FDA Revokes Emergency Authorization For COVID-19 Vaccines

 Recent changes in COVID-19 vaccine authorizations in the U. S. have led to significant shifts in public health policy and vaccine availability.

1. Emergency Use Authorization Rescinded:

The emergency use authorizations for COVID-19 vaccines, which were critical during the Biden administration, have been revoked. This affects approximately 240 million Americans.

2. New Approvals by FDA:

The FDA has now fully approved the Pfizer-BioNTech vaccine for older adults and children aged 5 and above with specific health risks. Moderna and Novavax vaccines have also received similar approvals.

3. Regulatory Standards:

The FDA's role involves ensuring products are safe and effective, as indicated by federal laws. Emergency authorizations are limited to public health emergencies and require evidence of potential effectiveness.

4. Ongoing Vaccination Strategies:

Regulators continue to authorize updated COVID-19 vaccines to address declining effectiveness and emerging variants, adopting a model similar to influenza vaccines, although recent approvals have relied on earlier data rather than new human trials.

5. Changing Recommendations:

The CDC has stopped recommending vaccinations for healthy children and pregnant women. However, the American Academy of Pediatrics advises vaccinations for young children, while the American College of Obstetricians and Gynecologists recommends it for pregnant women.

Kennedy mentioned plans to end vaccine mandates while ensuring vaccines remain accessible and emphasizing the need for more rigorous testing. The actions taken by the FDA reflect a step towards these goals, reshaping the COVID-19 vaccination landscape in the U. S.

https://www.zerohedge.com/covid-19/fda-revokes-emergency-authorization-covid-19-vaccines