Pharmacological mechanism-based drug safety assessment and prediction
- PMID: 21490594
- DOI: 10.1038/clpt.2011.55
Pharmacological mechanism-based drug safety assessment and prediction
Abstract
Advances in cheminformatics, bioinformatics, and pharmacology in the context of biological systems are now at a point that these tools can be applied to mechanism-based drug safety assessment and prediction. The development of such predictive tools at the US Food and Drug Administration (FDA) will complement ongoing efforts in drug safety that are focused on spontaneous adverse event reporting and active surveillance to monitor drug safety. This effort will require the active collaboration of scientists in the pharmaceutical industry, academe, and the National Institutes of Health, as well as those at the FDA, to reach its full potential. Here, we describe the approaches and goals for the mechanism-based drug safety assessment and prediction program.
Similar articles
-
Evaluation of serious adverse drug reactions: a proactive pharmacovigilance program (RADAR) vs safety activities conducted by the Food and Drug Administration and pharmaceutical manufacturers.Arch Intern Med. 2007 May 28;167(10):1041-9. doi: 10.1001/archinte.167.10.1041. Arch Intern Med. 2007. PMID: 17533207
-
Drugs and biologics in pregnancy and breastfeeding: FDA in the 21st century.Birth Defects Res A Clin Mol Teratol. 2008 Sep;82(9):605-9. doi: 10.1002/bdra.20500. Birth Defects Res A Clin Mol Teratol. 2008. PMID: 18704917 No abstract available.
-
Improving the reporting of adverse drug reactions in the hospital setting.Postgrad Med. 2010 Nov;122(6):154-64. doi: 10.3810/pgm.2010.11.2233. Postgrad Med. 2010. PMID: 21084792 Review.
-
FDA attempting to overcome major roadblocks in monitoring drug safety.J Natl Cancer Inst. 2005 Jun 15;97(12):872-3. doi: 10.1093/jnci/97.12.872. J Natl Cancer Inst. 2005. PMID: 15956645 No abstract available.
-
The effect of globalization of drug manufacturing, production, and sourcing and challenges for American drug safety.Clin Pharmacol Ther. 2008 Mar;83(3):494-7. doi: 10.1038/sj.clpt.6100493. Epub 2008 Feb 6. Clin Pharmacol Ther. 2008. PMID: 18253142 Review.
Cited by
-
The Systems Biology of Drug Metabolizing Enzymes and Transporters: Relevance to Quantitative Systems Pharmacology.Clin Pharmacol Ther. 2020 Jul;108(1):40-53. doi: 10.1002/cpt.1818. Epub 2020 Apr 11. Clin Pharmacol Ther. 2020. PMID: 32119114 Free PMC article. Review.
-
Advancing drug safety science by integrating molecular knowledge with post-marketing adverse event reports.CPT Pharmacometrics Syst Pharmacol. 2022 May;11(5):540-555. doi: 10.1002/psp4.12765. Epub 2022 Feb 20. CPT Pharmacometrics Syst Pharmacol. 2022. PMID: 35143713 Free PMC article. Review.
-
Leveraging Human Genetics to Identify Safety Signals Prior to Drug Marketing Approval and Clinical Use.Drug Saf. 2020 Jun;43(6):567-582. doi: 10.1007/s40264-020-00915-6. Drug Saf. 2020. PMID: 32112228 Free PMC article.
-
A rat RNA-Seq transcriptomic BodyMap across 11 organs and 4 developmental stages.Nat Commun. 2014;5:3230. doi: 10.1038/ncomms4230. Nat Commun. 2014. PMID: 24510058 Free PMC article.
-
Integrating Drug's Mode of Action into Quantitative Structure-Activity Relationships for Improved Prediction of Drug-Induced Liver Injury.J Chem Inf Model. 2017 Apr 24;57(4):1000-1006. doi: 10.1021/acs.jcim.6b00719. Epub 2017 Apr 10. J Chem Inf Model. 2017. PMID: 28350954 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical