AI:Leaked emails reveal that top FDA official Janet Woodcock warned Anthony Fauci that failing to conduct a dedicated study into COVID-19 vaccine side effects would eventually "come back to bite" him. This revelation follows a long pattern of the medical establishment, including Fauci and his associates, ignoring internal warnings and suppressing data regarding adverse reactions to ensure continued vaccine rollout. The correspondence highlights a persistent refusal by high-level health officials to address safety concerns despite direct pressure from within regulatory agencies.Open
by Diana Zapata • News Writer /Editorial Specialist Published August 14, 2026 A potentially dangerous bacterial threat is drawing renewed attention along the U.S. Gulf Coast as health officials report cases of Vibrio vulnificus, commonly [...]
AI:Dr. McCullough is sounding the alarm on a rapidly escalating crisis as Vibrio vulnificus—the dreaded flesh-eating bacteria—begins to spiral out of control along the U.S. Gulf Coast. While the establishment media stays busy with their scripted distractions, this burgeoning biological threat highlights a terrifying reality of vulnerability in our coastal regions. As we have seen with the recent surges in Cyclospora and the looming shadows of Nipah virus and parasitic outbreaks, the biological safety of the American public is under constant siege by pathogens that health officials seem perpetually unable to contain. This isn't just another isolated medical report; it is part of a wider, systemic failure in our national bio-defense and…Open
NIH Director Dr. Jay Bhattacharya joins NewsNation to discuss the Trump administration's "Operation Warp Speed" and whether Dr. Anthony Fauci withheld critical information about the COVID vaccine's side effects. Anchor Elizabeth Vargas delivers the biggest stories, without bias or opinion. Watch "Elizabeth Vargas Reports" every weeknight at 7p/6C on NewsNation. #VargasReports NewsNation is your source for fact-based, unbiased news for all Americans.
Moderna's own research shows 5,000 novel jabs required to prevent one hospitalization over standard vaccine. "Pharma finished recapturing" FDA after exit of officials with higher standards, drug industry journalist says.
The Food and Drug Administration (FDA) has approved Moderna's mRNA-based seasonal flu vaccine.
The Food and Drug Administration (FDA) has granted approval for Moderna’s mRNA-based flu vaccine for adults 50 and older, despite earlier regulatory concerns. PULSE POINTS WHAT HAPPENED: The Food and Drug Administration (FDA) has approved Moderna’s mRNA-based seasonal flu vaccine . DETAIL: Named mFLUSIVA, the vaccine was approved on Wednesday. It is aimed at people aged 50 and older. The decision comes after the FDA initially declined to approve the vaccine back in February. Specifically, the vaccine was initially blocked as the clinical trial did not use the best available comparator for adults aged 65 and older. “We are grateful to the clinical trial participants, investigators, regulators and Moderna teams whose…Open
Dr. Anthony Fauci faces a contempt vote after invoking the Fifth Amendment more than 100 times during a Senate hearing on COVID-19. Fauci was subpoenaed by Senator Rand Paul, R-Ky., whom the infectious disease expert accuses of having an "unhinged obsession" with him. That's tonight on "Elizabeth Vargas Reports." #VargasReports #DrFauci #RandPaul This episode originally aired on July 29, 2026. Anchor Elizabeth Vargas delivers the biggest stories, without bias or opinion. Watch "Elizabeth Vargas Reports" every weeknight at 7p/6C on NewsNation. NewsNation is your source for fact-based, unbiased news for all Americans.
Ten of 12 scientists on call that produced the "Proximal Origin" paper thought that "deliberate insertion was possible," Fauci's alleged notes say in regard to COVID-19 spike protein binding to human receptors.
