“[I’m] only looking at serious adverse events and deaths. There were almost no adverse events reported in some lots, and some lots had thousands and they had hundreds of deaths. And so, this is not good manufacturing practice-compliant product at all,” said Latypova. “I’m not endorsing flu vaccines or any vaccines anymore, because until this is investigated fully, nobody should be taking anything. That’s my professional opinion.”
The above graph shows Johnson & Johnson (Janssen), Moderna and Pfizer. Below is a graph for Moderna. The blue colour represents serious adverse events and the orange represents death post-vaccination. “A well-manufactured product should not look like this at all,” Latypova explained.
Explaining the significance of the lot labelled in the graph above, Latypova said:
“On January 18, Orange County, California Health Department flagged this particular lot of Moderna for what they called ‘excessive number of allergic reactions’. Nothing was done about it. The injections were not stopped. In fact, this lot was being sold all over the United States until it ran out in late March.
“And as you know, if there is salmonella in a salad, they will recall the entire product from all the shelves in the country. Right? That’s what you should do as a manufacturer. All manufacturers have systems to detect this. And the majority of recalls of products are voluntary because they don’t want this to happen.
“Yet [with this lot from Moderna], nobody stopped. Not the manufacturer, not the health authorities of Orange County, not the CDC, FDA, or whoever was supposed to monitor this, they continued selling this lot. It’s now associated with over 65 deaths in the US and over 3000 serious adverse events. So, after something like this happens, everything that follows is intentional.”
Every researcher that has questioned or challenged regulatory authorities has been told: “We looked at it. It’s safe and effective. Go get vaccinated.” Why were they all behaving this way? Why are they all following the same script the world over?
Latypova has been collaborating with legal researcher Katherine Watt, who publishes articles on a Substack page titled ‘Bailiwick News’, to reveal the legal structure – or rather the pseudo-legal structure as it’s not lawful – of this government, pharma, military criminal cartel. “It actually is operating all over the world,” Latypova said.
In the 1960s a contracting framework was put into place for NASA called ‘Other Transaction Authority’. “Now eleven federal agencies use it. [The] Department of Defence is a particularly huge user of this contracting method because it allows them to contract without following any federal procurement rules and regulations with a lot of secrecy,” Latypova said. “They typically use this framework to order weapons from defence contractors, but now they’re using the same framework to order what they tell us is a pharmaceutical product.”
In addition to this, there is a US code, which Latypova highlights in her presentation, which says that the use of emergency use authorised “countermeasures” is not a clinical investigation under a public health emergency. The significance of this, Latypova explained, is that if a countermeasure cannot be a clinical investigational product, then no pharmaceutical regulation applies to these products.
“So, here’s the lie that our government told to us and told to the world and the governments all over the world repeated to their citizens:
“They were claiming that it’s a health event. They were claiming that they’re producing pharmaceutical products to the good manufacturing standards when they perfectly well knew, I assure you, they were all aware of this. They perfectly well knew that no pharmaceutical regulations apply to these things, countermeasures.
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