The statement

‘We initially identified 678 studies and, after screening for our inclusion criteria, included 44 papers that contained 325 autopsy cases and one organ-restricted autopsy case (heart). The mean age of death was 70.4 years. The most implicated organ system among cases was the cardiovascular (49%), followed by hematological (17%), respiratory (11%), and multiple organ systems (7%). Three or more organ systems were affected in 21 cases. The mean time from vaccination to death was 14.3 days. Most deaths occurred within a week from last vaccine administration. A total of 240 deaths (73.9%) were independently adjudicated as directly due to or significantly contributed to by COVID-19 vaccination, of which the primary causes of death include sudden cardiac death (35%), pulmonary embolism (12.5%), myocardial infarction (12%), VITT (7.9%), myocarditis (7.1%), multisystem inflammatory syndrome (4.6%), and cerebral hemorrhage (3.8%).’

The source

Hulscher N, Alexander P E., Amerling R, Gessling H, Hodkinson R, Makis W et al (2024), A Systematic Review Of Autopsy Findings In Deaths After COVID-19 Vaccination, Science, Public Health Policy and the Law. 2024 Nov 17; v5.2019-2024; and related commentary by Hulscher as quoted by Steve Kirsch in his substack on 19 Nov 2024

My take on it

The TGA has from the outset of this scamdemic ignored calls for appropriate autopsies. That posture is culpable, and without merit. It is a fundamental failure of a duty of care. It has enabled the continuation of a ‘health’ policy that is literally murderous.

Others have now done what was required in that regard, and the results are no surprise.

We are blessed that the results of this analysis ever made it to print, given the multiple efforts to censor it as detailed by Steve Kirsch and lead author Nicholas Hulscher.

Hulscher calls on the FDA to respond immediately, in the public interest:

“Our study indicates that the COVID-19 injectable products must undergo an immediate Class I recall by the FDA to protect public safety. The U.S. Food and Drug Administration defines a Class I recall as: “A situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.”

I call on the TGA to do likewise, and for the same reasons.