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Yellow Card Scheme Reports re Covid-19 vaccinations

AnitaBreathe made this Freedom of Information request to Medicines and Healthcare Products Regulatory Agency This request has been closed to new correspondence. Contact us if you think it should be reopened.

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AnitaBreathe
Delivered

Dear Medicines and Healthcare Products Regulatory Agency,

Under the Freedom of Information Act, please provide the following information:

Since 8th December 2020, the date that the first covid vaccine was administered in the U.K., until 24th January 2021, how many Yellow Card Scheme reports of ADR have been reported and registered to MHRA?

Please provide
1. The total number of Yellow Card Scheme ADR reports MHRA has received during this period in regards to
a) the Pfizer-BioNTech vaccine?
b) the Oxford Astra-Zeneca vaccine?

2. A breakdown of these totals for each ADR received by MHRA during this period, by category, ie. Total number persons who reported vomiting after receiving
a) the Pfizer-BioNTech vaccine?
b) the Oxford Astra-Zeneca vaccine?

3. Total number of people who have died within 28 days of receiving
a) the Pfizer-BioNTech vaccine?
b) the Oxford Astra-Zeneca vaccine?

4. A breakdown of where these Yellow Card Scheme ADR are being reported from, and the total for each region ie. England, Scotland, Wales and NI, for
a) the Pfizer-BioNTech vaccine?
b) the Oxford Astra-Zeneca vaccine?

Yours faithfully,

Miss GB

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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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References

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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 21/095

Dear Miss GB,

RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000

Thank you for your enquiry which we received on 26 January 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.

Kind Regards,


MHRA Customer Service Centre

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

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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

FOI 21/095

Dear Miss GB,

Thank you for your email.

We can confirm that we have published the data and this is available to view at the following links of our website page below, please note this information will be published weekly moving forward:

https://www.gov.uk/government/publicatio...

https://www.gov.uk/government/publicatio...

Please find the following link below of our website page to register for our email alerting service.

https://www.gov.uk/government/organisati...

If you have a query about the information provided, please reply to this email.

If you are dissatisfied with the handling of your request, you have the right to ask for an internal review. Internal review requests should be submitted within two months of the date you receive this response and addressed to: [MHRA request email]

Due to the ongoing Covid-19 situation, we are not able to accept delivery of any documents or correspondence by post or courier to any of our offices

Please remember to quote the reference number above in any future communications.

If you were to remain dissatisfied with the outcome of the internal review, you would have the right to apply directly to the Information Commissioner for a decision. Please bear in mind that the Information Commissioner will not normally review our handling of your request unless you have first contacted us to conduct an internal review. The Information Commissioner can be contacted at:

Information Commissioner’s Office
Wycliffe House
Water Lane
Wilmslow
Cheshire
SK9 5AF

Yours sincerely

MHRA Customer Service Centre

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

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Pharmacovigilanceservice, Medicines and Healthcare Products Regulatory Agency

1 Attachment

Dear Miss GB,

Please find attached a letter for your attention.

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 

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