𝕁&𝕁’𝕀 ℂ𝕆𝕍𝕀𝔻 π•§π•’π•”π•”π•šπ•Ÿπ•– π•₯π•’π•œπ•–π•Ÿ 𝕓π•ͺ πŸ™πŸ‘ π•žπ•šπ•π•π•šπ• π•Ÿ π”Έπ•žπ•–π•£π•šπ•”π•’π•Ÿπ•€ π•šπ•€ β„™π•Œπ•ƒπ•ƒπ”Όπ”» 𝕆𝕦π•₯ 𝕓π•ͺ 𝔽𝔻𝔸

The Food and Drug Administration (FDA) has revoked authorization ofΒ Johnson & Johnson’s Covid vaccine after it was paused over rare blood clot concerns, which sent demand plummeting.Β 

The move was not unexpected because J&J’s parent company Jannsen had requested that federal regulators at the FDA withdraw authorization for its vaccine after it was revealed that the last tranche of doses – about 12.5 million – had expired.

As of year three of the Covid pandemic, nearly 231 million Americans have received either one J&J shot or two doses of an mRNA vaccine from Pfizer orΒ Moderna.

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