Public Health providers in Florida have been nudged by the State’s Department of Health and their Surgeon General. Informed consent demands we notify patients of the potential health risks associated with the COVID-19 “vaccines.”
The State Surgeon General is notifying the health care sector and public of a substantial increase in Vaccine Adverse Event Reporting System (VAERS) reports from Florida after the COVID-19 vaccine rollout. …
In Florida alone, there was a 1,700% increase in VAERS reports after the release of the COVID-19 vaccine, compared to an increase of 400% in overall vaccine administration for the same time period (Figure 1).
The reporting of life-threatening conditions increased over 4,400%. This is a novel increase and was not seen during the 2009 H1N1 vaccination campaign. There is a need for additional unbiased research to better understand the COVID-19 vaccines’ short- and long-term effects.
The findings in Florida are consistent with various studies that continue to uncover such risks. To further evaluate this, the Surgeon General wrote a letter to the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) illustrating the risk factors associated with the mRNA COVID-19 vaccines and emphasizing the need for additional transparency.
It’s a fun read if you’re not ideologically married to mRNA. In summary, the State Surgeon General is telling the state’s healthcare industry that there are safety signals and that they should notify patients of these risks (emphasis mine).
To support transparency, the State of Florida reminds health care providers to accurately communicate the risks and benefits of all clinical interventions to their patients, including those associated with the COVID-19 vaccine as additional risks continue to be identified and disclosed to the public.
A bit late, but it at least rises to the potential for informed consent.
One state down, 49 more to go.
