Propoxyphene and norpropoxyphene: influence of diet and fluid on plasma levels

Clin Pharmacol Ther. 1976 May;19(5 Pt 1):559-65. doi: 10.1002/cpt1976195part1559.

Abstract

The influence of various test meals and ingested fluid volumes on the bioavailability and pharmacokinetics of propoxyphene and its major metabolite norporpoxyphene has been studied in healthy human subjects. The absorption of drug was delayed by all test meals, but the overall efficiency of absorption was either not affected or was slightly increased. Increased fluid volume intake decreased propoxyphene bioavailability. Plasma levels of metabolite correlated well with levels of unchanged drug, particularly in the first 2 hr after dosing, but were not markedly influenced by treatments.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Biological Availability
  • Dextropropoxyphene / analogs & derivatives
  • Dextropropoxyphene / blood*
  • Diet
  • Female
  • Half-Life
  • Humans
  • Intestinal Absorption
  • Kinetics
  • Male
  • Time Factors

Substances

  • Dextropropoxyphene