Table 2.
Criteria | Korczowski et al. [13] | Blumer et al. [16] |
---|---|---|
Total number of patients included, n | 159 | 5 |
Patients with MRSA, n (%) | 18 (11%) | 1 |
Patients who received antibiotics prior to ceftaroline | 9 | 1 |
Duration of treatment with ceftaroline, median (range) | 3 days to 10 days | - |
Clinical success of MRSA patients, n (%) | 16/18 (89%) | 1 |
Safety outcome | 8% diarrhea 8% rash 7% vomiting 1% pruritis Serious adverse effects reported: 1 patient experienced hypersensitivity and another clostridium difficile colitis No death reported |
Anemia, pruritus and vomiting |