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To: metmom; ransomnote; Jane Long; bitt; bagster; numberonepal; Cletus.D.Yokel; Cathi; tatown; ...
https://www.usatoday.com/story/news/health/2022/08/22/pfizer-covid-booster-omicron-submitted-fda-emergency-authorization/7844312001/?

Money quote:

"In the study, eight mice that were given the BA.5 booster dose about 100 days after receiving two doses of Pfizer’s original vaccine generated an immune response.

“To rely only on mouse data (for authorization) would be unprecedented in my knowledge and would certainly raise eyebrows,” said John Moore, a vaccine and virology expert at Weill Cornell Medicine in New York. “It doesn’t mimic the human situation,” where many people were vaccinated more than a year ago and have since been boosted."

215 posted on 09/04/2022 9:48:03 PM PDT by grey_whiskers (The opinions are solely those of the author and are subject to change without notice.)
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To: grey_whiskers

Imagine if Dr. Malone or Pierre Kory had said that.

Some people would have labeled them a q conspiracy theorists or hucksters or some such nonsense.


216 posted on 09/04/2022 9:51:27 PM PDT by metmom (...fixing our eyes on Jesus, the Author and Perfecter of our faith…)
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To: grey_whiskers; ransomnote; Jane Long; bitt; bagster; numberonepal; Cletus.D.Yokel; Cathi; tatown; ..
Meanwhile, with the original trials:

https://www.bmj.com/content/375/bmj.n2635

Covid-19: Researcher blows the whistle on data integrity issues in Pfizer’s vaccine trial BMJ 2021; 375 doi: https://doi.org/10.1136/bmj.n2635 (Published 02 November 2021) Cite this as: BMJ 2021;375:n2635

Money quote:

In autumn 2020 Pfizer’s chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. “As I’ve said before, we are operating at the speed of science,” Bourla wrote, explaining to the public when they could expect a Pfizer vaccine to be authorised in the United States.1

But, for researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson (video 1), emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day.

217 posted on 09/04/2022 9:52:36 PM PDT by grey_whiskers (The opinions are solely those of the author and are subject to change without notice.)
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