Cefaloridine
General
- Type: 1st generation Cephalosporin
- Dosage Forms: powder for injection
- Dosage Strengths: 250mg, 500mg, 1g
- Routes of Administration: IV, IM
- Common Trade Names: Ceporin, Loridine
Adult Dosing
General
- Mild-Moderate: 250-500mg IM/IV q6h
- Severe: 1g IM/IV q6h
- Max: 4g/day (Strict limit due to nephrotoxicity risk)
UTI, Uncomplicated
- 500mg IM/IV q6h
Endocarditis Prophylaxis
- 1g IM/IV x1 (30-60 min before procedure)
Pediatric Dosing
General
- 30-50 mg/kg/day IM/IV divided q6-8h
- Max: 4g/day
Special Populations
- Pregnancy: B
- Lactation: Excreted in breast milk; use caution
- Renal
- Adult
- CrCl 30-50: Max 3g/day
- CrCl 10-29: Max 2g/day
- CrCl <10: Max 1g/day
- Note: Highly nephrotoxic; avoid in pre-existing renal impairment if possible.
- Pediatric
- Not well defined; avoid use.
- Adult
- Hepatic
- No adjustment usually required
Contraindications
- Allergy to class/drug
- Pre-existing significant renal impairment (Relative)
Adverse Reactions
Serious
- Nephrotoxicity (Dose-dependent proximal tubular necrosis)
- Anaphylaxis
- Neutropenia
- Leukopenia
- Seizures (accumulation in renal failure)
- Clostridium difficile
Common
- Rash
- Urticaria
- Nausea and Vomiting
- Injection site pain/phlebitis
- Pruritus
- Eosinophilia
Pharmacology
- Half-life: 1.1-1.5h
- Metabolism: Not significantly metabolized
- Excretion: Urine (glomerular filtration)
- 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
