Variable furosemide absorption and poor predictability of response in elderly patients

Michael D. Murray, Kathy M. Haag, Paula K. Black, Stephen D. Hall, D. Craig Brater

Research output: Contribution to journalArticle

85 Scopus citations


Study Objectives. To determine the between and within-patient variability of furosemide bioavailability and natriuretic response, and whether four marketed products differ in bioavailability and response. Design. Open-label, crossover study. Setting. General clinical research center at an academic medical center. Patients. Convenience sample of 17 patients age 65 ± 6 years receiving diuretics for the treatment of hypertension or congestive heart failure. Intervention. Each patient received each of five furosemide products (one intravenous and four oral tablet formulations) twice in random order for a total of 10 treatments. Measurements and Main Results. Measurements included absolute bioavailability using cumulative amounts of urinary furosemide collected over 8 hours after oral versus intravenous dosing, and cumulative amounts of urinary sodium. Extensive between- and within-patient variability in all measured values rendered any differences among the products neither clinically nor statistically significant. Mean (± SD) bioavailability was 49 ± 17% (range 12-112%) and coefficients of variation with different products were from 25- 43%. Coefficients of variation for urinary furosemide excretion and urinary sodium excretion were also large, 25-42% and 23-51%, respectively. Multivariate analyses that incorporated between- and within-patient effects tailed to reveal differences among the products for bioavailability (F=1.04, p=0.403), urinary furosemide excretion (F=l.09, p=0.371), or urinary sodium excretion (F=0.97, p=0.448). Correlation coefficients were 0.81-0.85 for the rates of sodium and furosemide excretion, and half-maximum response using a sigmoid E(max) model did not differ among products. Conclusion. Although furosemide concentration in urinary and natriuretic responses showed good correlation, variability in bioavailability considerably affects the drug's excretion into urine. Variability in absorption both among patients and within an individual patient is great anti overwhelms any differences in bioavailability amonng approved furosemide products. Switching from one formulation to another will not likely result in any predictable change in patient response.

Original languageEnglish (US)
Pages (from-to)98-106
Number of pages9
Issue number1
StatePublished - Jan 1997
Externally publishedYes

ASJC Scopus subject areas

  • Pharmacology (medical)

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    Murray, M. D., Haag, K. M., Black, P. K., Hall, S. D., & Brater, D. C. (1997). Variable furosemide absorption and poor predictability of response in elderly patients. Pharmacotherapy, 17(1), 98-106.