What is oral phynylephrine and why does the FDA want to remove it from cold medicine?
Oral phenylephrine is used in over-the-counter products like Sudafed and Dayquil to help temporarily relieve the common symptom of colds and allergies. Phenylephrine has been sold for more than 75 years, predating the agency’s own regulations on drug effectiveness.
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 wants to ban decongestant found in cold, allergy medicine
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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?
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
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Why compounders and telehealth providers are undeterred by the potential end of the weight-loss drug shortage
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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 ...
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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
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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 ...
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McDonald's and Boar's Head outbreaks may have you worried. Experts say the food supply is safe
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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 ...