A letter from the FDA—which quietly appeared on it’s website last week—shows that regulators have demanded Pfizer and Moderna update their labels to include findings of myocardial injury following vaccination.
The letter cites multiple long-term observational studies, including one showing 278 out of 331 patients experiencing post-vaccine cardiac symptoms.
It warns that failure to comply places the companies in violation of federal law (FDCA section 505(o)(4)). If ignored, their products will be labeled “misbranded,” opening the door to a full market recall. -
Few acronyms stir more visceral reactions among MAHA moms than this one: mRNA.
And with good reason.
We were sold the technology as a miracle, a revolutionary vaccine that would save lives and return us to normal. Most of us didn’t question it. We didn’t pause to ask how it differed from the traditional vaccines we grew up with. We assumed it had been tes…
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