“These providers failed Missouri’s children when they rejected even a diluted medical standard and subjected them to irreversible procedures. My office is not standing for it," says Missouri AG.
Neuralink has received the green light to initiate recruitment for its inaugural human clinical trial, dubbed the PRIME Study (Precise Robotically Implanted Brain-Computer Interface).
A panel from the Food and Drug Administration (FDA) unanimously decided that the ingredient phenylephrine is not effective in relieving cold and flu symptoms.
“FDA’s intentional withholding of information relating to the safety of the COVID-19 vaccines is outrageous and shows a complete disregard for the health and safety of the American people," says Wisconsin senator.
The Federal Court ruled last week that the U.S. Food and Drug Administration (FDA) abused its authority under law when advising Americans to stop using Ivermectin as a treatment for COVID.
Judicial Watch released a number of records last week revealing Pfizer tested the safety and efficacy of the COVID vaccine booster on only 23 people before it asked the FDA to approve the shots.
