FDA, CDC Guilty of Clinical Malpractice and Scientific Fraud by Inaction and Omission on mRNA Vaccine Safety Warnings

Today, unquestionably serious cardiovascular, thrombotic and neurologic adverse events related to the vaccine have occurred around the world. The FDA’s own vaccine adverse event tracking system (the Vaccine Adverse Event Reporting System or VAERS) shows substantial and serious risks from the vaccine, even though the FDA only collects an estimated 10% of all adverse events.

Still, federal agencies and manufacturers aren’t officially warning the American public about these risks, despite having been privy to this information for almost a whole year. Why? Because it would counter the narrative that taking endless vaccines and boosters is your patriotic duty.

It’s pretty clear today there are both safety and efficacy problems with vaccines and boosters. Because all of the FDA’s 18,000-plus employees had access to the same drug safety data we have, one must ask:

• Where is the updated Covid-19 labeling reflecting the latest safety and efficacy findings in VAERS?
• Where are the FDA “Dear Doctor” letters giving updated safety guidance?
• Where are the “Dear Pharmacist” letters to pharmacists who are still daily administering thousands of boosters to kids and other young healthy people?
• Why isn’t the FDA recommending follow-up symptom tracking to avoid further inflammatory neurologic/thrombotic/cardiovascular tragedies instead of its proposal to extend the dosing interval and cross fingers that it would mitigate risk (as there is no concrete clinical evidence that it will do anything?
• Why is the FDA ignoring internal drug safety epidemiologists who have stated during official FDA presentations that it only takes a single, well-documented adverse event to justify a safety signal investigation and warning to the American public of the risk?
• Why isn’t the FDA demanding studies addressing genotoxicity, teratogenicity, oncogenicity, the potential for reduced fertility in men and women, the clinical effects of spike proteins in donated blood, and the bioaccumulation of vaccine in women’s ovaries? Why isn’t the agency convening and dedicating a Data Safety Monitoring Board to surveil all these post-marketing effects and others?

Are Americans expected to believe that the $6.5 billion-per-year taxpayer-funded FDA lacks adequate funding to address all these public health issues?

Not Fully Disclosing Safety Risks to Patients Violates Ethics and States’ Licensing Standards

In order for a physician, pharmacist, and nurse, or anyone else with a clinical professional license to work at the FDA or CDC or any other public health agency, that person must have a “current, active, full, and unrestricted license or registration from any state in the US.” Not fully warning patients about the potential dangers from any drug before administering useless and potentially dangerous vaccines and boosters places these professionals’ licenses at risk, regardless of what the CDC, FDA, or White House says.

Physicians, pharmacists, and nurses have always been held to a higher standard. They are expected to think for themselves rather than simply take orders.

As the truth is elucidated about vaccine efficacy and safety, these federal employees and mRNA vaccine manufacturers who colluded to withhold information from the public will be held accountable, and the whole “I was just following orders” excuse will not cut it. Just keeping your head down and cruising through your job, handing out vaccines is not an option when it comes to the lives of your fellow Americans when licensures are...

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