ArticleFrontiers in drug safety and regulation2025
A national pharmacovigilance centre perspective on pandemic preparedness -
Article in Frontiers in drug safety and regulation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
3 citing papers in PubMed.
- Persistent rise in device-related errors for CGRP monoclonal antibodies: impact of the COVID-19 pandemic and post-pandemic implications.Naunyn-Schmiedeberg's archives of pharmacology · 2026Article
- GP Consultations for Herpes Zoster After COVID-19 Vaccination: A Self-Controlled Cohort Study Based on Electronic Health Record Data from the Netherlands.Drug safety · 2026Article
- Editorial: Pandemic preparedness in vaccine safety and regulation.Frontiers in drug safety and regulation · 2026Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The SARS-CoV-2 (COVID-19) pandemic highlighted the critical role of pharmacovigilance in ensuring vaccine and drug safety. This perspective from the Netherlands Pharmacovigilance Centre Lareb outlines key experiences and lessons learned during the pandemic. Lareb managed over 233,000 individual case safety reports (ICSRs) related to COVID-19 vaccines, with a considerable proportion submitted by consumers/vaccinated persons directly. Lareb employed both spontaneous reporting and cohort event monitoring (CEM) to gain a better understanding of the safety of these vaccines in a real-world setting. Challenges included the overwhelming volume of data, limited initial access to national vaccination and healthcare registries, underreporting of adverse reactions to SARS-CoV-2 treatments, and a strain on the trained staff to perform tasks while scaling up in personnel. Lareb addressed some challenges through further automation, although more work in this area is still needed. Communication efforts were expanded with a focus on transparency and timeliness. Key recommendations for future pandemic preparedness include investing in Artificial Intelligence for further automation in the reporting process and in signal detection, looking at ways to tackle underreporting for specific associations or medicines in innovative ways and enhancing timely linkage between vaccination and healthcare data. The article underscores the importance of transparent, independent communication and the need for a resilient pharmacovigilance system capable of rapid scale-up during health crises.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.