Xydalba
- Is potent and bactericidal
- Covers the most common Gram-positive pathogens in ABSSSI
- Is simple to use with two streamlined dosing regimens
- Plasma concentrations stay far above the susceptibility breakpoint for both dose regimens for at least 14 days
- Offers rapid resolution of fever and spread of erythema
- Has a low incidence of adverse events and low potential for drug/drug interactions
- Xydalba SmPC
- Vena A, et al. EP0175, Early clinical experience with dalbavancin in a tertiary hospital of Madrid, Spain. 27th European Congress on Clinical Microbiology and Infectious Diseases (ECCMID 2017), 22-25 April 2017, Vienna, Austria
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- FDA Briefing Presentation. Anti-infective Drugs Advisory Committee Meeting. March 31, 2014. NDA 21-883
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- Cubicin SPC 05/05/2015
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