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Review Article
Drug Therapy
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Volume 330:263-272 January 27, 1994 Number 4
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Oral Azole Drugs as Systemic Antifungal Therapy
Jackson A. Como, and William E. Dismukes

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Amphotericin B was the treatment of choice for patients with systemic fungal disease from the time of its introduction in the late 1950s until recently1. However, since the introduction of ketoconazole in 1981, fluconazole in 1990, and itraconazole in 1992, these antifungal azoles, which unlike amphotericin B can be given orally, have been increasingly used as therapy for the systemic mycoses. Despite the lack of direct comparisons of the efficacy of these drugs and amphotericin B in many fungal diseases, 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.

References


Related Letters:

Oral Azole Drugs as Systemic Antifungal Therapy
Schutze G. E., Etzel J. V., Como J. A., Dismukes W. E.
Extract | Full Text  
N Engl J Med 1994; 330:1759-1760, Jun 16, 1994. Correspondence

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