The FDA says it has no plans to add a black box warning to COVID-19 vaccines despite internal data linking the shots to reported deaths, including children. Critics argue the refusal undermines transparency and ignores documented harm tied to the injections.
Posts tagged as “FDA”
FDA leadership has declined to add a black box warning to COVID-19 mRNA injections despite a formal recommendation from its own safety division. Critics argue the decision ignores mounting peer-reviewed evidence of irreversible cardiac injury and institutional capture.
Children’s Health Defense (CHD) is asking the U.S. Food and Drug Administration (FDA) to revoke the licenses for all Pfizer-BioNTech and Moderna COVID-19 vaccines.
The U.S. Food and Drug Administration (FDA) has launched a renewed safety review of the RSV shots given to infants to protect against the virus, Reuters reported today.
By Tyler Durden By Zachary Stieber The doctor who led an investigation into deaths following COVID-19 vaccination is now the Food and Drug Administration’s (FDA) top drug…
by Brenda Baletti, Ph.D. In a leaked memo to staff, the U.S. Food and Drug Administration’s (FDA) top vaccine regulator said the agency will make changes to how…
By The WinePress In July, The WinePress reported that the Food and Drug Administration (FDA) approved the nation’s fifth fake meat company called Believer Meats,…
By Danielle The Food and Drug Administration (FDA) said drugmakers have recalled over 580,000 bottles of a blood pressure medication due to concerns it may include…
by Brenda Baletti, Ph.D. President Donald Trump on Monday advised pregnant women to avoid Tylenol during pregnancy based on evidence that its active ingredient, acetaminophen, may be associated…
by Michael Nevradakis, Ph.D. The FDA will approve leucovorin, a medication used in cancer treatments to counter the harmful side effects of other drugs, as an autism treatment after…
By Danielle The Food and Drug Administration (FDA) has removed multiple members of the committee that advises the agency on vaccines, including Paul Offit, a vocal…
by Brenda Baletti, Ph.D. The U.S. Food and Drug Administration (FDA) is considering ending the emergency use authorization (EUA) for Pfizer’s COVID-19 shot for children…
by Brenda Baletti, Ph.D. Dr. Vinay Prasad is returning to his job as the U.S. Food and Drug Administration’s (FDA) top vaccine regulator, less than two…
by Suzanne Burdick, Ph.D. The U.S. Food and Drug Administration (FDA) needs to do a better job of warning pregnant women that taking SSRIs, a…
by Brenda Baletti, Ph.D. The U.S. Food and Drug Administration (FDA) on Monday approved Merck’s new monoclonal antibody shot, which the company said is designed…
by Brenda Baletti, Ph.D. San Francisco-based ag-tech startup Wildtype Foods won approval from the U.S. Food and Drug Administration (FDA) for its lab-cultivated salmon last month. The company, backed…
By Danielle The U.S. Food and Drug Administration (FDA) approved the Biologics License Application for the Nuvaxovid (Novavax) COVID-19 jab in adults 65 years and…
by Brenda Baletti, Ph.D. The U.S. Food and Drug Administration is “initiating action” to remove children’s concentrated ingestible fluoride prescription drug products from the market. The drugs,…