Brivudine: a herpes virostatic with rapid antiviral activity and once-daily dosing

Drugs Today (Barc). 2003 May;39(5):359-71. doi: 10.1358/dot.2003.39.5.740221.

Abstract

Brivudine is an analog of thymidine, and is incorporated into the viral DNA. It blocks the action of DNA polymerases, thus inhibiting viral replication. It has a stronger antiviral effect against the varicella-zoster virus compared with reference compounds such as aciclovir or penciclovir. The efficacy of brivudine has been documented in a number of clinical trials in patients with herpesvirus-related infections, particularly in patients with herpes-zoster. At a dose of 125 mg once daily, brivudine has proved to be superior to aciclovir with respect to reducing the period of new blister production in patients with herpes-zoster, and has shortened the duration of post-herpetic neuralgia. Tolerability was equivalent to that of aciclovir or placebo, with occasional gastrointestinal disorders leading to treatment withdrawal in a minority of patients.

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / adverse effects
  • Antiviral Agents / pharmacokinetics
  • Antiviral Agents / pharmacology*
  • Antiviral Agents / therapeutic use
  • Antiviral Agents / toxicity
  • Bromodeoxyuridine / administration & dosage
  • Bromodeoxyuridine / adverse effects
  • Bromodeoxyuridine / analogs & derivatives*
  • Bromodeoxyuridine / pharmacokinetics
  • Bromodeoxyuridine / pharmacology*
  • Bromodeoxyuridine / therapeutic use
  • Bromodeoxyuridine / toxicity
  • Herpesviridae Infections / drug therapy*
  • Herpesviridae Infections / virology
  • Humans

Substances

  • Antiviral Agents
  • brivudine
  • Bromodeoxyuridine