-
Nearly 2,000 drug plants are overdue for FDA checks after COVID delays, AP finds
U.S. health inspectors are still struggling to address a massive backlog of pharmaceutical plants that went uninspected during disruptions caused by COVID-19. That’s according to an analysis of government data by the Associated Press. The data shows roughly 2,000 drug manufacturing sites around the world have not had a Food and Drug Administration inspection for quality since before the pandemic....
-
Teen vaping hits 10-year low in US, new data show
Youth vaping levels fell to the lowest in a decade this year, according to a new report from the Centers for Disease Control and Prevention and the Food and Drug Administration.
-
Doctors soon required to tell mammogram patients about breast density
Soon, doctors must tell their mammogram patients if they have dense breast tissue, a factor that can make it harder to detect breast cancer and put them at greater risk for cancer. The Food and Drug Administration released new standards in March of 2023 in an effort to help more women detect breast cancer sooner. The FDA gave providers until…
-
What to know about a new mammogram regulation
A D.C. woman who is a two-time breast cancer survivor says for a long time she didn’t know she had dense breast tissue. A new rule aims to provide more people with the knowledge about their breast density. News4’s Aimee Cho reports.
-
FDA approves new treatment for people with hemophilia B
There’s a new hope for people living with the rare blood disorder hemophilia B. The FDA recently approved a new gene therapy treatment for those who suffer from the debilitating condition. Dave Robinson, a 61-year-old IT consultant from Falls Church, Virginia, was born with the rare genetic blood disorder caused by an insufficient level of a protein known as...
-
FDA approves new treatment for people with hemophilia B
A man from Falls Church, Virginia who was born with Hemophilia B shares his reaction towards a clinical trial for a single infusion that changed the course of his life and could help others like him. News4’s Eun Yang has the story.
-
FDA warns against smelling salts claiming to boost energy
The FDA says the unapproved drugs can have some dangerous side effects.
-
FDA rejects psychedelic MDMA as treatment for PTSD, calling for additional study
Federal health officials have declined to approve the psychedelic drug MDMA as a therapy for PTSD. Drugmaker Lykos Therapeutics announced the FDA’s decision on Friday.
-
FDA approves first nasal spray to treat dangerous allergic reactions
U.S. health officials have approved the first nasal spray to treat severe allergic reactions, offering an alternative to injectable products like EpiPen.
-
FDA once again pushes back proposal to ban cancer-linked formaldehyde in hair relaxers
The Food and Drug Administration’s proposal to ban formaldehyde in hair care products has been pushed back once again, and the timeline for its release remains undetermined.
-
FDA OKs first menthol e-cigarettes, citing potential to help adult smokers
Friday’s action is the government’s strongest indication yet that switching to flavored vaping can reduce the harms traditional tobacco smoking.
-
The FDA reverses its ban on Juul e-cigarettes
Juul’s nicotine products have been allowed to stay in stores pending review of its application to sell them.
-
Panel rejects psychedelic drug MDMA as a PTSD treatment in possible setback for advocates
A first-of-a-kind proposal to begin using the mind-altering drug MDMA as a treatment for PTSD was roundly criticized Tuesday — a potentially major setback to psychedelic advocates who hope to win a landmark federal approval and bring the banned drugs into the medical mainstream.
-
Psychedelic drug MDMA faces questions as FDA considers approval for PTSD
Federal health regulators are set to review the first request to approve the mind-altering club drug MDMA as a treatment for PTSD. The Food and Drug Administration posted its review of the drug on Friday, raising questions about its effectiveness and potential risks, including heart problems.
-
Can yogurt reduce the risk of Type 2 diabetes?
The U.S. Food and Drug Administration recently said it’s OK for producers of yogurt to make that claim even though it’s based on limited evidence.
-
Bird flu is spreading to more farm animals. Are milk and eggs safe?
A bird flu outbreak in U.S. dairy cows has spread to more than two dozen herds in eight states. That comes weeks after the nation’s largest egg producer found the virus in its chickens. Health officials continue to stress that the risk to the public is low and that the U.S. food supply remains safe and stable.
-
Many cancer drugs remain unproven 5 years after accelerated approval, a study finds
Researchers have found that most cancer drugs granted accelerated approval by the U.S. Food and Drug Administration do not deliver on their early promise.
-
FDA approves Merck's drug for rare, deadly lung condition
The approval is a win for Merck, which is working to diversify its revenue stream as its blockbuster cancer drug Keytruda nears a loss of market exclusivity.
-
FDA warns about lead contamination in more cinnamon products in the US
The Food and Drug Administration issued a safety warning Wednesday, saying it identified additional cinnamon products in the United States that are contaminated with lead.
-
Watch out for fake Ozempic shots that are being sold through legitimate drug supply sources
The U.S. Food and Drug Administration says it has seized “thousands of units” of counterfeit Ozempic, the diabetes drug widely used for weight loss.