Pharmacogenomics and active surveillance for serious adverse drug reactions in children

Tenneille T. Loo, Colin J.D. Ross, Johanna Sistonen, Henk Visscher, Parvaz Madadi, Gideon Koren, Michael R. Hayden, Bruce C. Carleton

Research output: Contribution to journalReview articlepeer-review

18 Scopus citations

Abstract

Juxtaposing clinical pharmacology with human genetics, pharmacogenomics utilizes a patients genetic information to identify genetic variants that have the potential to provide clinically relevant predictions of toxicity and efficacy. The goal is to develop personalized and genetic-based predictions of an individuals drug response and likelihood of experiencing an adverse drug reaction. The Canadian Pharmacogenomics Network for Drug Safety (CPNDS) has implemented active adverse drug reaction surveillance to monitor and discover genetic markers related to serious adverse drug reactions in the pediatric population. Evidence-based pharmacogenomics research will inform public policy and influence drug benefit-risk decision-making. Regulatory processes and future challenges in pharmacogenomics research will be discussed.

Original languageEnglish
Pages (from-to)1269-1285
Number of pages17
JournalPharmacogenomics
Volume11
Issue number9
DOIs
StatePublished - Sep 2010
Externally publishedYes

Keywords

  • ADR
  • adverse drug reaction
  • children
  • clinical guidelines
  • drug regulation
  • drug safety
  • pediatrics
  • pharmacoeconomics
  • pharmacogenomics
  • pharmacovigilance
  • surveillance

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