Performance Comparison of Microfluidic and Immunomagnetic Platforms for Pancreatic CTC Enrichment
November 15, 2025
Brand Name :
Colestid
Synonyms :
colestipol
Class :
Bile Acid Sequestrants
Dosage forms & Strengths:Â
Adult:Â
Granules in bottleÂ
5 gmÂ
Granules in packetÂ
5 gmÂ
TabletÂ
1 gmÂ
Safety and efficacy are not seen in pediatricsÂ
Granules in bottleÂ
5 gmÂ
Granules in packetÂ
5 gmÂ
TabletÂ
1 gmÂ
Actions and Spectrum:Â
colestipol works by binding to bile acids in the intestine, which prevents them from being reabsorbed into the body. Bile acids are produced by the liver and stored in the gallbladder, where they are released into the small intestine to aid in the digestion of fats. By binding to bile acids, colestipol reduces the amount of cholesterol that is reabsorbed into the bloodstream, which can help lower cholesterol levels.Â
>10%:Â
1-10%:Â
BelchingÂ
FlatulenceÂ
DiarrheaÂ
Nausea/vomitingÂ
FatigueÂ
DizzinessÂ
VertigoÂ
AnxietyÂ
DrowsinessÂ
Black Box Warning:Â
It is essential to follow the dosage and administration instructions for the medication carefully.
Contraindication/Caution:Â
colestipol should not be used in people hypersensitive to the drug itself.Â
Pregnancy consideration:Â Â
Category CÂ
Breastfeeding warnings:Â Â
Use the drug with caution during breastfeeding. As it may interact with the absorption of vitamins in infants.Â
Pregnancy category:Â
PharmacologyÂ
colestipol works by binding to bile acids in the small intestine, forming a complex that is too large to be reabsorbed. This complex is then eliminated in the feces. Bile acids are synthesized in the liver from cholesterol and are necessary for the digestion of fats. colestipol’s binding to bile acids leads to an increased conversion of cholesterol to bile acids by the liver and a decrease in the amount of cholesterol available for reabsorption in the gut. This results in a decrease in the overall cholesterol levels in the body.Â
Pharmacodynamics:Â
colestipol pharmacodynamics involves binding to bile acids in the small intestine, forming a complex that is eliminated in the feces. Pharmacokinetics:Â Â
Pharmacokinetics is the study of how a drug is absorbed, distributed, metabolized, and eliminated by the body. The pharmacokinetics of colestipol can be described by the following parameters:Â
AbsorptionÂ
Not absorbed, just stays in the GITÂ
DistributionÂ
Not distributed into the bloodstreamÂ
MetabolismÂ
Not metabolizedÂ
Elimination and excretionÂ
The drug is excreted 100% in fecesÂ
Administration:Â
colestipol is taken orally. Â
The granules can be mixed with food or fluids. Â
Do not crush or chew the tablet. Â
Take one tablet at a time, with fluids or water.Â
Patient information leafletÂ
Generic Name: colestipolÂ
Pronounced: koe-LES-ti-polÂ
Why do we use colestipol?Â
colestipol is used to treat hyperlipidemia.Â