Cefradine
General
- Type: 1st generation Cephalosporin
- Dosage Forms: Capsules, Oral Suspension, Powder for injection
- Dosage Strengths: 250mg, 500mg; 125mg/5ml, 250mg/5ml; 500mg, 1g vials
- Routes of Administration: PO, IV, IM
- Common Trade Names: Velosef, Nicef
Adult Dosing
General
- Mild: 250-500mg PO q6h or 500mg-1g PO q12h
- Mod-Severe: 500mg-1g IM/IV q6h
- Max: 8g/day (IV), 4g/day (PO)
UTI, Uncomplicated
- 500mg PO q12h
Respiratory Tract Infections
- 250mg PO q6h or 500mg PO q12h
Skin and Soft Tissue
- 250mg PO q6h or 500mg PO q12h
Surgical Prophylaxis
- 1-2g IM/IV x1 (30-90 min before procedure)
- May repeat q4-6h for up to 24h
Pediatric Dosing
General (>9 Months)
- 25-50mg/kg/day PO/IM/IV divided q6h or q12h
- Severe: 75-100mg/kg/day PO/IM/IV divided q6h
- Max: 4g/day
Special Populations
- Pregnancy: B
- Lactation: Excreted in breast milk; use with caution
- Renal
- Adult
- CrCl >20: dose unchanged
- CrCl 5-20: 250-500mg q6h (PO) or 50% of dose (IV)
- CrCl <5: 250-500mg q12h (PO) or 25% of dose (IV)
- Hemodialysis: Give dose after dialysis (250mg start, then 250mg q12h)
- Peritoneal dialysis: Resistant to dialysis
- Pediatric
- Renal dosing adjustment required; specific guidelines vary, generally increase interval
- Adult
- Hepatic
- Not defined
Contraindications
- Allergy to class/drug (Cephalosporins)
- Immediate hypersensitivity to Penicillins
Adverse Reactions
Serious
- Anaphylaxis
- Stevens-Johnson Syndrome
- Neutropenia
- Thrombocytopenia
- Clostridium difficile
- Nephrotoxicity (rare)
- Seizures (in renal impairment)
Common
- Diarrhea
- Nausea and Vomiting
- Rash
- Abdominal Pain
- Urticaria
- Pruritus
- Transient rise in BUN/Creatinine
Pharmacology
- Half-life: 0.7 - 1.3h (Extended in renal failure)
- Metabolism: Not significantly metabolized
- Excretion: Urine (>90% 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
