Pharmacokinetics of a single dose of rimantadine in young adults and children

Antimicrob Agents Chemother. 1987 Jul;31(7):1140-2. doi: 10.1128/AAC.31.7.1140.

Abstract

Single doses of rimantadine were given to children and young adults to evaluate the safety and pharmacokinetics of this antiviral compound. The half-life of rimantadine in young adults was 27.7 +/- 4.9 h for tablets and 27.8 +/- 8.0 h for syrup preparations. A total of 10 children, 5 to 8 years old, received a syrup preparation of rimantadine. The half-life of rimantadine in children was 24.8 +/- 9.4 h. A single dose of rimantadine was well tolerated in young adults and children.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adamantane / analogs & derivatives*
  • Administration, Oral
  • Adult
  • Child
  • Child, Preschool
  • Half-Life
  • Humans
  • Kinetics
  • Male
  • Random Allocation
  • Rimantadine / administration & dosage
  • Rimantadine / metabolism*
  • Solutions
  • Tablets

Substances

  • Solutions
  • Tablets
  • Rimantadine
  • Adamantane