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Causality Assessment in Pharmacovigilance: Still a Challenge

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  • I. Ralph Edwards

    (WHO Collaborating Centre for International Drug Monitoring)

Abstract

Causality in pharmacovigilance is a difficult and time consuming exercise. This paper presents the challenges in determining causation by drug therapy. The first is that causation is complex and needs to be viewed from the context of the patient treated, rather than the drug product. Multiple causal vectors should be considered if we are to tackle the many issues involved in, for example, medication error and the many other factors that lead to bad outcomes from therapy, including failure to recognise known risk factors. The aim of pharmacovigilance is not only a bureaucratic exercise in public health norms, but is mainly concerned with small minorities of statistical outliers—and even individuals—whose experiences from harms may together form messages about causation that will prevent further at-risk patients from exposure, or at least assist with earlier recognition of drug-related harm and better management of such harm. This requires more time, more data, more analysis and more patient and clinical involvement in reporting useful clinical detail. The paradigm shift back towards gathering more case data relating to possible causation can be selective and would not be just retrogressive, nor necessarily too costly. Greater transparency of hypotheses and availability of anonymised case data will enrol more expertise into evaluations and hypothesis testing, and the provision of more complete and useful information should reduce clinical burdens from bad patient outcomes as well as their overall costs to society.

Suggested Citation

  • I. Ralph Edwards, 2017. "Causality Assessment in Pharmacovigilance: Still a Challenge," Drug Safety, Springer, vol. 40(5), pages 365-372, May.
  • Handle: RePEc:spr:drugsa:v:40:y:2017:i:5:d:10.1007_s40264-017-0509-2
    DOI: 10.1007/s40264-017-0509-2
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    Cited by:

    1. Oeystein Kjoersvik & Andrew Bate, 2022. "Black Swan Events and Intelligent Automation for Routine Safety Surveillance," Drug Safety, Springer, vol. 45(5), pages 419-427, May.
    2. de Boer, Alie & Geboers, Lisanne & van de Koppel, Sonja & van Hunsel, Florence, 2022. "Governance of nutrivigilance in the Netherlands: Reporting adverse events of non-registered products," Health Policy, Elsevier, vol. 126(8), pages 731-737.
    3. Florence Hunsel & Sonja de Koppel & Eugène Puijenbroek & Agnes Kant, 2018. "Vitamin B6 in Health Supplements and Neuropathy: Case Series Assessment of Spontaneously Reported Cases," Drug Safety, Springer, vol. 41(9), pages 859-869, September.

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