A new document from the Minnesota Department of Health titled “Ethical Framework for Allocation of Monoclonal Antibodies during the COVID-19 Pandemic” indicates that people of color get priority over others looking to get an antibody treatment.
Later this week, the FDA plans to approve, as the first outpatient COVID drugs, therapeutics that are extremely dangerous and unproven, even as the agency goes to war against cheap, safe, and proven drugs with a track record of no serious adverse events.
Epidemiologist compiles massive trove of research studies demonstrating "that Covid-19 lockdowns, shelter-in-place policies, masks, school closures, and mask mandates have failed in their purpose of curbing transmission or reducing deaths."
In an exclusive interview with The Defender, Dr. Paul Marik said patients are dying “unnecessarily and unlawfully” because the hospital where he is director of the ICU prioritizes expensive drugs like Remdesivir while banning more effective and less costly treatments.
X-Outloud is a growing network across Europe of people who are no longer LGBT and a collection of their testimonies can be found in the ministry's new book.
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.
Melissa Strickler, who previously worked for Pfizer as a quality inspector for 10 years, is blowing the whistle on how the brand's COVID vaccine has some toxic ingredients that make it "glow." These ingredients, however, are not in the label.
"One or more cell lines with an origin that can be traced back to human fetal tissue has been used in laboratory tests associated with the vaccine program."
