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QUESTIONS ON NOTICE

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

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

1. In regard to Covid vaccines, how many claims for deaths and injuries have been paid out on, how many outstanding claims are there for deaths and injuries and how many claims re deaths and injuries have been dismissed? 2. Is a non-disclosure agreement a condition of any of these payouts? 3. Is the Indemnity scheme going to be widened given there are more adverse events than recognised by Pfizer in their trials and in light of the fact that Pfizer has is trying to withhold data relating to the trials for up to 55 years? 193. What the conditions around vaccine indemnities given to pharmaceutical companies? If the companies have withheld data that is material to the safety and efficacy of the vaccine do the companies still receive indemnity?

24/02/2022

I note that on page 23 and 24 of the Pfizer post marketing surveillance data that the event latency was reported as <24 hours to 41 days with a median of 2 days for stroke, and for neurological events on page 21 range <24 hours to 48 days median 1 day, and for cardiovascular events including myocardial infarction and cardiac failure range a latency range of <24 hours to 21 days and median <24 hours. Because Pfizer failed to detect these vaccine injuries, victims have been denied proper medical attention and had their injuries ignored. Given this data will John Skerritt now admit the Pfizer vaccine can cause strokes and apologise to those who have suffered strokes and other adverse events?

24/02/2022

47. Will the TGA ask for the all the data from the Pfizer trial including the data the Pfizer is trying to prevent from releasing to the public for a period of up to 55 years? 48. Has the TGA ask Pfizer for an explanation of why the company does not want to release data for up to 55 years? 49. If the data that Pfizer does not want to release is shown to be materially different in terms of safety and efficacy will the TGA sue Pfizer for damages or does the Pfizer indemnity extend to fraud and or non-disclosure? 50. On what basis does John Skerritt say that the data relating to the vaccine trials is thorough when not all data has been released, individual data wasn’t looked at and several areas including carcinogenic risks, immunocompromised patients, pregnant women, breast feeding women, reactions to other drugs and longitudinal studies weren’t completed? 51. How can the TGA say the Pfizer trial was relevant to the vulnerable population when only 4% of the trial group was over 75 when over 75% of people over 75 were hospitalised or died from Covid? 52. Could the TGA provide measurements of clinical outcomes in the initial Pfizer trial such as hospitalisations and deaths and subclinical outcomes such as inflammation and clotting?

24/02/2022

4. Why is the Health Department allowing AHPRA (Australian Health Practitioner Regulation Agency) to censor Doctors and nurses on giving their views on the Covid vaccine? I have spoken to over 100 medical staff who are afraid of being suspended or have been suspended for giving their views on the dangers of the vaccine? 5. If AHPRA is not a government aligned body, then why isn’t the government protecting the right of medical staff to express their view freely without the threat of suspension? 6. I note neither the Chair or CEO of AHPRA are qualified doctors or nurses. Who gives AHPRA the authority to suspend doctors or nurses at a time there is a shortage of them in Australian hospitals for expressing their professional views based on their observations?

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

1. In regard to Covid vaccines, how many claims for deaths and injuries have been paid out on, how many outstanding claims are there for deaths and injuries and how many claims re deaths and injuries have been dismissed? 2. Is a non-disclosure agreement a condition of any of these payouts? 3. Is the Indemnity scheme going to be widened given there are more adverse events than recognised by Pfizer in their trials and in light of the fact that Pfizer has is trying to withhold data relating to the trials for up to 55 years? 193. What the conditions around vaccine indemnities given to pharmaceutical companies? If the companies have withheld data that is material to the safety and efficacy of the vaccine do the companies still receive indemnity?

24/02/2022

I note that on page 23 and 24 of the Pfizer post marketing surveillance data that the event latency was reported as <24 hours to 41 days with a median of 2 days for stroke, and for neurological events on page 21 range <24 hours to 48 days median 1 day, and for cardiovascular events including myocardial infarction and cardiac failure range a latency range of <24 hours to 21 days and median <24 hours. Because Pfizer failed to detect these vaccine injuries, victims have been denied proper medical attention and had their injuries ignored. Given this data will John Skerritt now admit the Pfizer vaccine can cause strokes and apologise to those who have suffered strokes and other adverse events?

24/02/2022

47. Will the TGA ask for the all the data from the Pfizer trial including the data the Pfizer is trying to prevent from releasing to the public for a period of up to 55 years? 48. Has the TGA ask Pfizer for an explanation of why the company does not want to release data for up to 55 years? 49. If the data that Pfizer does not want to release is shown to be materially different in terms of safety and efficacy will the TGA sue Pfizer for damages or does the Pfizer indemnity extend to fraud and or non-disclosure? 50. On what basis does John Skerritt say that the data relating to the vaccine trials is thorough when not all data has been released, individual data wasn’t looked at and several areas including carcinogenic risks, immunocompromised patients, pregnant women, breast feeding women, reactions to other drugs and longitudinal studies weren’t completed? 51. How can the TGA say the Pfizer trial was relevant to the vulnerable population when only 4% of the trial group was over 75 when over 75% of people over 75 were hospitalised or died from Covid? 52. Could the TGA provide measurements of clinical outcomes in the initial Pfizer trial such as hospitalisations and deaths and subclinical outcomes such as inflammation and clotting?

24/02/2022

4. Why is the Health Department allowing AHPRA (Australian Health Practitioner Regulation Agency) to censor Doctors and nurses on giving their views on the Covid vaccine? I have spoken to over 100 medical staff who are afraid of being suspended or have been suspended for giving their views on the dangers of the vaccine? 5. If AHPRA is not a government aligned body, then why isn’t the government protecting the right of medical staff to express their view freely without the threat of suspension? 6. I note neither the Chair or CEO of AHPRA are qualified doctors or nurses. Who gives AHPRA the authority to suspend doctors or nurses at a time there is a shortage of them in Australian hospitals for expressing their professional views based on their observations?

24/02/2022

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