Abstract
1 Twelve healthy volunteers received a single oral dose of tenoxicam 20 mg on six occasions separated by 3 weeks. 2 The six occasions were: fasted overnight; postprandial; fasting and 15 ml aluminium hydroxide gel; postprandial and 15 ml aluminium hydroxide gel; fasting and 15 ml aluminium and magnesium hydroxide gel; postprandial and 15 ml aluminium and magnesium hydroxide gel. 3 Twenty plasma samples were collected over 15 days following dosing with tenoxicam. 4 The following kinetic parameters for plasma tenoxicam were compared: peak concentrations, time taken to reach peak concentrations, area under the plasma concentration-time curve (AUC) and half-life of elimination. 5 Food lengthened the time taken to reach peak tenoxicam concentrations (5.82 +/- 4.6 vs 1.84 +/- 1.0 h in the fasting state; P less than 0.02) and marginally reduced the peak concentrations achieved. AUC was not affected by any of the different regimens. 6 These effects of food on tenoxicam bioavailability are unlikely to be of clinical significance during chronic dosing with the drug.
MeSH Terms
Adult
Aluminum Hydroxide/pharmacology
Antacids/pharmacology
Anti-Inflammatory Agents, Non-Steroidal/pharmacokinetics
Biological Availability
Female
Food
Humans
Intestinal Absorption/drug effects
Magnesium Hydroxide/pharmacology
Male
Middle Aged
Piroxicam/analogs & derivatives,pharmacokinetics
Chemicals
Antacids
Anti-Inflammatory Agents, Non-Steroidal
Piroxicam
Aluminum Hydroxide
Magnesium Hydroxide
tenoxicam
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Day R O
University of New South Wales, School of Physiology and Pharmacology, Department of Clinical Pharmacology and Toxicology, St Vincent's Hospital, Sydney, Australia.
Lam S
Paull P
Wade D
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