A Single Dose Study To Investigate The Pharmacokinetics and Safety Of Dalbavancin In Hospitalized Children Aged 3 Months to 11 Years.

* Hospitalized patients who will be receiving at least 24 hours of appropriate non-investigational intravenous anti-infective treatment for known or suspected bacterial infections with the exception of urinary tract infections. * Written parental informed consent. * Able to comply with the protocol for the duration of the study. * Expected to survive throughout the study. * Normal audiologic assessment within 3 days prior to the study drug infusion.

* Investigational drug within 30 days or 5 half-lives, whichever is longest, preceding the first dose of study medication. * History of fluctuant hearing, persistent tinnitus, balance disorder, otologic surgery or disease, tumor of the head, neck, or auditory system, head injury, Meniere's disease, autoimmune inner ear disease, perilymphatic fistula, CNS disorder resulting in hearing deficits, or significant noise exposure. * Significant exposure to aminoglycoside antibiotics or chemotherapy currently or within a week prior to enrollment into the study or current use of loop diuretics. * Patients continuing on vancomycin treatment or are anticipated to begin vancomycin or other glycopeptide treatment during the 7 day period after dalbavancin administration. * Patients with any clinically significant abnormality other than that associated with their underlying disease. Aminotransferases (AST, ALT) \>5 x ULN; total bilirubin and alkaline phosphatase) \>2 x ULN. * Albumin \< half lower limit of normal or physical exam evidence of malnutrition. * Patients who are less than one year of age, and were born with gestational age of less than 32 weeks. * Positive urine (or serum) pregnancy test at screening (post menarchal females only) or after admission (prior to dosing). * Known to have hypersensitivity to glycopeptides. * Calculated creatinine clearance \<30 ml/min using the Schwartz method. * Pregnant or nursing females. * Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.