Pravastatin and rosuvastatin are relatively hydrophilic and not significantly metabolized by cytochrome P 450 enzymes. 10 mg; 20 mg; 40 … STATIN INTENSITY CHART; DRUG INTERACTIONS; Drug interactions; Metabolism and clearance; PRICE ($) INFO; BIBLIOGRAPHY; OTHER RELATED PAGES; Statin review; Cholesterol treatment guidelines ; Cholesterol review; Cholesterol transport illustration; ACRONYMS AND DEFINITIONS; P = Drugs with approved pediatric dosing ; STATINS; Atorvastatin (Lipitor®) Dosage forms. In addition, they can exert antiatherosclerotic effects independently of their hypolipidemic action. And yes, you’d better believe it includes a statin intensity chart. Statin absorption, distribution, metabolism, and excretion are complex and vary from statin to statin. Statins differ mainly in the degree of metabolism and the number of active and inactive metabolites. Lipophilic statins are more susceptible to metabolism by the cytochrome P 450 system, except for pitavastatin, which undergoes limited metabolism via this pathway. All statins but pravastatin show highly active metabolites, the pharmacological activity depending on the kinetic profile of both parent compound and active metabolites. Muscle toxicity is one of the most widely recognized adverse effects of statin therapy, but it’s also a bit of a chameleon. They are the most common cholesterol-lowering drugs. The transporters and enzymes involved in these processes are now better understood and serve to explain the mechanisms of statin interactions with a variety of drugs that alter what is otherwise an excellent safety profile. Statins have antiatherosclerotic effects, that positively correlate with the percent decrease in LDL cholesterol. With the exception of pravastatin, which is mainly cleared by the kidneys, statins are metabolised in the cytochrome P450 isoenzyme system. Tablet. 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