Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Evolving pharmacovigilance requirements with novel vaccines and vaccine components

Bibliographic Data

ID21878674
AuthorsPatrick L F Zuber (0000-0002-8966-5054, World Health Organization, corresponding author), Marion Gruber (Center for Biologics Evaluation and Research), Marion F Gruber (Center for Biologics Evaluation and Research), David C Kaslow (0000-0003-3557-383X, Program for Appropriate Technology in Health), Robert T Chen (0000-0002-3094-8367, The Task Force for Global Health), Brigitte K Giersing (World Health Organization), Martin H Friede (World Health Organization), Martin Friede (World Health Organization)
Year2021
Volume6
IssueSuppl 2
Pagese003403
Publication date2021-05-01
Open AccessYes
TypeARTICLE
VenueBMJ Global Health (JOURNAL)
Journal identifiersISSN: 2059-7908 • E-ISSN: 2059-7908
PublisherBMJ (PUBLISHER • GB)
DOI10.1136/bmjgh-2020-003403
PMID34011500
OpenAlexW3160749742
LanguageEN
Citations received1
References cited61

This paper explores the pipeline of new and upcoming vaccines as it relates to monitoring their safety. Compared with most currently available vaccines, that are constituted of live attenuated organisms or inactive products, future vaccines will also be based on new technologies. Several products that include such technologies are either already licensed or at an advanced stage of clinical development. Those include viral vectors, genetically attenuated live organisms, nucleic acid vaccines, novel adjuvants, increased number of antigens present in a single vaccine, novel mode of vaccine administration and thermostabilisation. The Global Advisory Committee on Vaccine Safety (GACVS) monitors novel vaccines, from the time they become available for large scale use. GACVS maintains their safety profile as evidence emerges from post-licensure surveillance and observational studies. Vaccines and vaccine formulations produced with novel technologies will have different safety profiles that will require adapting pharmacovigilance approaches. For example, GACVS now considers viral vector templates developed on the model proposed by Brighton Collaboration. The characteristics of those novel products will also have implications for the risk management plans (RMPs). Questions related to the duration of active monitoring for genetic material, presence of adventitious agents more easily detected with enhanced biological screening, or physiological mechanisms of novel adjuvants are all considerations that will belong to the preparation of RMPs. In addition to assessing those novel products and advising experts, GACVS will also consider how to more broadly communicate about risk assessment, so vaccine users can also benefit from the committee’s advice

Adverse effect · Pharmacovigilance · Medicine · Pharmacovigilance and Adverse Drug Reactions · SARS-CoV-2 and COVID-19 Research · Vaccine Coverage and Hesitancy · Pharmacology · Virology

  • The impact of empowering community physicians to prescribe vaccines on public vaccination

    Open Access•Liqun Yao, Hailian Wang et al.•Frontiers in Public Health•2026

Citations per year1
Citation span2026 - 2026 (1)
Highly citedNo

Tools

Open DOIOpen Access
Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae