[Clinical studies on S 6472 granule preparation (sustained-release cefaclor) in chronic respiratory tract infections]

Jpn J Antibiot. 1988 Sep;41(9):1309-12.
[Article in Japanese]

Abstract

S 6472 granule preparation (sustained-release cefaclor) was orally administered to 15 patients with chronic respiratory tract infections (2 acutely exacerbated cases of chronic bronchitis, 13 cases of secondary infections consisting of 1 case of bronchial asthma, 2 cases of bronchial asthma/pulmonary emphysema, and 10 cases of bronchiectasis) at a daily dose of 750 mg divided into 2 doses administered after breakfast and dinner, for a duration of 14 days. The drug was ineffective in 3 of the 10 cases of bronchiectasis but was effective in the other 12 cases, with a rate of efficacy of 80%. There were no side effects of abnormal laboratory findings due to administration of this drug.

Publication types

  • English Abstract

MeSH terms

  • Administration, Oral
  • Aged
  • Aged, 80 and over
  • Cefaclor / administration & dosage
  • Cefaclor / therapeutic use*
  • Cephalexin / analogs & derivatives*
  • Chronic Disease
  • Delayed-Action Preparations
  • Drug Evaluation
  • Female
  • Humans
  • Male
  • Middle Aged
  • Respiratory Tract Infections / drug therapy*

Substances

  • Delayed-Action Preparations
  • Cefaclor
  • Cephalexin