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高收入国家的药品质量:比较患病率研究的障碍。

Medicine quality in high-income countries: The obstacles to comparative prevalence studies.

作者信息

Naughton Bernard David, Akgul Ebru

机构信息

Faculty of Health Sciences, School of Pharmacy and Pharmaceutical Sciences, Trinity College Dublin, Dublin, Ireland.

School of Pharmacy, University College London, London, UK.

出版信息

Med Access Point Care. 2021 Oct 21;5:23992026211052272. doi: 10.1177/23992026211052272. eCollection 2021 Jan-Dec.

Abstract

The entry of falsified and substandard medicines into the legitimate pharmaceutical supply chain has negative impacts on healthcare systems, patient safety, and patient access to medicine. The COVID-19 pandemic has highlighted the importance of access to safe medicine through legitimate pharmaceutical supply chains and the willingness of criminals to target medical products such as PPE (personal protective equipment) and COVID-19 treatments. In this article, we analyse data from the United Kingdom (UK) national medicine alert and recall database to identify and understand recent cases of substandard and falsified medicine in the UK's healthcare systems. Using the UK as a case study, we describe that national drug alert and recall data are useful in their current form to record and understand cases of substandard and falsified medicines in the supply chain. However, if regulatory agencies published further data, these drug recall databases may be useful to support longitudinal and international comparative medicine quality studies. We suggest that regulatory agencies publish the number of affected medicine packs in each recalled batch, as part of the recall process. This will help policy makers, practitioners, and researchers to better understand, monitor and compare the quality of medicines within legitimate supply chains.

摘要

假药和不合格药品进入合法药品供应链,会对医疗系统、患者安全以及患者获得药品的机会产生负面影响。新冠疫情凸显了通过合法药品供应链获取安全药品的重要性,也凸显了犯罪分子将个人防护装备(PPE)和新冠治疗药物等医疗产品作为目标的意愿。在本文中,我们分析了来自英国国家药品警报和召回数据库的数据,以识别和了解英国医疗系统中近期出现的不合格药品和假药案例。以英国为案例研究,我们描述了国家药品警报和召回数据在其当前形式下,对于记录和了解供应链中不合格药品和假药案例是有用的。然而,如果监管机构公布更多数据,这些药品召回数据库可能有助于支持纵向和国际比较药品质量研究。我们建议监管机构在召回过程中公布每个召回批次中受影响药品包装的数量。这将有助于政策制定者、从业者和研究人员更好地理解、监测和比较合法供应链内药品的质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6de/9413605/d1436046c625/10.1177_23992026211052272-fig1.jpg

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