
FDA authorizes COVID-19 booster for kids 12-15
The US Food and Drug Administration (FDA) made multiple changes to the emergency use authorization for the Pfizer/BioNTech vaccine.
The US Food and Drug Administration (FDA) made
Furthermore, the timing of the booster dose following the initial 2 dose vaccination has been shortened to a 5-month interval. Israeli data were also used to make this determination, with no negative safety effects found with the shorter time between doses. Additionally, the preliminary data indicate that a booster dose appears to increase antibody activity and be effective against the Omicron variant.
Finally, the amendments also include a third dose in the primary series for certain immunocompromised children aged 5 to 11 years. Any child who has received a solid organ transplant or who has a condition that is considered to be an equivalent level of immunocompromised may not have an adequate response to a 2-dose series. A third dose for all other children or a booster is still not currently recommended, but the FDA is monitoring the situation and will update the EUA if needed.
Acting FDA Commissioner Janet Woodcock, MD, stressed the importance of receiving both timely vaccination and booster in the release for the amendments, saying, “With the current wave of the Omicron variant, it’s critical that we continue to take effective, life-saving preventative measures such as primary vaccination and boosters, mask wearing, and social distancing to in order to effectively fight COVID-19.”
Reference
1. US Food and Drug Administration. Coronavirus (COVID-19) Update: FDA takes multiple actions to expand use of Pfizer-BioNTech COVID-19 vaccine. Published January 3, 2022. Accessed January 3, 2022.
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