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Genomics of Adverse Drug Reactions

Journal

TRENDS IN PHARMACOLOGICAL SCIENCES
Volume 38, Issue 1, Pages 100-109

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tips.2016.11.003

Keywords

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Funding

  1. Medical Research Council Centre for Drug Safety Science
  2. Wolfson Foundation
  3. European Commission Framework Program 7 and Horizon 2020 funding programs
  4. National Institutes of Health Research (NIHR) [II-LB-0313-20008] Funding Source: National Institutes of Health Research (NIHR)
  5. Epilepsy Research UK [P1105] Funding Source: researchfish
  6. Medical Research Council [MR/L006758/1] Funding Source: researchfish
  7. National Institute for Health Research [II-LB-0313-20008, NF-SI-0512-10064] Funding Source: researchfish
  8. MRC [MR/L006758/1] Funding Source: UKRI

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Adverse drug reactions (ADRs) are common, are associated with morbidity and mortality, and are costly to healthcare systems. Genomic factors predispose to ADRs, but these vary depending on the drug, patient, and disease. Genomic testing can not only help to predict and prevent ADRs but can also be used in other ways (diagnosis, closer monitoring of those at risk, pre-emptive genotyping, and understanding of mechanism), all of which will be important in the future to improve the benefit-risk ratio of drugs. In the era of precision medicine, such genomic data will need to be integrated with other forms of data to develop a comprehensive and integrated approach to improve responses to medicines used in patients.

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