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Advisers to the U.S. Food and Drug Administration (FDA) on Thursday recommended, by a vote of 10 to 4, that the agency approve Pfizer’s respiratory syncytial virus (RSV) vaccine for pregnant women, despite questions about the vaccine’s safety. During Thursday’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) meeting, committee members and medical experts raised concerns about premature births identified during Pfizer’s clinical trials. The FDA is expected to issue a final decision on the vaccine in August. If approved, it would become the first RSV vaccine authorized for pregnant women. The Centers for Disease Control and Prevention (CDC) must...

Open AI CEO Sam Altman will attend the secretive Bilderberg Meeting, an annual gathering of over 100 political and corporate leaders from Europe and North America, which has announced AI as a key item on its agenda this year. Altman isn’t the only Big Tech figure in attendance. Other participants include Microsoft CEO Satya Nadella, former Google CEO Eric Schmidt, and Google DeepMind head Demis Hassabis. Jen Easterly, director of the Cybersecurity and Infrastructure Security Agency (CISA), will also attend. As noted in a congressional hearing last week, CISA played a key role as a source of government pressure in...

The NIH has a newly nominated Pfizer rubber stamper in chief.Via The White House:Today, President Biden announced his intent to nominate Dr. Monica Bertagnolli as Director of the National Institutes of Health (NIH), the world’s preeminent biomedical research organization. Dr. Bertagnolli is a world-renowned surgical oncologist, cancer researcher, educator, and physician-leader who has the vision and leadership needed to deliver on NIH’s mission to seek fundamental knowledge and promote human health.Statement from President Biden: “Dr. Bertagnolli has spent her career pioneering scientific discovery and pushing the boundaries of what is possible to improve cancer prevention and treatment for patients, and...

James O’Keefe’s newly minted O’Keefe Media Group (OMG) has released new, undercover footage showing Fox News producer Sean Langille admitting that host Tucker Carlson’s firing was tied to the Dominion Voting Systems lawsuit, as well as aBig Pharma pressure campaign. “When it’s corporate media you’re beholden to advertisers… we take money from Pfizer,” Langille said. He was later confronted over the phone by James O’Keefe over the matter.

[H/T grey_whiskers ]Watch the full presentation here: https://rumble.com/v2m06ay-sonia-elijah-investigating-regulatory-failure-and-pharma-fraud.htmlOn Twitter 11:30 AM · May 4, 2023 https://soniaelijah.substack.com/p/regulatory-failure-and-pharma-fraudhttps://www.trialsitenews.com/a/startling-evidence-suggests-biontech-and-pfizer-falsified-key-data-part-1-e2595e7f https://www.trialsitenews.com/a/part-2-startling-evidence-suggests-biontechpfizer-falsified-key-data-further-scandals-24f4d743 https://www.trialsitenews.com/a/what-the-leaked-ema-emails-docs-reveal-major-concerns-with-pfizer-c-19-vaccine-batch-integrity-and-the-race-to-authorise-cdda0ba2On TwitterMay 5, 2023

Why didn't they warn us at the time? Instead, they remained silent. The mandates should have been the opposite: hospitals should have fired anyone who got vaccinated.Steve KirschApr 30, 2023 Most people didn’t read the September 17, 2021 FDA briefing document so let me highlight the top of page 22 for you. With a little simple math (shown here), it’s clear that you are 2X more likely to be infected during the time you are vaccinated. The p-value is <.001. This was not just a fluke. It was validated in the Cleveland Clinic study. Executive summaryThe Cleveland Clinic study, which...

Former Trump administration adviser Peter Navarro revealed that the ex-president was allegedly deceived into believing that Pfizer’s COVID-19 shot was a “true vaccine” while blaming Antony Fauci for hiding sensitive information regarding the COVID origin. Fauci and Pfizer “didn’t disclose the side effects of that [vaccine]” to Trump, Navarro said in a May 4 podcast by Patrick Bet-David on YouTube. “And they weren’t clear with him. They made him think that it was a true vaccine when it’s not. It’s mRNA technology.” Traditional vaccines work by introducing a harmless piece of bacteria or virus into the human body to trigger...

The Food and Drug Administration on Wednesday approved the world's first RSV vaccine: a shot for adults ages 60 and up, made by pharmaceutical giant GSK. The milestone was decades in the making. Researchers first attempted to develop a vaccine for respiratory syncytial virus roughly 60 years ago. In a late-stage clinical trial, the single-dose shot lowered the risk of symptomatic illness by 83% and of severe illness by 94%. The Centers for Disease Control and Prevention must still recommend the vaccine before it becomes available to the public. A CDC advisory committee is scheduled to meet in June to...

Pfizer’s latest quarterly results underscored the pressure the drugmaker is facing to sustain sales growth by hitting on drugs in development and recent acquisitions as demand wanes for its leading Covid-19 products. Pfizer’s first-quarter revenue and earnings were down by nearly a third from a year ago on plummeting demand for its Covid-19 vaccine, though the results topped Wall Street expectations. The company also faces sales declines for big-selling products in coming years due to expected patent expirations that will clear the way for lower-cost competition. Pfizer could lose $17 billion in sales from these patent losses.

Texas Attorney General Ken Paxton launched an investigation into Covid jab manufacturers on Monday to uncover whether these companies conducted gain-of-function research or misled the public about the efficacy of the experimental shots.“The development of the Covid-19 vaccine, and the representations made by and knowledge of Pfizer, Moderna, and Johnson & Johnson, are of profound interest to the public’s health and welfare. This investigation aims to discover the truth,” said Paxton in a statement. “If any company illegally took advantage of consumers during this period or compromised people’s safety to increase their profits, they will be held responsible.”According to a...

The court-mandated release of the documents related to what Pfizer and the FDA knew about the COVID-19 injections and when has unearthed evidence that they knew as early as April 2021 that the mRNA shots trigger adverse events (AEs) in breastfeeding babies.In the attempt to sell the COVID-19 vaccines to every man, woman, and child under the sun regardless of risk, age, underlying health conditions, etc., the corporate media claimed repeatedly, and continues to claim, that the vaccine was either not passed through the mother’s breast milk or, alternatively, that it was but it posed no risk to babies because...

On June 7, 2021, AGC Biologics announced that they were the supplier of plasmid DNA for the manufacturing of the BioNTech/Pfizer mRNA 'vaccines' ... : Recent experts have come forward confirming that plasmid DNA is in Pfizer’s mRNA vials and that plasmid DNA is for purposes of the expression on non-human DNA inside humans through cell transfection. I first reported on the existence of plasmid DNA as an ingredient in the Pfizer’s mRNA vials on October 20, 2021 on Brannon Howse. I begin my presentation on plasmid DNA at around the 32:25. ... We were never told what was in...

[H/T Mewzilla]On Twitter Apr 29, 2023

April 29, 2023 • by Amy Kelly, Program Director of the War Room/DailyClout Pfizer Documents Analysis ProjectThe April 2023 batch of Pfizer clinical trial documents released under court order by the Food and Drug Administration (FDA) contains a shocking, eight-page document titled, “Pregnancy and Lactation Cumulative Review.” The data in the Cumulative Review are “…from the time of drug product development to 28-FEB-2021,” and Robert T. Maroko of the FDA approved the Review on April 20, 2021. It reveals that Pfizer and the FDA knew in early 2021 that Pfizer’s mRNA COVID vaccine, BNT162b2, resulted in:Adverse events in over 54%...

‘So, these are monsters, and there's no way to avoid concluding that they're focused on disrupting human reproduction,’ the author conceded about the manufacturers of the COVID jab. 'It’s ‘a bioweapon and… we're under attack.’ ... In an extraordinary speech synthesizing several “headline” discoveries from analyses of thousands of Pfizer documents, Dr. Naomi Wolf presented how the COVID “vaccine” enterprise intentionally sought to not only “disrupt and impair human reproduction” but “attack” and “kill” large numbers of people, particularly in the West. Wolf, a lifelong Democrat, addressed the conservative citadel of Hillsdale College in March, confessing that events over the...

he decision to fire Tucker Carlson from his ratings juggernaut show on Fox News reportedly came straight from Rupert Murdoch. The exact factors which contributed to the anchor’s exit have not been officially confirmed by Fox, but sources have told various outlets that there were several factors involved in the decision. Persons familiar with the situation told the Los Angeles Times that Murdoch, the Fox Corporation chairman, was concerned about Carlson’s coverage of the attack on the Capitol on January 6, 2021, in which Carlson downplayed events as “mostly peaceful chaos” and promoted the notion that it was provoked by...

The Food and Drug Administration pulled the emergency use authorizations for the original COVID vaccines produced by Moderna and Pfizer on Tuesday. Both vaccines were authorized for emergency use more than two years ago after they were developed under Operation Warp Speed during the Trump administration. In a news release, the FDA explained the older vaccines no longer offer full protection from new strains of the virus. The agency said it had amended the emergency use authorizations of the initial Moderna and Pfizer-BioNTech vaccines in order to “simplify the vaccination schedule for most individuals.” “This action includes authorizing the current...

In a press release on Tuesday, the FDA has declared the monovalent Pfizer and Modena mRNA Covid-19 vaccines are no “longer authorized for use in the United States.”The decision was made through a recent amendment to the Emergency Use Authorizations of the Moderna and Pfizer Covid-19 bivalent vaccines.In the amendment, the FDA ruled the bivalent Moderna and Pfizer Covid-19 vaccines will be used for all doses and monovalent doses (targeted original strain) will no longer be authorized. The FDA claims the decision was made in order to simplify the vaccine process, but many people who have already received the monovalent...

There were 31% higher deaths in the vax group in the "gold standard" Phase 3 clinical trials. How do we know that none of those deaths were caused by the vaccine? Because Pfizer said so. No evidence. Executive summary.. There were 31.2% higher deaths in the "gold standard" Pfizer Phase 3 clinical trials. There is only one way to know whether or not the vaccine caused any of the deaths in the 21 vaccinated patients who died: proper histopathology. Pfizer never did it and the FDA never asked for it. This was the biggest mistake in the pandemic and nobody...

Documents reveal that the federal government and insurers incentivized healthcare providers in Kentucky and California to vaccinate Medicaid patients against COVID-19 by offering bonuses based on the percentage of patients successfully vaccinated. ... The federal government and insurers incentivized healthcare providers in Kentucky and California to vaccinate Medicaid patients against COVID-19 by offering bonuses based on the percentage of patients successfully vaccinated. “[This is] truly sickening and I am embarrassed for my profession by this,” Dr. Meryl Nass, an internist and biological warfare epidemiologist, wrote on her Substack, where she posted several documents relating to the COVID-19 vaccine provider incentive...