This is an HTML version of an attachment to the Official Information request 'CV TAG discussion papers regarding adverse effects of using a "leaky" COVID vaccine'.

133 Molesworth Street 
PO Box 5013 
Wellington 6140 
New Zealand 
T+64 4 496 2000 
6 October 2021
Simon Brown 
By email:  [FYI request #16617 email] 
Ref:  
H202111756 
Tēnā koe Simon 
Response to your request for official information 
Thank you for your request under the Official Information Act 1982 (the Act) on 4 September 
2021 for: 
“I would like to learn what discussions were had by the COVID Vaccine Technical 
Advisory Group regarding the potential long term detrimental safety implications of using a 
two-dose regimen of the BioNTech/Pfizer mRNA BNT162b2 vaccine. I am specifically 
interested in any and all discussions regarding the use of a "leaky" vaccine as described 
in Pfizers original application for FDA Emergency use Authorization, subsequently 
confirmed by numerous international studies, including the most recent Israeli study by 
Gazit et al 
(https://scanmail.trustwave.com/?c=15517&d=pNiy4Yvg__LcRQMMJH6LLgXtNWbyt2D80
FeJtlxGuw&u=https%3a%2f%2fwww%2emedrxiv%2eorg%2fcontent%2f10%2e1101%2f2
021%2e08%2e24%2e21262415v1) 

I specifically would like the minutes of meetings and any formal papers/submissions by 
CV-TAG members that address the following issues with the vaccinated and why they are
not considered either a short and/or long term public health risk:

1. increased risk of escape variants
2. disease reservoirs and increased risk for reverse zoonosis 3. high viral loads and
viraemia 4. increased risk of coagulopathies 5. increased risk of autoimmunities, antibody-
dependent enhancement (ADE) and acute lung injury (ALI).”

The stated concerns have not been identified through clinical trials or through the large number 
of real-world studies of the Pfizer vaccine, including before and after formal approval, at a 
sufficiently robust level that would trigger an assessment from COVID-19 Vaccine Technical 
Advisory Group. As such the Ministry of Health (the Ministry) does not hold the information you 
have requested. Therefore, your request is refused in full under section 18(g) of the Act on the 
grounds that the information sought is not held by the Ministry. 
Under section 28(3) of the Act you have the right to ask the Ombudsman to review any 
decisions made under this request. The Ombudsman may be contacted by email at: 
[email address] or by calling 0800 802 602. 


Please note that this response, with your personal details removed, may be published on the 
Ministry of Health website at: www.health.govt.nz/about-ministry/information-releases.  
 
Nāku noa, nā 
 
 
 
Nick Allan 
Manager, OIA Services 
Office of the Director-General 

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