Kia ora Hon. Dr. Verrall, Minister for COVID-19 Response and Rt. Hon. Prime Minister Hipkins (sent 31/01/2023)

I am following up on your email dated 15/12/2022 when you confirmed you were seeking advice from your officials for the evidentiary document sent to ex-PM Ardern and stated that I could expect a response, which has not been forthcoming.

While Prime Minister Ardern’s claimed resignation represents a shallow step in the right direction, Government has failed to notify unsuspecting New Zealanders of the lifelong health risks and enhanced susceptibility to SARS-CoV-2 variant infections, so they can mitigate these health risks. During this intervening period, the MOH administered approximately 70,000 COVID-19 vaccine doses, putatively resulting in a significant disbenefit over the unvaccinated (i.e., COVID-19 infections, excess deaths). Given the evidence, this would make the government knowingly complicit in the unnecessary killing and harming of New Zealanders since 05/12/2022, never mind before this date.

On 11/01/2023, Professor Blakely, the Chairman of New Zealand’s Royal Commission of Inquiry into the government’s COVID-19 response, was provided the evidentiary document and asked to investigate if a genetically modified SARS-CoV-2 bioweapon coupled with predictably unsafe COVID-19 vaccination was an intentional WHO-led global genocide strategy being implemented in New Zealand as part of this government’s COVID-19 response ( Significant concerns were raised with Professor Blakely about the strategic intent behind government’s COVID-19 response when viewed through the lens of predictable-preventable antibody-dependent enhancement of virus infection and antigenic imprinting, the MOH’s deceitful harm-hiding statistical biases, and the government’s multi-modal censorship of the global evidence of iatrogenic harm.

Furthermore, on 20/01/2023, NZ’s Media was requested to investigate the government’s COVID-19 response. They were asked if the government’s $55 million Public Interest Journalism Fund and the conditionality placed on recipient media firms undermined their independence and resulted in bias and censorship, among other issues. The media were requested to investigate the Department of Internal Affairs Face Book take-down portal. This portal confirms government censorship of New Zealanders under the guise of protecting them from non-government mis-/dis-information while permitting government mis-/dis-information. The media were also asked if the appointment of Caroline Flora as Chief Censor raised any alarm bells about the government’s intent to censor the harm it inflicted on New Zealanders while she was associate director general of the MOH (

The media were appraised of the 2022 draft Coroners Amendment Bill, making it possible for the government to hide the anticipated escalation of COVID-19 vaccine-associated excess mortality via the deployment of lesser qualified coroner associates able to classify vaccine-associated deaths as due to “unascertained natural causes” from behind a desk without a pathologist’s input. The media were also asked to investigate four highly evident examples of systematic UN/WHO member state government data fraud and falsifiable interpretative deceit of clinical outcomes – giving the notion of conspiracy theory absolute validity.

In my view, the Labor government, at best (unwittingly), failed to protect the public against irreparable and 100%-predictable vaccine-induced harm and, or at worst (intentionally), participated in an act of global genocide being implemented by WHO member- high income- nations, particularly. Given that this government and its system of health, justice, police, military, and media failed to protect New Zealanders, the Wakaminenga Māori Government was requested to intervene per their responsibility under He Wakaputanga and Ture Tikanga jurisdictional law.

I re-request that the Labor government urgently take responsibility for the irreparable life-shortening harm it has inflicted on the nation and notify the public so that they can mitigate their health and (re)infection risks and pressure you to withdraw these vaccines from use, while ensuring you are democratically removed from power in 2023. In the interim, the government is requested to ensure antivirals are stockpiled and made available for those at risk against the more pathogenic SARS-CoV-2 variants coming our way.

Recipients: TO: CC:;;;;;;;;;;;;;;;;;;;;;;;;;

Nga mihi

Dr. Carlton Brown BVSc MBA

Former CEO and co-innovator at Immune Targeting Systems Ltd (UK), “Vaccines for Mutating Viruses.”

Raising awareness for antibody-dependent enhancement of virus infection (ADE), vaccine-associated enhanced disease (VAED), and antigenic imprinting by COVID-19 vaccination.,,,

Download the Evidentiary Document:

Author: Revolution: Ice Age Re-Entry Amazon, Google Play (free).


Sent with Proton Mail secure email.

——- Original Message ——-
On Thursday, December 15th, 2022 at 9:59 AM, A Verrall (MIN) <> wrote:

Kia ora Dr Brown

On behalf of Hon Dr Ayesha Verrall, Minister for COVID-19 Response, thank you for your email on 5 December 2022. The Minister has noted your letter and has asked her officials for advice on the matters you have raised. You can expect a response from the Minister in due course.

Ngā mihi,

Private Secretary (COVID-19) | Office of Hon Dr Ayesha Verrall

Minister for COVID-19 Response

Minister of Research, Science and Innovation

Minister for Seniors

Associate Minister of Health

Private Bag 18041, Parliament Buildings, Wellington 6160, New Zealand

From: COVID19VaccineSafetyNZ []
Sent: Monday, 5 December 2022 4:36 PM
To: J Ardern (MIN) <>; A Little Office (MIN) <>; P Henare (MIN) <>; A Verrall (MIN) <>; A Sio (MIN) <>
Cc: C Sepuloni (MIN) <>; C Hipkins (MIN) <>; D OConnor (MIN) <>; D Parker (MIN) <>; D Clark (MIN) <>; Megan Woods (MIN) <>; G Robertson (MIN) <>; J Shaw (MIN) <>; J Tinetti (MIN) <>; K Davis (MIN) <>; K McAnulty (MIN) <>; K Allan (MIN) <>; M Davidson (MIN) <>; M Whaitiri (MIN) <>; M Wood (MIN) <>; N Mahuta (MIN) <>; P Twyford (MIN) <>; P Williams (MIN) <>; P Radhakrishnan (MIN) <>; S Nash (MIN) <>; W Jackson (MIN) <>;;
Subject: (3600-2022)Open Letter & Evidentiary Document for the Prime Minister and all Ministers: COVID-19 negative vaccine effectiveness and harm evidence in New Zealand and overseas (Results, Call to Action)

Dear Rt Hon Jacinda Ardern, Prime Minister, Hon Andrew Little, Minister of Health, Hon Dr. Ayesha Verrall, Minister of COVID-19 Response, and Hon Peeni Henare and Hon Aupito William Sio, Associate Ministers of Health

In this Open Letter and evidentiary document, I share my research results on overseas government and Ministry of Health (MoH) COVID-19 vaccine surveillance and pharmacovigilance data indicating irreparable vaccine-induced harm. Furthermore, I share important evidence that SARS-CoV-2 originated from gain-of-function research, remind you that no evidence exists for an animal-to-human origin, and highlight that its potential source lay beyond Wuhan, China. A series of requests for investigations are made below linked to this evidence, including the statisticalbiases evident in the Ministry of Health and other healthcare agencies’ calculable unvaccinated COVID-19 case rates. These biases essentially eliminated the negative vaccine effectiveness harm signal from ready public view. This evidentiary document is provided by a former European corporate venture capital-funded CEO/vaccine innovator (“Vaccines for Mutating Viruses”), veterinarian with 36 years of vaccine use experience, and a private researcher. It is supported by 525 unique data, scientific, and other citations.

According to New Zealand, England, Scotland, and Canada healthcare agencies and Global surveillance data (77 nations), these vaccines failed to prevent SARS-CoV-2 infection as initially touted. Significant negative vaccine effectiveness and vaccine failure were evident with the emergence of antigenically distinct strains (i.e., Delta, Omicron). The vaccine industry experienced antibody-dependent enhancement of virus infection (ADE) and vaccine-associated enhanced disease (VAED) with three other different coronaviruses and their spike protein vaccine prototypes in the last 30 years, giving my study results a predictable context. Furthermore, one year of US lot-numbered COVID-19 vaccine-associated deaths and hospitalizations equaled 32x (Comirnaty 15.4x) and 20x (Comirnaty 10.5x) of all US vaccine-associated deaths and hospitalizations, respectively. These adverse outcomes were highly skewed and peaked across vaccine lots and were associated with a minority of lots sent to a larger number of US States. This data highlights that there was an urgent need for investigation by the US and other regulatory and healthcare agencies before expanded population use.

A vast chasm exists between the vaccine safety and efficacy experienced in 2021-2022 and the falsifiable 95% vaccine efficacy and safety proclaimed by governments with Comirnaty’s first Emergency Use Authorization in 2020 (USA). This document reviews critical pharmacotoxicology and clinical safety package deficiencies evident in overseas regulatory reviews. This helps explain why Pfizer then struggled to cope with the sheer volume of Comirnaty adverse event reports in the first 90 days post-launch. This was uncharacteristic of a safe vaccine. Numerous vaccine-associated enhanced disease mechanisms are evident by which vaccine spike proteins can cause disease or exacerbate comorbidities common to severe COVID-19 outcomes.These mechanisms place upregulated furin and angiotensin-converting enzyme-2 receptors (ACE2) and prevalent comorbidities in tissues and organs common to all three center-stage. At the same time, SARS-CoV-2’s spike protein provides its uniquely encoded furin cleavage site for the furin to cleave its S1 and S2 sub-units and activate its ACE2-receptor-mediated infectivity and pathogenicity.

Of grave concern for global public health is a gain-of-function origin to SARS-CoV-2 is indicated by its spike protein incorporating human infectivity and pathogenicity enhancing features unprecedented in nature while synthetic biology left its fingerprints. Furthermore, there is no evidence supporting a Wuhan Huanan market zoonosis because no virus progenitor or animal host was ever identified. There are two reasons for detailing a coronavirus gain-of-function origin to SARS-CoV-2. Firstly, the negative vaccine effectiveness evident in governments’ COVID-19 surveillance data could have been enhanced by a genetically modified SARS-CoV-2. Secondly, the world will be left vulnerable to future pandemics if there was no accidental release from the Wuhan Institute of Virology. At least two other potential SARS-CoV-2 origins exist beyond Wuhan, with one of these potentially involving a WHO, Five Eyes, and NATO-spearhead member nation connected with Ukraine.

The US Department of Defense (DoD) and National Institutes of Health (NIH) funding of EcoHealth Alliance (EHA, $69 million) and its connections one-degree-removed were scrutinized because EHA’s leader led a failed attempt to cover up SARS-CoV-2’s gain-of-function origin. EHA directed research that genetically modified bat SARSr-CoVs that could not infect humans so that they could. EHA’s $14.2 million funding application to the DoD in 2018 showed its intent to insert a codon-optimized furin cleavage site (FCS) into bat SARSr-CoVs. A uniquely encoded Arginine-doublet containing FCS now sits between SARS-CoV-2’s spike protein S1 and S2 sub-units, which has no precedent in known viruses and may have infringed patents. Besides EHA’s long-standing collaborations with two coronavirus gain-of-function research epicenters in the USA and China, it had another with Metabiota. Metabiota’s Series-A lead investor was a Hunter Biden part-owned investment firm. The DoD-funded Metabiota operated in Pentagon Biolabs in Ukraine and US-funded Biolabs in Cameroon and researched corona-, monkeypox-, influenza-, and Ebola viruses. Metabiota has implemented major DoD and Homeland Security contracts across Central Africa while its surveillance role in Sierra Leone’s Ebola outbreak in 2014 created significant controversies.

You are requested to investigate: (1) this New Zealand and overseas evidence for negative vaccine effectiveness, vaccine failure, and toxic vaccine lots, (2) the statistical biases evident in the MoH and other healthcare agencies’ calculable unvaccinated COVID-19 case rates, which essentially eliminated the negative vaccine effectiveness signal, (3) the role of COVID-19 vaccination in exacerbating comorbidities most frequently associated with serious-severe COVID-19 outcomes, (4) SARS-CoV-2’s gain-of-function origin while internationally championing a punitive global ban on gain-of-function R&D, and (5) the conduct of the WHO during COVID-19 linked to seven critical points detailed in section 2.7. Would you please ensure New Zealanders are updated on their recently acquired life-long health risks and that informed consent guidelines associated with COVID-19 vaccination be urgently amended? Would government please prioritize clinical research into COVID-19 antibody-dependent enhancement of virus infection, vaccine-associated enhanced disease, and antigenic imprinting in the New Zealand population? Thank you.

Yours sincerely

Dr. Carlton Brown BVSc (1986, Massey University), MBA (1997, London Business School).

Former CEO and co-innovator at Immune Targeting Systems Ltd (UK), “Vaccines for Mutating Viruses.”

Raising awareness for antibody-dependent enhancement of virus infection (ADE), vaccine-associated enhanced disease (VAED), and antigenic imprinting.,,

Download the Open Letter and Evidentiary Document:

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