Prior to the Covid so-called “pandemic”, you (and I) thought the primary job of our Therapeutic Goods Administration (TGA) was to keep us safe. We could trust that the TGA employed highly qualified scientists and doctors to evaluate in fine detail all relevant data for every new therapeutic agent released for public use. We didn’t question the advice the TGA provided.
But all that changed dramatically with COVID and the COVID “vaccines” (or maybe even earlier but we didn’t notice).
The TGA became the cheer squad for Big Pharma. Reducing the usually required safety and efficacy data, rushing through release approvals and then fending off arguments that the Covid “vaccines” carried unacceptable safety risks and were associated with the highest incidence of serious adverse events ever reported for a new therapeutic agent. Listening to Senate Estimates questioning of TGA and Health Dept. staff by concerned Australian Senators such as Senators Roberts, Rennick and Antic over the last couple years might have lead you to think the TGA staff were working for Big Pharma and not for us. Responses to legitimate safety and efficacy questions were regularly met with distain, arrogance and dismissiveness.
We all now know the full extent of the lies and cover ups surrounding the COVID pandemic and the COVID “vaccines”. I’ve been detailing this appalling saga in my 400+ Substacks since January 2023.
Aside from the outrageous and totally fabricated mythical claims that millions of lives were saved by the COVID “vaccines”, the TGA clings to the incredible claim that they have judged that the COVID “vaccines” have caused only 14 deaths in Australia. How does the TGA come to this conclusion when there have been 1,042 suspected deaths reported to the Australian adverse event reporting system (DAEN - Drug Adverse Event Notification system) as of January 2025?
In fact, it is misleading to assume there have only been 1,042 deaths. Most doctors and health professionals have never reported an adverse event for any drug. Moreover, most would not even know how to report an adverse event and if they did they would not have the time and patience to do so. More importantly, prescribers are acutely aware of potential litigation so denial is common and, as we all know, doctors are not known for their willingness to admit error. For all these reasons and supported by published critical analyses, it is widely accepted that the under reporting factor for adverse drug reactions is probably greater than 30x. This means that in Australia there were more than 30,000 suspected cases of death following COVID “vaccinations”.
My Substack of 29 March 2024 addressed the various failings of the adverse event reporting system. CLICK HERE to view.
