Literature DB >> 30035271

Post-marketing Drug Safety Evaluation using Data Mining Based on FAERS.

Rui Duan1, Xinyuan Zhang2, Jingcheng Du2, Jing Huang1, Cui Tao2, Yong Chen1.   

Abstract

Healthcare is going through a big data revolution. The amount of data generated by healthcare is expected to increase significantly in the coming years. Therefore, efficient and effective data processing methods are required to transform data into information. In addition, applying statistical analysis can transform the information into useful knowledge. We developed a data mining method that can uncover new knowledge in this enormous field for clinical decision making while generating scientific methods and hypotheses. The proposed pipeline can be generally applied to a variety of data mining tasks in medical informatics. For this study, we applied the proposed pipeline for post-marketing surveillance on drug safety using FAERS, the data warehouse created by FDA. We used 14 kinds of neurology drugs to illustrate our methods. Our result indicated that this approach can successfully reveal insight for further drug safety evaluation.

Entities:  

Keywords:  Data mining; Post-marketing surveillance; Zero-truncated negative binomial regression model

Year:  2017        PMID: 30035271      PMCID: PMC6054455     

Source DB:  PubMed          Journal:  Data Min Big Data (2017)


  9 in total

1.  Psychotic experiences and suicide attempt risk in common mental disorders and borderline personality disorder.

Authors:  I Kelleher; H Ramsay; J DeVylder
Journal:  Acta Psychiatr Scand       Date:  2017-03       Impact factor: 6.392

2.  Dabigatran and postmarketing reports of bleeding.

Authors:  Mary Ross Southworth; Marsha E Reichman; Ellis F Unger
Journal:  N Engl J Med       Date:  2013-03-13       Impact factor: 91.245

Review 3.  Quinolones: review of psychiatric and neurological adverse reactions.

Authors:  Ana M Tomé; Augusto Filipe
Journal:  Drug Saf       Date:  2011-06-01       Impact factor: 5.606

4.  Predictors of spontaneous and systematically assessed suicidal adverse events in the treatment of SSRI-resistant depression in adolescents (TORDIA) study.

Authors:  David A Brent; Graham J Emslie; Greg N Clarke; Joan Asarnow; Anthony Spirito; Louise Ritz; Benedetto Vitiello; Satish Iyengar; Boris Birmaher; Neal D Ryan; Jamie Zelazny; Matthew Onorato; Betsy Kennard; Taryn L Mayes; Lynn L Debar; James T McCracken; Michael Strober; Robert Suddath; Henrietta Leonard; Giovanna Porta; Martin B Keller
Journal:  Am J Psychiatry       Date:  2009-02-17       Impact factor: 18.112

Review 5.  Comparative efficacy and acceptability of antimanic drugs in acute mania: a multiple-treatments meta-analysis.

Authors:  Andrea Cipriani; Corrado Barbui; Georgia Salanti; Jennifer Rendell; Rachel Brown; Sarah Stockton; Marianna Purgato; Loukia M Spineli; Guy M Goodwin; John R Geddes
Journal:  Lancet       Date:  2011-08-16       Impact factor: 79.321

Review 6.  Under-reporting of adverse drug reactions : a systematic review.

Authors:  Lorna Hazell; Saad A W Shakir
Journal:  Drug Saf       Date:  2006       Impact factor: 5.228

7.  CD-REST: a system for extracting chemical-induced disease relation in literature.

Authors:  Jun Xu; Yonghui Wu; Yaoyun Zhang; Jingqi Wang; Hee-Jin Lee; Hua Xu
Journal:  Database (Oxford)       Date:  2016-03-25       Impact factor: 3.451

8.  The Weber effect and the United States Food and Drug Administration's Adverse Event Reporting System (FAERS): analysis of sixty-two drugs approved from 2006 to 2010.

Authors:  Keith B Hoffman; Mo Dimbil; Colin B Erdman; Nicholas P Tatonetti; Brian M Overstreet
Journal:  Drug Saf       Date:  2014-04       Impact factor: 5.606

9.  A curated and standardized adverse drug event resource to accelerate drug safety research.

Authors:  Juan M Banda; Lee Evans; Rami S Vanguri; Nicholas P Tatonetti; Patrick B Ryan; Nigam H Shah
Journal:  Sci Data       Date:  2016-05-10       Impact factor: 6.444

  9 in total

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