COVID-19 vaccine supporters are fond of sneering at public figures who have called for the Food and Drug Administration to pull or at least re-evaluate the safety of the increasingly unpopular therapeutics, such as Health and Human Services secretary nominee Robert F. Kennedy Jr., cardiologist Peter McCullough and Florida Surgeon General Joseph Ladapo.
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Healthshare Org Urges Incoming Trump Admin to Make ‘Radical’ Change to FDA, Healthcare System
Solidarity HealthShare is calling on the incoming Trump Administration to fix the “nation’s broken healthcare system” with widespread changes to the Food and Drug Administration (FDA).
Read MoreSCOTUS Refused to Ban Federal Censorship Pressure; It Could Make Churches Complicit in Abortion
When the Supreme Court reversed a preliminary injunction against several federal agencies and officials in June for “coerc[ing] or significantly encourag[ing]” tech platforms to suppress content, Washington state saw a new way to protect its mandatory abortion coverage in maternity healthcare plans from religious freedom challenges.
Five years into a lawsuit by Cedar Park Assembly of God against SB 6219, which includes criminal penalties up to prison, the Evergreen State argues that insurers won’t necessarily offer abortion-free plans if the court permanently bars it from enforcing surgical- and chemical-abortion coverage against such religious ministries that are opposed to abortion.
Read MoreLawmakers Demand Investigation into U.S. Drug Companies Who Reportedly Worked with Chinese Military
A group of bipartisan lawmakers are demanding an investigation into U.S. drug companies with reportedly troubling ties to China, according to a letter obtained by the Daily Caller News Foundation.
The lawmakers raised alarm to the Food and Drug Administration (FDA) in a Monday letter that they had identified some U.S. pharmaceutical companies as having worked with the Chinese military, raising concerns that U.S. intellectual property is being siphoned off by Beijing. The lawmakers also pointed out that several U.S. pharmaceutical companies also conducted clinical trials in the Xinjiang province of China, a region known for “genocide” against religious minorities, according to a letter sent by the lawmakers to the agency.
Read MoreFDA Knew ‘Gender Affirming’ Puberty Blockers Increase ‘Suicidality’ in 2017, Promotes Them Today
Five months before the Food and Drug Administration issued a health warning on puberty blockers widely used off-label to treat minors with gender confusion, undermining a Department of Health and Human Services office that claimed “early gender affirming care is crucial to overall health and well-being,” an FDA leader acknowledged other health concerns.
Pediatric patients exposed to “gonadotropin-releasing hormone agonists,” most with central precocious puberty (CPP) and “a handful … transgender kids using the drugs off-label,” had an “increased risk of depression and suicidality, as well as increased seizure risk,” Division of General Endocrinology clinical team leader Shannon Sullivan told colleagues.
Read MoreLouisiana Abortion Pill Reclassification Bill Heads to Governor’s Desk
The Louisiana state Senate approved a bill on Thursday that would place two abortion pills on the state’s list of controlled dangerous substances, sending the legislation to the governor’s desk for his signature.
The state’s House of Representatives passed the bill on Tuesday, which could make possession of the drugs a crime punishable by jail time or a fine. Surgical and medical abortions are already illegal in the southern state except in extreme cases, meaning it is already difficult to obtain the drugs legally. But now the possession itself without a prescription could get an individual up to five years in prison.
Read MoreFDA Threatens Endangered Species with Shoddy Abortion-Drug Reviews: Lance Armstrong Investigator
Federal public health officials created strange bedfellows among animal-welfare advocates, scientists and vaccine skeptics for allegedly cutting corners in viral and COVID-19 vaccine research and oversight, possibly engineering a pathogen, then a cure that’s worse for some.
The Food and Drug Administration may be creating another odd couple in a case at the Supreme Court: environmental and pro-life activists.
Read MoreFeds Conceal Details About Anti-Ivermectin Campaign in Response to Doctors’ Reinstated Lawsuit
The Food and Drug Administration wants to continue its selective promotion of off-label drug use: good for COVID-19 vaccines, bad for alternatives to those vaccines. It just doesn’t want the public to see its full reasoning for the latter.
The FDA and the Department of Health and Human Services filed a renewed motion to dismiss a lawsuit by doctors claiming the agencies have a practice of demonizing ivermectin by conflating its human and animal doses and using “command” language, such as “stop it,” to discourage using the anti-parasite drug against COVID.
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