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

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From: OIA Requests


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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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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.

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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

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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

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

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

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From: OIA Requests


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Attachment H202107138 Response.pdf
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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]

 

 

show quoted sections

References

Visible links
1. mailto:[email address]

Link to this

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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