Ceforanide
General
- Type: 2nd generation Cephalosporin
- Dosage Forms: powder for injection
- Dosage Strengths: 500mg; 1g, 10g
- Routes of Administration: IV, IM
- Common Trade Names: Precef
Adult Dosing
General
- 0.5-1g IM/IV q12h
- Max: 4g/day
UTI, Uncomplicated
- 0.5-1g IM/IV q12h
Community Acquired Pneumonia
- 0.5-1g IM/IV q12h
Surgical Prophylaxis
- 0.5-1g IM/IV 1 hour prior to surgery
- Intraoperative: May repeat during lengthy procedures (>2hr)
- Postoperative: 0.5-1g IM/IV q12h for 24h
Pediatric Dosing
General (>1 Year)
- 20-40mg/kg/day IM/IV divided q12h
- Max: 4g/day
Special Populations
- Pregnancy: B
- Lactation: Excreted in breast milk; use caution
- Renal
- Adult
- CrCl >60: Standard dosing (q12h)
- CrCl 20-60: Give standard dose q24h
- CrCl <20: Give standard dose q48h
- Hemodialysis: Give supplement after dialysis
- Adult
- Hepatic
- No adjustment defined
Contraindications
- Allergy to class/drug (Cephalosporins)
- Caution in Penicillin allergy (cross-reactivity)
Adverse Reactions
Serious
- Anaphylaxis
- Stevens-Johnson Syndrome
- Clostridium difficile
- Hemolytic Anemia
- Neutropenia
- Thrombocytopenia
Common
- Injection site pain (IM) or phlebitis (IV)
- Diarrhea
- Rash
- Nausea and Vomiting
- Transient transaminitis
- Eosinophilia
Pharmacology
- Half-life: 2.9 - 3.0h
- Metabolism: Not metabolized
- Excretion: Urine (unchanged)
- Mechanism of Action: Bactericidal; inhibits cell wall mucopeptide synthesis
Antibiotic Sensitivities[1]
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
See Also
References
- ↑ Sanford Guide to Antimicrobial Therapy
