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  • {{Image|Pravastatin structure.jpg|right|350px|Pravastatin, a class I statin.}} ...n of HNG CoA reductases results in increased clearance of circulating LDL. Pravastatin also inhibits hepatic synthesis of VLDL, the precursor for LDL, reducing ci
    2 KB (200 words) - 08:45, 8 June 2009
  • 93 bytes (10 words) - 11:23, 6 July 2008
  • 12 bytes (1 word) - 17:48, 23 January 2008
  • {{r|pravastatin}}
    337 bytes (35 words) - 13:08, 8 July 2008

Page text matches

  • {{Image|Pravastatin structure.jpg|right|350px|Pravastatin, a class I statin.}} ...n of HNG CoA reductases results in increased clearance of circulating LDL. Pravastatin also inhibits hepatic synthesis of VLDL, the precursor for LDL, reducing ci
    2 KB (200 words) - 08:45, 8 June 2009
  • {{r|pravastatin}}
    337 bytes (35 words) - 13:08, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:09, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:09, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:10, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:10, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:06, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:07, 8 July 2008
  • {{r|pravastatin}}
    352 bytes (36 words) - 13:08, 8 July 2008
  • {{r|Pravastatin}}
    592 bytes (72 words) - 18:29, 11 January 2010
  • {{r|Pravastatin}}
    682 bytes (81 words) - 07:34, 8 January 2010
  • {{r|pravastatin}}
    340 bytes (38 words) - 08:59, 9 December 2008
  • {{r|Pravastatin}}
    1 KB (153 words) - 17:20, 11 January 2010
  • ...ing system present in the type I statins [[mevastatin]], [[lovastatin]], [[pravastatin]] and [[simvastatin]]. Suppression of HMG-CoA reductase decreases producti
    1 KB (185 words) - 08:03, 8 June 2009
  • ...] (Lipitor), [[cerivastatin]], [[fluvastatin]] (Lescol), [[lovastatin]], [[pravastatin]] (Pravachol), and [[simvastatin]] (Vytorin). Gemfibrizol increases the ef
    2 KB (208 words) - 09:09, 3 November 2009
  • ...ilar to the other class I [[statin]]s [[mevastatin]], [[lovastatin]] and [[pravastatin]]. Its IUPAC chemical name is [(1S,3R,7S,8S,8aR)-8-[2-[(2R,4R)-4-hydroxy-6-
    2 KB (221 words) - 08:33, 2 March 2012
  • ...kura H, ''et al'' |title=Primary prevention of cardiovascular disease with pravastatin in Japan (MEGA Study): a prospective randomised controlled trial |journal=L
    3 KB (339 words) - 09:11, 24 February 2010
  • {{r|Pravastatin}}
    4 KB (505 words) - 16:36, 11 January 2010
  • ...xymethylglutaryl-coenzyme A reductase inhibitor]]s (statins), except for [[pravastatin]] and [[rosuvastatin]], may also interact with [[warfarin]], although this ...xymethylglutaryl-coenzyme A reductase inhibitor]]s (statins), except for [[pravastatin]] and [[rosuvastatin]], are metabolized by this isoenzyme and may:
    22 KB (2,960 words) - 17:35, 10 February 2024
  • ...f a statin (the accompanying evidence report states "simvastatin, 40 mg/d; pravastatin, 40 mg/d; lovastatin, 40 mg/d; atorvastatin, 20 mg/d; or an equivalent dose ..., Toyota T et al.| title=Primary prevention of cardiovascular disease with pravastatin in Japan (MEGA Study): a prospective randomised controlled trial. | journal
    42 KB (5,816 words) - 10:22, 8 March 2015
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