| Literature DB >> 27955861 |
Ana Alfirevic1, Munir Pirmohamed2.
Abstract
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.Entities:
Keywords: adverse drug reactions; electronic medical records; pharmacogenomics; pre-emptive genotyping
Mesh:
Year: 2016 PMID: 27955861 DOI: 10.1016/j.tips.2016.11.003
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819