Adverse Effects of Covid "Vaccination"
Dear Medicines and Healthcare Products Regulatory Agency,
I too would like an answer to the points brought up in this letter. https://alethonews.com/2022/03/05/the-de...
The reported adverse effects is unprecedented at way nearly 1.5 million from the "vaccines". In particular the number of miscarriages and stillbirths is very worrying.
1. Is there recorded date to show that Dame June Raine, as CEO of the MHRA, and hence ultimately responsible for its decisions, is fully aware of the data recorded on the Yellow Card system in relation to the Covid-19 vaccines?
2. Is there any recorded data to show whether Dame June Raine consider it necessary to present the public with a full written analysis of the 1,458,428 adverse events relating to the Covid-19 vaccines which are recorded by the Yellow Card system.
3. Is there any recorded data to show that Dame June Raine does not consider the 1,458,428 adverse events recorded by the Yellow Card system serious enough to warrant immediate withdrawal of the Covid-19 vaccines.
4. Please give the duties and obligations of MHRA and what kind of entity it is,a nd when it started
Yours faithfully,
Barbara Jones
Our Ref: FOI 22/521
Dear Barbara Jones,
RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000
Thank you for your enquiry which we received on 7th March 2022.
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 Experience Centre
Communications and engagement team
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU
Telephone 020 3080 6000
Dear MHRA Customer Services,
You have failed to carry out your duty under the FOI Acts by a long way. Due to this long delay, failure to reply substantively in 3 working days will now result in a complaint to the ICO
Yours sincerely,
Barbara Jones
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: Barbara Jones
<[FOI #840956 email]> Sent: Thursday, April 28,
2022 8:21:51 PM To: MHRA Customer Services Subject: Re: FOI 22/521 - RE:
Freedom of Information request - Adverse Effects of Covid "Vaccination"
Dear MHRA Customer Services, You have failed to carry out your duty under
the FOI Acts by a long way. Due to this long delay, failure to reply
substantively in 3 working days will now result in a complaint to the ICO
Yours sincerely, Barbara Jones -----Original Message----- Our Ref: FOI
22/521 Dear Barbara Jones, RE: REQUEST UNDER THE FREEDOM OF INFORMATION
ACT 2000 Thank you for your enquiry which we received on 7th March 2022. 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 Experience Centre Communications and
engagement team Medicines and Healthcare products Regulatory Agency 10
South Colonnade, Canary Wharf, London E14 4PU Telephone 020 3080 6000
------------------------------------------------------------------- Please
use this email address for all replies to this request:
[FOI #840956 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...
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.
Dear Ms Jones,
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
Dear Pharmacovigilanceservice,
Thankyou for your reply.
However my request was made on 6 March 2022. The reply was made on 24 May 2022. No explanation is given nor even an apology. Please explain the delay which is a failing of duty to comply with the FOI Acts,
My questions were...
I too would like an answer to the points brought up in this letter. https://alethonews.com/2022/03/05/the-de...
1. Is there recorded data to show that Dame June Raine, as CEO of the MHRA, and hence ultimately responsible for its decisions, is fully aware of the data recorded on the Yellow Card system in relation to the Covid-19 vaccines?
2. Is there any recorded data to show whether Dame June Raine consider it necessary to present the public with a full written analysis of the 1,458,428 adverse events relating to the Covid-19 vaccines which are recorded by the Yellow Card system.
3. Is there any recorded data to show that Dame June Raine does not consider the 1,458,428 adverse events recorded by the Yellow Card system serious enough to warrant immediate withdrawal of the Covid-19 vaccines.
4. Please give the duties and obligations of MHRA and what kind of entity it is, and when it started
Question 4 was answered adequately, an attempt made was made at addressing the points in the letter, however there is no way on earth that these vaccines can be described as safe and effective and that is confirmed by the data released from Pfizer via the court case against the FDA in the USA.
However on questions that I labelled 1, 2,3 you have replied with "proof" (a recent email from Dr Raine, clearing the report for publication) written after the request. That of course is not how FOI works, and anything after the request could be written in reaction to the request.
Please therefore reply with actual recorded data from before my request date for questions 1,2,3 .
If this means an internal review on the whole request, so be it.
Yours sincerely,
Barbara Jones
Thank you for your email.
The Pharmacovigilance Service Team will aim to provide a response to your
query within seven working days – however where a contribution from a
specialist is required this may take longer; we endeavour to respond to
all requests within ten working days.
If you have not received a response within 10 working days, please feel
free to follow up via email.
If you are unsatisfied with the handling of your request, or for any
urgent matters, please contact the Service Team Manager Faiza Farooq on
0203 080 6511
All information provided is handled in line with our privacy policy, which
can be viewed on our website at
https://www.gov.uk/government/publicatio....
Kind Regards,
Pharmacovigilance Service Team
Vigilance and Risk Management of Medicines
MHRA
10 South Colonnade
Canary Wharf
London
E14 4PU
DISCLAIMER This email and any files transmitted with it are confidential.
If you are not the intended recipient, any reading, printing, storage,
disclosure, copying or any other action taken in respect of this email is
prohibited and may be unlawful. If you are not the intended recipient,
please notify the sender immediately by using the reply function and then
permanently delete what you have received. Incoming and outgoing email
messages are routinely monitored for compliance with the Department of
Health's policy on the use of electronic communications. For more
information on the Department of Health's email policy, click
[1]DHTermsAndConditions
References
Visible links
1. https://www.gov.uk/help/terms-conditions
Internal Review of FOI 22/521
Dear Ms Jones,
Thank you for your email.
We confirm that an internal review will be carried out on FOI 22/521. We normally aim to respond to requests for internal review within 20 working days of receipt. However, due to high volumes of queries we are currently receiving related to COVID-19 please be aware that responses may take longer than usual.
Kind Regards
MHRA Customer Experience Centre
Communications and engagement team
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf,
London E14 4PU
Telephone 020 3080 6000
Dear MHRA Customer Services,
I have still not received the results of my internal review request. It appers tht the department is deliberately delaying. Please do your duty
Yours sincerely,
Barbara Jones
Dear MHRA Customer Services,
I have no alternative but to report your lack of replies to the ICO
Yours sincerely,
Barbara Jones
Dear Ms Jones,
Please find the attached response to your Internal Review.
Kind Regards,
MHRA Customer Service Centre
Medicines and Healthcare products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU Telephone 0203 080 6000
DISCLAIMER This email and any files transmitted with it are confidential.
If you are not the intended recipient, any reading, printing, storage,
disclosure, copying or any other action taken in respect of this email is
prohibited and may be unlawful. If you are not the intended recipient,
please notify the sender immediately by using the reply function and then
permanently delete what you have received. Incoming and outgoing email
messages are routinely monitored for compliance with the Department of
Health's policy on the use of electronic communications. For more
information on the Department of Health's email policy, click
[1]DHTermsAndConditions
References
Visible links
1. https://www.gov.uk/help/terms-conditions
We work to defend the right to FOI for everyone
Help us protect your right to hold public authorities to account. Donate and support our work.
Donate Now