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2000
Volume 15, Issue 3
  • ISSN: 1389-2002
  • E-ISSN: 1875-5453

Abstract

Non-steroidal anti-inflammatory drugs (NSAIDs) are the most frequently used drugs, either on prescription or over-thecounter (OTC). Their daily dosage is based on randomised controlled trials and an empirical clinical assessment of their efficacy and toxicity that allows dose adjustment. The individual response can however be altered by environmental and genetic pharmacokinetic and pharmacodynamic factors. This review summarizes the available pharmacogenetic data that explains part of the variability in response and occurrence of adverse drug reactions to NSAIDs treatment, with a thorough focus on CYP2C9, uridine diphosphate glucuronosyltransferases (UGTs) and cyclooxygenases (COX1 and COX2). Other polymorphisms that are currently being studied and could also explain the interindividual variability in the efficacy and safety of NSAIDs will also be considered.

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/content/journals/cdm/10.2174/1389200215666140202214454
2014-03-01
2025-05-23
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  • Article Type:
    Research Article
Keyword(s): COX; CYP2C8; CYP2C9; genetic polymorphism; NSAIDs; PTGS; UDP glucuronsyltransferases; UGT
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