Source: Guest post by Todd Butterfield
Today the Pfizer COVID shot received FDA approval. The FDA has used Pfizer’s data from the Israeli population to support the safety and efficacy of the COVID shot, but as for reports made about thousands of Israelis who either died or were permanently disabled in association with the jab, the FDA has buried this data in a mass grave.
A group of Israeli and U.S. friends helped Israelis to report adverse events on VAERS, by promoting the public link where U.S. and non-U.S. people report these. Israelis living under their “Green Mark” vaccine passport system have perhaps experienced more coercion to take the COVID shot than others have so far. During a six-week period starting in June, we reached out to the social media pages of over 1 million English-speaking Israelis, and over 61,000 Israelis used this link we shared to go into the form where adverse event reports are made to the FDA.
4,420 additional deaths and 5,369 additional permanent disabilities were reported on VAERS for the 3-week period ending July 16. This was a dramatic increase compared to the prior period, which had averaged an additional weekly 312 deaths and 257 permanent disabilities from 12/14/20 until 7/2/21. After the initial surge in death reports on July 2, Children’s Health Defense did an individual-level count and determined that nearly every one of the 2,063 death reports made that week were on patients who had received the Pfizer shot—the only one used in Israel.
Children’s Health Defense also analyzed 5,739 deaths reported in VAERS as of July 30 (U.S. reports) and determined that 13% occurred within 24 hours of vaccination, 19% occurred within 48 hours of vaccination, and 34% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated. There now are over 34,000 deaths reported in association with the Pfizer, Moderna, AstraZeneca, and Janssen shots that cause people’s cells to mass produce the COVID-19 spike protein (VAERS + EudraVigilance death reports).
If you know anyone who experiences a heart attack or a stroke, any other blood clot related event, or other adverse event within 30 days of receiving the Pfizer shot, please use the FDA’s post-marketing surveillance system and make a report. Apparently we still need more voices, but the truth will set us free, and the FDA has not yet held the public meeting that it committed to hold prior to granting its approval to a COVID vaccine (Covid-19: FDA set to grant full approval to Pfizer vaccine without public discussion of data, BMJ 2021; 374 doi: , Published 20 August 2021).
Are you struggling to understand why there is such a worldwide push to get the COVID shots?
Consider that the vaccine-related I.D.s being issued can be compatible across borders as a single system where every person on the planet has a taxpayer I.D. number. The group of Israeli and U.S. friends who are helping people report their tragedies to the FDA receive their inspiration not from a few of the wealthiest people on the planet who seek to take from humanity, but from Jesus of Nazareth, who made the ultimate sacrifice to save us.