since I won’t jab period I have not followed this that closely but did they just approve vaporvax?
A vax that is not even available yet?
Yup - the FDA “approved” vax is not currently available. What they are trying to do is use up all the EUA vax so they don’t lose money on it .... plus, they haven’t worked out the liability issues on the ‘approved’ vax yet .... they have total immunity on the EUA vax.
Anyone being mandated to take the jab ... if it’s not the new vax name COMIRNATY on the bottle, it’s EUA, experimental, & you can REFUSE for that reason.
Article with info:
2 Things Mainstream Media Didn’t Tell You About FDA’s Approval of Pfizer Vaccine
https://childrenshealthdefense.org/defender/mainstream-media-fda-approval-pfizer-vaccine/
Excerpts:
EUA-approved COVID vaccines have an extraordinary liability shield under the 2005 Public Readiness and Preparedness Act. Vaccine manufacturers, distributors, providers and government planners are immune from liability. The only way an injured party can sue is if he or she can prove willful misconduct, and if the U.S. government has also brought an enforcement action against the party for willful misconduct. No such lawsuit has ever succeeded.
At least for the moment, the Pfizer Comirnaty vaccine has no liability shield. Vials of the branded product, which say “Comirnaty” on the label, are subject to the same product liability laws as other U.S. products.
When the Centers for Disease Control and Prevention’s (CDC) Advisory Committee for Immunization Practices places a vaccine on the mandatory schedule, a childhood vaccine benefits from a generous retinue of liability protections.
But licensed adult vaccines, including the new Comirnaty, do not enjoy any liability shield. Just as with Ford’s exploding Pinto, or Monsanto’s herbicide Roundup, people injured by the Comirnaty vaccine could potentially sue for damages.
And because adults injured by the vaccine will be able to show that the manufacturer knew of the problems with the product, jury awards could be astronomical.
Pfizer is therefore unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product.
Given this background, the FDA’s acknowledgement in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA Pfizer BioNTech jab, exposes the “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates.
The FDA’s clear motivation is to enable Pfizer to quickly unload inventories of a vaccine that science and the Vaccine Adverse Events Reporting System have exposed as unreasonably dangerous, and that the Delta variant has rendered obsolete.