257. Is the Federal government providing mental health support to those injured the vaccines?

Question Number: 186 PDR Number: SQ22-000189 Date Submitted: 24/02/2022 Department or Body: Department of Health Mental health and suicide prevention remains one of the Australian Government’s highest priorities. Australians who have concerns about vaccines have access to a wide range of mental health support services available to them. Since March 2020, the former government has […]

There are number of cases, 643515/680266 for example, where babies had seizures suspected to be from the vaccine because of exposure to breast milk. On what basis does the TGA dismiss these reports and continue to say it is safe for breast feeding women to get the Covid-19 vaccines?

Question Number: 139 PDR Number: SQ22-000187 Date Submitted: 24/02/2022 Department or Body: Department of Health To date, the Therapeutic Goods Administration (TGA) and other international regulators have not identified any safety signal for infants exposed to the breastmilk of vaccinated mothers. In Australia, and globally, vaccination against COVID-19 is recommended for breastfeeding women because of […]

A trial in Brazil on Ivermectin that went twice as long as the Pfizer study, with three times the number of participants showed a 44% reduction in risk of infection; 56% reduction in risk (sic) and a 68% reduction in risk of death. Given this is as high if not higher quality than the Pfizer trial where all data hasn’t been released and no active surveillance of trial group took place why isn’t the TGA allowing a safe drug to be used as an early treatment for Covid-19?

Question Number: 103 PDR Number: SQ22-000184 Date Submitted: 24/02/2022 Department or Body: Department of Health In Australia, the decision by the Therapeutic Goods Administration (TGA) was not to ban ivermectin, but to restrict the prescribing by general practitioners to TGA-approved indications such as scabies and certain parasitic infections. Ivermectin can be used as an early […]

Is the Covid-19 virus a retrovirus?

Question Number: 176 PDR Number: SQ22-000183 Date Submitted: 24/02/2022 Department or Body: Department of Health No. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the enveloped RNA virus that causes Coronavirus Disease 2019 (COVID-19), is not a retrovirus. Viruses are obligate intracellular mobile genetic elements. Viruses have a core of either DNA or RNA genetic material […]

Can all the documentation relating to meetings between the health minister and the TGA and the health minister and ATAGI please be provided?

Question Number: 172 PDR Number: SQ22-000182 Date Submitted: 24/02/2022 Department or Body: Department of Health The Therapeutic Goods Administration (TGA) meets with the Health Minister as a part of usual Portfolio briefings. There is no TGA specific documentation for these meetings. The Australian Technical Advisory Group on Immunisation (ATAGI) does not meet separately with the […]

If it takes three weeks for the body to produce antibodies to the Covid virus how much damage with the spike proteins produced by the vaccine do to the body and what organs will the spike protein enter/interfere with?

Question Number: 185 PDR Number: SQ22-000178 Date Submitted: 24/02/2022 Department or Body: Department of Health Antibodies are developed to COVID viruses on infection in most individuals much sooner than three weeks. There is no scientific evidence available that suggests that spike proteins created in our bodies from the COVID-19 vaccines are toxic or damaging our […]

Studies have shown that the risk of myocarditis increase (sic) after each booster shot. Can the TGA confirm that the risk of myocarditis or any adverse event especially clotting, doesn’t increase after each booster shot?

Question Number: 175 PDR Number: SQ22-000165 Date Submitted: 24/02/2022 Department or Body: Department of Health The Senator’s assertion is not backed up by Australian or global experience – safety monitoring does not indicate that the risk of adverse events increases after a booster. To 27 February 2022, approximately 11.4 million boosters or third doses have […]

On the 30th July 2021 the Advisory Coalition on Vaccines said Guillain-Barre Syndrome should be listed as a possible side effect. Why isn’t it and other nervous disorders in the indemnity scheme?

Question Number: 106 PDR Number: SQ22-000163 Date Submitted: 24/02/2022 Department or Body: Department of Health If this question relates to the COVID-19 Vaccine Claims Scheme, Guillain Barre Syndrome (GBS) is included as a recognised clinical condition related to Vaxzevria (Astra-Zeneca). Regarding ‘the indemnity scheme’, the Commonwealth funds health professional indemnity support programs. These programs are […]

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?

Question Number: 135 PDR Number: SQ22-000156 Date Submitted: 24/02/2022 Department or Body: Department of Health The Therapeutic Goods Administration (TGA) disagrees with the Senator’s assertions. The Pfizer post marketing surveillance data report does not indicate that its COVID-19 vaccine Comirnaty causes strokes, neurological events, myocardial infarction or cardiac failure. The report was submitted to the […]