(I) that the Secretary has authorized the emergency use of the product;
(II) of the significant known and potential benefits and risks of such use, and
of the extent to which such benefits and risks are unknown; and
(III) of the option to accept or refuse administration of the product, of the
consequences, if any, of refusing administration of the product, and of the
alternatives to the product that are available and of their benefits and risks.

EUA products are by definition experimental and thus require the right to refuse.
Under the Nuremberg Code, the foundation of ethical medicine, no one may be
coerced to participate in a medical experiment. Consent of the individual is
“absolutely essential.” A federal court held that even the U.S. military could not
mandate EUA vaccines to soldiers. Doe#1 v. Rumsfeld, 297 F.Supp.2d 119 (2003).
The Food and Drug Administration (FDA) has issued Emergency Use
Authorizations for over 200 diff