Acyclovir
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Last updated: June 2025
For educational purposes only
Clinical Reference
# Acyclovir
## Overview
- **Classification**: Antiviral, synthetic purine nucleoside analogue.
- **Mechanism**: Selectively inhibits viral DNA replication by interfering with viral DNA polymerase and terminating viral DNA chain elongation. Requires viral thymidine kinase for activation.
## Primary Indications
1. **Herpes Simplex Virus (HSV)** - Treatment and suppression of genital herpes, mucocutaneous infections (e.g., cold sores).
2. **Varicella-Zoster Virus (VZV)** - Treatment of herpes zoster (shingles) and varicella (chickenpox).
## Adult Dosing
### Standard Oral Dosing
**Genital Herpes (Initial Episode)**
- **Dose**: **200 mg**
- **Frequency**: 5 times/day (q4h while awake)
- **Route**: Oral
- **Duration**: 7-10 days
**Genital Herpes (Recurrent Episode)**
- **Dose**: **200 mg**
- **Frequency**: 5 times/day (q4h while awake)
- **Route**: Oral
- **Duration**: 5 days
- **Alternative**: **400 mg** PO TID for 5 days OR **800 mg** PO BID for 5 days.
**Genital Herpes (Chronic Suppression)**
- **Dose**: **400 mg**
- **Frequency**: BID
- **Route**: Oral
- **Duration**: Up to 12 months, then re-evaluate.
**Herpes Zoster (Shingles)**
- **Dose**: **800 mg**
- **Frequency**: 5 times/day
- **Route**: Oral
- **Duration**: 7-10 days
- **Special Considerations**: Initiate within **72 hours** of rash onset for optimal efficacy.
**Varicella (Chickenpox)**
- **Dose**: **800 mg**
- **Frequency**: QID
- **Route**: Oral
- **Duration**: 5 days
- **Special Considerations**: Initiate within **24 hours** of rash onset for optimal efficacy.
### Dose Adjustments
- **Renal Impairment**: Adjust frequency based on creatinine clearance (CrCl).
- CrCl 25-50 mL/min: Dose q8h for 200 mg, q12h for 400 mg, q8h for 800 mg.
- CrCl 10-25 mL/min: Dose q12h for 200 mg, q24h for 400 mg, q12h for 800 mg.
- CrCl <10 mL/min: Dose q24h for 200 mg, q24h for 400 mg, q24h for 800 mg.
- Hemodialysis: Administer dose after dialysis.
- **Hepatic Impairment**: No specific dose adjustment required.
- **Elderly Patients**: Monitor renal function closely; increased risk of CNS adverse effects.
## Pediatric Dosing (Oral)
### Neonates (0-28 days)
- **Primary Treatment**: IV acyclovir is preferred for active HSV infection.
- **HSV Suppression (after IV treatment)**: **300 mg/m²** PO BID-TID.
- **Duration**: Typically 6-12 months as directed by specialist.
- **Special Notes**: Dosing is highly specialized; consult with infectious disease.
### Infants (1-12 months)
- **Varicella (Chickenpox)**: **20 mg/kg** PO QID.
- **Maximum**: **800 mg** per dose.
- **Duration**: 5 days.
- **Special Notes**: Initiate within **24 hours** of rash onset.
### Children (1-12 years)
- **Varicella (Chickenpox)**: **20 mg/kg** PO QID.
- **Maximum**: **800 mg** per dose.
- **Duration**: 5 days.
- **Special Notes**: Initiate within **24 hours** of rash onset.
- **Oral HSV (Mucocutaneous)**: **20 mg/kg** PO TID-QID.
- **Maximum**: **400 mg** per dose (TID-QID) or **1000 mg** daily.
- **Duration**: 5-10 days.
### Adolescents (13-18 years)
- **Dose**: Generally follows **adult oral dosing** for specific indications.
- **Maximum**: Refer to adult maximum doses for each indication.
- **Special Notes**: Adjust for renal function if impaired.
## Safety Information
### Contraindications
- **Absolute**: Hypersensitivity to acyclovir or valacyclovir.
### Common Adverse Effects
- **Common (1-10%)**: Nausea, vomiting, diarrhea, headache, malaise.
- **Serious but Rare**:
- Acute renal failure (with rapid IV infusion, dehydration, or concurrent nephrotoxins).
- Neurotoxicity (confusion, hallucinations, seizures, tremors, coma), especially in elderly or renally impaired.
- Thrombotic Thrombocytopenic Purpura/Hemolytic Uremic Syndrome (TTP/HUS) in immunocompromised.
### Key Drug Interactions
- **Nephrotoxic drugs (e.g., NSAIDs, aminoglycosides, cyclosporine)**: Increased risk of renal dysfunction. Monitor renal function closely.
- **Probenecid, Cimetidine**: Increase acyclovir AUC and half-life. May require acyclovir dose reduction.
- **Mycophenolate Mofetil**: Acyclovir can increase mycophenolate levels. Monitor for mycophenolate toxicity.
## Monitoring & Follow-up
- **Before Treatment**: Assess baseline renal function (CrCl).
- **During Treatment**:
- Monitor renal function periodically, especially in patients with renal impairment, elderly, or on nephrotoxic drugs.
- Monitor hydration status (crucial with IV acyclovir).
- Observe for signs of CNS toxicity (confusion, lethargy, seizures).
- **Clinical Signs**: Assess for reduction in lesion count, pain, and progression of viral symptoms.
## Clinical Pearls
- 💡 **Early Initiation**: Acyclovir is most effective when initiated as early as possible after symptom onset (within 24h for varicella, 72h for zoster).
- 💡 **Hydration**: Advise patients to maintain adequate hydration, especially when taking high doses, to minimize the risk of renal effects.
- 💡 **Not a Cure**: Acyclovir helps manage symptoms and reduce the frequency/severity of herpes outbreaks but does not cure the infection.
- 💡 **Formulations**: Available as oral tablets, capsules, and suspension; IV formulation for severe infections.
> **⚠️ Important**: This information is for educational purposes only. Always consult current prescribing information, local guidelines, and clinical judgment before prescribing.