Secret CDC Reports confirm 535k American Children & Young Adults have died since the FDA approved the COVID-19 Vaccine, resulting in a shocking 50% increase in Excess Deaths

BY THE EXPOSÉ ON MARCH 5, 2023 • ( 10 COMMENTS ) A shocking report secretly released by the U.S. Centers for Disease Control (CDC) has revealed that COVID-19 vaccines, touted as the solution to the alleged SARS-CoV-2 virus, may actually be causing more harm than good to children and young adults in the United States. Let’s not lose touch…Your Government and

The greatest perpetrator of misinformation during the pandemic has been the United States government

Posted By Tim HainsOn Date March 1, 2023 Johns Hopkins University professor Dr. Marty Makary told the House Select Subcommittee on the Coronavirus Pandemic during its first hearing on Tuesday “the greatest perpetrator of misinformation during the pandemic has been the United States government” and listed multiple examples. DR. MARTY MAKARY: The greatest perpetrator of

It’s Time for the Scientific Community to Admit We Were Wrong About COVID and It Cost Lives

KEVIN BASS , MS MD/PHD STUDENT, MEDICAL SCHOOLON 1/30/23 AT 8:00 AM EST As a medical student and researcher, I staunchly supported the efforts of the public health authorities when it came to COVID-19. I believed that the authorities responded to the largest public health crisis of our lives with compassion, diligence, and scientific expertise. I

BREAKING NEWS: U.S. DOCTORS WARN THE WORLD TO STOP TAKING THE COVID VACCINES

December 27th, 2022 Dr. Pierre Kory, Dr. Ryan Cole, Dr. James Thorp, Dr. Peter McCullough – Vaccines are toxic, lethal, ineffective and must be stopped. They damage the brain, heart, liver, bone marrow, fetus, causing all sorts of harm in the body. CDC, FDA misinformation causing death and injury.

“WHAT HAVE WE DONE?” – “THIS IS UNCONSCIONABLE”: DR. PIERRE KORY RIPS APART PAUL OFFIT

January 12th, 2023. Dr. Offit voted in favor of the jab three times: ✅ 6 mo. to 5 yo (6/15/22)✅ 5 to 11 yo (11/26/21)✅ 12 to 15 yo (5/10/21) He admits if 100% of the world is jabbed, C19 would still circulate.

Pediatrician Dr. Renata Moon, MD explains how she came full circle on her views of the mRNA products.

December 28th, 2022 “We have trusted these regulatory agencies – I have, for my entire career, up until now. Something is extremely wrong.”

What I Wish The World Knew

23 dec 2022 When I teach about vaccines I start here: The media and excipient summary gives the list of ingredients. To which I then ask… “Would you let your child drink this concoction if it were on a spoon?” So why then would you let someone inject it into your child when they don’t

The FDA don’t give a f*** about you or your baby.

21 dec 2022 FDA doesn’t regulate what goes into baby lotion. Not that it regulates much else, but they pretend to…There are all kinds of toxic substances in products, even in products for babies and you’re going to trust FDA and governments with injections into your and your loved ones’ bodies?

DR. ROBERT MALONE – MRNA, FDA CRIMINALITY, DEPOPULATION AND WEF AGENDAS

November 24th, 2022  Why Dr. Malone invented key mRNA technologies decades ago – How the tech has been exploited by today’s pharma companies to harm billions – Dr. Malone unloads on FDA criminality and other sensitive topics – Dr. Malone answers false accusations about links to the CIA – How the mRNA tech really works

EXCESS MORTALITY: Over 2400 Americans are DYING each day following vaccine mandates… Ed Dowd unveils alarming, evidence-based data

Wednesday, November 16, 2022 by: Mike AdamsTags: badhealth, badmedicine, CDC, COVID, depopulation, Ed Dows, excess mortality, FDA, immunization, mRNA, pandemic, Plandemic, Vaccine deaths, Vaccine injuries, vaccines This article may contain statements that reflect the opinion of the author Copy URL 23KVIEWS (Natural News) Today we feature an interview with Ed Dowd, author of Unknown Causes: The Epidemic of Sudden Deaths in 2021 & 2022. Ed Dowd, along with his team of analysts,

WHISTLEBLOWER EXPOSES US DOD PLAN TO EXTERMINATE POPULATION

November 5th, 2022 Dear all,If this is new to you, it will COMPLETELY CHANGE YOUR UNDERSTANDING OF WHATS GONE ON.We’re barking up the wrong tree, it seems, in trying to hold the medicines regulators to account. Turns out the whole thing is a US military operation & they alone make all the decisions, legally (because

CDC Pressured FDA to Authorize COVID Boosters Without Clinical Trials

The Centers for Disease Control and Prevention pressured U.S. regulators to clear COVID-19 boosters without clinical trial data, according to emails obtained by Judicial Watch. By  The Epoch Times Link copied Miss a day, miss a lot. Subscribe to The Defender’s Top News of the Day. It’s free. By Zachary Stieber The Centers for Disease Control and

FDA “Approved” Drugs Killed 273 people yesterday!

31 oct 2022 For just about as long as pharmaceutical drugs have existed, so have side effects. Some of these are mild and considered worth the risk. Others are far more dangerous and even lethal.  The worst part? Many times, the manufacturers KNEW that the drugs were dangerous and sold them anyway. And the FDA

Megyn Kelly Interviews RFK, Jr.: How Pfizer Killed the Vaccine Safety Commission + More

10/27/22 In a two-hour conversation last week, Megyn Kelly, a journalist, lawyer and political commentator, and Robert F. Kennedy, Jr., discussed a wide range of topics including censorship and how Pfizer’s $1 million donation to former President Trump killed Trump’s vaccine safety commission. By  Suzanne Burdick, Ph.D. Miss a day, miss a lot. Subscribe to The

DR. PAUL OFFIT SPEAKS OUT AS FDA PANEL MEMBER Benefit of the vaccine?

19 oct 2022

Passing the blue pill “credibility test”

Here are some options to respond to people who claim I’m not credible because I’ve been “debunked” by “respected authorities” such as the authors of hit pieces. Steve Kirsch 4 oct 2022 I received an email recently that read: I sent out your email from yesterday and this is one response: How would you respond?

EXCLUSIVE: FDA Withholding Autopsy Results on People Who Died After Getting COVID-19 Vaccines

By Zachary Stieber September 29, 2022 Updated: September 30, 2022 The U.S. Food and Drug Administration (FDA) is refusing to release the results of autopsies conducted on people who died after getting COVID-19 vaccines. The FDA says it is barred from releasing medical files, but a drug safety advocate says that it could release the autopsies with personal information

I just learned why the Israeli Ministry of Health didn’t share the safety data

After they learned the vaccines were unsafe in March 2022, they said it was simply a manpower/budget issue that they weren’t able to inform the public. I’m serious! Steve Kirsch Sep 16 2022 On Sept 2, 2022, I wrote a long article about the medical corruption in Israel that was first exposed by an intrepid Israeli journalist Yaffa

We’re Coming For Them: “They Will Not Be Able to Hide from the Courts”

“Remember, after Nuremberg, seven physicians swung.” The Vigilant Fox 30 aug 2022 Before we start discussing crimes against humanity, let’s take a trip back in time. The year was 1976 when we saw a nationwide campaign to vaccinate every American against the swine flu. At that time, we had about 220 million Americans, and about

Big Pharma is very very VERY BAD, in terms of CORRUPTION

August 29th, 2022 Big Pharma is “very very VERY BAD..in terms of CORRUPTION..most of the major REGULATORS in western countries are FUNDED by the DRUG INDUSTRY. So the FDA takes about 65% of their money from the DRUG INDUSTRY, the MHRA in this country (UK) 86%” DR. JANE RUBY SHOW YOU CAN’T HIDE MASS GENOCIDE

Drug Co & Doctors: A Story of Corruption

december 2008 Drug Companies & Doctors: A Story of Corruption By Marcia Angell, MD, former Editor in Chief of The New England Journal of Medicine, is a review of three important books that examine corporate-academic liasons that have corrupted the integrity of American medicine. http://www.nybooks.com/articles/22237 Side Effects: A Prosecutor, a Whistleblower, and a Bestselling Antidepressant on

FDA executive exposed saying there’s financial incentives for drug companies to give more vaccines

aug 12 2022

Moderna Clinical Trials Terribly Flawed — and FDA Knew It, Former Pharma Executive Tells RFK, Jr.

08/09/22 There were “terrible flaws” in Moderna’s COVID-19 vaccine clinical trials — and the U.S. Food and Drug Administration knew it, Alexandra (Sasha) Latypova told Robert F. Kennedy, Jr., on a recent episode of “RFK Jr. The Defender Podcast.” By  Rachel Militello Miss a day, miss a lot. Subscribe to The Defender’s Top News of the

Biologically ‘Similar’: They Can Now Insert Anything Into These Injections They Like

July 17, 2022 Dr. Mike Yeadon: “They [FDA] just voted on it last week. There’s no requirement for any safety and efficacy studies in humans from these variant vaccines, which means a drug company’s computer can form any code they damn well like, press alt + print, manufacture a billion doses of something that FDA

Big Pharma Wants to Put an End to Vitamins and Supplements

By Dr. Joseph Mercola Global Research, July 20, 2022 Mercola 19 July 2022 Region: USA Theme: Law and Justice, Science and Medicine All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version). To receive Global Research’s Daily Newsletter (selected articles), click here. Follow us on Instagram and Twitter and

Latest FDA-Pfizer Document Dump: Why Did So Many Participants With ‘Minor’ Adverse Events Withdraw From Trial?

July’s release of U.S. Food and Drug Administration documents pertaining to the Emergency Use Authorization granted to the Pfizer-BioNTech COVID-19 vaccine included reports of a significant number of participants who withdrew from the trials — and the reasons for these withdrawals. By  Michael Nevradakis, Ph.D. Miss a day, miss a lot. Subscribe to The Defender’s Top

“It’s Like a Horror Movie I’m Being Forced to Watch and I Can’t Close My Eyes” – Senior FDA and CDC Officials Speak Out on “Political” Vaccine Decisions

BY WILL JONES 14 JULY 2022 Dr. Marty Makary, Professor at the Johns Hopkins School of Medicine, and Dr. Tracy Beth Høeg, an epidemiologist affiliated with the Florida Department of Health, have written a disturbing piece in Common Sense about the how the U.S. medicine regulatory agencies, the FDA, CDC and NIH, have been captured by a political narrative, leaving

FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal

According to Alexandra Latypova, an ex-pharmaceutical industry executive, documents obtained from the U.S. Department of Health and Human Services on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe. By  Megan Redshaw Miss a day, miss a lot. Subscribe to

Pharmaceutical Expert Says FDA Colluding with Pfizer and Moderna, Not Addressing Alarming Data

TrialSite Staff Staff at TrialSite | Quality Journalism Jun. 30, 2022, 7:30 a.m. Alexandra Latypova (“Sasha”) is a retired pharmaceutical industry executive and entrepreneur. She holds an MBA degree from Dartmouth College and spent approximately 25 years in pharmaceutical research and development. Sasha later co-founded several clinical research organizations working as a contractor for about

MORE JAB SIDE EFFECTS COMING

President of Brazil says Covid infection gives natural immunity and renders injection redundant – and reveals chilling FDA warning News Uncut Jul 4 2022 By Oliver May SEVERAL side effects from the Covid jab are “likely to emerge this year or next year” according to the President of Brazil Jair Bolsonaro. He also said that

Public Health and Medical Professionals for Transparency Pfizer

July 2022 This nonprofit, made up of public health professionals, medical professionals, scientists, and journalists exists solely to obtain and disseminate the data relied upon by the FDA to license COVID-19 vaccines. The organization takes no position on the data other than that it should be made publicly available to allow independent experts to conduct

From FDA to MHRA: are drug regulators for hire?

BMJ 2022; 377 doi: https://doi.org/10.1136/bmj.o1538 (Published 29 June 2022)Cite this as: BMJ 2022;377:o1538 Article Related contentMetrics Responses Maryanne Demasi, investigative journalist Author affiliations maryannedemasi@hotmail.com Patients and doctors expect drug regulators to provide an unbiased, rigorous assessment of investigational medicines before they hit the market. But do they have sufficient independence from the companies they are meant to regulate? Maryanne Demasi investigates Over the past

Possible causes of sudden adult death syndrome

https://vernoncoleman.org/articles/possible-causes-sudden-adult-death-syndrome

Where did Money Pock$ come from?

What a coincidence that FDA approved a sketchy monkeypox vaccine in 2019. Meryl Nass Jun 22 2022 There are now 2500 moneypox cases diagnosed in the current outbreak, in over 40 countries, and not a single death that anyone can point to, outside of Africa. Maybe ever. One moneypox death is said to have occurred

how do you miss the most blatant safety signal in vaccine history?

the trick, it would appear, is to ignore your own guidelines and never even look for it el gato malo Jun 22 2022 what’s worse than not having a helmet when playing football? thinking you have one when you don’t. it’s the worst of all worlds: the illusion of safety where there is none. you

The 2022 US Midterm Election Is About Stopping the Pharma Genocide

BY RHODA WILSON ON JUNE 22, 2022  The FDA and CDC have launched a reckless nationwide medical experiment on children, Dr. Toby Rogers wrote, this is a massacre of the innocents. “The federal government’s massacre of the innocents began Monday 19 June 2022.” He was referring to the meetings held by the US Food and Drug Administration (“FDA”)

FDA approve COVID Vaccine for 6-month-old Babies despite Data proving Vaccinated Children are 30,200%/303x more likely to die than Unvaccinated Children

BY THE EXPOSÉ ON JUNE 20, 2022  The U.S. Food & Drug Administration (FDA) has questionably authorised emergency use of both the Pfizer and Moderna mRNA Covid-19 injections for use among children aged 6 months and above despite data from the UK’s Office for National Statistics revealing that children are 82 to 303x more likely to die following

PFIZER PFRAUD

The information in this article was available to the Vaccine Advisory Committee before they made a decision. I pray that everyone reads this article and realizes the truth. James Roguski Jun 15 2022 First published at 2pm Eastern, Wednesday June 15, 2022. Last updated: 1pm Eastern, Friday June 17, 2022. Please share this article. It

FDA approves Pfizer infant vaccine after data altered to portray 80% efficacy

Posted by Eliyahu Tulshinski Thu, Jun 16, 2022 97% of COVID case data dropped from analysis Previously pulled request after disappointing trial results Frontline News shined light on Pfizer’s highly unusual initial request for FDA approval of its mRNA vaccine for use in 6-month-old infants and small children up to 4-years-old. The article title revealed what was so unusual: Pfizer vaccine

Top 10 Most Dystopian Things Pushed by the World Economic Forum: No.3 Pills That Contain Microchips

BY RHODA WILSON ON JUNE 12, 2022  Throughout the years, people at the World Economic Forum (“WEF”) have said some highly disturbing things, none of which garnered proper media attention. When one pieces together the topics championed by WEF, an overarching theme emerges – the total control of humanity using media, science, and technology while reshaping democracies to

Breaking: FDA Panel Recommends Moderna Two-Dose COVID Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns

06/14/22 The U.S. Food and Drug Administration’s vaccine advisory panel on Tuesday voted 22 – 0 to authorize Moderna’s COVID-19 vaccines for children ages 6 to 11 and 12 to 17 despite the lack of short- and long-term safety data and no evidence children are at risk of serious illness. By  Megan Redshaw Miss a

58 babies who received mRNA COVID-19 vaccines suffered life-threatening adverse events

An analysis of VAERS reports shows that contrary to the FDA’s briefing document claiming that the majority of adverse events in Pfizers’ clinical trial were non-serious – at least 58 cases of life-threatening side effects in infants under 3 years old who received mRNA vaccines were reported. For some, it is unclear if they survived.

The Pfizer clinical trial in kids 6 months to 4 years old is an embarrassment

Any VRBPAC member who votes Aye on this junk science application should be removed from his/her job Toby Rogers Jun 13 2022 On Sunday night, the FDA released its risk benefit assessment of Pfizer’s Emergency Use Authorization (EUA) application to inject mRNA into kids 6 months to four years years old. This application will be voted on

Pfizer Quietly Admits it Will NEVER Manufacture the Vaccine that was FDA Approved – Will Produce New “Tris-Sucrose Formulation” mRNA Vaccine Instead

By Julian ConradsonPublished June 9, 2022 It’s official – Pfizer’s “fully approved” and experimental mRNA vaccine, dubbed “Comirnaty,” was nothing more than a head-fake. Earlier this week, the notorious experimental vaccine maker quietly submitted an update to the CDC, admitting that its originally licensed “Comirnaty” vaccine will never be distributed for use. In other words, Pfizer has exclusively

Confidential Pfizer Documents reveal Covid-19 Vaccination is going to lead to Depopulation

BY THE EXPOSÉ ON JUNE 7, 2022 Covid-19 vaccination is going to lead to mass depopulation. This is a pretty bold claim to make. ‘Your Government is trying to kill you’ is even bolder. But unfortunately, these bold claims are now backed up with a mountain of evidence, and most of that evidence can be found in the

FDA Sued Over Hiding Records From Moderna COVID-19 Vaccine Approval.

JUNE 9, 2022 Defending the Republic, a Texas-based non-profit filed a Freedom of Information Act lawsuit against the Food and Drug Administration for refusing to turn over records related to the approval of Moderna’s COVID-19 vaccines. The group filed a Freedom of Information Act (FOIA) request seeking the production of records relating to the Food

Doctors Sue FDA, Allege Crusade Against Ivermectin ‘Unlawfully Interfered’ With Their Ability to Treat Patients

06/06/22 In a lawsuit filed June 2, Drs. Robert L. Apter, Mary Talley Bowden and Paul E. Marik argued the FDA acted outside of its authority by directing the public, including health professionals and patients, to not use ivermectin — even though the drug is fully approved by the FDA for human use. By  The

FDA ADMITS: SIGNIFICANTLY ELEVATED RISKS, X-FILES SHOWS NWO AGENDA

June 9th, 2022.

Dear Friends, Sorry to Announce a Genocide — It’s Really True: They Know they are Killing the Babies

by Dr Naomi Wolf So — I’ve been silent for some weeks. Forgive me. The truth is: I’ve been rendered almost speechless — or the literary equivalent of that — because in the last little while I’ve had the unenviable task of trying to announce to the world that indeed, a genocide — or what I’ve

Justice Department Announces Largest Health Care Fraud Settlement in Its History

29 may 2022 It’s hardly a secret that Pfizer has faced so many lawsuits throughout its industrious history that it’s difficult to count them all. It paid a record-breaking $2.3 billion fine for fraud in 2009. As part of that settlement, Pfizer paid a $1.13 billion criminal fine. To put a finer spin on it,

The Pfizer documents produce their first major results

But first…why haven’t you even heard of them? Phil Harper May 28 2022, “The Pfizer documents” are likely to become one of the largest stories of the decade, and yet, for those not actively working on it, you’re almost certain to have never heard about them. This article is my ‘on ramp’ to bring you

Over 500 Military Service Members Sue the Government for Mandating a Vaccine that Was Not FDA Approved and Should Not Have Been Administered

By Joe HoftPublished May 25, 2022 Over 500 service members filed a suit against the government on Monday.  These individuals argue that the vaccine mandate forced on the military was not approved and therefore should never have been administered to the military.  Around 520 military service members filed a suit on Monday against the government.  Their

Intent to Harm: The FDA and Pfizer Knew About Myocarditis Risks in Teens Months Before Letting Parents Know

May 5, 2022 Dr. Naomi Wolf: “There was a peer-reviewed article [in May of 2021] about [myocarditis] in a medical journal, and peer review had already gone on for several months. They found that 35 teens had had heart damage within a week of receiving [the] mRNA vaccine. Nonetheless, the FDA issued the emergency use

CDC and FDA ‘altered’ Covid guidance and even ‘suppressed’ findings while under political pressure, bombshell report suggests: Whistle-blower employees say they feared ‘retaliation’ if they spoke up

Federal investigators interviewed top-level directors and managers at agencies They also opened a hotline for employees to report ‘political interference’ Government Accountability Office uncovered widespread allegations of this They raised fears that Covid guidance may have been ‘altered or suppressed’ GAO warned none of the agencies had systems in place for reporting allegations Said they

My offer to share videos and blood clot tissue samples from multiple embalmers with the CDC and FDA

I want everyone to know that every time they have been offered to see evidence of harm, they refuse to see it. This is the latest offer. These clots are impossible to explain away. Steve Kirsch Apr 20 2022 Here’s the offer I made earlier today (at 12:20pm PST on April 20, 2022) to the

Pfizer Data From the FDA Reveals Conflicts of Interest in Vaccine Trials

By  Michelle Edwards April 13, 2022 In September 2020, Dr. Anthony Fauci declared in an interview that the U.S. Food and Drug Administration’s Data and Safety Monitoring Board (DSMB) “is an independent body.” Clarifying further, he explained that the board—which offers expert advice to the FDA on a range of issues, including the approval of the Pfizer jab—is “beholden to

$1M reward for a CDC or FDA whistleblower

The data was clear in January that the vaccines were unsafe. How come nobody at the CDC or FDA noticed? They ignored all attempts to alert them. If you have proof of corruption by insiders, let’s talk Steve Kirsch Apr 1 2022 I wrote an article earlier on how the safety signals in VAERS were flashing

Official Government data suggests the Fully Vaccinated are suffering Antibody-Dependent Enhancement; and the newly published Pfizer Documents prove Pfizer & the FDA knew it would happen

BY THE EXPOSÉ ON APRIL 3, 2022  An investigation of official Government data has uncovered that fully vaccinated individuals are up to 3 times more likely to be infected with Covid-19, 2 times more likely to be hospitalised with Covid-19, and 3 times more likely to die of Covid-19 than unvaccinated individuals. The question is, why? One possibility

Pfizer Confidential: 1 infant DEATH vs 1 Successful Birth

Pfizer and FDA Knew: Breastfeeding Sheds Vaccine to Infants Igor Chudov Apr 1 2022 Hat tip to Claus L who reminded me that new Pfizer documents were released. Summary: Only two births were recorded, one was successful and another resulted in infant death. Breastfeeding indeed affects infants and proves mRNA vaccine shedding by breastfeeding mothers. 1 Infant

Former BlackRock Advisor Tells RFK, Jr.: ‘FDA Is in on the Cover-Up’

03/18/22 In an interview with former BlackRock advisor Edward Dowd on “RFK Jr. The Defender Podcast,” Robert F. Kennedy, Jr. and Dowd discussed why they believe COVID vaccine makers committed fraud, and government agencies know it. By  David Marks In an interview with former BlackRock advisor Edward Dowd on “RFK Jr. The Defender Podcast,” Robert

Official documents reveal enormous gap between what FDA and Pfizer would attest to, compared to what the public was told about the Pfizer COVID vaccine

Meryl Nass Mar 13 2022 The label for COMIRNATY is a legal document updated on 12/20/21: 1.  CDC made the false claim on its website that anaphylactic reactions occur at rates  approximately the same after COVID vaccines as other vaccines.  I just looked for the citation and see the claim has recently been removed.  Now, CDC informs us that “safeguards are

Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

March 2, 2022 by Brian ShilhavyEditor, Health Impact News As the news cycle continues to focus on the Ukraine situation, the FDA complied with a court order to begin releasing 55,000 pages of Pfizer data per month that was used to authorize their COVID-19 vaccine produced with BioNTech, with the first batch quietly released yesterday, March

CDC is refusing to publish data it has collected on booster effectiveness for 33 MILLION Americans aged 18-49 over fears it might show the vaccines as ineffective: FDA expert tells CDC to ‘tell the truth’

Two weeks ago the Centers for Disease Control and Prevention (CDC) published data about the effectiveness of boosters against COVID-19 The CDC failed to publish a tranche of their data, however – omitting the impact on those aged 18-49, who are least likely to benefit from boosters The CDC are also being criticized for failing

FDA Executive Officer Exposes Close Ties Between Agency and Pharmaceutical Companies: ‘Almost a Billion Dollars a Year Going into FDA’s Budget from the People we Regulate’

feb 16 2022, FDA Executive Officer Chris Cole: “The drug companies, the food companies, the vaccine companies. So, they pay us hundreds of millions of dollars a year to hire and keep the reviewers to approve their products.” Cole on FDA fees: “Congress approved user fees for [the] FDA. Basically, we charge the industry millions

FDA Exec on Camera Reveals Future COVID Policy “Biden Wants To Inoculate As Many People As Possible”

FDA Executive Officer, Christopher Cole: “You’ll have to get an annual shot [COVID vaccine].  I mean, it hasn’t been formally announced yet ‘cause they don’t want to, like, rile everyone up.” Cole on President Joe Biden: “Biden wants to inoculate as many people as possible.” Cole on plans to approve vaccine for toddlers: “They’re not going

University That Funds Biden’s Think Tank And Hosts FactCheck.Org Has Contract With BioNTech, Gets Paid For Vaccine Sales And FDA Approvals

 By Patrick Howley  February 6, 2022 at 5:57am Documents obtained by NATIONAL FILE show that the University of Pennsylvania, which hosts and funds Joe Biden’s think tank called the Penn Biden Center, directly profits from the sale of Pfizer-BioNTech and Moderna Coronavirus vaccines. The University gets more money if more vaccines are sold. The University

Pharma Liability Shields Could Be at Risk if Fraud is Found, says Former Blackrock Investment Executive

BY PATRICIA HARRITY ON JANUARY 31, 2022  If Pfizer and the FDA do not release the data on their clinical trials, former Blackrock & Hedge Fund Guru Edward Dowd says he is assuming fraud, and Fraud Eviscerates all Contracts, that’s case-law. Dowd says that big pharma is supposed to be one of the most regulated industries, particularly with the

PCR test was developed without isolated samples

Jan 30 2022 Breaking news. share on all platforms: FDA document admits “Covid” PCR test was developed without isolated samples for test calibration, effectively admitting it’s testing something else.A document just released by the U.S. Food and Drug Administration (FDA) openly admits that the infamous PCR test for the Wuhan coronavirus (Covid-19) was developed not

MILITARY MED SKYROCKETING DISEASE DATA LEAKED! BIDEN REGIME KNOWINGLY CONTINUES DESTRUCTION OF FORCE

January 28, 2022 As researched and compiled by TerminalCWO: On January 25, 2022, Thomas Renz, the attorney for Doctors Peter Chambers, Theresa Long, and Samuel Sigoloff, testified before Congress regarding data leak directly from the Defense Health Agencies Defense Medical Epidemiology Database, otherwise known as DMED. Within DMED exists the Defense Medical Surveillance System’s DMSS, which contains up

Covid-19 vaccines and treatments: we must have raw data, now

19 jan 2022 Article Related content Metrics Responses Peter Doshi, senior editor,   Fiona Godlee, former editor in chief,   Kamran Abbasi, editor in chief Correspondence to: P Doshi Pdoshi@bmj.com Data should be fully and immediately available for public scrutiny In the pages of The BMJ a decade ago, in the middle of a different

Dr Wiseman’s damning ‘quasi-vaccine’ efficacy data ignored by the FDA and the CDC.

January 12, 2022 Video: https://rumble.com/vseupc-dr-wisemans-damning-quasi-vaccine-efficacy-data-ignored-by-the-fda-and-the-.html By Sonia Elijah Summary Tired, despondent, and confused CDC advisory committee recommend Pfizer boosters for 12-15-year-olds in hasty low-transparency meeting Decision is described as the “last whack-a-mole,” which is neither sustainable nor smart. Attempting to boost ourselves out of omicron where quasi-vaccine efficacy is negative, is the immunological equivalent of heroin

How Big Pharma pushes dangerous drugs and reaps profits

January 10th, 2022 Video: https://odysee.com/@Thecontentgather:3/The-Vatican%E2%80%99s-Unimaginable-Wealth:8

Rogan and Malone: Most Important Interview of Our Time?

4 jan 2022 In an interview with Joe Rogan, Dr. Robert Malone, mRNA vaccine expert and outspoken critic of our pandemic response, delivered a powerful message to the world. Yes, it’s three hours long, and yes, it’s worth every minute. By  Madhava Setty, M.D. 137 Miss a day, miss a lot. Subscribe to The Defender’s

There remains no FDA approved COVID vaccine in the United States

Is Pfizer is using children as legal human shields to get full authorization? Jordan SchachtelDec 29, 2021 I fact checked the fact checkers and couldn’t believe what I found. Despite the corporate press, Big Pharma, and the federal government telling us otherwise, it is absolutely true that there is no FDA approved COVID-19 vaccine available

FDA Should Need Only ‘12 Weeks’ to Release Pfizer Data, Not 75 Years, Plaintiff Calculates

12/17/21 The nonprofit group suing the U.S. Food and Drug Administration for the release of documents related to the approval of Pfizer’s Comirnaty vaccine calculated it should take the agency only 12 weeks with 19 reviewers working full-time to review and produce the documents. By  Seth Hancock 29 Miss a day, miss a lot. Subscribe

FDA just approved chips in pills! Says Pfizer CEO

17 dec 2021, imagine the potential for compliance that the health insurance company will know you took your pills automatically Video: https://odysee.com/@didchay:f/tmh-Vv47AxxqMMWV:1 Find others here: freedomscells.org

FDA’s forced hand drops Pfizer’s Bombshell Safety Document

SoniaElijah December 14, 2021 By Sonia Elijah The highly confidential Pfizer documents, which have been synonymous with the extreme lack of transparency revealed by the actions of pivotal governmental agencies, over the past 20 months, lead critics of the official narrative to demand “show us the data,” is finally being revealed–well sort of, the first

FDA and Pfizer conspired to hide thousands of adverse events and deaths caused by the COVID jab

by: Edit Lang, staff writer | December 6, 2021 FacebookEmailShare (NaturalHealth365)  While most doctors and scientists have gone along with the jab-pushing agenda, more and more physicians and medical experts are stepping forward to warn about the potential harm mRNA COVID injections inflict on the human body.  Despite their tireless efforts to alert the population,

Congressman Introduces Bill to Force FDA to Release Pfizer Documents Within 100 Days, Instead of 55 Years

U.S. Rep. Ralph Norman (R-S.C.) on Thursday introduced legislation to require the U.S. Food and Drug Administration (FDA) to release, within 100 days, all records of information related to Pfizer COVID vaccines. The FDA had asked to be allowed to take up to 55 years to release the documents. By  Seth Hancock 90 12/03/21 Miss

INFLUENZA PARADOX of the CRIME OF THE CENTURY

23 nov 2021 Is this Austria today? Meanwhile back west we see the INFLUENZA PARADOX of the CRIME OF THE CENTURY How come influenza “suddenly” disappeared, just as Covid-19 “suddenly” appeared? The FDA, CDC and NIH are inherently corrupt. They do not serve the interests of citizens, they are merely ‘licensing’ and marketing wings of

As Reports of Injuries After COVID Vaccines Near 1 Million Mark, CDC, FDA Clear Pfizer, Moderna Boosters for All Adults

11/19/21 VAERS data released today by the CDC included a total of 894,145 reports of adverse events from all age groups following COVID vaccines, including 18,853 deaths and 139,126 serious injuries between Dec. 14, 2020, and Nov. 12, 2021. By  Megan Redshaw 69 Miss a day, miss a lot. Subscribe to The Defender’s Top News

FDA Asks Federal Judge to Grant it Until the Year 2076 to Fully Release Pfizer’s COVID-19 Vaccine Data

November 17, 2021 by Brian ShilhavyEditor, Health Impact News Attorney Aaron Siri is a Vaccine Injury attorney, one of just a handful of such attorneys in the U.S. Since the passage of the 1986 National Vaccine Injury Compensation law, one cannot sue pharmaceutical companies for vaccine injuries and deaths. A special U.S. Vaccine Court handles

FDA’s Smoking Gun: Disinformation Campaign Targeting Ivermectin

SoniaElijah November 5, 2021 Note that views expressed in this opinion article are the writer’s personal views and not necessarily those of TrialSite. By Sonia Elijah It recently came to my attention that communication within the U.S. Food and Drug Administration (FDA) evidences the Gold Standard agency’s explicit involvement in the Ivermectin disinformation war. While

Gravitas: Was Pfizer’s Covid-19 vaccine trial “compromised”?

November 7th, 2021 Was Pfizer’s Wuhan Virus vaccine trial compromised? A whistleblower who worked for the company hired to run the trial spotted several lapses. She was …

FDA’s fraudulent modelling to justify vaccinating 5-11 year olds

November 1, 2021 Exaggeration of impact of COVID-19 on healthy children The FDA have published their reasoning behind justifying the vaccination of children aged 5 to 11 years old. The table, reproduced below, shows their estimates of risk of ICU admissions and deaths, in hypothetical future Covid waves, against the guaranteed risk from myocarditis if vaccination is

FDA Panel Votes 17-0 to Allow Experimental Pfizer Injections for Children 5-11 yrs

OCTOBER 27, 2021 BY NEWS WIRE Today the United States Food and Drug Administration (FDA) vaccines advisory committee voted 17-0, with one abstention, to allow pharmaceutical giant Pfizer access to America’s child population aged 5 to 11 years, paving the way for a new round of mass injections of the highly controversial experimental mRNA gene

Breaking: FDA Panel Endorses Pfizer Shots for 5- to 11-Year-Olds, Experts Say Vaccine for Kids Is ‘Unnecessary, Premature and Will Do More Harm Than Good’

The U.S. Food and Drug Administration’s advisory panel today voted to recommend the agency allow Pfizer to amend its Emergency Use Authorization for its COVID vaccine for children 5 through 11 years old, despite a host of objections from scientists and physicians. ByMegan Redshaw The Defender is experiencing censorship on many social channels. Be sure

FDA document admits “Covid” PCR test was developed without isolated samples for test calibration, effectively admitting it’s testing something else

A document just released by the U.S. Food and Drug Administration (FDA) openly admits that the infamous PCR test for the Wuhan coronavirus (Covid-19) was developed not with actual samples, but rather with what appears to be genetic material from a common cold virus. In the FDA document, it is clearly stated that ordinary seasonal

Scientists Sue the FDA for Data it Relied Upon to License Pfizer’s Covid-19 Vaccine

You can’t say no, you can’t sue for harm, and you can’t see the data underlying the government’s claim that the product is safe and effective. That seems fair. Aaron Siri Oct 11 The FDA repeatedly promised “full transparency” with regard to Covid-19 vaccines, including reaffirming “the FDA’s commitment to transparency” when licensing Pfizer’s Covid-19

The Plandemic (we still didn’t find the pandemic)

The events that have taken place over the past 19 months have all been in the pipeline for numerous years maybe even centuries. Strategic planning over multiple event scenarios and outcomes that our philanthropist overlords roll out on the human population without your vote or say so. To fit their specific agenda and reduce the

A Day After Our Investigative Reporter Mary Beth Pfeiffer Proved That the FDA Lied (And Thousands Likely Died) with the Ivermectin Horse-Dewormer Hoax, She Was Locked Out of Twitter

Please share the brave story by Mary Beth and Linda Bonvie far and wide, and help us beat the censors with the truth about IVM and early treatments. Michael Capuzzo Oct 17, 2021 Dear RESCUE Readers, Yesterday Teresa and I published an investigation, “Horse-Bleep,” by reporters Mary Beth Pfeiffer and Linda Bonvie documenting that the FDA

Proof that the CDC is lying to the world about COVID vaccine safety

SteveKirsch October 15, 2021 Note that views expressed in this opinion article are the writer’s personal views and not necessarily those of TrialSite. FREE to read and SHARE without paying. The CDC and the FDA claim that we can safely ignore the huge spike in event rates reported to the VAERS system this year (this is

Whistleblower Physician Assistant Says NY Hospital Admissions Were 90% Vaccinated, Not Being Reported to VAERS

She reached out to the FDA and CDC and was ignored. BY LEAH ANAYAOCTOBER 18, 2021 Physician Assistant Deborah Conrad had the hospital where she works track the patients admitted and their COVID-19 vaccination status. The hospital is United Memorial Medical Center, within the Rochester Regional Health System in New York. Conrad’s community reportedly has a less than

Is There Plausible Basis For Fertility Concerns?

sept 30, 2021 In my own community, the most prominent concern on the minds of many of the vaccine hesitant, especially young women of childbearing age, is the fear of an adverse effect on fertility. Possibly because of this, fertility concerns have also been derisively dismissed by the doctors with more passion and vengeance than

FDA Open Public Hearing, 1000% Increase in Adverse Reactions for 2021 Already

September 27th, 2021 NEW – Dr. Jessica Rose at the FDA Open Public Hearing: “There’s an over 1000% increase in the total number of adverse events just for 2021 and we are not done with 2021 … In my opinion [the risks] outweigh any potential benefits…with these products, especially in children.” https://odysee.com/@Robert-Self:a0/Dr.-Jessica-Rose-FDA-Open-Public-Hearing,-1000-Increase-in-Adverse-Reactions-for-2021-Already:4

Major Law Firm Confirms FDA Deceived America With Its ‘Approval’ Of Pfizer Vax

Published on September 6, 2021 Written by leohohmann.com When the U.S. Food and Drug Administration announced Aug. 23 it had granted full approval to the first Covid “vaccine” under the brand name Comirnaty, the mainstream media immediately ran with the narrative. Joe Biden jumped in front of a microphone and told businesses they needed to “step

House of COVID Cards Collapses: FDA Vaccine Panel Comes Out Against Deadly Injections

Bombshell testimony from top scientists at vaccine hearing reveals injections killing more people than saving and driving surge of variants. Image Credits: Pavlo Gonchar/SOPA Images/LightRocket via Getty Images. By Jamie White | INFOWARS.COM Saturday, September 18, 2021 Several doctors from the Food and Drug administration’s (FDA) vaccine hearing on Friday claimed in explosive testimony that the COVID-19 vaccine is

The Meaning of the FDA Resignations

BY JEFFREY A. TUCKER   SEPTEMBER 14, 2021   POLICY, PUBLIC HEALTH   9 MINUTE READ How significant is it that the two top FDA officials responsible for vaccine research resigned last week and this week signed a letter in The Lancet that strongly warns against vaccine boosters? This is a remarkable sign that the project of government-managed virus mitigation is in the final stages

Bayer Loses Again! Heads to Supreme Court for Glyphosate Lawsuits

By Ty & Charlene BollingerSeptember 2, 2021 TTAC is experiencing heavy censorship on many social media channels since we’ve been targeted by the mainstream media sellouts, social media bullies, and political turncoats.  Be sure to get the TRUTH by subscribing to our email list.  It’s free. In a final, desperate attempt to avoid billions of dollars of liability, Bayer has

2 Top FDA Vaccine Officials Resign, Raising Questions About Pressure From White House to Approve Boosters

Dr. Marion Gruber, director of the U.S. Food and Drug Administration’s vaccines office, and her deputy, Dr. Philip Krause, reportedly said they don’t believe there is data to support the Biden administration’s push to offer COVID booster shots later this month. By Megan Redshaw The Defender is experiencing censorship on many social channels. Be sure to stay

Children’s Health Defense to sue FDA over fraudulent Pfizer covid vaccine “approval”

The U.S. Food and Drug Administration’s (FDA) recent decision to “fully approve” the Wuhan coronavirus (Covid-19) “vaccine” from Pfizer was “premature, arbitrary, and capricious,” says Children’s Health Defense (https://thenewamerican.com/childrens-health-defense-to-challenge-full-approval-of-pfizer-covid-vaccine/) (CHD), which is now filing a legal challenge against the corrupt federal agency. On August 23, the FDA decided to approve Comirnaty, a rebranded version of

Why is the FDA Funded in Part by the Companies It Regulates?

Nearly half the agency’s budget now comes from ‘user fees’ paid by companies seeking approval for medical devices or drugs The Food and Drug Administration has moved from an entirely taxpayer-funded entity to one increasingly funded by user fees paid by manufacturers that are being regulated. Today, close to 45% of its budget comes from these

Does the FDA think these data justify the first full approval of a covid-19 vaccine?

August 23, 2021 The FDA should demand adequate, controlled studies with long term follow up, and make data publicly available, before granting full approval to covid-19 vaccines, says Peter Doshi On 28 July 2021, Pfizer and BioNTech posted updated results for their ongoing phase 3 covid-19 vaccine trial. The preprint came almost a year to the day

Former Pfizer Employee: “Checkmate. Game Over. We WIN”

BY STEW PETERS SHOWAUGUST 25, 2021 Biotech Analyst DESTROYS Big Pharma in BOMBSHELL EXCLUSIVE! Karen Kingston is a former Pfizer employee, a pharmaceutical marketing expert and biotech analyst. Kingston joins Stew Peters, and brings the receipts! Kingston reveals how the FDA “approval” is sure to be the “checkmate” move to end the shots that have caused

2 Things Mainstream Media Didn’t Tell You About FDA’s Approval of Pfizer Vaccine

08/24/21 Buried in the fine print of Monday’s approval by the U.S. Food and Drug Administration of the Pfizer Comirnaty COVID vaccine are two critical facts that affect whether the vaccine can be mandated, and whether Pfizer can be held liable for injuries. By Robert F. Kennedy, Jr.Meryl Nass, M.D. The Defender is experiencing censorship on many

Microbiologist Explains COVID Jab Effects

Analysis by Dr. Joseph MercolaFact Checked STORY AT-A-GLANCE  The FDA can only grant emergency use authorization for a pandemic drug or vaccine ifthere’s no safe and effective preexisting treatment or alternative. Since there are severalsuch alternatives, the FDA is legally required to revoke the emergency authorization forthese shots  While the COVID injections have

7 Reasons why the COVID vaccines and vaccine mandates should not be approved

Here’s a solid set of reasons to be very concerned about what corrupt FDA is rumoured to be about to do. The vaccines kill more people than they save. Although the vaccines reduce the number of COVID deaths, that benefit comes at a steep price: death from other causes. Pfizer’s own Phase 3 study (6

FDA set to grant full approval to Pfizer vaccine without public discussion of data

BMJ 2021; 374 doi: https://doi.org/10.1136/bmj.n2086  (Published 20 August 2021)Cite this as: BMJ 2021;374:n2086 Article Related content Metrics Responses Gareth Iacobucci Transparency advocates have criticised the US Food and Drug Administration’s (FDA) decision not to hold a formal advisory committee meeting to discuss Pfizer’s application for full approval of its covid-19 vaccine. Last year the FDA said it was “committed to use

Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19

Authors Stephanie SeneffComputer Science and Artificial Intelligence Laboratory, MIT, Cambridge MA, 02139, USA Greg NighNaturopathic Oncology, Immersion Health, Portland, OR 97214, USA Keywords:  antibody dependent enhancement, autoimmune diseases, gene editing, lipid nanoparticles, messenger RNA, prion diseases, reverse transcription, SARS-CoV-2 vaccines Abstract Operation Warp Speed brought to market in the United States two mRNA vaccines, produced

BREAKING: CDC, FDA faked “covid” testing protocol by using human cells mixed with common cold virus fragments… PCR tests are merely detecting the common cold

By Mike AdamsJuly 31, 2021 This article was originally published by Mike Adams on NaturalNews.com. It has been reposted here with permission from the author. In a shocking revelation first reported by Dan Dicks of Press for Truth (Canada), an FDA document admits that the CDC and FDA conspired to fabricate a covid-19 testing protocol using human cells

The truth about vaccines that the CDC doesn’t want you to know

vaccinetruth July 11, 2021 On July 15, 2021, the US Surgeon General called COVID misinformation an “urgent threat.” The White House also is working with social media companies to ban medical disinformation. But what both Dr. Vivek Murthy and Press Secretary Jen Psaki neglect to say is that the biggest misinformation is coming from the CDC, FDA, and NIH.

Vaccine side effects shown at a FDA presentation in 2020

The following list of jab side effects appeared for a split second at 2:33:40 in an FDA presentation on October 22, 2020. The specific slide appears only for a split second. It was scrolled through and not presented properly. During that split second, this screen, which shows the adverse effects of the jab that the

U.S. Medicines Regulator Will Decide Whether to Fully Approve the Pfizer Covid Vaccine by January 2022

The Food and Drug Administration (FDA) will decide on whether to fully approve the use of the Pfizer Covid vaccine in the U.S. for those aged 16 and over no later than January 2022, it has been announced. The vaccine is currently only authorised for emergency use in Americans aged 12 and over and has

Thousands of victims of the COVID-19 “vaccine” in the United States ask for help

Kathy Vittetoe | BLes.com 11/07/21 🔴 Avoid censorship follow us on Rumble and Telegram . Drafting BLes – After more than six months of the mass immunization campaign with the COVID-19 experimental vaccines, not approved by the FDA, tens of thousands of victims are speaking, regretting their decisions and asking for help. In the past, the protesters were mostly parents of vaccine-damaged children. Now

How Pfizer Manipulated COVID Vaccine Trial Protocols To Obtain Emergency FDA Authorisation For Children

July 5, 2021 Analysis and comparison of the review document submitted by Pfizer to the US Food and Drug Administration, on the basis of which the FDA gave the green light to expand the emergency permit for vaccination also for children aged 12-15 (1), as opposed to the study protocol in children (2, 3), reveal

New report stuns the world: The vast majority of those now dying with covid are people who were VACCINATED against it

Public Health England just released a new report showing that at least 62 percent of all deaths associated with the Wuhan coronavirus (Covid-19) are occurring in people who were already “vaccinated.” The news just so happened to come out the same day that the mainstream media ran a distraction story about British politician Matt Hancock

Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Innova SARS-CoV-2 Antigen Rapid Qualitative Test (also distributed under the names Innova COVID-19 Self-Test Kit (3T Configuration), Innova SARS-CoV-2-Antigen Rapid Qualitative Test (7T Configuration), and Innova SARS-CoV-2-Antigen Rapid

U.S. health officials report higher-than-expected heart inflammation cases following Covid-19 vaccination

By Andrew Joseph  June 10, 2021 Federal health officials said Thursday they’re seeing rare but higher-than-expected cases of a heart issue called myocarditis among adolescents and young adults who received their second shot of one of the mRNA Covid-19 vaccines. The data are preliminary and limited, and experts are still trying to determine if there is indeed

COVID hospitalizations, deaths for the vaccinated more than triple in one month, CDC reports

A total of 10,262 SARS-CoV-2 vaccine ‘breakthrough infections’ – defined as coronavirus infections in fully vaccinated people – were reported to the CDC from 46 U.S. states and territories between January 1 and April 30, 2021. Mon Jun 7, 2021 By Celeste McGovernFOLLOW CELESTE June 7, 2021 (LifeSiteNews) – Deaths and hospitalizations for COVID-19 infection

86% of Children suffered an Adverse Reaction to the Pfizer Covid Vaccine in Clinical Trial

BY THE DAILY EXPOSE ON MAY 30, 2021 • The FDA granted emergency use authorisation of the Pfizer mRNA Covid vaccine for use in children aged 12 and over in the USA back on the 10th May 2021. The EMA has recently followed suit, recommending the Pfizer jab should be administered to children aged 12 and over in EU

Push back against Mandatory COVID-19 vaccinations

May 25, 2021 Push back against Mandatory COVID-19 vaccinations! Here is information based on publicly available sources – that you can use to write a letter or with which to seek the assistance of legal counsel: There are No Licensed COVID-19 Vaccines in the U.S presently[1]. All COVID-19 vaccines are currently approved only as Emergency

HARD DATA PROVES BIG PHARMA KNEW COVID VACCINES WOULD WORSEN AND PROLONG THE PANDEMIC

By Ty BollingerMay 24, 2021 +1TweetShare322Share322 Shares (Reposted from stateofthenation.co) What the many graphs below clearly indicate are two crucial data points about the Covid Super Vaccination Agenda. First, that virtually every country in the world was trending downward — precipitously — as the world community of nations started to approach natural herd immunity for COVID-19

No jab for me

Deutsche Español Statements in this site are substantiated with facts that will stand in a court of law. Informed Consent requires a flow of information. Click on the hyperlinked sections to direct you to primary sources such as CDC, WHO, FDA documents. Anyone trying to take down this site will be named as codefendant in Nuremberg

Side Effects Of The Moderna Vaccine For COVID-19 Explained

Three vaccines against COVID-19 have been made available to the public as of March 2021. None have yet earned formal approval by the U.S. Food and Drug Administration (via FDA), but each is subject to an “emergency use authorization” (EUA). That means members of the public may receive the vaccine in advance of FDA approval.