The U.S. Food and Drug Administration’s decision to limit COVID vaccines to people 65 and older and others with underlying health conditions has alarmed some medical experts who worry the change will lead to more infections and more deaths.

SHELTON, CT / ACCESS Newswire / May 22, 2025 / Dr. Anil Diwan, President of NanoViricides, Inc. (NYSE Amer.:NNVC ) (the “Company”), comments on the new COVID Vaccine policy adopted by the US FDA. The new FDA COVID Vaccine Booster Shots policy [1] is based on the findings that the groups that benefit from repeat

Federal health officials will no longer routinely approve annual COVID-19 shots for younger adults and children who are healthy

Frank DeStefano, MD, MPH, was there when the CDC's Vaccine Safety Datalink (VSD) first came online in 1990, when the agency convinced four health maintenance organizations (HMOs) to contribute data to assess vaccine safety.

As the Trump administration’s FDA moves to limit approval for COVID-19 booster shots, millions of Americans under 65 may find themselves without access this fall. However, until Friday, there’s still time to influence this decision, pro or con, through the FDA’s public comment portal.

Peter A. McCullough, a former cardiologist who promoted unproven treatments like ivermectin and hydroxychloroquine at the height of the pandemic, posted a video to Instagram claiming that Biden’s cancer was “turbo cancer.”

The FDA’s new approach to boosters could mean that kids will no longer be able to get vaccinated against the disease to begin with.

The shift was a marked departure from previous FDA guidance, which recommended an annual COVID vaccine for everyone 6 months and older.