Even FDA-funded research acknowledges “safety signal” for serious heart inflammation in 12-17 year-olds. Agency ignores federal law by demanding proven “causality,” medical researchers claim.
Researchers around the world continue documenting potentially severe side effects from COVID-19 mRNA vaccines in certain demographics, but the Food and Drug Administration refuses to label them or even tell recipients the shots can’t stop transmission of an increasingly immune-evasive virus.
Autopsies and reviews of medical records revealed a much higher incidence of Pfizer and Moderna vaccine-associated heart deaths than officially categorized in South Korean, Japanese and Qatari government registries, particularly in younger people at lower risk from COVID. That echoes a German autopsy study of healthy people who died within 20 days of jabs.
An FDA-funded study in the Journal of the American Medical Association Pediatrics on May 22 also found a “safety signal” for myocarditis and pericarditis — forms of serious heart inflammation — following vaccination in 12-17 year-olds. It was based on “near-real-time monitoring using commercial claims databases” for more than 3 million children ages 5-17 who took Pfizer’s vaccine.
Three weeks earlier, the Nature journal NPJ Vaccines published a Taiwanese study that found a much higher risk of “all forms of retinal vascular occlusion” — visual impairment — among vaccinated populations both 12 weeks and two years later, with “no disparity … between brand and dose” among mRNA vaccines.
and yet TV, RADIO, BILLBOARDS, want you to get yours shots or get your booster shots WTH