They don't file VAERS reports either. That's a violation of federal law. I had a bunch of questions for their media relations department, but they ghosted me. Here's what I wanted to know.

Moderna CEO Stéphane Bancel testifies at 10:00 a.m. ET on March 21 to U.S. Senate Health Committee on ...

Pfizer examined possible ways its COVID-19 vaccine causes heart inflammation, a newly disclosed document shows. The company in ...

Dr Judy A Mikovits, co-author of Plague, Plague of Corruption and Ending Plague. In her forty-year quest to understand the causes, prevent and treat chronic diseases, Dr. Judy has co-authored seminal papers culminating at least a decade of research in each of four fields: immunology, natural products chemistry, epigenetics, and HIV/AIDs drug development.

John Beaudoin is calling for a criminal investigation into remdesivir citing data that it may have killed 100,000 people in America. The US Food and Drug Administration (“FDA”) authorised the experimental antiviral drug remdesivir, brand name Veklury, for emergency use against covid-19 in May 2020. By October 2020, it had received full approval. It remains a primary treatment for covid-19 in hospitals, despite research showing it lacks effectiveness and can cause high rates of organ failure. In mid-February, Beaudoin called for a criminal investigation into the drug, citing data for Massachusetts he estimates remdesivir may have killed 100,000 people in the US. “They know,” he tweeted, “or they wilfully refuse to know. Either way, it’s homicide.”

WASHINGTON—President Joe Biden on March 20 signed into law a bill mandating declassification of COVID origin-related intelligence, saying ...

The U.S. Food and Drug Administration’s decision Tuesday to allow infants and children 6 months through age 4 to get Pfizer’s bivalent booster shot drew harsh criticism from pediatricians and others who said children don’t need any COVID-19 vaccines, let alone four doses.

Physician assistant fired for reporting to VAERS tells her story.