But the FDA chose to ignore it.
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.
Even then, the vaccine failed.
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....<<<Read More>>>...
