To print: Select File and then Print from your browser's menu

Title: Gemfibrozil Increases Plasma Concentrations of Rosiglitazone

URL: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=R
Retrieve&db=PubMed&dopt=Abstract&list_uids=12898007

Diabetologia 2003 Jul 29;[Epub ahead of print]. "Gemfibrozil considerably increases the plasma concentrations of rosiglitazone"
09/10/2003 11:48:21 AM
By Jill Taylor

ERRATUM: Gemfibrozil Contraindicated in Diabetics Patients Taking Rosiglitazone There was an error in the title of a review (Aug. 6, 2003) of a paper in Diabetologia. The original title read: Gemfibrozil Contraindicated in Diabetics Patients Taking Rosiglitazone The corrected text now reads: Gemfibrozil Increases Plasma Concentrations of Rosiglitazone We apologise to the manufacturer for having published inaccurate information on their product. We are committed to providing the most accurate, relevant and balanced information for physicians worldwide and have devoted considerable resources to ensuring this. We deeply regret this error. -------------------------------------------------------- Administration of usual therapeutic doses of gemfibrozil considerably increases the plasma concentrations of rosiglitazone, an insulin-sensitising drug used to treat patients with Type 2 diabetes mellitus. Gemfibrozil, a lipid-lowering agent, was recently demonstrated to dangerously increase the plasma concentrations of another antidiabetic drug, repaglinide. Because fibrates are commonly used to lower triglyceride levels in diabetics, M. Niemi and colleagues of the Helsinki University Central Hospital in Finland, investigated a possible interaction between gemfibrozil and rosiglitazone. The investigators performed a randomised, placebo-controlled crossover study in which 10 healthy volunteers (9 men, 1 woman) took 600 mg gemfibrozil or placebo orally twice daily for 4 days, and a single 4 mg dose of rosiglitazone on day 3. Day 3 food intake was standardised, and patients received food at 3 hours and 7 hours after rosiglitazone administration. Venous blood samples were collected before and for up to 48 hours after rosiglitazone administration. Gemfibrozil was found to raise the mean area under the plasma rosiglitazone concentration-time curve 2.3-fold, as well as increase the elimination half-life from 3.6 to 7.6 hours. Additionally, while gemfibrozil had only a minor effect on peak plasma rosiglitazone concentration (a 1.2-fold increase), the plasma rosiglitazone concentration measured at 24 hours post administration increased almost 10-fold. Considerable variability between individuals in the extent of drug interaction was noted, with the relative increase in rosiglitazone concentration ranged from 51 to 179%. Concomitant administration of the two drugs may enhance rosiglitazone efficacy, but may also increase the risk of concentration-dependent adverse effects. "Due to the possibility of an increased risk of adverse effects, it could be advisable to avoid co administration of gemfibrozil and rosiglitazone," researchers say. The researchers recommend that rosiglitazone dose be reduced by about 50 to 70% if gemfibrozil treatment is started on a patient using rosiglitazone, and the patient carefully monitored for signs and symptoms of adverse effects.

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=R
Retrieve&db=PubMed&dopt=Abstract&list_uids=12898007

Copyright © 2009 P\S\L Consulting Group Inc. All rights reserved. Republication or redistribution of P\S\L content is expressly prohibited without the prior written consent of P\S\L. P\S\L shall not be liable for any errors, omissions or delays in this content or any other content on its sites, newsletters or other publications, nor for any decisions or actions taken in reliance on such content.