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U.S. FDA retweeted

FDA Drugs and Biologics

NEWS: Today, FDA approved a new treatment for metastatic androgen pathway modulation-naïve or -sensitive prostate cancer. fda.gov/drugs/resources-info…

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U.S. FDA retweeted

𝐈𝐭'𝐬 𝐑𝐞𝐝 𝐑𝐢𝐛𝐛𝐨𝐧 𝐖𝐞𝐞𝐤! DEA Administrator Cole shares a powerful message about the legacy of Special Agent Enrique “Kiki” Camarena and the spirit of #RedRibbonWeek: "Make A Difference, Be A Hero, Stay Drug Free! Learn more about #DEARedRibbon at DEA.gov/redribbon. @DEATerryCole @TheJusticeDept

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The FDA is responsible for ensuring the U.S. seafood supply is safe, sanitary, wholesome, and properly labeled. To support the America First Seafood Strategy, the agency published draft guidance to help companies proudly and accurately label seafood of U.S. origin. If finalized, the guidance would provide examples of statements, such as “U.S.-Caught,” and graphics featuring the American flag to help consumers identify and choose U.S. seafood.

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HHS Rapid Response

@HHSResponseOct 22

🗣️ @FDA_KyleD announces the launch of the latest @FDA initiative: the Alzheimer's Prevention Accelerator Learn more 👇

HHS Rapid Response

@HHSResponseOct 22

MAJOR ANNOUNCEMENT: @SecKennedy announces 2026 update for the National Plan to Address Alzheimer's Disease and Related Dementias. 4 Commitments ⬇️ 1️⃣ Reduce dementia risk by confronting long-term risk factors 2️⃣ Accelerate discovery through investment in robust science 3️⃣ Improve care for patients to get clear answers and care they can afford 4️⃣ Strengthen services for families caring for loved ones to help preserve independence

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Reminder: FDA is holding a hybrid meeting on Oct. 28 from 1-5 pm ET to seek input on its Rare Disease Framework Initiative reimagining the agency’s approach to rare disease drug development. Find out how to register: fda.gov/news-events/fda-meet…

FDA Rare Disease Framework Initiative Public Meeting

On October 28, 2026, the U.S. Food and Drug Administration, in partnership with the Reagan-Udall Foundation for the FDA, will convene a hybrid public meeting to seek input related to the FDA’s Rare...

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NAIN’s first initiative, the Alzheimer’s Prevention Accelerator, will focus on delaying and preventing Alzheimer’s disease, one of the most urgent public health challenges of our time.

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The FDA is launching the Neuroscience Advancement and Innovation Nexus (NAIN), a new cross-center program to advance medical products for conditions affecting the brain and nervous system. fda.gov/news-events/press-an…

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Under the Trump administration, the FDA is issuing new draft action levels to guide manufacturers in lowering cadmium in packaged foods for babies and young children, advancing our Closer to Zero initiative to make these foods safer.

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FDA Advances Closer to Zero Initiative to Safeguard Food for Children

FDA Advances Closer to Zero Initiative to Safeguard Food for Children

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#ICYMI FDA’s #Testosterone Use in Menopausal Women Public Workshop recording is now available on FDA’s YouTube channel. Learn about the current scientific evidence, knowledge gaps, & more. youtube.com/watch?v=mJQz5WBB…

ALT The image is a promotional poster by the FDA Office of Women’s Health and Center for Drug Evaluation and Research. It announces the availability of a workshop recording titled "Testosterone Use in Menopausal Women." The poster features the FDA logo and circular photos of five individuals, including a person in a lab coat.

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Are you or someone you love showing signs of #depression? It can affect #women at any stage of life. Help is available. Talk with your health care provider about your symptoms and learn more about FDA-approved treatments. fda.gov/consumers/womens-hea…

ALT A healthcare professional holding a tablet speaks with a seated individual. The image contains text that reads, "Learn about FDA-approved treatments for depression," and features the FDA logo.

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This #DrugTakeBackDay, take a few minutes to check your medicine cabinet. Unused #opioids don't need to be saved "just in case." Safe disposal protects your whole family, especially your teens. 🗓 Saturday, October 24 | 10 a.m. - 2:00 p.m. 📍 Find a convenient, confidential drop-off location near you: dea.gov/takebackday

Gather all unneeded, unused or expired medications for #DEATakeBackDay. Safely dispose of them at one of the 4,200 drop-off locations to prevent misuse and protect our communities. #TakeBackDay dea.gov/takebackday @TheJusticeDept

DEA National Take Back program offers nearly 4,200 locations nationwide for safe medication disposal.

ALT DEA National Take Back program offers nearly 4,200 locations nationwide for safe medication disposal.

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🦴 Strong bones support healthy aging. On #WorldOsteoporosisDay, learn how FDA-approved biosimilars may be an option for some bone-related conditions, including certain forms of osteoporosis: Learn more: fda.gov/drugs/biosimilars/ba…

ALT Image of two individuals engaging in an exercise using a small dumbbell. The person on the left is raising the dumbbell, assisted by the other. Text reads "World Osteoporosis Day." The FDA logo is visible at the bottom right.

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Food fraud can cost consumers more than money—it can undermine confidence in what’s on the label. FDA testing of 195 domestic and import samples of lemon juice found 7 imported products that did not meet the U.S. standard of identity for lemon juice. This work builds on recent FDA sampling to detect economically motivated adulteration in foods including honey and seafood. Learn more about the results of FDA’s testing of lemon juice samples.

ALT The image features a blue background with text stating, "The FDA tested 195 samples of domestic and imported lemon juice for authenticity. See what we found." Below the text is an illustration of lemon branches with leaves and lemons. The FDA logo is at the bottom left.

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FDA Releases Sampling Results on Economically Motivated Adulteration i

FDA Releases Sampling Results on Economically Motivated Adulteration in Lemon Juice

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This #BreastCancerAwarenessMonth, pink ribbons come with real reason for hope. In the past year alone, FDA approved 10 new breast cancer treatments. The FDA is working every day to get life-saving breakthroughs to patients faster. washingtonexaminer.com/op-ed…

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⚠️ FDA is warning consumers about counterfeit OTC eye drops found in Florida and Georgia, with possible distribution in other states. Some products tested positive for bacterial contamination, posing risks of eye infections, injury, and vision problems. FDA is working to identify and remove unlawful products.

A blue background features a small white eye drop bottle with its cap removed. White text on a dark blue banner reads: "FDA warns consumers about counterfeit eye drops." Below, in white text on a blue background: "Some products have tested positive for bacterial contamination.

ALT A blue background features a small white eye drop bottle with its cap removed. White text on a dark blue banner reads: "FDA warns consumers about counterfeit eye drops." Below, in white text on a blue background: "Some products have tested positive for bacterial contamination.

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Learn more: fda.gov/drugs/counterfeit-me…

Counterfeit versions of eye drops found in several states

Counterfeit versions of over-the-counter eye drops have been found in Florida and Georgia in stores serving primarily Spanish-speaking customers. These products also may be in Louisiana, Mississippi,...

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