COVID-19 vaccines
Dear European Medicines Agency,
Under the right of access to documents in the EU treaties, as developed in Regulation 1049/2001, I am requesting documents which contain the following information:
- Correspondence (including emails and their attachments) involving officials/representatives from the European Medicines Agency and all the national competent authorities of the Member States of the European Union (EU) and the European Economic Area (EEA) responsible for human medicines which refer to the issue of Vaxzevria (formerly COVID-19 Vaccine AstraZeneca).
- Correspondence (including emails and their attachments) involving officials/representatives from the European Medicines Agency and all the national competent authorities of the Member States of the European Union (EU) and the European Economic Area (EEA) responsible for human medicines which refer to the issue of COVID-19 Vaccine Janssen.
- Data related to the cases of unusual blood clots with low blood platelets found after the administration of any of the authorised COVID-19 vaccines in the Member States of the European Union (EU) and the European Economic Area (EEA), including information regarding gender and age of the people affected by these unusual events.
Yours faithfully,
Ángela Bernardo
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