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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 […]
Read the whole story at www.americanthinker.com
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