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QUESTIONS ON NOTICE

Questions are currently being updated, please check back soon for previous questions.

135. Given the TGA failed to review the gene technology around the Pfizer vaccine did the TGA seek advice and analysis from the Office of Gene Technology Regulator before approving the Pfizer vaccine which involves gene technology? If not why not? 136. Was the TGA required to get authorisation from the Office of the Gene Technology Regulator before approving the Pfizer vaccine? 137. Did the Office of the Gene Technology Regulator provide analysis to the TGA for either of the Astra Zeneca or Pfizer vaccines? If so, could copies please be provided.

24/02/2022

45. Why do people have to lodge a FOI to get serious adverse event data from the TGA – shouldn’t it be made available with weekly reports? I refer to FOI-3520 that had to be lodged in order to get the total number of serious adverse events following Covid-19 vaccine injections? 46. Can the TGA point out where on the weekly reports are the total of serious adverse events listed as per John Skerritts comments in estimates that they are listed? There is nowhere that specifically states how many of the total adverse events reported are serious.

24/02/2022

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?

24/02/2022

128. Has the TGA assessed the risk of, and presence of micro-RNA sequences comprised within the Pfizer vaccine? 129. Has the TGA assessed the risk of and or presence of Stop Codon read- through arising as a result of the use pseudouridine in the Pfizer miRNA active ingredient? 130. Do the mRNA strands have stop codons embedded in them? If not, how will the cell stop producing spike proteins? 131. Has the TGA tested the quality of the mRNA strands in the vaccine to determine how many are mal-coded or damaged for every given inoculation? 132. Can the TGA guarantee that no other protein is transcribed by the mRNA vaccine other the purported Covid-19 spike protein? If not why not? 133. How many mRNA strands are in one dose of the Pfizer vaccine? 134. How can Pfizer/TGA guarantee that each does of the Pfizer vaccine will have the same number of mRNA strands?

24/02/2022

Senator RENNICK: Okay; that’s fine. When you review that data, can you please tell me how many people in the placebo trial were hospitalised, how many in the inoculation trial were hospitalised and how many died in the initial Pfizer trial?Dr Skerritt: Senator, we’ll put the data on deaths in the placebo and active arm as an answer to a question on notice.Senator RENNICK: I know the answer to that now; it’s actually zero and zero, because the initial Pfizer trial had no clinical outcomes in terms of hospitalisations and death and it had no-Dr Skerritt: Senator, I do not believe that is correct.Senator RENNICK: In the initial Pfizer trial, in the six-month data, there are different numbers, but-Dr Skerritt: Senator, I do not believe that you are correct-Senator RENNICK: Okay. We can move on.Dr Skerritt: I’m happy to, on notice. I do not believe that the Pfizer trial for the COVID-19 vaccine lacked data on hospitalisations. I do not believe that your assertion is correct.Senator RENNICK: Okay. I did not say it lacked data; I asked how many went to hospital. I’m asking you how many went to hospital and how many died in the inoculation group and the placebo group.Dr Skerritt: We will provide that information on notice.Senator RENNICK: Could you also provide subclinical outcomes regarding clotting and inflammation.Dr Skerritt: We’ll provide that additional information from the trial data, on notice.Senator RENNICK: Yes, on the initial trial data and not the six-month trial data.Dr Skerritt: Yes, on the initial. As long as-Senator RENNICK: Okay. Thanks, Chair.

24/02/2022

105. What was the absolute efficacy (not relative efficacy) in reducing people catching Covid of the Pfizer vaccine in the initial trials conducted by Pfizer? 106. To what extent did the vaccine reduce transmission in the initial Pfizer trials? Please provide in terms of absolute numbers? 107. To what extent did the vaccine reduce hospitalisation admissions in the initial Pfizer trials? Please provide the data in terms of absolute numbers. 108. To what extent did the vaccine reduce deaths in the initial Pfizer trials? Please provide the data in terms of absolute numbers. 109. To what extent the vaccine cause inflammation in the initial Pfizer trials? Please provide the data backing up the result? 110. To what extent did the vaccine cause clotting in the initial Pfizer trials? Please provide the data backing up the result. 113. On the 4th of January 2021, the CEO of Pfizer said the Pfizer vaccine was 100% effective in stopping transmission. This claim was repeated by Health experts in Australia. Will the TGA and the Health Department provide an apology to the Australian people for misleading them?

24/02/2022

98. In the initial Pfizer trials why no testing was done on the carcinogenic properties of the vaccine and why didn’t the TGA request it be performed?99. In the initial Pfizer trials why was no testing was done on pregnant women, breastfeeding women or immunocompromised people and why didn’t the TGA request it be performed?100. In the initial Pfizer trial why was the placebo group was unblinded after 2 months when best practice required the group to stay blinded until the end of the trial 2-3 years later?101. Given the lack of quality assurance and data derived from the Pfizer trials on what basis does John Skerrit say that the data was thoroughly assessed for safety?

24/02/2022

29. If John Skerritt and the TGA doesn’t believe the medical experts who suspect the vaccines are the cause of death are wrong, then why won’t the TGA acknowledge the deaths as being from the vaccine? 30. Why does the TGA and its experts who never examined the patient think they have a better understanding of the cause of death than the experts who actually examined the body and/or dealt with the patient symptoms as they were dying? 31. How can a board of remote ”experts” making a subjective assessment without examining the body overrule the physician who did examine the body and ticked the box ”likely” to be an adverse effect or reported death?

24/02/2022

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?

24/02/2022

135. Given the TGA failed to review the gene technology around the Pfizer vaccine did the TGA seek advice and analysis from the Office of Gene Technology Regulator before approving the Pfizer vaccine which involves gene technology? If not why not? 136. Was the TGA required to get authorisation from the Office of the Gene Technology Regulator before approving the Pfizer vaccine? 137. Did the Office of the Gene Technology Regulator provide analysis to the TGA for either of the Astra Zeneca or Pfizer vaccines? If so, could copies please be provided.

24/02/2022

45. Why do people have to lodge a FOI to get serious adverse event data from the TGA – shouldn’t it be made available with weekly reports? I refer to FOI-3520 that had to be lodged in order to get the total number of serious adverse events following Covid-19 vaccine injections? 46. Can the TGA point out where on the weekly reports are the total of serious adverse events listed as per John Skerritts comments in estimates that they are listed? There is nowhere that specifically states how many of the total adverse events reported are serious.

24/02/2022

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?

24/02/2022

128. Has the TGA assessed the risk of, and presence of micro-RNA sequences comprised within the Pfizer vaccine? 129. Has the TGA assessed the risk of and or presence of Stop Codon read- through arising as a result of the use pseudouridine in the Pfizer miRNA active ingredient? 130. Do the mRNA strands have stop codons embedded in them? If not, how will the cell stop producing spike proteins? 131. Has the TGA tested the quality of the mRNA strands in the vaccine to determine how many are mal-coded or damaged for every given inoculation? 132. Can the TGA guarantee that no other protein is transcribed by the mRNA vaccine other the purported Covid-19 spike protein? If not why not? 133. How many mRNA strands are in one dose of the Pfizer vaccine? 134. How can Pfizer/TGA guarantee that each does of the Pfizer vaccine will have the same number of mRNA strands?

24/02/2022

Senator RENNICK: Okay; that’s fine. When you review that data, can you please tell me how many people in the placebo trial were hospitalised, how many in the inoculation trial were hospitalised and how many died in the initial Pfizer trial?Dr Skerritt: Senator, we’ll put the data on deaths in the placebo and active arm as an answer to a question on notice.Senator RENNICK: I know the answer to that now; it’s actually zero and zero, because the initial Pfizer trial had no clinical outcomes in terms of hospitalisations and death and it had no-Dr Skerritt: Senator, I do not believe that is correct.Senator RENNICK: In the initial Pfizer trial, in the six-month data, there are different numbers, but-Dr Skerritt: Senator, I do not believe that you are correct-Senator RENNICK: Okay. We can move on.Dr Skerritt: I’m happy to, on notice. I do not believe that the Pfizer trial for the COVID-19 vaccine lacked data on hospitalisations. I do not believe that your assertion is correct.Senator RENNICK: Okay. I did not say it lacked data; I asked how many went to hospital. I’m asking you how many went to hospital and how many died in the inoculation group and the placebo group.Dr Skerritt: We will provide that information on notice.Senator RENNICK: Could you also provide subclinical outcomes regarding clotting and inflammation.Dr Skerritt: We’ll provide that additional information from the trial data, on notice.Senator RENNICK: Yes, on the initial trial data and not the six-month trial data.Dr Skerritt: Yes, on the initial. As long as-Senator RENNICK: Okay. Thanks, Chair.

24/02/2022

105. What was the absolute efficacy (not relative efficacy) in reducing people catching Covid of the Pfizer vaccine in the initial trials conducted by Pfizer? 106. To what extent did the vaccine reduce transmission in the initial Pfizer trials? Please provide in terms of absolute numbers? 107. To what extent did the vaccine reduce hospitalisation admissions in the initial Pfizer trials? Please provide the data in terms of absolute numbers. 108. To what extent did the vaccine reduce deaths in the initial Pfizer trials? Please provide the data in terms of absolute numbers. 109. To what extent the vaccine cause inflammation in the initial Pfizer trials? Please provide the data backing up the result? 110. To what extent did the vaccine cause clotting in the initial Pfizer trials? Please provide the data backing up the result. 113. On the 4th of January 2021, the CEO of Pfizer said the Pfizer vaccine was 100% effective in stopping transmission. This claim was repeated by Health experts in Australia. Will the TGA and the Health Department provide an apology to the Australian people for misleading them?

24/02/2022

98. In the initial Pfizer trials why no testing was done on the carcinogenic properties of the vaccine and why didn’t the TGA request it be performed?99. In the initial Pfizer trials why was no testing was done on pregnant women, breastfeeding women or immunocompromised people and why didn’t the TGA request it be performed?100. In the initial Pfizer trial why was the placebo group was unblinded after 2 months when best practice required the group to stay blinded until the end of the trial 2-3 years later?101. Given the lack of quality assurance and data derived from the Pfizer trials on what basis does John Skerrit say that the data was thoroughly assessed for safety?

24/02/2022

29. If John Skerritt and the TGA doesn’t believe the medical experts who suspect the vaccines are the cause of death are wrong, then why won’t the TGA acknowledge the deaths as being from the vaccine? 30. Why does the TGA and its experts who never examined the patient think they have a better understanding of the cause of death than the experts who actually examined the body and/or dealt with the patient symptoms as they were dying? 31. How can a board of remote ”experts” making a subjective assessment without examining the body overrule the physician who did examine the body and ticked the box ”likely” to be an adverse effect or reported death?

24/02/2022

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?

24/02/2022

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