What is the recommended renal dose of meropenem for a patient with impaired renal function?

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Last updated: January 7, 2026View editorial policy

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Meropenem Renal Dosing

For adults with impaired renal function, reduce both the dose and/or extend the dosing interval of meropenem based on creatinine clearance: maintain the full recommended dose (500 mg or 1 gram depending on infection type) but extend to every 12 hours for CrCl 26-50 mL/min, reduce to half the recommended dose every 12 hours for CrCl 10-25 mL/min, and reduce to half the recommended dose every 24 hours for CrCl <10 mL/min. 1

Standard Renal Dosing Algorithm for Adults

The FDA-approved dosing adjustments are structured as follows 1:

  • CrCl >50 mL/min: Full dose (500 mg for cSSSI, 1 gram for intra-abdominal infections) every 8 hours 1
  • CrCl 26-50 mL/min: Full recommended dose every 12 hours 1
  • CrCl 10-25 mL/min: Half the recommended dose every 12 hours 1
  • CrCl <10 mL/min: Half the recommended dose every 24 hours 1

Critical distinction: The FDA recommends maintaining the full individual dose and extending the interval for moderate impairment (CrCl 26-50 mL/min), rather than reducing the dose itself. 1 This preserves the concentration-dependent bactericidal activity of meropenem. 2

Special Considerations for Pseudomonas aeruginosa

When treating infections caused by P. aeruginosa, use 1 gram every 8 hours in patients with normal renal function, then apply the same renal adjustment algorithm to this higher base dose. 1 For example, a patient with CrCl 26-50 mL/min treating Pseudomonas would receive 1 gram every 12 hours. 2

Hemodialysis Dosing

For patients on intermittent hemodialysis, administer meropenem after each dialysis session, as approximately 50% of the drug is removed during a dialysis session. 2, 3, 4 The recommended approach is to give half the recommended dose every 24 hours, with dosing timed immediately post-dialysis. 4 Administering before dialysis leads to premature drug removal and subtherapeutic levels. 2

The elimination half-life during hemodialysis shortens from approximately 7.0 hours (off dialysis) to 2.9 hours (during dialysis). 4

Continuous Renal Replacement Therapy (CRRT)

For patients on CRRT, use 1 gram every 8-12 hours to compensate for continuous drug removal. 2 CRRT removes 25-50% of meropenem, while CVVHDF removes 13-53%, creating substantial variability. 2, 3 The wide range reflects differences in:

  • CRRT modality (CVVHF vs CVVHDF) 3
  • Effluent flow rates 2
  • Residual renal function 2

Therapeutic drug monitoring is strongly recommended for all patients on CRRT to ensure adequate exposure and prevent toxicity. 2

Sustained Low-Efficiency Dialysis (SLED)

For SLED patients, maintain the full 1 gram dose every 12 hours. 2 The rationale is to preserve concentration-dependent killing while accounting for the prolonged elimination half-life (2.5-8.7 hours) in this setting. 2 Do not reduce the individual dose below 1 gram, as smaller doses may compromise efficacy. 2

Pediatric Renal Dosing

There is no established pediatric renal dosing for meropenem. 1 The FDA label explicitly states "there is no experience in pediatric patients with renal impairment." 1 For pediatric patients 3 months and older with normal renal function, standard dosing is 10 mg/kg (cSSSI), 20 mg/kg (intra-abdominal), or 40 mg/kg (meningitis) every 8 hours. 5, 1

Resistant Organisms and Extended Infusions

When treating organisms with MIC ≥4-8 mg/L, use extended 3-hour infusions even in renal impairment to optimize time above MIC. 2 For carbapenem-resistant Enterobacterales with meropenem MIC ≥8 mg/L, specifically use 1 gram over 3 hours every 8 hours (adjusted for renal function per the standard algorithm). 2

Extended infusions maximize the percentage of time that free drug concentrations remain above the MIC, which is the critical pharmacodynamic parameter for beta-lactams. 2

Common Pitfalls to Avoid

  • Do not use meropenem with probenecid, as probenecid inhibits renal excretion and is not recommended. 1
  • Monitor for neurological toxicity in renal impairment, particularly when trough concentrations exceed 64 mg/L. 2 However, meropenem has lower pro-convulsive activity than imipenem, making it safer in renal dysfunction. 2
  • Reassess renal function regularly (every 2-3 days in unstable patients) to adjust dosing appropriately. 2
  • Avoid underdosing in CRRT patients due to variable drug removal—when in doubt, use therapeutic drug monitoring. 2, 3

Evidence Quality Considerations

The FDA label provides the highest quality dosing guidance for standard renal impairment. 1 Research confirms that recommended dose reductions for meropenem result in drug exposure 158-286% higher than patients with normal renal function receiving regular doses, indicating the adjustments are appropriate and prevent toxicity. 6 Meropenem is the only renally cleared antibiotic with good-quality evidence supporting its dose reduction recommendations. 6

References

Guideline

Meropenem Dosing in Adults with Impaired Renal Function

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Does dose reduction of renally cleared antibiotics in patients with impaired renal function lead to adequate drug exposure? A systematic review.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2021

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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