The Pfizer vaccine uses mRNA technology, which was never authorized before December 2020 for human use – and for a reason. During animal trials for SARS and MERS viruses, it had the opposite of its intended effect and worsened the disease by inducing antibody-dependent enhancements.
Eighteen months after the injections were administrated in trials, all the animals died. Yet somehow, the vaccine was granted emergency use authorization around the world and administered to millions to protect them against a disease that statistically kills only less than 0.2 percent of those affected, the majority being the elderly, the vulnerable and those who already had existing underlying conditions.
An example is Australia. In June, nearly 90 percent of Australia is considered fully vaccinated, but the country is still riding its largest wave of COVID-19 deaths since March. According to data, at least 4 in 5 of the COVID-19 deaths recorded were among the fully vaccinated
This suggests that the COVID-19 injections don’t work. Moreover, it suggests that the injections make the recipients more vulnerable to infection.
Data revealed that all of the deaths could have been avoided if the FDA bothered to read the documents submitted by Pfizer. Instead, the FDA attempted to delay the release of the company’s vaccine safety data for 75 years, despite approving the injection after only 108 days of safety review.
Thanks to Federal Judge Mark Pitton, the FDA was forced to release 55,000 pages of the Pfizer documents every month. Nonprofit group Public Health and Medical Professionals for Transparency posted all of the released documents on its website, with the latest uploaded on June 1.
Documents in the data dump include information on important potential risks, one of which is VAED.
VAED occurs when an individual who has received a vaccine develop more severe presentations of the disease he or she was exposed to.
Disease enhancement has usually been associated with dengue virus infection and was previously observed in humans with inactivated whole-virus vaccines against the respiratory syncytial virus (RSV) and measles.
While it can be difficult to distinguish between vaccine failure (also called a breakthrough disease) and VAED, the latter requires recognition that a clinical presentation is different, atypical, modified or more severe compared to the natural presentation of the disease.
TOP SECRET PFIZER DOCUMENT LEAKS ONLINE…
VAED cases not definitive, claims Pfizer
Pfizer made sure to use this confusion between breakthrough infections to VAED to their advantage, claiming that the identified potential VAED cases are not definitive.
In an FAQ on the U.K. government website, VAED is identified as a potential risk for both Pfizer and AstraZeneca vaccines and should be kept under close review.
Real-world data showed that Pfizer is likely committing fraud, and it won’t be the first time. In 2009, the company paid $2.3 billion in a massive health care fraud settlement for “mis-promoting” the drug Neurotonin for uses that have not been approved by medical regulators and for paying kickbacks to those who had been compliant.
In the U.K., the Pfizer vaccine was granted emergency use authorization on December 8, 2020, with the first injection administered the following day. Five months later, in April 2021, the company admitted that it did not have a clue if its vaccines caused VAED and that they will know once they have more data. This means that the general public could be taking part in the largest pharmaceutical experiment ever conducted.
Pfizer also admitted that VAED is a theoretical risk associated with its experimental COVID-19 vaccine, which has been injected into hundreds of millions of people around the world since December 2020.
Follow Vaccines.news for more information about Pfizer’s documents in connection with the COVID vaccine.
Dr Eddy Bettermann MD focus on Biological Medicine (Biologische Medizin) #Biological #Medicine #videos http://bit.ly/2LF3Ro3, Darkfield Microscopy (Dunkelfeld Mikroskopie), Orthomolecular Medicine (Orthomolekulare Medizin), Ayurvedic Medicine (Ayurveda), Psychosomatic Medicine (Psychosomatische Medizin), raw food (Rohkost), fasting (Fasten):
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Dr. Eddy Bettermann MD, physician from Germany, consultant and teacher in biological medicine, especially dark field microscopy known as Live Blood Analysis in Thailand, Malaysia, Hong Kong, Singapore and the Philippines. But he lecture also in the USA, Canada and the U.A.E. He speaks english and german.
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Our Mission:
The mission of the Integrative Medicine is to search for the most effective treatments for patients by combining both conventional and alternative approaches that address all aspects of health and wellness – biological, psychological, social and spiritual. Biological Medicine is a big part of my work and so is Dark field Microscopy, what I use in my daily practice and what I teach more then 15 years in Asia and around the world: Live Blood Analysis in dark field based on Haematology.
We utilize Live blood analysis since 2004, conventional as well as specialty laboratories for a thorough diagnostic work up of the disease in question. Our integrative medicine treatment regimens are especially unique and are tailored specifically to the individual needs of each patient.
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Heavy metal poisoning
Heavy metal poisoning is much more common than most people realize, and if you’re thinking that it doesn’t apply to you because you haven’t been exposed to any, think again. If you’ve eaten fish regularly, had amalgam fillings, received vaccinations, drank contaminated water, or done industrial or agricultural work or pharmaceutical manufacturing, there’s a good chance that you have a fair amount of toxic metals in your system..
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