What is the recommended dose of Augmentin (amoxicillin/clavulanate) for a patient with End-Stage Renal Disease (ESRD) on hemodialysis?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: February 4, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Augmentin Dosing in ESRD on Hemodialysis

For patients with end-stage renal disease on hemodialysis, administer Augmentin (amoxicillin/clavulanate) at a reduced dose of 250-500 mg every 24 hours, with supplemental dosing immediately after each dialysis session.

Pharmacokinetic Rationale

The dosing adjustment is necessary because both amoxicillin and clavulanic acid are significantly removed during hemodialysis:

  • Amoxicillin has a dialysis clearance of 77.1 mL/min, with 64% of the drug removed during a 4-hour hemodialysis session, and a prolonged half-life of 13.6 hours on non-dialysis days (compared to 1-1.5 hours in normal renal function) 1

  • Clavulanic acid has a dialysis clearance of 92.8 mL/min, with 65% removed during dialysis, and a half-life of 3.05 hours on non-dialysis days 1

  • Both components demonstrate reduced non-renal clearance in ESRD patients, suggesting some degree of hepatic impairment that further necessitates dose reduction 1

Specific Dosing Recommendations

Standard Dosing Schedule

  • Non-dialysis days: 250-500 mg orally every 24 hours 1, 2

  • Dialysis days: Administer the regular dose plus a supplemental dose (250-500 mg) immediately after the dialysis session 3, 1

Timing Considerations

  • Post-dialysis administration prevents premature drug removal by the dialysis machine and facilitates directly observed therapy 3

  • Administering before dialysis wastes drug and reduces therapeutic efficacy 4

Dosage Adjustment Principles

The general rule for antibiotics in renal impairment is to reduce the dose by approximately 30% for each level of renal impairment 2. For ESRD specifically:

  • The dose reduction accounts for the dramatically prolonged elimination half-life (nearly 10-fold increase for amoxicillin) 1

  • Hemodialysis efficiently clears both components due to their low molecular weight, reduced protein binding, and small volume of distribution 2

Clinical Monitoring

  • Renal function monitoring is essential, though in ESRD patients this primarily involves tracking dialysis adequacy 5

  • Watch for signs of drug accumulation, particularly on non-dialysis days when clearance is minimal 1

  • The drug is generally well-tolerated even in patients with chronic renal insufficiency, though careful monitoring remains important 6

Common Pitfalls to Avoid

  • Do not use standard dosing (875 mg twice daily or 500 mg three times daily) as this will lead to excessive drug accumulation and potential toxicity 1, 5

  • Do not administer before dialysis as this results in immediate drug removal and therapeutic failure 3, 4

  • Do not assume peritoneal dialysis requires the same approach—peritoneal dialysis removes substantially less drug than hemodialysis, and dosing for pre-dialysis ESRD patients may be more appropriate 7

References

Research

[Antibiotic use in patients with renal or hepatic failure].

Enfermedades infecciosas y microbiologia clinica, 2009

Guideline

Dosing Recommendations for IV Cefazolin and Azithromycin in ESRD on Hemodialysis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Meropenem Dosing Considerations in End-Stage Renal Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Pharmacokinetics and dosage adjustment in patients with renal dysfunction.

European journal of clinical pharmacology, 2009

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.