Amphotericin B was the treatment of choice for patients withsystemic fungal disease from the time of its introduction inthe late 1950s until recently1. However, since the introductionof ketoconazole in 1981, fluconazole in 1990, and itraconazolein 1992, these antifungal azoles, which unlike amphotericinB can be given orally, have been increasingly used as therapyfor the systemic mycoses. Despite the lack of direct comparisonsof the efficacy of these drugs and amphotericin B in many fungaldiseases, physicians have been influenced by the efficacy, safety,and ease of administration of the azoles. For many of the . . . [Full Text of this Article]
Chemistry
Mechanism of Action
Pharmacology
Spectrum of Activity and Resistance
Adverse Effects
Drug Interactions
Clinical Indications
Candidiasis
Cryptococcosis
Endemic Mycoses (Blastomycosis, Coccidioidomycosis, and Histoplasmosis)
Aspergillosis
Antifungal Prophylaxis in Patients with Neutropenia
Summary
Source Information
From the Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham School of Medicine (W.E.D.), and the Department of Pharmacy, University Hospital, University of Alabama at Birmingham (J.A.C.), Birmingham.
Address reprint requests to Dr. Dismukes at the University of Alabama at Birmingham, Division of Infectious Diseases, THT 229, Birmingham, AL 35294-0006.
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