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Under-Reporting of Adverse Drug Reactions

A Systematic Review

Drug Safety volume 29, pages 385–396 (2006)Cite this article

Abstract

The purpose of this review was to estimate the extent of under-reporting of adverse drug reactions (ADRs) to spontaneous reporting systems and to investigate whether there are differences between different types of ADRs. A systematic literature search was carried out to identify studies providing a numerical estimate of under-reporting. Studies were included regardless of the methodology used or the setting, e.g. hospital versus general practice. Estimates of under-reporting were either extracted directly from the published study or calculated from the study data. These were expressed as the percentage of ADRs detected from intensive data collection that were not reported to the relevant local, regional or national spontaneous reporting systems. The median under-reporting rate was calculated across all studies and within subcategories of studies using different methods or settings.

In total, 37 studies using a wide variety of surveillance methods were identified from 12 countries. These generated 43 numerical estimates of under-reporting. The median under-reporting rate across the 37 studies was 94% (interquartile range 82–98%). There was no significant difference in the median under-reporting rates calculated for general practice and hospital-based studies. Five of the ten general practice studies provided evidence of a higher median under-reporting rate for all ADRs compared with more serious or severe ADRs (95% and 80%, respectively). In comparison, for five of the eight hospital-based studies the median under-reporting rate for more serious or severe ADRs remained high (95%). The median under-reporting rate was lower for 19 studies investigating specific serious/severe ADR-drug combinations but was still high at 85%.

This systematic review provides evidence of significant and widespread under-reporting of ADRs to spontaneous reporting systems including serious or severe ADRs. Further work is required to assess the impact of under-reporting on public health decisions and the effects of initiatives to improve reporting such as internet reporting, pharmacist/nurse reporting and direct patient reporting as well as improved education and training of healthcare professionals.

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Acknowledgements

The Drug Safety Research Unit (DSRU) is a registered independent charity (No. 327206) associated with the University of Portsmouth. The DSRU receives donations and grants from pharmaceutical companies; however, the companies have no control on the conduct or publication of its studies.

This systematic review was not externally funded. Lorna Hazell has no conflicts of interest with regard to this review. Dr Shakir has provided consultancies and received lecturing fees from pharmaceutical companies but none of these are related to this review.

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  1. Drug Safety Research Unit, Bursledon Hall, Blundell Lane, Southampton, 31 1AA, UK

    Lorna Hazell & Saad A.W. Shakir

  2. University of Portsmouth, Portsmouth, UK

    Saad A.W. Shakir

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  1. Lorna Hazell
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  2. Saad A.W. Shakir
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Correspondence to Lorna Hazell.

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Hazell, L., Shakir, S.A. Under-Reporting of Adverse Drug Reactions. Drug-Safety 29, 385–396 (2006). https://doi.org/10.2165/00002018-200629050-00003

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Keywords

  • Spontaneous Reporting
  • Selective Reporting
  • Spontaneous Reporting System
  • Proportional Reporting Ratio
  • Public Health Decision