Interview with Nadya Swart of BizNews, Nov. 1
CDC has scheduled its ACIP Advisory Committee meeting for Sept. 1 and 2 to sign off on the new Omicron boosters. The normal notice was not provided in advance of this meeting. In accordance with 41 CFR 102-3.150(b), less than 15 calendar days’ notice is being given for this meeting due to the exceptional circumstances…
https://blogs.bmj.com/bmj/2021/06/08/why-we-petitioned-the-fda-to-refrain-from-fully-approving-any-covid-19-vaccine-this-year/ We are part of a group of clinicians, scientists, and patient advocates who have lodged a formal “Citizen Petition” with the United States Food and Drug Administration (FDA), asking the agency to delay any consideration of a “full approval” of a covid-19 vaccine. The message of our petition is “slow down and get the science right—there…
Here is the preprint: Ineffective neutralization of the SARS-CoV-2 Mu variant by convalescent and vaccine sera Here is how I know the forced vaccination program is not intended to protect me and others from Covid but has some other, unspoken purpose(s): 1. People with pre-existing immunity are being required to get the vaccine, though it…
Children’s Health Defense and Global Research discuss the letter here. A copy of the letter Senator Johnson sent is here: https://childrenshealthdefense.org/wp-content/uploads/2021-08-26-Letter-to-FDA-re-Comirnaty.pdf
https://www.statnews.com/2020/03/10/simple-math-alarming-answers-covid-19/ Medical staff wait outside rooms at the Red Cross hospital in Wuhan, China.AFP VIA GETTY IMAGES Much of the current discourse on — and dismissal of — the Covid-19 outbreak focuses on comparisons of the total case load and total deaths with those caused by seasonal influenza. But these comparisons can be deceiving, especially in the…
Thanks to Shannon Brownlee and Jeanne Lenzer, well known health journalists, for this erudite piece on the limitations of epidemiological data for flu vaccines and antiviral drugs. They are brave women to tackle and publish this piece: kudos! A new GAO report on FDA’s reliance on surrogate endpoints (such as using antibody levels generated by…