Why is there an ingredient blacked out that's listed on the FDA document used for approval for the BioNtech Comniraty vaccine?? (AKA the Pfizer vaccine that was just FDA approved).
To protect “confidential corporate information,” the FDA routinely redacts information in warning letters, using (b)(4) to indicate where information has been blacked out.
Cross referencing the ingredients on the FDA documentation used to obtain FDA approval with the package insert for the FDA approved vaccine, the blacked out/redacted ingredient isn't listed at all on the package insert.
This unknown liquid ingredient makes up about 20% of the vaccine.
How is informed consent able to be properly given when important details (an ingredient‼️) seem to be intentionally left out? What is this ingredient? Is it just water? If it was no big deal, why is it redacted and not listed on the package insert?
Legal teams are on this, hopefully we will all be informed soon!
FDA document for approval :
Package insert :
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