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The Latest Breaking News from FDA

10 Times Brands Promised “Lower Sugar” But Didn’t Deliver

We all celebrate when a product boasts “lower sugar,” thinking we’re making a healthier choice—only to be disappointed (and maybe even misled). The promise of sweetness with less cost to our health feels smart, but in many cases, it’s more marketing than truth. From sneaky labeling to lawsuits over deceptive…

Grocery Coupon Guide

What’s Behind the Sudden Rise in “Plant-Based” Labels—With No Plants?

Have you ever grabbed a product labeled “plant-based,” expecting something leafy, only to find it’s greenwashed marketing—not actual plants? You’re not alone. The trend of plant-based labels with no plants is growing fast and causing plenty of confusion for shoppers. Understanding why this happens—from marketing spin to lax regulation—can help…

Grocery Coupon Guide

Tylenol maker's stock lost billions after a rumor linking the medicine to autism. Wall Street says buy the dip as one bank sees a 'major overreaction'

Canaccord Genuity went on social media to gauge the reaction. Even the MAHA crowd was mixed on this one.

Fortune

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Broad ‘MAHA’ proposal largely calls for studies, awareness - Roll Call

The Trump administration on Tuesday presented a "Make America Healthy Again" plan to tackle rising chronic disease.

Roll Call

Ionis Pharmaceuticals To Expedite Development Of Rare Neurological Disease Candidate With FDA Breakthrough Status

On Tuesday, the U.S. Food and Drug Administration (FDA) granted Breakthrough Therapy designation to Ionis Pharmaceuticals Inc.’s (NASDAQ:IONS) ION582 for Angelman syndrome (AS), a rare neurological disorder.

Benzinga

Soap, deodorant and sanitiser recalls over sepsis concerns - full list revealed

Customers are eligible for a full refund

Evening Standard

Advocates of MDMA-Assisted Psychotherapy Complain that 'the FDA Moved the Goalposts'

The agency's puzzling concerns about the Lykos Therapeutics drug application

Reason

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As Covid surges in the US, Americans can’t get vaccinated: ‘terrified I might kill somebody’

The FDA is allowing the vaccine for people 65 and older, but younger people need to have an underlying condition

The Guardian - US

FDA To Expedite Nicotine Pouch Reviews In Pilot Program Under Trump Pressure: Report

The U.S. Food and Drug Administration (FDA) is reportedly set to launch a pilot program to fast-track the review of nicotine pouches from four major tobacco companies amid mounting pressure from the Trump administration.

Benzinga

FDA Tightens Grip On Safe Weight Loss Drugs, WHO Adds Them To Essential Medicines List

The U.S. Food and Drug Administration on Friday established a "green list" import alert to help stop potentially dangerous GLP-1 (glucagon-like peptide-1) active pharmaceutical ingredients (APIs) from unverified foreign sources from entering the U.S. market.

Benzinga

Two brothers have the same genetic disorder. Their insurance only covered life-altering treatment for one of them

Exclusive: Alison Joseph's sons Noah and Hunter both have Duchenne muscular dystrophy. She tells Rhian Lubin the heartbreaking reality of watching one thrive while the other suffers

The Independent UK

Maryland screwworm case has US officials bracing for return of an old foe

Rise in cases south of the border prompts concern over US livestock as Trump budget cuts hit research and foreign aid

The Guardian - US

LSD shows promise for reducing anxiety, shows drugmaker's study

The psychedelic drug LSD showed positive results for easing symptoms in people with generalised anxiety disorder, a recent study has shown.

Euronews

Florida surgeon general Ladapo's vaccine mandates opposition goes against medical mainstream

Dr_ Joseph Ladapo, a Nigerian-born physician with impeccable U_S_ medical credentials, says that requiring vaccinations for diseases like measles, polio and chickenpox amounts to government-imposed “slavery.”

The Independent UK

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Grocery Coupon Guide

6 Times a Recalled Product Was Still on the Shelf

Picture this: a product is recalled for safety, yet it somehow ends up still sitting on store shelves. It’s alarming, and potentially dangerous—and yes, it happens more often than you’d think. Learning about each recalled product on the shelf instance helps you stay alert, know what to check for, and…

Benzinga

Regenxbio Unveils 12-Month Data For Gene Therapy Soon After FDA Delays Review Date

On Friday, REGENXBIO Inc. (NASDAQ:RGNX) shared new data from the Phase 1/2/3 CAMPSIITE trial of clemidsogene lanparvovec (RGX-121) for the treatment of patients with Mucopolysaccharidosis Type II (MPS II), also known as Hunter syndrome, at the International Congress of Inborn Errors of Metabolism (ICIEM) 2025.

International Business Times UK

US Senator Claims Eating Radioactive Shrimp Will Make You An Alien - Is Video Real Or AI? The Answer Will Surprise You

Senator John Kennedy claims radioactive shrimp could turn people into aliens, sparking viral debate while experts confirm risks are real but not sci-fi extreme.

The Independent UK

Why did a republican take a giant photo of the alien from ‘Alien’ to the Senate?

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The Independent UK

Republican senator suggests eating radioactive shrimp will turn you into an alien

Louisiana Republican John Kennedy claimed that eating recalled radioactive shrimp could make people resemble the creature from the sci-fi horror movie Alien – or even grow an extra ear

Benzinga

Syndax Gains Attention With Strong Drug Portfolio, Path To Leukemia Market Growth

Investors are increasingly looking to biotechnology companies for potential breakthroughs and profitable returns, as the sector shows resilience and growth amid broader market volatility. Within this landscape, Syndax Pharmaceuticals Inc. (NASDAQ:SNDX) is capturing attention with its promising drug portfolio and financial performance.

The Guardian - US

RFK Jr accused of ‘reckless disregard for science and the truth’ in Senate hearing

Health secretary defends his leadership as Democrats attack his vaccine policy and demand his resignation

Benzinga

FDA Outlines Process To Speed Up Rare Disease Therapy Approvals

The U.S. Food and Drug Administration on Thursday introduced the Rare Disease Evidence Principles (RDEP) to provide greater speed and predictability in the review of therapies intended to treat rare diseases with very small patient populations.

The Guardian - US

RFK Jr hints access to key abortion drug could be cut back

Health secretary claims Biden officials ‘twisted the data’ despite research showing mifepristone is safe and effective

Benzinga

FDA Breakthrough Status Awarded To Lilly-Merck Combo Drug For Advanced Non-Small Cell Lung Cancer

The U.S. Food and Drug Administration (FDA) on Thursday granted Breakthrough Therapy designation to Eli Lilly and Co.’s (NYSE:LLY) olomorasib, in combination with Merck Co. Inc.’s (NYSE:MRK) anti-PD-1 therapy Keytruda (pembrolizumab), for the first-line treatment of unresectable advanced or metastatic non-small cell lung cancer (NSCLC) with a KRAS G12C mutation…

Benzinga

FDA Confirms Direct Review Path For Aquestive's Allergy Treatment

The U.S. Food and Drug Administration (FDA) on Thursday informed Aquestive Therapeutics, Inc. (NASDAQ:AQST) that an advisory committee meeting is not required for Anaphylm (dibutepinephrine) Sublingual Film.

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