MEDSAFE COMITTED MEDICAL FRAUD WHEN THEY KNOWINGLY AND INTENTIONALLY MISREPRESENTED A BIOSYNTHETIC PATHOGEN AS A VACCINE, THESE BIOLOGICAL, CHEMICAL, TOXINS AND POISONS ARE DANGEROUS. IT IS A VIOLATION OF BIOLOGICAL WEAPONS, CHEMICAL WEAPONS AND BIOTERRORISM LAWS.
It is well-established through the FDA, Pfizer and BioNTech clinical trials, for the ‘COVID-19 vaccines’ (hereafter referred to as ‘COVID-19 nanoparticle injections’ or ‘mRNA nanoparticle injections’ or ‘COVID-19 injections’) were not designed to clinically and statistically demonstrate that the COVID-19 nanoparticle injections prevent infection, prevent transmission, or protect against SARS-CoV-2 or the disease known as COVID19, or hospitalizations, and death. This crime of MEDICAL FRUAD, giving false information and hoaxes will apply to the Sections herein on bioweapons, fraud, domestic terrorism and murder. MEDSAFE HAVE BEEN involve acts dangerous to human life that are a violation of the criminal laws of NEW ZEALAND.
When MEDSAFE provided provisional consent, it involved an act dangerous to human life. There must be accountability. In the January 2021, MEDSAFE New Medicine Application Evaluation Report – Quality there should never have been any Provisional Consent for Pfizer's Poison. Some of the information within MEDSAFE New Medicine Application Evaluation Report – Quality was withheld under the following sections of the Act: • section 6(b)(ii) as its release would prejudice information entrusted to the Government of New Zealand on a basis of confidence by any international organisation; and • section 9(2)(b)(ii). I will go through some of the information MEDSAFE should have known prior to January 2021.
WHEREAS since 2002 experimental mRNA, researchers have been trying to develop a corona virus vaccine since acute respiratory syndrome (SARS-1) outbreak in 2002. mRNA had never been licensed for use in humans. (The Truth About Covid-19, Joseph Mercola, Ronnie Cummins, Chelsea Green Publishing, 2021, p. 129) “To expect these experimental fast-tracked coronavirus vaccines to succeed when others that have been tested over far longer periods of time have failed miserably is pure folly.”
WHEREAS on BioNTech’s own 2019 annual report filing to the SEC describes the company as follows: "We are a clinical-stage biopharmaceutical company with NO pharmaceutical products approved for commercial sale. We have incurred significant losses since our inception and we anticipate that we will continue to incur significant losses for the foreseeable future, which makes it difficult to assess our future viability. We have incurred net losses in each year since our inception in 2008, including net losses of €179.2 million and €48.3 million for the years ended December 31, 2019 and December 31, 2018, respectively. As of December 31, 2019, we had accumulated losses of €424.8 million (€245.8 million as of December 31, 2018)." BioNTech is responsible for manufacturing all the mRNA for the New Zealand supply of the Pfizer vaccine.
WHEREAS between January and August 2019 Operation Crimson Contagion, a joint exercise conducted by the Department of Health and Human Services unfolded, led by Robert Kadlec and involving numerous national, state, local government and public and private organizations testing response to a simulated severe pandemic of influenza originating in China.
WHEREAS October 18, 2019, John Hopkins Center for Public Safety (Bloomberg) in collaboration with Bill and Melinda Gates Foundation and the World Economic Forum (Schwab) conducted Event 201, a 3.5-hour table-top pandemic war game simulation featuring an immune resistant novel respiratory corona virus with devastating impact and rapid spread countered by blitzkrieg roll-out of vaccines but with a total exclusion of treatments with already licensed repurposed medicines. The Event included the director general of Chinese CDC.
WHEREAS November 2019 concern grew in China over the outbreak of a new disease. News reports around the world said the novel Covid-19 virus came from human exposure to a bat supposedly in a wet market in Wuhan, China. In a short time, the disease was elevated to a world-wide pandemic status, although then and to this day the “virus” has not been isolated and purified for proper identification purposes.
WHEREAS on December 17th 2019, the EU’s European Investment Bank, under the direction of former German foreign office official Werner Hoyer, provided BioNTech €50 million in debt financing for manufacturing mRNA.
WHEREAS on 12 January 2020, China shared the genetic sequence of the novel coronavirus for countries to use in developing specific diagnostic kits, according to the WHO Novel Coronavirus (2019-nCoV) SITUATION REPORT - 1 21 JANUARY 2020.
WHEREAS on January 14th 2020, BioNTech began animal testing the COVID19 vaccine. BIOTECH SAFETY STUDY 14TH Jan 2020 till 23 Jan 2020. They injected the (b) (4) “state-of-the-art technology within a U.S. weapon system” (Redaction Codes | National Archives) into the mice they became sick and then they euthanized them on day nine.
WHEREAS in mid-January 2020 the first PCR test confirmed cases of COVID-19 around the World. The PCR tests are not accurate in diagnosing live virus but nonetheless were used to deceptively inflate the numbers of people sick with COVID-19. The inventor of the PCR, Kary Mullis, a Nobel Prize Winner was a staunch opponent of Anthony Fauci and his misuse of the PCR test during the HIV/Aids outbreak and the administration of toxic AZT. He said that the PCR test should not be used in the manner in which Fauci was using it. Mullis died shortly before the Wuhan outbreak. https://rumble.com/vhu4rz-kary-mullis-inventor-of-the-pcr-test.html
WHEREAS on 23rd January 2020 Journalist Stafan Stanford discusses the evidence for it being a Bioweapon based on patents for it and funding receipts for gain of function research at Wuhan Lab.
WHEREAS on 30th of January 2020, In the “Uncanny similarity of unique inserts in the 2019-nCov spike protein to HIV-1 gp 120 and Gag” nine Scientists, find that the 2019-nCov spike protein causes the HIV virus. The Scientists claim that “All the insertions got aligned with Human Immunodeficiency Virus-1 (HIV-1).”
WHEREAS on 14 February 2021, at 11:59 pm, Auckland moved up to alert level 3 and the rest of New Zealand to level 2 after new community cases were detected in Auckland during level 1.
WHEREAS February 19, 2020 article in Science, authored by the inventors of coronavirus S-2P spike proteins, Barney Graham and Jason McClellan, the authors state that the S-2P ‘spike protein’ has stronger binding affinity to the ACE-2 receptors (in the hearts, lungs, kidneys, and endothelial cell line of blood vessels) than the original SARS-CoV-2 (S) spike protein. Graham and McLellan also tested synthetically recreated antibodies for coronaviruses (SARS-CoV-2) against the S-2P spike proteins. Their research showed that none of the antibodies for coronaviruses bound to the new trimeric two-proline spike (S-2P) proteinsandno coronavirus antibodies were able to neutralize it. This scientific evidence (authored by the inventors of the spike proteins) confirms that the COVID-19 mRNA vaccines; DO NOT produce antibodies to SARS-CoV-2, and are resistant to the antibodies for SARS-CoV-2, and therefore - It is scientifically and clinically IMPOSSIBLE for Pfizer’s FDA-approved mRNA vaccines TO PROVIDE ANY PROTECTION AGAINST SARS-CoV-2 infection, or any coronavirus, including ‘VARIANTS’. The Inventors of the S-2P ‘spike protein’ say that “currently, there are no effective prophylactic or therapeutic measures” to prevent SARS-CoV-2 infection.They say that their technology has been used for HKU1-CoV, SARS-CoV and MERS-CoV. The Inventors is technology is applicable for delivery via other platforms, such as mRNA. The Inventors say that “the stabilised perfusion coronavirus spike protein can be used as a vaccine antigen to elicit robust neutralising antibody responses.” Antigens are chemical and biological toxics and poisons foreign to the body like cancer cells, parasites, viruses, fungi, and bacteria. The immune system identifies and attacks "non-self" external antigens. The Inventors say that their S-2P ‘spike protein’ elicit robust neutralising antibody responses this means that it makes antibodies made in the white blood cell ineffective; it counteract; destroys, kills, or nullify them, so they are unable to identify and neutralize foreign objects such as pathogenic bacteria and viruses.
WHEREAS on March 16, 2020 NIAID announced beginning a clinical trial of new investigational vaccine at the Kaiser Permanente Washington Research Institute (KPWHRI) Seattle, Moderna Inc. mRNA -1273 supported by CEPI (The Courage to Face Covid-19, Peter McCullough and John Leake, p.30) implementing CEPI plan, five days after the pandemic declaration.
WHEREAS April 2020 Li-Meng Yan, an experienced Chinese virologist at the Hong Kong School of Public Health escaped to the United States. She claimed that the virus is not actually from nature but a man-made virus created in a lab. She claimed Wuhan Institute possess the world’s largest collection of corona viruses and that there is a link to the Chinese military.
WHEREAS on 17 June 2020, the European Commission presented the EU Vaccines Strategy to accelerate the development, manufacturing and deployment of vaccines against COVID-19.
WHEREAS June and July 2020, in Pfizer’s short 6 week study, TWO RATS DIED after being injected with the Bioweapon. We know that it is a Bioweapon because of (b) (4 and (b) (6). (b) (4) means “Reveal information that would impair the application of state-of-the-art technology within a U.S. weapon system” and (b) (6) means “Reveal information, including foreign government information, that would cause serious harm to relations between the United States and a foreign government, or to ongoing diplomatic activities of the United States.” Redaction Codes | National Archives Of particular concern is the increased fibrinogen concentration among the rats; fibrinogen is made in your liver and helps your blood clot. Increased fibrinogen is associated with blood clotting, heart disease, blood vessel dysfunction, and stroke. REPEAT-DOSE TOXICITY STUDY OF THREE LNP-FORMULATED RNA PLATFORMS ENCODING FOR VIRAL PROTEINS BY REPEATED INTRAMUSCULAR ADMINISTRATION TO WISTAR HAN RATS (Final Report dated 01 July 2020) 125742_S1_M4_4.2.3.2-38166.pdf (icandecide.org).
WHEREAS on 7th of August 2020 according to Nick Allan the Director General in the Ministry of Health New Zealand. “The Ministry does not hold records that describes the isolation of the SARS-COV-2 virus.” There is no scientific evidence or records that describe the isolation/purification of the alleged “COVID-19 virus” from any unadulterated sample taken from a diseased patient. Without this step having been performed and followed by characterization, sequencing and controlled experiments, all claims of this alleged “virus” is nothing, but wild speculation backed only by fraudulent science, fraudulent tests and fraud-based diagnoses.
WHEREAS on 24 September 2020 the COVID-19 mRNA MEDSAFE Resubmission Meeting some of the information is being kept secret. It was released with some information withheld under the following sections of the Act: • section 9(2)(a) to protect the privacy of natural persons; • section 9(2)(b)(ii) where its release would likely unreasonably prejudice the commercial position of the person who supplied the information; and • section 9(2)(ba)(i) to protect information that is subject to an obligation of confidence and making it available would likely prejudice the supply of similar information, or information from the same source, and it is in the public interest that such information should continue to be supplied; or would be likely otherwise to damage the public interest. h202106950_-_response.pdf (health.govt.nz)
WHEREAS on 24 September 2020 MEDSAFE knew as per Resubmission Meeting the non-clinical safety package to support initiation of clinical testing for the BNT162b2 vaccine, that there was NO vaccine to protect against SARS-CoV-2 infections or the disease it causes COVID-19, NO genotoxicity studies were performed, NO carcinogenicity studies were performed, NO carcinogenicity studies were performed, NO dedicated immunotoxicity study was conducted, that specific fertility and embryofetal development studies are ongoing and that NO Quality Data is available (Ref 1). The Pfizer Injections are a NON-Complying Product. h202106950_-_response.pdf (health.govt.nz)
WHEREAS in September 2020 BioNTech, which is the mRNA specialist in the Pfizer-BioNTech alliance and is the actual owner and legal manufacturer of the vaccine, which had never previously brought any product to market. Arranged to purchase its main manufacturing facility in Marburg being conditional upon the COVID19 vaccine emergency authorization which it would only obtain in December 2020.
WHEREAS on October 21, 2020, it was known by MEDSAFE THAT the COVID-19 mRNA nanoparticle injections were NEVER proven to prevent infection, disease, hospitalization or death. As per the New Medicine Application it states that "There are currently no available vaccines to protect against SARS-CoV-2 infections or the disease it causes COVID-19" (Ref 1). h202106950_-_response.pdf (health.govt.nz)
WHEREAS on October 22, 2020, the FDA and ‘vaccine’ manufacturers (i.e. Pfizer) clinically established that the COVID-19 injections would cause an unprecedented incidence of disease, permanent disabilities, and death, when on October 22, 2020 (before the ‘COVID-19 vaccine rollout’) the FDA met with the manufacturers and reviewed this ‘working list’ of harmful clinical outcomes caused by the injections; nervous system disease (convulsions, seizures, Guillain-Barre syndrome myelitis encephalitis, encephalopathy, encephalomyelitis, narcolepsy, cataplexy, meningitis, meningoencephalitis acute demyelinating diseases), cardiac disease (acute myocardial infarction myocarditis, pericarditis, stroke), blood and circulatory disease (disseminated intravascular coagulation, thrombocytopenia, venous thromboembolism), musculoskeletal disease (arthritis, joint pain), reproductive and pregnancy disorders (adverse pregnancy outcomes, adverse birth outcomes), autoimmune disease (VAED, multisystem inflammatory syndrome), and death. https://www.fda.gov/media/143557/download?
WHEREAS on November 9, 2020 the New Zealand Department of the Prime Minister and Cabinet still did not have any scientific evidence or records that describe the isolation/purification of the alleged “COVID-19 virus” from any unadulterated sample taken from a diseased patient.
WHEREAS on November 11, 2020 the European Commission approved a fourth contract with pharmaceutical companies BioNTech and Pfizer, which provides for the initial purchase of 200 million doses on behalf of all EU Member States. In the Advance Purchase Agreement they are referred to as "product," "vials," and "doses" and making a vaccine is said to be aspirational.
WHEREAS on November 20, 2020, Pfizer stated in writing that the risk-benefit ratio of their COVID-19 mRNA nanoparticle injections were not favorable (unfavorable) for children 12 to 15 years of age, based on FDA submitted data from 100 injected children from their Phase 3 trial.
WHEREAS in 2020 and 2021 Dr. Luc Montagnier Medicine Nobel Prize 2008 winner and a French virologist who discovered the virus that causes AIDS, said “Presence of elements of HIV and germ of malaria in the gemone of coronavirus is highly suspect and the characteristics of the virus could not have arisen naturally.” After studying the constituents of the COVID19 vaccines he said "They will all die from antibody-dependent enhancement” “Everything is very simple. Variants come from vaccination ,” the Nobel laureate replied. “The virus has a very strong ability to change, like other RNA viruses. The flu virus is another such example .” “It’s confirmed ,” Montagnier said, stressing that SARS-CoV-2 is a “chimera” engineered virus. Although the starting point for its construction was a natural virus.” Montagnier stressed that mass vaccination against coronavirus is, “so to speak, a scientific error and medical negligence,” “This is an unforgivable historical mistake. One day we will summarize this ,” the scientist said. “Because it was vaccination that gave rise to the emergence of the SARS-CoV-2 mutations .”
WHEREAS on December 11, 2020, emergency use authorization meeting for the Pfizer COVID-19 mRNA vaccines, FDA committee members pointed out that the mRNA vaccines appear to provide no clinical benefit, specifically regarding severe disease. “Some committee members raised concerns about the small number of severe COVID-19 cases and limited conclusions about the prevention of severe disease based on the study endpoints. FDA pointed out that vaccine development has a long history and that FDA is not aware of an example of any vaccine that is effective against mild disease that is not also effective against severe disease and that even though limited, data for Pfizer-BioNTech COVID-19 Vaccine suggest efficacy against severe disease.” - FDA EUA Review Committee for Pfizer EUA COVID-19 mRNA vaccines, Dec 11, 2020 Emergency Use Authorization for Pfizer-BioNTech COVID-19 Vaccine Review Memo (fda.gov)
WHEREAS on December 11, 2020, per the data discussed during that same FDA meeting, not only do Pfizer’s COVID-19 mRNA vaccines NOT prevent severe disease, Pfizer’s mRNA vaccines cause SEVERE COVID-19 within 7 days of being injected. Page 41 of PFIZER’s EUA submission, states that there were 409 patients who had COVID-19 symptoms within 7 days of getting their first (1st) or second (2nd) PFIZER shot, BUT these patients did not have a positive PCR-test for SARS-CoV-2.
WHEREAS on December 11, 2020, Pfizer-BioNTech was first COVID-19 vaccine authorized under EUA.
WHEREAS on January 23, 2021, in a public statement at the Washington DC. Defeat the Mandates Rally Dr. Robert Malone said, "genetic vaccines don’t work and are not completely safe, vaccines do not protect against Omicron infection, viral replication or spread to others…vaccines are leaky, have poor durability can not achieve herd immunity and stop COVID. Not completely safe and their full risks are unknown.” This is the man responsible for the mRNA gene therapy patent which comprises the COVID vaccine. He said they don’t work.
WHEREAS January 2021 as per the New Medicine Application Evaluation Report MEDSAFE said that the BNT162b2 vaccine is a Higher-risk medicine - Vaccine. "This vaccine contains a new biological entity, so data protection period will apply for 5 years from the date of the gazette." "This new medicine application is for a new biological entity, hereafter referred to as BNT162b2[mRNA] (Pfizer code number PF-07302048) or by the trade name Comirnaty, which has been developed by Pfizer and BioNTech." h202106950_-_response.pdf (health.govt.nz)
WHEREAS January 2021 MEDSAFE knew that the engineered nanoparticle technologies in COVID-19 mRNA injections are gene-editing nanotechnologies as per the MEDSAFE New Medicine Application Evaluation Report the BNT162b2 vaccine they use cationic liposome technologies to alter human DNA through RNA transfection; as has been described in Pfizer’s biological license application (BLA). As in this document "MEDSAFE will seek expert advice from the Medicines Assessment Advisory Committee (MAAC) to determine what information is required prior to approval for distribution in New Zealand, and what can be accepted post-approval". h202106950_-_response.pdf (health.govt.nz)
WHEREAS in January 2021 MEDSAFE allowed a labelling exemption to Pfizer. There was NO packaging leaflet, the information on the vial label does not mention the drug substance name or strength. The absence of the statement of active substance has been allowed by MEDSAFE despite the labelling does NOT meet New Zealand Medicines Regulations 1984 for the labelling of medicines. The carton label does not state the name and strength/potency of the drug substance on either of the two panels, this represents an area of non-compliance with New Zealand Medicines Regulations. The dose form description on the carton label is ‘suspension for intramuscular injection’ and does not mention that the product is a vaccine concentrate. The label includes the statement ‘Rx only’, which is recognised in New Zealand as meaning the product is a Prescription Only medicine. h202106950_-_response.pdf (health.govt.nz)
WHEREAS in January 2021 MEDSAFE's document PFIZER'S Drug product manufacture, packaging and testing is kept secret. Section 9(2)(b)(ii) where its release would likely unreasonably prejudice the commercial position of the person who supplied the information. h202106950_-_response.pdf (health.govt.nz)
WHEREAS in January 2021 MEDSAFE's knew that the mRNA ‘spike proteins’ and ‘lipid’ nanoparticles cross the barrier membranes of the cardiovascular, respiratory, reproductive, and central nervous system (including the brain); causing inflammation that can result in disease, disability, and death, per peer-reviewed publications and research and development Pfizer documents. h202106950_-_response.pdf (health.govt.nz)
WHEREAS in January 2021 MEDSAFE's knew that the BNT16b2 drug product is NOT safe. h202106950_-_response.pdf (health.govt.nz)
WHEREAS in MEDSAFE's 2 February 2021 document it states, "New Zealand does not have an emergency use authorisation pathway and currently does not have the public health emergency situation." A new medicine application was submitted by Pfizer New Zealand Limited for Comirnaty (COVID-19 mRNA vaccine) (Pfizer-BioNTech) 0.5 mg/ml concentrate for injection (TT50 10853) under section 20 of the Medicines Act 1981. There are several aspects of the data required to support quality, safety and efficacy that are not available at the time of completion of the evaluation. It is also proposed that any provisional consent be granted for a period of nine months, before which time all additional data should be received. It is considered that the safety specification for this product is currently inadequate and does not accurately reflect the important known risks, important potential risks or missing information. The RMP should be updated to include the additional risks and state how the missing information will be addressed. The additional studies appear to generally address the information gaps, but the company should state specifically how they will provide information on the NZ concerns raised above and listed at the beginning. In addition the provision of the results of these studies and provision of safety updates should be made a condition of approval. h202106950_-_response.pdf (health.govt.nz)
WHEREAS on 20 February 2021, The NEW ZEALAND national roll-out of COVID-19 vaccines commenced with Pfizer-BioNTech (Comirnaty).
WHEREAS through to 28 February 2021, there were 42086 serious adverse reactions according to Pfizer's document. 5.3.6-postmarketing-experience.pdf (phmpt.org)
WHEREAS on June 10, 2021, the FDA Vaccine and Biological Products Advisory Committee (VRBPAC) stated in writing that it would not be infeasible (it would be impossible) to conduct a clinical trial that could clinically and statistically prove that any vaccine could prevent SARS-CoV-2 infection and/or COVID-19 disease in pediatric populations because teenagers, children, and infants rarely (if ever) become infected or present with symptoms.
WHEREAS by June 18, 2022 there were 696,605 nervous system disorders, 539,299 musculoskeletal and connective tissue disorders (92,942 pain in extremities), and 317,811 gastrointestinal disorders, 224,633 skin, hair and nail disorders, 190,720 respiratory and chest disorders, 178,353 female and male reproductive system disorders (erectile dysfunction, infertility, heavy menstrual bleeding), 167,382 victims developed bacterial, viral, or parasitic infections (24,9010 herpetic infections), 126,993 cardiac disorders, 100,970 blood and lymphatic system disorders, 77,148 psychiatric disorders, 73,542 vascular disorders, 61,518 eye disorders, 47,038 ear and labyrinth disorders (15,833 tinnitus), 31,895 autoimmune disorders, 13,647 kidney and urinary disorders, 3,711 cancers and benign cysts, 4,056 pregnancy complications (1,859 spontaneous abortion complications, 1,143 genetic disorders, and 3,814 deaths were documented in an internal Pfizer documents.
WHEREAS on the 30 November 2022, MEDSAFE committed medical FRUAD when they said that "the protective benefits of vaccination against COVID-19 far outweigh the potential risks of vaccination." Safety Report #46 – 30 November 2022 (medsafe.govt.nz)
WHEREAS by June 16, 2023, 17,560 deaths, 83,092 hospitalizations, 116,479 urgent care visits,194,594 doctor visits, 36,014 anaphylaxis/severe allergic reactions, 13,515 cardiac events/conditions, 17,076 permanent disabilities, and an additional 14,494 life threatening events have been reported into the CDC’s VAERS database, with an estimated 100-fold underreporting factor per a Harvard Pilgrim Healthcare Analysis commissioned by HHS.
The COVID-19 mRNA nanoparticle injections were administered to civilian adults and children through unlawful human experimentation, specifically whereas the clinical safety risks were known by the MEDSAFE and FDA to outweigh any potential clinical benefits and the COVID-19 injections were administered without informed consent regarding;
the composition and variability of the COVID-19 nanoparticle injections’ vials,
the gene-editing mechanism of action of COVID-19 nanoparticle technologies, and
the known harmful, permanently disabling and/or sometimes deadly clinical outcomes of being injected with engineered COVID-19 nanoparticle technologies.