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TGA Makes COVID Shot Report Public

Recently, Australia’s Therapeutic Goods Administration (TGA) made a report from 2021 available to the public. Titled “Nonclinical Evaluation Report BNT162b2 [mRNA] COVID-19 Vaccine (COMIRNATYTM)” the document provides inputs from the preclinical work involving the Pfizer-BioNTech mRNA vaccine BNT162b2 (Comirnaty) via Pfizer Australia pty Ltd.  A bombshell actually, the TGA, the agency that is supposed to “safeguard and enhance the health of the Australian community through effective and timely regulation of therapeutic goods” seemingly let the pharmaceutical company dictate the risk-benefit analysis. At the height of the pandemic and the onset of the mass COVID-19 “vaccination” rollout starting February 22, 2021, the data in this document wasn’t shared with the public. But why not? Would the data (or lack thereof) associated with this report lead to more “vaccine” hesitancy?

You bet it would.

Take a look at the graph where it’s clear the “vaccine” spreads into the brain, liver, bone marrow, spleen, thyroid, small intestine, ovaries and virtually everywhere in the body.  Dr. Byram Bridle obtained the biodistribution data nearly two years ago from the Japanese government through a FOIA and made this information known back then but was vilified mercilessly over it.  Video Here (Approx. 11 Min)

COVID Injections Accentuates Comorbidities &

The spike proteins within the “vaccine” have destroyed the ability to repair single and double stranded DNA. This will cause the body to adapt and attempt survival as the body fails at replenishing vital cells that need to be repaired. The result will be accelerated aging due to the inability to repair damaged DNA. The “vaccine” will exploit and accentuate any and all comorbidities leading to deterioration of health. Although most “vaccinated” individuals know that something has gone terribly wrong within their bodies, they want to “cure” this feeling with another booster. Unfortunately, with every shot, their minds are becoming more forgetful, body aches are becoming painful, dizziness episodes increase as well as periodic fluttering heart events, and exhaustion.  The study at the end looked at how the spike protein inhibits repair pathways which would affect women who inherit a specific gene mutation (BRCA1) and have a much higher risk (over 70%) of developing breast cancer, as well as causes an aberrant expression of a specific gene (53BP1) which contributes to tumor occurrence and development – which will affect a host of cancers.

For a deeper dive into the research, read independent researcher Walter M Chesnut’s article:  Persistence of the Spike Protein May be Inducing Systemic Autoimmune Disease MIMICKING Sjogren’s, Arthritis, Vasculitis, Diabetes, etc.

The spike protein, in essence, works as the perfect bioweapon sowing seeds of self-destruction via most efficient endothelial delivery.


…the Spike Protein is a designed viral fragment that has been attached to a coronavirus as a delivery mechanism. This viral fragment causes ARDS, multiple organ failure and death in a very few due to the initial phase of the Syndrome it induces. This is what I have called SPED. Spike Protein Endothelial Disease.

The second phase of this Syndrome I had initially thought was a Progeria syndrome. I now no longer believe that to be the case. However, Phase II would certainly be PART of a Progeria syndrome. I now believe that, given recent evidence, Phase II is the induction of a SYSTEMIC AUTOIMMUNE DISEASE which I will call Spike Protein Autoimmune Syndrome.

Interestingly, the complete virus is NOT found in those with Long COVID – the spike protein IS.

Chesnut feels the key is in clearing the body of the Spike Protein, but he is concerned that the Spike’s mRNA has been retrotranscribed into DNA.

The diabolical scheme of course is that this induced illness will not be attributed back to the “vaccines.”

Read on how the “vaccine” causes DIC, and ADE.

Please see FLCCC’s Recovery protocols which included the use of intermittent fasting, ivermectin, LDN, nattokinase, aspirin, melatonin, magnesium, methylene blue, sunlight, and resveratrol along with numerous second line and third line therapies.  Please note that many of these treatments have been attacked by ‘the powers that be’:


TGA Document Revelations

March 25, 2023

Dr. John Campbell goes through the document thoroughly showing the shots were approved on scant data filled with a multitude of holes in understanding, and the fact lung inflammation was observed in both infected animal controls and immunized animals.  Page 45 shows the lipid nanoparticles are systemically distributed but there is no data on how long the spike protein persists or any investigation into potential for autoimmune diseases.

Please see:

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