Cefuzonam
General
- Type: 2nd generation Cephalosporin
- Dosage Forms: powder for injection
- Dosage Strengths: 250mg, 500mg, 1g
- Routes of Administration: IV, IM
- Common Trade Names: Cosmosin
Adult Dosing
General
- 1-2g/day IM/IV divided q12h
Severe Infections
- Up to 4g/day IM/IV divided q12h
Pediatric Dosing
General
- 40-80mg/kg/day IM/IV divided q6-8h
- Max: 150mg/kg/day for severe infections (do not exceed 4g/day)
Special Populations
- Pregnancy: Safety not established (Use only if clearly needed)
- Lactation: Excreted in breast milk (Caution advised)
- Renal
- Adult
- CrCl 30-50: 500mg q12h
- CrCl 10-29: 500mg q24h
- CrCl <10: 500mg q48h
- Hemodialysis: Give dose after dialysis
- Pediatric
- Renal impairment: Reduce dose or extend interval
- Adult
- Hepatic
- No specific adjustment defined
Contraindications
- Allergy to class/drug
- Previous shock to Cefuzonam
Adverse Reactions
Serious
- Anaphylaxis / Shock
- Stevens-Johnson Syndrome
- Toxic Epidermal Necrolysis
- Pancytopenia / Agranulocytosis
- Interstitial Pneumonia (PIE syndrome)
- Pseudomembranous colitis (Clostridium difficile)
- Acute Renal Failure
Common
- Diarrhea
- Rash
- Nausea and Vomiting
- Elevated LFTs (AST/ALT)
- Eosinophilia
- Injection site pain/phlebitis
Pharmacology
- Half-life: ~1 hour (extended in renal failure)
- Metabolism: Not significantly metabolized
- Excretion: Urine (largely unchanged)
- Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis
Antibiotic Sensitivities
Key
- S susceptible/sensitive (usually)
- I intermediate (variably susceptible/resistant)
- R resistant (or not effective clinically)
- S+ synergistic with cell wall antibiotics
- U sensitive for UTI only (non systemic infection)
- X1 no data
- X2 active in vitro, but not used clinically
- X3 active in vitro, but not clinically effective for Group A strep pharyngitis or infections due to E. faecalis
- X4 active in vitro, but not clinically effective for strep pneumonia
