Tulobuterol: one-month intravenous safety studies in rats and dogs

Drug Chem Toxicol. 1984;7(3):283-98. doi: 10.3109/01480548409035109.

Abstract

Tulobuterol was given intravenously to rats and dogs at dosages of 1, 5, or 25 mg/kg/day and 0.6, 2, or 6 mg/kg/day, respectively. The no-toxic-effect dosages were 5 mg/kg/day in rats and 6 mg/kg/day in dogs. Two rats died at 25 mg/kg/day. Convulsions, jerking movements, hyperactivity, tremors, hypoactivity and ptyalism were observed in rats given 25 mg/kg/day. Restlessness, ptyalism and hypoactivity were also observed in dogs at 2 and 6 mg/kg/day. Cutaneous and/or mucosal erythema were observed in rats and dogs at all dosages. Increased body weight gain occurred in drug-treated rats and in mid- and high-dose female dogs. Slight elevations in serum creatinine and BUN were seen in rats and dogs at the highest dosages. Heart weights were increased in rats at all dosages after 1 month of treatment and in rats given 25 mg/kg/day after 2 weeks of recovery. There were no treatment-related morphologic changes in either species.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Blood Urea Nitrogen
  • Body Weight / drug effects
  • Bronchodilator Agents / administration & dosage
  • Bronchodilator Agents / toxicity*
  • Creatinine / blood
  • Dogs
  • Eating / drug effects
  • Female
  • Hydrogen-Ion Concentration
  • Infusions, Parenteral
  • Male
  • Organ Size / drug effects
  • Rats
  • Rats, Inbred Strains
  • Salivation / drug effects
  • Species Specificity
  • Specific Gravity
  • Terbutaline / administration & dosage
  • Terbutaline / analogs & derivatives*
  • Terbutaline / toxicity
  • Terbutaline / urine
  • Time Factors

Substances

  • Bronchodilator Agents
  • tulobuterol
  • Creatinine
  • Terbutaline