Proketazin
Brand names,
Proketazin
Analogs
Proketazin
Brand Names Mixture
Proketazin
Chemical_Formula
No information avaliable
Proketazin
RX_link
http://www.rxlist.com/cgi/generic2/colesevelam.htm
Proketazin
fda sheet
Proketazin
msds (material safety sheet)
Proketazin
Synthesis Reference
No information avaliable
Proketazin
Molecular Weight
618.248 g/mol
Proketazin
Melting Point
No information avaliable
Proketazin
H2O Solubility
Insoluble
Proketazin
State
Solid
Proketazin
LogP
No information avaliable
Proketazin
Dosage Forms
Tablets (off-white, film-coated, solid tablets containing 625 mg colesevelam)
Proketazin
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).
Proketazin
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.
Proketazin
Absorption
Not hydrolyzed by digestive enzymes and is not absorbed.
Proketazin
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.
Proketazin
Patient Information
Proketazin
Organisms Affected
Humans and other mammals