FOI release

Freedom of Information request

Case reference FOI2024/00560

Received 19 September 2024

Published 29 October 2024

Request

As per Freedom of Information Act, I request details of the three batch numbers that appear most often in the Adverse Drug Reaction (ADR) reports, including those with a fatal outcome, reported to the Yellow Card scheme in association with the COVID-19 Pfizer/BioNTech Vaccine, COVID-19 Vaccine AstraZeneca, COVID-19 Vaccine Moderna and GSK/Sanofi VidPrevtyn Beta vaccine, including separate aggregated tables for patient age and patient sex, for all the three batches combined, for each of the four COVID-19 vaccines requested, up to the date of this email which is 19/9/2024

Response

see attached

Documents

This is Medicines and Healthcare products Regulatory Agency's response to a freedom of information (FOI) or environmental information regulations (EIR) request.

You can browse our other responses or make a new FOI request.