Ceftaroline fosamil
Cephalosporin · Antibiotic
Mechanism
Ceftaroline fosamil, a cephalosporin antibiotic, exhibits pharmacology similar to penicillins, acting as a beta-lactam to inhibit bacterial cell wall synthesis. It specifically targets penicillin-binding proteins (PBPs), which are enzymes crucial for the transpeptidation step in peptidoglycan cross-linking. This interference compromises the structural integrity of the bacterial cell wall, leading to osmotic instability and subsequent cell lysis.
Indications
Dosing
- Adult
- 600 mg IV Q8-12 hr
- Pediatric
- Infant <2 months (ABSSSI indication only): 6 mg/kg/dose IV Q8 hr; 2 months to <2 years: 8 mg/kg/dose IV Q8 hr; 2 years to <18 years and ≤33 kg: 12 mg/kg/dose IV Q8 hr; 2 years to <18 years and >33 kg: 400 mg IV Q8 hr or 600 mg IV Q12 hr; Child ≥6 years and adolescent (Cystic fibrosis): 15 mg/kg/dose IV Q8 hr infused over 2 hr
- Renal adjustment
- 100% of normal dose if creatinine clearance >30 mL/min. 50% of normal dose if creatinine clearance approximately 10 mL/min.
- Max dose
- 600 mg/dose (pediatric cystic fibrosis)
Contraindications
- Immediate hypersensitivity to penicillin
Side effects
- Hypersensitivity
- Direct Coombs test seroconversion
Pregnancy & lactation
B
Drug interactions
12 additional unreviewed or low-confidence interactions hidden because their provenance or source detail is insufficient.
Related guidelines
Other Cephalosporin drugs
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Textbook-sourced·Sources: Katzung, BNF, Harriet Lane·Updated: 2026-05-10