Atorvastatin: Difference between revisions

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*Atorpic  
*Atorpic  
*Liprimar
*Liprimar
== Drug interactions ==
* [[Amprenavir]] can possibly increase the statin
* [[Atazanavir]] increases the effect and toxicity of the statin
* [[Bezafibrate]] increases the risk of [[myopathy]]/[[rhabdomyolysis]]
* [[Bosentan]] could decrease atorvastatin
* [[Carbamazepine]] decreases the effect of the statin
* [[Colchicine]] increases the risk of rhadbomyolysis with this combination
* [[Clarithromycin]] possibly increases the statin toxicity
* [[Cyclosporine]] may cause [[myopathy]] and [[rhabdomyolysis]]
* [[Delavirdine]] an [[NNRT inhibitor]] increases the effect and toxicity of the statin
* [[Diltiazem]] increases the effect and toxicity of atorvastatin
* [[Efavirenz]], an NNRT inhibitor, increases the effect and toxicity of the statin
* [[Erythromycin]] possibly increases the statin toxicity
* [[Fenofibrate]] Increasing risk of myopathy/rhabdomyolysis
* [[Fluconazole]] Increases the risk of myopathy/rhabdomyolysis
* [[Fosamprenavir]] Amprenavir can possibly increase the statin toxicity
* [[Gemfibrozil]] Increases the risk of myopathy/rhabdomyolysis
* [[Imatinib]] increases the effect and toxicity of atorvastatin
* [[Indinavir]] increases the effect and toxicity of atorvastatin
* [[Itraconazole]] Increases the risk of myopathy/rhabdomyolysis
* [[Josamycin]], a macrolide, possibly increases the statin toxicity
* [[Ketoconazole]] increases the risk of myopathy/rhabdomyolysis
* [[Nefazodone]] increases the effect and toxicity of the statin drug
* [[Nelfinavir]] increases the effect and toxicity of the statin
* [[Nevirapine]], an NNRT inhibitor, increases the effect and toxicity of the statin
* [[Quinupristin]] presents an increased risk of toxicity
* [[Rifabutin]], a [[rifamycin]], decreases the effect of the statin drug
* [[Rifampin]], a rifamycin, decreases the effect of the statin drug
* [[Ritonavir]] increases the effect and toxicity of the statin
* [[Saquinavir]] increases the effect and toxicity of atorvastatin
* [[Tacrolimus]] increases the effect and toxicity of the statin
* [[Telithromycin]] may possibly increase statin toxicity
* [[Verapamil]] increases the effect and toxicity of the statin

Revision as of 11:23, 24 January 2008

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(CC) Image: David E. Volk
Atorvastatin, a class II statin.

Atorvastatin, commonly called Lipitor, is a class II statin used to treat high cholesterol (hypercholesterolemia), prevent heart attacks and strokes, and to lessen the formation of artial plaque. It is a HMG-CoA reductase inhibitor that decreases the synthesis of mevalonate, a key chemical precursor of cholesterol. Although the structure is based on an indole ring, as are the other class II statins fluvastatin and rosuvastatin, its longer half-life and specificity for the liver makes atorvastatin a better drug for lowering LDL-cholesterol levels. The metabolites of atorvastatin, ortho- and parahydroxylated derivatives and various beta-oxidation products, are equivalent HMG-CoA reductase inhibitors. The drug should be taken with a low fat meal and alcohol and grapefruit juice should be avoided. Atorvastatin can be toxic, leading to liver problems, rhabdomyolysis and eye hemorrhages.

Its official IUPAC chemical name is (3R,5R)-7-[2-(4-fluorophenyl)-3-phenyl-4-(phenylcarbamoyl)-5-propan-2-ylpyrrol-1-yl]-3,5-dihydroxyheptanoic acid and it has chemical formula C33H35FN2O5.

brand names

  • Cardyl
  • Lipitor
  • Sotis
  • Torvast
  • Tozalip
  • Xavator
  • Sortis
  • Torvacard
  • Totalip
  • Tulip
  • Xarator
  • Atorpic
  • Liprimar


Drug interactions