• February 5, 2023

HUGE: Lead Author of Peer-Reviewed Research Re-Examining Pfizer and Moderna mRNA Vaccine Trials Calls for Immediate Suspension Due to Serious Adverse Events (VIDEO)

 HUGE: Lead Author of Peer-Reviewed Research Re-Examining Pfizer and Moderna mRNA Vaccine Trials Calls for Immediate Suspension Due to Serious Adverse Events (VIDEO)

Dr. Joseph Fraiman calls for immediate suspension of mRNA COVID vaccine due to serious adverse events.

During a COVID-19 EU hearing last October, Pfizer’s President of International Developed Markets, Janine Small, admitted that the vaccine had never been tested on its ability to prevent transmission, contrary to what was previously advertised.

During the hearing, when asked by Dutch politician Ross if the Pfizer COVID vaccine tested on stopping the transmission of the virus before it entered the market, Janine Small responded while smiling,

“Regarding the question around did we know about stopping immunization before it entered the market? No. We have to really move at the speed of science to really understand what is taking place in the market.”

This statement was confirmed by an unredacted Pfizer agreement from a FOIA request with the Slovenian government.

“The Participating Member State acknowledges that the Vaccine and materials related to the Vaccine, and their components and constituent materials are being rapidly developed due to the emergency circumstances of the COVID-19 pandemic and will continue to be studied after provision of the Vaccine to the Participating Member States under the APA,” according to the documents.

“The Participating Member State further acknowledges that the long-term effects and efficacy of the Vaccine are not currently known and that there may be adverse effects from the Vaccine that are not currently known.”

Pfizer clearly states in the supply contract that the injections are not going to be the same as the clinical trial injections AND it has no clue as to long-term effects or efficacy AND there may be unknown adverse effects that are, presumably, ABOVE and BEYOND the adverse event rate of 24% in the injected group of 21,900 in the Pfizer phase 3 clinical trials v 6% in the 21,900 placebo group in those trials.

According to FDA Surveillance Data, the Pfizer COVID vaccine increases the risk of lung blood clots by 50%.

FDA finally admitted Pfizer’s COVID-19 vaccine had been linked to blood clotting in older individuals based on the result of one of the largest studies of elderly persons aged 65 years and above.

In November, The Gateway Pundit reported that big pharmaceutical companies Pfizer and Moderna have both begun clinical tests to investigate whether or not the use of their experimental COVID vaccines may have any long-term adverse effects on a person’s health.

On Monday, Dr. Joseph Fraiman, the lead author of peer-reviewed research re-examining Pfizer and

Source: The Gateway Pundit

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