(Tyler Durden) The Centers for Disease Control and Prevention (CDC) confirmed in late 2021 that a person died from blood clotting after receiving a COVID-19 vaccine that had been linked with an increased risk of blood clotting, but did not alert the public for two weeks, newly obtained emails show.
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Doctors Unite to Send Powerful Message to CDC & FDA: Stop Targeting Kids Because ‘Emergency Phase of COVID-19 is Over’
(Kyle Becker) Doctors are uniting across the country to tell the Centers for Disease Control and Prevention and the Food and Drug Administration to stop targeting children with Covid-19 vaccines and mask recommendations, because the “emergency phase of Covid-19 is over.”
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Over 500 Military Service Members Sue the Government for Mandating a Vaccine that Was Not FDA Approved and Should Not Have Been Administered
(Joe Hoft) 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.
FDA Commissioner: ‘Don’t Think We Need the Defense Production Act’ – ‘There Is Formula out There’
(Ian Hanchett) On Monday’s broadcast of ABC’s “Good Morning America,” FDA Commissioner Dr. Robert M. Califf argued that invoking the Defense Production Act isn’t needed to fix the baby formula shortage because baby formula manufacturers have already increased production, there has been more formula purchased over the last month than the month before the recall, and “there is formula out there. It’s just not in the right place at the right time.” Because of supply chain disruptions due to Abbott shutting down one of its plants.
FDA Issues Warning As Women Abort Healthy Babies Due To False Positives On Prenatal Genetic Screening Tests
(Dr Leonard Coldwell) The FDA is warning that certain prenatal screening tests used to detect genetic abnormalities have a high chance of returning a false positive, and the stakes could not be higher as the results of these tests lead some women to get abortions.
FDA Director: “The Fda Does Not Regulate Cell Towers Or Cell Tower Radiation” And “Has No Studies Or Information On Cell Towers…”
(B.N. Frank) Decades of peer-reviewed published research has determined that exposure to sources of wireless “Wi-Fi” radiation including cell phones and cell towers can cause symptoms, illnesses, and injuries. In some parts of the world, government agencies are warning residents about this but not in the U.S. In fact, last year, a federal court ruled in favor of organizations and petitioners that sued the Federal Communications Commission (FCC) for NOT adequately protecting Americans from wireless radiation exposure (including 5G). Despite the ruling, the FCC has continued to instead promote and fund the deployment of unreliable and unsafe wireless radiation emitting infrastructure (see 1, 2, 3, 4, 5, 6, 7)
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Federal Investigators Reveal ‘Bombshell’ Findings CDC & FDA Undertook Politically Motivated Actions During Covid Pandemic
(Kyle Becker) A federal investigation into Health and Human Services, National Institutes of Health, the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA) found that public health officials suppressed Covid study findings for political reasons, the Government Accountability Office (GAO) has revealed in a 37-page report.
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FDA Limits Johnson and Johnson COVID Shot Due to Rare Blood-Clotting Syndrome
(Abby Liebing, The Western Journal) Though the U.S. is starting to get back to a semblance of normalcy more than two years after COVID-19 became part of life, vaccine manufacturers are still competing to dominate the market and the general debate over the coronavirus vaccine continues, with validity to both skeptics’ and advocates’ arguments.
FDA Limits J&J’s COVID-19 Vaccine Over Blood Clot Risk
(Tyler Durden) The Food and Drug Administration (FDA) on Thursday strictly limited who can receive Johnson & Johnson’s Covid-19 vaccine due to a rare but serious risk of blood clots.
FDA Vaccine Advisors Discuss Waning Efficacy of Boosters, Ignore Pleas by Vaccine-Injured
(Madhava Setty, MD) Wednesday’s nine-and-a-half-hour meeting of the U.S. Food and Drug Administration’s vaccine advisory committee was riddled with technical issues and punctuated by a sobering 60-minute long public hearing, as committee members sought, but failed to answer basic questions.
FDA Approves First and Only Covid-19 Treatment for Pediatric Patients as Young as 28 Days Old
(Jim Hoft) The Food and Drug Administration on Monday granted its full approval of the COVID-19 antiviral treatment Veklury (remdesivir) for infants and young children. The treatment was previously under emergency use authorization for children.
FDA Launches Investigation Into Popular Breakfast Cereal After Numerous Reports of People Falling Ill
(Julian Conradson) The U.S. Food and Drug Administration has reportedly opened an investigation into Lucky Charms Cereal after hundreds of people have filed reports claiming to have gotten sick after eating it.
How the Criminal FDA Protects Big Pharma by Controlling the Media
(Brian Shilhavy) The British Medical Journal (BMJ) has released a video of whistleblower Brook Jackson, who was a regional director employed by Ventavia Research Group in Texas in 2020 to monitor the Pfizer COVID-19 vaccine trials.
Another GMO Salmon Related Lawsuit Filed Against FDA
(BN Frank) Concerned about potential health risks from consuming GMO foods? Earlier this year, the U.S. Department of Agriculture announced that GMO foods will start being labelled “Bioengineered” or they will include a QR code, website, or phone number for verification. Additionally, a food safety group recently filed another lawsuit against the Food and Drug Administration (FDA) regarding its approval of highly controversial GMO Salmon (aka “Frankenfish”).
FDA Limits Use of COVID-19 Monoclonal Antibody Treatment in 8 States
(Madeleine Hubbard) The U.S. Food and Drug Administration is no longer authorizing the monoclonal antibody treatment sotrovimab in 10 states and territories due to questions about its effectiveness against the BA.2 Omicron subvariant.
