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Questions re vaccines

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Dear Medicines and Healthcare Products Regulatory Agency,

Some further questions I require answers to:

1. In what way are the MHRA hoping to update the Reporting system? Please can you give an account of what the changes will be and what their purpose is?

2. Will the new database used in future ensure that an analysis of the vaccine safety data will be regularly passed to the public?

3. Do the MHRA follow up on all reports to the Adverse Events database? If not what percentage of Reports do they follow up on?

4. Why is the only contraindication to receiving a vaccine anaphylaxis to previous vaccine of same type? Surely if one has had an adverse reaction of a somewhat serious nature to a coronavirus vaccine one ought to be at liberty to be exempt from further vaccines at all?

5. Please provide the exact breakdown of ingredients in each vaccine not just an 'it contains' or 'it includes' list ie list all excipients for all vaccines currently available in the UK.

6. If someone has had a severe adverse reaction to ANY vaccine in their lifetime surely it is reasonable for them to claim exemption from a coronavirus vaccine? If not please explain why not.

7. If a vulnerable person is not a meat eater and does not eat GMO products and does not have capacity why does it appear that you would support legislation/ judicial decisions to force them to receive an injection containing GMO organisms and foetal matter and monkey cell lines?

Yours faithfully,
s.o'donnell

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Thank you for your email.  This auto-response is to inform you that your
email has been received and will be reviewed by our Customer Service Team.
We will respond to you as soon as possible. 
 
Please note that we may not respond if your query: 
 
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• is illegible
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• is for information only 
 
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, 
Canary Wharf, 
London 
E14 4PU
gov.uk/mhra
Stay connected 
 
For information on how the Agency uses your personal data and your data
protection rights, please see our three centres’ Privacy Notices: MHRA,
CPRD and NIBSC. 
 
The UK has left the EU, and the transition period ends on 31 December
2020. Ourguidance and information can be accessed here.

________________________________________ From: Sally Anne
<[FOI #814446 email]> Sent: Tuesday, December 7,
2021 6:11:22 PM To: MHRA Customer Services Subject: Freedom of Information
request - Questions re vaccines Dear Medicines and Healthcare Products
Regulatory Agency, Some further questions I require answers to: 1. In what
way are the MHRA hoping to update the Reporting system? Please can you
give an account of what the changes will be and what their purpose is? 2.
Will the new database used in future ensure that an analysis of the
vaccine safety data will be regularly passed to the public? 3. Do the MHRA
follow up on all reports to the Adverse Events database? If not what
percentage of Reports do they follow up on? 4. Why is the only
contraindication to receiving a vaccine anaphylaxis to previous vaccine of
same type? Surely if one has had an adverse reaction of a somewhat serious
nature to a coronavirus vaccine one ought to be at liberty to be exempt
from further vaccines at all? 5. Please provide the exact breakdown of
ingredients in each vaccine not just an 'it contains' or 'it includes'
list ie list all excipients for all vaccines currently available in the
UK. 6. If someone has had a severe adverse reaction to ANY vaccine in
their lifetime surely it is reasonable for them to claim exemption from a
coronavirus vaccine? If not please explain why not. 7. If a vulnerable
person is not a meat eater and does not eat GMO products and does not have
capacity why does it appear that you would support legislation/ judicial
decisions to force them to receive an injection containing GMO organisms
and foetal matter and monkey cell lines? Yours faithfully, s.o'donnell
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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 21/1319

Dear S.O'Donnell,

RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000

Thank you for your enquiry which we received on 8 December 2021.

I confirm that your request is now being handled under the Freedom of Information Act and you should receive a reply within 20 working days from our date of receipt.

If you need to contact us again about this request, please quote the reference number above.

Please be aware that we publish FOIs replies and these are redacted and are located on our website at the following link below.
https://www.gov.uk/government/collection...

Kind Regards,

MHRA Customer Service Centre

Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU Telephone 0203 080 6000

show quoted sections

Dear MHRA Customer Services,

by law, the authority should normally have responded promptly and by 7 January 2022

Yours sincerely,

Sally Anne

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Thank you for your email.  This auto-response is to inform you that your
email has been received and will be reviewed by our Customer Service Team.
We will respond to you as soon as possible. 
 
Please note that we may not respond if your query: 
 
• contains offensive language
• has already been answered in a previous reply to you
• is illegible
• is selling or promoting a product
• is for information only 
 
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, 
Canary Wharf, 
London 
E14 4PU
gov.uk/mhra
Stay connected 
 
For information on how the Agency uses your personal data and your data
protection rights, please see our three centres’ Privacy Notices: MHRA,
CPRD and NIBSC. 
 
The UK has left the EU, and the transition period ends on 31 December
2020. Ourguidance and information can be accessed here.

________________________________________ From: Sally Anne
<[FOI #814446 email]> Sent: Saturday, January 8,
2022 9:07:27 AM To: MHRA Customer Services Subject: Internal review of
Freedom of Information request - Questions re vaccines Dear MHRA Customer
Services, by law, the authority should normally have responded promptly
and by 7 January 2022 Yours sincerely, Sally Anne -----Original
Message----- Our Ref: FOI 21/1319 Dear S.O'Donnell, RE: REQUEST UNDER THE
FREEDOM OF INFORMATION ACT 2000 Thank you for your enquiry which we
received on 8 December 2021. I confirm that your request is now being
handled under the Freedom of Information Act and you should receive a
reply within 20 working days from our date of receipt. If you need to
contact us again about this request, please quote the reference number
above. Please be aware that we publish FOIs replies and these are redacted
and are located on our website at the following link below.
https://eur01.safelinks.protection.outlo...
Kind Regards, MHRA Customer Service Centre Medicines and Healthcare
products Regulatory Agency 10 South Colonnade, Canary Wharf, London E14
4PU Telephone 0203 080 6000
------------------------------------------------------------------- Please
use this email address for all replies to this request:
[FOI #814446 email] Disclaimer: This message and
any reply that you make will be published on the internet. Our privacy and
copyright policies:
https://eur01.safelinks.protection.outlo...
For more detailed guidance on safely disclosing information, read the
latest advice from the ICO:
https://eur01.safelinks.protection.outlo...
Please note that in some cases publication of requests and responses will
be delayed. If you find this service useful as an FOI officer, please ask
your web manager to link to us from your organisation's FOI page.

show quoted sections

Pharmacovigilanceservice, Medicines and Healthcare Products Regulatory Agency

1 Attachment

Dear Ms O'Donnell,

Please find attached the response to your FOI request.

Kind regards,

FOI Team
Vigilance and Risk Management of Medicines Division
Medicines and Healthcare Products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU

show quoted sections

We don't know whether the most recent response to this request contains information or not – if you are Sally Anne please sign in and let everyone know.