Telavancin: A Novel Lipoglycopeptide

Telavancin, a derivative of vancomycin, is a lipoglycopeptide antibiotic that has been shown to be effective for the treatment of complicated skin and skin-structure infections. It has also been effective in the treatment of gram-positive pneumonia. This antibiotic has a dual mechanism of action by...

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Published inClinical infectious diseases Vol. 49; no. 12; pp. 1908 - 1914
Main Authors Saravolatz, Louis D., Stein, Gary E., Johnson, Leonard B.
Format Journal Article
LanguageEnglish
Published Oxford The University of Chicago Press 15.12.2009
University of Chicago Press
Oxford University Press
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ISSN1058-4838
1537-6591
1537-6591
DOI10.1086/648438

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Summary:Telavancin, a derivative of vancomycin, is a lipoglycopeptide antibiotic that has been shown to be effective for the treatment of complicated skin and skin-structure infections. It has also been effective in the treatment of gram-positive pneumonia. This antibiotic has a dual mechanism of action by inhibiting peptidoglycan synthesis and causing membrane depolarization. Telavancin is consistently active against Staphylococcus aureus , including methicillin-resistant S. aureus , vancomycin-intermediate S. aureus , linezolid-resistant S. aureus , and daptomycin-nonsusceptible strains. The drug is usually administrated intravenously at 10 mg/kg every 24 h. Telavancin is excreted by the kidneys, and thus, dosage adjustments are required in cases of renal failure. Clinical trials have demonstrated non-inferiority, compared with vancomycin, in the treatment of complicated skin and skin-structure infections and pneumonia. Telavancin is associated with higher rates of renal events, altered taste, nausea, and vomiting but lesser rates of pruritus and infusion-related events, compared with vancomycin.
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ISSN:1058-4838
1537-6591
1537-6591
DOI:10.1086/648438