Source:http://linkedlifedata.com/resource/pubmed/id/17301736
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2007-4-17
|
pubmed:abstractText |
The aim of this study was to determine the influence of amiodarone on the pharmacokinetics of simvastatin and pravastatin in humans. This was a prospective, crossover, randomized, open-label study performed in 12 healthy volunteers comparing the pharmacokinetics of a single oral dose of simvastatin (40 mg) or pravastatin (40 mg) taken alone and after 3 days of amiodarone (400 mg/day). Amiodarone increased simvastatin acid AUC (area under the plasma concentration-time curve)0-24 h, peak plasma concentration (Cmax), and t1/2 by 73% (P=0.02), 100% (P=0.02), and 48% (P=0.06), respectively, whereas it did not significantly alter pravastatin pharmacokinetics. Point estimates and 90% confidence intervals for simvastatin acid, simvastatin lactone, and pravastatin AUC0-24 h were 154% (109-216%), 155% (109-227%), and 86% (63-118%), respectively. If amiodarone and a statin have to be simultaneously prescribed, pravastatin should be preferred to simvastatin in order to avoid a drug interaction.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Amiodarone,
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Arrhythmia Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA...,
http://linkedlifedata.com/resource/pubmed/chemical/Organic Anion Transporters,
http://linkedlifedata.com/resource/pubmed/chemical/Pravastatin,
http://linkedlifedata.com/resource/pubmed/chemical/SLCO1B1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Simvastatin
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0009-9236
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
81
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
679-84
|
pubmed:meshHeading |
pubmed-meshheading:17301736-Adult,
pubmed-meshheading:17301736-Amiodarone,
pubmed-meshheading:17301736-Anti-Arrhythmia Agents,
pubmed-meshheading:17301736-Area Under Curve,
pubmed-meshheading:17301736-Biotransformation,
pubmed-meshheading:17301736-Cross-Over Studies,
pubmed-meshheading:17301736-Drug Interactions,
pubmed-meshheading:17301736-Female,
pubmed-meshheading:17301736-Humans,
pubmed-meshheading:17301736-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:17301736-Male,
pubmed-meshheading:17301736-Organic Anion Transporters,
pubmed-meshheading:17301736-Polymorphism, Genetic,
pubmed-meshheading:17301736-Pravastatin,
pubmed-meshheading:17301736-Prospective Studies,
pubmed-meshheading:17301736-Simvastatin,
pubmed-meshheading:17301736-Tissue Distribution
|
pubmed:year |
2007
|
pubmed:articleTitle |
Amiodarone interacts with simvastatin but not with pravastatin disposition kinetics.
|
pubmed:affiliation |
Assistance Publique Hôpitaux de Paris, Hôpital Bicêtre, Service de Génétique Moléculaire et Pharmacogénétique, and Départment de Pharmacologie, Université Paris-Sud (XI), Le Kremlin Bicetre, France. laurent.becquemont@bct.aphp.fr
|
pubmed:publicationType |
Journal Article,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't
|