Literature DB >> 16381072

Extending the methods used to screen the WHO drug safety database towards analysis of complex associations and improved accuracy for rare events.

G Niklas Norén1, Andrew Bate, Roland Orre, I Ralph Edwards.   

Abstract

Post-marketing drug safety data sets are often massive, and entail problems with heterogeneity and selection bias. Nevertheless, quantitative methods have proven a very useful aid to help clinical experts in screening for previously unknown associations in these data sets. The WHO international drug safety database is the world's largest data set of its kind with over three million reports on suspected adverse drug reaction incidents. Since 1998, an exploratory data analysis method has been in routine use to screen for quantitative associations in this data set. This method was originally based on large sample approximations and limited to pairwise associations, but in this article we propose more accurate credibility interval estimates and extend the method to allow for the analysis of more complex quantitative associations. The accuracy of the proposed credibility intervals is evaluated through comparison to precise Monte Carlo simulations. In addition, we propose a Mantel-Haenszel-type adjustment to control for suspected confounders.

Mesh:

Year:  2006        PMID: 16381072     DOI: 10.1002/sim.2473

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  45 in total

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Authors:  Johan Hopstadius; G Niklas Norén; Andrew Bate; I Ralph Edwards
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4.  A web-based quantitative signal detection system on adverse drug reaction in China.

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Journal:  Eur J Clin Pharmacol       Date:  2009-03-05       Impact factor: 2.953

5.  Early detection of pharmacovigilance signals with automated methods based on false discovery rates: a comparative study.

Authors:  Ismaïl Ahmed; Frantz Thiessard; Ghada Miremont-Salamé; Françoise Haramburu; Carmen Kreft-Jais; Bernard Bégaud; Pascale Tubert-Bitter
Journal:  Drug Saf       Date:  2012-06-01       Impact factor: 5.606

6.  Prospective data mining of six products in the US FDA Adverse Event Reporting System: disposition of events identified and impact on product safety profiles.

Authors:  Steven Bailey; Ajay Singh; Robert Azadian; Peter Huber; Michael Blum
Journal:  Drug Saf       Date:  2010-02-01       Impact factor: 5.606

7.  A computerized system for detecting signals due to drug-drug interactions in spontaneous reporting systems.

Authors:  Yifeng Qian; Xiaofei Ye; Wenmin Du; Jingtian Ren; Yalin Sun; Hainan Wang; Baozhang Luo; Qingbin Gao; Meijing Wu; Jia He
Journal:  Br J Clin Pharmacol       Date:  2010-01       Impact factor: 4.335

8.  Impact of stratification on adverse drug reaction surveillance.

Authors:  Johan Hopstadius; G Niklas Norén; Andrew Bate; I Ralph Edwards
Journal:  Drug Saf       Date:  2008       Impact factor: 5.606

9.  Detecting unexpected adverse drug reactions in children.

Authors:  Kristina Star
Journal:  Paediatr Drugs       Date:  2011-04-01       Impact factor: 3.022

10.  Signal Detection Based on Time to Onset Algorithm in Spontaneous Reporting System of China.

Authors:  Tianyi Zhang; Xiaofei Ye; Xiaojing Guo; Guizhi Wu; Yongfang Hou; Jinfang Xu; Wentao Shi; Tiantian Zhu; Yuan Zhang; Xinji Zhang; Jiaqi Song; Jia He
Journal:  Drug Saf       Date:  2017-04       Impact factor: 5.606

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