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FDA Advisory Committee (VRBPAC) did not follow FDA published guidelines for communicating risks and benefits to the public, and the committee failed to report absolute risk reduction measures in authorizing the BNT162b2 and mRNA-1273 vaccines for emergency use. Such examples of outcome reporting bias mislead and distort the public’s interpretation of COVID-19 mRNA vaccine efficacy and violate the ethical and legal obligations of informed consent.

FDA Advisory Committee (VRBPAC) did not follow FDA published guidelines for communicating risks and benefits to the public, and the committee failed to report absolute risk reduction measures in authorizing the BNT162b2 and mRNA-1273 vaccines for emergency use. Such examples of outcome reporting bias mislead and distort the public’s interpretation of COVID-19 mRNA vaccine efficacy and violate the ethical and legal obligations of informed consent.

(post is archived)

[–] • 1 pt

Pfizer did publish the all cause mortality in their trial reports. In the they clearly reported 17 deaths in the placebo group and 21 deaths in the vaccinated group (see page 23). Thankfully, I was following the kinds of people who read these long reports to find the important parts that everyone else was trying to hide or ignore.

[–] • 0 pt

Thankfully I was following SGT Report, David Icke, and others including AJ. So I was aware of the beast system being inaugurated with the mark of the beast (injection).