Literature DB >> 12269853

Rosuvastatin.

Christopher I Carswell1, Greg L Plosker, Blair Jarvis.   

Abstract

Rosuvastatin is a hydroxymethylglutaryl coenzyme A (HMG-CoA) reductase inhibitor used in the treatment of patients with dyslipidaemia. Rosuvastatin is not extensively metabolised and has a low propensity for drug interactions. In well designed trials of between 6 and 52 weeks' duration, rosuvastatin was superior to atorvastatin, simvastatin and pravastatin in improving the lipid profile of patients with hypercholesterolaemia. In a 1-year dose-titration study, rosuvastatin 13.4mg daily (mean dose) allowed more patients to achieve US National Cholesterol Education Program (Adult Treatment panel II)[NCEP] target low-density lipoprotein (LDL)-cholesterol levels than atorvastatin 20.8mg daily (98 vs 87%) with the difference most marked in high-risk patients (97 vs 61%). Similarly, when compared with pravastatin and simvastatin 20 mg/day in a further 1-year trial, 88% of rosuvastatin recipients [9.5 and 13.8 mg/day (mean doses)] achieved NCEP target serum LDL-cholesterol levels compared with 60 and 73% of pravastatin and simvastatin recipients, respectively, with the difference more marked in high-risk patients. In further clinical trials, rosuvastatin improved the lipid profile of patients with heterozygous or homozygous familial hypercholesterolaemia, hypertriglyceridaemia or mixed dyslipidaemias. Rosuvastatin was well tolerated in clinical trials of up to 1 years' duration.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12269853     DOI: 10.2165/00003495-200262140-00008

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  19 in total

Review 1.  Drug treatment of lipid disorders.

Authors:  R H Knopp
Journal:  N Engl J Med       Date:  1999-08-12       Impact factor: 91.245

2.  Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III).

Authors: 
Journal:  JAMA       Date:  2001-05-16       Impact factor: 56.272

3.  Summary of the second report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II)

Authors: 
Journal:  JAMA       Date:  1993-06-16       Impact factor: 56.272

Review 4.  Coronary heart disease: reducing the risk: the scientific background to primary and secondary prevention of coronary heart disease. A worldwide view. International Task force for the Prevention of Coronary Heart disease.

Authors:  G Assmann; P Cullen; F Jossa; B Lewis; M Mancini
Journal:  Arterioscler Thromb Vasc Biol       Date:  1999-08       Impact factor: 8.311

5.  Synthesis and biological activity of methanesulfonamide pyrimidine- and N-methanesulfonyl pyrrole-substituted 3,5-dihydroxy-6-heptenoates, a novel series of HMG-CoA reductase inhibitors.

Authors:  M Watanabe; H Koike; T Ishiba; T Okada; S Seo; K Hirai
Journal:  Bioorg Med Chem       Date:  1997-02       Impact factor: 3.641

Review 6.  The cost of treating dyslipidaemia using National Cholesterol Education Program (NCEP) guidelines.

Authors:  J M McKenney
Journal:  Pharmacoeconomics       Date:  1998       Impact factor: 4.981

7.  The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators.

Authors:  F M Sacks; M A Pfeffer; L A Moye; J L Rouleau; J D Rutherford; T G Cole; L Brown; J W Warnica; J M Arnold; C C Wun; B R Davis; E Braunwald
Journal:  N Engl J Med       Date:  1996-10-03       Impact factor: 91.245

8.  Prevention of cardiovascular events and death with pravastatin in patients with coronary heart disease and a broad range of initial cholesterol levels.

Authors: 
Journal:  N Engl J Med       Date:  1998-11-05       Impact factor: 91.245

9.  Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. West of Scotland Coronary Prevention Study Group.

Authors:  J Shepherd; S M Cobbe; I Ford; C G Isles; A R Lorimer; P W MacFarlane; J H McKillop; C J Packard
Journal:  N Engl J Med       Date:  1995-11-16       Impact factor: 91.245

10.  Comparative effects of rosuvastatin and atorvastatin across their dose ranges in patients with hypercholesterolemia and without active arterial disease.

Authors:  Dennis W Schneck; Robert H Knopp; Christie M Ballantyne; Ruth McPherson; Rohini R Chitra; Steven G Simonson
Journal:  Am J Cardiol       Date:  2003-01-01       Impact factor: 2.778

View more
  5 in total

1.  Race differences: modeling the pharmacodynamics of rosuvastatin in Western and Asian hypercholesterolemia patients.

Authors:  Juan Yang; Lu-jin Li; Kun Wang; Ying-chun He; Yu-cheng Sheng; Ling Xu; Xiao-hui Huang; Feng Guo; Qing-shan Zheng
Journal:  Acta Pharmacol Sin       Date:  2010-12-13       Impact factor: 6.150

2.  Pharmacokinetics and tolerability of multiple-dose rosuvastatin: An open-label, randomized-sequence, three-way crossover trial in healthy Chinese volunteers.

Authors:  Ruoqi Zhang; Yunxia Li; Xuehua Jiang; Ling Wang
Journal:  Curr Ther Res Clin Exp       Date:  2009-10

3.  Drug discovery from natural sources.

Authors:  Young-Won Chin; Marcy J Balunas; Hee Byung Chai; A Douglas Kinghorn
Journal:  AAPS J       Date:  2006-04-14       Impact factor: 4.009

4.  More potent lipid-lowering effect by rosuvastatin compared with fluvastatin in everolimus-treated renal transplant recipients.

Authors:  Ida Robertsen; Anders Asberg; Tone Granseth; Nils Tore Vethe; Fatemeh Akhlaghi; Mwlod Ghareeb; Espen Molden; Morten Reier-Nilsen; Hallvard Holdaas; Karsten Midtvedt
Journal:  Transplantation       Date:  2014-06-27       Impact factor: 4.939

5.  No effects of pantoprazole on the pharmacokinetics of rosuvastatin in healthy subjects.

Authors:  J Huguet; J Lu; F Gaudette; J-L Chiasson; P Hamet; V Michaud; J Turgeon
Journal:  Eur J Clin Pharmacol       Date:  2016-05-05       Impact factor: 2.953

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.