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Absolutely NOT safe and NOT effective: FDA and CDC lied about vaccine efficacy to obtain ’emergency authorized use’ (EAU) for highly-suspect human medical experiment using mRNA

As they say, the proof is in the pudding. COVID-19 shots have been the deadliest inoculations ever documented, by far, and that’s according to the CDC’s very own data. More people have died from Covid vaccines (approaching 5,000 now) than all vaccine deaths totaled since the 1950s. No wonder why. They couldn’t even reach the EAU (emergency authorized use) 50 percent efficacy threshold for approval, and that is pretty sad, but worst of all, these ‘treatments’ are super dangerous and haphazard.

Safety thresholds have been thrown out the window with all of these Covid jabs from all three manufacturers. They always assume that none of us can remember what happened last month or last year, but some of us can (the unvaccinated) and do, and we review the data and the findings too. Investigative journalists who support clean living and healthy living must expose the truth to the masses, or the “fence riders” (those not sure whether to vax-up or not) have no chance at all.

Scamdemic Alert: Gene-tampering Covid jabs offer ZERO safety or effectiveness proof, while causing blood clots around the world

In the summer of 2020, the FDA’s commissioner stated that in order for the vaccine manufacturers to even get just emergency authorized use, they had to cross the minimum threshold of 50 percent efficacy, that’s according to their own documented standard, and even if they did, that would only be considered a medical experiment, not some mass campaign to inoculate more than 70 percent of the world’s populace in less than 6 months. So how did they even get 50 percent efficacy, when the shots haven’t proven that ANYBODY at all is yet immune to Covid? Easy. Fake the research. Fake the results. Fake everything.

All Covid vaccines are actually a crime right now because none of them even meet the EAU threshold. FDA testing reveals more than half of the test-subject participants came down with Covid-19 within 7 days post vaccination, but the symptoms were labeled “reactogenicity” to alter the results in order to gain emergency approval. In other words, the FDA/CDC created a gray area where they say symptoms of Covid overlap with symptoms and adverse reactions or “side effects” of the inoculations.

So what did the vaccine manufacturers do to solve this little dilemma, and in their favor? They never bothered to verify whether those test subjects (human guinea pigs) even had Covid, they just chalked up all the symptoms they had as common reactogenicity.

They simply never checked to see if the vaccinated sheeple really caught Covid, because they didn’t want those results (and records), as they would demolish their chances of reaching the 50 percent EAU acceptable medical experiment threshold. And when will the worldwide “test” of vaccine “efficacy” cross the blood clot threshold of 50 percent?