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Titlebook: Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials; Tony K.L. Kiang,Kyle John Wilby,Mary H.H. En

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发表于 2025-3-21 18:16:09 | 显示全部楼层 |阅读模式
书目名称Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials
编辑Tony K.L. Kiang,Kyle John Wilby,Mary H.H. Ensom
视频video
概述Discusses the clinical pharmacokinetic and pharmacodynamic drug interactions involving antimalarial drugs recommended by the WHO.Addresses the clinical significance of the interactions and provides a
图书封面Titlebook: Clinical Pharmacokinetic and Pharmacodynamic Drug Interactions Associated with Antimalarials;  Tony K.L. Kiang,Kyle John Wilby,Mary H.H. En
描述.This comprehensive review provides a systematic, unbiased analysis, critique and summary of the available literature and generates novel clinical decision-making algorithms which can aid clinicians and scientists in practice management and research development. Potential mechanisms for the identified drug interactions are deduced from available preclinical and in vitro data which are interpreted in the context of the in vivo findings. Current limitations and gaps in the literature are summarized, and potential future research directions / experimentations are also suggested.  In addition to the main objective to review the available clinical pharmacokinetic and pharmacodynamic drug interactions associated with WHO-recommended antimalarial drugs on the market today (i.e. chloroquine, amodiaquine, sulfadoxine, pyrimethamine, mefloquine, artemisinin, artemether, artesunate, dihydroartemisinin, artemotil, lumefantrine, primaquine, atovaquone, proguanil, piperaquine and quinine), this book also provides succinct chapter summaries on the epidemiology of malaria infection, diagnosis and therapeutics, in vivo pharmacology and chemistry, preclinical pharmacology, in vitro pharmacodynamics,
出版日期Book 2015
关键词Pharmacodynamics; Pharmacokinetics; antimalarial drugs; interactions; malaria
版次1
doihttps://doi.org/10.1007/978-3-319-10527-7
isbn_softcover978-3-319-38193-0
isbn_ebook978-3-319-10527-7
copyrightSpringer International Publishing Switzerland 2015
The information of publication is updating

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Drug Interaction Potential of Antimalarial Drugs Based on Known Metabolic Properties of Antimalariaalarials include the following: chloroquine, amodiaquine, sulfadoxine and pyrimethamine, mefloquine, primaquine, atovaquone, proguanil, quinine, artemisinin, artesunate, artemether, and dihydroartemisin.
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The Roles of SUMO in Metabolic Regulationb) suggest there were approximately 207 million cases of malaria in 2012 and 627,000 deaths related to the disease. Most deaths occurred among children living in Africa. However, since 2000, deaths due to malaria have decreased by 42 % worldwide and rates of malaria-related deaths among children in Africa have decreased by 54 % (WHO 2014a).
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发表于 2025-3-23 01:29:53 | 显示全部楼层
Introduction,b) suggest there were approximately 207 million cases of malaria in 2012 and 627,000 deaths related to the disease. Most deaths occurred among children living in Africa. However, since 2000, deaths due to malaria have decreased by 42 % worldwide and rates of malaria-related deaths among children in Africa have decreased by 54 % (WHO 2014a).
发表于 2025-3-23 06:49:37 | 显示全部楼层
Pharmacology of Recommended Antimalarial Agents,loroquine, amodiaquine, sulfadoxine, pyrimethamine, mefloquine, quinine/quinidine, artemisinin (the artemisinin agents, artemether, artesunate, and dihydroartemisin, are closely related and summarized as a class, where applicable), lumefantrine, primaquine, atovaquone, and proguanil.
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