What is oral phynylephrine and why does the FDA want to remove it from cold medicine?
The U.S. Food and Drug Administration (FDA) is proposing to remove a common ingredient in nasal decongestants used by millions of Americans, citing data that shows it’s not effective. Oral phenylephrine is used in over-the-counter products like Sudafed ...
FDA wants to ban decongestant found in cold, allergy medicine
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FDA Claims Ingredients In Cold Medicines Is Ineffective
FDA Claims Ingredients In Cold Medicines Is Ineffective
FDA proposes pulling ineffective cold medicine from shelves
When you're feeling under the weather, you likely grab your go-to cough and cold medicine. But are all the ingredients helping you fight off that cold?
The FDA Is Finally Pulling a Useless Cold Medicine From the Market
Phenylephrine is both the most common decongestant on pharmacy shelves, and arguably the worst at its job. Last year, the FDA's advisory panel ruled it should no longer be considered an effective drug.
FDA Plans to Ban Ineffective Cold Medicine Ingredient—How It Will Affect You
The FDA has proposed removing phenylephrine, a widely used ingredient to treat nasal congestion, from over-the-counter cold medications.Last year, an FDA advisory committee concluded that the oral version of the medication is not effective at treating nasal congestion.
FDA Reviews Efficacy of Common Cold Medicines
The U.S. Food and Drug Administration (FDA) is currently evaluating the effectiveness of widely-used decongestants found in popular over-the-counter cold remedies such as Sudafed, Dayquil, and Mucinex.
Robert F. Kennedy Jr.’s Views Now Matter for the Nation. Here’s How He Could Influence Food and Drug Policy
Robert F. Kennedy Jr is known as a persistent critic of vaccine safety and is a longtime antagonist of the Food and Drug ...
Why compounders and telehealth providers are undeterred by the potential end of the weight-loss drug shortage
Online health platforms continue to advertise access to copycat versions of blockbuster weight-loss drugs Wegovy and Zepbound ...
Food, fluoride and funding: How a new Trump term might affect health in California
From family planning to hospital bills, the new Trump administration has the potential to affect a wide range of policies in ...
Fast Company9mon
food and drug administration
The Food and Drug Administration could now revoke over-the-counter designations for phenylephrine, an active ingredient in Benadryl and Sudafed. Pfizer’s COVID-19 pill: Here’s the latest on ...
Ars Technica1mon
Drug makers can’t make knockoff weight-loss drugs anymore—and they’re mad
Compounding pharmacies are suing the Food and Drug Administration so they can keep making imitation versions of popular—and lucrative—tirzepatide drugs, namely knockoffs of Mounjaro for ...
National Catholic Register20d
3 States Pick Up Abortion-Pill Lawsuit Against Food and Drug Administration
Three states have picked up a lawsuit previously dismissed by the U.S. Supreme Court earlier this year against the Food and Drug Administration (FDA) over its removal of safety restrictions on ...
Business Wire1mon
U.S. Food and Drug Administration (FDA) accepts New Drug Application for elinzanetant
BERLIN--(BUSINESS WIRE)--Bayer today announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s New Drug Application (NDA) for the investigational compound ...
The Associated Press - Business News on MSN16d
McDonald's and Boar's Head outbreaks may have you worried. Experts say the food supply is safe
according to the Food and Drug Administration. “The U.S. food supply remains one of the safest in the world,” FDA ...
Fluoride, vaccines and food dye are part of RFK Jr.'s plan to 'Make America Healthy Again.' What do experts think?
And on Wednesday, Kennedy said he’d cut “entire departments” of the Food and Drug Administration. But what does that mean for the American people? Here’s what to know about the former ...
Business Wire1mon
Alnylam Submits Supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration for Vutrisiran for the Treatment of Transthyretin Amyloidosis with Cardiomyopathy
to the U.S. Food and Drug Administration (FDA) for vutrisiran, an investigational RNAi therapeutic in development for the treatment of ATTR amyloidosis with cardiomyopathy (ATTR-CM). Vutrisiran ...