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Link: https://www.naturalnews.com/2025-01-25-fda-refused-monitor-select-covid-19-vaccine-injuries.html
Newly released FDA emails reveal inconsistent monitoring of COVID-19 vaccine injuries, with frequent alerts for the Janssen vaccine but few for Pfizer and Moderna. Despite over 1.4 million adverse event reports in VAERS, the FDA failed to detect widely recognized risks like myocarditis and pericarditis for mRNA vaccines. The CDC and FDA relied solely on one data analysis method, ignoring another that flagged hundreds of potential safety signals. Critics argue the agencies’ oversight was inadequate, raising concerns about transparency and accountability in vaccine safety monitoring.