What is the recommended dose of Meropenem (generic name) for adults with impaired renal function?

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Last updated: August 9, 2025View editorial policy

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Meropenem Dosing in Adults with Impaired Renal Function

For adults with impaired renal function, meropenem dosage should be reduced based on creatinine clearance: 500 mg-1 g every 12 hours for CrCl 26-50 mL/min, half the recommended dose every 12 hours for CrCl 10-25 mL/min, and half the recommended dose every 24 hours for CrCl <10 mL/min. 1

Dosing Algorithm Based on Renal Function

The FDA-approved meropenem dosing adjustments for adults with renal impairment are as follows:

Creatinine Clearance (mL/min) Dose Dosing Interval
>50 mL/min Recommended dose (500 mg for cSSSI and 1 gram for intra-abdominal infections) Every 8 hours
26-50 mL/min Recommended dose Every 12 hours
10-25 mL/min One-half recommended dose Every 12 hours
<10 mL/min One-half recommended dose Every 24 hours

Special Considerations for Specific Infections

For different types of infections, the base dosing (before renal adjustment) varies:

  • Complicated skin and skin structure infections: 500 mg every 8 hours
  • Complicated intra-abdominal infections: 1 gram every 8 hours
  • For infections caused by Pseudomonas aeruginosa: 1 gram every 8 hours 1

When treating severe infections such as meningitis or those caused by resistant organisms:

  • For bacterial meningitis (in the UK guidelines): 2 g IV every 8 hours 2
  • For ESBL-producing organisms: 2 g IV every 8 hours 2

Administration Methods

Meropenem can be administered in several ways:

  • Intravenous infusion over 15-30 minutes (standard)
  • Intravenous bolus injection over 3-5 minutes
  • Extended infusion over 3 hours (recommended for severe infections or high MICs) 3

Patients on Renal Replacement Therapy

For patients on continuous renal replacement therapy (CRRT):

  • Pharmacokinetic studies show that CRRT contributes significantly to meropenem elimination
  • For patients on continuous venovenous hemofiltration (CVVH), the dose should be increased by approximately 100% compared to anuric patients not on CRRT 4
  • Residual diuresis (remaining urine output) is an important factor affecting clearance in patients on CRRT 5

Clinical Pearls and Pitfalls

  1. Calculate creatinine clearance accurately: When only serum creatinine is available, use the Cockcroft-Gault equation:

    • Males: CrCl (mL/min) = Weight (kg) × (140 - age) / (72 × serum creatinine [mg/dL])
    • Females: CrCl (mL/min) = 0.85 × male value 1
  2. Monitoring considerations:

    • Regular monitoring of renal function is essential during therapy
    • For prolonged therapy, monitor for superinfection and emergence of resistance
  3. Safety profile:

    • Meropenem is generally well-tolerated even in patients with renal impairment when properly dosed
    • The most common adverse events include diarrhea, nausea, vomiting, headache, rash, and injection site inflammation 6
    • Unlike imipenem, meropenem has a lower risk of seizures and does not require co-administration with cilastatin 7
  4. Extended infusion consideration:

    • For severe infections or when targeting organisms with higher MICs, consider extended infusion (3 hours) to optimize the time above MIC
    • This approach may be particularly beneficial in critically ill patients 3
  5. Avoid underdosing in CRRT:

    • Patients on CRRT may require higher doses than those with similar degrees of renal impairment not on CRRT 4

By following these evidence-based dosing recommendations, clinicians can optimize meropenem therapy in patients with impaired renal function, balancing efficacy against the risk of toxicity.

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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