Evidence of Risk, Harms Mount as FDA Forces new Covid Booster Without Human Testing
Jefferey Jaxen … Throughout the pandemic response, the US Food and Drug Administration (FDA) has become increasingly reckless rubber stamping Covid shots into circulation. At the start of the FDA’s vaccine vetting process, the agency promised transparency. We’ve went from rushing experimental vaccines onto the market with short, improper testing during an emergency to rushing […]
The Declining Standards of FDA Drug Approvals
Maryanne Demasi The US Food and Drug Administration (FDA) has a legal obligation to protect the public and ensure that the benefits of medicines outweigh the harms before being marketed to people. But the agency’s increasing reliance on pharmaceutical industry money has seen the FDA’s evidentiary standards for drug approvals significantly decline. … Industry fees […]
Big Pharma Wants to Put an End to Vitamins and Supplements
Joseph Mercola One of the latest attempts to thwart your ability to access nutritional supplements comes in the form of draft legislation that would require premarket approval for dietary supplements. In short, it would require supplements — which are food — to undergo the same approval process as drugs. In the past, the drug industry […]
FDA Colluded With Moderna to Bypass COVID Vaccine Safety Standards, Documents Reveal
Megan Redshaw According to an ex-pharmaceutical industry and biotech executive, documents obtained from the U.S. Department of Health and Human Services (HHS) on Moderna’s COVID-19 vaccine suggest the U.S. Food and Drug Administration (FDA) and Moderna colluded to bypass regulatory and scientific standards used to ensure products are safe. Alexandra Latypova has spent 25 years in pharmaceutical […]
Letter to UK Health Authorities, Re: 6 Month to 4 Years Covid Vaccines
the children’s union We are writing to you urgently concerning the announcement that the FDA has granted an Emergency Use Authorisation for both Pfizer and Moderna Covid-19 vaccines in preschool children. We would urge you to consider very carefully the move to vaccinate ever younger and younger children against SARS-CoV-2, despite the gradual but significant […]
FDA Panel Votes to Waive Clinical Trials for New COVID Boosters
Megan Redshaw The U.S. Food and Drug Administration’s (FDA) vaccine advisory panel on Tuesday voted 19 to 2 to recommend new COVID-19 booster shots that include the Omicron variant this fall. The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) did not issue guidance on whether additional data would be needed to recommend an updated composition of the primary-series vaccines authorized for […]
Why Big Pharma is Desperate to Get COVID Jab Into Babies
Joseph Mercola The rate of COVID-19 associated hospitalization among children aged 5 to 11 is just 0.0008%. In real-world terms, that’s so close to zero you basically cannot lower it any further. Despite that, the U.S. Food and Drug Administration’s vaccine advisory panel — the Vaccines and Related Biological Products Advisory Committee (VRBPAC) — on […]
FDA Briefing Document: Vaccines and Related Biological Products Advisory Committee Meeting
June 28, 2022 At a previous Vaccines and Related Biological Products Advisory (VRBPAC) meeting on April 6, 2022, the committee discussed considerations that should inform strain composition decisions to ensure that available COVID-19 vaccines continue to meet public health needs, when and how frequently to consider strain composition changes, and the process that should be […]
