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Table representation of search results timeline featuring number of search results per year.

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1970 1
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1973 9
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1975 11
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1980 22
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1982 21
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1984 12
1985 14
1986 19
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1988 24
1989 21
1990 33
1991 20
1992 16
1993 17
1994 14
1995 24
1996 11
1997 10
1998 12
1999 7
2000 7
2001 8
2002 7
2003 3
2004 4
2005 6
2006 6
2007 8
2008 4
2009 2
2010 3
2011 4
2012 5
2013 3
2014 8
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2017 6
2018 1
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560 results

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Page 1
Colestipol.
[No authors listed] [No authors listed] 2017 Sep 28. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012–. 2017 Sep 28. LiverTox: Clinical and Research Information on Drug-Induced Liver Injury [Internet]. Bethesda (MD): National Institute of Diabetes and Digestive and Kidney Diseases; 2012–. PMID: 31643751 Free Books & Documents. Review.
Colestipol is a nonabsorbed bile acid sequestrant that is used a therapy of hyperlipidemia and for the pruritus of chronic liver disease and biliary obstruction. Colestipol has not been associated with clinically apparent liver injury....
Colestipol is a nonabsorbed bile acid sequestrant that is used a therapy of hyperlipidemia and for the pruritus of chronic liver dise
Colestipol.
[No authors listed] [No authors listed] 2022 Sep 19. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. 2022 Sep 19. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. PMID: 30000452 Free Books & Documents. Review.
Colestipol is a nonabsorbable resin. Because it does not enter the mother's bloodstream, it will not reach the infant via breastmilk. ...
Colestipol is a nonabsorbable resin. Because it does not enter the mother's bloodstream, it will not reach the infant via breastmilk.
Clinical pharmacokinetics of diclofenac. Therapeutic insights and pitfalls.
Davies NM, Anderson KE. Davies NM, et al. Clin Pharmacokinet. 1997 Sep;33(3):184-213. doi: 10.2165/00003088-199733030-00003. Clin Pharmacokinet. 1997. PMID: 9314611 Review.
Significant drug interactions have been demonstrated for aspirin (acetylsalicylic acid), lithium, digoxin, methotrexate, cyclosporin, cholestyramine and colestipol....
Significant drug interactions have been demonstrated for aspirin (acetylsalicylic acid), lithium, digoxin, methotrexate, cyclosporin, choles …
Colestipol.
Hameed MH, Patel P, Farzam K. Hameed MH, et al. 2024 Jan 30. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2024 Jan 30. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 36508523 Free Books & Documents.
Colestipol is an antihyperlipidemic drug approved by the United States Food and Drug Administration (FDA) as an adjunctive therapy to lower elevated low-density lipoprotein cholesterol in patients with primary hypercholesterolemia unresponsive to dietary modifications alon
Colestipol is an antihyperlipidemic drug approved by the United States Food and Drug Administration (FDA) as an adjunctive therapy to
Lipid-lowering drugs.
[No authors listed] [No authors listed] Med Lett Drugs Ther. 2022 Sep 19;64(1659):145-152. Med Lett Drugs Ther. 2022. PMID: 36094548 No abstract available.
Lipid-lowering drugs.
[No authors listed] [No authors listed] Med Lett Drugs Ther. 2019 Feb 11;61(1565):17-24. Med Lett Drugs Ther. 2019. PMID: 30845106 No abstract available.
Colestipol-induced hepatotoxicity.
Sirmans SM, Beck JK, Banh HL, Freeman DA. Sirmans SM, et al. Pharmacotherapy. 2001 Apr;21(4):513-6. doi: 10.1592/phco.21.5.513.34501. Pharmacotherapy. 2001. PMID: 11310528
One week after discontinuing colestipol, serum transaminases fell dramatically, with some returning to normal limits. Four weeks after colestipol was discontinued, all liver function tests were normal. Rechallenge was not attempted. ...
One week after discontinuing colestipol, serum transaminases fell dramatically, with some returning to normal limits. Four weeks afte …
Pruritus.
Franco J. Franco J. Curr Treat Options Gastroenterol. 1999 Dec;2(6):451-456. doi: 10.1007/s11938-999-0048-8. Curr Treat Options Gastroenterol. 1999. PMID: 11097728
The treatment of patients with pruritus of liver disease poses a challenge to the clinician. Resins (cholestyramine or colestipol) in quantities of 4 to 16 grams a day should be the initial agents used. In those who remain refractory, diphenhydramine should be added, altho …
The treatment of patients with pruritus of liver disease poses a challenge to the clinician. Resins (cholestyramine or colestipol) in …
Treatment of hypercholesterolemia.
Grundy SM. Grundy SM. Am J Clin Nutr. 1977 Jun;30(6):985-92. doi: 10.1093/ajcn/30.6.985. Am J Clin Nutr. 1977. PMID: 326023 Review. No abstract available.
Bile acid sequestrants.
Ast M, Frishman WH. Ast M, et al. J Clin Pharmacol. 1990 Feb;30(2):99-106. doi: 10.1002/j.1552-4604.1990.tb03447.x. J Clin Pharmacol. 1990. PMID: 2179278 Review.
The bile acid sequestrants, cholestyramine and colestipol, are the drugs of choice for the treatment of patients with hypercholesterolemia caused by increases in LDL-cholesterol levels without concurrent hypertriglyceridemia (type IIA and type IIB hyperlipoproteinemia). .. …
The bile acid sequestrants, cholestyramine and colestipol, are the drugs of choice for the treatment of patients with hypercholestero …
560 results