On 13 July, Australia’s drug regulator quietly granted full approval for Pfizer’s Comirnaty “vaccine.” This is the same product that currently has 81,361 reported adverse events, with 443 deaths.
Why would the Australian Therapeutic Goods Administration (“TGA”) give full approval to a drug that has a bad safety profile? Is it because the TGA receives nearly all its funding from the companies that it is supposed to regulate?
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