US2012053239A1PendingUtilityA1
Treatment for intestinal gas, bloating, microscopic colitis, inflammatory bowel disease and traveler's diarrhea using colloidal bismuth subcitrate
Est. expiryDec 7, 2026(~0.3 yrs left)· nominal 20-yr term from priority
Inventors:Eli D. Ehrenpreis
A61K 33/245A61K 45/06A61K 31/29
59
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
A method of treatment for intestinal gas bloating, microscopic colitis, traveler's diarrhea and inflammatory bowel disease, said method comprising ingesting an effective quantity of a composition comprising colloidal bismuth subcitrate to eliminate gastrointestinal discomfort.
Claims
exact text as granted — not AI-modifiedI claim:
1 . A method of treatment for intestinal gas bloating, microscopic colitis and traveler's diarrhea, said method comprising ingesting an effective quantity of a composition comprising colloidal bismuth subcitrate to eliminate gastrointestinal discomfort.
2 . The method according to claim 1 , wherein the composition contains at least 125 mg of colloidal bismuth subcitrate.
3 . The method according to claim 2 , wherein the composition is administered once daily.
4 . The method according to claim 2 , wherein the composition is administered twice daily.
5 . The method according to claim 2 , wherein the composition is administered up to six times a day.
6 . The method according to claim 1 , wherein the composition contains between 125 mg and 900 mg of colloidal bismuth subcitrate.
7 . A topical oral dosage selected from the group consisting of chewing gums, lozenges, troches, and combinations thereof, wherein the topical oral dosage form comprises a pharmaceutically active agent effective against intestinal gas bloating, microscopic colitis and traveler's diarrhea, wherein the pharmaceutically active agent comprises colloidal bismuth subcitrate.
8 . The topical oral dosage of claim 7 wherein the dosage form is a chewing gum.
9 . The topical oral dosage of claim 7 wherein the dosage form is a lozenge.
10 . The topical oral dosage of claim 7 wherein the dosage form is a troche.
11 . The topical dosage of claim 7 wherein the topical dosage form is chewing gum.
12 . The topical dosage of claim 11 wherein the chewing gum comprises between about 125 mg and about 900 mg of colloidal bismuth subcitrate.
13 . The method according to claim 1 , wherein the composition contains ranitidine bismuth citrate at a dose of 400 mg, administered daily or up to three times per day.
14 . The method according to claim 1 , wherein the composition contains ranitidine bismuth citrate at a dose of 800 mg, administered daily or up to three times per day.
15 . The method according to claim 1 , wherein the composition further contains one or more of the following simethicone, a steroid, an anti-inflammatory, and an antibiotic.Join the waitlist — get patent alerts
Track US2012053239A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.