Tolerability of 3-day, once-daily azithromycin suspension versus standard treatments for community-acquired paediatric infectious diseases

Int J Antimicrob Agents. 2001 Nov;18(5):427-31. doi: 10.1016/s0924-8579(01)00439-3.

Abstract

Tolerability of azithromycin oral suspension, 10 mg/kg once daily for 3 days, was assessed in paediatric patients (< or = 18 years) with respiratory or skin and soft-tissue infections. Of 2425 patients evaluated, 1213 received azithromycin and 1212 received standard regimens of amoxycillin/clavulanic acid, cefaclor, cefixime, ceftriaxone, clarithromycin, erythromycin, or penicillin V. The incidence of treatment-related adverse events was significantly lower in patients receiving azithromycin than comparators (7.9 vs. 11.5%, P=0.003), while discontinuation rates were similar (1.0 and 1.1%, respectively). Significantly fewer gastrointestinal events were recorded for azithromycin than comparators (6.5 vs. 9.9%, P=0.002), and their duration was significantly shorter (mean 2.3 vs. 5.0 days, P=0.0001). Azithromycin paediatric oral suspension is well tolerated and associated with significantly fewer adverse events than comparators.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Anti-Bacterial Agents / administration & dosage*
  • Anti-Bacterial Agents / adverse effects*
  • Azithromycin / administration & dosage*
  • Azithromycin / adverse effects*
  • Bacterial Infections / drug therapy*
  • Child
  • Child, Preschool
  • Community-Acquired Infections / drug therapy*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Multicenter Studies as Topic
  • Randomized Controlled Trials as Topic
  • Respiratory Tract Infections / drug therapy
  • Skin Diseases, Infectious / drug therapy
  • Soft Tissue Infections / drug therapy

Substances

  • Anti-Bacterial Agents
  • Azithromycin