What is the recommended dose of Meropenem (generic name) for intravenous administration?

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Meropenem Intravenous Dosing

The standard dose of meropenem for adults is 1 gram IV every 8 hours for most serious infections, administered as an infusion over 15-30 minutes, with higher doses (2 grams every 8 hours) reserved for meningitis, severe pneumonia, or infections with resistant organisms. 1

Standard Adult Dosing by Infection Type

Complicated Intra-Abdominal Infections

  • 1 gram IV every 8 hours is the recommended dose for complicated intra-abdominal infections 1, 2
  • Treatment duration is typically 5-7 days based on source control adequacy and clinical response 2, 3
  • This provides excellent anaerobic coverage without requiring additional agents 4

Skin and Soft Tissue Infections

  • 500 mg IV every 8 hours for uncomplicated skin and skin structure infections 1
  • 1 gram IV every 8 hours when treating infections caused by P. aeruginosa 1
  • For necrotizing infections requiring broad-spectrum coverage, use 1 gram IV every 8 hours as part of combination therapy 2

Pneumonia and Respiratory Infections

  • 2 grams IV every 8 hours for hospital-acquired or ventilator-associated pneumonia 2
  • Extended infusion over 3 hours is recommended for critically ill patients 2, 4
  • Treatment duration is at least 7 days 2

Central Nervous System Infections

  • 2 grams IV every 8 hours for meningitis caused by Enterobacteriaceae or suspected ESBL organisms 5
  • Treatment duration varies by pathogen: 10 days for H. influenzae, 21 days for Enterobacteriaceae or Listeria 2

Administration Methods

Standard Infusion

  • Administer over 15-30 minutes for most infections 1
  • Doses of 1 gram may also be given as an IV bolus over 3-5 minutes 1

Extended Infusion (Critical for Optimization)

  • Administer over 3 hours when treating carbapenem-resistant Enterobacteriaceae (CRE) 2, 4
  • Use 3-hour infusion when the pathogen MIC is ≥8 mg/L 2, 4
  • Extended infusion is preferred for critically ill patients with healthcare-associated infections 2, 4
  • This maximizes the time above MIC, which is the key pharmacodynamic parameter for beta-lactam efficacy 2

Dosing for Resistant Organisms

Carbapenem-Resistant Enterobacteriaceae (CRE)

  • 1 gram IV every 8 hours by 3-hour extended infusion as part of combination therapy 2
  • For high MIC organisms (≥16 mg/L), increase to 2 grams IV every 8 hours by 3-hour infusion 2
  • Combination therapy is mandatory for CRE infections 2

Carbapenem-Resistant Acinetobacter baumannii (CRAB)

  • 2 grams IV every 8 hours in combination with colistin for CRAB with meropenem MIC ≤8 mg/L 2
  • Extended infusion over 3 hours is recommended 2

Renal Dose Adjustments

Dosage reduction is required when creatinine clearance falls below 50 mL/min: 1

  • CrCl 26-50 mL/min: Give recommended dose every 12 hours 1
  • CrCl 10-25 mL/min: Give half the recommended dose every 12 hours 1
  • CrCl <10 mL/min: Give half the recommended dose every 24 hours 1

Continuous Renal Replacement Therapy (CRRT)

  • 1 gram IV every 8 hours is appropriate for most patients on CRRT 6, 7
  • Residual diuresis significantly impacts clearance: patients with preserved urine output may require higher doses or extended infusions 7
  • CRRT intensity (dialysate flow rate) does not significantly modify clearance 7

Pediatric Dosing

Children ≥3 Months and ≤50 kg

  • 10 mg/kg every 8 hours (maximum 500 mg) for skin/soft tissue infections 1
  • 20 mg/kg every 8 hours (maximum 1 gram) for intra-abdominal infections 1
  • 40 mg/kg every 8 hours (maximum 2 grams) for meningitis 1
  • Administer as infusion over 15-30 minutes 1

Children >50 kg

  • Use adult dosing: 500 mg every 8 hours for skin infections, 1 gram every 8 hours for intra-abdominal infections, 2 grams every 8 hours for meningitis 1

Infants <3 Months

  • Dosing is based on gestational age (GA) and postnatal age (PNA) 1
  • Infants <32 weeks GA and PNA <2 weeks: 20 mg/kg every 12 hours 1
  • Infants <32 weeks GA and PNA ≥2 weeks: 20 mg/kg every 8 hours 1
  • Infants ≥32 weeks GA and PNA <2 weeks: 20 mg/kg every 8 hours 1
  • Infants ≥32 weeks GA and PNA ≥2 weeks: 30 mg/kg every 8 hours 1

Critical Pitfalls and Caveats

Coverage Gaps

  • Meropenem does NOT cover MRSA or VRE 2, 4
  • Add vancomycin or linezolid if MRSA coverage is needed empirically 4
  • Do not use meropenem alone for suspected polymicrobial infections involving these organisms 4

Loading Dose

  • No loading dose is required for meropenem, unlike colistin or tigecycline 2, 4
  • Standard dosing achieves therapeutic levels rapidly 2

Stability Concerns

  • Extended 3-hour infusions are stable and recommended 2, 4
  • True 24-hour continuous infusions may have stability issues and are not routinely recommended 4

Antimicrobial Stewardship

  • Avoid empiric use based solely on HCAP criteria; only use when locally validated risk factors for resistant organisms exist 4
  • De-escalate to narrower-spectrum agents when susceptibilities allow 2
  • For perioperative prophylaxis in patients colonized with ESBL organisms, ertapenem is preferred over meropenem due to single-dose administration 3

Therapeutic Drug Monitoring

  • Consider TDM in critically ill patients, those with altered pharmacokinetics, or when treating organisms with elevated MICs 8
  • Target trough concentrations depend on infection severity and pathogen MIC 8

References

Guideline

Meropenem for Complicated Bacterial Infections

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Meropenem and Azithromycin Dosage and Duration Recommendations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Meropenem Empiric Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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