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Volumn 45, Issue 7, 2005, Pages 802-809

Effect of hepatic impairment on the multiple-dose pharmacokinetics of ranolazine sustained-release tablets

Author keywords

Hepatic impairment; Pharmacokinetics; Ranolazine

Indexed keywords

CVT 2512; CVT 2514; CVT 2738; DRUG METABOLITE; MIDAZOLAM; RANOLAZINE; UNCLASSIFIED DRUG;

EID: 21044458297     PISSN: 00912700     EISSN: None     Source Type: Journal    
DOI: 10.1177/0091270005276739     Document Type: Article
Times cited : (43)

References (9)
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  • 2
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    • Chaitman BR, Pepine CJ, Parker JO, et al. Effects of ranolazine with atenolol, amlodipine, or diltiazem on exercise tolerance and angina frequency in subjects with severe chronic angina: a randomized controlled trial. JAMA. 2004;291:309-316.
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    • Chaitman, B.R.1    Pepine, C.J.2    Parker, J.O.3
  • 3
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    • Anti-ischemic effects and long-term survival during ranolazine monotherapy in subjects with severe coronary artery disease and chronic angina: The MARISA trial
    • Chaitman BR, Skettino SL, Parker JO, et al. Anti-ischemic effects and long-term survival during ranolazine monotherapy in subjects with severe coronary artery disease and chronic angina: the MARISA trial. J Am Coll Cardiol. 2004;43:1375-1382.
    • (2004) J Am Coll Cardiol , vol.43 , pp. 1375-1382
    • Chaitman, B.R.1    Skettino, S.L.2    Parker, J.O.3
  • 4
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    • A controlled trial with a novel anti-ischemic agent, ranolazine, in chronic stable angina pectoris that is responsive to conventional antianginal agents
    • Ranolazine Study Group
    • Pepine CJ, Wolff AA. A controlled trial with a novel anti-ischemic agent, ranolazine, in chronic stable angina pectoris that is responsive to conventional antianginal agents. Ranolazine Study Group. Am J Cardiol. 1999;84:46-50.
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    • Pepine, C.J.1    Wolff, A.A.2
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    • Food and Drug Administration. Guidance for Industry: Pharmacokinetics in Subjects With Impaired Hepatic Function-Study Design, Data Analysis, and Impact on Dosing and Labeling. Washington, DC: US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Biologics Evaluation and Research (CBER). Available at: http://www.fda.gov/cder/guidance/3625fnl.pdf.
    • Guidance for Industry: Pharmacokinetics in Subjects with Impaired Hepatic Function-Study Design, Data Analysis, and Impact on Dosing and Labeling
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    • Clinical pharmacokinetic and pharmacodynamic considerations in subjects with liver disease: An update
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  • 9
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    • In vitro metabolism of ranolazine
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    • (2003) Drug Metab Rev , vol.35 , Issue.SUPPL. 2 , pp. 182
    • Chu, N.1    Soohoo, D.2    Sun, H.-L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.