Risk Management Plan
Virginia Crawford made this Official Information request to Ministry of Health
Response to this request is long overdue. By law Ministry of Health should have responded by now (details and exceptions). The requester can complain to the Ombudsman.
From: Virginia Crawford
Dear Ministry of Health,
Your Risk Management Plan mentioned the following "missing information"
Use in pregnancy and while breast feeding
Use in immunocompromised patients
use in frail patients with co-morbidities
use in patients with autoimmune or inflammatory disorders
interaction with other vaccines
Could you please provide an update on each of the above? Is that information coming solely from Pfizer or are other sources included?
What information do you have regarding VAED/VAERD?
Yours faithfully,
Virginia Crawford
From: OIA Requests
Kia ora
Please find attached a letter regarding your request for information.
Ngā mihi
OIA Services
Government Services
Office of the Director-General
Ministry of Health
E: [1][email address]
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From: Virginia Crawford
Dear OIA Requests,
Please supply in full any further information you have regarding the "missing information" or any other similar matters arising from the Risk Management Plan, in accordance with the latest MARC committee meeting minutes.
https://medsafe.govt.nz/profs/adverse/Mi... (3rd May 2021)
Yours sincerely,
Virginia Crawford
From: OIA Requests
Kia ora Virginia Crawford,
Thank you for your request for official information received 14 June 2021
for:
"Please supply in full any further information you have regarding the
"missing information" or any other similar matters arising from the Risk
Management Plan, in accordance with the latest MARC committee meeting
minutes".
The Ministry's reference number for your request is: H202107138
As required under the Official Information Act 1982 we will endeavour to
respond to your request no later than 15 July 2021, being 20 working days
after the day your request was received.
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 Team
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From: Virginia Crawford <[FYI request #15189 email]>
Sent: Sunday, 13 June 2021 13:11
To: OIA Requests <[email address]>
Subject: Re: Your request for information - H202104627
Dear OIA Requests,
Please supply in full any further information you have regarding the
"missing information" or any other similar matters arising from the Risk
Management Plan, in accordance with the latest MARC committee meeting
minutes.
[1]https://medsafe.govt.nz/profs/adverse/Mi... (3rd
May 2021)
Yours sincerely,
Virginia Crawford
-----Original Message-----
Kia ora
Please find attached a letter regarding your request for information.
Ngā mihi
OIA Services
Government Services
Office of the Director-General
Ministry of Health
E: [1][email address]
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From: OIA Requests
Kia ora Virginia,
Please find attached a letter regarding your request for information.
Ngā mihi
OIA Services
Government Services
Office of the Director-General
Ministry of Health
E: [1][email address]
****************************************************************************
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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From: Virginia Crawford
Dear OIA Requests,
Given the seriousness of the situation and the alarming number of adverse reactions and deaths reported around the world, it is essential that you follow up with Pfizer on the outstanding information. Please confirm that you will be doing this and reporting the results as appropriate,
Yours sincerely,
Virginia Crawford
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Virginia Crawford left an annotation ()
One would have thought that a request to the vaccine company for further information would have been obligatory, as the missing information is absolutely CRUCIAL.
Two requests have been merged into one, for the second one, see below:
Answering the question as to why the Ministry has made a decision which is contrary to ordinary common sense is apparently not part of its remit.
Link to this