Titlebook: Drug Interactions in Infectious Diseases: Antimicrobial Drug Interactions; Manjunath P. Pai,Jennifer J. Kiser,Keith A. Rodvol Book 2018Lat

Scleroderma

Drug Interactions of Non-HIV Antiviral Agents,higher risk for severe viral infections such as those caused by cytomegalovirus (CMV), adenovirus, and disseminated herpes simplex virus (HSV). Infection with hepatitis C virus (HCV) is common, and many new antiviral regimens have come into use for management of infected patients. Influenza continue

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Drug-Drug Interactions of Antimalarial Drugs,of Africa, Asia, and the Americas. Combination chemotherapy is recommended for treatment of acute uncomplicated malaria as a result of widespread drug resistance. Tuberculosis (Tb) is also widespread and combination therapy is its standard of care. Treatment of malaria in an individual on antituberc

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Antiprotozoal and Anthelmintic Agents,therapy with the wish to minimize emergence of drug resistance. Throughout the past few decades, the clinical pharmacokinetics and metabolism of many antiparasitic agents have been elucidated, particularly the role of drug-metabolizing enzymes, notably cytochromes P450, and drug transporter proteins

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Drug Interactions in Infectious Diseases: Antimicrobial Drug Interactions

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Drug Interactions in Infectious Diseases: Antimicrobial Drug Interactions978-3-319-72416-4

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Book 2018Latest edition interactions in hepatitis B virus (HBV) and hepatitis C virus (HCV)-relatedinfections is included.  Two new chapters are dedicated to the management of human immunodeficiency virus (HIV) drug-drug interactions given the breadth of antiretroviral class-specific effects. This comprehensive review of

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Beta-Lactam Antibiotics,umentation is needed and/or potential harm to the patient is less. Minor interactions are either poorly documented, present minimal potential harm to the patient, or occur with a low incidence..The drug interactions of most concern with the beta-lactam antibiotics are those with oral contraceptive p

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Quinolones,ee less widely available FQs (antofloxacin, nemonoxacin, and prulifloxacin) act as moderate cytochrome P450 enzyme inhibitors and may increase serum concentrations of theophylline and caffeine. Warfarin pharmacodynamics are variably affected by the FQs. The pharmacodynamic interactions between NSAID