What is the renal adjusted dose of acyclovir (Antiviral medication) for patients with impaired renal function?

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Last updated: December 14, 2025View editorial policy

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Acyclovir Renal Dose Adjustment

For patients with renal impairment, acyclovir requires dose reduction based on creatinine clearance, with oral dosing adjusted to 200 mg every 12 hours for CrCl <10 mL/min and intravenous dosing reduced to 2.5-5 mg/kg every 24 hours for the same level of renal function, with supplemental dosing required after each hemodialysis session. 1, 2

Oral Acyclovir Dosing Adjustments

Standard Dosing by Indication and Renal Function

  • For CrCl >10 mL/min: Standard dosing applies based on indication (200 mg every 4 hours for genital herpes, 400 mg every 12 hours for suppressive therapy, or 800 mg every 4 hours for herpes zoster) 2

  • For CrCl <10 mL/min: Reduce all oral regimens to 200 mg every 12 hours regardless of indication 1, 2

  • For hemodialysis patients: Administer 200 mg every 12 hours, with the first daily dose given after dialysis 1, 2

Specific Adjustments by Standard Regimen

  • 200 mg every 4 hours regimen: No adjustment needed for CrCl >10 mL/min; reduce to 200 mg every 12 hours for CrCl 0-10 mL/min 2

  • 400 mg every 12 hours regimen: No adjustment needed for CrCl >10 mL/min; reduce to 200 mg every 12 hours for CrCl 0-10 mL/min 2

  • 800 mg every 4 hours regimen: No adjustment for CrCl >25 mL/min; reduce to 800 mg every 8 hours for CrCl 10-25 mL/min; reduce to 800 mg every 12 hours for CrCl 0-10 mL/min 2

Intravenous Acyclovir Dosing Adjustments

Dose Reduction by Creatinine Clearance

  • For CrCl 25-50 mL/min: Reduce to 5-10 mg/kg IV every 12 hours 1

  • For CrCl 10-24 mL/min: Reduce to 5-10 mg/kg IV every 24 hours 1

  • For CrCl <10 mL/min: Reduce to 2.5-5 mg/kg IV every 24 hours 1

Hemodialysis Considerations

  • Timing of administration: Administer the dose post-dialysis on dialysis days, as hemodialysis removes approximately 60% of acyclovir over a 6-hour dialysis period with a dialysis clearance of 81.8 mL/min 1, 3

  • Supplemental dosing: An additional dose is required after each dialysis session 1, 2

  • Terminal half-life during dialysis: Acyclovir half-life decreases from 19.5 hours in anuric patients to 5.7 hours during hemodialysis 3

Critical Administration Guidelines to Prevent Nephrotoxicity

Infusion Rate and Hydration

  • Avoid rapid IV bolus: Administer IV acyclovir as a slow infusion over 1 hour to prevent crystalluria and acute renal failure 1

  • Ensure adequate hydration: Maintain at least 1.5 liters of water intake daily during treatment 1

  • Monitor renal function: The risk of acyclovir-induced nephrotoxicity increases with bolus administration and inadequate hydration 4, 5

Common Pitfalls and Caveats

Neurotoxicity Risk in Renal Failure

  • Increased risk with impaired clearance: Patients with end-stage renal disease have a terminal plasma half-life of 19.5 hours (compared to 2-3 hours in normal renal function), leading to drug accumulation and potential neurotoxicity if doses are not adjusted 3, 6

  • Clinical presentation: Neurotoxicity manifests as reversible neuropsychiatric symptoms and occurs more frequently when standard doses are used in renal impairment 7, 6

  • CSF penetration: While renal impairment does not alter the CSF-to-plasma ratio, the higher systemic concentrations result in proportionally higher CSF concentrations, increasing neurotoxicity risk 7

Peritoneal Dialysis

  • No supplemental dosing required: Unlike hemodialysis, peritoneal dialysis does not require additional dosing after the dosing interval is adjusted 2

  • Recommended regimen for CAPD patients: Use a loading dose of 400 mg followed by maintenance dosing of 200 mg twice daily 6

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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