No Mandatory Injections
First responder law suit against county officials in New Mexico
That the vaccine being forced upon Plaintiff is “unapproved” cannot be disputed. Even though the FDA granted emergency use authorizations for the Pfizer/BioNTech and Moderna vaccines
in December, 2020, the clinical trials the FDA will rely upon to ultimately decide whether to license
these vaccines are still underway and are designed to last for approximately two years to collect
adequate data to establish if these vaccines are safe and effective enough for the FDA to license. The
abbreviated timelines for the emergency use applications and authorizations means there is much the
FDA does not know about these products even as it authorizes them for emergency use, including their
effectiveness against infection, death, and transmission of SARS-CoV-2, the virus that is allegedly the
cause of the COVID disease. Given the uncertainty about the two vaccines, their EUAs (emergency use
authorizations) are explicit that each is “an investigational vaccine not licensed for any indication” and
require that all “promotional material relating to the Covid-19 Vaccine clearly and conspicuously …
state that this product has not been approved or licensed by the FDA, but has been authorized for
emergency use by FDA”. See Exhibit C, EUA letter for Pfizer.
https://d697c6dd-b94d-4c33-8cef-d36ec2a5eb54.filesusr.com/ugd/218232_bf2db48a88ae42b8b4500c1c1a42742a.pdf