Literature DB >> 14632590

The quality of published adverse drug event reports.

William N Kelly1.   

Abstract

BACKGROUND: Case reports of adverse drug events (ADEs) are an important source of information.
OBJECTIVE: To determine what variables are reported in ADE case reports, how causality was assessed for each report, and what criteria are specified for publishing ADE case reports.
METHODS: A descriptive analysis of highly significant ADE case reports published in English over a 20-year period was performed. Main outcome measures included frequency distributions for the types of variables reported. The presence of causality assessment and the criteria for submitting an ADE report to practitioner journals were also examined.
RESULTS: A highly significant ADE was described in 1520 published case reports during the study period. Three patient variables were reported >90% of the time, while 12 others were reported <25% of the time. Only 1 drug variable was reported >90% of the time; 6 others were reported 14-74% of the time. Most of the relevant ADE variables were reported most often. Added information for drug interactions, medication errors, and allergic drug reactions were reported 61-99% of the time. Less than 1% of ADE reporters objectively assessed the probability of the ADE. All but one journal publishing the most ADE reports did not require such assessment.
CONCLUSIONS: Professional journals might consider stricter requirements for publishing ADE reports. As a minimum, requirements should include an objective assessment of ADE causality, with explicit recognition in the published text and abstract of the report.

Entities:  

Mesh:

Year:  2003        PMID: 14632590     DOI: 10.1345/aph.1D202

Source DB:  PubMed          Journal:  Ann Pharmacother        ISSN: 1060-0280            Impact factor:   3.154


  24 in total

Review 1.  Toxicity from repeated doses of acetaminophen in children: assessment of causality and dose in reported cases.

Authors:  Kennon Heard; Alison Bui; Sara L Mlynarchek; Jody L Green; G Randall Bond; Richard F Clark; Eran Kozer; Raymond S Koff; Richard C Dart
Journal:  Am J Ther       Date:  2014 May-Jun       Impact factor: 2.688

2.  Completeness of published case reports on suspected adverse drug reactions: evaluation of 100 reports from a company safety database.

Authors:  Piero Impicciatore; Massimiliano Mucci
Journal:  Drug Saf       Date:  2010-09-01       Impact factor: 5.606

3.  Comparison of three pharmacovigilance algorithms in the ICU setting: a retrospective and prospective evaluation of ADRs.

Authors:  Sandra L Kane-Gill; Elizabeth A Forsberg; Margaret M Verrico; Steven M Handler
Journal:  Drug Saf       Date:  2012-08-01       Impact factor: 5.606

Review 4.  Important elements for the diagnosis of drug-induced liver injury.

Authors:  Vijay K Agarwal; John G McHutchison; Jay H Hoofnagle
Journal:  Clin Gastroenterol Hepatol       Date:  2010-02-17       Impact factor: 11.382

Review 5.  Statins and pancreatitis: a systematic review of observational studies and spontaneous case reports.

Authors:  Sonal Singh; Yoon K Loke
Journal:  Drug Saf       Date:  2006       Impact factor: 5.606

Review 6.  Case reports of suspected adverse drug reactions--systematic literature survey of follow-up.

Authors:  Yoon Kong Loke; Deirdre Price; Sheena Derry; Jeffrey K Aronson
Journal:  BMJ       Date:  2006-01-18

7.  The international intravitreal bevacizumab safety survey.

Authors:  F Ziemssen; S Grisanti; K U Bartz-Schmidt
Journal:  Br J Ophthalmol       Date:  2006-11       Impact factor: 4.638

Review 8.  Methods for causality assessment of adverse drug reactions: a systematic review.

Authors:  Taofikat B Agbabiaka; Jelena Savović; Edzard Ernst
Journal:  Drug Saf       Date:  2008       Impact factor: 5.606

9.  Guidelines for submitting adverse event reports for publication.

Authors:  William N Kelly; Felix M Arellano; Joanne Barnes; Ulf Bergman; Ralph I Edwards; Alina M Fernandez; Stephen B Freedman; David I Goldsmith; Kui A Huang; Judith K Jones; Rachel McLeay; Nicholas Moore; Rosie H Stather; Thierry Trenque; William G Troutman; Eugene van Puijenbroek; Frank Williams; Robert P Wise
Journal:  Drug Saf       Date:  2007       Impact factor: 5.606

Review 10.  Bisphosphonates and nonhealing femoral fractures: analysis of the FDA Adverse Event Reporting System (FAERS) and international safety efforts: a systematic review from the Research on Adverse Drug Events And Reports (RADAR) project.

Authors:  Beatrice J Edwards; Andrew D Bunta; Joseph Lane; Clarita Odvina; D Sudhaker Rao; Dennis W Raisch; June M McKoy; Imran Omar; Steven M Belknap; Vishvas Garg; Allison J Hahr; Athena T Samaras; Matthew J Fisher; Dennis P West; Craig B Langman; Paula H Stern
Journal:  J Bone Joint Surg Am       Date:  2013-02-20       Impact factor: 5.284

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