By Nancy Thorner -
The Pfizer vaccine that was fully approved by the USA, FDA on Monday, August 23, 2021 now has a new name, Comirnaty COVID-19 Vaccine (BioNTech – Pfizer BNT162b2). It has an ingredient called BNT162b2 and reports that it is an "experimental mRNA vaccine"… intended to prevent COVID-19 in humans aged 12-85 [FDA literature says age 16-85].
COMIRNATY is also an mRNA (messenger ribonucleic acid) vaccine. It has a warning "Do not administer Pfizer-BioNTech, Germany COVID-19 Vaccine to individuals with a known history of a severe allergic reaction (e.g., anaphylaxis)."
- mRNA lipids((4-hydroxybutyl)azanediyl)bis(hexane 6,1-diyl)bis(2-hexyldecanoate),
- 2 [(polyethylene glycol)-2000]-N,
- N ditetradecylacetamide,
- 1,2-Distearoyl-sn-glycero-3-phosphocholine, and cholesterol),
- potassium chloride,'monobasic potassium phosphate,sodium chloride
- dibasic sodium
- phosphate dihydrate,
- and sucrose.
Check out the two links below:
Pfizer-BioNTech COVID-19 Vaccine EUA Fact Sheet for Recipients and Caregivers (fda.gov)
Package Insert – COMIRNATY (fda.gov) New Phizer name for Covid – MRNA vaccine
Wisconsin U.S. Senator Ron Johnson questions expedited approval of Covid vaccines
In a press release on Sunday, August 22, 2021, U.S. Sen. Ron Johnson (R-Wis.) sent a letter to Dr. Francis Collins, Director of the National Institutes of Health (NIH), Dr. Rochelle P. Walensky, Director of Centers for Disease Control and Prevention (CDC), and Dr. Janet Woodcock, Acting Commissioner of the Food and Drug Administration (FDA) on the FDA’s decision not to hold a formal advisory committee meeting to discuss Pfizer’s application for full approval of its Covid-19 vaccine.
“I see no need to rush the FDA approval process for any of the three Covid-19 vaccines,” the senator wrote. “Expediting the process appears to only serve the political purpose of imposing and enforcing vaccine mandates. The observational phases of FDA approval take time, because there is no substitute for time in detecting and determining possible long-term harm. Additionally, we are already experiencing a severe health care worker shortage. Frontline doctors and nurses that are contacting me are expressing grave concerns about vaccine mandates which will only exacerbate the shortage.”
“Over the last year and a half, the decisions of federal health agencies have dramatically affected the lives of all Americans. The impact of these decisions has been felt in Americans’ treatment options, employment, schools, housing and travel, and in countless other ways. The human toll of the social restrictions and economic devastation is incalculable. Unfortunately, your federal health agencies have not been transparent with the American people about how these life altering decisions have been made or what science and data they are based upon. I urge you to provide the information I have requested in my previous letters and to reconsider your decision not to assemble a VRBPAC public meeting prior to the granting of any to assemble a VRBPAC public meeting prior to the granting of any final Covid-19 vaccine approval.”
The full text of the letter can be found here.
Why the rush for FDA approval?
As posted on Natural News on August 23, 2021 by Mike Adams:
“The insane, fraudulent rushing of the Pfizer vaccine into “full approval” status by the FDA — just announced today — was ordered by the collapsing Biden regime. The purpose of this accelerated approval is to allow Biden’s puppet masters to roll out medical martial law as a means to control the population and suppress the massive uprising that will soon commence against the illegitimate Biden regime.”
But do you really think amoral, money-grubbing big biz/ big tech didn’t collude with the revolving door FDA/Big Pharma camora?
The Defender has a great take on the corruption and scam the fake FDA approval is here. Following is a brief snippet from the article: "Between 2000 and 2010, pharmaceutical companies paid the FDA $3.4 billion to gain rapid drug approvals. Today, Pharma companies underwrite three-quarters of FDA’s budget for scientific reviews (ProPublica) and fund nearly 50% of the FDA’s total annual budget through PDUFA fees. In exchange, the agency increasingly fast-tracks expensive drugs and vaccines with significant side effects and unproven health benefits . No one at FDA wins kudos for slowing down those money flows. To the contrary, according to FDA’s own employees, drug company payments bias regulators, with “an inclination toward approval.”
Despite the fact that the vaccinated people can still contract the virus, and despite the fact that the original safety trials aren’t scheduled to be completed until 2023, according to The Washington Post this vaccine approval was the fastest in FDA history, coming less than four months after Pfizer/BioNTech filed for licensing in May. The FDA has zero long-term data in hand, while emerging short-term data shows the COVID-19 jab is deadly, and by the FDA’s own flawed counting system actually increasing COVID-19 cases.”
This is at the same time as Pfizer is expanding its recall of anti-smoking drug Chantix after testing found high levels of carcinogenic material in the pill. The leading prescription for smoking secession, Chantix is prescribed to over half a million people each year and accounts for $1.1 BILLION in revenue for Pfizer each year.
Until today the fastest approval for a vaccine ever took 5 years – which was for Ebola, that kills ~50% of its victim. By contrast, we have around just six months of safety data for the Covid shot until approval, and the survival rate is 99.997 if you are under 21, and not far below that even up to age 70. Yes, we do need to be careful of those with serious co-morbidities and elderly.
It’s all the more surprising that Pfizer received approval by the FDA on Monday, August 23, 2021, as it was reported on August 6, 2021:
“The Moderna and Pfizer vaccine tests were conducted, as customary, with a control group; a group within the trial who were given a placebo and not the test vaccine. However, during the trial -and after the untested vaccines were given emergency use authorization- the vaccine companies conducting the trial decided to break protocol and notify the control group they were not vaccinated. Almost all the control group were then given the vaccine."
“Purposefully dissolving the placebo group violates the scientific purpose to test whether the vaccine has any efficacy; any actual benefit and/or safety issues. Without a control group there is nothing to compare the vaccinated group against. According to NPR, the doctors lost the control group in the Johnson County Clinicial Trial (Lexena, Kansas) on purpose."
Fully vaccinated in Israel account for 85-90% of all new hospitalizations
As both Gateway Pundit reported, and Israel’s Channel 13 News, “According to Dr. Haviv, the vaccinated account for 85-90% of all new hospitalizations and 95% of “severe” cases at the Herzog Medical Center in Jerusalem.
"…According to their health officials, the majority of Israelis have been fully vaccinated, including 85% of those who are eligible. Out of the estimated 9.3 million citizens, 5.8 million have received at least one shot and 5.4 million are fully vaccinated."
Interestingly, the same week the news about Israel came out, it was also announced that 40% of migrants bused in through Texas test positive for COVID-19 (of those they actually did test.) So, no worries for the Delta if you are an illegal. They’ll put you on a plane then, too, to fly you somewhere to boot…if not on a bus to towns across the U.S.
