What is the recommended dosage of Cefepime (Intravenous Cefepime) for infections?

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Last updated: September 25, 2025View editorial policy

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Cefepime Dosage Recommendations for Infections

The recommended dosage of intravenous cefepime for adults with normal renal function is 2 g every 8-12 hours for most serious infections, while pediatric patients should receive 50 mg/kg every 12 hours (every 8 hours for febrile neutropenia). 1

Adult Dosing

Standard Dosing by Infection Type

  • Moderate to Severe Pneumonia: 1-2 g every 8-12 hours for 10 days 1
  • Empiric therapy for febrile neutropenic patients: 2 g every 8 hours for 7 days or until resolution of neutropenia 1
  • Mild to Moderate UTIs: 0.5-1 g every 12 hours for 7-10 days 1
  • Severe UTIs: 2 g every 12 hours for 10 days 1
  • Moderate to Severe Skin/Skin Structure Infections: 2 g every 12 hours for 10 days 1
  • Complicated Intra-abdominal Infections: 2 g every 8-12 hours for 7-10 days (used with metronidazole) 1

Important Considerations for Adult Dosing

  • For Pseudomonas aeruginosa infections, use the higher dose of 2 g every 8 hours 1
  • Higher doses may be needed in critically ill patients with preserved renal function due to increased clearance and volume of distribution 2
  • Prolonged or continuous infusions may be beneficial for infections caused by bacteria with high MICs 2

Pediatric Dosing

Standard Pediatric Dosing

  • Children (2 months to 16 years): 50 mg/kg every 12 hours 1, 3
  • For febrile neutropenia: 50 mg/kg every 8 hours 1
  • Maximum individual dose: 2 g 3

Special Pediatric Populations

  • Infants >14 days of age and children ≤40 kg: 50 mg/kg every 12 hours 2
  • Neonates ≤14 days of age: 30 mg/kg every 12 hours 2

Dosage Adjustments for Renal Impairment

Cefepime requires dose adjustment in patients with renal impairment:

  • Significant linear relationship exists between total body clearance and creatinine clearance 4
  • Dosage should be reduced in proportion to the decline in creatinine clearance 4
  • For patients on continuous renal replacement therapy (CRRT), higher doses may be needed than typically recommended in clinical resources 5

Pharmacokinetic Considerations

  • Elimination half-life is approximately 2 hours in patients with normal renal function 6, 3
  • Volume of distribution at steady state in healthy adults is about 20.5 liters 4
  • In pediatric patients, elimination half-life averages 1.7 hours 3
  • Bioavailability after intramuscular administration averages 82% 3

Clinical Pearls and Pitfalls

Potential Pitfalls

  • Underdosing in critically ill patients: Standard doses may be insufficient in critically ill patients with preserved renal function due to increased clearance and volume of distribution 2
  • Neurotoxicity risk: When cefepime concentrations exceed eight times the MIC, there is risk of neurological deterioration, particularly in ICU patients 2
  • Inadequate dosing for resistant organisms: For infections caused by bacteria with high MICs, standard dosing may not achieve adequate drug concentrations 2

Monitoring Recommendations

  • Consider therapeutic drug monitoring in critically ill patients to ensure optimal dosing 2
  • Monitor renal function regularly to adjust dosing as needed 4
  • For patients receiving aminoglycosides with cefepime, individualized daily administration according to lean body mass and estimated extracellular fluid volume is preferred 2

By following these evidence-based dosing recommendations and considering patient-specific factors like renal function and severity of infection, clinicians can optimize cefepime therapy to improve outcomes while minimizing adverse effects.

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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