'Today's actions demonstrate our commitment to public health in proactively fighting against the COVID-19 pandemic,' the FDA commissioner said.
) announced Wednesday that it had authorized booster doses for both the Moderna and Johnson & Johnson COVID-19 vaccines.
For example, a person who received an initial Johnson & Johnson vaccine may receive a dose of either theGuidelines were released by the FDA for the distribution and use of booster vaccines by various at-risk groups, mainly including the elderly and those with significant pre-existing conditions. The Johnson & Johnson vaccine booster may be given two months after the initial vaccination was completed to people 18 and older.
"As the pandemic continues to impact the country, science has shown that vaccination continues to be the safest and most effective way to prevent COVID-19, including the most serious consequences of the disease, such as hospitalization and death," said acting FDA commissioner Janet Woodcock."The available data suggest waning immunity in some populations who are fully vaccinated.
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