Australia’s medicines regulator, the Therapeutic Goods Administration (TGA), holds 2 databases for the reporting of adverse events on medicines or vaccines. One is their internal database for the initial reports, then after 3 months to allow for their investigations into the reported cases, the data is de-identified and a summary of the data is made public in their Database of Adverse Event Notifications or DAENs database. The DAENs data is available online for public searching as needed.<\/p>\n
I searched the DAENs database for all reported adverse events on all vaccines going back to the start of their data in 1971. I did not include the reported events for the CV-19 shots as I wanted to compare the number of reported adverse events and deaths of other vaccines to the current ones.<\/p>\n
What I found was shocking… Especially when compared to the statistics of the current adverse events, and the fact that these results are only based on 3 months of CV-19 reports, with the data of the other 3 months of their use not being available yet.<\/p>\n
My findings are here:
\nAdverse events for non-CV-19 vaccines reported to TGA (1971-2021) – 18,080
\nReported deaths for non-CV-19 vaccines (1971-2021) – 57
\nAdverse events for CV-19 vaccines reported to TGA (2021) – 43,811
\nReported deaths for CV-19 vaccines (2021) – 407
\nOr in short, the current CV-19 vaccines in approximately 6 months (but only 3 months of TGA data on the CV-19 shots) since being introduced have caused:
\n– Approx 2.5x times as many adverse events from the CV-19 shots compared to ALL other vaccines combined over the past 50 YEARS
\n– Over 7x times as many deaths from the CV-19 shots compared to ALL other vaccines combined over the past 50 YEARS. 7 TIMES MORE in just 3 months of TGA data.<\/p>\n
On an annual basis, the CV-19 shots have caused a 2800% increase in deaths compared to all other shots combined over the last 50 years of vaccines.<\/p>\n
Does this really seem safe to you?<\/p>\n","protected":false},"excerpt":{"rendered":"
Australia’s medicines regulator, the Therapeutic Goods Administration (TGA), holds 2 databases for the reporting of adverse events on medicines or vaccines. One is their internal database for the initial reports, then after 3 months to allow for their investigations into the reported cases, the data is de-identified and a summary of the data is made … <\/p>\n