Pharmacokinetics and adverse effects of oral meloxicam tablets in healthy adult horses.
Abstract: The objective of this study was to assess the pharmacokinetic profile and determine whether any adverse effects would occur in seven healthy adult horses following oral meloxicam tablet administration once daily for 14 days at a dose of 0.6 mg/kg·bwt. Horses were evaluated for health using physical examination, complete blood count, serum chemistry, urinalysis, and gastroscopy at the beginning and end of the study. Blood was collected for the quantification of meloxicam concentrations with liquid chromatography and mass spectrometry. The mean terminal half-life was 4.99 ± 1.11 h. There was no significant difference between the mean Cmax , 1.58 ± 0.71 ng/mL at Tmax 3.48 ± 3.30 h on day 1, 2.07 ± 0.94 ng/mL at Tmax 1.24 ± 1.24 h on day 7, and 1.81 ± 0.76 ng/mL at 1.93 ± 1.30 h on day 14 (P = 0.30). There was a statistically significant difference between the Tmax on the sample days (P = 0.04). No statistically significant increase in gastric ulcer score or laboratory analytes was noted. Oral meloxicam tablets were absorbed in adult horses, and adverse effects were not statistically significant in this study. Further studies should evaluate the adverse effects and efficacy of meloxicam tablets in a larger population of horses before routine use can be recommended.
© 2012 John Wiley & Sons Ltd.
Publication Date: 2012-10-15 PubMed ID: 23067209DOI: 10.1111/jvp.12021Google Scholar: Lookup
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- Clinical Trial
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The study evaluated the effects of oral meloxicam tablets in healthy adult horses. Results indicated the drug was well-absorbed and did not significantly cause adverse effects, though the authors recommend further investigations before routine use.
Objective of the Study
- The study aimed to measure the pharmacokinetic behavior (the way the body processes the drug) of meloxicam tablets in healthy adult horses.
- The researchers also wanted to identify if there were any negative effects associated with the medication.
Methodology of the Study
- Seven healthy adult horses were chosen for the experiment and they were given oral meloxicam tablets daily for 14 days at a specific dosage.
- The horses were thoroughly examined at the start and end of the study. This involved carrying out physical examinations, complete blood counts, serum chemistry, urinalysis, and gastroscopy.
- The amount of meloxicam present in their bloodstream was determined using liquid chromatography and mass spectrometry, methods that allow for the precise detection and quantification of chemicals.
Findings of the Study
- The half-life of the drug (the time taken for the drug’s concentration in the body to reduce to half) was found to be approximately 5 hours.
- The maximum concentration of the drug in the body did not differ significantly across the sample days – day 1, day 7, and day 14 of administering the drug.
- The time taken to reach maximum concentration, however, was different across the sample days.
- Furthermore, no considerable increase in gastric ulcer score or laboratory analytes (markers in the blood that indicate the function of the body) was found.
- Overall, the tablets were absorbed well in the adult horses and did not cause a statistically significant increase in any adverse effects.
Conclusions and Recommendations
- The research concludes that oral meloxicam tablets were tolerated well by the healthy adult horses in the study.
- Despite the positive results, the team suggested extending this research to a larger population of horses, as this would generate a more robust understanding of the potential side effects and effectiveness of meloxicam tablets in horses. This will help determine whether meloxicam can be recommended for routine use in this population.
Cite This Article
APA
Vander Werf KA, Davis EG, Kukanich B.
(2012).
Pharmacokinetics and adverse effects of oral meloxicam tablets in healthy adult horses.
J Vet Pharmacol Ther, 36(4), 376-381.
https://doi.org/10.1111/jvp.12021 Publication
Researcher Affiliations
- Department of Clinical Sciences, Veterinary Teaching Hospital, University of Illinois, Champaign-Urbana, IL, USA. kvanderw@illinois.edu
MeSH Terms
- Administration, Oral
- Animals
- Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
- Anti-Inflammatory Agents, Non-Steroidal / adverse effects
- Anti-Inflammatory Agents, Non-Steroidal / blood
- Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
- Area Under Curve
- Female
- Half-Life
- Horse Diseases / chemically induced
- Horses
- Male
- Meloxicam
- Stomach Ulcer / chemically induced
- Stomach Ulcer / veterinary
- Tablets
- Thiazines / administration & dosage
- Thiazines / adverse effects
- Thiazines / blood
- Thiazines / pharmacokinetics
- Thiazoles / administration & dosage
- Thiazoles / adverse effects
- Thiazoles / blood
- Thiazoles / pharmacokinetics
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