Strengthening the Pharmacovigilance System in Mexico: Implementation of VigiFlow and VigiLyze, as ICSR and Signal Detection Management Systems.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY Pharmaceutical Medicine Pub Date : 2023-11-01 Epub Date: 2023-10-07 DOI:10.1007/s40290-023-00490-y
Gandi Rayón-Ramírez, Salvador Alvarado-López, Rosa Camacho-Sandoval, Miriam J Loera, Alejandro E Svarch, Jorge Alcocer-Varela
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Abstract

Pharmacovigilance (PV) activities aim to identify potential risks of medicines and vaccines after they have been authorised in the market by collecting and analysing information on suspected adverse events from different stakeholders. These can be captured and transmitted electronically in the form of Individual Case Safety Reports (ICSRs). Hence, up-to-date ICSRs management systems, like VigiFlow and signal detection and management systems as VigiLyze, have an important role in the PV system of a country. In 2019, after various attempts to establish a PV database that could fulfil the needs of the country, Mexico's National Regulatory Authority, COFEPRIS (Federal Commission for the Prevention against Sanitary Risks) decided to implement these tools. This has been a successful project that is still ongoing, it has involved national and international organisations, and has required the participation and integration of different components of the national PV system. The implementation of these tools has allowed COFEPRIS to increase its reporting trends and quality of reporting, while contributing to make more efficient interactions and processes with PV stakeholders, even during the COVID-19 pandemic. It has also allowed them to strengthen their commitment to the WHO-Programme for International Drug Monitoring, while highlighting opportunities for improvement in the national PV scenario and in the PV tools themselves. The aim of this article is to describe the implementation process, give an overview of current results regarding ICSR data and processes, and highlight the achievements, challenges, and opportunities for improvement after the three years since the beginning of the project.

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加强墨西哥的药物警戒系统:VigiFlow和VigiLyze作为ICSR和信号检测管理系统的实施。
药物警戒(PV)活动旨在通过收集和分析来自不同利益相关者的疑似不良事件信息,确定药物和疫苗在市场上获得授权后的潜在风险。这些信息可以以个人病例安全报告(ICSR)的形式进行电子捕获和传输。因此,最新的ICSRs管理系统,如VigiFlow和信号检测和管理系统VigiLyze,在一个国家的光伏系统中发挥着重要作用。2019年,在多次尝试建立一个能够满足国家需求的光伏数据库后,墨西哥国家监管局COFPRIS(联邦卫生风险预防委员会)决定实施这些工具。这是一个仍在进行中的成功项目,涉及国家和国际组织,需要国家光伏系统不同组件的参与和整合。这些工具的实施使COFPRIS能够提高其报告趋势和报告质量,同时有助于与PV利益相关者进行更有效的互动和流程,即使在新冠肺炎大流行期间也是如此。这也使他们能够加强对世界卫生组织国际药物监测方案的承诺,同时突出国家PV情景和PV工具本身的改进机会。本文的目的是描述实施过程,概述ICSR数据和过程的当前结果,并强调自项目开始以来三年的成就、挑战和改进机会。
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来源期刊
Pharmaceutical Medicine
Pharmaceutical Medicine PHARMACOLOGY & PHARMACY-
CiteScore
5.10
自引率
4.00%
发文量
36
期刊介绍: Pharmaceutical Medicine is a specialist discipline concerned with medical aspects of the discovery, development, evaluation, registration, regulation, monitoring, marketing, distribution and pricing of medicines, drug-device and drug-diagnostic combinations. The Journal disseminates information to support the community of professionals working in these highly inter-related functions. Key areas include translational medicine, clinical trial design, pharmacovigilance, clinical toxicology, drug regulation, clinical pharmacology, biostatistics and pharmacoeconomics. The Journal includes:Overviews of contentious or emerging issues.Comprehensive narrative reviews that provide an authoritative source of information on topical issues.Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by PRISMA statement.Original research articles reporting the results of well-designed studies with a strong link to wider areas of clinical research.Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Pharmaceutical Medicine may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.All manuscripts are subject to peer review by international experts. Letters to the Editor are welcomed and will be considered for publication.
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