Health
FDA to look into the future of COVID booster doses
March 21, 2022-Today’s FDA announcement this is vaccination The advisory board met on April 6 to discuss the future of COVID-19 booster doses and specific strains. coronavirus You need your own vaccine.
Representatives from the CDC and the National Institute of Health will participate in the independent experts of the Vaccine and Related Biological Products Advisory Board. According to the FDA’s statement, no votes will be cast and no specific company’s vaccine will be discussed.
“Prevention in the following ways to prepare for future needs to address COVID-19: vaccination Dr. Peter Markes, MD, director of the FDA’s Center for Biologics Evaluation and Research, said in a statement.
Conference experts will discuss why vaccine prescriptions should be changed to target specific variants and when and to whom booster immunization should be given.
Infectious disease experts are monitoring BA.2, a subvariant of Omicron that appears to be more contagious than the first strain. BA.2 is promoting outbreaks throughout Europe and is becoming more common throughout the United States
BA.2 accounted for 23% of the new COVID-19 cases for the week ending March 12. Latest quote From the CDC, it increased from 13.7% last week.
FDA grants public access to background material at least two business days prior to the meeting.
The meeting will be livestreamed at Agency YouTube channel Now available as a webcast on the FDA’s website.
The CDC currently recommends vaccination and boost immunization for all people over the age of 12, and two doses for children ages 5-11. People with weakened immunity are already being encouraged to get a second boost.
Moderna and Pfizer last week requested FDA approval for their second COVID-19 booster shot. Moderna’s request was for all adults, and Pfizer’s request was for users over the age of 65.
Moderna wants to offer a fourth dose to a wide range of age groups to give health authorities “flexibility” in deciding which age group will benefit most.
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