A federal judge in Texas ordered the Food and Drug Administration to make public the data it relied on to license Pfizer’s COVID-19 vaccine.
It is the first time the public are allowed to access the data Pfizer submitted to FDA from its clinical trials in support of a COVID-19 vaccine license.
When Pfizer applied for FDA approval, they were aware of almost 158,000 adverse events from their vaccine and requested these documents remain sealed for 75 years.
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