203. Professors from UCLA and Stanford have highlighted the risk of vaccine injuries at 11 in 10000. How can the TGA refute these prestigious institutions – Serious Adverse Events of Special Interest Following mRNA Vaccination in Randomized Trials by Joseph Fraiman, Juan Erviti, Mark Jones, Sander Greenland, Patrick Whelan, Robert M. Kaplan, Peter Doshi :: SSRN 219. In a previous QON the TGA stated “Since these vaccines were granted provisional approval, more than 11 billion people have received doses of COVID-19 vaccines worldwide. Data on real-world use of the COVID-19 vaccines approved in Australia provides reassurance about their safety and that the trials were carried out correctly. This is supported by reviews of safety data by international medicines regulators in countries with extensive COVID-19 vaccine experience who have found no new safety concerns associated with the use of COVID-19 vaccines. In addition, the TGA’s monitoring program has not detected any new safety signals in relation to COVID-19 vaccines to date?” This reply is a blatant lie that will be reported for contempt. A number of side effects have been reported such as myocarditis and heavy menstrual bleeding. Why is the TGA covering up serious side effects from the mRNA Covid vaccines? 280. Given the Covid vaccine trials were so short in duration why does the TGA take the sponsors word as to what side effects are and ignore real world data being reported
Question Number: 208 PDR Number: SQ22-000578 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 203 It is incorrect and misleading to infer that the paper by Fraiman et al ‘highlights the risk of vaccine injuries at 11 in 10000”. This paper was not designed to confirm vaccine-related harm and is not a formal […]
174. Will the Health department run a study to determine if Covid antibodies are higher in the vaccinated or unvaccinated? If not, why not – isn’t this critical to determine the long term of effects of multiple Covid vaccines on the immune system to find out if repeated vaccine shots lower the body’s immune defences? 201. Has the TGA or the sponsor tested the modifications to the mRNA in the vaccine spike protein to ensure that it is capable of being broken down by the body’s immune system? If so, can studies please be provided and the number of days taken to break down the spike protein be stated? 269. How much confidence is there that the proline insertions keep the spike protein in its prefusion shape? What studies have been completed that demonstrate this? Does the TGA accept that if the spike is not replicated in its prefusion shape then the immune system will recognise it as a different pathogen to the virus spike protein?
Question Number: 205 PDR Number: SQ22-000575 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 174 The Therapeutic Goods Administration (TGA) does not conduct clinical trials or serological surveys on any medicine or vaccines, however the TGA is aware that studies to assess immunity derived from both vaccination and natural infection (or a hybrid […]
105. If the Federal Health Department doesn’t support mandates, then why is ATAGI restricting exemptions to just a few conditions based on inadequate trials from sponsor who has an inherent conflict of interest? Given the Australian Immunisation Handbook says people can’t be coerced into taking a vaccine how can ATAGI override that by setting rules that completely ignore a person’s individuals characteristics? 106. Myocarditis and Pericarditis are now two well-known risks for young men from the vaccine. Doctors are still refusing to write exemptions for these indications, and I have been contacted by people who have lost their jobs even with an exemption. When will ATAGI lift the exemptions on mandates so doctors are free to issue exemptions subject to their own discretion? 107. Given myocarditis was a known risk for young men as far back as May 2021 why has ATAGI allowed vaccines to be mandated and furthermore still encourage booster uptake knowing it can cause such harm? 108. Dr Christoper Blyth said ATAGI has not provided a recommendation for mandates – is that correct – if so when then why has ATAGI defined the exemptions so narrowly?
Question Number: 203 PDR Number: SQ22-000573 Date Submitted: 21/11/2022 Department or Body: Department of Health 105. The Australian Government does not impose COVID-19 vaccination mandates and maintains that COVID-19 vaccination is voluntary, as are all vaccinations in Australia. During the COVID-19 pandemic some state and territory enacted public health orders that set mandatory vaccination requirements […]
189. DARPA funded and basically built Moderna. Will the new Moderna facility be involved with the production of bio-weapons? 199. Australia has signed a ten year deal with Moderna for 100 million vaccines. Is this true and if so, why has Australia committed to buying so many mRNA vaccines given they have yet to be proved safe and effective?
Question Number: 201 PDR Number: SQ22-000571 Date Submitted: 21/11/2022 Department or Body: Department of Health 189. No. Moderna’s Australian facility will produce respiratory mRNA vaccines and pandemic mRNA vaccines as they are developed and registered by Australia’s Therapeutic Goods Administration (TGA). 199. In a pandemic scenario, the facility will be capable of producing up to […]
102. Regarding vaccine injury claims how can the TGA override specialists when they have examined the patient and the TGA hasn’t? 103. Regarding reported deaths from the vaccine how can the TGA override specialists when they have examined the patient and the TGA hasn’t? Especially when the specialists or health professional has ticked the “suspected” box that indicates they believe the death was caused by the vaccine? 104. Regarding reported injuries from the vaccine how can the TGA override specialists or health professionals when they have examined the patient and the TGA hasn’t? Especially when the specialists or health professional has ticked the “suspected” box that indicates they believe the death was caused by the vaccine?
Question Number: 199 PDR Number: SQ22-000569 Date Submitted: 21/11/2022 Department or Body: Department of Health Answer 102 The Therapeutic Goods Administration (TGA) does not provide specialist clinical opinion on any vaccine injury claim. The claimant’s diagnosis (and therefore clinical eligibility under the scheme) is dependent on the treating doctor’s specialist opinion. There is no process […]
175. What law gives ATAGI the authority to issue rules around Vaccine exemptions to doctors? 176. Studies have shown that natural immunity from Covid has been found to last up to 20 months after infection. Why doesn’t ATAGI recognise natural immunity and antibody tests as a reason to grant an exemption to getting a Covid vaccine? 193. Does Nigel Crawford work for the Murdoch Children’s Research Institute? 194. How much do the the Bill and Melinda Gates Foundation and other big Pharma organisations pay Nigel Crawford’s employers? 195. Why are there so many Monash employees on the ATAGI board, given Monash receives money from Big Pharma and the Bill and Melinda Gates foundation? 210. Section 10 then says an advertisement cannot be inconsistent with a public health campaign. If a public health campaign is failing to acknowledge risks, then why is it not okay to highlight those risks – take myocarditis for example where ATAGI knew about the risks but failed to highlight them? 242. Chair of ATAGI, Prof Nigel Crawford – “Previous animal trials of experimental vaccines against SARS-CoV-1 and MERS-CoV have also been shown to induce a more serious disease when subsequently exposed to the diseases – https://mvec.mcri.edu.au/references/vaccine-associated-enhanced-disease-vaed/ – given this knowledge why is ATAGI encouraging more booster given what is known about immune imprinting? 288. Is ATAGI aware that students are running hospital wards because of their mandates resulting in staff shortage?
Question Number: 197 PDR Number: SQ22-000567 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 175 The role of the Australian Technical Advisory Group on Immunisation (ATAGI) is to advise the Minister for Health and Aged Care on the medical administration of vaccines available in Australia, including COVID-19 vaccines and those available through the […]
100. The Australian government bought around 250 million doses and has used around 70 million doses to date. Why did the government buy so many given Australia only has a population of 25 million? 101. Will the government get a refund on the $8 billion given the vaccines didn’t work?
Question Number: 195 PDR Number: SQ22-000565 Date Submitted: 21/11/2022 Department or Body: Department of Health 100. The Australian Government has invested in a diverse portfolio of COVID-19 vaccines to secure early access, provide Australian’s flexibility of choice and enable the government to address variants of concern in the future. Quantities were procured well above population […]
186. Regarding Ivermectin, is this the first time in Australian history that the Federal Government has instructed the withdrawal of a medicine in the context of a public health emergency? 187. What evidence was there that taking Ivermectin could be a risk to the community either directly, or indirectly by discouraging vaccination. Given vaccination doesn’t stop transmission how was taking Ivermectin a threat to others? 188. What evidence was considered by the committee when recommending that Ivermectin was a risk to individual patient health. Did the Committee and Minister review any evidence of death or injury through inappropriate use of Ivermectin? I note Dr Skerritt stated 12mg was an unsafe dose in a previous conversation yet the sponsors of the drug have claimed that one off does of 120mg and 30,60 and 90mg doses on day 1, day 4 and day 7 are safe.
Question Number: 194 PDR Number: SQ22-000564 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 186 There was no ‘withdrawal of ivermectin”; the decision to instruct restrictions on off-label prescribing was made by a delegate of the Secretary of Health and Aged Care on the strong advice of the Advisory Committee for Medicines Scheduling. […]
178. On average how many strands of mRNA are in 30 micrograms of mRNA? Given there are 5 doses in each vial how can the TGA be sure that each dose will contain the same amount of mRNA? 179. What is the margin of error administering 30 uml (.3mL) from a vial with 5 doses? 180. Why didn’t the TGA make Pfzier measure out the 30 microns evenly instead of leaving it to the person who administers the vaccine – the margin of error for such a small dose would be huge would it not? 181. Given the TGA measures mRNA by mass how does it know if they or the administrators of the vaccine are measuring mRNA and not solution?
Question Number: 192 PDR Number: SQ22-000562 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 178 A single dose of COMIRNATY COVID-19 vaccine containing 30 micrograms of mRNA has approximately 1.30 × 1013 ‘strands’ of mRNA. The Therapeutic Goods Administration (TGA) reviews the ability of the manufacturer to produce consistent batches as part of […]
98. Real world data is starting to show negative efficacy from repeated booster shots. Why is the TGA ignoring immune imprinting or Original Antigenic sin?
Question Number: 190 PDR Number: SQ22-000560 Date Submitted: 21/11/2022 Department or Body: Department of Health We disagree with the assertion that studies are showing negative efficacy from booster shots. The Therapeutic Goods Administration (TGA) is not aware any reputable evidence to support the view that vaccination against COVID-19 lowers the body’s immune response to the […]
