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Pfizer Vaccine Consistency

Chuck Schooner made this Official Information request to Ministry of Health

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From: Chuck Schooner

Dear Ministry of Health,

Latest statistics shows that a large amount of the New Zealand population has been vaccinated. A lot of them have been vaccinated safely yet there are now 126,679 adverse reports that have been reported including the below very serious side effects.

- strokes
- at least one death
- cardiac arrest
- myocarditis & pericarditis
- haemmorrage

Despite all of these very serious side effects the Ministry of Health, and I say this in gest given statistics can you please state if

- Medsafe has done any batch sampling of the Pfizer vaccines to assess consistency?
- If not, why not?
- Does the Pfizer document preclude any and all testing of the contents in the vial? This is a yes no answer and does not require any sensitive information being disclosed
- Are Medsafe aware that in Japan 1.6m doses of the vaccine were discarded due to contamination - how does Medsafe determine if any of the Pfizer vaccines are contaminated?
- What quality controls are completed by Medsafe to ensure the vaccine doses are consistent and not contaminated?
- Would very serious side effects in some versus no side effects in others raise any flags at Medsafe and how would that be investigated?
- Are there clauses in the Pfizer contract that preclude any investigation of the vials at all? Yes or No
- In the 1970's 1/3 of the American population were vaccinated against swine flu - there were 26 suspicious deaths and then the vaccine was stopped. Pfizers cumulative analysis report recently released under Official Information by the FDA confirms that over 1,200 people died in the first 90 days of the Pfizer roll out directly from the vaccine (and to date thousands more globally). What has changed from the 70's versus now? Given it is now categorically known from Pfizers own documentation that this vaccine/gene therapy can kill you could any criminal charges be laid against the persons approving this vaccine if they were knowingly aware of the Pfizer cumulative analysis report?

Yours faithfully,

Chuck Schooner

Link to this

From: OIA Requests

Kia ora,

 

Thank you for your Official Information Act (the Act) request. This is
an automatic reply to let you know we received it.

 

Due to the COVID-19 global pandemic response, the Ministry is experiencing
significantly higher volumes of queries and requests for information. We
will endeavour to acknowledge your request as soon as possible. Further
information about COVID-19 can be found on our
website: [1]https://www.health.govt.nz/our-work/dise...

 

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)

 

If you'd like to calculate the due date for your request, you can use the
Ombudsman's online calculator here: [2]http://www.ombudsman.parliament.nz/

If you have any questions while we're processing your request, please let
us know via [3][email address]

 

Ngā mihi  

OIA Services Team  

   

[4]Ministry of Health information releases  

[5]Unite against COVID-19 

 

 

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References

Visible links
1. https://www.health.govt.nz/our-work/dise...
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/

Link to this

From: OIA Requests


Attachment image001.png
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Kia ora Chuck,

 

Thank you for your request for official information. The Ministry's
reference number for your request is: H202117155.

 

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 18
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]

 

show quoted sections

Link to this

From: OIA Requests


Attachment image001.png
7K Download


Kia ora Chuck, 

  

Thank you for your request for official information received on 6 December
for: 

  

"Medsafe has done any batch sampling of the Pfizer vaccines to assess
consistency?
- If not, why not?
- Does the Pfizer document preclude any and all testing of the contents in
the vial? This is a yes no answer and does not require any sensitive
information being disclosed
- Are Medsafe aware that in Japan 1.6m doses of the vaccine were discarded
due to contamination - how does Medsafe determine if any of the Pfizer
vaccines are contaminated?
- What quality controls are completed by Medsafe to ensure the vaccine
doses are consistent and not contaminated?
- Would very serious side effects in some versus no side effects in others
raise any flags at Medsafe and how would that be investigated?
- Are there clauses in the Pfizer contract that preclude any investigation
of the vials at all? Yes or No
- In the 1970's 1/3 of the American population were vaccinated against
swine flu - there were 26 suspicious deaths and then the vaccine was
stopped. Pfizers cumulative analysis report recently released under
Official Information by the FDA confirms that over 1,200 people died in
the first 90 days of the Pfizer roll out directly from the vaccine (and to
date thousands more globally). What has changed from the 70's versus now?
Given it is now categorically known from Pfizers own documentation that
this vaccine/gene therapy can kill you could any criminal charges be laid
against the persons approving this vaccine if they were knowingly aware of
the Pfizer cumulative analysis report?"

  

A secondary request for official information was received on 8 December
for: 

  

"On receipt of a trove of Pfizer documents released by the FDA.

              Please state if Pfizer provided the following document to
Medsafe for their safety assessment.
              5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE
EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021
              If so, when did Medsafe receive this document. If not, why
was this document not provided given the date. Now that Medsafe is       
                                          aware of the document and the
vaccine has caused death and 10 pages of other serious side effects can
you honestly say proper due                                         
diligence was completed"

  

The Ministry of Health has consolidated your requests under reference
number: H202117155. 

  

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

  

 

--------------------------------------------------------------------------

From: OIA Requests <[email address]>
Sent: Tuesday, 7 December 2021 10:42
To: Chuck Schooner <[FOI #17850 email]>
Subject: Acknowledgement of your request for official information (ref:
H202117155)
 

Kia ora Chuck,

 

Thank you for your request for official information. The Ministry's
reference number for your request is: H202117155.

 

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 18
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: [2][email address]

 

show quoted sections

Link to this

From: OIA Requests


Attachment image001.png
7K Download

Attachment image.png
13K Download


Kia ora Chuck, 
Further to our email below we will also be responding to the following
request under this reference: H202117155.

 

"Please state if the following report was used in the assessment to
approve the Pfizer/Biontech vaccine when Medsafe first approved this gene
therapy/vaccine.

5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT
REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021

If the report was not available can you please state if Medsafe requested
any real time safety reports from Pfizer in advance of approving this gene
therapy. 

By the time Medsafe approved this gene therapy the vaccine had been widely
used globally and so there would be real time statistics.  If not, did you
rely on Pfizer trial information only?

Medsafe then approved the gene therapy for two more years and stated
Pfizer had met a number of safety conditions following their provisional
approval.  Please provide all reports/evidence that Pfizer provided
Medsafe that prove that they met their safety conditions that were part of
the first gazette notice.

The above report was dated early 2021 - please state if Pfizer had
provided this to Medsafe at all when they have completed any of their due
diligence in assessing this gene therapy.

Please state if on the release of the documents by the FDA has Medsafe
requested all of the Pfizer documents that have been released - please
provide a list of all the Pfizer documents that Medsafe have relied upon
in approving this gene therapy.

This document is now available and if you approve this in children who
will ultimately be responsible for illnesses in children? Medsafe or
Ministry of Health.

Were Medsafe responsible for approving Remdesivir as a Covid-19 treatment.

Is Medsafe/Ministry of Health using Remdesivir as a Covid-19 treatment?
What studies were used to say Remdesivir was safe?

An Ebola study using Remdesivir showed that it was pulled from use in a 12
month trial after six months because it killed 54% of the trial subjects
it used.

The Remdesiver study also showed that patients were having the following
side effects

- 10 day treatment of Covid-19 showed 23% had serious adverse events were
organ dysfunction syndrome, septic shock, acute kidney failure and kidney
failure.

Please state how many Covid patients have been treated with Remdesiver in
New Zealand and how many of them had the above side effects and died.  It
appears Remdesiver will kill you.  Did Medsafe do any due diligence for
Remdesiver as it will likely poison patients."

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]

 

--------------------------------------------------------------------------

From: OIA Requests <[email address]>
Sent: Monday, 13 December 2021 11:40
To: Chuck Schooner <[FOI #17850 email]>
Subject: Re: Acknowledgement of your request for official information
(ref: H202117155)
 

Kia ora Chuck, 

  

Thank you for your request for official information received on 6 December
for: 

  

"Medsafe has done any batch sampling of the Pfizer vaccines to assess
consistency?
- If not, why not?
- Does the Pfizer document preclude any and all testing of the contents in
the vial? This is a yes no answer and does not require any sensitive
information being disclosed
- Are Medsafe aware that in Japan 1.6m doses of the vaccine were discarded
due to contamination - how does Medsafe determine if any of the Pfizer
vaccines are contaminated?
- What quality controls are completed by Medsafe to ensure the vaccine
doses are consistent and not contaminated?
- Would very serious side effects in some versus no side effects in others
raise any flags at Medsafe and how would that be investigated?
- Are there clauses in the Pfizer contract that preclude any investigation
of the vials at all? Yes or No
- In the 1970's 1/3 of the American population were vaccinated against
swine flu - there were 26 suspicious deaths and then the vaccine was
stopped. Pfizers cumulative analysis report recently released under
Official Information by the FDA confirms that over 1,200 people died in
the first 90 days of the Pfizer roll out directly from the vaccine (and to
date thousands more globally). What has changed from the 70's versus now?
Given it is now categorically known from Pfizers own documentation that
this vaccine/gene therapy can kill you could any criminal charges be laid
against the persons approving this vaccine if they were knowingly aware of
the Pfizer cumulative analysis report?"

  

A secondary request for official information was received on 8 December
for: 

  

"On receipt of a trove of Pfizer documents released by the FDA.

              Please state if Pfizer provided the following document to
Medsafe for their safety assessment.
              5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE
EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021
              If so, when did Medsafe receive this document. If not, why
was this document not provided given the date. Now that Medsafe is       
                                          aware of the document and the
vaccine has caused death and 10 pages of other serious side effects can
you honestly say proper due                                         
diligence was completed"

  

The Ministry of Health has consolidated your requests under reference
number: H202117155. 

  

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: [2][email address

  

 

--------------------------------------------------------------------------

From: OIA Requests <[email address]>
Sent: Tuesday, 7 December 2021 10:42
To: Chuck Schooner <[FOI #17850 email]>
Subject: Acknowledgement of your request for official information (ref:
H202117155)
 

Kia ora Chuck,

 

Thank you for your request for official information. The Ministry's
reference number for your request is: H202117155.

 

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 18
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: [3][email address]

 

show quoted sections

Link to this

From: OIA Requests


Attachment H202117069 Chuck Schooner FINAL.pdf
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Kia ora Chuck
Please find attached a response to your requests for official information.

Ngâ mihi 

 

OIA Services 

Office of the Director-General | Ministry of Health  

  

E: [1][email address]  

 

Do your bit to keep New Zealand COVID free; get vaccinated; wear a mask;
practice good hygiene (includes washing your hands often and coughing into
your elbow), sign using the NZ COVID Tracer app, if you’re unwell stay
home and get tested. 

 

show quoted sections

References

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1. mailto:[email address]

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