mesalamine or a salt thereof. In certain embodiments, the aminosalicylate comprises mesalamine and further wherein the mesalamine is administered in an amount of about 4.8 g/day. In certain embodiments, the mammalian male subject is a human male. In certain embodiments, the mammalian male subject is less than about 65 years of age. In certain embodiments, the mammalian male subject is a non-smoking subject. In certain embodiments, the mammalian male subject is Caucasian. In certain embodiments, the mammalian male subject is a previous or current steroid user. In some embodiments, the step of orally administering comprises orally administering tablets comprising about 800 milligrams of mesalamine or a salt thereof. In some embodiments wherein tablets comprising about 800 milligrams of mesalamine or a salt thereof are orally administered, the tablets are delayed-release tablets. In some embodiments, the step of orally administering comprises orally administering tablets comprising about 1.2 g mesalamine or a salt thereof. In some embodiments wherein tablets comprising about 1.2 g of mesalamine or a salt thereof are orally administered, the tablets are delayed-release tablets. In some embodiments, the aminosalicylate comprises a component selected from the group consisting of mesalamine, a salt of mesalamine, olsalazine, a salt of olsalazine, balsalazide, a salt of balsalazide, sulfasalazine, a salt of sulfasalazine, or any pharmaceutically acceptable combination thereof. In some embodiments, the step of orally administering comprises orally administering once per day, twice per day, three times per day, or four times per day. In another aspect of the present invention, there is method of treating moderate ulcerative colitis in a mammalian male subject comprising the step of administering to the mammalian male subject an aminosalicylate in an amount to deliver greater than about 2.4 g/day but less than or equal to about 4.8 g/day of 5-aminosalicylic acid to the subject. In certain embodiments, the step of administering comprises rectal administration. In some embodiments, the step of administering an aminosalicylate comprises administering an aminosalicylate in an amount to deliver about 4.8 g/day of 5-aminosalicylic acid to the subject. In some embodiments wherein about 4.8 g/day of 5-aminosalicylic acid is delivered to the subject, the aminosalicylate comprises mesalamine or a salt thereof. In some embodiments wherein about 4.8 g/day of 5-aminosalicylic acid is delivered to the subject, the step of administering comprises administering once per day, twice per day, three times per day, or four times per day. In some embodiments, the aminosalicylate comprises mesalamine or a salt thereof. In some embodiments, the aminosalicylate comprises mesalamine and further wherein the mesalamine is administered in an amount of about 4.8 g/day. In certain embodiments, the mammalian male subject is a human male. In certain embodiments, the mammalian male subject is less than about 65 years of age. In certain embodiments, the mammalian male subject is a non-smoking subject. In certain embodiments, the mammalian male subject is Caucasian. In certain embodiments, the mammalian male subject is a previous or current steroid user. In certain embodiments, the step of administering comprises administering a rectal composition comprising about 800 milligrams or about 1.2 g of mesalamine or a salt thereof. In some embodiments, the rectal composition is an enema. In some embodiments, the rectal composition is a foamed composition. In some embodiments wherein a rectal composition is administered, the rectal composition is a suppository. In some embodiments, the aminosalicylate comprises a component selected from the group consisting of mesalamine, a salt of mesalamine, olsalazine, a salt of olsalazine, balsalazide, a salt of balsalazide, sulfasalazine, a salt of sulfasalazine, or any pharmaceutically acceptable combination thereof. In some embodiments, the step of administering comprises administering once per day, twice per day, three times per day, or four times per day. The foregoing has outlined the features and technical
advantages of the present invention in order that the detailed description
of the invention that follows may be better understood. Additional features
and advantages of the invention will be described hereinafter which form
the subject of the claims of the invention. It should be appreciated by
those skilled in the art that the conception and specific embodiment disclosed
may be readily utilized as a basis for modifying or designing other structures
for carrying out the same purposes of the present invention. It should
also be realized by those skilled in the art that such equivalent constructions
do not depart from the spirit and scope of the invention as set forth in
the appended claims. The novel features which are believed to be characteristic
of the invention, both as to its organization and method of operation,
together with further objects and advantages will be better understood
from the following description when considered in connection with the accompanying
figures. It is to be expressly understood, however, that each of the figures
is provided for the purpose of illustration and description only and is
not intended as a definition of the limits of the present invention.
There are also herbal medicines which can very effectively treat colitis
& ulcerative colitis. Boswellia is an
Ayurvedic (Indian traditional medicine) herb, used as a natural alternative
to drugs. Many studies have found that the effectiveness of Boswellia is similar and even superior to sulfasalazine based prescription drugs.
(Source Wikipedia: We recommend taking a
4 months course of our Boswellia Serrata Extract.
Order Boswellia - Shallaki - 4 Months course
Total
of 4 bottles- of Boswellia
- 4 Months course - Taken 2 capusles twice a day.
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