Chlormeroprin en es it fr

Chlormeroprin Brand names, Chlormeroprin Analogs

Chlormeroprin Brand Names Mixture

  • No information avaliable

Chlormeroprin Chemical_Formula

C11H28ClN5O

Chlormeroprin RX_link

http://www.rxlist.com/cgi/generic/colestipol.htm

Chlormeroprin fda sheet

Chlormeroprin msds (material safety sheet)

Chlormeroprin MSDS

Chlormeroprin Synthesis Reference

No information avaliable

Chlormeroprin Molecular Weight

281.826 g/mol

Chlormeroprin Melting Point

No information avaliable

Chlormeroprin H2O Solubility

Insoluble

Chlormeroprin State

Solid

Chlormeroprin LogP

-2.206

Chlormeroprin Dosage Forms

Tablets containing 1 gram of colestipol hydrochloride (light yellow in color and are tasteless and odorless)

Chlormeroprin Indication

For use, as adjunctive therapy to diet, for the reduction of elevated serum total and LDL-C in patients with primary hypercholesterolemia (elevated LDL-C) who do not respond adequately to diet.

Chlormeroprin Pharmacology

Cholesterol is the major, and probably the sole precursor of bile acids. During normal digestion, bile acids are secreted via the bile from the liver and gall bladder into the intestines. Bile acids emulsify the fat and lipid materials present in food, thus facilitating absorption. A major portion of the bile acids secreted is reabsorbed from the intestines and returned via the portal circulation to the liver, thus completing the enterohepatic cycle. Only very small amounts of bile acids are found in normal serum. Colestipol hydrochloride binds bile acids in the intestine forming a complex that is excreted in the feces. This nonsystemic action results in a partial removal of the bile acids from the enterohepatic circulation, preventing their reabsorption. Since colestipol hydrochloride is an anion exchange resin, the chloride anions of the resin can be replaced by other anions, usually those with a greater affinity for the resin than the chloride ion.

Chlormeroprin Absorption

Not absorbed from the gastrointestinal tract.

Chlormeroprin side effects and Toxicity

Oral LD50 in rats is > 1000 mg/kg. Symptoms of overdose may include eye irritation, constipation, abdominal cramps, nausea, vomiting, diarrhea, and hypersensitivity. However, as colestipol is not absorbed, the risk of systemic toxicity is low.

Chlormeroprin Patient Information

Chlormeroprin Organisms Affected

Humans and other mammals