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GENERAL PEDIATRICS DRUG INFORMATION
Acyclovir
Antiviral
Herpes simplex encephalitis IV: 3 months - 12 years: 10 - 15 mg/kg (maximum: 1 g/dose) Q8H 13 years or older: 10 mg/kg (maximum: 1 g/dose) Q8H
Neonatal HSV IV: Treatment: 20 mg/kg Q8H for at least 14 days for skin/ocular/mouth disease (mucous membrane involvement) and a minimum of 21 days for CNS disease.
PO: Suppressive therapy following Neonatal HSV: 300 mg/m2 TID for 6 months Suppressive therapy should be offered to infants with CNS disease. Data is less convincing for skins, eyes and mucous membrane or disseminated disease, but can be offered.
Varicella (severe) or in immunocompromised IV: 10 mg/kg (maximum: 1 g/dose) Q8H Therapy not always indicated in immunocompetent host.
PO: 20 mg/kg (maximum: 800 mg/dose) QID Therapy not always indicated in immunocompetent host.
Mucotaneous HSV infection (Mild to moderate) PO: 10 - 20 mg/kg (usual maximum: 200 mg/dose) QID Treat for 5-7 days.
Mucotaneous HSV infection (Severe e.g. eczema herpeticum or immunocompromised hosts) IV: 5 - 10 mg/kg Q8H
PO: Following IV therapy: 15 - 20 mg/kg (usual maximum: 400 mg/dose) QID
HSV Prophylaxis in selected hematology-oncology patients PO: 20 mg/kg BID Alternative dosing: 15 mg/kg TID
Chronic suppressive therapy for recurrent mucocutaneous or genital HSV episodes PO: 15 mg/kg (usual maximum: 400 mg/dose) TID
Base dose on ideal body weight. Ensure adequate hydration and urine output (especially on high dose IV therapy). Monitor renal function and extend dosing interval to q12h or q24h in renal impairment
Availability: Tablets: 200, 400 mg.
See valACYclovir if liquid required as acyclovir suspension requires compounding, has poor oral bioavalability, and needs for frequent dosing.
Pharmacology: Antiviral agent effective against herpes simplex 1 and herpes simplex 2, and varicella. Synthetic nucleoside analogue that inhibits viral DNA synthesis. Largely excreted unchanged by kidney therefore needs dose adjustments in renal failure
Updated: 06/01/2026
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