I have two concerns about this point, one extremely compelling.
The first concern is why are the Moderna and Johnson & Johnson vaccines still being administered under the Emergency Use Authorization when the FDA itself says:
What is an Emergency Use Authorization (EUA)?Wouldn't the availability of the FDA-approved Pfizer vaccine invalidate the need for the Moderna and Johnson & Johnson EUA?An Emergency Use Authorization (EUA) is a mechanism to facilitate the availability and use of medical countermeasures, including vaccines, during public health emergencies, such as the current COVID-19 pandemic. Under an EUA, FDA may allow the use of unapproved medical products, or unapproved uses of approved medical products in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions when certain statutory criteria have been met, including that there are no adequate, approved, and available alternatives. Taking into consideration input from the FDA, manufacturers decide whether and when to submit an EUA request to FDA.
Secondly, and more importantly, the EUA vaccines require a patient informed consent form to be signed. United States case law says that any consent given under duress is not consent under the law.
It seems to me that forcing someone to get a vaccine or lose their jobs, their pay, and their family security, is the utmost coercive duress possible on someone.
Nobody can give a legally binding consent under these conditions, and for that reason these mandates to take the EUA vaccines should be challenged in court.
-PJ
The fda approved a Pfizer "vaccine", supposedly, similar to the one in use here, but it's not the same one.
TITLE 21 - FOOD AND DRUGS
21 U.S. Code § 355 - New drugs
(…)
(i) Exemptions of drugs for research; discretionary and mandatory conditions; direct reports to Secretary
(…)
(4) Regulations under paragraph (1) shall provide that such exemption shall be conditioned upon the manufacturer, or the sponsor of the investigation, requiring that experts using such drugs for investigational purposes certify to such manufacturer or sponsor that they will inform any human beings to whom such drugs, or any controls used in connection therewith, are being administered, or their representatives, that such drugs are being used for investigational purposes and will obtain the consent of such human beings or their representatives, except where it is not feasible, it is contrary to the best interests of such human beings,….
(…)
[ EMPHASIS: “…informed consent…except where it is not feasible, it is contrary to the best interests of such human beings,…” ]
{ ===> They decided informed consent is not in your best interest. }