Proketazine
Brand names,
Proketazine
Analogs
Proketazine
Brand Names Mixture
Proketazine
Chemical_Formula
No information avaliable
Proketazine
RX_link
http://www.rxlist.com/cgi/generic2/colesevelam.htm
Proketazine
fda sheet
Proketazine
msds (material safety sheet)
Proketazine
Synthesis Reference
No information avaliable
Proketazine
Molecular Weight
618.248 g/mol
Proketazine
Melting Point
No information avaliable
Proketazine
H2O Solubility
Insoluble
Proketazine
State
Solid
Proketazine
LogP
No information avaliable
Proketazine
Dosage Forms
Tablets (off-white, film-coated, solid tablets containing 625 mg colesevelam)
Proketazine
Indication
For use, alone or in combination with an HMG-CoA reductase inhibitor, as adjunctive therapy to diet and exercise for the reduction of elevated LDL cholesterol in patients with primary hypercholesterolemia (Fredrickson Type IIa).
Proketazine
Pharmacology
Colesevelam is a high capacity bile-acid binding molecule. Colesevelam binds to bile acids in the intestine which reduces the amount of bile acids that are returned to the liver via enterohepatic circulation. Clinical studies have demonstrated that elevated levels of total cholesterol (total-C), LDL-C, and apolipoprotein B (Apo B, a protein associated with LDL-C) are associated with an increased risk of atherosclerosis in humans. Similarly, decreased levels of high-density lipoprotein cholesterol (HDL-C) are associated with the development of atherosclerosis. Epidemiological investigations have established that cardiovascular morbidity and mortality vary directly with the levels of total-C and LDL-C, and inversely with the level of HDL-C. The combination of colesevelam and an HMG-CoA reductase inhibitor is effective in further lowering serum total-C and LDL-C levels beyond that achieved by either agent alone.
Proketazine
Absorption
Not hydrolyzed by digestive enzymes and is not absorbed.
Proketazine
side effects and Toxicity
Symptoms of overdose may include eye irritation, constipation, abdominal cramps, nausea, vomiting, diarrhea, and hypersensitivity. However, as colesevelam is not absorbed, the risk of systemic toxicity is low. Doses in excess of 4.5 g per day have not been tested.
Proketazine
Patient Information
Proketazine
Organisms Affected
Humans and other mammals