𝔽𝔻𝔸 𝔸𝕑𝕑𝕣𝕠𝕧𝕖𝕀 π•’π•Ÿπ•• 𝔸𝕦π•₯π•™π• π•£π•šπ•«π•–π•€ π•Œπ•‘π••π•’π•₯𝕖𝕕 π•žβ„β„•π”Έ ℂ𝕆𝕍𝕀𝔻-πŸ™πŸ‘ π•π•’π•”π•”π•šπ•Ÿπ•–π•€ π•₯𝕠 𝔹𝕖π•₯π•₯𝕖𝕣 ℙ𝕣𝕠π•₯𝕖𝕔π•₯ π”Έπ•˜π•’π•šπ•Ÿπ•€π•₯ β„‚π•¦π•£π•£π•–π•Ÿπ•₯𝕝π•ͺ β„‚π•šπ•£π•”π•¦π•π•’π•₯π•šπ•Ÿπ•˜ π•π•’π•£π•šπ•’π•Ÿπ•₯𝕀

Today, the U.S. Food and Drug Administration approved and granted emergency use authorization (EUA) for updated mRNA COVID-19 vaccines (2024-2025 formula) to include a monovalent (single) component that corresponds to the Omicron variant KP.2 strain of SARS-CoV-2.

The mRNA COVID-19 vaccines have been updated with this formula to more closely target currently circulating variants and provide better protection against serious consequences of COVID-19, including hospitalization and death. Today’s actions relate to updated mRNA COVID-19 vaccines manufactured by ModernaTX Inc. and Pfizer Inc.

π•Œ.π•Š. 𝔽𝔻𝔸
ℝ𝕒π•ͺπ•žπ• π•Ÿπ••

Global excess deaths

𝔻𝕣. π•π• π•™π•Ÿ β„‚π•’π•žπ•‘π•“π•–π•π•

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