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Antimicrobial Agents and Chemotherapy, November 2008, p. 4172-4174, Vol. 52, No. 11
0066-4804/08/$08.00+0 doi:10.1128/AAC.00805-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Nadine Albermann,2,
Walter E. Haefeli,1* and
Friedrich Ebinger3
Department of Internal Medicine VI, Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Im Neuenheimer Feld 410, D-69120 Heidelberg, Germany,1 Department of Pediatrics, Neonatology, Im Neuenheimer Feld 153, D-69120 Heidelberg, Germany,2 Department of Pediatrics, Pediatric Neurology, Im Neuenheimer Feld 153, D-69120 Heidelberg, Germany3
Received 19 June 2008/ Returned for modification 31 July 2008/ Accepted 7 September 2008
For an adolescent with bacterial meningitis and subsequent cerebral aspergillosis, intravenous voriconazole dose requirements substantially decreased during coadministration with intravenous chloramphenicol and considerably rose after discontinuation of the antibiotic. In agreement with in vitro evidence, these data suggest that chloramphenicol is a rather significant inhibitor of hepatic CYP3A4 and/or CYP2C19.
Published ahead of print on 15 September 2008.
Both authors contributed equally to this work.
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