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The percentage of participants in the Solicited Safety Set who reported local (A) or systemic (B) solicited adverse reactions is shown for 330 participants who received a booster dose of mRNA-1273 (50 g) after a primary series of two doses of 50 or 100 g of mRNA-1273 in Part B, 198 participants who received a booster dose of mRNA-1273 (50 g) after a primary series of two doses of 100 g of mRNA-1273 in Part B, and 14691 participants who received two doses of 100 g of mRNA-1273 in the phase 3 COVE trial

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