Analysis of paired reports from the Norwegian ADR Registry suggests merging consumer and healthcare professional accounts of the same adverse event may improve causality assessment
19 August 2026
By building adverse drug reaction reporting directly into clinicians' existing patient records system, two Sydney hospitals turned years of near-silence into over 1,600 reports.
13 August 2026
A review of PBRERs assessed between 2023 and 2025 reflects how the SFDA has gradually refined its approach to monitoring medicine safety.
10 July 2026
In Portugal's decentralised pharmacovigilance system, regional units work close to the people who report. Experience from Coimbra suggests that this can improve ADR reporting.
05 November 2026
Can human factors science help pharmacovigilance deliver on its promise? Eight guiding principles offer a shared framework for turning safety signals into real-world protection.
22 October 2026
Mexico's new pharmaceutical waste framework puts One Health into practice, from hazardous-waste handling in hospitals to expired pills in the kitchen drawer.
27 August 2026
Analysis of paired reports from the Norwegian ADR Registry suggests merging consumer and healthcare professional accounts of the same adverse event may improve causality assessment
19 August 2026
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