Why Aren’t The FDA And CDC Informing The Public About Documented Adverse Events After mRNA Injections?
By: David Gortler
March 25, 2022
Properly evaluating any kind of drug safety — let alone that of presidentially mandated vaccines— involves carefully examining all of the available data. While Americans still haven’t been given full access to the full Pfizer “Comirnaty” license application, we do have access to the Food and Drug Administration’s medical officer review.
This comparatively spartan 107-page FDA review document purportedly contained everything the FDA believed was important to release to the public from the original Pfizer application of 329,000 pages. The FDA review conspicuously notes “clinically important serious adverse reactions [included] anaphylaxis and myocarditis/pericarditis”— that is, severe allergic reactions and inflammation of the heart and or the sac containing the heart, respectively.
Likewise, Moderna’s “Spikevax” vaccine was given its Emergency Use Authorization in late 2020, and was fully approved by the FDA on January 31, 2022. Following approximately a month of time to redact its review from “trade secrets,” the FDA released an even leaner 30-page review. Like the Pfizer vaccine, there were clear indications of myocarditis and pericarditis in the initial study, demonstrating the potential for risk going forward.
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https://thefederalist.com/2022/03/25/why-arent-the-fda-and-cdc-informing-the-public-about-documented-adverse-events-after-mrna-injections/
