December 10, 2020 (LifeSiteNews) — An FDA advisory panel voted 17-4 today to recommend emergency use authorization (EUA) of the Pfizer-BioNTech COVID-19 vaccine, favoring the opinion that its benefits “outweigh its risks for use in individuals 16 years of age and older.”
Diana Zuckerman, Ph.D, president of the National Center for Health Research, stressed during the panel meeting that “the EUA is not approval, and it should have more restrictions than you’d have for approval.” The EUA, which would allow select groups of people to take the Pfizer vaccine before a months-long full approval process, is completed.
“We need long-term data to fully understand if the benefits outweigh the risks for frail patients, and for all races and ethnicities, and for all patients,” said Zuckerman.
Rossi Hassad, a professor at Mercy College with expertise in epidemiology, acknowledged that during Pfizer vaccine trials “there were frequent mild and moderate adverse effects, which are recognized as common side effects of vaccines.”
“Ongoing monitoring of this vaccine is imperative,” Hassad noted.
On Wednesday, the NHS medical director in England advised that “people with a significant history of allergic reactions do not receive this vaccination after two people with a history of significant allergic reactions responded adversely” to the Pfizer-BioNTech vaccine.
Pfizer is notable for being one of several vaccine producers that Robert F. Kennedy, the nephew of John F. Kennedy and an environmental attorney, called “convicted serial felon(s)” during a July debate with Alan Dershowitz.
“In the past 10 years, just in the last decade, those companies have paid $35 billion in criminal penalties, damages, fines, for lying to doctors, for defrauding science, for falsifying science, for killing hundreds of thousands of Americans knowingly,” Kennedy said.
In January 2020, a class-action lawsuit was filed “accusing Pfizer of hiding the fact that Zantac contains a carcinogen,” reported Becker’s Hospital Review.
In 2009, Pfizer Inc. paid $2.3 billion, “the largest health care fraud settlement in the history of the Department of Justice,” according to the DOJ, for illegally promoting drugs for off-label use or at unapproved dosages.
According to the U.K.’s Independent, Pfizer, the owner of the COVID-19 mRNA vaccine BNT162b2, has been given indemnity in the United Kingdom, which means that people who suffer damage from the vaccine will not be able to sue the company.
U.K. government-provided safety instructions for the Pfizer COVID-19 vaccine state that there is “no or limited data” on the vaccine regarding fertility, pregnancy and lactation, and “it is unknown whether COVID-19 mRNA Vaccine BNT162b2 has an impact on fertility.”
The guide advises that women avoid pregnancy before vaccination and “for at least two months after their second dose.” The guide also specifies that the vaccine “should not be used during breast-feeding,” because “a risk to the newborns/infants cannot be excluded.”
The guide also noted that side effects were commonly experienced by the vaccine trial volunteers, including chills experienced by over 30 percent, headache (over 50 percent), and fatigue (over 60 percent). According to the Daily Mail, one of the participants in Pfizer’s vaccine trial “said she suffered a headache, fever and aches all over her body that became ‘more severe’ after the second dose.”
Pfzier’s vaccine must be stored at -70°C (-94°F) – nearly twice as cold as the North Pole’s average temperature in the winter, and “20 degrees colder than extreme winter temperatures at the South Pole,” as CBS News has noted.
This is because, as Fast Company reminded readers, the Pfizer vaccine will be the first-ever vaccine to use “an as-yet-unproven technology platform that relies on something called messenger RNA, usually shortened to mRNA.”
According to Margaret Liu, a vaccine researcher who chairs the board of the International Society for Vaccines, the reason the Pfizer vaccines needs to be kept at such an extremely cold temperature is because mRNA is “really easily destroyed,” NPR reported.
The mRNA vaccine works by injecting mRNA, which is a kind of “blueprint” for proteins that triggers cells to produce their own protein antibodies to block and destroy the virus so the person will not become infected.
Pfizer is one of 15 companies that has partnered with the Bill & Melinda Gates Foundation to “to accelerate the development” of “treatments for COVID-19.” The Bill & Melinda Gates Foundation also provides funding to Pfizer for its injectable contraceptive product “Sayana.”
“We’ve never created a new vaccine in less than five years,” Bill Gates said while explaining how the RNA vaccine works. “So this is urgent. It’s gonna have to go to seven billion people,” he said.
PETITION UPDATE (12/16/2020) -
Operation Warp Speed—the HHS’s program to accelerate the development, manufacture, and distribution of COVID-19 therapeutics—has spent billions of our tax dollars to bring a COVID vaccine to market.
Now, the FDA has granted emergency approval to roll out the Pfizer/BioNTech vaccine, and people in the UK and the US are already receiving it.
Though the Pfizer vaccine was not designed or produced using aborted fetal cells, it was tested using the HEK293 fetal cell line to create humanized mice.
And, more unethical vaccines are reaching the finish line and are being funded and promoted by the HHS with our tax dollars.
We must continue to demand that this stop and that a fully ethical vaccine be brought to market instead!
SIGN and SHARE our petition with the Personhood Alliance to demand that the HHS stop using our money to support the grisly connection between abortion and biomedical science.
Operation Warp Speed—the HHS’s program to accelerate the development, manufacture, and distribution of COVID-19 therapeutics—is spending billions of our tax dollars to bring a COVID vaccine to market as quickly as possible.
Now, two of the Operation Warp Speed vaccines (one created by Pfizer/BioNTech and one created by Moderna/NIH) are nearing the finish line, soon to be applying for emergency FDA approval for mass distribution.
And, while LifeSite neither advocates for or against voluntary vaccination, there are several apparent problems with the vaccines being fast-tracked by HHS’ Operation Warp Speed.
First among the vaccines’ major problems: they were tested using aborted fetal cells.
Please SIGN and SHARE LifeSite’s urgent petition with the Personhood Alliance to demand that the HHS stop funding and promoting this unethical practice, and bring a fully ethical vaccine to market instead.
The production and testing of vaccines that use the remains of aborted children, regardless of when they were killed and at what point they were used in the process, is morally unacceptable and must be consistently opposed by the whole pro-life movement.
And, although the Pfizer and Moderna vaccines were not designed or produced using aborted fetal cells, the Personhood Alliance recently reported that the vaccines’ testing phases used the HEK293 aborted fetal cell line to create humanized mice.
This stomach-churning practice transferred immortalized cells from a child killed in 1973 into mouse embryos, so that when the mice were born, they had tiny human lungs that researchers infected with COVID to test the vaccines.
This type of Frankenscience has no place in a civilized society, certainly not one whose citizens are forced to fund it!
Sign our petition with the Personhood Alliance to demand that the HHS stop supporting the grisly connection between abortion and biomedical science.
We can make a difference if we raise our voices together, but we’re running out of time!
Thank you for SIGNING and SHARING this urgent petition today!
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