COVID19 efficacy/safety data

Mr D Tait a fait une demande de Accès à l'information à Agence européenne des médicaments

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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:

1- All randomised control trial data in your possession that demonstrates COVID-19 vaccines reduce deaths and hospitilisations from the disease COVID-19.

2- Total number of reports of adverse events including deaths within the EUDRA database and any other adverse events databases available for COVID-19 vaccines.

3- All documents that mention safety concerns in relation to the frequent administration of COVID-19 boosters.

Yours faithfully,

Mr D Tait

Agence européenne des médicaments

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