Tag Archives: FDA deception

DEBORAH BIRX UNMASKED – I BET YOU DON’T KNOW THIS ABOUT THE SCARF LADY

Birx is a pivotal member of the Medical Mafia – here are some stories you might not know about the evil scarf lady. Can you support this channel with a financial gift? Visit my website: https://amazingpolly.net/contact-support.php Birx now says she knew all along that the Covid vaccines wouldn’t work and admitted to subverting the US government (and tricking the world!) in multiple ways while on the COVID-19 Task Force.

Dr. Deborah Birx reveals LIVE who is running the CORONA HOAX

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​Healthcare workers win $10.3 million in lawsuit after being fired for refusing Covid vaccine

​Healthcare workers win $10.3 million in lawsuit after being fired for refusing Covid vaccine

FULL STORY: https://fightingthecommies.com/GCR

Unprecedented jab class action lawsuit awards over 500 healthcare workers 10 million and their jobs back.

https://www.redvoicemedia.com/2022/07/unprecedented-jab-class-action-lawsuit-awards-over-500-healthcare-workers-10-million-and-their-jobs-back/ref/6/

Source:

https://lc.org/newsroom/details/080122-class-action-settlement-over-shot-mandate-is-a-wakeup-call

https://lc.org/newsroom/details/072922-health-care-workers-settle-covid-shot-mandate-for-dollar103-million

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Deborah Birx Should be ARRESTED AND HUNG

Deborah Birx should be indicted for premeditated mass genocide, brought before a citizen tribunal and tried, and if convicted, hung.

Dr. Deborah Birx admits she deceived Trump to push COVID measures

She also told us WHO (GATES) was running the CORONA HOAX. Yes, it is a HOAX.

Dr. Deborah Birx reveals LIVE who is running the CORONA HOAX

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FDA’s Advisory Committee Ignores Member’s Conflict of Interest and Allows Him to Attend Meetings and Vote

On June 14-15, 2022, the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) convened and voted to recommend an emergency use authorization for both Moderna’s COVID-19 vaccine for children ages 6 months to 17 years and Pfizer’s COVID-19 vaccine for children 6 months to 4 years.
After the members introduce themselves, one of the first things done at these VRBPAC meetings is the reading of VRBPAC’s Conflict of Interest Statement which includes a statement that the “FDA has determined that all members of this advisory committee, both regular and temporary members, are in compliance with federal ethics and conflicts of interest law.”
During the reading of the Conflict of Interest Statement on June 14, it was noted that one temporary voting member, Dr. James Hildreth, had received a waiver allowing him to participate in the VRBPAC meeting. In his Acknowledgement of Financial Interests form, Dr. Hildreth disclosed that both he and his employer had financial interests that could be affected by the matter he was planning to voting on at VRBPAC.
Namely, Dr. Hildreth’s employer, Meharry Medical College, is a COVID-19 vaccine trial site and expected to receive between $1.5 million to $2 million for conducting that trial. Additionally, Meharry Medical College enrolled participants in the trials for the very product that was being considered by him at VRBPAC – Moderna’s pediatric COVID-19 trials – for which it was to receive $400,000 – $600,000. Finally, Dr. Hildreth disclosed that he would personally make up to $5,000 for enrolling participants in one of those trials.
ICAN, through its attorneys, demanded that VRBPAC immediately remove Dr. Hildreth as a temporary voting member, bar him from participating the following day, and discard his vote from that day’s meeting. Regardless of Dr. Hildreth’s experience or expertise, it was completely inappropriate for VRBPAC to proceed with Dr. Hildreth’s participation given the nature of these conflicts of interest.
VRBPAC instead, unbelievably, recited the very same Conflict of Interest Statement the next day, assuring the public that “all members” of VRBPAC “are in compliance with federal ethics and conflicts of interest laws.” Not surprisingly, Dr. Hildreth voted “yes” to all three products being considered, two of which were Moderna pediatric vaccines.
ICAN will continue to build the record and case against the improper actions by our federal “health” agencies so that they cannot claim ignorance when judgment day arrives.

To share this legal update, please use this link: https://www.icandecide.org/ican_press/fdas-advisory-committee-ignores-members-conflict-of-interest-and-allows-him-to-attend-meetings-and-vote/ 

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CDC Director Violates FDA’s Emergency Use Authorizations and Posts Misinformation about COVID-19 Vaccines

While Twitter has suspended and permanently blocked numerous individuals for posting so-called “misinformation” concerning COVID-19 vaccines, it has not done so to “health” authorities – those who arguably should be held to an even higher standard – when they blatantly share inaccurate information.
On June 18, 2022, CDC Director Rochelle Walensky posted a tweet with a video of herself discussing the CDC’s recent recommendation of the COVID-19 shots for children under 5. In the video, Dr. Walensky made the following two claims:
  • “We now know based on rigorous scientific review that the vaccines available here in the United States can be used safely and effectively in children under 5.”
  • “We have taken another important step together on our fight against COVID-19 by making safe and effective vaccines available for our little ones.”
But as Dr. Walensky should certainly be aware, in issuing Emergency Use Authorizations (EUAs), the FDA has not (under its ridiculously low standards) made a finding that these vaccines are “safe and effective.” Instead, the grant of an EUA means only that the FDA has determined “it is reasonable to believe that [each vaccine] may be effective” and that “it is reasonable to conclude, based on the totality of scientific evidence available, that the known and potential benefits of [each vaccine] outweigh the known and potential risks of the vaccine.”

By claiming – two separate times – that these vaccines are “safe and effective,” Dr. Walensky is misleading the public by suggesting these vaccines have met the legal standard required for licensure.

Worse yet, because her tweet is “descriptive printed matter” that is both advertising and promoting Pfizer’s and Moderna’s vaccines, the tweet itself is in violation of both EUAs issued to these companies because it does not “clearly and conspicuously” contain the required disclaimer that these products have not yet been licensed as safe and effective by the FDA.

ICAN, through its attorneys, has sent Dr. Walensky a formal letter demanding that she immediately remove the misleading tweet and we will keep you posted on the CDC’s response.

To share this legal update, please use this link: https://www.icandecide.org/ican_press/cdc-director-violates-fdas-emergency-use-authorizations-and-posts-misinformation-about-covid-19-vaccines/

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DOD and Pfizer Sending Fake Comirnaty Vials to Coast Guard

Dr. Jane Blows open the DOD’s dirty tricks being played on our military as they shuffle and race to ship out Pfizer Biontech EUA vials of God knows what, and slapping on labels with conflicting temperature instructions, untraceable manufacturing origination sites, and made up LOT numbers, many of these vials are showing up at military bases with their internal temperature alarms having gone off, and they’re being told by Ft. Detrick personnel to “just change the expiration dates” randomly.
And in the Natural Health Series, Bee Pollen – what is it and how can it help you remain medically independent and healthy without traditional medicine; and the show concludes with a recap of 3 embalmers – out of many that are pulling never before seen clots out of the jabbed – first seen on the Dr. Jane Ruby show in February.

Pfizer Fraud Exposed: Vaccine Advisory Committee Lied To Get FDA Approval For Babies

REP. JIM JORDAN EXPOSES THE BIDEN ADMIN’S LIES ON VACCINE EFFICACY

23/6/2022 – Watch as Rep. Jim Jordan exposes the Biden Admin’s lies on vaccine efficacy, as Deborah Birx testimony throws a monkey wrench into the narrative.

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YOU DID NOTHING: TRUTH BOMB ON FDA

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COVID-19 Vaccine Manufacturers Fail to Properly Investigate Adverse Events Reports

Vaccine manufacturers, like the rest of the public, must submit a FOIA to the FDA to obtain additional information regarding serious adverse events, including deaths, submitted to VAERS. The problem: they are not doing it.
 
At the CDC’s Advisory Committee on Immunization Practices (ACIP) meeting in April 2021, Janssen’s Chief Medical Officer gave a presentation regarding the safety of its J&J COVID-19 vaccine. During his presentation, he indicated that pharma companies, like the public, only gain access to VAERS reports each Friday when they are released, and that, because “there is significant redaction of some of the data fields,” “it is not possible for [vaccine manufacturers] to follow-up for further information,” except that they “can attempt to do so through Freedom of Information [Act] applications.” Implying this was a common practice, Dr. Maree stated that the “FDA has been very supportive in helping [them] try to expedite these requests.”

ICAN set out to determine if vaccine manufacturers were, in fact, investigating VAERS reports of serious injuries by making FOIA requests to the FDA. Through its attorneys, ICAN requested that  the FDA provide copies of all FOIA requests submitted by ModernaJohnson & Johnson, and Pfizer since the inception of the companies’ COVID-19 vaccines.

For those familiar with these companies’ history, the results will not be all that surprising. Based on the FDA’s response so far, two of the three vaccine manufacturers did not submit a single FOIA request to the FDA regarding reports of adverse events to their COVID-19 vaccines.

  • Moderna filed one single FOIA request in April 2021 for a copy of the FDA’s site visit report of its facility in Massachusetts – but not a single FOIA about an adverse event following vaccination.
  • Johnson & Johnson submitted one single FOIA request in July 2021 for the FDA’s risk assessment regarding benzene levels in aerosol sunscreen – but again, not a single FOIA about an adverse event following vaccination.
  • Pfizer submitted only four FOIA requests for VAERS reports related to its COVID-19 vaccine between December 18, 2020 and February 7, 2021, at least three of which were apparently at the FDA’s prompting. Two of Pfizer’s requests related to anaphylaxis and syncope indicated they were in response to an FDA “query,” that specifically told Pfizer it “may request a copy of redacted VAERS report[s] via FOIA.”  Pfizer has not filed a single FOIA request since February 2021, nor has it filed any requests related to any other adverse event following vaccination, including myocarditis.
Unfortunately, as the experiences of many vaccine-injured individuals have proven, these companies do not appear to be adhering to their claims of taking adverse events to their products seriously. ICAN, however, does and we will continue to hold these companies accountable.

To share this legal update, please use this link: https://www.icandecide.org/ican_press/covid-19-vaccine-manufacturers-fail-to-properly-investigate-adverse-events-reports/

Source: https://www.icandecide.org

The Marburg pathogen: It will be the excuse used to force the unvaxxed into quarantine camps (FEMA) where kill-shots will be administered.

Todd Callender joined the The Prather Point to discuss the next Plandemic (the Marburg pathogen_. It will be the excuse used to force the unvaxxed into quarantine camps (FEMA) where kill-shots will be administered. — https://www.bitchute.com/video/4ajhXs6ykjhs/

Todd Callender joins the The Prather Point to discuss the next PLANdemic (the Marburg pathogen), which will be the excuse used to force the unvaxxed into quarantine camps (FEMA) where kill-shots will be administered.

He also says that those who received the Covid shots already have the dormant Marburg virus encapsulated in lipid nanoparticles, which can be activated via 5G frequencies. Those who have Marburg will then become zombie-like, because it affects frontal cortex brain function.

Coming Marburg, 5G & Mind Control – Maria Zeee w/ Todd Callendar and Dr. Peter Chambers (48:23)
https://www.bitchute.com/video/3GGXZS3uvz2t/

Nov. 28, 2021 Swiss Referendum – NO to Green Pass – Marburg Virus is the Next Planned Pandemic (52:18)
https://www.bitchute.com/video/Z8QN90S8DZa5/

Source: AgentOfChange

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This is a serial killer

This is a serial killer

She KNOWS what she’s doing, that’s the scary part of it

Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for “fair use” for purposes such as criticism, comment, news reporting, teaching, scholarship, and research. Fair use is a use permitted by copyright statute that might otherwise be infringing. Non-profit, educational or personal use tips the balance in favor of fair use.