What is the recommended pediatric dose of cefdinir (Omnicef) for treating ear infections in children?

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Pediatric Dosage of Cefdinir for Treating Ear Infections

For treating acute otitis media (ear infections) in children, the recommended dosage of cefdinir (Omnicef) is 14 mg/kg/day given once daily or 7 mg/kg twice daily for 5 to 10 days, with a maximum daily dose of 600 mg. 1

Dosing Guidelines

  • The FDA-approved dosage for acute bacterial otitis media in pediatric patients (6 months through 12 years) is:

    • 7 mg/kg every 12 hours for 5 to 10 days, OR
    • 14 mg/kg once daily for 10 days 1
  • Once-daily dosing for 10 days has been shown to be as effective as twice-daily dosing for ear infections 1, 2

  • The maximum daily dose should not exceed 600 mg, regardless of weight 1

Weight-Based Dosing Chart

For the 125 mg/5 mL suspension:

  • 9 kg (20 lbs): 2.5 mL every 12 hours or 5 mL once daily 1
  • 18 kg (40 lbs): 5 mL every 12 hours or 10 mL once daily 1
  • 27 kg (60 lbs): 7.5 mL every 12 hours or 15 mL once daily 1
  • 36 kg (80 lbs): 10 mL every 12 hours or 20 mL once daily 1
  • ≥43 kg (95 lbs): 12 mL every 12 hours or 24 mL once daily 1

For the 250 mg/5 mL suspension:

  • 18 kg (40 lbs): 2.5 mL every 12 hours or 5 mL once daily 1
  • 27 kg (60 lbs): 3.75 mL every 12 hours or 7.5 mL once daily 1
  • 36 kg (80 lbs): 5 mL every 12 hours or 10 mL once daily 1
  • ≥43 kg (95 lbs): 6 mL every 12 hours or 12 mL once daily 1

Clinical Efficacy and Treatment Duration

  • The American Academy of Pediatrics recommends cefdinir as an alternative treatment for acute otitis media when patients have penicillin allergy 3

  • Clinical studies have shown that a 5-day course of cefdinir at 14 mg/kg/day is as effective as a 10-day course of cefprozil for treating acute otitis media in children 4

  • However, comparative studies have shown that high-dose amoxicillin/clavulanic acid for 10 days has a better cure rate (86.5%) than cefdinir for 5 days (71.0%) in children with acute otitis media 5

Special Considerations

  • For children with renal insufficiency (creatinine clearance <30 mL/min/1.73 m²), the dose should be reduced to 7 mg/kg (up to 300 mg) given once daily 1

  • Cefdinir is stable against commonly occurring plasmid-mediated beta-lactamases and retains good activity against beta-lactamase-producing strains of H. influenzae and M. catarrhalis, which are common causes of otitis media 6

  • For children with recurrent or persistent otitis media at high risk of treatment failure, some studies have investigated higher doses of cefdinir (25 mg/kg once daily for 10 days), though this is not an FDA-approved dosing regimen 7

  • Cefdinir can be administered without regard to meals, which improves compliance in pediatric patients 1

  • The suspension should be shaken well before each administration and can be used for 10 days after mixing, after which any unused portion must be discarded 1

Potential Pitfalls and Caveats

  • Diarrhea is the most common adverse event reported with cefdinir treatment in pediatric patients 6

  • The efficacy of cefdinir decreases against penicillin-nonsusceptible S. pneumoniae strains, with eradication rates of 91% for penicillin-susceptible strains but only 43% for penicillin-resistant strains 7

  • In areas with high prevalence of penicillin-resistant S. pneumoniae, cefdinir may not be the optimal first-line choice for treating otitis media 5, 7

  • For children on hemodialysis, the dose should be adjusted to 7 mg/kg every other day, with an additional dose after each hemodialysis session 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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