3 years ago

538

Brianne Dressen took part in the Utah-based portion of the U.S.
AstraZeneca trial in 2020.
She suffered significant neurological injury after the first dose and withdrew from the trial. She spoke to KUTV News reporter Jim Spiewak Tuesday, saying her kids will not receive a COV vaxxine, if approved.

Dressen told the FDA advisory panel their “decision is being rushed, based on incomplete data from underpowered trials, insufficient to predict rates of severe and long-lasting adverse reactions.”

He urged the committee to reject the EUA modification and direct Pfizer to perform trials “that will decisively demonstrate that the benefits outweigh the risks for children.”

Utah scientist testifies before FDA panel, asks not to approve COV vaxxine for kids

https://kutv.com/news/local/utah-scientist-testifies-before-fda-panel-asks-not-to-approve-covid-19-vaccine-for-kids

PFIZER'S TOP SECRET DOCUMENT LEAKED

https://rumble.com/vwbs0f-pfizers-top-secret-document-leaked.html

5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021

https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf?fbclid=IwAR2q7wQwL_b7ISUkQ-OGm4wgO8G_1cQL_2lKgCjRWiqVfnpTtqBxtyIRqZo

Pfizer vaxxine data. Of particular interest is page 30

Twitter Thread

Pfizer was forced to release the information they wanted sealed for 75 years. This information includes 8 pages of adverse effects from the cov liability free chemical experiment. 1/2

https://twitter.com/Shmeemom/status/1498754221910470660?ref_src=twsrc%5Etfw%7Ctwcamp%5Etweetembed%7Ctwterm%5E1498760269144551424%7Ctwgr%5E%7Ctwcon%5Es3_&ref_url=https%3A%2F%2Fdontspeaknews.com%2F2022%2F03%2F02%2Fthe-official-data-pfizer-and-the-cdc-were-trying-to-hide-from-you%2F

THE OFFICIAL DATA PFIZER AND THE CDC WERE TRYING TO HIDE FROM YOU

https://dontspeaknews.com/2022/03/02/the-official-data-pfizer-and-the-cdc-were-trying-to-hide-from-you/

My wife was severely neurologically injured by a single COV vaxxine in a clinical trial here in the United States last November.
Because study protocol requires two doses, she was dropped from the trial,
her access the study app deleted. Her reaction is not described in the recently released clinical trial report. 266 participants are described as having an AE leading to discontinuation, 56 neurological reactions are tallied.

Clinical trail Dropped people with sever reactions to the jabberwalkie and all their information was gone from the history.

The second dose was required to keep participating in the trial.

Her experience was NOT included from the trail results, and her access to the tracking app was denied.

Negative reactions were supposed to be monitored closely they ABANDONED these People.

They ARE MANIPULATING THE DATA AT OUR EXPENSE!!!

Safety and Efficacy of the BNT162b2 mRNA Cov VaXXine

https://www.nejm.org/doi/pdf/10.1056/NEJMoa2034577?articleTools=true

Differential dropout and bias in randomized controlled trials: when it matters and when it may not

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4688419/?report=printable

Impact of COV on clinical trials and clinical research: A systematic review

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538012/pdf/nje-10-878.pdf

Safety and Efficacy of the BNT162b2 mRNA Cov VaXXine