FDA Grants Emergency Use to Johnson & Johnson COVID-19 Vaccine
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Alabama could reach herd immunity as early as May, UAB researcher estimates
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Johnson & Johnson vaccine: Why Americans shouldn t turn their noses up at J&J s coronavirus vaccine
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This article has been reviewed and updated as of April 13, 2021.
On April 13, 2021, the U.S. Food and Drug Administration (FDA) and U.S. Centers for Disease Control and Prevention (CDC) asked states to temporarily halt using the Johnson & Johnson’s COVID-19 vaccine “out of an abundance of caution” after receiving six reports of a rare and severe type of blood clot forming in individuals after receiving the vaccine. CreakyJoints is monitoring this news closely and will keep readers updated as more information is released.
Now that that the U.S. Food and Drug Administration (FDA) has issued emergency use authorization (EUA) for the Johnson & Johnson COVID-19 vaccine, people who take immunosuppressant medications, are immunocompromised, or who have autoimmune conditions have questions and concerns about what this development means for them.