[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"doc-detail-45616-en":3,"doc-seo-45616-105":30,"detail-sidebar-cat-0-en-105":91},{"code":4,"msg":5,"data":6},0,"success",{"doc_id":7,"user_id":8,"nickname":9,"user_avatar":10,"doc_module":4,"category_id":11,"category_name":12,"doc_title":13,"doc_description":14,"doc_content":15,"file_id":16,"file_url":17,"file_type":18,"file_size":19,"view_count":20,"is_deleted":4,"is_public":21,"is_downloadable":21,"audit_status":21,"page_count":22,"language":23,"language_code":24,"site_id":25,"html_lang":24,"table_of_contents":26,"faqs":27,"seo_title":13,"seo_description":14,"update_tm":28,"read_time":29},45616,4810365810221,"Aurora","https://ap-avatar.wpscdn.com/davatar_155a257f0dc6eb9ab79c44ca47cae57d",7,"Healthcare","Covid Medical Network Letter to ATAGI","A formal letter from the Covid Medical Network and co-signatories to ATAGI and related Australian health officials follows up on prior correspondence and FOIA requests regarding gene-based Covid-19 vaccines. The letter alleges limited scope of safety and efficacy data, late and heavily redacted FOIA responses, and unanswered questions about reproductive toxicology and molecular genetics. It cites peer-reviewed in vitro concerns, adverse event reporting, adverse event database analysis, mortality correlations, and additional clinician and researcher reports, urging immediate withdrawal of claims of safety.","8 March 2022  \nAssociate Professor Nigel Crawford  \nChair, Australian Therapeutics Advisory Group on Immunisation (ATAGI)  \nOther voting members ofATAGI:  \nProfessor Michelle Giles  \nProfessor Allen Cheng  \nMs Karen Bellamy  \nProfessor Katie Flanagan  \nDr Katherine Gibney  \nDr Penelope Burns  \nProfessor Cheryl Jones  \nAdjunct Professor Tony Korman  \nAssociate Professor Bette Liu  \nDr Nicholas Silberstein  \nDr James Wood  \nMs Diane Walsh  \nProfessor Tom Snelling  \nMs Kristy Cooper  \nDr Brendan Murphy  \nSecretary, Department of Health  \nProfessor Paul Kelly  \nChief Medical Officer, Department of Health  \nProfessor John Skerritt  \nDeputy Secretary, Health Products Regulatory Group (Therapeutics Goods Administration, TGA)  \nTGA’s Advisory Committee on Vaccines (ACV)  \nProfessor Allen Cheng, Chair  \nProfessor Jim Buttery  \nDr Jeanine Bygott  \nMs Madeline Hall  \nProfessor Kristine Macartney  \nDr Ines Rio  \nDr Vicky Sheppeard  \nAssociate Professor Adrienne Torda  \nProfessor Joseph Torresi  \nMs Diane Walsh  \nThe Honorable Greg Hunt  \nMinister for Health & Aged Care  \nDear A/Prof Crawford, Dr Murphy, Prof Kelly, Prof Skerritt, Hon Minister Hunt, members of ATAGI and ACV,  \nWe, the Covid Medical Network and co-signatories, are writing to you to follow up on prior correspondence to ATAGI, the TGA and the Health Minister, and FOIA requests to the TGA, where answers have either been not forthcoming or have indicated the TGA has lacked  \ncritical information for making its provisional approval of the gene-based vaccines, namely  \nPfizer’s BNT162b2 & Comirnaty, AstraZeneca’s ChAdOx1-S and Moderna’s Spikevax/mRNA-1273.  \nThis letter pertains to:  \n1. Correspondence you and the TGA received that the Pfizer (and AstraZeneca and Moderna) data via the companies themselves or via the FDA was likely too limited in scope to make a proper determination of safety and efficacy.  \n2. FOIA requests to the TGA with respect to reproductive toxicology issues that have been responded to late and with heavily redacted documents.  \n3. FOIA request with respect to micro-RNA sequences and related molecular genetic issues as to whether the TGA had assessed these.  \n4. Peer-reviewed published in vitro research that gene-based vaccine generated spike proteins can migrate into human cell nuclei to disrupt DNA repair mechanisms, and vaccine-derived RNA can be reverse transcribed with evidence pointing to possible integration of this sequence into human genome.  \n5. That a release of some Pfizer data from a FOIA request to the FDA in the US indicated high adverse events reporting by 28 February 2021.  \n6. Analysis ofthe TGA’s own Database of Adverse Events Notifications (DAEN) data and what Australian clinicians are increasingly witnessing as a high rate of injuries from these gene-based vaccines.  \n7. Extrapolating from German insurance company actuarial data, backed up by multiple US insurance company actuarial data, Australia’s DAEN Covid-19 adverse event data is likely to be under-reported by 9-fold. To date, 2,422, and possibly as high as 6,501 Australians dying as results of the Covid-19 gene-based vaccines is a justifiable calculation.  \n8. All-cause mortality data from official UK, EU and US databases indicate a positive correlation with the Covid-19 gene-based vaccine rollouts during 2021.  \n9. US military doctors have provided data from the US military electronic medical records database (DMED) showing an almost 10-fold increase in registered diagnosis episodes since gene-based vaccines were given to personnel.  \n10. German pathologists described pathological aggregates of spike proteins and  \nlymphocyte infiltrations in inflamed organs in autopsies related to deaths postvaccination. Has the TGA provided guidance and resources for autopsies of postvaccine deaths of Australians?  \n11. Reports of inadequacies, irregularities and possible fraudulent practices in the Pfizer vaccine trial provided by whistleblowers to the BMJ.  \n12. The correspondence you receive","cbCaivheA3yFvavs","https://ap.wps.com/l/cbCaivheA3yFvavs","pdf",2466901,2,1,52,"English","en",105,"# Follow-up context\n# Specific issues raised\n## Data limitations and FOIA delays\n## Molecular and reproductive toxicology questions\n## Safety signal evidence cited\n# Requests and urgency","[{\"question\":\"What is the purpose of the letter to ATAGI and associated health officials?\",\"answer\":\"The letter is written to follow up on earlier correspondence and FOIA requests, and to raise concerns about safety and efficacy determinations for gene-based Covid-19 vaccines.\"},{\"question\":\"What does the letter claim about FOIA responses from the TGA?\",\"answer\":\"It alleges responses were late and heavily redacted, and that critical information required for provisional approval was missing, including details relevant to reproductive toxicology and molecular genetic questions.\"},{\"question\":\"What actions does the letter request regarding gene-based vaccine safety statements and use?\",\"answer\":\"It calls for immediate withdrawal of any statements claiming these vaccines are “safe,” and argues that normal decision-making would require halting gene-based vaccines to the 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is the purpose of the letter to ATAGI and associated health officials?","Question",{"text":75,"@type":76},"The letter is written to follow up on earlier correspondence and FOIA requests, and to raise concerns about safety and efficacy determinations for gene-based Covid-19 vaccines.","Answer",{"name":78,"@type":73,"acceptedAnswer":79},"What does the letter claim about FOIA responses from the TGA?",{"text":80,"@type":76},"It alleges responses were late and heavily redacted, and that critical information required for provisional approval was missing, including details relevant to reproductive toxicology and molecular genetic questions.",{"name":82,"@type":73,"acceptedAnswer":83},"What actions does the letter request regarding gene-based vaccine safety statements and use?",{"text":84,"@type":76},"It calls for immediate withdrawal of any statements claiming these vaccines are “safe,” and argues that normal decision-making would require halting gene-based vaccines to the 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