FDA May Investigate DNA Contamination in COVID Shots
The U.S. Food and Drug Administration (FDA) is considering investigating potential DNA contamination in mRNA COVID-19 shots. Tracy Beth Hoeg, MD, senior adviser to FDA commissioner Marty Makary, MD, MPH, confirmed that the investigation is “something that’s being discussed.”1 Retsef Levi, PhD, chair of the U.S. Centers for Disease and Prevention’s (CDC) COVID-19 immunization workgroup, […]
Flu Vaccine Effectiveness Pegged at About 50 Percent
Each year, the influenza vaccine is promoted across the country—recommended by public health authorities, advertised widely, and often required by medical workplaces, schools, and childcare centers. Yet, the vaccine’s effectiveness remains uncertain, as it is formulated months in advance based on predictions of which influenza virus strains will predominately circulate. This season, the flu shot’s […]
Cancer Treatments Using mRNA Technology Targeted as COVID Shots Sales Decline
BioNTech SE and Moderna, Inc., two leading pharmaceutical companies that developed the mRNA COVID-19 biological, are facing new financial and regulatory challenges as demand for COVID booster shots continues to fall and U.S. health policy changes reshape the vaccine market.1 Moderna cut its 2025 sales forecast to between $1.5 billion and $2.2 billion, down as […]
Autism Symptoms Could Be Added to U.S. Vaccine Injury Program
On July 28, 2025, Secretary of Health and Human Services Robert F. Kennedy, Jr. said he planned to overhaul the National Vaccine Injury Compensation Program (VICP. In September, the U.S. Department of Health and Human Services (DHHS) announced it may add certain symptoms of autism to the official list of vaccine side effects eligible for […]
FDA Questions Safety of Giving Multiple Vaccines at Once
The U.S. Food and Drug Administration (FDA) is re-evaluating the long-standing federal vaccine use policy that allows multiple vaccines to be given during the same visit—particularly COVID-19, influenza and RSV shots. In a memo last month, Vinay Prasad, MD, MPH, director of the FDA’s Center for Biologics Evaluation and Research (CBER), wrote that the agency […]
Withheld: Real-World Infant Deaths from RSV Antibody Shot
As ACIP deliberated without access to full trial data, an even more alarming pattern was already unfolding in the real world. Now, analysis of the FDA’s FAERS database reveals 37 infant deaths out of just 991 reports—a fatality signal nearly twice that of other routine vaccines. Why was this not disclosed? The warning sign was […]