TGA Workload Explodes 1,000% in Just One Year

In 2021, there were 100 times more deaths reported in Australia following vaccination compared to 2020. With the TGA investigating each and every case resulting in death - can they keep up?

The Therapeutic Goods Administration (TGA) is responsible for overseeing and regulating the use of theraputic medicines and devices in Australia. In 2021 the TGA provisionally approved a number of anti-SARS-CoV-2 drugs as a means of bringing these drugs to market as soon as possible.

The idea of a provisional approval is that the TGA will monitor real-world data on the safety and efficacy of the drugs - ensuring that the real-world performance of the drugs are in line with the clinical trial data submitted by the drug’s sponsor.

Effectively this means that passive, self-reported data will be relied upon by the TGA to make these judgements in lieu of active clinical surveilance data.

The Database of Adverse Event Notifications (DAEN) is a national system for patients and medical professionals to report unintended side effects following the use of a therapeutic medicine or medical device. This database is a primary source of safety information for regulators and drug makers alike, and should be integral in the TGA’s decision to fully approve a drug or not.

The DAEN is administered and monitored by the TGA, which they say…

"The TGA uses adverse event reports to identify when a safety issue may be present."

Unlike VAERS (Vaccine Adverse Event Reporting System) in the United States, the TGA has made a concerted effort to restrict the public's access to the DAEN, and to withhold critical variables from the publicly accessible database.

Although the DAEN can be searched by the public, the results can only be viewed on the TGA website - making it virtually impossible for anyone to analyse the data in a meaningful way.

Typically, one would expect to be able to download these search results as a CSV file so the data can then be analysed in a spreadsheet. From a technical standpoint, there is no reason to suggest the TGA is incapable of making search results available for download. In fact, they already do this when performing a search of the Australian Recall Actions Database on the TGA website.

So if the TGA is capable of providing search results for download as a CSV, then why aren't they doing it? Sadly, the only conclusion could be that the TGA is purposefully creating barriers to obtain this information.

Despite these barriers - where there's a will, there's a way. We've managed to find a way to transcribe DAEN search results, line by line into CSV format to make this information openly available and accessible for the Australian public.

DAEN Reports and Deaths Over The Years

The information and graphs presented below demonstrate an unprecedented number of reports of deaths, hospitalisations and severe adverse events following vaccination in Australia.

In my personal opinion, these statistics alone should be sufficient evidence for the TGA to revoke the provisional approval of the Astrazeneca, Pfizer and Moderna COVID-19 injections - until such time that the TGA has commissioned clinical trials to conclusively address each and every one of the severe safety signals being reported following these injections.

This first graph shows the total number of adverse events and deaths reported following a vaccination (excluding covid injections) in Australia from 1971 to the end of 2021.

As you can see, there is moderate growth in the number of reports over time. This is in line with the adoption of a reporting system, population growth, and the increasing prevalence of vaccinations.

While there are a few annomolous years with a spike in the number of reports and deaths, intervention by regulators and manufacturers seem to address these issues and the number of reports in the following years tend to return to their "natural" rate.

Adverse Event Overload

The next graph is not for the feint of heart - it is truly disturbing to see how many Australians have died or been injured following a vaccination in just one year alone. The number of reports in 2021 is so large that the reports from the past 40 years are barely distinguishable from zero.

In order to make this graph readable, we have had to change the scale to an exponential "logarithmic" scale. So keep in mind that each horizontal line on this next graph represents a value ten times greater than the line below it.

One way to look at this chart, is to see how many years it has taken for the number of reports to grow ten-fold. For example, from 1973 through to 1991 the number of yearly reports grew from 10 to 100 - about 18 years. Then from 1991 to 2016, yearly reports grew from 100 to 1,000 - roughly 27 years.

Now let’s take a look at the difference between 2020 (approx. 1,000 reports and 9 deaths) and 2021 (approx. 100,000 reports and 900 deaths).

What took 45 years historically, has been achieved by just three provisionally approved drugs in less than one year. Am I the only one who thinks this is insane?

To sum up, the TGA claim that they use the DAEN to "identify when a safety issue may be present" - If this one graph isn't enough to cause alarm or to suggest a safety issue may be present, trust me - there are far more shocking revelations about these covid injections to come when we deep-dive into the data.

Stay tuned, in the next post we will be releasing CSV files containing over 100,000 adverse event reports and symptom summaries relating to the Astrazeneca, Pfizer and Moderna covid injections up until December 31, 2021.

Leave your thoughts and comments below. Also, please share this email with anyone you know who might find this article, or the upcoming data drop of interest.