Pharmacokinetics of famotidine, a new H2-receptor antagonist, in relation to renal function

Eur J Clin Pharmacol. 1985;28(3):327-31. doi: 10.1007/BF00543332.


The pharmacokinetics of a new, potent H2-receptor antagonist, famotidine, 20 mg i.v. was studied in 7 subjects with normal renal function and in 24 patients with varying degrees of renal impairment. The volume of distribution at steady state was 1.141/kg in normal subjects and was not altered in renal failure. The half-life of elimination was 2.59 h in normal subjects and was unchanged in mild renal failure (creatinine clearance, CLCR 90-60 ml/min/1.48 m2) but was increased to 4.72 h in moderate renal failure (CLCR 60-30 ml/min/1.48 m2), and to 12.07 h in severe renal failure (CLCR below 30 ml/min/1.48 m2). The cumulative urinary excretion and renal clearance of famotidine were correspondingly reduced in patients with impaired kidney function. In normal subjects and in patients with mild to moderate renal failure, about 70% of famotidine was excreted through the kidney, mainly by tubular secretion. In patients with a CLCR above 60 ml/min/1.48 m2 the normal daily dose of famotidine can be employed, but in those with a CLCR between 60 and 30 ml/min/1.48 m2 the dose should be reduced by half, and in patients with a CLCR below 30 ml/min/1.48 m2 a reduction by three quarters of the normal dose is recommended.

MeSH terms

  • Adult
  • Aged
  • Famotidine
  • Female
  • Histamine H2 Antagonists / metabolism*
  • Humans
  • Kidney / metabolism
  • Kidney Diseases / metabolism*
  • Kinetics
  • Male
  • Metabolic Clearance Rate
  • Middle Aged
  • Thiazoles / metabolism*


  • Histamine H2 Antagonists
  • Thiazoles
  • Famotidine