Press Release December 14, 2020 For immediate release    WASHINGTON, DC — The Food and Drug Administration’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) recently voted to approve Emergency Use Authorization of BioNTech and Pfizer’s Covid-19 vaccine despite recent reports of anaphylactic reactions among recipients. The vaccine contains polyethylene glycol (PEG) which has been identified as the … Continue reading FDA Ignores RFK, Jr.’s Pleas for Vaccine Safety Oversight Concerning PEG, Suspected To Cause Anaphylaxis