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Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus

Daptomycin is a lipoglycopeptide antibacterial drug that is rapidly bactericidal for methicillin-resistant Staphylococcus aureus (MRSA) infection and has antibiotic activity against a wide range of Gram-positive organisms. It has been approved by the Ministry of Health, Labor and Welfare in Japan fo...

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Detalles Bibliográficos
Autores principales: Hagihara, Mao, Umemura, Takumi, Mori, Takeshi, Mikamo, Hiroshige
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284219/
https://www.ncbi.nlm.nih.gov/pubmed/22368449
http://dx.doi.org/10.2147/TCRM.S23875
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author Hagihara, Mao
Umemura, Takumi
Mori, Takeshi
Mikamo, Hiroshige
author_facet Hagihara, Mao
Umemura, Takumi
Mori, Takeshi
Mikamo, Hiroshige
author_sort Hagihara, Mao
collection PubMed
description Daptomycin is a lipoglycopeptide antibacterial drug that is rapidly bactericidal for methicillin-resistant Staphylococcus aureus (MRSA) infection and has antibiotic activity against a wide range of Gram-positive organisms. It has been approved by the Ministry of Health, Labor and Welfare in Japan for the treatment for bacteremia, right-sided endocarditis, and skin and skin-structure infections, such as necrotizing fasciitis, due to MRSA on the basis of a Phase III trial conducted in Japan since July, 2011. In Japanese Phase I and III trials, daptomycin therapy given at 4 mg/kg and 6 mg/kg once per day was well tolerated and effective as standard therapy for the treatment of acute bacterial skin and skin-structure infections and bacteremia caused by MRSA, but side effects remain to be evaluated in large-scale trials.
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spelling pubmed-32842192012-02-24 Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus Hagihara, Mao Umemura, Takumi Mori, Takeshi Mikamo, Hiroshige Ther Clin Risk Manag Review Daptomycin is a lipoglycopeptide antibacterial drug that is rapidly bactericidal for methicillin-resistant Staphylococcus aureus (MRSA) infection and has antibiotic activity against a wide range of Gram-positive organisms. It has been approved by the Ministry of Health, Labor and Welfare in Japan for the treatment for bacteremia, right-sided endocarditis, and skin and skin-structure infections, such as necrotizing fasciitis, due to MRSA on the basis of a Phase III trial conducted in Japan since July, 2011. In Japanese Phase I and III trials, daptomycin therapy given at 4 mg/kg and 6 mg/kg once per day was well tolerated and effective as standard therapy for the treatment of acute bacterial skin and skin-structure infections and bacteremia caused by MRSA, but side effects remain to be evaluated in large-scale trials. Dove Medical Press 2012 2012-02-17 /pmc/articles/PMC3284219/ /pubmed/22368449 http://dx.doi.org/10.2147/TCRM.S23875 Text en © 2012 Hagihara et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Hagihara, Mao
Umemura, Takumi
Mori, Takeshi
Mikamo, Hiroshige
Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus
title Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus
title_full Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus
title_fullStr Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus
title_full_unstemmed Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus
title_short Daptomycin approved in Japan for the treatment of methicillin-resistant Staphylococcus aureus
title_sort daptomycin approved in japan for the treatment of methicillin-resistant staphylococcus aureus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284219/
https://www.ncbi.nlm.nih.gov/pubmed/22368449
http://dx.doi.org/10.2147/TCRM.S23875
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