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@RepMTG Sign me on! I’ve called out the risky and ineffective COVID-19 vaccines from the very beginning. Recently, I held a hearing with top experts on the countless injuries caused by these experimental jabs. It’s time to say NO to COVID-19 vaccines and remove FDA approval.

A lawsuit attempting to punish the FDA for denouncing ivermectin as a COVID cure could have dangerous consequences In 2021, a bizarre cure for COVID-19 began to emerge on social media, the anti-parasite drug ivermectin. The Food and Drug Administration (FDA) is now under fire for its efforts to refute claims that the drugs could stop the deadly virus. A group of doctors is now suing the FDA, saying the agency’s efforts to refute claims about the drug’s effectiveness against COVID caused them personal harm. Some experts fear that punishment the FDA could face for refuting false information about the...

The Food and Drug Administration (FDA) released an advisory Thursday warning customers not to use counterfeit Ozempic shots found in the drug supply chain. The administration said it is investigating occurrences of fake semaglutide — the drug found in weight-loss medications such as Ozempic and Wegovy — and said it has already seized thousands of units of the counterfeit product. The agency advised wholesalers, retail pharmacies, health care practitioners and patients to check the products they receive and to not distribute, sell or use products labeled with NAR0074 and serial number 430834149057, as some counterfeit products may still be available.

A physician with more than 25 years of experience, Dr. Mary Talley Bowden is board-certified in otolaryngology and sleep medicine. In 2019, she founded BreatheMD in Houston. Educated at the University of North Carolina in Chapel Hill, the Medical College of Georgia at Augusta University, and the University of Texas Medical Branch, Dr. Bowden completed her residency at Stanford University. She is one of the few direct care specialists in the U.S. who does not contract with any health insurance companies and strives to offer affordable care with clear pricing. Dr. Bowden was targeted after speaking out against prescribed protocols...

FDA is not a physician. It has authority to inform, announce, and apprise — but not to endorse, denounce, or advise. Appeals Court.. An appeals court has ruled that the FDA overstepped its authority in telling the public not to use ivermectin to treat Covid. The lawsuit was filed by Dr. Mary Tally Bowden and two others. Dr. Bowden says ivermectin is safe and effective to treat Covid, and, like many doctors, prescribed it to patients. But the FDA controversialized the medicine in infamous tweets that referred to the veterinary form of ivermectin. One tweet read, "You are not a...

The U.S. Food and Drug Administration could not provide information on a confirmed side effect of the Pfizer COVID-19 vaccine, according to a newly disclosed document.FDA staffers said in the document, from 2021, that one of the agency's top surveillance systems was unable to provide details on heart inflammation after Pfizer vaccination.The FDA's Sentinel program was described in the document as "NOT sufficient to identify the outcomes of myocarditis and pericarditis due to reasons identified." Pericarditis is inflammation of the pericardium, or the membrane around the heart.There weren't enough people in the program to assess the risk for 12- to...

The Biden administration gave $86 million to a company accused of peddling counterfeit COVID test kits manufactured in China, according to records obtained by the Washington Free Beacon. The U.S. Department of Health and Human Services announced the funding to CorDx, a COVID test kit manufacturer, in September. The deal will finance free testing products to American households and is intended to "bolster U.S. manufacturing."But records obtained by the Free Beacon raise questions about CorDx's testing kits and its domestic manufacturing capabilities. One of the company's competitors claimed CorDx sold knockoff kits stamped with a false brand name, in violation...

The recent findings of DNA fragments in the Pfizer and Moderna Covid-19 vaccines has led many to question why the FDA, which is responsible for monitoring the quality and safety of the vaccines, has failed to sound the alarm.For years, the FDA has known about the risk posed by residual DNA in vaccines. Its own guidance to industry states:“Residual DNA might be a risk to your final product because of oncogenic and/or infectivity potential. There are several potential mechanisms by which residual DNA could be oncogenic, including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration.”Put...

The Supreme Court seemed concerned Monday that blowing up Purdue Pharma’s bankruptcy settlement — a plan the Biden administration challenged based on the immunity it granted the company’s owners from facing future lawsuits — could mean victims of the opioid crisis never see a cent in compensation. The settlement requires the Sackler family to provide up to $6 billion to address the opioid crisis in exchange for immunity from future lawsuits. While skeptical of the arrangement, multiple justices voiced concerns during oral arguments Monday in Harrington v. Purdue Pharma that changing it would put victims, who overwhelmingly support the settlement...

What could be more dangerous in the field of medicine than government officials knowingly licensing dangerous medical experiments on the population, and then suddenly taking up new positions with the pharmaceutical companies that they were supposed to regulate? This revolving door of corruption is currently taking place between the Food and Drug Administration (FDA) and Moderna, one of the manufacturers of COVID-19 “vaccines.” This collusion is the real public health threat, because it means there is no true regulatory oversight, no accountability for gross medical error and unchecked medical fraud. When a little-known pharmaceutical company named Moderna was awarded $4.94...

"The FDA's regulations related to animal testing no longer fully conform with applicable law," writes the Kentucky senator.Congress unanimously passed the FDA Modernization Act 2.0 in December 2022. The law allows drug companies to find alternative methods of assessing their products, without testing them on animals or human beings. The bill was sponsored by Sens. Rand Paul (R–Ky.) and Cory Booker (D–NH). Its goal was to speed up the drug approval process, and to let scientists experiment with approaches methods that are more humane than testing on live subjects. Reason's Elizabeth Nolan Brown aptly summarized the bill's achievements, noting that...

A world-renowned vaccine expert has presented evidence during congressional testimony showing that pharmaceutical giant Moderna knows its Covid mRNA shots cause cancer. Dr. Robert Malone, the inventor of mRNA vaccine technology, testified during a hearing on Capitol Hill led by Republican Rep. Marjorie Taylor Greene (R-GA). During his testimony, Malone presented the patent for Moderna’s Covid vaccine. Moderna’s patent shows that its COVID-19 vaccine vials contain billions of DNA fragments. Those fragments, along with other contaminants, are linked to birth defects and cancer. In the patent, Moderna admits that contaminants in the shots cause cancer. However, as Malone highlights in...

Several former officials with the U.S. Food and Drugs Administration (FDA) took high-paying jobs with pharmaceutical companies after playing key roles in pushing those Big Pharma firms’ Covid shots through the regulation process. The “revolving door” was exposed during an investigation by the renowned peer-reviewed British Medical Journal (BMJ). The discovery is reminiscent of former FDA official Curtis Wright IV. Wright played a central role in the FDA’s approval of the dangerously addictive opioid OxyContin for Purdue Pharma in 1995. Shortly after, he left the FDA for a job at Purdue and a massive salary with the company. The actions...

Federal public health agencies are reportedly withholding the most accurate and up-to-date reports of vaccine injury from the public, allegedly to protect privacy. Patients don't necessarily see it that way, and it's not clear the feds told Congress. The Vaccine Adverse Events Reporting System, jointly managed by the CDC and FDA, has a secret "back end" privy only to regulators, an FDA official told advocates of VAERS reform nearly a year ago, according to a British Medical Journal investigation published Friday. "Anything derived from medical records by law" cannot be included in the "front end system" accessible to the public,...

The U.S. Food and Drug Administration (FDA) on Thursday announced its approval of Ixchiq, the first chikungunya vaccine. The vaccine, which is made by Valneva, is approved for anyone age 18 and older who has a risk of being exposed to the virus. The chikungunya virus is transmitted to people through bites from infected mosquitoes. "This virus is in a similar category as dengue or Zika and is carried by the same mosquitoes," noted Dr. Marc Siegel, clinical professor of medicine at NYU Langone Medical Center and a Fox News medical contributor. The FDA described chikungunya as an "emerging global...

[10/30/2023] FDA is updating the list of over-the-counter eye drop products consumers should not purchase or use to include Equate Hydration PF Lubricant Eye Drop 10 mL sold by Walmart in stores and online. Walmart is removing the product from their store shelves and website. [10/27/2023] FDA is warning consumers not to purchase and to immediately stop using 26 over-the-counter eye drop products due to the potential risk of eye infections that could result in partial vision loss or blindness. Patients who have signs or symptoms of an eye infection after using these products should talk to their health care...

The Food and Drug Administration (FDA) has issued a dire warning to customers NOT to purchase more than two dozen eye drop products being sold at some of the nation’s most prominent retailers. While this is undoubtedly critical public information, this new revelation should also raise some serious questions about the FDA itself. As ABC News reported Monday, the FDA in a press release Friday revealed that the eye drop products were manufactured in a facility with “insanitary conditions” and carry a “potential risk of eye infections that could result in partial vision loss or blindness.” These products are intended...

Anewly discovered “anti-CRISPR” system in viruses could help us control CRISPR gene-editing technologies and lead to better weapons against antibiotic-resistant superbugs. The background: Your immune system has ways to remember viruses you’ve encountered before and help defend you if they appear again — and, amazingly, some single-celled bacteria do, too. These microbes evolved the CRISPR system to protect themselves from the viruses that infect bacteria, called phages. The bacteria will take a little bit of a virus’ DNA sequence and add it to their own genome, like a memory of past infections. They then create CRISPR-associated (Cas) proteins containing copies...

Sheesh, talk about the timing of two different articles. Politico reported yesterday that CDC officials admit only 3% of eligible Americans have chosen to get the latest COVID-19 booster shot, although there could be some delay in reporting.WASHINGTON – The Biden administration’s campaign to convince Americans to get an annual Covid shot is off to a very slow start. Even so, the nation’s top disease-fighting official says the U.S. remains “on track” to hit last year’s uptake levels, which crested at just 17 percent of the U.S. population. (more)Today, the FDA announces when COVID booster is combined with Flu shot,...

An accurate reporting by Pfizer would have shown equal numbers of clinical trial deaths in the vaccine and placebo groups and thus, no benefit of vaccination. To obtain emergency use authorization (EUA) for its COVID-19 vaccine, Pfizer and BioNTech submitted a data package in 2020 to the U.S. Food and Drug Administration (FDA) so the agency could evaluate the safety and efficacy of its vaccine. A recently published peer-reviewed study by the DailyClout Pfizer/BioNTech Documents Investigations Team suggests Pfizer excluded known deaths in the vaccine arm of its clinical trial from its data filing and withheld information from the agency...