Scott Free (@ScottFreeforQ)

In January a federal judge in the US ordered that the Food and Drug Administration (FDA) release the data it relied on to approve Pfizer’s Covid-19 vaccine. The FDA had requested that they only release 500 pages a month, meaning the full release would have taken over 75 years! The reason given for this long timescale was that the FDA was short-staffed and only had the bandwidth to review 500 pages a month. However, in a win for transparency, the judge ordered that the FDA needed to publish 55,000 pages a month, meaning that all of the data will be published by the end of summer 2022, rather than by 2097. The first tranche of documents was released which contained all the known adverse effects. Pages 30-38 are a 'LIST OF ADVERSE EVENTS OF SPECIAL INTEREST'' - {9 PAGES of ADVERSE EFFECTS} The first one on the list is "1p36 deletion syndrome" - the deletions of chromosome 1p36. In other words permanent altering of your DNA !!!!!!!!!!!!!!! https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf