Informed Consent #12 - Adverse Effects Reporting
Annie Weston made this Official Information request to Ministry of Health
The request was refused by Ministry of Health.
From: Annie Weston
Dear Ministry of Health,
In NZ there are currently more deaths attributable to the Pfizer vaccine than from Covid-19.
My question please: why is there no Govt mandate to report adverse effects from the vaccines?
This is especially important now the Govt has mandated vaccination - surely the Govt will want to mitigate its responsibility for killing people.
Yours faithfully,
Annie Weston
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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From: OIA Requests
Kia ora Annie,
Thank you for your email.
Your first statement is incorrect and based on misinformation. There has
been one death linked to the COVID-19 Pfizer vaccine.
It is also important to note that while anyone can report an AEFI –
doctor, nurse, pharmacist, vaccinator, government agency, consumer, or
member of the public – reporting is voluntary. The form to do so is
available at: [1]https://report.vaccine.covid19.govt.nz/s/. Both the
Ministry and Medsafe encourage everyone to report AEFI.
While all AEFI occur after vaccination, that does not mean they are caused
by vaccination. That is why AEFI are investigated by the Centre for
Adverse Reactions Monitoring (CARM), at the University of Otago, which
undertakes pharmacovigilance in New Zealand under contract to the
Ministry. Reported adverse events for the COVID-19 vaccine are evaluated
according to whether they are serious or non-serious according to certain
criteria, such as if the person required hospitalisation. All reports are
verified to check that:
• The person had a COVID-19 vaccine
• There is an identifiable person in the report
• An adverse event following immunisation (AEFI) has been
reported
• There is a reporter who can be contacted for more
information
It is not uncommon that a report is received about the same event from
both the vaccinator and the consumer, so there are checks to ensure an
event is not reported twice.
Significant reports are medically assessed by CARM according to the World
Health Organization guidance and if needed follow up is conducted to seek
further information. Significant reports are also reviewed by the COVID-19
Vaccine Independent Safety Monitoring Board (CV-ISMB), which provides
expert advice on a potential link to the vaccine. All potential safety
signals investigated in New Zealand for the COVID-19 vaccine are presented
and discussed with the CV-ISMB, with Medsafe providing an update on these
in its regular safety report available
at: [2]www.medsafe.govt.nz/COVID-19/vaccine-report-overview.asp.
If the investigation of a new side effect of the COVID-19 vaccine is
found, this will be communicated to everyone through an alert
communication and an update to the data sheet and CMIS, for example, with
Medsafe’s report about myocarditis, available
at: [3]www.medsafe.govt.nz/safety/Alerts/comirnaty-myocarditis-alert.htm.
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: [4][email address] or by calling 0800
802 602.
Ngâ mihi
OIA Services Team
[5]Ministry of Health information releases
[6]Unite against COVID-19
[FYI request #17819 email]>
Sent: Friday, 3 December 2021 11:37
To: OIA Requests <[email address]>
Subject: Official Information request - Informed Consent #12 - Adverse
Effects Reporting
Dear Ministry of Health,
In NZ there are currently more deaths attributable to the Pfizer vaccine
than from Covid-19.
My question please: why is there no Govt mandate to report adverse effects
from the vaccines?
This is especially important now the Govt has mandated vaccination -
surely the Govt will want to mitigate its responsibility for killing
people.
Yours faithfully,
Annie Weston
-------------------------------------------------------------------
This is an Official Information request made via the FYI website.
Please use this email address for all replies to this request:
[FYI request #17819 email]
Is [Ministry of Health request email] the wrong address for Official Information requests
to Ministry of Health? If so, please contact us using this form:
[7]https://scanmail.trustwave.com/?c=15517&...
Disclaimer: This message and any reply that you make will be published on
the internet. Our privacy and copyright policies:
[8]https://scanmail.trustwave.com/?c=15517&...
If you find this service useful as an Official Information officer, please
ask your web manager to link to us from your organisation's OIA or LGOIMA
page.
-------------------------------------------------------------------
****************************************************************************
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legal privilege.
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distribute or copy this message or attachments.
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immediately and delete this message.
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References
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2. http://www.medsafe.govt.nz/COVID-19/vacc...
3. http://www.medsafe.govt.nz/safety/Alerts...
4. mailto:[email address]
5. https://www.health.govt.nz/about-ministr...
6. https://covid19.govt.nz/
7. https://scanmail.trustwave.com/?c=15517&...
8. https://scanmail.trustwave.com/?c=15517&...
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From: Annie Weston
Dear OIA Requests,
Thank you for your prompt reply.
The misinformation you refer to is from Medsafe's webpage:
"Up to and including 6 November 2021, a total of 103 deaths were reported to CARM after the administration of the Comirnaty vaccine."
I understand the average time to resolve these coronial cases is 540 days so in the meantime I'd like to be as informed as possible please before being coerced into taking an experimental vaccine and risking death.
I understand that AEFI reporting is voluntary hence my original question, here again:
Why is there no Govt mandate to report adverse effects from the vaccines?
Yours sincerely,
Annie Weston
From: OIA Requests
Kia ora Annie,
Thank you for your follow up email.
The sentence you have referred to below is for AEFIs after vaccination.
There has only been one linked death. Further information can be found
here: [1]https://www.health.govt.nz/news-media/me....
These are mainly coincidental events that people have reported. As
approximately 90 percent of the people in New Zealand over the age of 12
have now received at least one dose of the Comirnaty vaccine, there is a
high probability that anyone who has an illness or condition in New
Zealand will have been vaccinated.
While the Act allows New Zealanders to ask for information from Ministers
and government agencies, there is no requirement for agencies to prove or
provide an opinion or comment on a statement. Your last question appears
designed to engage in a debate about the Government’s COVID-19 vaccination
programme, rather than a request for official information. The Act does
not support requests where an opinion, comment, argument, or hypothetical
statement is put to the Ministry for response, couched as a request for
information. These questions are therefore refused 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: [2][email address] or by calling 0800
802 602.
Ngā mihi
OIA Services Team
[3]Ministry of Health information releases
[4]Unite against COVID-19
--------------------------------------------------------------------------
From: Annie Weston <[FOI #17819 email]>
Sent: Friday, 3 December 2021 15:32
To: OIA Requests <[email address]>
Subject: Re: Response to your correspondence 3 December 2021
Dear OIA Requests,
Thank you for your prompt reply.
The misinformation you refer to is from Medsafe's webpage:
"Up to and including 6 November 2021, a total of 103 deaths were reported
to CARM after the administration of the Comirnaty vaccine."
I understand the average time to resolve these coronial cases is 540 days
so in the meantime I'd like to be as informed as possible please before
being coerced into taking an experimental vaccine and risking death.
I understand that AEFI reporting is voluntary hence my original question,
here again:
Why is there no Govt mandate to report adverse effects from the vaccines?
Yours sincerely,
Annie Weston
-----Original Message-----
Kia ora Annie,
Thank you for your email.
Your first statement is incorrect and based on misinformation. There has
been one death linked to the COVID-19 Pfizer vaccine.
It is also important to note that while anyone can report an AEFI –
doctor, nurse, pharmacist, vaccinator, government agency, consumer, or
member of the public – reporting is voluntary. The form to do so is
available at: [1]https://report.vaccine.covid19.govt.nz/s/. Both the
Ministry and Medsafe encourage everyone to report AEFI.
While all AEFI occur after vaccination, that does not mean they are
caused
by vaccination. That is why AEFI are investigated by the Centre for
Adverse Reactions Monitoring (CARM), at the University of Otago, which
undertakes pharmacovigilance in New Zealand under contract to the
Ministry. Reported adverse events for the COVID-19 vaccine are evaluated
according to whether they are serious or non-serious according to certain
criteria, such as if the person required hospitalisation. All reports are
verified to check that:
• The person had a COVID-19 vaccine
• There is an identifiable person in the report
• An adverse event following immunisation (AEFI) has been
reported
• There is a reporter who can be contacted for more
information
It is not uncommon that a report is received about the same event from
both the vaccinator and the consumer, so there are checks to ensure an
event is not reported twice.
Significant reports are medically assessed by CARM according to the World
Health Organization guidance and if needed follow up is conducted to seek
further information. Significant reports are also reviewed by the
COVID-19
Vaccine Independent Safety Monitoring Board (CV-ISMB), which provides
expert advice on a potential link to the vaccine. All potential safety
signals investigated in New Zealand for the COVID-19 vaccine are
presented
and discussed with the CV-ISMB, with Medsafe providing an update on these
in its regular safety report available
at: [2]www.medsafe.govt.nz/COVID-19/vaccine-report-overview.asp.
If the investigation of a new side effect of the COVID-19 vaccine is
found, this will be communicated to everyone through an alert
communication and an update to the data sheet and CMIS, for example, with
Medsafe’s report about myocarditis, available
at: [3]www.medsafe.govt.nz/safety/Alerts/comirnaty-myocarditis-alert.htm.
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: [4][email address] or by calling 0800
802 602.
Ngâ mihi
OIA Services Team
[5]Ministry of Health information releases
[6]Unite against COVID-19
[FYI request #17819 email]>
Sent: Friday, 3 December 2021 11:37
To: OIA Requests <[email address]>
Subject: Official Information request - Informed Consent #12 - Adverse
Effects Reporting
Dear Ministry of Health,
In NZ there are currently more deaths attributable to the Pfizer vaccine
than from Covid-19.
My question please: why is there no Govt mandate to report adverse
effects
from the vaccines?
This is especially important now the Govt has mandated vaccination -
surely the Govt will want to mitigate its responsibility for killing
people.
Yours faithfully,
Annie Weston
-------------------------------------------------------------------
This is an Official Information request made via the FYI website.
Please use this email address for all replies to this request:
[FYI request #17819 email]
Is [Ministry of Health request email] the wrong address for Official
Information requests
to Ministry of Health? If so, please contact us using this form:
[7]https://scanmail.trustwave.com/?c=15517&...
Disclaimer: This message and any reply that you make will be published on
the internet. Our privacy and copyright policies:
[8]https://scanmail.trustwave.com/?c=15517&...
If you find this service useful as an Official Information officer,
please
ask your web manager to link to us from your organisation's OIA or LGOIMA
page.
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2. [6]http://www.medsafe.govt.nz/COVID-19/vacc...
3.
[7]http://www.medsafe.govt.nz/safety/Alerts...
4. [8]mailto:[email address]
5. [9]https://www.health.govt.nz/about-ministr...
6.
[10]https://scanmail.trustwave.com/?c=15517&...
7.
[11]https://scanmail.trustwave.com/?c=15517&...
8.
[12]https://scanmail.trustwave.com/?c=15517&...
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[FOI #17819 email]
Disclaimer: This message and any reply that you make will be published on
the internet. Our privacy and copyright policies:
[13]https://scanmail.trustwave.com/?c=15517&...
If you find this service useful as an Official Information officer, please
ask your web manager to link to us from your organisation's OIA or LGOIMA
page.
-------------------------------------------------------------------
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legal privilege.
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distribute or copy this message or attachments.
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5. https://scanmail.trustwave.com/?c=15517&...
6. http://www.medsafe.govt.nz/COVID-19/vacc...
7. http://www.medsafe.govt.nz/safety/Alerts...
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From: Annie Weston
Dear Ministry of Health & OIA Requests,
It is a simple question on your policy - it does not require opinion, comment, argument, or a hypothetical statement.
I simply want to know why the Govt does not require anyone to report adverse effects from taking the vaccines.
Yours faithfully,
Annie Weston
From: OIA Requests
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Kia ora Annie,
Thank you for your requests for official information. The Ministry of
Health has consolidated your requests received on 3 December 2021, 6
December 2021 and 7 December 2021 under reference number: H202117251.
We will be responding to the following requests under this reference:
Official Information request - Informed Consent #12 - Adverse Effects
Reporting
Official Information request - Informed Consent #13 - Post Vaccine Symptom
Check
Official Information request - Informed Consent #15 - New Information from
Pfizer
Official Information request - Informed Consent #17 - New list of adverse
events
Official Information request - Informed Consent #19 - Pfizer drug
interactions
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 21
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]
-----Original Message-----
From: Annie Weston <[FOI #17819 email]>
Sent: Friday, 3 December 2021 5:27 pm
To: OIA Requests <[email address]>
Subject: Re: Official Information request - Informed Consent #12 - Adverse
Effects Reporting
Dear Ministry of Health & OIA Requests,
It is a simple question on your policy - it does not require opinion,
comment, argument, or a hypothetical statement.
I simply want to know why the Govt does not require anyone to report
adverse effects from taking the vaccines.
Yours faithfully,
Annie Weston
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[2][FOI #17819 email]
Disclaimer: This message and any reply that you make will be published on
the internet. Our privacy and copyright policies:
[3]https://scanmail.trustwave.com/?c=15517&...
If you find this service useful as an Official Information officer, please
ask your web manager to link to us from your organisation's OIA or LGOIMA
page.
-------------------------------------------------------------------
****************************************************************************
Statement of confidentiality: This e-mail message and any accompanying
attachments may contain information that is IN-CONFIDENCE and subject to
legal privilege.
If you are not the intended recipient, do not read, use, disseminate,
distribute or copy this message or attachments.
If you have received this message in error, please notify the sender
immediately and delete this message.
****************************************************************************
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References
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hide quoted sections
From: OIA Requests
Kia ora Annie,
Thank you for your requests for official information. The Ministry of
Health has consolidated your requests received on 3 December 2021, 6
December 2021, 7 December 2021, 9 December 2021 and 11 December 2021 under
reference number: H202117251.
We will be responding to the following requests under this reference:
Official Information request - Informed Consent #12 - Adverse Effects
Reporting
Official Information request - Informed Consent #13 - Post Vaccine Symptom
Check
Official Information request - Informed Consent #15 - New Information from
Pfizer
Official Information request - Informed Consent #17 - New list of adverse
events
Official Information request - Informed Consent #19 - Pfizer drug
interactions
Official Information request - Informed Consent #21 - Gene Therapy
Official Information request - Informed Consent #22 - Definition of
Vaccination
Official Information request - Informed Consent #23 - Consequences of
Lockdown
Official Information request - Informed Consent #28 - Inconsistent
Information on Pfizer Vaccine
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 21
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: Wednesday, 8 December 2021 15:09
To: Annie Weston <[FOI #17819 email]>
Subject: Acknowledgement of your request for official information (ref:
H202117251)
Kia ora Annie,
Thank you for your requests for official information. The Ministry of
Health has consolidated your requests received on 3 December 2021, 6
December 2021 and 7 December 2021 under reference number: H202117251.
We will be responding to the following requests under this reference:
Official Information request - Informed Consent #12 - Adverse Effects
Reporting
Official Information request - Informed Consent #13 - Post Vaccine Symptom
Check
Official Information request - Informed Consent #15 - New Information from
Pfizer
Official Information request - Informed Consent #17 - New list of adverse
events
Official Information request - Informed Consent #19 - Pfizer drug
interactions
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 21
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]
-----Original Message-----
From: Annie Weston <[FOI #17819 email]>
Sent: Friday, 3 December 2021 5:27 pm
To: OIA Requests <[email address]>
Subject: Re: Official Information request - Informed Consent #12 - Adverse
Effects Reporting
Dear Ministry of Health & OIA Requests,
It is a simple question on your policy - it does not require opinion,
comment, argument, or a hypothetical statement.
I simply want to know why the Govt does not require anyone to report
adverse effects from taking the vaccines.
Yours faithfully,
Annie Weston
-------------------------------------------------------------------
Please use this email address for all replies to this request:
[3][FOI #17819 email]
Disclaimer: This message and any reply that you make will be published on
the internet. Our privacy and copyright policies:
[4]https://scanmail.trustwave.com/?c=15517&...
If you find this service useful as an Official Information officer, please
ask your web manager to link to us from your organisation's OIA or LGOIMA
page.
-------------------------------------------------------------------
****************************************************************************
Statement of confidentiality: This e-mail message and any accompanying
attachments may contain information that is IN-CONFIDENCE and subject to
legal privilege.
If you are not the intended recipient, do not read, use, disseminate,
distribute or copy this message or attachments.
If you have received this message in error, please notify the sender
immediately and delete this message.
****************************************************************************
--------------------------------------------------------------------------
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by the Ministry of Health's Content and Virus Filtering Gateway
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References
Visible links
1. mailto:[email address]
2. mailto:[email address]
3. mailto:[FOI #17819 email]
4. https://scanmail.trustwave.com/?c=15517&...
hide quoted sections
From: OIA Requests
Kia ora Annie,
Further to our email below we will also be responding to the following
requests under this reference: H202117251.
Official Information request - Informed Consent #26 - Vaccine-Associated
Enhanced Disease (VAED)
Official Information request - Informed Consent #27 - Miscarriage and
Still Birth Rates
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 12:23
To: Annie Weston <[FOI #17819 email]>
Cc: OIA Requests <[email address]>
Subject: Re: Acknowledgement of your request for official information
(ref: H202117251)
Kia ora Annie,
Thank you for your requests for official information. The Ministry of
Health has consolidated your requests received on 3 December 2021, 6
December 2021, 7 December 2021, 9 December 2021 and 11 December 2021 under
reference number: H202117251.
We will be responding to the following requests under this reference:
Official Information request - Informed Consent #12 - Adverse Effects
Reporting
Official Information request - Informed Consent #13 - Post Vaccine Symptom
Check
Official Information request - Informed Consent #15 - New Information from
Pfizer
Official Information request - Informed Consent #17 - New list of adverse
events
Official Information request - Informed Consent #19 - Pfizer drug
interactions
Official Information request - Informed Consent #21 - Gene Therapy
Official Information request - Informed Consent #22 - Definition of
Vaccination
Official Information request - Informed Consent #23 - Consequences of
Lockdown
Official Information request - Informed Consent #28 - Inconsistent
Information on Pfizer Vaccine
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 21
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: Wednesday, 8 December 2021 15:09
To: Annie Weston <[FOI #17819 email]>
Subject: Acknowledgement of your request for official information (ref:
H202117251)
Kia ora Annie,
Thank you for your requests for official information. The Ministry of
Health has consolidated your requests received on 3 December 2021, 6
December 2021 and 7 December 2021 under reference number: H202117251.
We will be responding to the following requests under this reference:
Official Information request - Informed Consent #12 - Adverse Effects
Reporting
Official Information request - Informed Consent #13 - Post Vaccine Symptom
Check
Official Information request - Informed Consent #15 - New Information from
Pfizer
Official Information request - Informed Consent #17 - New list of adverse
events
Official Information request - Informed Consent #19 - Pfizer drug
interactions
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)
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Ngā mihi
OIA Services
Government Services
Office of the Director-General
Ministry of Health
E: [3][email address]
-----Original Message-----
From: Annie Weston <[FOI #17819 email]>
Sent: Friday, 3 December 2021 5:27 pm
To: OIA Requests <[email address]>
Subject: Re: Official Information request - Informed Consent #12 - Adverse
Effects Reporting
Dear Ministry of Health & OIA Requests,
It is a simple question on your policy - it does not require opinion,
comment, argument, or a hypothetical statement.
I simply want to know why the Govt does not require anyone to report
adverse effects from taking the vaccines.
Yours faithfully,
Annie Weston
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From: OIA Requests
Kia ora Annie
Please find a request from the Ministry of Health to rescope your
consolidated requests.
Ngā mihi
OIA Services
Office of the Director-General | Ministry of Health
E: [1][email address]
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From: OIA Requests
Kia ora Annie
Please find attached a response to your request 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.
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Report this requestAct on what you've learnt
Similar requests
Informed Consent #29 - When did the PM receive the post-marketing info from Pfizer
To Department of the Prime Minister and Cabinet by Annie Weston
victor left an annotation ()
As you are gaining from the responses to your OIA requests, Annie.
- MOH and medsafe are misinformation
- Nobody in NZ will be held responsible or accountable because 'they are following orders' from offshore
- 'Idependent' means conflicted
- Coincidental doesn't extend to those that have died or suffered severe ill health event while in a waiting facility to be injected because there aren't any
MOH and medsafe are using corporate defined frameworks for which they will not publish the top to bottom process for while repeatedly refusing to provide the risk analysis in age and specialist group stratified format
They are hiding the contract hiding the ingredients and hiding the risks profile while mandating the product destroying countless lives in a myriad of ways
Of course they are 'minimizing' the serious adverse events including death behind the imported guidance the people involved know they are, and that is now undeniable in the data collected during 2021
What would be the incentive of anyone involved in the disaster to speak up as opposed to the incentive not to do so?
Medsafe MOH parliament are all part of the industry following industry directives.
Thousands of deaths in the observed group are dismissed behind unpublished calculations and formulas , it all follows the same patterns while peoples lives are ruined and ended
Thousands of deaths are now recorded as 'monitored' as are tens of thousands of serious adverse events due underrporting factor which is also unpublished but exists.
Link to this