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Adverse drug reactions for AstraZeneca COVID-19 vaccine(s)

Aiden Chang made this Freedom of Information request to Medicines and Healthcare Products Regulatory Agency

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Dear Medicines and Healthcare products Regulatory Agency,

To define the terms of this request:

1. "Inoculations" refers to presently recorded number of AstraZeneca COVID-19 inoculations of members of the public, outside of clinical trials

2. "ADR types" refers to the adverse drug response type, immunologic and non-immunologic, and sub-types of both types

3. "Data" refers to a raw table of official un-adjusted aggregate numbers of the requested information recorded by the government agency, not sourced from non-government bodies

I hereby request the Data of Inoculations, including the months of December 2020 thru March 2021, categorized by ADR type and month.

Data is to be gathered from the United Kingdom, unless the MHRA holds government-recorded Data from identical agencies in other countries.

In the latter case, a table is of Data is to be provided for each country, in addition to the United Kingdom.

Yours faithfully,
Aiden Chang

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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References

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1. https://www.gov.uk/government/collection...

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Our Ref: FOI 21/384

Dear Aiden Chang,

RE: REQUEST UNDER THE FREEDOM OF INFORMATION ACT 2000

Thank you for your enquiry which we received on 9 April 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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Pharmacovigilanceservice, Medicines and Healthcare Products Regulatory Agency

1 Attachment

Dear Mr Chang,

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

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