“Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritised the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity.”

From the leaked Pfizer trials documents showing they knew their product killed and seriously injured people.

Not only did the company know, but every regulatory advisory body that approved them also saw those documents and still went ahead, including the EMA where the data hack happened.

This should be front page news across every media platform in the world, shouldn’t it?

Link to all documents are below, the one you really want is 5.3.6 – ‘postmarketing experience’.

• Darren Smith xxx

@TheLightTruthPaper