FDA Panel Recommends Approval of Moderna Virus Vaccine for Emergency Use
A U.S. Food and Drug Administration (FDA) advisory panel on Thursday voted to recommend the emergency use approval of the Moderna vaccine.
A U.S. Food and Drug Administration (FDA) advisory panel on Thursday voted to recommend the emergency use approval of the Moderna vaccine.
Workers at Pfizer’s Michigan headquarters paused for a moment and erupted into a round of applause early Sunday morning as the first shipments of the coronavirus vaccine were being moved to a loading dock.
The CDC warned Wednesday that the Chinese coronavirus would make the next few months “the most difficult” in U.S. “public health history.”
The Food and Drug Administration (FDA) approved Eli Lilly’s coronavirus antibody treatment for emergency use.
The U.S. Food and Drug Administration (FDA), overcoming the White House’s initial opposition, released new safety guidelines Tuesday for drugmakers working for months on developing a Chinese virus vaccine. The move could prevent or delay introducing a potentially safe and effective final product before Election Day and beyond.
More than 90 members of Congress have written to Food and Drug Administration (FDA) Commissioner Stephen Hahn, urging him to classify the abortion drug Mifeprex (mifepristone) as a “hazard” or “threat of danger” in order to have it removed from the U.S. market.
“The deep state, or whoever, over at the FDA is making it very difficult for drug companies to get people in order to test the vaccines and therapeutics,” Trump wrote on Twitter, specifically calling out FDA administrator Dr. Stephen Hahn.
A parasite linked to bagged salad mixes has sickened 641 people in 11 states, federal health officials said Friday.
The Food and Drug Administration (FDA) has put out a warning about nine potentially harmful hand sanitizers made in Mexico that contain a toxic ingredient.
The U.S. Food and Drug Administration (FDA), citing the latest science and data, rescinded its emergency use authorization (EUA) for chloroquine and hydroxychloroquine, the anti-malaria drugs touted by President Donald Trump and some doctors to combat the Chinese coronavirus.
The American Civil Liberties Union (ACLU) filed a federal lawsuit Wednesday challenging a Food and Drug Administration (FDA) rule that requires women to have an in-person clinic visit in order to obtain drugs to induce an abortion.
The acting CEO of Planned Parenthood said the “silver lining” of the pandemic is that her abortion chain has used telehealth technology to provide drug-induced, at-home abortions.
The U.S. Food and Drug Administration (FDA) issued an emergency use authorization on Friday for a blood purification treatment for coronavirus patients with confirmed or imminent respiratory failure.
Food and Drug Commissioner (FDA) Commissioner Stephen Hahn said on Tuesday that serological tests could help determine who is no longer “susceptible” to coronavirus infection and who can return to work.
The Food And Drug Administration (FDA) issued an emergency authorization Sunday for hydroxychloroquine, a drug already used to treat malaria and other ailments, which has shown anecdotal efficacy against coronavirus.
Centers for Medicare and Medicaid Services (CMS) Administrator and White House coronavirus task force team member Seema Verma told Breitbart News Daily how America can “overcome” the coronavirus and what the Donald Trump administration is doing to help Americans throughout the crisis.
Studies are showing malaria drug chloroquine can both “prevent and treat coronavirus” in the cells of primates, but it is not FDA-approved for COVID-19.
Sen. Marsha Blackburn (R-TN) has pushed for the Trump administration to enact reforms that would expand access to telehealth, thus protecting Americans from exposure to the coronavirus.
A Utah-based diagnostic testing company claimed Monday that it has the resources to produce 50,000 Chinese coronavirus tests daily.
India, the world’s leading supplier of generic drugs, is cutting down exports of vital medicines and ingredients due to supply shortages amid the growing Chinese coronavirus threat.
Sen. Josh Hawley (R-MO) introduced the Medical Supply Chain Security Act on Thursday to combat potential American drug shortages created in the wake of the coronavirus outbreak in China and to reveal America’s reliance on Chinese manufacturing of pharmaceuticals and medical devices.
The Centers for Disease Control and Prevention (CDC) is warning consumers of an E. coli outbreak linked to salad sold in three states and Canada.
Nestlé USA announced a recall of its ready-to-bake refrigerated cookie dough on Thursday, due to the possible presence of food-grade rubber pieces.
CVS Pharmacy has pulled Zantac from its shelves due to a concern that the medication might contain a substance that causes cancer, reports said.
A European doctor who supplies drugs for inducing abortion to American women online has filed a lawsuit against the Food and Drug Administration (FDA).
The U.S. Food and Drug Administration released a list of dog food brands Thursday that could potentially lead to canine heart disease.
A Kellogg’s worker was handed a ten-month prison sentence for urinating on a conveyor belt filled with Rice Krispies cereal at a Memphis plant
Florida Gov. Ron DeSantis continues to push a bill that would make it easier to import prescription drugs from Canada despite concerns over increased fraud that might come with the bill; one advocate for the bill has faced accusations of faking prescriptions.
The Obama-appointed director of the National Institutes of Health (NIH) says that human fetal tissue from elective abortions “will continue to be the mainstay” for federal research.
The National Institutes of Health (NIH) — part of the Department of Health and Human Services (HHS) — announced Monday it would be seeking to find and develop human tissue models that do not rely on the use of aborted fetal tissue.
Rene Craighead blames her daughter’s cholecystectomy on the multiple bags of “hot” snack foods she consumed every week.
Thirty-five people in nine states have fallen ill with salmonella poisoning caused by contaminated eggs, prompting authorities to recall more than 207 million eggs.
The House has scheduled a vote for Tuesday on the “Right to Try Act,” which would enable sick patients to try medical treatments not yet approved by the Food and Drug Administration (FDA).
The U.S. Food and Drug Administration (FDA) is warning dog owners that store-bought bone treats can kill their four-legged companions.
The pharmaceutical industry, which has financially backed Luther Strange’s political career, doesn’t care about whether Americans become addicted to dangerous prescription painkillers, charged Breitbart News reporter Aaron Klein in a radio segment.
NEW YORK — During a period he served as Alabama Attorney General, Luther Strange received more campaign contributions than any other U.S .attorney general from members of a controversial lobby group peddling the dangerous prescription pain medication business amid an ongoing opioid crisis in Alabama.
The National Institutes of Health (NIH) is spending roughly $200,000 to study tweets about electronic cigarettes.
Texas public health officials issued an advisory this week following a spike in the number of cases of a parasitic foodborne intestinal illness often linked to the consumption of imported produce tainted with human fecal matter.
The Food and Drug Administration banned 19 chemicals used in antibacterial soaps, saying that companies have failed to prove they are safe and effective.
The U.S. Food and Drug Administration recently gave clearance to an Israeli-developed contact lens used to treat corneal edema, a painful eye condition commonly caused by eye surgery, trauma, or aging.