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. 2024 Dec 16;20(1):2439031. doi: 10.1080/21645515.2024.2439031

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© 2024 GSK. Published with license by Taylor & Francis Group, LLC.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

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Figure 3. — Number* and proportion of participants reporting at least one MAE (a) or SAE (b) within 30 days after vaccination, stratified by dose and overall.

* The numbers below each graph (N) correspond to numbers of participants reporting a given adverse event; CI, confidence interval; MAE, medically attended adverse event; SAE, serious adverse event.

The term “Total” refers to all reported MAEs or SAEs, “Grade 3” refers to MAEs with a grade 3 intensity, “related” refers to MAEs or SAEs assessed by the investigator to be related to vaccination. Error bars represent 95% CIs.