Department of General Practice and Primary Health Care, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Drug Saf. 2020 Dec;43(12):1205-1210. doi: 10.1007/s40264-020-01002-6. Epub 2020 Sep 30.
Vaccines against COVID-19 are being developed at speeds not previously achieved. With this unprecedented effort comes challenges for post-marketing safety monitoring and challenges for vaccine safety communication. To deploy these new vaccines fast across diverse populations, it is vital that robust pharmacovigilance and active surveillance systems are in place. Not all countries have the capability or resources to undertake adequate surveillance and will rely on data from those who can. The tools exist to assess COVID-19 vaccines as they are deployed such as surveillance systems, administrative data and case definitions for adverse events of special interest. However, stitching these all together and using them effectively requires investment and collaboration. This paper provides a high-level overview of some of the facets of modern vaccine safety assessment and how they are, or can be, applied to COVID-19 vaccines.
针对 COVID-19 的疫苗正在以前所未有的速度开发。在这一前所未有的努力下,出现了对上市后安全性监测的挑战,以及对疫苗安全性沟通的挑战。为了在不同人群中快速推出这些新疫苗,建立强大的药物警戒和主动监测系统至关重要。并非所有国家都有能力或资源进行充分的监测,将依赖于有能力进行监测的国家的数据。有一些工具可以在部署 COVID-19 疫苗时评估其安全性,例如监测系统、行政数据和特别关注的不良事件病例定义。然而,将所有这些工具整合并有效地利用它们需要投资和合作。本文概述了现代疫苗安全性评估的一些方面,以及如何将其应用于 COVID-19 疫苗。