FDA

At the request of the Nebraska Department of Health, on Oct. 15, Nebraska Attorney General Doug Peterson issued a legal opinion that Nebraska healthcare providers can legally prescribe ivermectin and hydroxychloroquine for the treatment of COVID, so long as they obtain informed consent from the patient.

A tale of two drugs. One has become the standard of care at an astronomical cost despite studies showing negative efficacy, despite causing severe renal failure and liver damage, and despite zero use outpatient. The other has been safely administered to billions for river blindness and now hundreds of millions for COVID throughout the world and has turned around people at death's doorstep for pennies on the dollar.

(Information Liberation) The FDA approved the rollout of Moderna mRNA booster shots based off "a gut feeling" rather than any "really truly serious data,"...

The U.S. Food and Drug Administration announced Friday it would delay its decision on administration of the Moderna vaccine to adolescents, citing concerns the shot may lead to a heightened risk of a rare heart condition.

VAERS data released Friday by the CDC included a total of 798,636 reports of adverse events from all age groups following COVID vaccines, including...

There is a massive propaganda push against those choosing not to vaccinate against COVID-19 with the experimental mRNA vaccines. Mainstream media, the big tech...

FDA notes lack of data regarding Moderna's booster vaccine "[u]se in pregnancy and while breastfeeding, long term safety, use in immunocompromised subjects, interaction with other vaccines, use in frail subjects and unstable health conditions and comorbidities, and use in subjects with autoimmune or inflammatory disorders."

Merck made headlines in early October when it announced the trial results of a newly developed antiviral pill that effectively reduced the risk of hospitalization and death by up to 50%.

Gupta admits he did not perform his job duties as CNN's health expert

Senators Kim Thatcher and Dennis Linthicum have gathered thousands of signatures to support their petition to launch a grand jury investigation into the Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration's (FDA) methods of measuring COVID statistics.