Dear colleagues, health professionals!
I know that this is a hot topic at the moment, but as a pharmacist with some (albeit a bit dusty) knowledge of safety protocols for the approval of new medicines, I am forced to respond.
It is clear to me that you as pharmacists, as opposed to politicians, make a significant distinction between an authorised medicine and a conditionally authorised medicine. All "covid" vaccines have only conditional marketing authorisation in the EU. For full approval, the marketing authorisation holders have to supply the conclusions of many studies still in progress, which will be individually evaluated in months or years!
Just to illustrate:
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