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FDA clears the way for additional bivalent boosters for certain vulnerable individuals

By Eric November 30, 2025

In a significant move to bolster public health efforts ahead of the upcoming fall vaccination campaigns, the U.S. Food and Drug Administration (FDA) has amended the emergency use authorizations (EUAs) for the bivalent COVID-19 vaccines developed by Pfizer and Moderna. This update, announced on Tuesday, specifically permits individuals aged 65 and older, as well as certain immunocompromised individuals, to receive additional doses of these vaccines. The decision comes as health officials aim to enhance protection against COVID-19, particularly with the anticipated rise in cases as the colder months approach.

The revised authorization allows for these additional doses to be administered in light of growing evidence that older adults and those with weakened immune systems may not achieve optimal protection from the virus with the standard vaccination schedule. For instance, studies have indicated that the immune response in older populations can diminish over time, making them more susceptible to severe illness and hospitalization. By facilitating access to extra doses, the FDA is addressing these concerns and reinforcing the importance of vaccination as a key strategy in combating the ongoing pandemic. This proactive approach also aligns with public health recommendations, which emphasize the need for vulnerable populations to stay up-to-date with their vaccinations to mitigate the risk of severe outcomes from COVID-19.

The FDA’s decision underscores the ongoing evolution of the vaccination strategy in response to the pandemic, particularly as new variants of the virus continue to emerge. With the bivalent vaccines designed to target both the original strain of the virus and newer variants, these additional doses are expected to provide enhanced immunity and help curb the spread of COVID-19 during the fall and winter seasons. As the nation prepares for a potential surge in cases, this amendment to the emergency use authorization serves as a critical step in ensuring that the most vulnerable populations have access to the protection they need. Health officials encourage eligible individuals to consult with their healthcare providers about the timing and necessity of these additional doses, reinforcing the message that vaccination remains a vital tool in safeguarding health and preventing the spread of COVID-19.

The U.S. Food and Drug Administration amended the terms of its emergency use authorizations for the Pfizer and Moderna bivalent vaccines on Tuesday, allowing people ages 65 and older and certain people with weakened immunity to get additional doses before this fall’s vaccination campaigns.

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Eric

Eric is a seasoned journalist covering US Politics news.

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