“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.
