[Must See!] Aussie GP – Dr Melissa McCann – Stands up [Part I]
THIS IS OUTRAGEOUS. This is a must-listen-to important speech by QLD GP Dr. Melissa McCann. UNBELIEVABLY TRAGIC & CRIMINAL. (Video + Transcript + Screenshots + REFS)
(Darn it, my host can’t handle the size of this post, split into two Parts. See also—Part II)
Good evening Sydney. I’d just like to welcome you all here this evening. My name is James Lutton, and I’m a member of the United Australia Party team that have helped house these events for you. Craig Kelly will be your guest MC this evening.
Thank you so much, and what a wonderful crowd we have tonight. As you’re all aware, the COVID-19 pandemic response has divided opinion around Australia and the world, but as a former leader of the United Australia Party, Sir Robert Menzies once said, today’s truth is frequently tomorrow’s error. If truth is to be triumphant, the process of free debate must go on, and that is the spirit that we’re here in tonight. Now we know there have been many adverse effects attributed to the COVID-19 vaccines, which until recently have had limited publication. We’re here today to assist in the understanding of the COVID vaccines and the side effects of this so-called immunisation. To get the ball rolling, our first speaker tonight is Queensland GP, Dr Melissa McCann. Dr McCann comes from a pharmaceutical background, is a registered general practitioner and a practice owner. She is an incredible woman with an incredible story, and trust me. She has some extremely important information to share with us all tonight. Dr McCann started as a pharmacist working on before commencing postgraduate medical education in Western Australia. Since completing her medical training, she has worked around Australia and has now settled on the Whitsunday coast where she has built a reputation as a caring and highly competent general practitioner. Please give a big welcome to Dr Melissa McCann.
Thank you so much, everyone, and thank you, Craig, for such a generous introduction. I just want to start this final talk tonight by sincerely and humbly thanking Mr Clive Palmer and the United Australia Party, for so generously hosting this important event. It has been an absolutely humbling and so hopeful to have spent a few days with this incredible professional and competent group of people, the other international expert speakers, Dr Peter McCullough and his beautiful wife. Dr Pierre Kory, and Mr John Leake.
And also, Mr Clive Palmer’s amazing team. I actually don’t know how this incredible team has managed to pull off this event, but I do know that these people literally should be running this country. They are the most capable, dedicated, caring and professional team of people that I’ve ever worked with, and we’ve been so generously accommodated by Mr Palmer, and I’ve been struck by the thought that someone with the vast resources and influence that he has, he could much more easily be bunkering down on a luxurious private island with his family and friends, whilst the rest of us face whatever dystopian future the unelected elites have planned for us, and instead, this quite incredible man has cared enough about the fate of his fellow Australians to challenge the COVID narrative and to use his resources to support the vaccine injured and to provide this forum for all of us to share the truth.
So from the philosopher Arthur Schopenhauer:
All truth passes through three stages. First, it is ridiculed. Second, it is violently opposed. Third, it is accepted as being self-evident.
As I consider this truth self-evident, I will speak as such.
I will be discussing severe adverse events and deaths following vaccines, and I apologise for any distress that may cause. So 2020 to 21, to me, was defined largely by fear, media images of coffins, body bags, and ICU scenes out of Italy and Wuhan, and stories of healthcare workers dying from COVID.
Next, the somewhat threatening statement from AHPRA, the regulator for all health practitioners on the 9th of March 21, which brought a new type of fear that any discussion unfavourable to the COVID vaccine programme could be career-ending. (01) (02)
I think it’s true to say that despite all of that, we first look forward to the COVID vaccine and that for the most part, doctors, nurses, and healthcare workers were first in line for ourselves, our parents, and grandparents, myself included, but as the programme rolled out more broadly in my rural area from around the end of 21, I started to see more adverse events than ever before.
For context, my clinic has always given a lot of vaccines, and has deliberately encouraged childhood and flu vaccines for many years by offering these to all patients without any fee.
For the COVID vaccines, I incidentally did very few due to the arrangements for pharmacies, and the government funded respiratory clinics to do these, and from around the end of 21, none at all.
My patients would still come in after having had their vaccine given elsewhere, and I had never seen anything like this.
One young patient with extensive blood clot after vaccination, several patients with strokes, patient after patient with miscarriages, and these at later gestation requiring DNC.
Patients with chest pain and unusual debilitating neurological symptoms.
In one week, four patients with confirmed myocarditis. In a region with a population of maybe 15,000, and my patient group, just a small fraction of that, the numbers just did not add up. By chance, maybe I would see one.
Multiple cases of myocarditis? This was impossible.
So in mid-November of 21, I sat down to do an informal practice audit, and look at some of those adverse events, and found there was a clear increase compared to previous years.
I went on to the TGA DAEN database and was horrified to see the reported death in a 14-year-old, reports of cardiac arrest in teenagers, at least some of those with death as a reported outcome.
Case after case of severe cardiac events in young people.
And literally thousands of severe events, strokes, blood plots, neurological events, blindness, heart attacks….
So I immediately wrote to Minister Greg Hunt and Prof John Skerritt describing what I had observed in my patients and highlighting this serious adverse event on the DAEN. I requested the immediate suspension of the vaccination program and a review of the safety issues. (03)
From John Skerritt the response:
“For the fatal outcome of the teenage girl, they did not believe the death was related to vaccination, and there was no safety signal for sudden or unexpected death in young people.” He advised that there are around “150 sudden cardiac deaths in young people each year, so it was inevitable that there would be growing numbers of reports of death to the database,” and finally, “the TGA’s focus remains on keeping Australians as safe as possible from a dangerous and very contagious virus that has killed millions of people globally.”
Frankly, I would have preferred the TGA’s focus remain on the vigilant and competent regulation of therapeutic goods, including adverse events surveillance, and I think I was naïve enough then, that I was quite put out by this response.
To compare, in 2010 in Western Australia, the halting of the childhood flu vaccines after several nurses and doctors had noticed an increase in events such as Febrile convulsions compared to previous years, a detailed report later reviewed the timeline and within weeks the program was suspended. (04) (05)
The safety signal was identified based on the reports of just a few doctors and nurses recognising a change to the usual pattern of events and an increase in the proportionality reporting ratio.
This ratio is one way of comparing reports to the database from a particular product compared to similar products and takes into account the number of doses given.
Normally, a ratio of more than one suggests a higher than expected rate of adverse events. In fact, prior to the COVID vaccine rollout in Australia, a ratio of one was selected to allow for faster detection of signals and the ratios were to be reported weekly rather than bi-monthly.
|9 January 2023||COVID Pharmacovigilance activities including ACV and VSIG minutes. (06)|
|FOI 4029||FOI 4029 document 1 (pdf,184kb)|
FOI 4029 document 2 (pdf,173kb)
FOI 4029 document 3 (pdf,228kb)
FOI 4029 document 4 (pdf,186kb)
FOI 4029 document 5 (pdf,152kb)
FOI 4029 document 6 (pdf,278kb)
FOI 4029 document 7 (pdf,81kb)
FOI 4029 document 8 (pdf,122kb)
FOI 4029 document 9 (pdf,250kb)
|FOI 4029 document 3 (pdf,228kb) (see p.10)||Advisory Committee on Vaccines Minutes Meeting 25, held 29 September 2021 COMMITTEE IN CONFIDENCE TRIM Reference no. D21-3141615 (07)|
Documents recently released on the freedom of information show this analysis was not done weekly but continued by monthly and show ratios of not only more than one but well over two for cardiac arrest for the vaccines across the period.
|29 November 2022||Proportionality Reporting Ratio analyses for the COVID-19 vaccines to 22 October 2022 (08)|
|FOI 4032||FOI 4032 document 1 (pdf,88kb)|
FOI 4032 document 2 (pdf,324kb)
FOI 4032 document 3 (pdf,241kb)
FOI 4032 document 4 (pdf,165kb)
FOI 4032 document 5 (pdf,217kb)
FOI 4032 document 6 (pdf,315kb)
FOI 4032 document 7 (pdf,285kb)
FOI 4032 document 8 (pdf,220kb)
FOI 4032 document 9 (pdf,197kb)
For other serious events such as intestinal ischemia, pulmonary infarction, ratios of more than 20 and up to 50 during the time of highest uptake, ratios over 20 for myocarditis again during the peak of the vaccine rollout, rare and serious events such as vertebral artery dissection, aortic dissection and rupture, aneurysms, strokes, intracranial haemorrhages were shockingly high given these are such rare events. (09)
Compare again with just 11 years prior, with the reporting ratio just edging over two, and within one month of that signal being detected the national suspension of the program.
In addition, deciding causality versus coincidence does not just involve looking at ratios or background rates. The WHO Handbook for Adverse Events Surveillance, provides a simple method and a flow chart.
- WHO User Manual Adverse Events 2019-2021 Edition (see p.22) (10)
- WHO User Manual Adverse Events 2018 Edition | PDF (see p.26) (11) (12)
- WHO User Manual Adverse Events 2013 Edition (13)
- Is there a strong temporal relationship? That is that the event started soon after the vaccine.
- In this patient can we confirm another cause for the event?
- Is there evidence in the published literature that the vaccine may cause such an event?
- Is there a biological causeability that the vaccine may cause such an event?
Complicating the issues was that even doctors who had themselves had severe adverse events often remained of the belief that they should not discuss their often life-changing events with others, and that they should continue to encourage vaccination, and so these doctors and other health professionals suffered in silence, unable to even discuss with their own colleagues for fear of ridicule or reprimand.
Mandates in this or any environment were and are a catastrophe of medical ethics that deserves a talk all of its own.
I saw patients who had presented months after the vaccine with ongoing chest pain and breathlessness, especially when they exercised, who resorted to paying a $1,000 to have an MRI done privately, and finally, they would get a diagnosis of myocarditis—months and months after vaccination—and I often reflected that had these patients died from a heart attack or a cardiac arrest at any point in the months between the vaccine and finally getting an MRI and the myocarditis diagnosis, that there is no way that their death would have ever been attributed to the vaccine.
I would describe waking up for me, the way John Green described falling asleep or falling in love — “slowly, and then all at once,” and in 2022, I woke up and all at once.
In March of 2022, I wrote to Minister Hunt and John Skerritt again, this time with 14 other doctors from various specialties co-signing again requesting in the strongest terms the immediate suspension of the program and a review of the safety issues. (17)
In summary: I wrote to Minister Hunt and John Skerritt in November 2021 requesting immediate suspension of the covid 19 vaccination program and urgent review of the safety issues. I presented a number of reports from the DAEN database, and also described a number of safety issues that had been observed in m y rural patient cohort which were vastly in excess of expected rates based on the published literature and the TGA weekly safety reports. I do not consider these concerns were adequately addressed, and in the three months following this correspondence colleagues and I continue to observe high numbers of adverse events amongst our patients and we remain extremely concerned regarding the adverse events reported on DAEN, including many with death as a reported outcome.
I request in the strongest possible terms an an immediate suspension of the covid 19 vaccination program pending an urgent review of the adverse event reports. The high number of observed adverse events constitute a serious safety signal and in my view, continuation of approval represents an abrogation of our duty of care in relation to medication safety and regulatory approval.
Dr Melissa McCann, 20 Mar 2022
I raised again the reports of cardiac events and the risks potentially related to the genetic sequences of the vaccines, including risk due to impacts of microRNA sequences and potential Oncomir’s, which are small RNA sequences that cause cancer, and for which the TGA acknowledged in a freedom of information response that they had not evaluated. (18) (19)
I raised the unknown metabolism of the lipid nanoparticle adjuvants, and these metabolic animal studies were stopped at just four hours in animals, and at that time, almost none of the lipids had been metabolised from the liver at all—how long these products stay in the body or their metabolic pathway is entirely unknown! (20) (21) (22) (23)
These are highly inflammatory and cross the blood brain barrier and into the neuro tissues, into the spinal cord, into the ovaries and the testes, and of course, genotoxicity and carcinogenic studies had not been performed with dubious justification for this oversight, in my opinion, which also deserves another talk all to itself. (24) (25)
Finally, I raised the concerns of safety and pregnancy, and with an assessment obtained by freedom of information, (26) first suggesting a Category B2 for the Pfizer product, noting the abnormalities in the animal reproductive study of supernumerary, lumbar ribs in foetuses from COMIRNATY-treated female rats, which then, without explanation, was revised to remove this sentence and to change to a category B1 in the publicly available product information, (27) (28) and the preclinical studies also demonstrate a number of other foetal anomalies and a doubling of the risk of miscarriages in these animal studies, and this reflected what I was seeing in my patients.(29) (30) (31) (32) (33)
Unsatisfied with the responses of coincident adverse events and deaths following vaccination, I undertook a freedom of information requests process with the TGA, and following an unexpectedly arduous consultation process, I received 10 documents containing the TGA causality assessments. Amongst them:
- a 21-year-old female who died from myocarditis and cardiac arrest with the assessment outcome awaiting, which has since been determined, causal by VC, and now appears on the TGA safety report
- this beautiful young lady named Natalie died after a long and traumatic ICU battle with weeks on ECMO after developing vaccine-induced myocarditis. She was in her final year of law school and just two weeks after her 21st birthday when she died. Today would have been Natalie’s 23rd birthday, and instead her mother and brother are spending her birthday today grieving her life lost too soon. (34)
- I also received the case report of a 14-year-old female who died and the assessment decision—unlikely causality
- A 21-year-old male who died and the assessment outcome decision was—question mark ? causality
- A 24-year-old female who died of cardiac arrest where the assessment decision was—causality
- A 9-year-old child who died of cardiac arrest and the assessment outcome decision was— causality
- A 7-year-old boy who died of cardiac arrest and the causality outcome decision was—causality
And just to be completely clear, I requested these documents under freedom of information because I wanted clarity on the TGA assessment of the reports of deaths. I was confused that the safety report say 900 plus cases of death but only 14 confirmed causal. (35) (36)
|22 July 2022|
|TGA Case Assessment summaries in relation to specific case numbers on the Database of Adverse Event Notifications (DAEN), and data on the numbers of adverse events reported to Pfizer.|
FOI 3727 document 1 (pdf,155kb)
FOI 3727 document 2 (pdf,181kb)
FOI 3727 document 3 (pdf,97kb)
FOI 3727 document 4 (pdf,92kb)
FOI 3727 document 5 (pdf,130kb)
FOI 3727 document 6 (pdf,129kb)
FOI 3727 document 7 (pdf,317kb)
FOI 3727 document 8 (pdf,97kb)
FOI 3727 document 9 (pdf,136kb)
FOI 3727 document 10 (pdf,133kb)
FOI 3727 document 11 (pdf,890kb)
When I discussed this with other medical colleagues, they all draw the conclusion that all the other deaths have been reviewed and are not causal. But the language is misleading. The TGA implies this but does not explicitly state this. So I was requesting the actual TGA assessments of these reports of death, and these documents are factal adverse events, team meetings. The names are redacted but there are multiple people present at these meetings, and the opinion of this TGA team in some of these cases, including in young children, was causal. (37)
Or in other words, the vaccine is the likely cause of death, and when I asked the TGA freedom of information team why these documents were not published to the public disclosure log, I was advised the decision maker determined that disclosure of the documents could undermine public confidence, and reduce the willingness of the public to report adverse events to the TGA.
This is outrageous.
Doctors and the public have relied on the fact that out of millions of vaccines—only 14 deaths—and this appears to be completely misleading and deliberately non-transparent to the public.
Before the vaccine roll out, there were also reported deaths in the elderly in Norway, and the media release by the TGA in January of 21 announced that an investigation into these deaths was underway. (38) (39)
Three weeks later, the investigation was complete, and there was no causal link between vaccination and the deaths in the elderly. (40)
I recently obtained under freedom of information the correspondences related to that investigation:
These report the Norway regulator stating that adverse reactions from the vaccine, such as nausea and diarrhoea, had caused a turn for the worse as the people were already so fragile and that one in 1,000 people had died, (41) (42) and John Skerritt wrote that for the 30 fatal cases, a uniform picture, nausea, vomiting, diarrhoea leading to acute kidney injury in frail patients. (43) (44)
See: Part II
|01||Govt Policy Gag Order https://pennybutler.com/govt-policy-gagorder/|
|02||Senator Gerard Rennick Help Me Stop The Mandates And Help Those That Have Been Negatively Impacted By Them https://gerardrennick.com.au/mandates-reporting/|
|03||Letter addressed to Health Minister Greg Hunt and Adj. Professor John Skerritt, 18 November 2021; Letter addressed to Adj. Professor John Skerritt, TGA, 20 November 2021;|
|04||Clothier HJ, Lawrie J, Russell MA, Kelly H, Buttery JP. Early signal detection of adverse events following influenza vaccination using proportional reporting ratio, Victoria, Australia. PLoS One. 2019 Nov 1;14(11):e0224702. doi: 10.1371/journal.pone.0224702. PMID: 31675362; PMCID: PMC6824574. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0224702 (See Fig 6. Timeline of 2010 influenza vaccine and fever AEFI signal detection.)|
|05||Gold MS, Effler P, Kelly H, Richmond PC, Buttery JP. Febrile convulsions after 2010 seasonal trivalent influenza vaccine: implications for vaccine safety surveillance in Australia. Med J Aust. 2010 Nov 1;193(9):492-3. doi: 10.5694/j.1326-5377.2010.tb04029.x. Erratum in: Med J Aust. 2010 Nov 15;193(10):617. PMID: 21034379. https://pubmed.ncbi.nlm.nih.gov/21034379/|
|06||9 January 2023 FOI 4029 COVID Pharmacovigilance activities including ACV and VSIG minutes. https://www.tga.gov.au/foi-disclosure-log|
|07||TGA Advisory Committee on Vaccines Minutes Meeting 25, held 29 September 2021 COMMITTEE IN CONFIDENCE TRIM Reference no. D21-3141615 https://www.tga.gov.au/sites/default/files/2023-01/foi-4029-03.PDF|
|08||TGA 29 November 2022 FOI 4032 Proportionality Reporting Ratio analyses for the COVID-19 vaccines to 22 October 2022 https://www.tga.gov.au/foi-disclosure-log|
|09||Senator Gerard Rennick – FOI shows injury rate significantly higher than other vaccines 12 December 2022 https://gerardrennick.com.au/foi-shows-injury-rate-significantly-higher-than-other-vaccines|
|10||WHO Handbook 2019 Edition – Causality assessment of an adverse event following immunization (AEFI): user manual for the revised WHO classification, 2nd ed., 2019 updated 16 April 2021 | Manual (see page 22) https://www.who.int/publications/i/item/9789241516990|
|11||WHO Handbook 2018 Edition – CAUSALITY ASSESSMENT OF AN ADVERSE EVENT FOLLOWING IMMUNIZATION (AEFI) https://apps.who.int/iris/handle/10665/259959 | PDF (See Page 26) https://apps.who.int/iris/bitstream/handle/10665/259959/9789241513654-eng.pdf|
|12||Puliyel J, Naik P. Revised World Health Organization (WHO)’s causality assessment of adverse events following immunization-a critique. F1000Res. 2018 Feb 28;7:243. doi: 10.12688/f1000research.13694.2. PMID: 30026925; PMCID: PMC6039921. https://pubmed.ncbi.nlm.nih.gov/30026925/|
|13||WHO Handbook 2013 Edition Tozzi AE, Asturias EJ, Balakrishnan MR, Halsey NA, Law B, Zuber PL. Assessment of causality of individual adverse events following immunization (AEFI): a WHO tool for global use. Vaccine. 2013 Oct 17;31(44):5041-6. doi: 10.1016/j.vaccine.2013.08.087. Epub 2013 Sep 8. PMID: 24021304. https://pubmed.ncbi.nlm.nih.gov/24021304/|
|14||Australia records highest excess death rates since WWII https://pennybutler.com/australia-records-highest-excess-deaths-since-wwii/|
|15||Died Suddenly Posts https://pennybutler.com/died-suddenly/|
|16||18% excess mortality in Australia is a disaster but media is silent https://pennybutler.com/dowd-excess-mortality-australia/|
|17||Letter 20 March 2022 addressed to Minister Hunt with copy to Adj. Prof Skerrit, Dr Cook TGA medical advisor, Prof Cheng of ATAGI and the members of the TGA Advisory Committee on vaccines; Letter addressed to Health Minister Mark Butler, Adj. Professor John Skerritt, Dr Robyn Langdon of the TGA, and Prof Cheng of ATAGI, 26 August 2022. https://news.rebekahbarnett.com.au/p/breaking-australias-drug-regulator#footnote-2-102751449|
|18||TGA FOI 3604 FREEDOM OF INFORMATION REQUEST FOI 3604 Highlighted (with the original FOI request from the COVID Medial Network attached) https://www.covidmedicalnetwork.com/open-letters/AnnexJ%20D22-5167274%20%20FOI%203604%20-%20s24A%20Decision%20Letter_Redacted.pdf|
|19||Australian Medical Network – Open Letter To Atagi & TGA https://pennybutler.com/open-letter-atagi-tga/|
|20||What Your Doctor Won’t Tell You About The Pfizer Docs https://pennybutler.com/pfizer-data-dump-summary/ “The materials in the Pfizer vaccine, including lipid nanoparticles and polyethylene glycol, are designed to distribute throughout the body and can accumulate in organs such as the brain, liver, adrenals, spleen, and ovaries. The lipid nanoparticles in the Pfizer vaccine can cross every membrane in the human body. Pfizer knew about the potential bio-distribution of these materials. Dr. Robert Chandler, a Ret. Orthopaedic Surgeon, has shown that these materials accumulate in organs over time. There is concern about the potential long-term effects, especially for women, as there is no known mechanism for the body to release the lipid nanoparticles from the ovaries.”|
|21||200+ Aussie Doctors Request Health Reform (AMPS Summit 2022) https://pennybutler.com/amps-summit-2022/ “The approval pathway was granted not through their mode of action – gene therapy – but through their title – that of vaccines. These products lacked data on: safety, full pharmacokinetics, biodistribution, genotoxicity, reproductive toxicity, and carcinogenicity.”|
|22||Double-Jabbed TV Doctor Is Waking Up [Cardiologist, Dr. Aseem Malhotra] https://pennybutler.com/draseemmalhotra/ “In response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), several new pharmaceutical agents have been administered to billions of people worldwide, including the young and healthy at little risk from the virus. Considerable leeway has been afforded in terms of the pre-clinical and clinical testing of these agents, despite an entirely novel mechanism of action and concerning biodistribution characteristics.”|
|23||Finally, An Australian Paper On COVID Vaccines… https://pennybutler.com/covid-vaccines-australian-review/ “Pfizer’s documents show lipid nanoparticles with their mRNA cargo being distributed throughout the entire body and passing through the blood brain, placental and foetal blood brain barriers and concentrate in the ovaries.”|
|24||TGA FOI 2389 [Video & Doc] https://pennybutler.com/tga-foi-2389/|
|25||TGA FOI 2389 – Safety Studies Skipped https://pennybutler.com/tga-foi-2389-part3/ “Safety testing skipped on toxicity, genotoxicity, carcinogenicity (cancer-causing), immunotoxicology, juvenile paediatric, novel excipients, vaccine-induced autoimmune disease”|
|26||TGA FOI 2389 Delegate’s Overview and Request for ACV’s Advice Active ingredient (s): BNT162b2 [mRNA] Proprietary Product Name: COMIRNATY COVID 19 vaccine Sponsor: Pfizer Australia Pty Ltd https://www.tga.gov.au/sites/default/files/foi-2389-01.pdf (Page 27)|
|27||AusPAR: BNT162b2 (mRNA) Australian Public Assessment Report https://www.tga.gov.au/resources/auspar/auspar-bnt162b2-mrna|
|28||Australian Public Assessment Report for BNT162b2 (mRNA) Proprietary Product Name: Comirnaty Sponsor: Pfizer Australia Pty Ltd https://www.tga.gov.au/sites/default/files/auspar-bnt162b2-mrna-210722.pdf “Pregnancy Category B1 — page 7“|
|29||TGA FOI 2389 – Spike Protein In Any Cell In The Body https://pennybutler.com/tga-foi-2389-part2/|
|30||10 Posts tagged “TGA FOI 2389” https://pennybutler.com/tag/tga-foi-2389/|
|31||Australian Medical Network – Open Letter To Atagi & TGA https://pennybutler.com/open-letter-atagi-tga/ “Fully-referenced grave concerns for vaccines in Australia from Covid Medical Network and Australian pathologists. Despite clear evidence from government-compiled data that the cure is worse than the disease, government officials continue the Safe & Effective Narrative.”|
|32||200+ Aussie Doctors Request Health Reform (AMPS Summit 2022) https://pennybutler.com/amps-summit-2022/ “The approval pathway was granted not through their mode of action – gene therapy – but through their title – that of vaccines. These products lacked data on: safety, full pharmacokinetics, biodistribution, genotoxicity, reproductive toxicity, and carcinogenicity.” “In the biodistribution study that Pfizer wanted to keep hidden, the lipid nanoparticles accumulated in the ovaries. The true impact on female fertility is yet to be elucidated. The effect on women’s periods is only now being studied. The fertility studies were done on lab-rats, and the baby rats were only followed up until lactation (not a long-term follow-up).”|
|33||Australian Jab Update – Miscarriages & Serious Injuries https://pennybutler.com/tga-foi-3727-miscarriages/ | Download PDF: TGA FOI # 3727 (170 Pages | Pfizer) https://www.tga.gov.au/sites/default/files/foi-3727-01.pdf?fs=e&s=cl|
|34||‘We were all forced’: Mum of ‘healthy’ 21-year-old who died after Moderna blames vaccine mandates https://www.news.com.au/lifestyle/health/health-problems/we-were-all-forced-mum-of-healthy-21yearold-who-died-after-moderna-blames-vaccine-mandates/news-story/63d221adaa84ccdfc5acc7d6c33f16f3 “The mum of a “fit and healthy” 21-year-old from Melbourne who died after taking the Moderna vaccine has blasted authorities for mandating Covid injections.”|
|35||TGA FOI 3727 “TGA Case Assessment summaries in relation to specific case numbers on the Database of Adverse Event Notifications (DAEN), and data on the numbers of adverse events reported to Pfizer.” https://www.tga.gov.au/foi-disclosure-log|
|36||Where’s the TGA’s transparency? Russell Broadbent MP https://youtu.be/xD1ZV4xBl-o “Last year a Queensland GP obtained documents from the TGA under the FOI Act, No. FOI 3727. These documents contained nine assessments conducted by the TGA following reports of someone dying from the COVID-19 vaccine. The deceased people listed on these reports were aged seven, nine, 14, 19, 21, 21, 24, 46 and 44.”|
|37||Dissecting the DAEN TGA Database of Adverse Events in Children 5-11 https://followingthescience.substack.com/p/dissecting-the-daen-tga-database|
|38||Norwegian investigation of COVID-19 vaccination risks for elderly, very frail patients In recent days the TGA has received reports of about 30 deaths in over 40,000 elderly individuals in Norway vaccinated with the Pfizer BioNTech vaccine Published 17 January 2021 https://www.tga.gov.au/news/media-releases/norwegian-investigation-covid-19-vaccination-risks-elderly-very-frail-patients|
|39||Wyller TB, Kittang BR, Ranhoff AH, Harg P, Myrstad M. Nursing home deaths after COVID-19 vaccination. Tidsskr Nor Laegeforen. 2021 May 19;141. English, Norwegian. doi: 10.4045/tidsskr.21.0383. PMID: 34018389. https://pubmed.ncbi.nlm.nih.gov/34018389/|
|40||Investigation reveals no specific risk of COVID-19 vaccinations in elderly patients The TGA has concluded that there is no specific risk of vaccination with the Pfizer-BioNTech COVID-19 vaccine in elderly patients. Published 2 February 2021 https://www.tga.gov.au/news/media-releases/investigation-reveals-no-specific-risk-covid-19-vaccinations-elderly-patients|
|41||TGA FOI 4073 – Madsen: “Only 1/1000” – (Madsen = Medical director of the Norwegian Medicines Agency: Dr Steinar Madsen) https://www.tga.gov.au/sites/default/files/2023-01/foi-4073-03.pdf|
|42||Torjesen I. Covid-19: Norway investigates 23 deaths in frail elderly patients after vaccination. BMJ. 2021 Jan 15;372:n149. doi: 10.1136/bmj.n149. PMID: 33451975. https://www.bmj.com/content/372/bmj.n149|
|43||TGA FOI 4073 Email from Prof John Skerritt regarding the review of 13 cases https://www.tga.gov.au/sites/default/files/2023-01/foi-4073-08.pdf “review of 13 cases triggered the Press Release (currently in NO there are over 30 reports of fatal cases; under review); uniform picture – nausea, vomiting, diarrhoea leading to acute kidney injury in frail patients; some additional details in the attached below; PR aimed to flag to HCP to carefully consider B/R of vaccination in frail patient; no updated communication expected at this stage”|
|44||EMA report on the same issue: EMA – 28 Jan 2021 – COMIRNATY — BioNTech Manufacturing GmbH https://www.ema.europa.eu/en/documents/covid-19-vaccine-safety-update/covid-19-vaccine-safety-update-comirnaty-28-january-2021_en.pdf “The latest safety data for this vaccine are in line with the known side effect profile, and the related reviews are presented in this update. Reports of suspected severe allergic reaction have not identified new aspects regarding the nature of this known side effect. No specific safety concern has been identified for vaccine use in frail elderly individuals. Review of reports of suspected side effects with fatal outcome, specifically in frail elderly individuals. On 28 January 2021, PRAC concluded that the safety data reviewed for Comirnaty are in line with the vaccine’s known benefit-risk profile. Given concerns which arose from Norway about deaths reported in frail elderly individuals after vaccination with Comirnaty, PRAC reviewed the current reports of suspected side effects with fatal outcome in individuals of any age. This review did not suggest a safety concern. In many cases concerning individuals above 65 years of age, progression of (multiple) pre-existing diseases seemed to be a plausible explanation for death. In some individuals, palliative care had already been initiated (WTF??? WHY!!!!???) before vaccination. PRAC concluded that based on the current data there was no need to amend the product information regarding how Comirnaty should be used, including in frail elderly individuals. “ Fucking murderers.|