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Date of receipt of Pfizer Cumulative Analysis of Adverse Event Reports

Paul Roberts made this Official Information request to Ministry of Health

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From: Paul Roberts

Dear Ministry of Health,

In recent news Pfizer confidential documents have been released with the title "5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT
REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021" with the document located in the following link https://pdfhost.io/v/LNN0hIyYb_536postma...

Under the Official Information Act would you please provide the date the Ministry/Medsafe received such documentation from Pfizer showing the Cumulative Analysis of Post-authorization Adverse Event Reports, the same or similar to what was released in the above referenced document?

Yours faithfully,

Paul Roberts

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From: OIA Requests

Kia ora,

 

Thank you for your Official Information Act (the Act) request. This is
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Due to the COVID-19 global pandemic response, the Ministry is experiencing
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[4]Ministry of Health information releases  

[5]Unite against COVID-19 

 

 

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2. http://scanmail.trustwave.com/?c=15517&a...
3. mailto:[email address]
4. https://www.health.govt.nz/about-ministr...
5. https://covid19.govt.nz/

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From: OIA Requests


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Kia ora Paul,

 

Thank you for your request for official information. The Ministry's
reference number for your request is: H202117154.

 

Please be advised that due dates for requests received from 29 November
2021 onwards take into account the following periods:

 

Christmas (25 December 2021)

Summer Holidays (25 December to 15 January)

New Year's Day (1 January 2022)

Day after News Year's Day (2 January 2022)

 

Your request has been logged and you can expect a reply no later than 24
January 2022 as required under the Official Information Act 1982.

 

Due to the COVID-19 global pandemic response, the Ministry is experiencing
significantly higher volumes of queries and requests for information. If
we are unable to respond to your request within this time frame, we will
notify you of an extension of that time frame.

 

If you have any queries related to this request, please do not hesitate to
get in touch.

 

Ngā mihi

 

OIA Services

Government Services

Office of the Director-General

Ministry of Health

E: [1][email address]

 

 

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Jonathan Wood left an annotation ()

Is this what you are after? https://phmpt.org/wp-content/uploads/202... (Link courtesy of "NZ Doctor" article, "Take One, with a dash of Optimism" accessed 10/12/21)

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From: OIA Requests


Attachment H202117154 Paul Roberts FINAL.pdf
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Kia ora Paul
Please find attached a response to your request for official information.

 

Ngā mihi 

 

OIA Services 

Office of the Director-General | Ministry of Health  

  

E: [1][email address]  

  

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Chuck Schooner (Account suspended) left an annotation ()

Hi Paul,

Given this data is now available and not commercially sensitive can you follow up and request a copy of what they allude to below and how it was implemented into their application for the original provisional consent and subsequent follow up application?

"as the response also notes as a part of the provisional consent for the Comirnaty COVID-19 vaccine granted in New Zealand under the Medicines Act 1981, Pfizer has provided the same data, albeit in a form that meets the
company’s legal obligations in New Zealand"

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