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food and drug administration

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Apr 15

FDA to weigh easing limits on unproven peptides favored by RFK Jr. and MAHA supporters

By Matthew Perrone, Associated Press

The Food and Drug Administration will hold a meeting this summer to consider easing restrictions on more than a half dozen peptide injections, a group of unapproved therapies that have become popular among wellness influencers, fitness gurus and celebrities.

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Mar 29

Makers of dietary supplements push the FDA to allow peptides and other new ingredients

By Matthew Perrone, Associated Press

Makers of dietary supplements are pushing the Food and Drug Administration to expand the types of ingredients they can put in their products.

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Mar 16

7 people in the U.S. sickened by E. coli linked to cheese made from raw milk, FDA says

By JoNel Aleccia, Associated Press

At least seven people in three states, including young children, have been sickened by E. coli food poisoning linked to cheddar cheese made from raw milk, federal health officials said Monday.

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Mar 14

What are peptides, and are they safe? Here's what to know

By Grace Abels, PolitiFact

Lots of people are talking about peptides. But what are they? Here’s a quick primer on the health trend and what we know about peptides’ safety.

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Feb 18

Moderna says FDA will now consider its new mRNA flu shot after initial refusal

By Lauran Neergaard, Associated Press

Moderna announced the change Wednesday, about a week after revealing that the FDA’s vaccine chief was refusing to review the new vaccine, made with Nobel Prize-winning mRNA technology.

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Jan 18

FDA's new expedited drug program raises legal questions and concerns

By Matthew Perrone, Associated Press

The FDA commissioner's effort to drastically shorten the review of drugs favored by President Donald Trump's administration is causing alarm across the agency.

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Jan 11

Watch 5:15
Investigation raises concerns about lack of FDA quality testing for generic drugs

By John Yang, Andrew Corkery

By some estimates, about 90% of prescriptions in the U.S. are filled with generic drugs. The Food and Drug Administration says that all agency-approved generic drugs “have the same high quality” as brand-name drugs, but a ProPublica investigation found that…

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Nov 23

What to know about menopause hormone therapy after FDA removed 'black box' warnings

By Grace Abels, PolitiFact

The FDA removed safety warnings from several hormone drugs used to treat menopause symptoms. Here’s what you need to know about these treatments before your next doctor's appointment.

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Nov 19

What are biologics and can the Trump administration make them cheaper with biosimilars?

By Madison Czopek, PolitiFact

Biologics represented 5% of the drugs prescribed in the U.S. in 2024, but they accounted for more than half of the country’s total prescription medicine spending, according to health data analysis company IQVIA. The Trump administration said it hopes to…

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Nov 10

WATCH: RFK Jr. says FDA will remove long-standing warning from hormone-based menopause drugs

By Matthew Perrone, Associated Press

The change announced Monday is a break from more than 20 years of FDA policy, in which the drugs carried the agency's most severe warning label.

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