Category Archives: TGA
Covid: US DoD and other world governments’ bioterrorism program confirmed by Twitterfiles releases
By Alexandra Bruce
According to Sasha Latypova, a retired pharma executive who started the websites, HowBad.Info and HowBadIsMyBatch.com, where you can check your vaxxine batch number to see if you got saline or if you got a Death Shot, she says that from a legal perspective, including the actual contracts signed by Pfizer with the DoD, as well as other internal documents that she’s acquired, Operation Warp Speed is a DoD project and the vaxx is under Emergency Use Authorization. Therefore, it is not subject to FDA regulation. Any pretense that we have seen of regulation is pure theater. It is a total PSYOP, because the vaxx is not a commercial pharmaceutical product.
This is why, in the face of all of the overwhelming evidence of injury and death, the FDA and its counterparts all over the world have not stopped this program. Legally, these shots are not clinical investigational products and they are not subject to any normal pharmaceutical regulations and there can be no other conclusion than that these are bioweapons that are intended to maim and kill.
Per contracts with the US Government, the product is shipped to the DoD, which retains ownership of the vials until the product is injected into people. These contracts are very detailed and they specify the manufacturing data to be delivered to the DoD but they don’t require any of the routine sampling that takes place per FDA regulations.
It is a regulatory requirement to retain samples of each batch produced, and these samples of vials should exist and be available for examination, for purposes of verification of their contents vs the label. However, the DoD contracts expressly forbid any such tests!
Despite the disturbing prohibition on independent vial testing, covert random testing of the mRNA vials has been ongoing worldwide – and the consistent finding among all is that there is yet to be a single vial found in full conformance to the manufacturer’s label.
Some batches which have tested as “blanks” have also been associated with those batches having almost no reported adverse events. This is why some people who’ve been injected are fine and why this was reported to be especially true of the earliest batches of 2021. They couldn’t have people dying suddenly, right off the bat.
According to Sasha Latypova, whose Substack is absolutely MUST-READ, she says that the American People and the peoples of the world have been subjected to a conspiracy to commit mass murder through bioterrorism and informational warfare operations by the DoD, HHS, other US government agencies – as well as other world governments, along their conspirators in the Mainstream Media and in Big Tech, who we’ve recently learned through the Twitterfiles have been enacting their unprecedented censorship on Americans, about the vaxx, about the elections, about transsexuals, etc. on the direct orders of our intelligence agencies.
Naomi Wolf was on with Steve Bannon yesterday and she echoed these thoughts but it looks like she isn’t quite ready yet to go on the record and say that large swathes of our own government – like many, many governments around the world – are committing genocide against their own people. This is not something that China is doing to us or that Big Pharma is inflicting on us and that our poor little government is asleep at the wheel. No.
My own source tells me that a big part of how this has occurred – not all of it but a big part of this infiltration of the US Government has been through the Senior Executive Service aka “The Keystone”, which is a kind of union for DC bureaucrats, where they’re not subject to the same degree of vetting, which is how we got Sam Brinton, the gender-fluid kleptomaniac in the Department of Energy and how it’s nearly impossible to fire them.
“It has been shown how deeply the son of the current US president, Hunter Biden, is involved in funding the US DoD-controlled company, Metabiota.
“However, some participants in closed projects remain in the shadows, although they are key players in Ukraine’s military-biological programme,” stated Major General Igor Kirillov, the head of the Russian military’s radiation, biological and chemical protection troops.Arrogant TGA head Dr John Skerritt ducks for cover as Roberts accuses him of vaccine impropriety
Federal Police should be investigating Professor John Skerrit’s onshore and offshore bank accounts. Former PM Scott Morrison accrued $52 Million while PM. How much has Bro John salted away? (https://cairnsnews.org/2022/02/23/scott-morrison-under-the-microscope/)
Senator ROBERTS: Can you tell me how many medicines were approved under the provisional approval pathway during the COVID period 1 July 2020 to date? My numbers are 13 vaccines and six drugs; is that correct?
Dr Skerritt: Are you talking specifically about COVID treatments and COVID vaccines?
Senator ROBERTS: No, any vaccines or drugs that have been approved using the provisional pathway.
Dr Skerritt: I will start with COVID vaccine treatments. There have been seven COVID vaccines and eight COVID treatments. I’ll just check whether I’ve got the numbers for other medicines during that period. You’re talking about the provisional approval pathway?
Senator ROBERTS: Yes.
Dr Skerritt: From 1 July this year there have been five provisional approvals. From the period 1 July 2021 to 30 June 2022 there have been 23. That would include those COVID treatments. What it does show is a lot of other medicines, such as cancer medicines, such as medicines for rare conditions, have also been approved. In the financial year 2021, from 1 July 2021 to 30 June 2022, there were five. Over the period you’re talking about, that would add up to 33.
Senator ROBERTS: How many drugs have been approved under the normal process during that same period?
Dr Skerritt: During the same period? I will add the three financial years and I’ll check my mental arithmetic. So 36 this current financial year, and 117. These are either new approvals or new indications approved. And 95 the year before. So, it is a significant percentage, but not most of them.
Senator ROBERTS: Is the maximum provisional approval period six years because it can take that long to get drugs approved under the old approval system?
Dr Skerritt: A provisional approval is only valid for two years and then the company either has to come back and show why they cannot obtain all the data within the period and apply for an extension.
Senator ROBERTS: No, the maximum provisional approval?
Dr Skerritt: They can apply for further lots of two years.
Senator ROBERTS: Is the maximum provisional approval—
Dr Skerritt: Overall the maximum period is six years, but it’s not six years off the bat.
Senator ROBERTS: It’s two years with extensions.
Dr Skerritt: They are possible extensions; they’re not guaranteed.
Senator ROBERTS: How much money do you save pharmaceutical companies by switching from full approval to express approval? I understand it’s hundreds of millions per approval?
Dr Skerritt: It actually costs the pharmaceutical companies more in regulatory fees for provisional approval.
Senator ROBERTS: No, I didn’t say regulatory fees. How much are you saving the pharmaceutical companies by giving them express or provisional approval rather than going through the six-year period for getting proper approval?
Dr Skerritt: No, you’ve misinterpreted the system. It’s not a six-year period to get full regulatory approval.
Senator ROBERTS: It varies. I accept that.
Dr Skerritt: Most of our approvals are submitted as a standard approval, especially, for example, if it wasn’t a public health emergency or it’s a drug that already has others in the same category. They’re submitted as a standard approval.
Senator ROBERTS: Dedicated trials for their drugs, I understand, can be hundreds of millions of dollars. How much time and money would they save by going express?
Dr Skerritt: We would not give a provisional approval to a medicine unless there were clinical trials.
Senator ROBERTS: How much money does it save if they do a provisional without doing a formal or normal approval process? How much money does it save the drug company?
Dr Skerritt: I don’t believe there are necessarily savings. The situation would be different for every drug. It’s really important to emphasise there were very extensive clinical trials for the vaccines and treatments that have been through provisional approval.
Senator ROBERTS: My understanding is that it can cost hundreds of millions of dollars to get the full approval process. Without the dedicated trial, they could save hundreds of millions of dollars per drug?
Dr Skerritt: I don’t necessarily agree with you.
Senator ROBERTS: When does the provisional approval for Pfizer expire?
Dr Skerritt: The two-year period will be two years from the anniversary of the first approval. I would emphasise that in certain countries—
Senator ROBERTS: What is that date?
Dr Skerritt: The products are now fully approved.
Senator ROBERTS: What is the date of provisional approval expiry?
Dr Skerritt: For the very first approval, for 16 years and over, the two-year period finishes on 25 January 2023.
Senator ROBERTS: I have in front of me a document called the Australian Public Assessment Report for Tozinameran, from Comirnaty (Pfizer), dated December 2021. Is this the approval application for the paediatric version of the Pfizer vaccine?
Dr Skerritt: No, it is not. An Australian Public Assessment Report is a summary of the assessment that we did of the application. You mentioned Pfizer. The actual application is over 220,000 thousand pages of paper from Pfizer for that particular group of vaccines.
Senator ROBERTS: I reference page 61, which states:
Limitations of the current application data. Safety follow-up is currently limited to median 2.4 months post dose 2 in cohort 1, and 2.4 weeks for the safety expansion cohort.
What is the safety expansion cohort?
Dr Skerritt: Remember, also, this was going back to the time of approval. We now have hundreds of millions, actually more than a billion, people who have been vaccinated with that vaccine and experience going on since December 2020, when the first vaccination was done. The safety expansion cohort is in a clinical trial where individuals are monitored closely and the data reported back to regulators for periods of months, leading to years, after their vaccination.
Senator ROBERTS: Did you recommend this substance based on 2.4 weeks of safety testing or did you get more in? If so, over what period? How many months?
Dr Skerritt: Remember the initial approval from TGA was based on that two months of follow-up, but we also had the experience of other countries that had more than a month before starting mass vaccination campaigns. When we approved Pfizer on 25 January2021, we were in almost daily contact with the British, who by that stage had vaccinated millions of British people by 25 January 2021. Real-world evidence played a very important role in both the approvals and in the ongoing safety monitoring of these vaccines.
Senator ROBERTS: So you relied on data from other countries and you relied for periods of months, merely months. It can’t be more than six months, because there’s a gap between application and approval and to give time for collection of data and analysis. There should be years of data before we start putting this stuff into our children, yet it’s months.
Dr Skerritt: I disagree in the context of a pandemic and a public health crisis. Regulators globally felt that it was appropriate to do initial approvals—
Senator ROBERTS: You’re the Australian regulator.
Dr Skerritt: As the head of the Australian regulator, I would do precisely the same if I had my time again. The alternative would have been to leave Australians unvaccinated through the course of 2020, 2021 and 2022, and there would have been tens of thousands more Australian deaths.
Senator ROBERTS: Can I reference a letter from the Commonwealth Department of Health and Aged Care, signed by Radha Khiani, Director, Governance and Coordination section, in which the department makes this claim. The letter from 4 November 2022, just last week, states:
A large team of technical and clinical experts at the TGA carefully evaluated the data submitted by the sponsor. A treatment or vaccine is only provisionally approved if this rigorous process is completed.
This document concerned the use of Pfizer stages 2 to 3 cynical trial data in support of their application for provisional approval. Did the TGA check the stage 2 and stage 3 clinical trial data from Pfizer? Did you check it?
Dr Skerritt: We did check the phase 2 and phase 3 clinical trial data from Pfizer and we also took it to independent external medical experts as well as consumer representatives.
Senator ROBERTS: Referencing Freedom of Information No. 2289, in which the applicant requested a copy of the stage 2 and stage 3 clinical trial data, the TGA responded that the ‘TGA does not hold any relevant documents relating to the request’. That was a request for stages 2 to 3 clinical trial data.
Dr Skerritt: Without seeing what’s in your hand, I believe that you asked for individual patient data rather than the phase 2 and phase 3 clinical trial data. I can give you my word that we assessed the phase 2 and phase 3 clinical trial data; otherwise, what else did we do? Look at the colour of the label on the bottle? That is the main thing our team of several thousand clinicians look at in reviewing a new vaccine, the phase 2 and phase 3 clinical trial data. It is the centrepiece.
Senator ROBERTS: The freedom-of-information request then asked for ‘any documents confirming the process of analysing this data to a decision, including meetings, notes, dates and times’. Again the TGA replied, ‘We have no relevant documents.’ Did you review the stage 2 and stage 3 data or not, and, if you did, why did you tell this freedom-of-information applicant you did not have these documents? Which document is the lie? One of them is.
Dr Skerritt: I don’t have that document in front of me. We can review it on notice. But we reviewed the phase 2 and phase 3 clinical trial data at length.
CHAIR: This really needs to be the last one so I can share the call.
Senator ROBERTS: I just want you to think about this and confirm it or otherwise: and ‘the trail data contained sufficient proof the vaccines were safe and effective, sufficient to meet the criteria for provisional approval’; is that correct?
Dr Skerritt: Correct. Yes.
Covid Medical Network letter is indictment of medical authorities
Letter to the Editor
Dear Australian Community
In the midst of your grief and sorrow and utter exhaustion from the devastating effects of the unnatural catastrophic weather events we have just been subjected to, we ask that you pause for 15 minutes to read and digest this message and linked letter and take action.
This letter exposes the COVID-19 and “vaccine” mandate Fraud and serves as an indictment of Australia’s purported health leaders, those men and women who were and are meant to guide all Australians in living the healthiest life possible … a mission they have failed to perform for over two years now.
It is a stunning document we ardently request you share everywhere, so our Australian Community can learn and confirm the facts many have come to know or suspect, while gaining strength in the knowledge that hundreds of Australia’s leading doctors, scientists, and academics have also had enough and are fed-up!
North Coast NSW, Australia, barrister Julian Gillespie is a co-author and signatory to this 52-page Letter, with hundreds of pages of supporting evidence, in collaboration with the Australian Covid Medical Network.
Here is the letter:
https://www.covidmedicalnetwork.com/open-letters/open-letter-to-atagi.aspx
It comes from the combined effort of Australia’s leading clinical doctors, scientists,
research academics, health care professionals, overseas specialists, and lawyers working together over many months.
The material presented has been ‘fact checked’ by the vigorous peer-review process to present the Truth.
This Letter has also been received by every Federal, State, and Territory MP and Senator, in order to inform them of a variety of scientific Truths being flagrantly ignored by both these health ‘leaders’, and the Ministers responsible for overseeing their conduct.
We urge you to please take a small amount of time out of your demanding day to call and email your Federal and State/Territory representatives and get them to ask the same Questions, and Demand the same Answers you will see in the Letter.
Armed now with the facts, the history, and the evidence of a litany of wilful instances of malfeasance, it is now time for the wider Community to say ‘enough is enough’ and call an end to all “vaccine” mandates and false COVID narratives.
We need our doctors, nurses, teachers, lawyers, transport industry, farmers, military, police, religious leaders, government employees, corporations, business people, ordinary workers, and everyday community members – vaxxed and unvaxxed – to stand together and demand an end to all COVID “vaccine” mandates, ban any further rollout of this experimental gene-based treatment, and demand a full and transparent public enquiry.
Australia’s future is in our own hands. What you and I do right now, today, will determine what kind of world we end up living in, and the world our children and grandchildren inherit.
They are trying to divide and conquer us, and silence all opposition. Already, planned protests in all capital cities are being impacted as millions of people struggle with the utter devastation caused by these incredibly harmful and destructive weather events being rolled out across the East Coast of Australia.
Please understand the gravity of the situation we are currently facing and take action NOW. Thank you and may the Divine Creator’s Light and Love be with us all at this dark and challenging time for humanity.
Once again, here is the link to the Letter together with supporting Annexures:
https://www.covidmedicalnetwork.com/open-letters/open-letter-to-atagi.aspx
from Diane Drayton Buckland
Queensland
An ode to Harry, and brickbats for false pandemic
Letter to the Editor
Thank you, Harry, for all you’ve done. Banging your head against walls gets to be very tiring.
I’m surprised that this COVID scam has lasted as long as it has. It just needed someone to ask the government for proof that there actually was a pandemic. Why has no-one even questioned the existence of the ‘pandemic’?
A check of ABS death figures for 2019-2021 shows there was NO pandemic due to COVID-19. It’s a total fraud! Also, Virologists have shown that the SARS-Cov2 (COVID-19) virus has never been isolated. It doesn’t exist! The COVID-19 “vaccines” do not list a viral component (because it doesn’t exist) and therefore they are not vaccines. They contain a computer-generated mRNA genetic sequence which alters human DNA, causes the immune system to attack itself, creating spike proteins, causing blood to clot. Vaccinated people have created a spike in coronary heart deaths and deaths from strokes and many other blood clot related injuries in lungs and limbs, besides many other vaccine-caused deaths and injuries.
All over the world, more vaccinated people are dying than unvaccinated people. The TGA would be well aware of this and is not transparent with Australian vaccine-related deaths. They continue to coerce people to vaccinate and now children as young as 5 years are targeted. This is pure evil! The government’s own figures show that young people are in no danger of dying from COVID-19 and, instead, face death and injuries from the ‘vaccines’ which are neither safe nor effective..
The COVID-19 “vaccines” were hurriedly produced, given ’emergency authority’ to be dispensed with long-term safety completely unknown. The ‘vaccines’ are experimental gene-altering medications which violate the Nuremberg Code and gullible Australians, blindly trusting the government, have been used as guinea pigs without proper informed consent. Our government and Health Dept heads have committed treason and murder. Why have vaccinations not been stopped? Any other vaccine would have been stopped after 25 deaths, Covid “Vaccine” deaths are now over 700, possibly a lot more as the TGA is hiding the actual figures as ‘Covid deaths’.
I have proof to back up my statements, and if this was exposed in a court, the government would have no legs to stand on. Current court cases have all started on the assumption that there is a pandemic and that the ‘vaccines’ are safe and effective vaccines. Coming up before Free Mason judges, we haven’t a chance!
The mainstream media is strictly controlled as to what it can/cannot say and hence the majority of the public has no idea as to what is going on. It is only alternative news sites, like yours, which divulge this information. Generally dismissed as ‘conspiracy theory’, the truth will come out eventually, so, Harry, as difficult as it is, just know that you are needed and very much appreciated. We are fighting a conspiracy so massive and evil that it is unbelievable, and many refuse even to contemplate it. Time will show that it is true – but will it be too late then? Please everyone, help to expose this massive fraud being perpetrated around the globe.
from smootoo
NSW
Senator Malcolm Roberts takes down TGA Public Servant Professor Skerritt
Professor John Skerritt deputy secretary of health at TGA showed his bureaucratic self opinionated flagrant arrogance to Senator Malcolm Roberts questions as to why he had not complied with many requests as to who is responsible for recording covid deaths at the TGA
How the duopoly government is controlled by unelected unaccountable public servants.
Big-Pharma sponsored TGA after importer of Ivermectin
The Big Pharma -sponsored Therapeutic Goods Administration and its Chairman Professor John Skerritt are prosecuting anyone who imports Ivermectin for any purpose. Big Pharma has tied up the TGA and politicians so well that any alternative treatment for ‘Covid’ will be prevented no matter what.
A reader imported Ivermectin tablets from India for animal treatment but TGA’s Sam, no surname, informed him he cannot bring the Covid cure in without a permit.
Endemic corruption festers in the ranks of all bureaucracy and politics and it begs the question, how did PM Scott Morrison accumulate $52million in assets on a $450,000 per annum salary?
Cairns News is doing an investigation of Skerritt’s wealth over the past two years and will publish the results.
Therapeutic Goods Authority, AHPRA answerable only to WHO
by Alison Ryan
Are these Government bureaucracies contemptuous of investigation and accountability because they are WHO affiliated?
ATAGI members include Director of the National Centre for Immunisation Research and Surveillance, itself a member of the WHO-led project Vaccine Safety Net (VSN).
https://en.wikipedia.org/wiki/Australian_Technical_Advisory_Group_on_Immunisation
https://www.who.int/teams/regulation-prequalification/regulation-and-safety/pharmacovigilance/vaccine-safety-net/vsn-members/national-centre-for-immunisation-research-and-surveillance-of-vaccine-preventable-diseases
TGA is a WHO Collaborating Centre for Drug Quality Assurance
https://apps.who.int/whocc/List.aspx?K5BSqfJdqi0s4VqVDkw8cA==
and AHPRA (Ahpra) is a designated World Health Organization (WHO) Collaborating Centre for Health Workforce Regulation.
https://www.ahpra.gov.au/about-ahpra/our-engagement-activities/who-collaboration.aspx
Read on from Senator Malcolm Roberts, Queensland
“The Therapeutic Goods Administration (“TGA“) and their buddies, the Australian Technical Advisory Group on Immunisation (“ATAGI“) and the unaccountable Australian Health Practitioner Regulation Agency (“AHPRA“), have enabled the distortion of science in Australia that has seen COVID vaccines mandated, the minimising of vaccine reactions, banning of alternative treatments and general COVID mismanagement.
“In this final Senate Estimates session before the election is inevitably called I tried to desperately get straight answers out of Australia’s Chief Health bureaucrats about how they could do so much of this without evidence.
“Watch here as the TGA ducks and weaves in interrogation.
“Doctors and other health professionals feel great pressure to not report adverse events or sentiment which could undermine the vaccine rollout. Health Bureaucrats continue to deny such pressure exists despite official guidelines saying that Doctors could be de-registered for opposing supposed public health measures from the government. AHPRA threatens to deregister Doctors but is a private corporation with no accountability to the Senate or the Australia Public.
“The TGA has been morally deficient in their blind acceptance of overseas data provided by the pharmaceutical companies to approve COVID vaccines. Despite this, they bat away any criticism or safety concerns as simply a conspiracy theory. As I said, conspiracy theory is “used as a term to ridicule the person asking the question” and what did one of our Chief Health Officers respond to that? “It is and I’ll be using it that way”. The contempt these bureaucrats have for openness and transparency is palpable.
“AHPRA is an unaccountable private organisation that holds the threat of de-registration over the head of any Doctor who dares give advice against vaccination counter to the Government line. They must be held accountable and the primacy of the confidential doctor-patient relationship must be restored.
Copied from: http://www.malcolmrobertsqld.com.au/questioning-the-tga-at-senate-estimates
See the latest from Senator Malcolm Roberts here: http://www.malcolmrobertsqld.com.au/latest-news
Covid vaxx spike protein detox protocol
Glutathione (most important for body detoxification) or better
NAC = N-Acetyl-Cysteine 600-750mg (causes the body to produce glutathione itself)
Zinc
Astaxantin 5mg (also improves vision)
Quercetin
vitamin D3
Milk thistle (also liver and stomach protection)
Melatonin 1mg to 10mg (against 5G)
Alternatively CDS/CDL and zeolite
Dr. Zelenko’s Protocol contains Ivermectin, Hydroxychloroquine (HCQ), Zinc, Vitamin D3, and Quercetin.
Spike protein detoxification
David Wolf’s Shop, order here: http://bit.ly/SpikeProtein
This is the updated Nutrition protocol to protect those who’ve been injected with spike protein, graphene oxide and mRNA and the same protocol is useful to protect those concerned with the spike protein and graphene oxide shedding (transmission) coming off those who’ve been injected. We now have evidence of the latest injections containing: mRNA, spike protein, graphene oxide, SM-102, and numerous other potentially toxic substances (also: some—but not all—injections, appear to be higher in graphene oxide and some appear to be saline placebos).
If you know someone who has been injected and requires help, please provide them with this Nutrition Protocol:
Most Important Elements of the Protocol (Shortlist Summary)
Spike Protein: Shikimate neutralizes the Spike Protein
This is the Nutrition Protocol to Prevent Damage from Spike Protein and Derivatives due to Injection and to Protect from Spike Protein Shedding (transmission):
Shikimate Main Sources to Detox Spike Protein
• Pine Needle Tea for Shikimic Acid or Shikimate (from green edible pine needles) There are toxic pine needles, be careful! When drinking pine needle tea, drink the oil/resin that accumulates too!
And/Or
• Fennel and/or Star Anise Tea
And/Or
• Schizandra Berry Tea
• Iodine* (dosage depends on brand, more is not better). Iodine is a product you have to start with small dosages and build up over time.
• Vitamin D3* (10,000 IU’s per day)
Graphene Oxide Detox:
• C60 (1-3 droppers full per day): One of the issues we are seeing with those who have been injected is disturbances in their energetic field (magnetism) and hot spots of inflammation. C60 is a rich-source of electrons and acts like a fire extinguisher to inflammation and simultaneously (because it bio-distributes throughout the body) drives a normalization of electron flow throughout the body. In this category, we offer two products, the traditional C60 product* is made by yours truly and the C60 Super Concentrate* is made by a carbon scientist friend of mine and contains a higher concentration of electrons. C60 is recommended to neutralize spike protein, detoxify graphene oxide and SM-102.
• Kohlbitr Activated Charcoal: Take between 400-2000mg (1-5 capsules) a day with water.
• NAC: N-Acetyl Cystiene is the best precursor to glutathione in the body which has the best research for neutralizing graphene oxide. Take 900-1800mg a day. Get it while you can. The US Federal communist government is trying to make NAC illegal unless you have a doctor’s prescription.
• Enzymes (especially those containing serrapeptase and nattokinase such as VeganZyme— dosage for VeganZymes is 3 caps, twice daily):
Serrapeptase: Serrapeptase provides the anti-inflammatory breakdown of excess and unusual protein. Dosage: 100-200 mg on an empty stomach per day.
Nattokinase: Nattokinase has a long history of being used to prevent blood clots. 2000-4000 Fibrinolytic Units per day (2-4 capsules) with or without food.
Special Note: Ivermectin is showing great promise against hydrogels containing graphene oxide and found on PCR test swabs, but it is a pharmaceutical, so I do not include it.
Here is the Complete Protocol
•Coated Silver (1-6 drops per day, depending on degree of exposure) (Coated silver blocks the sulfur-bearing protein on the spikes from entering the cell. Sulfur-rich amino acids on the spike protein interact with silver causing them to fold incorrectly).
• NAC (N-acetyl cysteine) (accelerates detoxification and is considered a producer of the super detoxifier glutathione in the body) Dosage: 1200-2400 mg per day on an empty stomach. NAC is recommended to detoxify graphene oxide and SM-102. NAC is tough to find after the FDA recently made it illegal to purchase over the counter in the USA. Request NAC from your doctor!
• Zinc (30-80mg per day depending on immunological pressure)
• Vitamin D3* (10,000 IU’s per day)
• Lyposomal Vitamin C (30ml, twice daily)*
• Quercetin (500-1000 mg, twice daily)*
• Iodine* (dosage depends on brand, more is not better). Iodine is a product you have to start with small dosages and build up over time.
• PQQ* (20-40 mg per day)
Additional recommendations:
• Fennel and/or Star Anise Tea: These are also an excellent source of shikimate or shikimic acid (which is known to neutralize the spike protein)
Hesperidin sources to help disable spike protein:
• Citrus fruit (especially blood oranges, due to their high hesperidin content — hesperidin is a chalcone like quercetin that deactivates spike protein)
• Peppermint (very high in hesperidin)
Superherbs to help disable spike protein:
• Triphala formulations: In Sanskrit, the word Triphala means “three fruits”: a combination of Indian gooseberry (Emblica officinalis), black myrobalan (Terminalia chebula) and belleric myrobalan (Terminalia belerica). The terminalia fruits are rich in shikimate.
• St. John’s Wort (shikimate is found throughout the entire plant and in the flowers)
• Comfrey Leaf (rich in shikimate)
• Feverfew (leaves and flowers are rich in shikimate)
• Gingko Biloba Leaf (rich in shikimate)
• GiantHyssop or Horsemint (Agastache urtifolia) (rich in shikimate)
• LiquidAmbar (Sweet Gum tree) A tea of the spiky seed pods is rich in shikimate.
•Glycyrrhiza glabra (Chinese medicine’s licorice root): Glycyrrhizic acid is extracted from the root of the licorice plant inhibits spike protein.
TGA demands $350k from Australian vaxx manufacturer threatened with arrest for developing first, safe, sub-protein vaxx
from The Spectator
Professor Nikolai Petrovsky has just developed Australia’s first successful vaccine in 40 years. In any approximation of a normal world, he would be feted as the living incarnation of the government’s much trumpeted aspiration to be an ‘innovation nation’. Instead, he has been stood down by his university and threatened with arrest if he sets foot in his office. Why? For refusing to be immunised with one of the vaccines approved by the Therapeutic Goods Administration (TGA).
It’s ironic. Petrovsky was immunised with his own vaccine more than a year ago. Recently concluded phase III trials show it is far safer than any vaccine approved by the TGA and better at preventing infection with and transmission of the Sars-Cov-2 virus. This week, the TGA recognised the Chinese Sinopharm and the Indian Covaxin vaccines as effective. Yet the TGA refuses to look at Petrovsky’s Australian vaccine until he pays a fee of $350,000.
The travails of Petrovsky are a cautionary tale of governments picking losers and punishing winners. Aside from being professor of medicine at Flinders University, director of endocrinology at the Flinders Medical Centre and vice-president and secretary-general of the international Immunomics Society, Petrovsky is the founder of Vaxine, an Australian biotech company that has won numerous awards, developed successful vaccines against Sars and Mers and is funded by the US National Institutes of Health.
Despite an outstanding record of achievement, Petrovsky’s application for funding to develop a Covid vaccine was rejected by the federal government. Instead, the government funded a project developed by the University of Queensland and backed by CSL, the only vaccine manufacturer in Australia. Before phase I trial results had even been completed, federal health minister Greg Hunt announced an investment of $1.7 billion to pre-order 84.8 million doses of the UQ and AstraZeneca vaccines. The project never made it beyond the phase I trial, but CSL still refuses to manufacture Petrovsky’s vaccine and the federal government refuses to fund a vaccine that is not manufactured in Australia.
The results of Petrovsky’s trials in monkeys, ferrets and hamsters showed not only that his vaccine was safe but that vaccinated animals produced neutralising antibodies in the nose and throat, blocking transmission to animals which had not been immunised. Before injecting the vaccine into a single person, Petrovsky injected it into himself to demonstrate his confidence in the product. Compare that with the CEO of Pfizer, Albert Bourla who began dosing people with its experimental vaccine on April 23, 2020. Bourla didn’t get his first shot of the Pfizer vaccine until 21 March 2021.
Vaxine was the first Covid sub-protein vaccine in the world to gain regulatory approval, on 8 October, beating Swiss-American pharmaceutical giant Novartis, which teamed up with the Bill Gates-backed Coalition for Epidemic Preparedness Innovations (CEPI) and this week gained regulatory approval for its Novavax vaccine. Yet rather than being a great Australian success story, Petrovsky has had to team up with an Iranian manufacturer to produce his Covax-19 vaccine, sending Australian manufacturing jobs offshore, and is using a GoFundMe site to raise the $350,000 to pay the TGA fees which go directly to the Commonwealth Department of Health.
Why has Petrovsky faced so many hurdles? There is no doubt that there is a highly influential vaccine establishment which has played along with the fiction that Sars-Cov-2 could not have leaked from the Wuhan Institute of Virology. Petrovsky was one of the first major Western scientist to say that having studied the virus, it was highly unlikely that it could have acquired its unusual characteristics other than in a laboratory. That would have angered powerful and influential people.
But is there something murkier? Petrovsky says a government MP told him that doors would remain closed to him in Canberra unless he paid a lobbyist to open them. Pfizer, AstraZeneca, Merck, Novartis and Sanofi on the other hand all have the deepest pockets to smooth their way. Whatever the truth, this week, the nation’s most successful vaccinologist was stood down during a global pandemic and South Australia sacked ten per cent of its healthcare workforce because they refused to comply with the same draconian, unscientific and unethical vaccine mandate. And this, a fortnight before the state’s borders will open to wide-scale infection which will inevitably lead to increased hospitalisations of vulnerable people.
Petrovsky was sacked even though he may well have better immunity than those who are sacking him. And the vaccine mandates remain in place even though the most recent vaccine surveillance report in the UK states that vaccine effectiveness wanes after ‘the first three to four months’ and that the AstraZeneca (AZ) vaccine, even at its peak, only provides 65-75 per cent protection and both AZ and Pfizer wane to no effective immunity within six months. Indeed, in every age group over 30, the vaccinated are more likely to get infected than the unvaccinated. The mandates also refuse to acknowledge that infection-acquired immunity is as robust as vaccine acquired immunity, even though this is backed by 102 research studies, and according to Johns Hopkins University School of Medicine professor Dr Marty Makary, data from Israel shows that natural immunity is 27 times more effective than vaccinated immunity.
‘We know they are lying, they know they are lying, they know we know they are lying, we know they know we know they are lying, but they are still lying’ wrote Aleksandr Solzhenitsyn. How did it come to pass so quickly that Australia feels like a former Eastern bloc country where virological Lysenkoism is an official doctrine, dissidents are sacked, the newspapers report propaganda and the truth is relegated to social media samizdat?
In his 1961 farewell address to the nation, President Dwight Eisenhower warned that ‘the prospect of domination of the nation’s scholars by Federal employment, project allocations, and the power of money is ever present and is gravely to be regarded’, and ‘in holding scientific research and discovery in respect, as we should, we must also be alert to the equal and opposite danger that public policy could itself become the captive of a scientific-technological elite’. Eisenhower said it was the task of statesmen to balance these forces within the principles of our democratic system so that security and liberty could prosper together.
Sadly, there is no one to hold a candle to him today. If we are to get out of this mess, we must save ourselves.
Dr Tenpenny warns parents to prepare for thousands of deaths of young children after Pfizer shot
“Maybe people will start to wake up when there are millions of dead six and seven-year-olds. When it affects them personally. It’s their own children, and we’re coming up on Christmas. Now suddenly, we’ve got millions without even 1000s or 10s of 1000s, or hundreds of 1000s of dead first graders, and second graders, and seventh graders.
So what did I tell people they need to do the most of us they need to get mentally prepared for that. Think of what our children have been through as a society in the last year and a half. With masks, social distancing, the spike of psychiatric illness and depression, suicide, their world’s devastated and destroyed in terms of going, graduating from high school, graduating from college, participating in sports. Their whole worlds have been decimated.
And now, when they start looking around at some of their classmates dead, it may be the very chill classmates who were saying I got the shot and it didn’t even hurt, and I got ice cream. You should get the shot too.
And then they say to their parents. I thought you told me the shot was okay. I thought you got me the shot, right? Am I going to die next? These are the things I think we need to get prepared for. Seriously. And if that’s planned for the worst and hope for the best, you know, maybe none of that stuff happens. But at least you’ve been psychologically, mentally, spiritually prepared.” – Dr. Sherri Tenpenny
Craig Kelly asks TGA head John Skerritt why he allowed dangerous Moderna vaxx for kids when the US banned it
Dear Professor Skerritt,
Further to my email of the 19th October 2021, in regards to my concerns that the TGA had approved the Moderna (Spikevax) Covid vaccine to be injected into Australian teenagers aged 12-17, despite the fact that in the country of manufacture (the USA) that the American regulators have refused to allow Moderna to be injected into American teenagers, and your reply of the 25th October 2021, advising that the TGA believes that American regulators are wrong and that;
“The TGA decided that the Moderna vaccine is effective and safe for use in adults and adolescents aged 12 years and above”
I would like to draw to your most urgent attention, that your Database of Adverse Event Notifications (DAEN) lists a case where a death has been reported on the 20th October 2021, as having been suspected of being caused by the Moderna (Spikevax) covid vaccine. It also appears that this death was that of a 14 year-old girl (Case no.647663)
- Can you confirm, that this reported death, suspected as a result of the Moderna (Spikevax) covid vaccine, is in fact that of a 14 year-old Australian girl ?
- If so, following the death of this 14 year-old girl, together with the 626 other adverse events already reported (from the 1st Oct 2021 – 22nd Oct 2021) suspected to be caused by the Moderna vaccine – does the TGA continue to maintain the stance that the Moderna vaccine is “effective and safe for use in adults and adolescents aged 12 years and above” ?
- I assume that the TGA is urgently investigating this death, and therefore assuming that TGA adheres to the ‘Precautionary Principle’ can you confirm if the TGA will immediately suspend any further injections of the Moderna Vaccine into Australian teenagers until the completion of the investigation in the death of this 14 year-old girl ?
- If the TGA continues to maintain the stance that the Moderna vaccine is “effective and safe for use in adults and adolescents aged 12 years and above” (contrary to the views of the American regulators), how many deaths of young Australians aged 12-17 (suspected to be a result of Moderna covid vaccine – and reported to DAEN) would it take for the TGA to change its view ?
- Given the principle of ‘Informed Consent’, can you confirm if the parents of this deceased 14 year-old girl where informed that the Moderna (Spikevax) covid vaccine had not been given approval in the USA for injection into American 14 year-old girls due to safety concerns ?
- Do you have any concerns that TGA’s conduct of rejecting and acting contrary to the advice of the American medical regulators on Moderna (especially when Moderna is manufactured in the USA) and continuing to allow the injections of Moderna into Australian teenagers, following the death of this 14 year-old Australian girl, may expose Australian taxpayer’s to substantial claims for compensation and/or that private action may be commenced against the decision makers at the TGA ?
I look forward to most urgent reply.
Regards,
Craig Kelly MP
Member for Hughes
Leader, United Australia Party
Cairns News 