These Discoveries Will Make You Think Twice About COVID Vaccinations
I don’t write enough about the adverse events from COVID vaccines. The reason is that I like to be accurate, but most of the data on vaccine side effects is hidden from us. So, while I have pointed out the many databases that FDA and CDC have available and are supposed to be using to assess vaccine safety, only 1 is publicly available: VAERS. Officially, it is the joint FDA-CDC Vaccine Adverse Event Reporting System. Steve Kirsch and Jessica Rose have done the best job analyzing the VAERS data, so I suggest you go to their Substacks and read what they have to say.
Both the FDA and CDC each have about ten other databases that taxpayers pay for, but most of them we never hear about. Here are the FDA databases:
Below, then-head of Immunizations at CDC, Dr. Nancy Messonier, told the public about the databases that would be used to assess COVID vaccines’ safety just before the rollout, on December 10, 2020.
Both agencies provided the public with promises of what these vaccine safety databases could provide. The databases FDA rents include more than 100 million Americans, for example. But since the rollout, the federal agencies have been almost silent on what they reveal.
However, yesterday I came across 3 very important items about COVID vaccine safety that I had not seen discussed elsewhere. Each one is an important, though limited, piece of the COVID vaccine safety puzzle — but together, they give us a very good idea of what we are all dealing with as we traverse this data desert, touching small bits of the elephant like the blind men, but never being able to grasp the picture in its entirety.
Item 1 was posted on the FDA website on July 12, 2021 with no fanfare. It revealed that the FDA was indeed using its Medicare beneficiary database to look for potential vaccine adverse reactions, and it found four related to Pfizer’s vaccine, which is the most widely used COVID vaccine:
FDA has routinely been using screening methods to monitor the safety of COVID-19 vaccines and to evaluate potential adverse events of interest (AEI) related to these vaccines. One of these methods, called near real-time surveillance, detected four potential AEIs in the Medicare healthcare claims database of persons aged 65 years and older who had received the Pfizer/BioNTech COVID-19 vaccine. The four potential AEI are pulmonary embolism, acute myocardial infarction, immune thrombocytopenia, and disseminated intravascular coagulation. The screening methods have not identified these AEI after vaccination in persons 65 years and older who received the two other authorized COVID-19 vaccines…
These events have not been identified as safety concerns or signals in the CDC Vaccine Safety Datalink (VSD) or the Veterans Administration (VA) Healthcare data systems screening methods. The Vaccine Adverse Event Reporting System (VAERS), another government monitoring system, also has not identified any association between any COVID-19 vaccine and these AEI.
FDA continues to closely monitor the safety of the COVID-19 vaccines and will further investigate these findings by conducting more rigorous epidemiological studies. FDA will share further updates and information with the public as they become available.
If the vaccine caused blood clots and bleeding, as suspected, those are the four diagnoses I would expect to see indicating vaccine injuries. The claim that FDA has not seen them in its other databases, including VAERS, is curious because people who independently study VAERS have, in fact, reported higher rates of myocardial infarctions and pulmonary emboli.
Six weeks after the FDA posted about these very serious warning signs, they issued a full, unrestricted license for Pfizer’s vaccine, the very one they were warning about. The FDA website where the above information is posted has never been updated, and the FDA has not revealed what the last 8 months of “more rigorous epidemiological studies” show.
Item 2 is an academic paper published by the CDC in its own, non-peer reviewed journal, the Morbidity and Mortality Weekly Report. It was written by CDC scientists with researchers at various sites that participated in a CDC-funded data collection on COVID.
The paper concludes that while myocarditis is known to occur after COVID vaccinations, it is more common after getting the disease COVID. This is an unusual claim, since myocarditis rates as high as 1 in 2000 males aged 18-24 have been reported after the second COVID shot, and no one has claimed that such rates apply after getting the disease.
So what did the CDC do? It chose to examine this issue using a database that admittedly misattributed most vaccinations!
The CDC has access to everyone’s vaccination data and could have easily used an accurate dataset, but chose not to. Instead, the CDC admitted in the paper’s fine print that while 82% of Americans over age 5 have reportedly received at least one COVID vaccine, in the 15 million person dataset it used, only 28% were recorded as vaccinated. The only reasonable interpretation is that a large number of vaccinated individuals were incorrectly assigned to the unvaccinated category. It seems a case could be made that this is scientific fraud.
Item 3 came from the Pfizer documents that were released on April 1. Huge thanks to all the volunteers who have been digging through these documents to piece together the truth about the vaccines. Huge thanks also to the scientists and attorneys who had to file suit and win in court to force FDA to release them.
This information, I think, could be crucial.
It turns out that Pfizer had to hire 600 new full-time employees simply to process the adverse event reports that were coming in regarding vaccine injuries and deaths: 600 new hires in the first 2 1/2 months of the vaccine rollout. Pfizer further said it planned to hire another 1800. Eighteen hundred more! Just to manage the paperwork resulting from its vaccine-caused carnage.
The FDA knew. But the FDA wanted it buttoned up for 75 years. The CDC also knew, since the deaths reported to VAERS caused by COVID vaccines exceed all death reports for the past 30 years for all other vaccines put together. Both agencies hid what they knew. The CDC even played tricks with data to mislead us. Pfizer knew. The DHHS must have known.
There is no Public Health without public honesty. Our public health agencies have become public trickery agencies. Why should anyone believe anything they say now? Why would anyone do what they recommend?
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Dr. Meryl Nass is an internal medicine physician who has been challenging the official dogma for over 30 years. She is the first person to have investigated an epidemic and proved it was due to biological warfare. She challenged the Defense Department regarding the causes of Gulf War Syndrome, and helped lead the fight against the military’s forced anthrax vaccinations. More recently, she has investigated all aspects of the COVID pandemic: identifying a coverup of the pandemic’s origin, revealing over 50 ways hydroxychloroquine treatment of COVID was suppressed, and providing patients with effective early care. In January 2022, her medical license was suspended for spreading misinformation and prescribing hydroxychloroquine and ivermectin for patients.