196. What percentage of adverse events relating to Covid vaccines were prepared by medical professionals v consumers? 197. What percentage of adverse events relating to Covid vaccines were suspected to be caused by the vaccine? 198. What percentage of reported deaths relating to Covid vaccines were prepared by medical professionals v consumers? 199. What percentage of reported deaths relating to Covid vaccines were suspected to be caused by the vaccine?
Question Number: 138PDR Number: SQ22-000159Date Submitted: 24/02/2022Department or Body: Department of Health This provides information on the reporter type for adverse event reports for COVID-19 vaccines received up to 6 March 2022: All adverse event reports, including those with a fatal outcome, remain in the Therapeutic Goods Administration (TGA) database even if they have not […]
200. Where does the Centre for Innovation in Regulatory Science, of which John Skerritt is chair get its funding from? 201. Where does the International Coalition of Medicines Regulatory Authority of which the John Skerrit is the vice chair get its funding from?
Question Number: 112 PDR Number: SQ22-000160 Date Submitted: 24/02/2022 Department or Body: Department of Health Response to Question 200 • The Centre for Innovation in Regulatory Science (CIRS) provides an international forum for industry, regulators, Health Technology Assessment (HTA) and other healthcare stakeholders to meet, debate and develop regulatory and reimbursement policy through the innovative […]
204. Prior mRNA vaccine studies in rats resulted in the rats producing super numerary ribs. These are a sign of maternal distress are they not? 205. Given that animals studies indicated maternal distress from the mRNA vaccines why didn’t Pfizer perform more comprehensive studies on pregnant and breastfeeding women before rolling it out to the general population? Furthermore, why didn’t the TGA ask that Pfizer be more thorough in its investigations before approving for pregnant and breast feeding women in Australia?
Question Number: 165 PDR Number: SQ22-000162 Date Submitted: 24/02/2022 Department or Body: Department of Health 204. Supernumerary ribs naturally occur in rats and it is common in this species and the number of animals with supernumerary ribs may vary between studies. In the rat study with the Pfizer vaccine, supernumerary ribs were seen in both […]
241. Is there a legal requirement within any Australian jurisdiction that requires an autopsy to be performed if someone passes away within 28 days of receiving a virus (sic)? If not, why not? 242. Given the Covid-19 vaccines are only provisionally approved shouldn’t any death within 28 days of the receiving the vaccine be exanimated (sic) to (sic) in order to determine if the vaccine was the cause of death?
Question Number: 122 PDR Number: SQ22-000181 Date Submitted: 24/02/2022 Department or Body: Department of Health There is no legal requirement within any Australian jurisdiction that explicitly requires an autopsy to be performed if death occurs within 28 days of vaccination. Decisions about coronial processes and procedures, such as performing autopsies and selecting the type of […]
253. Regarding Freedom of Information 3586 on reported deaths why is so much data redacted? 254. Regarding Freedom of Information 3586 on reported deaths why is there almost another 150 deaths on the file that isn’t listed as a reported death?
Question Number: 154 PDR Number: SQ22-000188 Date Submitted: 24/02/2022 Department or Body: Department of Health Question 253 Documents published under the Freedom of Information Act 1982 (FOI Act) may have redactions applied for a number of reasons. They may, for example, contain information that is not relevant to the FOI request, or information which is […]
115. There are fifty adverse event reports in children under 17 years old for Moderna Spikevax (100 ug of mRNA) and roughly the same amount in the 5 to 11 year old group where an adult dose of 30 ug was given instead of the provisionally authorised 10 ug all since January 10 – Feb 3. That’s roughly 100 children incorrectly given a much stronger dose and unauthorised for their age. What is the TGA doing about the administrators of vaccines giving wrong dosage amounts to children. I note Phase I dose finding studies halted the 30 ug dose in the sentinel group after a safety committee deemed it too unsafe to continue in that dose for that age group? 217. Why did ATAGI approve the Pfizer vaccine for children given it wasn’t powered to detect rare adverse events? 218. How can ATAGI guarantee that there will no long-term adverse events in children if no long-term testing was carried out on the vaccine? 219. How can ATAGI guarantee that there will no long-term adverse events in children if no long-term testing was carried out on the vaccine? 220. There have already been reports of severe adverse events in children aged 5-11 that weren’t detected in the initial children’s trials including strokes, tardive dyskinesia, chest pain, myocarditis and pericarditis. Given the large number and the broad range of adverse events will ATAGI withdraw its recommendation that the vaccine be rolled out to children?
Question Number: 104 PDR Number: SQ22-000244 Date Submitted: 24/02/2022 Department or Body: Department of Health 115. In the rare event that a vaccine administration error occurs, appropriate clinical management is provided to the patient by their health care provider. Regular communication directly to peak bodies, Primary Health Networks and health care practitioners reinforces appropriate administration […]
146. Is blood being donated to the Red Cross being tested for the presence of toxins in vaccinated bloods such as spike proteins, denuded mRNA or lipid nanoparticles? If not, why not? 147. Can CSL and the Federal government guarantee that vaccinated blood donated to Red Cross is safe?
Question Number: 119 PDR Number: SQ22-000252 Date Submitted: 24/02/2022 Department or Body: National Blood Authority 146. The Australian Red Cross Lifeblood (Lifeblood) does not test donated blood for trace vaccine components as this is not necessary for safety reasons. Screening tests for donated blood must be appropriately licensed in accordance with the Therapeutic Goods Administration […]
202. Do poisons stimulate a person’s immune system to produce antibodies? 203. How does stimulating antibodies in itself prove that a vaccine works? Should the vaccine sterilize the antigen completely to ensure it doesn’t mutate into a stronger variant?
Question Number: 166 PDR Number: SQ22-000161 Date Submitted: 24/02/2022 Department or Body: Department of Health Question 202 It is unclear by what is meant by a poison in this context. Biological substances such as anti-COVID-19 antigen proteins and proteins of animal origin, which are foreign to the human body, can stimulate a person’s immune system […]
151. Why were Early Treatments withheld from the Australian public from even being tried? 152. Why has the health department failed to actively pursue getting effective affordable Early Treatment protocols for Covid, especially given they could reduce viral loads and transmission unlike the Covid vaccines? 153. Was it a legal reason that did not allow the experimental vaccines to be used at all if there was already a treatment that works? 154. Were there any terms and conditions in the Pfizer contract with the Australian government for the Covid vaccines that prevented early treatments from being used? 255. Can the TGA guarantee there have been no lives lost by obstructing the use of early treatments as compared to allowing them?
Question Number: 163 PDR Number: SQ22-000147 Date Submitted: 24/02/2022 Department or Body: Department of Health The Department of Health and Aged Care funds the National COVID-19 Clinical Evidence Taskforce, which is continuously identifying and analysing research on various treatments for COVID-19 in order to provide national evidence-based guidelines for the clinical care of people with […]
195. Can the TGA guarantee that there were (sic) no long-term damage to people’s immune system from the mRNA vaccines and repeated booster shots? 196. Has the TGA conducted studies on the impact of receiving multiple booster (sic)
Question Number: 168 PDR Number: SQ22-000146 Date Submitted: 24/02/2022 Department or Body: Department of Health 195. The COVID-19 mRNA vaccines are designed to make human cells produce the SARS-CoV-2 spike protein and thus trigger human immune systems to create antibodies and specific T cells against SARS-CoV-2 virus. The mRNA and spike protein are quickly degraded […]
