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The Vaccine Adverse Event Reporting System
https://vaers.hhs.gov
On February 1, 2022, US Senator Ron Johnson sent a letter to Secretary of Defense Lloyd Austin on February 1 highlighting the dramatic rise in adverse events reported in the Defense Medical Epidemiology Database (DMED) after the vaccines were rolled
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Not Gene Tech Are COVID-19 vaccines experimental gene technology that is still under development? No, that’s not true: The Medicines and Healthcare products Regulatory Agency (MHRA) in the United Kingdom says none of the vaccines authorized in the U.K. —
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Via Blue State Conservative What should receive far greater attention is the formation of microscopic blood clots throughout bodies caused by spike proteins. These are not found through conventional medical scanning and imaging technologies. Know this: They result from COVID
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Guest Post by Steve Kirsch I read in the media that Spotify has a fact-based COVID-19 hub. So I thought I’d create my own so you’d have a choice on which facts you want to believe. Spotify made a press
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Summary DHS is getting tough on COVID misinformation spreaders, i.e., people who spread information that “undermines public trust in government institutions.” Since DHS has finite resources to pursue all these perpetrators, as a public service, I have created a list
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The United States military’s official database for vaccine adverse events is overflowing with evidence to show a massive uptick in serious illnesses due to Wuhan coronavirus (Covid-19) injections. The Defense Medical Epidemiology Database, or DMED for short, clearly reveals a
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No Admission Does Pfizer admit in confidential documents that its COVID-19 vaccine may cause vaccine-associated enhanced disease (VAED)? No, that’s not true: The document, called 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021, lists
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No Admission Does Pfizer admit in confidential documents that its COVID-19 vaccine may cause vaccine-associated enhanced disease (VAED)? No, that’s not true: The document, called 5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021, lists
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*** February 1, 2022, Pfizer/BioNTech asked the U.S. Food and Drug Administration to grant emergency use authorization (EUA) for their COVID shot to babies and children aged 6 months through 4 years The EUA will be for a two-dose regimen,
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The millions of health impacts being reported in conjunction with Wuhan coronavirus (Covid-19) “vaccines” have one common link: microscopic blood clots triggered by spike proteins. It is now known that the jabs damage blood vessels throughout the body. They are
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