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. 2021 Dec 27;11(1):463–483. doi: 10.1007/s40121-021-00571-y

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© The GSK group of companies 2021

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 2 — Number of enrolled participants (cumulative, by ISO week) with proportion reporting at least one AE after dose 1 or dose 2 (safety set). AE, adverse event; ISO, International Organization for Standardization. Cumulative number of enrolled participants by week and by country, with the proportion reporting at least one AE. Participants in Germany and Belgium were adults and therefore received only one dose of GSK’s inactivated quadrivalent seasonal influenza vaccine, while some participants in Spain were children eligible for two doses. Participants were enrolled from ISO week 40, 2020 (28 September–4 October 2020) to ISO week 2, 2021 (11–17 January 2021)