What is the dosage of Meropenem for bacterial infections?

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Meropenem Dosage for Bacterial Infections

For bacterial infections, meropenem is typically dosed at 1 gram IV every 8 hours for most serious infections, with adjustments based on infection type, severity, and patient factors. 1

Standard Adult Dosing

  • For complicated skin and skin structure infections: 500 mg IV every 8 hours (increase to 1 gram every 8 hours if treating Pseudomonas aeruginosa) 1
  • For complicated intra-abdominal infections: 1 gram IV every 8 hours 1, 2
  • Administration should be via intravenous infusion over 15-30 minutes, or as an intravenous bolus injection over 3-5 minutes 1

Special Populations and Conditions

Renal Impairment (Adults)

  • Creatinine clearance >50 mL/min: Standard recommended dose 1
  • Creatinine clearance 26-50 mL/min: Standard dose every 12 hours 1
  • Creatinine clearance 10-25 mL/min: Half the recommended dose every 12 hours 1
  • Creatinine clearance <10 mL/min: Half the recommended dose every 24 hours 1

Pediatric Dosing

  • Children ≥3 months: 1

    • Complicated skin/skin structure infections: 10 mg/kg every 8 hours (max 500 mg/dose)
    • Complicated intra-abdominal infections: 20 mg/kg every 8 hours (max 1 gram/dose)
    • Meningitis: 40 mg/kg every 8 hours (max 2 grams/dose)
  • Children <3 months with intra-abdominal infections: 1

    • Dosing based on gestational age and postnatal age, ranging from 20-30 mg/kg every 8-12 hours

Special Clinical Scenarios

Carbapenem-Resistant Infections

  • For carbapenem-resistant Enterobacteriaceae (CRE): 1 gram IV every 8 hours by extended infusion (3 hours) in combination therapy 3, 2
  • Extended infusion (3 hours) is recommended when meropenem MIC ≥8 mg/L 3, 2
  • For patients with CRAB (carbapenem-resistant Acinetobacter baumannii) infections with meropenem MIC <8 mg/L, consider carbapenem combination therapy with high-dose extended-infusion 4

Treatment Duration

  • For complicated intra-abdominal infections: Typically 5-7 days, individualized based on infection site, source control, and clinical response 2

Clinical Pearls

  • Meropenem has excellent activity against most clinically significant aerobic and anaerobic pathogens 5
  • For critically ill patients with healthcare-associated infections, consider prolonged or continuous infusions to optimize pharmacodynamic targets 2
  • Meropenem is stable to human dehydropeptidase-I (DHP-I) and does not require co-administration with cilastatin (unlike imipenem) 6
  • Common adverse events include diarrhea (2.3%), rash (1.4%), nausea/vomiting (1.4%), and injection site inflammation (1.1%) 7
  • Meropenem has a favorable safety profile with low seizure risk compared to imipenem 7, 6

Combination Therapy Considerations

  • For severe CRAB infections, combination therapy with two in vitro active antibiotics is suggested 4
  • Polymyxin-meropenem combination therapy is not recommended for CRAB infections 4
  • For necrotizing skin and soft tissue infections, meropenem (1 gram every 8 hours IV) can be used as part of broad empiric coverage 4

References

Guideline

Carbapenem-Resistant Enterobacteriaceae Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Meropenem for Complicated Bacterial Infections

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Meropenem: a microbiological overview.

The Journal of antimicrobial chemotherapy, 1995

Research

Meropenem: evaluation of a new generation carbapenem.

International journal of antimicrobial agents, 1997

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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