Doctors release vaccine recommendations for RSV, influenza, COVID-19
Medical groups have released vaccine recommendations this fall in lieu of guidance from the CDC. File Photo by…
U.S. FDA Accepts Teva’s New Drug Application (NDA) and Grants Priority Review for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Patients with Tourette Syndrome
Teva Pharmaceutical Industries Ltd Ecopipam (EBS-101) is a first-in-class selective D1 (dopamine) receptor antagonist with Orphan Drug designation NDA…
The FDA Issued a Recall on Bladder Medication Nationwide
Key Points A nationwide recall was issued for mirabegron tablets due to an impurity in the active ingredient.…
FDA says recalled blood thinner sold across the US is unlikely to cause serious harm
A recalled generic blood thinner has drawn national attention. But the U.S. Food and Drug Administration says the…
Blood Pressure Drug Recalled Nationwide, FDA Announces
When a prescription drug is recalled, often it’s a generic version that’s being pulled from market. But this…
Medicare’s Drug-Pricing Proposal Carries A Hidden Cost
“CMS’s proposal would encourage one thing above all else: investing less in improving existing medicines,” says health expert…
Major VA study to examine effectiveness of psilocybin on depression, PTSD
The Department of Veterans Affairs is launching research to determine whether psilocybin — the psychoactive ingredient in “magic…
Antihistamine Recall: 34,000 Bottles at Highest Risk Level
It’s not the first recall we’ve seen for antihistamine, but it might be one of the first with…
FDA Approves Mannkind’s At-Home Treatment Option for Heart Failure or Kidney Disease
Benzinga and Yahoo Finance LLC may earn commission or revenue on some items through the links below. Mannkind…
KVUE Stock Rises As FDA Approves Tylenol Combination Despite Trump Administration’s Pushback
The green light arrives in spite of continued pressure on the Tylenol brand. In September 2025, President Donald…
FDA panel reviewing some peptides to consider loosening regulations for unapproved therapies
A Food and Drug Administration advisory panel will spend the next two days discussing whether compounding pharmacies can…
Popular Supplement Recalled Due to Salmonella Risk: Nausea and Bloody Diarrhea Possible
Your morning supplement could make you sick. The U.S. Food and Drug Administration (FDA) announced that Moringa Leaf…