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Publication | Open Access

WHO Strategy for Collecting Safety Data in Public Health Programmes: Complementing Spontaneous Reporting Systems

230

Citations

9

References

2013

Year

TLDR

Spontaneous reporting is the most common, low‑cost pharmacovigilance approach worldwide, yet it suffers from poor‑quality, under‑reporting and makes it difficult to estimate adverse drug reaction rates. Public health programmes must quantify and characterize medicine‑related risks to protect individuals and communities, maintain confidence, and detect medication errors, necessitating quantitative safety monitoring methods beyond spontaneous reporting. The WHO introduces cohort event monitoring and targeted spontaneous reporting as complementary methods to capture quantitative safety data within its public health programmes. The paper discusses the strengths and limitations of these methods and outlines how each can be applied in clinical practice.

Abstract

Globally, national pharmacovigilance systems rely on spontaneous reporting in which suspected adverse drug reactions (ADRs) are reported to a national coordinating centre by health professionals, manufacturers or patients. Spontaneous reporting systems are the easiest to establish and the cheapest to run but suffer from poor-quality reports and underreporting. It is difficult to estimate rates and frequencies of ADRs through spontaneous reporting. Public health programmes need to quantify and characterize risks to individuals and communities from their medicines, to minimize harm and improve use, to sustain public confidence in the programmes, and to track problems due to medication errors and poor quality medicines. Additional methods are therefore needed to monitor the quantitative aspects of medicine safety, to better identify specific risk factors and high-risk groups, and to characterize ADRs associated with specific medicines and in specific populations. The present paper introduces two methods, cohort event monitoring and targeted spontaneous reporting, that are being implemented by the WHO, in its public health programmes, to complement spontaneous reporting. The advantages and disadvantages of these methods and how each can be applied in clinical practice are discussed.

References

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