Pharmacokinetics of acyclovir suspension in infants and children

Antimicrob Agents Chemother. 1987 Nov;31(11):1722-6. doi: 10.1128/AAC.31.11.1722.

Abstract

Eighteen children from 3 weeks to 6.9 years of age were given an oral acyclovir suspension for herpes simplex or varicella-zoster virus infections. Thirteen patients who were 6 months to 6.9 years old received 600 mg/m2 per dose, and three infants and two children less than 2 years old were given 300 mg/m2 per dose. The drug was given four times a day, except to one infant who was treated with three doses a day. Among the 13 children who received the 600-mg/m2 dose, the maximum concentration in plasma (Cmax) was 0.99 +/- 0.38 microgram/ml (mean +/- standard deviation), the time to maximum concentration (Tmax) was 3.0 +/- 0.86 h, the area under the curve (AUC) was 5.56 +/- 2.17 micrograms.h/ml, and the elimination half-life (t1/2) was 2.59 +/- 0.78 h. The three infants less than 2 months of age who received the 300-mg/m2 dose had a Cmax of 1.88 +/- 1.11 micrograms/ml, a Tmax of 4.10 +/- 0.48 h, an AUC of 6.54 +/- 4.32 micrograms.h/ml, and a t1/2 of 3.26 +/- 0.33 h. The acyclovir suspension was well tolerated by young children. No adverse effects requiring discontinuation of the drug occurred.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyclovir / adverse effects
  • Acyclovir / pharmacokinetics*
  • Acyclovir / therapeutic use
  • Age Factors
  • Child
  • Child, Preschool
  • Herpesviridae Infections / drug therapy
  • Humans
  • Infant
  • Infant, Newborn
  • Suspensions

Substances

  • Suspensions
  • Acyclovir