Coronavirus

[Dachsie]

https://blog.nomorefakenews.com/2021...-transparency/

Breaking: FDA to give full approval to COVID vaccines; no public hearing; no transparency; no open review of vaccine data
Aug
23

by Jon Rappoport

It’s all happening behind closed doors

by Jon Rappoport

August 23, 2021

(To join our email list, click here.)

The fix is in.

We’re racing from “emergency use authorization” of experimental vaccines to “full approval.” Boom.

Despite the promise of “transparency” prior to giving full approval to the COVID vaccines, the FDA is set to give its final green light today, or later this week. It’s a slam-dunk.

And there is NO public hearing.

This means the vaccine marketing/intimidation/mandate campaigns will ramp up much higher. “Well, now there is NO reason for anyone to refuse the shot. The FDA states it is completely safe and effective.”

Obviously, the FDA didn’t want to allow even mainstream “experts” to speak in a public hearing before approval; the agency is running a very tight ship. No slip-ups. No defections.

An 8/20 article in the BMJ (“Covid-19: FDA set to grant full approval to Pfizer vaccine without public discussion of data”) quotes a few of these dissenting mainstream pros. For example:

“Kim Witczak, a drug safety advocate who serves as a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee, said the decision removed an important mechanism for scrutinising the data.”

“’These [FDA] public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightning speed under emergency use authorisation,’ she said. ‘The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems tackled, and data scrutinised in advance of an approval’.”

“Witczak is one of the more than 30 signatories of a citizen petition calling on the FDA to refrain from fully approving any covid-19 vaccine this year to gather more data. She warned that without a [public FDA] meeting ‘we have no idea what the data looks like’.”

“’It is already concerning that full approval is being based on 6 months’ worth of data despite the clinical trials designed for two years,’ she said. ‘There is no control group after Pfizer offered the product to placebo participants before the trials were completed’.”

“’Full approval of covid-19 vaccines must be done in an open public forum for all to see. It could set a precedent of lowered standards for future vaccine approvals’.”

Understand—this devastating criticism of the FDA is coming from a person who operates WITHIN the public-health establishment.

Amidst a tsunami of reports of vaccine injuries and deaths from around the world, the FDA is proving it is an agency that will certify maiming and killing without hesitation.

[monty]

Just prior to posting his announcement that FDA approved the poison Jon Rappoport posted a link to this video

Yes, Trump did tell RFK Jr. to investigate vaccine dangers—and why it matters

Aug23by Jon Rappoport
by Jon Rappoport
August 23, 2021


Exerpt from Jon Rappoport

In this explosive 12 minute Theo Von video interview with Robert Kennedy Jr., we get details of the 2016 Trump-Kennedy meeting, at which Trump gave Kennedy the go-ahead to investigate vaccine dangers.

This isn’t simply “setting the record straight” on what went down. The latest official figures on autism? 1 in 54 American children are autistic. So we are talking about the MASSIVE destruction of life, and the ongoing internal destruction of the country.


Investigating and detailing the role vaccines play in this horrific reality should be the highest priority.


Robert Kennedy, in the video interview, explains that shortly after Trump was elected in November of 2016, the new president contacted him (Kennedy) and invited him for a meeting at Trump Tower in New York.


During the two-hour sit-down with Trump, Kennedy explained that a comprehensive investigation of vaccines could be done without any heavy lifting by government. There was a well-known Vaccine Safety Datalink which, when opened, would give independent researchers access to a vast trove of US medical records. From those records, a convincing case could be made about vaccine safety/dangers.


Trump gave Kennedy the green light to move ahead.


However, roadblocks then appeared.

[Dachsie]

Rappaport's annoncement spoke in future tense -- "FDA to give full approval" so it's not a done deal yet. Wait for official announcement.

We have a full communist breakdown of every societal institution and all we are given is lies, lies, and more lies.

[Dachsie]

Notice how the FDA gives favored sanction to only the Pfizer killshot.

Here is the Associated Press announcement

https://apnews.com/article/coronavir...a08a7cc0683a72

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https://apnews.com/article/coronavir...a08a7cc0683a72
Click to copy
US regulators give full approval to Pfizer COVID-19 vaccine
By LAURAN NEERGAARD and MATTHEW PERRONE17 minutes ago


WASHINGTON (AP) — The U.S. gave full approval to Pfizer’s COVID-19 vaccine Monday, a milestone that could lift public confidence in the shots and spur more companies, universities and local governments to make vaccinations mandatory.

The formula made by Pfizer and its German partner BioNTech now carries the strongest endorsement from the Food and Drug Administration, which has never before had so much evidence to judge a shot’s safety.

More than 200 million Pfizer doses have been administered in the U.S. — and hundreds of millions more worldwide — since December. But up to now, they were dispensed in this country under what is known as emergency use authorization from the FDA.
________________

Here is the WeThePatriots.org email announcement but I am having problems getting their website link on this.


BREAKING: FDA GIVES FULL APPROVAL TO EXPERIMENTAL PFIZER SHOT
As expected, this morning the Food and Drug Administration (FDA) gave full approval to the experimental Pfizer COVID-19 injection for individuals 16 years of age and older. Despite thousands upon thousands of reports from all over the world of serious adverse effects, the puppet agency turned a blind eye and pushed full steam ahead to full approval, which was always its intent from the start.

With this news, employers and colleges all across the nation are emboldened to mandate the jab for workers and students respectively, and they will likely dig in their heels when reviewing exemption requests. As reported by the Associated Press today:

“Mandating becomes much easier when you have full approval,” said Dr. Carlos del Rio of Emory University. “I think a lot of businesses have been waiting for it.”

This opens the door not only for mandates at work and school, but for widespread mandates for travel, entertainment, shopping, and even food access. WE HAVE TO STOP THIS NOW. We have a talented network of attorneys across the country, and our goal is to file lawsuits in every Circuit in the nation. The only thing holding us back at this point is funding. This has all happened so fast, and already the amount of legal work we have has far outpaced our financial support. Please consider a monthly donation today (we are a 501(c)(3) nonprofit organization, so for most donors gifts are tax-deductible). While we appreciate any kind of gift, monthly donations allow us to have a predictable stream of income so we know just how much we can take on. Without that, we are basically flying by the seat of our pants from month to month, which is a recipe for disaster.

Please forward this email to everyone you know who doesn't want to live in a world where your ability to obtain an education, earn a living, or even buy food for your family is conditioned on your submission to a medical dictate by the government or a corporation. Thank you in advance for your generosity.

[EE_]

Approved but still in trial until 2023. A lot of working people are fucked!

Study Type : Interventional (Clinical Trial)
Estimated Enrollment : 43998 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Prevention
Official Title: A PHASE 1/2/3, PLACEBO-CONTROLLED, RANDOMIZED, OBSERVER-BLIND, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, IMMUNOGENICITY, AND EFFICACY OF SARS-COV-2 RNA VACCINE CANDIDATES AGAINST COVID-19 IN HEALTHY INDIVIDUALS
Actual Study Start Date : April 29, 2020
Estimated Primary Completion Date : May 2, 2023
Estimated Study Completion Date : May 2, 2023

https://clinicaltrials.gov/ct2/show/NCT04368728

[Dachsie]

Know what this approval means,.

This opens the door not only for mandates at work and school, but for widespread mandates for travel, entertainment, shopping, and even food access. WE HAVE TO STOP THIS NOW.

[EE_]

Know what this approval means,.

This opens the door not only for mandates at work and school, but for widespread mandates for travel, entertainment, shopping, and even food access. WE HAVE TO STOP THIS NOW.

Once you submit to tyranny, there is no stopping what they will do to you. How long before these tyrants come for your guns?
They will claim there is an epidemic of gun violence in the US and you will have to register your firearms for the good of the country.
Registration is the last step before confiscation

[Dachsie]

Once you submit to tyranny, there is no stopping what they will do to you. How long before these tyrants come for your guns?
They will claim there is an epidemic of gun violence in the US and you will have to register your firearms for the good of the country.

Exactly. The continual cycle of problem-reaction-solution is now in full force.

Beware the Needle Nazis

They are hoping for a revolution in the streets as that will really expedite their program.

[monty]

This letter to Pfizer from FDA says it is an extension of the EUA agreement

https://t.me/silverreportforum/12166

FDA APPROVAL WAS JUST AN INDEFINITE EXTENSION OF EMERGENCY USE AUTHORIZATION (EUA) AND IS BASED ON 3 LIES


Denise M. Hinton, Chief Scientist at the FDA signed this letter (https://www.fda.gov/media/150386/download), not granting full approval, but extending emergency use authorization "indefinitely." If you read the letter, these were her reasons:
▪️A. SARS-CoV-2 can cause a serious or life-threatening disease or condition, including severe respiratory illness, to humans infected by this virus; [ Primarily in those with co-morbities (https://t.me/westcoastintel/12668) ]

▪️B. Based on the totality of scientific evidence available to FDA, it is "REASONABLE TO BELIEVE" that the Pfizer (jab) MAY BE effective in preventing COVID-19, and that, when use d under the conditions described in this authorization, the known and potential benefits outweigh its known and potential risks; and [ WRONG (https://t.me/westcoastintel/13355) ]

▪️C. There is no adequate, approved, and available alternative to the emergency use of Pfizer [ LIES (https://t.me/rockymountain_intel/4598) ]


On the last page it reads:
This EUA will be effective until the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic is terminated under Section 564(b)(2) of the Act or the EUA is revoked under Section 564(g) of the Act.

[Dachsie]

This letter to Pfizer from FDA says it is an extension of the EUA agreement

https://t.me/silverreportforum/12166

FDA APPROVAL WAS JUST AN INDEFINITE EXTENSION OF EMERGENCY USE AUTHORIZATION (EUA) AND IS BASED ON 3 LIES


Denise M. Hinton, Chief Scientist at the FDA signed this letter (https://www.fda.gov/media/150386/download), not granting full approval, but extending emergency use authorization "indefinitely." If you read the letter, these were her reasons:
▪️A. SARS-CoV-2 can cause a serious or life-threatening disease or condition, including severe respiratory illness, to humans infected by this virus; [ Primarily in those with co-morbities (https://t.me/westcoastintel/12668) ]

▪️B. Based on the totality of scientific evidence available to FDA, it is "REASONABLE TO BELIEVE" that the Pfizer (jab) MAY BE effective in preventing COVID-19, and that, when use d under the conditions described in this authorization, the known and potential benefits outweigh its known and potential risks; and [ WRONG (https://t.me/westcoastintel/13355) ]

▪️C. There is no adequate, approved, and available alternative to the emergency use of Pfizer [ LIES (https://t.me/rockymountain_intel/4598) ]


On the last page it reads:
This EUA will be effective until the declaration that circumstances exist justifying the authorization of the emergency use of drugs and biological products during the COVID-19 pandemic is terminated under Section 564(b)(2) of the Act or the EUA is revoked under Section 564(g) of the Act.

I have to wonder whats in it for Pfizer and the FDA to keep the EUA in extended indefinite "limbo" status.

The first thing that comes to my mind is that if they remove EUA status they no longer have total immunity from liability if something goes wrong with their vaccines.

And the phony government program to reimburse victims of the vaccine if it can be proven that they sustained serious injury from the vaccine. That phony program has paid almost nothing out to all the many victims of various vaccines over the last several years. So removing EUA stus to full-approval status would no doubt result in many cases against this government vaccine injury compensation progam.

But probably another idea to consider is that the FDA's decision to leave the vaccine in EUA status is part of their sophisticated long-term plan on how to play out the fake plandemicc to their benefit and objectives.

They do not appear to be primarily after dollars but they do appear to want to kill people for worldwide population reduction and control.