Rey E, Luquel L, Richard M O, Mory B, Offenstadt G, Olive G
Département de pharmacologie clinique, Hôpital Saint-Vincent de Paul, Université René Descartes, Paris, France.
Eur J Clin Pharmacol. 1989;37(4):387-9. doi: 10.1007/BF00558505.
Salbutamol was administered intravenously to 5 patients with renal function impairment for estimation its pharmacokinetic parameters. The mean terminal half-life was 256 min, similar to previously reported values in healthy adults. The mean clearance (167 ml/min) and the mean volume of distribution (551) were decreased. These parameters were not correlated with the creatinine clearance. A slight but significant decrease was observed in the plasma potassium level up to 125 min after the salbutamol infusion. The heart rate was significantly increased, and the increase in 3 patients was correlated with the salbutamol concentration. The biological effects of the drug were less marked than expected.