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<\/figure>\nFDA Documents Confirm Pfizer\u2019s 2021 mRNA Vaccine Lots Had Different Formulations Based on Lot#<\/h2>\nFDA documents confirm different Pfizer EUA mRNA formulations were injected into over a hundred million Americans. US government patent shows many more mRNA bioweapon formulations<\/em><\/h4>\n\n\n\n\n![](\"https:\/\/i0.wp.com\/substackcdn.com\/image\/fetch\/w_64,c_limit,f_auto,q_auto:good,fl_progressive:steep\/https%3A%2F%2Fbucketeer-e05bbc84-baa3-437e-9518-adb32be77984.s3.amazonaws.com%2Fpublic%2Fimages%2Ffb7487a3-a300-4dac-b786-2f59f66145eb_2048x1365.jpeg?w=678&ssl=1\")
\u00a0\u00a0KAREN KINGSTON<\/a><\/h3>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\nWhen the emergency use (EUA) COVID-19 mRNA vaccines were first rolled out in the United States, many Americans questioned\u00a0if different formulations were being distributed<\/strong>. Why? Because some people became severely injured or died after vaccination, while others seemed completely fine. Furthermore,\u00a0some vaccine lots had higher incidences of severe injuries and deaths<\/strong>, while other lots and little to no adverse events per the VAERS database.<\/p>\nIn a court of law, it would be difficult to argue that the incidence of adverse events by lot number is evidence that the EUA mRNA vaccines varied in formulation. One could simply counter argue that people respond differently to biologics and drugs. The varying rates of adverse events can easily be dismissed as a coincidence or potentially attributed to some other factor affecting residents in that region, such as higher rates of obesity.<\/p>\n
What one can\u2019t argue against is<\/strong>\u00a0Pfizer\u2019s and the FDA\u2019s (CBER)\u00a0<\/strong>own\u00a0admission<\/a>\u00a0<\/strong><\/em>that Pfizer\u2019s EUA mRNA vaccines vary in formulations.<\/strong><\/h4>\nPer the FDA\u2019s approval of Pfizer\u2019s Biological License Application (BLA<\/a>); Dr. Ramachandra Naik, of the FDA\/CBER, specifically asked Pfizer, \u201cWhat EUA mRNA vaccine lots are the same as the\u00a0FDA approved<\/strong>\u00a0formulation of COMIRNATY?\u201d<\/p>\nPfizer\u2019s answer should have been, \u2018All of them.\u2019 Why? Because in 2021 the American people were told that there was\u00a0only one formulation for Pfizer\u2019s EUA COVID-19 mRNA vaccines.<\/em><\/strong>\u00a0But that wasn\u2019t Pfizer\u2019s response. Not even close.<\/p>\nInstead, Pfizer responded to Dr. Naik and the FDA by saying,\u00a0\u201cHere\u2019s a list of lot numbers for EUA mRNA vaccines that are the same formulation as COMIRNATY.\u201d<\/strong><\/p>\n\n\n\n![\"\"](\"https:\/\/i0.wp.com\/substackcdn.com\/image\/fetch\/w_1456,c_limit,f_auto,q_auto:good,fl_progressive:steep\/https%3A%2F%2Fbucketeer-e05bbc84-baa3-437e-9518-adb32be77984.s3.amazonaws.com%2Fpublic%2Fimages%2F8f8693dd-a693-4852-b7e4-05ea4e50c056_920x511.png?resize=678%2C377&ssl=1\")
<\/picture>\n<\/div>\n<\/div>\n<\/figure>\n<\/div>\nThis means that throughout 2021, there were some Pfizer EUA mRNA lots that had the same formulation as\u00a0COMIRNATY<\/a>\u00a0and\u00a0a whole bunch of lots that had different mRNA formulations.<\/strong><\/p>\nPfizer\u2019s and the FDA\u2019s own\u00a0BLA document<\/a>\u00a0confirms that Pfizer unleashed\u00a0multiple COVID-19 mRNA formulations\u00a0on the American people and our children.<\/strong><\/h4>\n
\u00a0\u00a0KAREN KINGSTON<\/a><\/h3>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n\n\n\nWhen the emergency use (EUA) COVID-19 mRNA vaccines were first rolled out in the United States, many Americans questioned\u00a0if different formulations were being distributed<\/strong>. Why? Because some people became severely injured or died after vaccination, while others seemed completely fine. Furthermore,\u00a0some vaccine lots had higher incidences of severe injuries and deaths<\/strong>, while other lots and little to no adverse events per the VAERS database.<\/p>\nIn a court of law, it would be difficult to argue that the incidence of adverse events by lot number is evidence that the EUA mRNA vaccines varied in formulation. One could simply counter argue that people respond differently to biologics and drugs. The varying rates of adverse events can easily be dismissed as a coincidence or potentially attributed to some other factor affecting residents in that region, such as higher rates of obesity.<\/p>\n
What one can\u2019t argue against is<\/strong>\u00a0Pfizer\u2019s and the FDA\u2019s (CBER)\u00a0<\/strong>own\u00a0admission<\/a>\u00a0<\/strong><\/em>that Pfizer\u2019s EUA mRNA vaccines vary in formulations.<\/strong><\/h4>\nPer the FDA\u2019s approval of Pfizer\u2019s Biological License Application (BLA<\/a>); Dr. Ramachandra Naik, of the FDA\/CBER, specifically asked Pfizer, \u201cWhat EUA mRNA vaccine lots are the same as the\u00a0FDA approved<\/strong>\u00a0formulation of COMIRNATY?\u201d<\/p>\nPfizer\u2019s answer should have been, \u2018All of them.\u2019 Why? Because in 2021 the American people were told that there was\u00a0only one formulation for Pfizer\u2019s EUA COVID-19 mRNA vaccines.<\/em><\/strong>\u00a0But that wasn\u2019t Pfizer\u2019s response. Not even close.<\/p>\nInstead, Pfizer responded to Dr. Naik and the FDA by saying,\u00a0\u201cHere\u2019s a list of lot numbers for EUA mRNA vaccines that are the same formulation as COMIRNATY.\u201d<\/strong><\/p>\n\n\n\nThis means that throughout 2021, there were some Pfizer EUA mRNA lots that had the same formulation as\u00a0COMIRNATY<\/a>\u00a0and\u00a0a whole bunch of lots that had different mRNA formulations.<\/strong><\/p>\nPfizer\u2019s and the FDA\u2019s own\u00a0BLA document<\/a>\u00a0confirms that Pfizer unleashed\u00a0multiple COVID-19 mRNA formulations\u00a0on the American people and our children.<\/strong><\/h4>\n
When the emergency use (EUA) COVID-19 mRNA vaccines were first rolled out in the United States, many Americans questioned\u00a0if different formulations were being distributed<\/strong>. Why? Because some people became severely injured or died after vaccination, while others seemed completely fine. Furthermore,\u00a0some vaccine lots had higher incidences of severe injuries and deaths<\/strong>, while other lots and little to no adverse events per the VAERS database.<\/p>\n In a court of law, it would be difficult to argue that the incidence of adverse events by lot number is evidence that the EUA mRNA vaccines varied in formulation. One could simply counter argue that people respond differently to biologics and drugs. The varying rates of adverse events can easily be dismissed as a coincidence or potentially attributed to some other factor affecting residents in that region, such as higher rates of obesity.<\/p>\n Per the FDA\u2019s approval of Pfizer\u2019s Biological License Application (BLA<\/a>); Dr. Ramachandra Naik, of the FDA\/CBER, specifically asked Pfizer, \u201cWhat EUA mRNA vaccine lots are the same as the\u00a0FDA approved<\/strong>\u00a0formulation of COMIRNATY?\u201d<\/p>\n Pfizer\u2019s answer should have been, \u2018All of them.\u2019 Why? Because in 2021 the American people were told that there was\u00a0only one formulation for Pfizer\u2019s EUA COVID-19 mRNA vaccines.<\/em><\/strong>\u00a0But that wasn\u2019t Pfizer\u2019s response. Not even close.<\/p>\n Instead, Pfizer responded to Dr. Naik and the FDA by saying,\u00a0\u201cHere\u2019s a list of lot numbers for EUA mRNA vaccines that are the same formulation as COMIRNATY.\u201d<\/strong><\/p>\n This means that throughout 2021, there were some Pfizer EUA mRNA lots that had the same formulation as\u00a0COMIRNATY<\/a>\u00a0and\u00a0a whole bunch of lots that had different mRNA formulations.<\/strong><\/p>\nWhat one can\u2019t argue against is<\/strong>\u00a0Pfizer\u2019s and the FDA\u2019s (CBER)\u00a0<\/strong>own\u00a0admission<\/a>\u00a0<\/strong><\/em>that Pfizer\u2019s EUA mRNA vaccines vary in formulations.<\/strong><\/h4>\n
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<\/picture>\nPfizer\u2019s and the FDA\u2019s own\u00a0BLA document<\/a>\u00a0confirms that Pfizer unleashed\u00a0multiple COVID-19 mRNA formulations\u00a0on the American people and our children.<\/strong><\/h4>\n
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