168. I note FOI 3717 pertaining to metallic particle contamination in Moderna vaccines has not been displayed in the FOI Disclosure log. I note in the correspondence dated 27/08/21 that someone (can’t tell because the TGA redacted it) was concerned about visual testing and the fact that the TGA was not looking at or analysing the contents of the vial. When exactly did the TGA start analysing vials and in what way? Were they analysing from the start? If not, why not?
Question Number: 188 PDR Number: SQ22-000558 Date Submitted: 21/11/2022 Department or Body: Department of Health The Therapeutic Goods Administration (TGA) can confirm that it analyses the contents of vaccine vials from each batch through batch release testing of the COVID-19 vaccines. Each batch of COVID-19 vaccine must undergo independent assessment by the TGA Laboratories before […]
96. There is no evidence that the blood lung barrier will allow IgG antibodies which weight around 150,000 Daltons to cross from the blood into the alveolar space of the lungs where Covid is infecting the epithelial cells. Given this is the case why do authorities claim the Covid vaccine can fight Covid which is present in the lungs? 97. I note that the TGA non-clinical report on the Pfizer vaccine showed there was very little difference in lung inflammation after 8 days in between vaccinated an unvaccinated monkeys. Given they weight 10kgs and got three times the dose of humans on what basis did this trial proof the vaccine was effective noting there was an IgG response for only 35 days. I note the weight to dose ratio for the monkeys was 20 times higher than humans so on that basis there may have been an IgG response for two days (35/20) or a lower IgG response.
Question Number: 187 PDR Number: SQ22-000557 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 96 Vaccination and infection induce immune responses to pathogens in the lymphoid system including mucosa-associated lymphoid tissues. Lung based responses can occur by a number of mechanisms, some of which involve antibodies. Resident memory lymphocytes (T cells and B […]
172. What is Methotrexate used for and why has there been 46 reported deaths from it in the last 2 and a half years?
Question Number: 186 PDR Number: SQ22-000556 Date Submitted: 21/11/2022 Department or Body: Department of Health Methotrexate tablets are used to treat rheumatoid arthritis, severe psoriasis and some types of cancer. Since 2020, the Therapeutic Goods Administration (TGA) has received 48 adverse event reports for methotrexate that include a fatal outcome. Reporting an adverse event does […]
89. In the TGA non-clinical report it states “the S protein is synthesised and processed within the ER for surface expression or secretion.” Why is the vaccine stimulating the human body to export the spike protein from the cell – shouldn’t it be sterilising the virus rather than reproducing it? 90. What impact does the secretion of spike proteins have on the endothelium and other sensitive body organs? 91. Has the TGA done any research on the secretion of proteins from the cell as a result of the vaccine? If not, why not? 92. What evidence does the TGA have to prove that proteins secreted from the cells don’t cause clots and damage to body organs? 93. How does the TGA know that the ribosome translates the mRNA code 100% accurately and no mutations occur if no mutagenic studies have been done? 94. Has the TGA done any distribution and degradation studies to determine the potential toxicity of the secreted spike protein. If not, why not?
Question Number: 185 PDR Number: SQ22-000555 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 89 The expressed spike protein in vitro (in HEK293 cells) co-localised with an endoplasmic reticulum (ER) marker, suggesting the S protein is synthesised and processed within the ER for surface expression. This study did not show that the vaccine […]
88. FOI 2565 requested “Histopathology/microscopic evaluation of gonads (ovaries/testes) of vaccinated animals in relation to Pfizer and AstraZeneca COVID-19 vaccines”. This application has been rejected three times, and was rejected finally by the internal reviewers on 27 Sep 2021. Why is the TGA withholding reports of ovarian and testicular effects of an investigational (provisionally registered) vaccine. Particularly in the context of vaccine mandates being imposed upon men and women of reproductive age in various occupational sectors, and now on children and teens with their reproductive years ahead of them?
Question Number: 184 PDR Number: SQ22-000554 Date Submitted: 21/11/2022 Department or Body: Department of Health The request under FOI 2565 was a request for “histopathology/microscopic evaluation of gonads in relation to the Pfizer and AstraZeneca COVID-19 vaccines”. In order to respond to this request the full, nonclinical study reports would need to be supplied to […]
166. The AusVax safety data showed over 5 million people reported side effects 3 days after taking the Covid-19 vaccine and around 1 in 100 had to see a doctor or go to emergency just 3 days after taking a vaccine. How can the TGA justify the rollout of the Covid-19 vaccine when the adverse event rate is so high? 167. The AusVax safety data says 8% reported missing work, study or routine duties after dose 1 of the Covid vaccine, 21% after dose 2 of the Covid vaccine and 15% after dose 3 of the Covid vaccine. How can the TGA justify the rollout of the Covid-19 vaccine when the adverse event rate is so high?
Question Number: 182 PDR Number: SQ22-000552 Date Submitted: 21/11/2022 Department or Body: Department of Health The safety of the Australian population has always been the Australian Government’s highest priority. For this reason, decisions regarding COVID-19 vaccines have been, and continue to be, based on the expert medical advice of the Australian Technical Advisory Group on […]
163. Hasn’t Pfizer and Co broken the Therapeutic Goods Act 1989 by failing to report all the adverse events from their trials and post marketing surveillance (refer to patient records)? Under paragraph 28(5)(ca) of the Act, you MUST retain records pertaining to the reporting requirements and safety for your medicine. (page 29 of 44) 164. What is the legislation that details the TGAs responsibilities in regard to post market safety surveillance data? Why hasn’t the TGA sought to allay the publics fear over data that shows an alarming number of adverse events and poor quality assurance practices? 202. Does the TGA do post marketing surveillance at all over and above that of the sponsor? If not, why not? What is the point of having an independent regulator if it doesn’t do independent safety testing?
Question Number: 181 PDR Number: SQ22-000551 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 163 The Therapeutic Goods Administration (TGA) is not aware of any failure by Pfizer to comply with their reporting or record-keeping obligations related to adverse events and post market surveillance. Question 164 The Therapeutic Goods Act 1989 contains a […]
80. In the prior set of estimates Prof Skerrit said that the lipids used in the vaccine are like the lipids you have in a steak for breakfast. This is not the case – as per Pfizers own website they are special ionised lipids designed to cross the cell membrane. Will Prof Skerritt withdraw his prior remark? 81. Lipids are hydrophobic not hydrophilic – by cationising them you have completely changed their characteristics from inactive to active -why did Prof Skerritt mislead the senate when he said the lipids were like the lipids you find in sausages/steak for breakfast? 82. Given these lipids are ionised and therefore an active ingredient what studies have been undertaken to ensure they were not harmful to the human body? 83. What studies were undertaken to ensure that the cationic lipids don’t create reactive oxygen species which can cause irreversible damage to DNA? 84. If the ionic lipids can enter any cells via electroporation or transfection then aren’t they more infectious than the virus which can only enter cells that contain ACE and TMPRRS enzymes that facilitate the virus entering the cell? 85. Can the lipids enter both white and red blood cells? I note that lipids entered both the spleen and bone marrow in the rat studies? 86. Given the lipids are taken up by the ovaries what guarantees can the TGA give that eggs are not being damaged. Obstetricians are reporting that they are seeing clusters of low Anti-Mullerian Hormone (AMH) levels in young women 95. The bone marrow, spleen, and lymph nodes are responsible for producing white blood cells and regulating the while blood cells in the blood and the lymphatic system. Given that lipids can enter these organs and induce an autoimmune response against the cells in these body organs isn’t there a serious risk that the vaccine can induce autoimmune diseases?
Question Number: 180 PDR Number: SQ22-000550 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 80 Lipid nanoparticles (LNPs) in the COVID-19 vaccines consist of four lipids and all four are structurally similar to natural lipids. ALC-0315 and SM-102 are similar in structure and help encapsulate mRNA. ALC-0159 and PEG200-DMG are lipids attached to […]
71. Has the TGA now got comprehensive and exhaustive data that determines how long the body produces the Spike protein. If not, then why are they allowing the rollout of the vaccine to continue? 72. Has the TGA now got comprehensive and exhaustive data that determines how long the spike protein or any other related prions, mutations stay in the body and by body organ type. If not, then why are they allowing the rollout of the vaccine to continue? 73. Do expressed spike proteins stay in the cell membrane or are they secreted via exosomes? 74. The ribosomes on the endoplasmic reticulum produce protein for export while ribosome in the cytoplasm produce proteins for use inside the cell. Given the TGA non-clinical report says the spike protein is produced via the endoplasmic reticulum then isn’t evidence that spike proteins will be exported from the cell and potentially re-enter the circulatory system? 76. Which part of the mRNA code tells the mRNA to attach to the Endoplasmic Reticulum? 77. What evidence does the TGA have that the spike protein doesn’t go into the nucleus – the delivery of the spike protein was never tested. There were no studies carried out so how would the TGA know with 100% certainty the mRNA or the spike protein doesn’t enter the nucleus? 78. Is there any evidence that the spike protein does not inhibit the P53 gene? Were studies carried out to prove this? 79. “Another study revealed that extracellular vesicles decorated with S-proteins persist up to 4 months after vaccination… This raises the possibility that LNP–mRNA remain in circulation for extended periods of time, retaining their ability to induce S-protein expression….”. Does the TGA refute this study? www.mdpi.com/2227- 9059/10/7/1538/htm 87. Have studies been conducted by the TGA to determine if the spike protein interferes with oocytes?
Question Number: 179 PDR Number: SQ22-000549 Date Submitted: 21/11/2022 Department or Body: Department of Health Question 71 At present, there is no evidence suggestive of long-term accumulation of the provisionally approved COVID-19 vaccines or their associated proteins or effects in the body. The mRNA and spike protein are quickly degraded and removed via normal cellular […]
161. “Pfizer has asked a U.S. court to throw out a lawsuit from a whistle-blower who revealed problems at sites that tested Pfizer’s COVID-19 vaccine. Pfizer stated that the regulations don’t apply to its vaccine contract with the U.S. Department of Defence because the agreement gives contract holders the ability to skirt many rules and laws that typically apply to contracts.” Pfizer Moves to Dismiss Lawsuit From COVID-19 Vaccine Trial, Citing ‘Prototype’ Agreement (theepochtimes.com) – Has Australia signed a Covid-19 contract with Pfizer that has similar conditions? 162. Why are you penalising Australians $10,000 of dollars for importing Ivermectin worth $40 but doing nothing about Pfizer not living up to its promise about the safety and efficacy of the vaccine? 165. Can the TGA provide all correspondence with Pfizer regarding the Covid vaccine in regards to purchase agreements, testing and safety concerns? 183. Is the vaccine injury scheme going to be updated to include additional side effects that have been reported to the TGA by Health Professionals rather than Pfizer who have a conflict of interest in reporting side effects from their own drugs? 191. The normal default for contracts is to reserve a “right” to buy. Are these the terms the Pfizer Covid vaccine contract was based on, or do have an “obligation” to buy the Covid vaccines regardless of performance? If so, why did the health department deviate from the normal procedure for a contract that covers Australia’s needs many times over, for a period where all would already be vaccinated (2022 and 2023). 262. The contract between Pfizer and the US government prohibits independent researchers from studying the vaccines. They claim it would ‘divert’ these precious resources away from their intended use fulfilling an ‘urgent’ need. Is this true? If so, then why is Pfizer hiding from independent scrutiny?
Question Number: 178 PDR Number: SQ22-000548 Date Submitted: 21/11/2022 Department or Body: Department of Health 161 The details of Advance Purchase Agreements with pharmaceutical companies for the purchase of COVID-19 vaccines are commercial-in-confidence. 162 The controls on the importation of therapeutic goods exist to ensure that only goods subject to regulatory oversight are supplied in […]
