Serious questions have been raised as to why medicine regulators have not pulled the Covid-19 vaccines from distribution to the general public after data on the Australian Government site revealed that there have been nine times as many deaths reported as adverse reactions to the Covid-19 vaccines over a period of 7 months than deaths due to all other available vaccines combined over a period of 50 years.
The Department of Health Therapeutic Goods Administration (TGA) is the medicine regulator for the Australian Government, and as part of the Department of Health, the TGA regulates the quality, supply, and advertising of medicines, pathology devices, medical devices, blood products and most other therapeutics.
However, a Freedom of Information request made by Doctors for Covid Ethics back in February 2021 revealed that the TGA never saw the extremely limited study data for the Pfizer mRNA Covid-19 vaccine prior to granting it emergency approval and deeming it safe to be injected into the arms of Australians.
The TGA originally attempted to suppress the FOI request by requesting a 6-month extension in view of the amount of work required to respond satisfactorily. But after a complaint was made to the Office of the Information Commissioner the TGA responded confirming that they had never seen or requested the patient data from Pfizer and simply accepted Pfizer’s report of their study as fact, despite their proven history of fraudulent claims.
