On October 26th 2021, the Food and Drug Adminstration (FDA) held a meeting of the Vaccines and Related Biological Products Advisory Committee (VRBPAC) to review the safety and efficacy of the Pfizer mRNA Covid-19 injection and decide whether or not to extend the Emergency Use Authorisation of the Pfizer vaccines for children aged 5 to 11.
Steve Kirsch, Executive Director of the Covid-19 Early Treatment Fund was invited to speak at the meeting and due to the short time frame given to speak he felt it was best to prepare 30 slides which asked some extremely serious questions on the safety of giving an experimental injection to children.
Every question asked by the Executive Director of the Covid-19 Early Treatment Fund were questions that he feels need to be answered before any vote to authorise Covid-19 vaccination for 5 to 11-year-old children, and they were as follows…
The full slide show presented by Steve Kirsch to the FDA can be viewed here. At the time of writing the FDA meeting is still ongoing and no vote on extending the emergency use authorization of the Pfizer vaccine for children aged 5-to 11 has taken place.
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The Liberty Beacon Project is now expanding at a near exponential rate, and for this we are grateful and excited! But we must also be practical. For 7 years we have not asked for any donations, and have built this project with our own funds as we grew. We are now experiencing ever increasing growing pains due to the large number of websites and projects we represent. So we have just installed donation buttons on our websites and ask that you consider this when you visit them. Nothing is too small. We thank you for all your support and your considerations … (TLB)
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Following a three-year study, the FDA reported VAERS was “seriously underreporting” drug side effects. The worst offender was vaccines, with only around 1% adverse events reported. They proposed further work with the CDC to find a way to automate reporting so both government and drug makers would have accurate data about harmful side effects. Unfortunately, the CDC dropped the ball entirely and nothing was ever done. Ten years later, and they are still making drug approvals based on the same 1% of data.