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The clinical positioning of telavancin in Europe
Telavancin was the first marketed lipoglycopeptide. Although licensed in Europe in 2011 for the treatment of nosocomial pneumonia caused by meticillin-resistant Staphylococcus aureus (MRSA), it did not become clinically available until March 2014.
Antoni Torres +2 more
exaly +2 more sources
Telavancin: A novel lipoglycopeptide antimicrobial agent
Purpose. The pharmacology, activity, pharmacokinetics, pharmacodynamics, clinical efficacy, safety, dosage, and place in therapy of telavancin are reviewed. Summary.
exaly +2 more sources
Staphylococcus aureus bacteremia (SAB) is one of the most common serious bacterial infections and the most frequent invasive infection due to methicillin-resistant S. aureus (MRSA).
Matteo Bassetti +2 more
exaly +2 more sources
The pharmacodynamics of telavancin and vancomycin were compared using neutropenic murine thigh and lung infection models. Four Staphylococcus aureus strains were included.
Alexander J Lepak +2 more
exaly +2 more sources
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Telavancin: mechanisms of action, in vitro activity, and mechanisms of resistance.
Clinical Infectious Diseases, 2015James A. Karlowsky, Kim Nichol
exaly
Dalbavancin and telavancin: novel lipoglycopeptides for the treatment of Gram-positive infections
Expert Review of Anti-Infective Therapy, 2008James A. Karlowsky +1 more
exaly
Outpatient treatment of osteomyelitis with telavancin
International Journal of Antimicrobial Agents, 2017Claudia P Schroeder, Lucinda Van Anglen
exaly

