Did Pfizer Do Any Safety Studies for mRNA Injections?
A pharmaceutical data analyst dove into the Pfizer preclinical studies released by the FDA. This is what she found.
A pharmaceutical data analyst dove into the Pfizer preclinical studies released by the FDA. This is what she found.
The Food and Drug Administration (“FDA”) has released Pfizer’s report on adverse events to its Covid injection for the first two-months and 12 days since post-emergency authorisation. Over this period Pfizer had received more than 42,000 reports, mostly from the United States. Almost 30,000 of these adverse event reports were from women and 26,000 related to nervous system disorders.
Maddie De Garay was 12 when she enrolled (along with her 2 older brothers) in the Pfizer Phase 3 Trial for Kids, and was Paralyzed for life. She’s 13 years old now and 9 months later, Maddie’s mum Stephanie gives an update warning parents “if this happens to your child – you are on your own – doctors, pharmaceutical companies, and the government will not help you”.
So remember how Pfizer & the FDA blocked a FOI request and requested from the courts to delay handing over documents that the FDA used to approve it… that it would take them over half a century (2076) to fulfil the request? Here’s the first batch of released pages (only 54 years, 11 months to go…)