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Titlebook: Drug Interactions in Infectious Diseases; Stephen C. Piscitelli (Director),Keith A. Rodvold Book 20052nd edition Humana Press 2005 HIV.HI

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發(fā)表于 2025-3-21 16:12:43 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Drug Interactions in Infectious Diseases
編輯Stephen C. Piscitelli (Director),Keith A. Rodvold
視頻videohttp://file.papertrans.cn/284/283094/283094.mp4
概述Includes supplementary material:
叢書名稱Infectious Disease
圖書封面Titlebook: Drug Interactions in Infectious Diseases;  Stephen C. Piscitelli (Director),Keith A. Rodvold  Book 20052nd edition Humana Press 2005 HIV.HI
描述Over the past 25 years, the world’s population has witnessed an explosion in kno- edge about infectious diseases. The global population is coming to the realization that diseases long recognized to cause substantial suffering, such as malaria, tuberculosis, schistosomiasis, and hepatitis, can be diagnosed and treated, and that transmission can be prevented using tools that are available, and which may be becoming increasingly affordable. The global population is recognizing that few infections are local: the travel of humans, other animals, insects, and food transport pathogens around the world, often with astonishing rapidity. New pathogens are appearing, either newly recognized or newly developing, such as severe acute respiratory syndrome (SARS), avian inf- enza, metapneumovirus, or hepatitis C, which are causing human morbidity and m- tality. Finally, there is growing fear that dangerous pathogens may be intentionally introduced into human populations by deranged individuals or terrorist organizations. The potential to use drugs or biologic agents to treat and prevent infectious diseases has increased dramatically over the past quarter century as we have learned more about the
出版日期Book 20052nd edition
關(guān)鍵詞HIV; HIV infection; Malaria; antibiotics; infection; infections; infectious; infectious disease; infectious
版次2
doihttps://doi.org/10.1385/1592599249
copyrightHumana Press 2005
The information of publication is updating

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發(fā)表于 2025-3-21 22:17:09 | 只看該作者
Antifungal Agents,ics when tailoring therapy to treat a specific systemic fungal infection. Systemically acting antifungal agents can cause drug—drug interactions by a variety of mechanisms. Therefore, they have the potential to interact with a vast array of medicines. Given the patient populations in whom systemic m
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發(fā)表于 2025-3-22 03:12:45 | 只看該作者
Drug-Cytokine Interactions,availability or responsiveness (.). A report put a novel twist on the drug-cytokine interaction definition. Brooks et al. (.) reported that the β-lactam antibiotic benzylpenicillin conjugated with interferon-γ and reduced the cytokine’s immune responses.
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發(fā)表于 2025-3-22 07:36:43 | 只看該作者
Circumventing Drug Interactions,kinetic or pharmacodynamic interactions, resulting in decreased therapeutic efficacy, increased incidence of drug toxicities, or potential for increased antimicrobial resistance. Thus, the ability to prevent or minimize adverse drug interactions is of vital importance in optimizing the appropriate a
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Virtual Trade and Comparative Advantageics when tailoring therapy to treat a specific systemic fungal infection. Systemically acting antifungal agents can cause drug—drug interactions by a variety of mechanisms. Therefore, they have the potential to interact with a vast array of medicines. Given the patient populations in whom systemic m
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發(fā)表于 2025-3-22 17:33:23 | 只看該作者
Distance, Production, and Virtual Tradeavailability or responsiveness (.). A report put a novel twist on the drug-cytokine interaction definition. Brooks et al. (.) reported that the β-lactam antibiotic benzylpenicillin conjugated with interferon-γ and reduced the cytokine’s immune responses.
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發(fā)表于 2025-3-23 02:20:43 | 只看該作者
Book 20052nd editionrous pathogens may be intentionally introduced into human populations by deranged individuals or terrorist organizations. The potential to use drugs or biologic agents to treat and prevent infectious diseases has increased dramatically over the past quarter century as we have learned more about the
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