Reduction in fever and symptoms in young adults with influenza A/Brazil/78 H1N1 infection after treatment with aspirin or amantadine

Antimicrob Agents Chemother. 1983 Apr;23(4):577-82. doi: 10.1128/AAC.23.4.577.

Abstract

During an outbreak of influenza A/Brazil/78 H1N1 infection, 47 volunteers with clinical and virological influenza of less than 2 days duration were treated in a randomized double-blind fashion for 5 days with 100 or 200 mg of amantadine daily or with 3.25 g of aspirin daily. The aspirin treatment group defervesced more rapidly (10.3 h versus 21.5 h and 23.6 h; P less than 0.01), but by the second daily follow-up visit, both groups of amantadine recipients exhibited greater symptomatic improvement. Bothersome side effects resulted in discontinuation of therapy by 35% of the aspirin treatment group but only 3% of the amantadine treatment group (P less than 0.05). Individuals who present to a physician during an influenza A epidemic with characteristic symptoms will experience symptomatic benefit from amantadine treatment, with negligible toxicity.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Amantadine / adverse effects
  • Amantadine / therapeutic use*
  • Aspirin / adverse effects
  • Aspirin / therapeutic use*
  • Female
  • Fever / drug therapy*
  • Humans
  • Influenza A Virus, H1N1 Subtype
  • Influenza A virus / isolation & purification
  • Influenza, Human / drug therapy*
  • Male

Substances

  • Amantadine
  • Aspirin