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Telavancin is a lipoglycopeptide antibacterial agent that is a synthetic derivative of vancomycin. This antibiotic inhibits bacterial wall synthesis and disrupts the bacterial membrane barrier function. Telavancin was approved on September 2009, for the treatment of complicated skin and skin–structure infections (cSSSIs) caused by susceptible isolates of the gram–positive microorganisms Staphylococcus aureus (methicillin–susceptible and methicillin–resistant isolates), Streptococcus pyogenes, Streptococcus agalactiae, the Streptococcus anginosus group,

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