Respiratory syncytial virus prevention is finally here: An overview of safety

被引:0
作者
Laemmle-Ruff, Ingrid [1 ,2 ]
Crawford, Nigel W. [1 ,2 ,3 ]
机构
[1] Murdoch Childrens Res Inst, Surveillance Adverse Events Following Vaccinat Com, Melbourne, Vic, Australia
[2] Royal Childrens Hosp, Dept Gen Med, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
关键词
UNITED-STATES; IMMUNIZATION PRACTICES; ADVISORY-COMMITTEE; NIRSEVIMAB; VACCINE; PRETERM; INFANTS; RSV; RECOMMENDATIONS; DISEASE;
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
BackgroundA number of respiratory syncytial virus (RSV) prevention products have recently been approved in Australia. These products focus on highest risk groups, aiming to prevent RSV disease in young infants and older adults. While not currently included in the National Immunisation Program (NIP), an RSV vaccine (Arexvy, GlaxoSmithKline [GSK]) is available privately for adults >= 60 years, and some Australian jurisdictions have commenced RSV monoclonal antibody (nirsevimab) programs for infants in 2024. ObjectiveThis article summarises safety data regarding RSV prevention products approved in Australia, including vaccines for adults >= 60 years, maternal vaccines and monoclonal antibodies for infants. DiscussionClinical trial data found these products were largely well tolerated, with most local and systemic reactions being mild-moderate and short-lived. Proportions of serious adverse events were low. While very rare, potential safety signals being further assessed include risk of preterm birth following the maternal vaccine (Abrysvo, Pfizer) and Guillain-Barr & eacute; syndrome (GBS) following RSV vaccines in older adults (Abrysvo and Arexvy). Close monitoring of these adverse events of special interest via post-licensure surveillance is underway.
引用
收藏
页码:704 / 708
页数:5
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