"Follow the Science?"

Larry A. Law

Jessica Rose, Ph.D., holds degrees in applied mathematics, immunology, computational biology, molecular biology, and biochemistry. In a podcast interview on September 18, 2021 with The Covexit she discussed data from the U.S. Vaccine Adverse Events Reporting System (VAERS) which called into question the safety of COVID shots. You can see a copy of her slides here. Her analysis shows that the number of VAERS reports varied from a low of 25,408 per year to a high of 49,412 per year during the last decade (2011 to 2020). In the first ten months of 2021 the number of reports shot up to 521,667 just for COVID shots! The total number of deaths ranged from a low of 120 per year to a high of 183 per year during that same period. As of September 3, 2021, the reported death toll just in the U.S. is 7,662! Why isn't that raising a red flag?

Cardiovascular, immunological, and neurological adverse events have all increased exponentially as well. She estimates the "under-reporting factor" (URF) to be 31. This is the calculated multiplier that accounts for the fact that less than 1% of adverse events are reported to VAERS. Taking the URF into account, the death toll from COVID shots rises from 7,662 to 205,809! Historically, 50 deaths has been the cutoff point where a vaccine is pulled from the marketplace. There seems to be no ceiling anymore for which death or disability are considered unacceptable. Why?  

The U.S. Food and Drug Administration (FDA) used to be funded strictly by taxpayer money. Currently, approximately 45% of the FDA annual budget comes from user fees paid by Big Pharma. The trend from public funding to corporate funding is seen in drug approvals. Only 38% of drugs were approved by the FDA in 2005. By 2018 the rate rose to 61%. The pharmaceutical industry is not paying the bill for nothing. The pressure to move drugs forward and create a return on their investment is high. A 2017 study by Yale documents the downside of that rush for approval. Fully one-third of all FDA approved drugs end up having significant safety issues and 21% of them are ultimately removed from the market or given a black box warning. The journal Science looked at 107 FDA physician advisors and found that 40 of them received more than $10,000, 26 got more than $100,000, and 6 got more than $1 million in post-approval earnings from the drug company. Doesn't that represent a conflict of interest? A 2016 study found that 15 of 26 employees left the agency to work or consult for the pharmaceutical industry. Clearly, the FDA does not work in the public's best interest.  

The FDA has a Vaccines and Related Biologic Products Advisory Committee (VRBPAC) responsible for vaccine safety. This committee never met to consider the effectiveness of the Pfizer COVID-19 shot (it was decreed effective by the Biden Administration) but they did meet to consider the booster on September 17, 2021. At the end of the day, 16 of the 18 committee members voted "No" on whether to administer the booster. This was a result of expert testimony received during the day.

One of those experts, Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, presented data showing the Pfizer shot kills two people for every person it saves! He reviewed data showing there were four times as many heart attacks in the treatment group in the Pfizer 6-month trial report. This wasn't bad luck as VAERS showed heart attacks happen 71 times more often following these vaccines compared to any other vaccine. Kirsch stated, "If the net all-cause mortality from the vaccines is negative, then vaccines, boosters and mandates are all nonsensical." He calculated that at least 115,000 people have died from the COVID shots. He quoted the data for 90+ year olds coming from Israel. They went from 94.4% vaccinated to 82.9% vaccinated in just 4 months.  If you read between the lines, that means at least 50% of the vaccinated people died while 0% of the unvaccinated people died. That statistic alone means they should not approve the booster.  

Later in the day, an unscheduled second vote was called for by the FDA. This time, the VRBPAC was told to consider "the totality of scientific evidence available," not just Pfizer's booster dose clinical trial. And to consider just those over age 65, health care workers, and others deemed high risk. So, the FDA bowed to the pressure and declared the Pfizer shot safe and effective enough to warrant a third booster for certain groups. The politically appointed CDC director overruled the first vote by the VRBPAC a few days later (September 24, 2021). No science justified her actions. She just did it because she had the power to do it. No one is allowed to stop this train until everyone is forced to be vaccinated. "Follow the science" is their mantra and no other science is permitted except that which supports the politically correct narrative. Not only are the unvaccinated being targeted but children are also. It won't stop until parents rise up and say, "Not me and NOT MY CHILD."