Commentary Recently, revelations by outstanding artist and writer/researcher/investigator Sasha Latypova about COVID genetic vaccines have shed light on the shady, and as she calls it criminal, process by which the vaccine products were manufactured and authorized. Medical Countermeasures With No Regulatory Oversight Latypova combed through FOIA-extracted and leaked documents to find convincing evidence that COVID vaccine manufacture and…
Vaccine Harms Are Biodefense Plan’s Collateral Damage
February 24, 2023
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‘Normalization’ of Emergency Use Authorizations Concerns Health Experts
January 12, 2023
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The Food and Drug Administration (FDA) has approved an unprecedented number of emergency use authorizations (EUAs) for drugs, tests, and medical devices since the beginning of the pandemic. Between March 2020 and June 2021, more than 600 EUAs were authorized, according to Fortune. This has caused concern among healthcare professionals, with some studies claiming that…
End the National Emergency and Public Health Emergency Declarations
The National COVID-19 Emergency, first declared by President Trump in March 2020 in response to the COVID-19 pandemic, was formally extended a second time by President Biden on February 18, 2022 and will come up for a third consideration by Biden in February, 2023. In January 2020, the U.S. Department of Health and Human Services…
Safety of Millions of Americans Hinge on Data From 8 Mice: Pfizer’s New Formulation Had No Human Trials Prior to Approval | Facts Matter
October 16, 2022
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Drug regulators over at the FDA granted a new Emergency Use Authorization to both Moderna and Pfizer for their updated COVID vaccine booster shots despite having no human clinical trial data for the modified formulations. This video is brought to you by Sekur: https://ept.ms/3yW0Wul Stay tuned for our newsletter so you won’t miss out on our exclusive…
[Premiering 10/17 at 1PM ET] Safety of Millions of Americans Hinge on Data From 8 Mice: Pfizer’s New Formulation Had No Human Trials Prior to Approval | Facts Matter
October 16, 2022
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Drug regulators over at the FDA granted a new Emergency Use Authorization to both Moderna and Pfizer for their updated COVID vaccine booster shots despite having no human clinical trial data for the modified formulations. This video is brought to you by Sekur: https://ept.ms/3yW0Wul Stay tuned for our newsletter so you won’t miss out on our exclusive…
Drastic Increase in Non-Infectious Diseases in Military Explained as Data Glitch: Whistleblower
August 23, 2022
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A medical Army officer who discovered a sudden increase in disease coinciding with reports of side effects alongside COVID-19 vaccines—which the Army has dismissed as a data glitch—said he faces involuntary separation after being convicted but not punished for disobeying COVID-19 protocol. In January 2022, First Lt. Mark Bashaw, a preventive medicine officer at the…
80K New Pfizer Docs: Why Did So Many Participants With ‘Minor’ Adverse Events Withdraw From Trial? | Facts Matter
The latest trove of Pfizer documents was released by the FDA. These documents reveal information about the clinical trials that Pfizer was running prior to getting emergency use authorization. This was actually the fifth batch of Pfizer documents released by the FDA thus far. The backstory is that the FDA has in their possession approximately…
Is There a Medical Emergency?
Let’s look at the data. Senator Rand Paul has accused Dr. Fauci and the White House (which is captured by the HHS Administrative State) of “emotionalism and sensationalism” leading up to the renewal of the determination of a continuing medical emergency attributable to COVID-19 disease and SARS-CoV-2 infection. Is this medical emergency justified, or does it reflect…
The Never Ending Medical Emergency.
Are hospitals in USA full of COVID-19 Cases? No. Let’s look at the data. Senator Rand Paul has accused Dr. Fauci and the White House (which is captured by the HHS Administrative State) of “emotionalism and sensationalism” leading up to the renewal of the determination of a continuing medical emergency attributable to COVID-19 disease and SARS-CoV-2 infection….
Novavax COVID-19 Vaccine May Be Issued Emergency Use Authorization in June: FDA
The U.S. Food and Drug Administration (FDA) announced Friday that it will have its advisory panel meet to discuss Novavax’s request for emergency use authorization (EUA) of its COVID-19 vaccine in June. “On June 7, FDA intends to convene VRBPAC [Vaccines and Related Biological Products Advisory Committee] to discuss an EUA request for a COVID-19…
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