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Í klínískum iii. stigs rannsóknum sem tóku til 1680 sjúklinga (751 með spítalalungnabólgu og 929 með cssti), sem fengu 10 mg/kg af telavancíni á sólarhring, var greint frá aukaverkunum hjá 47,3% sjúklinga.
in phase 3 clinical trials involving 1680 patients (751 and 929, np and cssti, respectively) who received telavancin at a daily dose of 10 mg/kg, adverse reactions were reported in 47.3% of patients.