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 says some cold and allergy drugs have an ineffective key ingredient
There are new concerns that phenylephrine, an ingredient in common over-the-counter cold and allergy medicines is ineffective. The FDA said the ingredient is safe but many popular medicines are being pulled off the shelves.
FDA moves to pull popular decongestant from shelves amid effectiveness concerns
The safety of phenylephrine isn’t a concern, but its effectiveness has been debated for years. Patrick T. Fallon/AFP/ via CNN Newsource
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?
FDA wants to ban decongestant found in cold, allergy medicine
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Four Major Cold, Allergy Meds May Get Pulled Because They Don't Work
Ugh, that explains it! No wonder so many of us never felt better. More than 80 million people across the country deal with seasonal allergies. That’s 25 percent of the United States according to the Center for Disease Control,
FDA Claims Ingredients In Cold Medicines Is Ineffective
FDA Claims Ingredients In Cold Medicines Is Ineffective
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 ...
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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 ...