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. 2013 Mar;57(3):1192–1200. doi: 10.1128/AAC.02192-12

Table 5.

Adverse events possibly or probably related to daptomycina

Age range (yr), sex Wt (kg) Underlying disease(s)b DAP dosec Adverse event Onset of event/total DAP duration (days) DAP DC Outcome
31–50, M 141 CLCR of 30 to <50, OM, DM, HTN, GI disease (no statin) 6 mg/kg q24h CPK increase 8/13 Yes Resolved
51–65, F 71 CLCR of 30 to <50, HTN, COPD, anemia/hematologic disease, acute renal failure, solid organ cancer (no statin) 6 mg/kg q24h CPK increase 7/11 Yes Resolved
51–65, F 85 CLCR of <30 4 mg/kg q48h Vaginal candidiasis 8/unknownd No Unknown
66–80, M 80 CLCR of <30 ml/min, IE, cardiac arrhythmias, HTN, COPD, renal disease 6 mg/kg q48h Anemia 1/7 No Resolved with residual effects
a

None of the reported adverse events were serious. Abbreviations: CHF, congestive heart failure; COPD, chronic obstructive pulmonary disease; CLCR, creatinine clearance; CPK, creatine phosphokinase; DAP, daptomycin; DC, discontinued; GI, gastrointestinal; CV, cardiovascular; HTN, hypertension; PVD, peripheral vascular disease; IE, infective endocarditis; OM, osteomyelitis; DM, diabetes mellitus; M, male; F, female.

b

Start-of-treatment and end-of-treatment CLCR groups did not change for the 4 patients during daptomycin therapy.

c

Initial and final daptomycin doses did not change for the 4 patients.

d

The patient was monitored for 19 days after the onset of the adverse event; nothing about the vaginal candidiasis outcome was documented.