Previous Article | Next Article ![]()
Antimicrobial Agents and Chemotherapy, July 2009, p. 3122-3125, Vol. 53, No. 7
0066-4804/09/$08.00+0 doi:10.1128/AAC.00361-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Division of Infectious Diseases, Los Angeles Biomedical Research Institute at Harbor-University of California at Los Angeles (UCLA) Medical Center, Torrance, California,1 the David Geffen School of Medicine at UCLA, Los Angeles, California,2 Departments of Medicine and Medical Microbiology and Immunology, University of Wisconsin School of Medicine, Madison, Wisconsin,3 Division of Infectious Diseases, University of Southern California (USC) School of Medicine Department of Medicine, Los Angeles, California,4 Long Beach Public Department of Health, Long Beach, California,5 Summa Health System, Akron, Ohio,6 Division of Infectious Diseases, Olive View-UCLA Medical Center, Sylmar, California,7 Immunocompromised Host Section, Pediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland8
Received 16 March 2009/ Returned for modification 21 April 2009/ Accepted 4 May 2009
We sought to describe the safety profile of open-label, adjunctive deferasirox iron chelation therapy in eight patients with biopsy-proven mucormycosis. Deferasirox was administered for an average of 14 days (range, 7 to 21) at 5 to 20 mg/kg of body weight/day. The only adverse effects attributable to deferasirox were rashes in two patients. Deferasirox treatment was not associated with changes in renal or liver function, complete blood count, or transplant immunosuppressive levels. Thus, deferasirox appears safe as an adjunctive therapy for mucormycosis.
Published ahead of print on 11 May 2009.
Copyright © 2010 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»