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Therapeutic Goods Administration: “It would not be practical to follow up on every individual report [of the 140,000 adverse events for Covid 19 mRNA vaccines]” Do the TGA understand what they just said?
226,503 просмотров • 1 год назад •via X (Twitter)
Комментарии: 9

It gets worse…

Skerrit is a scary human being

140,000 adverse event reports! 140,000!! How many Australians does the experimental gene therapy need to kill or injure before @TGAgovau and @healthgovau declare a moratorium? The TGA's determination to treat this as normal is simply wicked - and it makes me wonder why? Perhaps the simplest explanation is the best.

@TGAgovau @healthgovau royal commission asap

That's comforting to know. They can't properly assess the safety because there are too many indicators of the lack of safety.

If they had any integrity, they would pull all vaccines from the market whilst they researched the 140,000 reports of adverse events. The fact that they can acknowledge 140,000 and continue to allow them to be administered is unconscionable at best, criminal at worst.

Who cares if they follow up or not. The thing nobody wanted to ever admit was how many adverse reactions there was!! 140k!!!!

There is a major maleficence issue here. The TGA fully admitting there was a known problem with the injectables (lots of them 140K) So rather than sit on your hands TGA, what may have been the most logical thing to do, considering your role in Australia's health? Maybe raise a warning to the public or ban the poisons? This is beyond stupid, this is beyond simple negligence, this is criminal negligence, and by the way this is all taxpayer funded criminal negligence by our government bodies. A Royal Commission is required, commencing February 2025.

agreed
