Kennedy says FDA is reviewing safety of abortion pill mifepristone
Conservatives have criticized the abortion medication, particularly after it became available through telehealth.
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Conservatives have criticized the abortion medication, particularly after it became available through telehealth.
President Trump's announcement this week about an alleged link between Tylenol and autism has drawn pushback from medical experts.
Health Secretary Robert F. Kennedy Jr. has launched an FDA review of mifepristone, the drug used in two-thirds of all abortions. Abortion rights advocates are worried the FDA could restrict access to the pill even in states where abortion is legal. Dr. Celine Gounder explains.
President Trump's warning about Tylenol use during pregnancy, claiming it's linked with an increased risk of autism, rattled the medical community and is getting major pushback. Jericka Duncan has more.
The Food and Drug Administration is looking to shift away from policies dating back decades of having outside experts and panels review new drug applications. These external committees have been used since the 1970s in order to better advise health officials facing difficult decisions. Arthur Allen, senior correspondent for KFF Health News, joined CBS News to discuss.
Advisory committee meetings help FDA scientists make decisions and increase public understanding of drug regulation, and abandoning them doesn't make sense, former officials said.
President Trump ordered the FDA to enforce rules on direct-to-consumer drug ads, after HHS Secretary Robert F. Kennedy Jr. released a report on the administration's approach to healthy outcomes for children and families.
Earlier this week, a European Union ban on an ingredient widely used in many gel nail polishes went into effect. The chemical known as TPO gives gel polish a glossy shine as it quickly hardens under UV or LED lights. TPO has not been banned in the U.S. Kelly Dobos, a cosmetic chemist at the University of Cincinnati, joins "The Daily Report" to discuss.
Health and Human Services Secretary Robert F. Kennedy Jr. appeared before the Senate Finance Committee on Thursday to discuss President Trump's "Make America Healthy Again" agenda. CBS News' Nikole Killion reports and disease expert Dr. Michael Osterholm joins "The Takeout" to discuss.
The Food and Drug Administration authorized updated COVID-19 vaccines on Wednesday, but the agency has limited who is allowed to get the shots.
The Food and Drug Administration rescinded the emergency use authorization that made COVID-19 shots available for healthy children under 5 years old.
There's a growing concern about kratom, a southeast Asian plant that has made its way into everything from diet supplements, alcohol and even synthetic drugs. Lilia Luciano reports.
Some packages of Great Value frozen shrimp sold at Walmart are at risk for potential for Cesium-137 contamination, the FDA says.
Mousse sunscreens made by Supergoop!, Vacation and others pose risk to consumers, FDA says.
Wegmans is recalling its brand of medium camembert cheese and products that contain it due to potential listeria contamination, which can lead to serious illness.
DermaRite Industries announced on Friday that it was voluntarily recalling three skin-cleansing products and an anti-itch lotion over microbial contamination concerns.
Found in a variety of products, the supplement known as kratom is currently banned in six states and Washington, D.C., as it faces scrutiny over addiction concerns.
In a Phase 3 trial, drugmaker Eli Lilly and Company said it's oral GLP-1 pill showed similar results to injectable weight loss options after a 72-week period.
Beverage brand High Noon is recalling some of its beach variety packs due to some cans being mislabeled as non-alcoholic Celsius energy drinks.
Dr. Vinay Prasad had been serving as the FDA's director of the Center for Biologics Evaluation and Research since May, and was later named chief medical and scientific officer.
FDA regulators said Juul's studies show its e-cigarettes are less harmful for adult smokers, who can benefit from switching completely to vaping.
More than 67,000 cases of Power Stick deodorant were recalled over manufacturing defects, according to the FDA.
Plastic pieces were discovered in the dome toppers of YoCrunch products, the FDA said in a recall alert.
The U.S. Food and Drug Administration approved a new blue color additive derived from the fruit of the gardenia, a flowering evergreen, for use in a variety of drinks and candies.
Several lots of Hartford Bakery, Inc.'s "Lewis Bake Shop Artisan Style 1/2 Loaf" may contain undeclared hazelnuts, the company said.