Adverse reactions to Seasonal Flu Vaccine. Enzira/ Pfizer from 2008-2018

R Legal made this Rhyddid Gwybodaeth request to Medicines and Healthcare Products Regulatory Agency

This request has been closed to new correspondence from the public body. Contact us if you think it ought be re-opened.

Roedd y cais yn llwyddiannus.

Dear Medicines and Healthcare products Regulatory Agency,

Please provide details of adverse reactions to influenza vaccines from Pfizer/ Enzira from 2008 -2018.

Yours faithfully,
R Legal

MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

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MHRA Customer Services, Medicines and Healthcare Products Regulatory Agency

Dear Enquirer,

Thank you for your email which we have referred onward for consideration. We will respond to you as soon as possible.
The reference number for your enquiry is GCEP-00130022; please quote this number in any future correspondence on this matter.
Our maximum response time is 18 working days, but the vast majority of our enquiries are responded to before this time.

Kind Regards,
 
Yvonne Smith
Customer Services
Communications division
Medicines and Healthcare Products Regulatory Agency
10 South Colonnade, Canary Wharf, London  E14 4PU
Telephone: 020 3080 6000
Email: [MHRA request email]
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Yellow Card Mailbox, Medicines and Healthcare Products Regulatory Agency

3 Atodiad

Dear R Legal,

Thank you for your enquiry, please see the attached documents.

Kind Regards

Vigilance and Risk Management of Medicines Division
Medicines and Healthcare Products Regulatory Agency
10 South Colonnade, Canary Wharf, London E14 4PU
Email: [email address]
Stay connected: mhra.gov.uk/stayconnected

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Have you done our new 45 minute e-learning module on ADRs for doctors (CPD accredited) and healthcare professionals?

Seen our animation? www.youtube.com/watch?v=3et5LdYLc8M
Share it on social media to help MHRA raise awareness about reporting suspected adverse drug reactions (ADRs) to the Yellow Card Scheme.

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