Literature DB >> 17566621

Creating knowledge about adverse drug reactions: a critical analysis of the Danish reporting system from 1968 to 2005.

Lise Aagaard1, Birthe Soendergaard, Elin Andersen, Jens Peter Kampmann, Ebba Holme Hansen.   

Abstract

Data on adverse drug reactions (ADRs) have been collected in Denmark since 1968 and the process is ongoing. This article explores knowledge created by the system, including how the collected data have been used to monitor the safety of licensed drugs. Nonaka's theory of knowledge creation was used to discriminate between tacit and explicit knowledge. A total of 56,802 ADR case reports were received from 1968 to 2005. The analysis shows a rather stable number of ADR cases from 1980, with about 2000 reports per year. The distribution of cases into serious and non-serious ADRs has been one to four throughout the period under study, but with large variations. Analysis of selected ADR cases shows that the system lacked the potential to capture available knowledge. Consequently the ADR reports have had limited value and significance in the process of creating scientific knowledge. Thus, the analysis questions the way available data can become explicit as a basis for regulatory decisions and whether all data can become knowledge, including who decides what knowledge is.

Mesh:

Year:  2007        PMID: 17566621     DOI: 10.1016/j.socscimed.2007.04.026

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  9 in total

1.  Knowledge creation about ADRs--turning the perspective from the rear mirror to the projector?

Authors:  Lise Aagaard; Birthe Soendergaard; Doris I Stenver; Ebba Holme Hansen
Journal:  Br J Clin Pharmacol       Date:  2007-10-24       Impact factor: 4.335

2.  Consumer reporting of adverse drug reactions: a retrospective analysis of the Danish adverse drug reaction database from 2004 to 2006.

Authors:  Lise Aagaard; Lars Hougaard Nielsen; Ebba Holme Hansen
Journal:  Drug Saf       Date:  2009       Impact factor: 5.606

3.  Adverse drug reactions in the paediatric population in Denmark: a retrospective analysis of reports made to the Danish Medicines Agency from 1998 to 2007.

Authors:  Lise Aagaard; Camilla Blicher Weber; Ebba Holme Hansen
Journal:  Drug Saf       Date:  2010-04-01       Impact factor: 5.606

Review 4.  Pharmacovigilance in China: development and challenges.

Authors:  Ying Zhao; Tiansheng Wang; Guangyao Li; Shusen Sun
Journal:  Int J Clin Pharm       Date:  2018-07-26

Review 5.  How Effective Are Incident-Reporting Systems for Improving Patient Safety? A Systematic Literature Review.

Authors:  Charitini Stavropoulou; Carole Doherty; Paul Tosey
Journal:  Milbank Q       Date:  2015-12       Impact factor: 4.911

Review 6.  Using text-mining techniques in electronic patient records to identify ADRs from medicine use.

Authors:  Pernille Warrer; Ebba Holme Hansen; Lars Juhl-Jensen; Lise Aagaard
Journal:  Br J Clin Pharmacol       Date:  2012-05       Impact factor: 4.335

7.  Structures and processes in spontaneous ADR reporting systems: a comparative study of Australia and Denmark.

Authors:  Lise Aagaard; Doris Irene Stenver; Ebba Holme Hansen
Journal:  Pharm World Sci       Date:  2008-03-19

8.  Identification of possible adverse drug reactions in clinical notes: The case of glucose-lowering medicines.

Authors:  Pernille Warrer; Peter Bjødstrup Jensen; Lise Aagaard; Lars Juhl Jensen; Søren Brunak; Malene Hammer Krag; Peter Rossing; Thomas Almdal; Henrik Ullits Andersen; Ebba Holme Hansen
Journal:  J Res Pharm Pract       Date:  2015 Apr-Jun

Review 9.  Information about ADRs explored by pharmacovigilance approaches: a qualitative review of studies on antibiotics, SSRIs and NSAIDs.

Authors:  Lise Aagaard; Ebba Holme Hansen
Journal:  BMC Clin Pharmacol       Date:  2009-03-03
  9 in total

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