WASHINGTON, DC: Rep. Andy Harris, M.D. (MD-01) and fellow physician Members of Congress called upon the acting HHS Secretary to utilize his statutory authorities to consider immediately revising the COVID-19 mRNA vaccination Emergency Use Authorizations (EUA) based upon the growing body of scientific data and studies indicating that changes to vaccine administration regiments could save tens of thousands of lives.
Congressman Harris issued the following statement:
“When tens of thousands of lives are at stake, the Biden Administration must not drag its feet, get bogged down in bureaucracy, and ignore the latest real-world science. That is why I echo the sentiments of President Biden’s former COVID-19 Advisory Board member, who called for an immediate review of all the data, including from abroad, in the CIDRAP report published this past week.
The U.S. should be leading in this effort to increase vaccine supply, but it is the United Kingdom, France, and others who are adjusting dosing regiments to expand supply and save lives. If the Biden Administration won’t lead, maybe they will follow. Thousands of lives depend on it.”
A copy of the Harris-led letter to the Acting HHS Secretary is attached. The scientific body of evidence continues to grow daily.
This will not happen. Sorry Andy. The pharmaceutical companies have carte blanche on doing their experimentation on real live humans without any liability to themselves if something goes wrong. In other words people they can’t be sued if they screw you up. Just like the big tech companies tat can’t be sued because of that article 230 or whatever number it is that protects them from being sued.