Dozens of drugs are now available at discounted prices on TrumpRx.gov, a government website that officially launched on Thursday.
The site currently features 43 drugs &#8212; including those that tackle weight loss, autoimmune issues, fertility, addiction, and high cholesterol &#8212; at discounted prices for anyone who has a prescription.
The discounted prices were negotiated by the Trump administration, and the number of offered drugs are expected to rise in the coming weeks and months.
Consumers can browse through the <a href="https://trumprx.gov/browse">available drugs here</a>, or view them below (as <a href="https://www.cbsnews.com/news/trumprx-drugs-website-discount/">compiled</a> by CBS News):
<ul>
<li>Abrilada Pen (autoimmune) — TrumpRx price: $207.60</li>
<li>Airsupra (respiratory) — TrumpRx price: $201</li>
<li>Azulfidine Tabs (rheumatology) — TrumpRx price: $99.60</li>
<li>Azulfidine En Tabs (rheumatology) — TrumpRx price: $130.80</li>
<li>Bevespi (respiratory) — TrumpRx price: $51</li>
<li>Cetrotide (IVF) — TrumpRx price: $22.50</li>
<li>Chantix (smoking cessation) — TrumpRx price: $106.20</li>
<li>Cleocin (antibiotic) — TrumpRx price: $94.35</li>
<li>Colestid (cholesterol) — TrumpRx price: $127.91</li>
<li>Cortef (inflammation) — TrumpRx price: $45</li>
<li>Cytomel (thyroid) — TrumpRx price: $6</li>
<li>Diflucan (antifungal) — TrumpRx price: $14.06</li>
<li>Duavee (women&#8217;s health) — TrumpRx price: $30.30</li>
<li>Estring (women&#8217;s health) — TrumpRx price: $249</li>
<li>Eucrisa (dermatologic) — TrumpRx price: $158.48</li>
<li>Farxiga (diabetes, cardiovascular) — TrumpRx price: $181.59</li>
<li>Genotropin (human growth hormone) — TrumpRx price: $89.67</li>
<li>Gonal F (fertility) — TrumpRx price: $168</li>
<li>Insulin Lispro (high blood sugar) — TrumpRx price: $25</li>
<li>Levoxyl (hypothyroidism) — TrumpRx price: $35.10</li>
<li>Lopid (cholesterol) — TrumpRx price: $39.60</li>
<li>Medrol (inflammation) — TrumpRx price: $3.15</li>
<li>Ngenla (human growth hormone) — TrumpRx price: $2,217</li>
<li>Nicotrol (smoking cessation) — TrumpRx price: $271.16</li>
<li>Ovidrel (fertility) — TrumpRx price: $84</li>
<li>Ozempic Pen (diabetes, weight loss) — TrumpRx price: $199</li>
<li>Premarin (women&#8217;s health) — TrumpRx price: $99</li>
<li>Premarin Vaginal Cream (women&#8217;s health) — TrumpRx price: $236.65</li>
<li>Prempro (women&#8217;s health) — TrumpRx price: $98.84</li>
<li>Pristiq (antidepressant) — TrumpRx price: $200.10 </li>
<li>Protonix (heartburn) — TrumpRx price: $200.10</li>
<li>Tikosyn (cardiovascular) — TrumpRx price: $336</li>
<li>Toviaz (bladder control) — TrumpRx price: $43.50</li>
<li>Vfend (antifungal) — TrumpRx price: $306.98</li>
<li>Viracept (antiviral) — TrumpRx price: $607.20</li>
<li>Wegovy (weight loss) — Pen TrumpRx price: $199</li>
<li>Wegovy Pill (weight loss) — TrumpRx price: $149</li>
<li>Xeljanz (rheumatology) — TrumpRx price: $1,518</li>
<li>Xigduo XR (diabetes) — TrumpRx price: $181.59</li>
<li>Zarontin (anticonvulsant) — TrumpRx price: $71.10</li>
<li>Zavzpret (migraine treatment) — TrumpRx price: $594.84</li>
<li>Zepbound (weight loss, sleep apnea) — TrumpRx price: $299</li>
<li>Zyvox (antibiotic) — TrumpRx price: $122.74</li>
</ul>
Currently, the drugs are for those buying out-of-pocket, as insurance is not accepted.
Trump announced his intention to lower prescription drug prices for Americans months ago. He&#8217;s repeatedly said that it&#8217;s &#8220;unacceptable&#8221; that Americans pay far more for drugs than other developed nations, arguing that these nations are being subsidized by the U.S.
Following through on his promise, Trump announced the official launch of TrumpRx on Thursday, as reported by <a href="https://www.dailywire.com/news/trumprx-officially-launches-with-promise-to-dramatically-cut-drug-costs-for-americans?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=2&amp;row=0&amp;rowType=Vertical+List&amp;title=TrumpRx+Officially+Launches+With+Promise+To+Dramatically+Cut+Drug+Costs+For+Americans">The Daily Wire</a>.
“For years, politicians from both parties have promised to bring down prescription drug prices and make health care more affordable, but they all failed. It was all words, as usual,” Trump said at the rollout. “But I’m actually getting it done; it is done, actually.”
Related: <a href="https://www.dailywire.com/news/trumprx-officially-launches-with-promise-to-dramatically-cut-drug-costs-for-americans?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=2&amp;row=0&amp;rowType=Vertical+List&amp;title=TrumpRx+Officially+Launches+With+Promise+To+Dramatically+Cut+Drug+Costs+For+Americans">TrumpRx Officially Launches With Promise To Dramatically Cut Drug Costs For Americans</a>

Trump Vows US Drug Price Cuts Of Up To 80% In Industry Blow

Here Are The 43 Drugs Now Offered At Discounted Prices On TrumpRx

Health

Prescription Drugs

Trump Administration

TrumpRx

U.S.

The U.S. Food and Drug Administration said on Friday it would take action against telehealth provider Hims &amp; Hers for its $49 weight-loss pill, including restricting access to the drug&#8217;s ingredients and referring the company to the Department of Justice for potential violations of federal law.
Federal action to limit the production of compounded drugs would be a win for Novo Nordisk, which has been losing share in the weight-loss market to rival Eli Lilly and telehealth firms like Hims. However, the FDA did not make clear whether it could quickly halt the sale of Hims&#8217; product, the cheapest GLP-1 therapy on the U.S. market.
Shares of Hims fell 14.1% in after-hours trade.
The FDA said it plans to restrict GLP-1 ingredients used in non-approved compounded drugs that companies such as Hims and other compounding pharmacies have marketed as alternatives to authorized treatments. The agency cited concerns over quality, safety and potential violations of federal law.
On Thursday, Reuters was first to report that Hims would begin offering copies of Novo Nordisk&#8217;s new Wegovy pill at an introductory price of $49 per month, about $100 less than the brand name.
Novo Nordisk later said it would take legal action against the telehealth company over its plan to sell compounded copies of the drug.
The U.S. Department of Health and Human Services&#8217; General Counsel, Mike Stuart, also said on Friday he has referred Hims &amp; Hers to the Department of Justice for investigation over potential violations.
Hims said in a statement that the company &#8220;has always operated with a deep commitment to the safety and best interests of consumers and in compliance with applicable law.
&#8220;We have a long history of successfully working with regulators, and look forward to continuing to engage with the FDA to ensure safe access to affordable healthcare.&#8221;
A Lilly spokesperson said the company applauded the FDA action. &#8220;For years, compounders have been putting patients at risk by unlawfully mass-producing knockoff drugs using substandard ingredients from illicit foreign suppliers and selling them without clinical evidence that they’re safe or even work. Patients deserve better, and we look forward to decisive action by FDA, other regulators, and law enforcement.”
Compounding, in which pharmacies mix ingredients for specialized medicines or to copy a drug but at different dosages, has flourished as Americans chase cheaper prices for drugs.
The practice is legal under the Federal Food, Drug and Cosmetic Act in certain circumstances, like when prescribed by a physician to address patient side effects or during a drug shortage.
Hims&#8217; compounded drug is not FDA-approved and has not gone through clinical trials to prove efficacy.
The FDA&#8217;s enforcement actions against Hims could include sending a warning letter, pursuing a court injunction or conducting an administrative seizure of products, said Joanne Hawana, a member at Mintz, Levin, Cohn, Ferris, Glovsky and Popeo, P.C.
The agency would need the help of the Justice Department to pursue an injunction, as it lacks independent litigation authority, Hawana said.
The FDA&#8217;s statements suggest that &#8220;this announcement by Hims, to the government, is concerning enough that they decided they’re going to escalate,&#8221; Hawana said.
Thus far, the FDA&#8217;s actions on weight-loss drugs have been limited to warning letters sent in the fall of 2025 to combat misleading direct-to-consumer advertising and marketing.
Commissioner Marty Makary said in a statement on Friday that the agency will &#8220;use all available compliance and enforcement tools within its authorities to address unsubstantiated claims and associated public health concerns.&#8221;
The health regulator said that, in promotional materials, companies cannot claim that non-FDA-approved compounded products are generic versions or the same as drugs approved by FDA.
It added that &#8220;they also cannot state compounded drugs use the same active ingredient as the FDA-approved drugs or that compounded drugs are clinically proven to produce results for the patient.&#8221;
(Reporting by Siddhi Mahatole in Bengaluru and Leah Douglas in Washington; additional reporting by Amina Niasse in New York; Editing by Alan Barona and David Gregorio)

Pharmaceutical Companies in India

Hims Stock Tumbles As FDA Targets Its Discounted Weight-Loss Drugs

Ozempic

President Donald Trump on Thursday officially launched the federal government&#8217;s highly anticipated direct-to-consumer medication website called TrumpRx.
The site, which Trump lauded as a major win for his administration, will give Americans access to big discounts on popular and high-priced medicines. Now, consumers can pay low prices that are comparable to those in other developed nations, keeping in line with the Trump Most-Favored Nation policy.
&#8220;America was being overcharged for medicine. The same drugs, made in the same factories, at the same dosages, are costing Americans up to 1,000% more than in any other country,&#8221; the live <a href="https://trumprx.gov/">TrumpRx site</a> reads. &#8220;This is unacceptable.&#8221;
&#8220;Starting tonight, dozens of the most commonly used prescription drugs will be available at dramatic discounts for all consumers throughout our new website, it&#8217;s called TrumpRx.gov,&#8221; the president announced at Thursday&#8217;s launch.
&#8220;For years, politicians from both parties have promised to bring down prescription drug prices and make health care more affordable, but they all failed. It was all words, as usual,&#8221; he added. &#8220;But I&#8217;m actually getting it done; it is done, actually.&#8221;
<blockquote class="twitter-tweet" data-media-max-width="560">
🚨 <a href="https://twitter.com/POTUS?ref_src=twsrc%5Etfw">@POTUS</a>: &#8220;Starting tonight, dozens of the most commonly-used prescription drugs will be available at dramatic discounts for all consumers throughout a new website: <a href="https://t.co/QSJ4wskHM1">https://t.co/QSJ4wskHM1</a>.&#8221; <a href="https://t.co/tB9FdIZMWZ">pic.twitter.com/tB9FdIZMWZ</a>
— Rapid Response 47 (@RapidResponse47) <a href="https://twitter.com/RapidResponse47/status/2019566096836366586?ref_src=twsrc%5Etfw">February 6, 2026</a></blockquote>
<div>
According to the White House, Trump was able to make deals with major companies like AstraZeneca, Eli Lilly, EMD Serono, Novo Nordisk, and Pfizer to get the lower drug prices for Americans.
&#8220;Additional drugs from other companies that have signed MFN pricing deals will be made available through TrumpRx.gov in the coming months,&#8221; a press release said, adding, &#8220;Depending on the manufacturer of a given drug, patients with valid prescriptions will be able to access savings through user-friendly coupons that can be printed or downloaded onto their phones or through channels set up by the manufacturer and integrated into TrumpRx.gov.&#8221;
</div>
<div id="attachment_1039745" style="width: 935px" class="wp-caption alignnone"><img loading="lazy" decoding="async" aria-describedby="caption-attachment-1039745" class="wp-image-1039745 size-large" src="https://dw-wp-production.imgix.net/2026/02/Screenshot-2026-02-05-at-7.33.51-PM-925x576.png" alt="" width="925" height="576" srcset="https://dw-wp-production.imgix.net/2026/02/Screenshot-2026-02-05-at-7.33.51-PM-925x576.png 925w, https://dw-wp-production.imgix.net/2026/02/Screenshot-2026-02-05-at-7.33.51-PM-300x187.png 300w, https://dw-wp-production.imgix.net/2026/02/Screenshot-2026-02-05-at-7.33.51-PM-768x478.png 768w, https://dw-wp-production.imgix.net/2026/02/Screenshot-2026-02-05-at-7.33.51-PM-1536x956.png 1536w, https://dw-wp-production.imgix.net/2026/02/Screenshot-2026-02-05-at-7.33.51-PM-2048x1275.png 2048w" sizes=" (max-width: 925px) 100vw, 925px" />Screenshot: Trump RX</div>
A White House fact-sheet sent to The Daily Wire listed the following examples of reduced-price medications:
<ul>
<li>The monthly prices of Ozempic and injectable Wegovy will fall from $1,028 and $1,349, respectively, to an average price of $350 and as low as $199, depending on dosage strength.</li>
<li>The monthly price of the Wegovy pill will fall from $1,349 to as low as $149, depending on dosage strength.</li>
<li>The monthly price of Zepbound will fall from $1,088 to an average price of $346 and as low as $299, depending on dosage strength.</li>
<li>Gonal-F, one of the most commonly-used fertility drugs, will see its price reduced to as low as $168 per pen, depending on dosage strength.</li>
<li>The price of Cetrotide, another commonly used fertility medicine, will drop from $316 to $22.50.</li>
<li>The price of Ovidrel will fall from $251 to $84.</li>
<li>Bevespi Aerosphere, an inhaler used to treat chronic obstructive pulmonary disease (COPD), will be discounted from $458 to $51.</li>
<li>Airsupra, an inhaler used to treat asthma symptoms and attacks, will see a price drop from $504 to $201.</li>
<li>Eucrisa, a topical ointment for atopic dermatitis, will be discounted from $792 to $158.</li>
<li>Insulin Lispro will be available for as low as $25 per month.</li>
<li>Duavee, a medication used to treat hot flashes and osteoporosis, will see its price cut from $202 to $30.</li>
</ul>
America&#8217;s HealthShare (AHS), a popular health sharing ministry, praised the development from the administration.
<div>
“America&#8217;s healthcare system is broken, and people are simply paying too much for medicine and hospital visits. America’s HealthShare enthusiastically supports the effort to offer working families and elderly people on fixed incomes access to more affordable prescription drugs,&#8221; America’s HealthShare President David Lejeune said in a statement sent to The Daily Wire.
&#8220;Our law and policy makers can and should work with this Administration, in bipartisan fashion, to address long-term solutions to America’s healthcare system,&#8221; he added. &#8220;At America&#8217;s HealthShare, we are proud to support the Make America Healthy Again movement by restoring freedom and accountability in healthcare through an innovative approach.&#8221;
Related: <a href="https://www.dailywire.com/news/trumprx-trump-scores-significantly-lower-prices-for-popular-weight-loss-drugs">TrumpRx: Trump Scores Significantly Lower Prices For Popular Weight Loss Drugs</a>
</div>

US-VOTE-TRUMP

TrumpRx Officially Launches With Promise To Dramatically Cut Drug Costs For Americans

Donald Trump

Executive

Health Care

Politics

Editor’s note: This week, we’re reprinting some of our best stories from the past year. This piece, originally published in September, discusses the dangerous drug sold at gas stations across the country derived from kratom.
U.S. Food and Drug Administration Commissioner Dr. Marty Makary says his agency is working to get ahead of what could be the “fourth wave” of the deadly opioid crisis by targeting a substance derived from the kratom plant that is being sold to young people in gas stations and vape shops all across the nation.
The concentrated compound, 7-hydroxymitragynine, known as 7-OH, is up to 13 times more potent than morphine, according to Makary. Deceptive marketing and easy access are helping fuel its spread, luring in an increasing number of young Americans.
“We can’t get caught flat-footed again,” Makary recently <a href="https://www.youtube.com/watch?v=5-9RKbVl_m8">warned</a>. “We got burned with fentanyl, we got burned with prescription drugs. We cannot get behind the eight ball again. This may be the fourth wave of the opioid epidemic. Concentrated, synthetic, 7-OH may be the fourth wave of the opioid epidemic.”
“7-OH, people need to know, is an opioid,” he emphasized. “You can walk down the street in almost any neighborhood in America and buy an opioid.”
The kratom plant is native to Southeast Asia. In its natural state, some people find it to have healthful and medicinal qualities. The FDA has made clear that it’s not focusing on the natural kratom leaf. They’re targeting concentrated and synthetic forms of kratom, or 7-OH.
At the end of July, the FDA recommended that 7-OH be classified as a Schedule I controlled substance, making it illegal to sell or possess. The agency says it’s an opioid that comes with significant health risks, including addiction and overdose.
Some people may not have even heard of kratom before, but they’ve likely seen kratom-derived 7-OH products in gas stations, corner stores, vape shops, or even online. Kratom, overall, is a billion-dollar industry in the U.S. – and it’s growing fast. In just a few years, the industry is expected to almost double in size.
7-OH is sold in a variety of forms, including powders, vapes, drinks, pills, and products that appeal to children, such as <a href="https://www.fda.gov/news-events/press-announcements/fda-takes-steps-restrict-7-oh-opioid-products-threatening-american-consumers?utm_source=chatgpt.com">fruit-flavored gummies and even ice cream cones</a>.
<div id="attachment_967745" style="width: 874px" class="wp-caption alignnone"><img loading="lazy" decoding="async" aria-describedby="caption-attachment-967745" class="wp-image-967745 size-large" src="https://dw-wp-production.imgix.net/2025/09/GettyImages-530276352-864x576.jpg" alt=" In this photo illustration, a bottle with Kratom liquid and bags of capsules with the herbal supplement Kratom inside are seen on May 10, 2016 in Miami, Florida. " width="864" height="576" srcset="https://dw-wp-production.imgix.net/2025/09/GettyImages-530276352-864x576.jpg 864w, https://dw-wp-production.imgix.net/2025/09/GettyImages-530276352-300x200.jpg 300w, https://dw-wp-production.imgix.net/2025/09/GettyImages-530276352-768x512.jpg 768w, https://dw-wp-production.imgix.net/2025/09/GettyImages-530276352.jpg 1024w" sizes=" (max-width: 864px) 100vw, 864px" />Joe Raedle/Getty Images</div>
These products are often inaccurately labeled concerning their 7-OH content, and can be disguised or marketed as merely the kratom plant. There’s also no federal age restriction on these products, though <a href="https://www.nbcnews.com/health/health-news/kratom-targeted-crackdowns-states-cities-rcna166661">several states</a> now prohibit the sale of such products to minors.
As far as widespread harm, especially to young Americans, the data are mixed – or perhaps underreported, and too early to tell.
The CDC says there have been some overdose deaths associated with kratom products, but often other substances were also involved. There was also a <a href="https://project.tampabay.com/investigations/deadly-dose/kratom-overdose-deaths-florida-mitragynine-testing/">recent report</a> from the Tampa Bay Times that links kratom products to hundreds of deaths just in the state of Florida, over the past decade. Additionally, more and more anecdotal accounts of 7-OH-related addictions and deaths fill the web, though they remain unverified.
A toxicologist and emergency physician from Albany Medical Center, Dr. Alicia Tudor, believes kratom-related harms are being underreported, specifically regarding overdoses.
“I’ll see it in the emergency department and then probably more often in the addiction clinic that I work at as well,” Tudor <a href="https://cbs6albany.com/news/wellness-watch/ballston-spa-mother-advocates-for-kratom-regulation-after-sons-death-controlled-substance-legislation-bill-protest-overdose-toxicology">told</a> WRGB.
Toxicology tests are not always given when patients come in for an overdose, she said. “Then the results would come back, you know, weeks later, and at that point, the patient’s been discharged and doing better,” Tudor added.
<div id="attachment_967751" style="width: 874px" class="wp-caption alignnone"><img loading="lazy" decoding="async" aria-describedby="caption-attachment-967751" class="wp-image-967751 size-large" src="https://dw-wp-production.imgix.net/2025/09/GettyImages-2228201310-864x576.jpg" alt="Cari Scribner with photos of her son, Nickolas, on Thursday, July 31, 2025, in her home Ballston Spa, NY. " width="864" height="576" srcset="https://dw-wp-production.imgix.net/2025/09/GettyImages-2228201310-864x576.jpg 864w, https://dw-wp-production.imgix.net/2025/09/GettyImages-2228201310-300x200.jpg 300w, https://dw-wp-production.imgix.net/2025/09/GettyImages-2228201310-768x512.jpg 768w, https://dw-wp-production.imgix.net/2025/09/GettyImages-2228201310.jpg 1024w" sizes=" (max-width: 864px) 100vw, 864px" />Jim Franco/Albany Times Union via Getty Images</div>
New York mother Cari Scribner wants action taken on these highly concentrated kratom products. Her 27-year-old son, Nickolas, died last year from what appears to have been a kratom-related death.
Scribner <a href="https://cbs6albany.com/news/wellness-watch/ballston-spa-mother-advocates-for-kratom-regulation-after-sons-death-controlled-substance-legislation-bill-protest-overdose-toxicology">says</a> her son started using the products to manage anxiety, depression, and insomnia, believing it was merely an “all natural herbal, energy, and health supplement.”
In a similar tragedy, Makary relayed the contents of a letter from a grieving stepfather of a young man who had finally quit addiction, only to purchase 7-OH without being aware of its contents.
“He called me on May 31 to tell me he had stopped at the vape shop to buy a vape and was offered a fruity pill, and was told that it was kratom,” Makary read the letter aloud. “He said that he took the pill and became addicted, and should have done his research. He died the night he took two 20 mg 7-OH pills. The wrapper was at his bedside. There were no other drugs or alcohol in the house.”
While kratom has been widely used in the U.S. for some time, concentrated 7-OH has only risen in popularity within the last five years. Ultimately, the FDA is moving to stop the substance from causing more widespread harm before it’s too late.
And it’s not just the FDA taking action. Florida is leading the way on the state level. Earlier this month, Florida AG James Uthmeier announced an emergency rule to classify 7-OH as a Schedule I controlled substance. GOP Gov. Mike DeWine has also <a href="https://governor.ohio.gov/media/news-and-media/governor-dewine-calls-on-pharmacy-board-to-schedule-+kratom-compounds-as-illegal-drugs">urged</a> the Ohio Board of Pharmacy to designate synthetic and natural kratom compounds as illegal drugs. Additionally, a number of other states have moved to add age restrictions for 7-OH or limitations on concentrations of the compound.
The Drug Enforcement Administration (DEA) is currently reviewing the FDA’s recommendation to effectively ban 7-OH.

Kratom

Best Of 2025: This Drug Is Sold in Your Gas Station. It May Trigger the ‘Fourth Wave’ Of The Opioid Crisis.

Drugs

Perhaps the only thing Democrats and Republicans seem to agree on these days is that the pharmaceutical industry is bad. In particular, there has been bipartisan movement in recent years to ban direct-to-consumer drug ads, which are only permitted in the United States and New Zealand. Some supporters, like The Daily Wire&#8217;s Matt Walsh, have called these ads <a href="https://www.dailywire.com/news/all-the-reasons-why-big-pharma-commercials-should-be-banned">dangerous</a>.
But even those who don&#8217;t feel that strongly about the issue aren&#8217;t jumping up to defend these ads, which generally feature a bunch of shiny, happy stock-photo models dancing around while a narrator speed-reads through a list of side effects ranging from nausea to death.
In this provocative piece, Stephen Moore does just that. A noted economist and political commentator, Moore served as a senior economic adviser to President Donald Trump and was instrumental in crafting the Tax Cuts and Jobs Act of 2017. Moore not only argues that pharmaceutical ads help patients, but that banning them could have negative downstream consequences. We hope you enjoy. — Tim Rice
***
Chevrolet’s newest <a href="https://x.com/chevrolet/status/1993694235552595978?s=46" target="_blank" rel="noopener">holiday ad</a> is tugging at America’s heartstrings.
The spot follows a family’s classic Chevy Suburban through decades of memories — kids tumbling around the backseat, tearful college drop-offs, and that quiet, bittersweet moment when the house becomes an empty nest. The ad ends as the couple parks their old Suburban beside a shiny new one, welcoming their grown children and grandchildren home for the holidays.
It’s the kind of commercial American companies have long excelled at: emotionally evocative in all the right ways, tapping into nostalgia, family, and the warmth of the season — and, yes, selling a product. Holiday ads have become part of our cultural fabric. Think of Coca-Cola&#8217;s polar bears, or the Budweiser Clydesdales. These ads don’t just market products; they help set the tone for the season.
Ads like these may not survive if Washington continues down a troubling road of restricting TV commercials for politically unpopular — but legal — products. At the top of this list is pharmaceutical ads, which Senator Bernie Sanders (I-VT) wants removed from the airwaves. In that fight he has an unlikely ally: Health and Human Services Secretary Robert F. Kennedy Jr.
This may seem like a rare instance of bipartisan cooperation. And in today’s political climate, dinging pharmaceutical companies is almost certain to prove popular.
But we already have strict advertising laws against including false or misleading claims in ads, and severe penalties for violations — and appropriately so. Banning pharmaceutical ads would be regulatory overkill, and could have negative consequences its advocates aren’t considering.
Contrary to what critics say, prescription drugs preserve life and improve health. Because of this, advertising can be a social good. An ad that makes people aware of a new drug’s benefits can literally save lives and alleviate suffering.
Some politicians and regulators say these ads only serve to artificially drive up demand. And they do drive up demand — for treatments that work. That’s a good thing.
Think about what would happen if we had a new wonder drug to help cure or stop the spread of breast cancer. Now imagine that the government prevented the pharmaceutical company from promoting this treatment to patients.
It could take months before patients get access to this miracle cure.
Plus, if lawmakers succeed in chipping away protections for advertisers, it will only empower future government censors. Imagine a future Democrat administration that wants to ban ads for gas-powered cars or disposable diapers in the name of “protecting the environment.”
Pharmaceutical ads may not be the most popular thing in the world. But that doesn’t change the fact that they have a real benefit — or the fact that banning them would do more harm than good.
Stephen Moore is a co-founder of Unleash Prosperity and a former senior economic advisor to President Donald Trump.
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The views expressed in this piece are those of the author and do not necessarily represent those of The Daily Wire.
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Prescription drugs

Bernie Sanders’s Latest Crusade Could Kill Your Favorite Christmas Commercials

advertising

Bernie Sanders

Robert F. Kennedy Jr.

Televison

The U.S. Food and Drug Administration confirmed on Friday that toxic cough syrups linked to children&#8217;s deaths in India had not been shipped to the United States.
The World Health Organization has said India has a &#8220;regulatory gap&#8221; in screening locally sold syrup medicines.
The U.S. FDA said it was aware of news reports of devastating, ongoing diethylene glycol and ethylene glycol contamination in children&#8217;s cough and cold medicine in India.
Indian authorities advised the public to avoid two more brands of cough syrup on Wednesday following the deaths of 17 children under age five, linked to a toxic ingredient.
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The children died in India over the past month after consuming cough medicine containing toxic diethylene glycol in quantities nearly 500 times the permissible limit, officials said. The deaths were all linked to the Coldrif medicine brand, which was banned after a test confirmed the presence of the chemical on October 2.
India&#8217;s health authority, the Central Drugs Standard Control Organization, informed the U.S. regulator that these products were not exported from India to any other country, the FDA said.
The FDA also said it remains vigilant to prevent contaminated drugs from entering the U.S. and asked manufacturers to ensure that drugs marketed in the U.S. are safe and of the highest quality.
(Reporting by Sneha S K in Bengaluru; Editing by Pooja Desai)

Cough Syrup

Cough Syrups Linked To Child Deaths Not Shipped To U.S., FDA Makes Clear

India

World

President Donald Trump unveiled a deal with U.K.-based drugmaker AstraZeneca on Friday under which the company will sell some medicines at a discount to the government&#8217;s Medicaid health plan in exchange for tariff relief, similar to a drug pricing pact reached last week with Pfizer.
The deals set a framework the White House will use to try to reach its goal of lowering U.S. prescription medicine prices. The president sent letters to 17 leading drugmakers in July telling them to slash prices. Pfizer and Astra are the first two companies to reach a deal with the administration.
AstraZeneca will also offer some of its drugs at up to 80% off their list price through the TrumpRx website planned for next year, CEO Pascal Soriot said at an event in the Oval Office.
He said the company will receive a three-year tariff exemption &#8220;to localize the remainder of our products.&#8221;
U.S. patients currently pay by far the most for prescription medicines, often nearly three times more than in other developed nations, and Trump has been pressuring drugmakers to lower their prices to what patients pay elsewhere or face stiff tariffs.
Last month, Trump threatened 100% tariffs, ratcheting up pressure on the pharmaceutical industry to agree to price cuts and shift manufacturing to the U.S., after negotiations broke down earlier this year, lobbyists and executives told Reuters following the Pfizer deal.
More than 70 million people are covered by Medicaid, the state and federal government program for low-income people. Drug spending in that program is dwarfed by that of Medicare, which covers people aged 65 and older or those with disabilities and is not included in Friday&#8217;s announcement.
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Medicare&#8217;s drug spending reached $216 billion in 2021, while Medicaid&#8217;s gross spending was around $80 billion.
The Medicaid program already receives the lowest drug prices in the U.S., so the additional savings may be modest, said Craig Garthwaite, a professor at Northwestern University&#8217;s Kellogg School of Management.
&#8220;If you look at AstraZeneca&#8217;s portfolio, I don&#8217;t think there are a bunch of drugs that exist where that&#8217;s going to involve them giving a very big discount to Medicaid,&#8221; Garthwaite said.
AstraZeneca&#8217;s Pfizer‑like deal may spare it tariffs, but will not move the needle on U.S. rising health insurance premiums and out‑of‑pocket drug costs, said Rena Conti, an associate professor at Boston University.
&#8220;It&#8217;s good for the companies, and has very uncertain if any benefit for Americans struggling with the affordability of prescription drugs,&#8221; Conti said.
Soriot has worked to keep his company close to Washington while pursuing its growth strategy.
AstraZeneca in July announced it will invest $50 billion in U.S. manufacturing and research and development by 2030. It will build its biggest site worldwide in Virginia, and expand facilities in five other U.S. states.
In September, the company announced it will sell its diabetes and asthma drugs direct to cash-paying U.S. patients at a discount of up to 70% off list prices, another move in response to Trump&#8217;s pressure campaign.
Soriot this year has played up the company&#8217;s U.S. credentials. He described the Anglo-Swedish firm as a &#8220;very American company,&#8221; highlighting its identity shift toward its largest market. AstraZeneca will list its shares in the United States as well as its current markets in the UK and Europe.
(Reporting by Steve Holland in Washington and Michael Erman in New Jersey; Additional reporting by Jarrett Renshaw and Ahmed Aboulenein in Washington, Maggie Fick in London, Patrick Wingrove in New York and Mariam E Sunny in Bengaluru; Editing by Caroline Humer and Bill Berkrot)

Trump Announces U.S. Drug Pricing Deal With AstraZeneca

Economy

Pfizer

U.K.

White House

The U.S. Food and Drug Administration said on Friday it has launched a new pilot program to speed up the review process for generic drugs that are tested and manufactured entirely in the United States.
The program is designed to encourage companies to invest in domestic drug production and research by offering faster approvals for products made with U.S.-sourced ingredients and tested within the country.
Earlier this week, the FDA held a public meeting to discuss its broader efforts to support U.S. pharmaceutical manufacturing, including the PreCheck program, which aims to help set up high-priority drug facilities more quickly.
The FDA said these steps will help strengthen the U.S. drug supply chain and bring high-quality, U.S.-made generic drugs to market more quickly.
More than half of the pharmaceuticals distributed in the United States are made overseas, according to the health regulator.
As of 2025, only 9% of companies that produce the key ingredients in drugs &#8211; known as active pharmaceutical ingredients &#8211; are based in the U.S., compared to 22% in China and 44% in India, the FDA said.
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&#8220;Over-reliance on foreign drug manufacturing and testing creates risks both to national security and patient access, and undermines investments in U.S. research, manufacturing and production,&#8221; said George Tidmarsh, Director of FDA&#8217;s Center for Drug Evaluation and Research.
&#8220;It also slows down reviews and costs taxpayers more money,&#8221; he added.
The FDA also noted many important studies used to approve drugs &#8211; including tests to show that generic drugs work the same as brand-name ones &#8211; are now often done outside the U.S., which is weakening the country&#8217;s ability to lead in drug research and development.
(Reporting by Siddhi Mahatole in Bengaluru; Editing by Shailesh Kuber)

FDA Launches Pilot Program To Fast-Track Review Of Generic Drugs Made In U.S.

President Donald Trump announced on Tuesday that popular medications will be offered at massively discounted prices — known as &#8220;most-favored-nation&#8221; prices — as pharmaceutical behemoth Pfizer commits to a $70 billion investment to manufacture drugs in the U.S.
<blockquote class="twitter-tweet">
President Trump: &#8220;All new medications introduced by Pfizer to the American market will be sold at the reduced, most favored nation cost.&#8221; <a href="https://t.co/S2CQxh7PKC">pic.twitter.com/S2CQxh7PKC</a>
— CSPAN (@cspan) <a href="https://twitter.com/cspan/status/1973055450980503972?ref_src=twsrc%5Etfw">September 30, 2025</a></blockquote>
A new website, called TrumpRX, will allow Americans to purchase drugs directly from the government rather than going through insurance. Virtually all drugs will be discounted on TrumpRX, the White House said.
Pfizer stepped up with a $70 billion investment, a shift toward making drugs in the U.S., which the Trump administration has addressed as a national security issue. 
The company is also offering all medications to Medicaid at most favored nations prices &#8212; which are prices comparable to or less than the cost of other nations&#8217; drug prices. Additionally, all new medications will be offered at most-favored-nation prices.
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Dermatitis medication, for example, will be discounted by 80% &#8212; and that refers to the net price, which is what consumers are actually paying. Meds for post-menopausal osteoporosis, which is extremely common, will be discounted by 85%. Migraine medication and rheumatoid arthritis drugs will be discounted by 50% and 40%, respectively.
<blockquote class="twitter-tweet">
PROMISES MADE, PROMISES KEPT: President Trump Delivers LOWER DRUG PRICES for Americans <a href="https://t.co/nA4tPrmcXt">pic.twitter.com/nA4tPrmcXt</a>
— Rapid Response 47 (@RapidResponse47) <a href="https://twitter.com/RapidResponse47/status/1973062430591692829?ref_src=twsrc%5Etfw">September 30, 2025</a></blockquote>
Health officials, including Food and Drug Administration (FDA) Commissioner Dr. Marty Makary, emphasized that research and development will not stop, but instead, will no longer be funded by only American citizens while the rest of the world benefits.
Makary, for instance, called the changes the &#8220;end of the great American ripoff.&#8221; He noted that drug price offsets will be directed to developed nations like France, Germany, and the U.K.
&#8220;Today marks the end of the great American ripoff, and it also marks the beginning of the end of a great American tragedy, something I’ve seen as a physician at the bedside — patients getting spun up into a financial rage &#8230; to try to get enough money to pay for a drug &#8230; a drug that&#8217;s five or ten times more expensive than the same drug in France or Germany or the U.K.,&#8221; he said.
<blockquote class="twitter-tweet" data-media-max-width="560">
.<a href="https://twitter.com/DrMakaryFDA?ref_src=twsrc%5Etfw">@DrMakaryFDA</a>: &#8220;Today marks the the beginning of the end of the great American rip off, and it also marks the beginning of the end of a great American tragedy; something I’ve seen as a physician at the bedside — patients getting spun up into a financial rage&#8230; to try to get… <a href="https://t.co/SD0iKsZR2B">pic.twitter.com/SD0iKsZR2B</a>
— Rapid Response 47 (@RapidResponse47) <a href="https://twitter.com/RapidResponse47/status/1973063636395373048?ref_src=twsrc%5Etfw">September 30, 2025</a></blockquote>
Dr. Mehmet Oz, who is the administrator of the Centers for Medicare &amp; Medicaid Services (CMS), echoed the sentiment, noting that the administration is &#8220;protecting medical advances for the future, while at the same time securing the drug prices Americans want, today.&#8221;
<blockquote class="twitter-tweet">
.<a href="https://twitter.com/DrOzCMS?ref_src=twsrc%5Etfw">@DrOzCMS</a>: &#8220;In July, President Trump demanded that manufacturers make a firm commitment to lower their prices “or else.” Last week, we made a major breakthrough. Protecting medical advances for the future, while at the same time securing the drug prices Americans want today.&#8221; <a href="https://t.co/56dvAt1OHi">pic.twitter.com/56dvAt1OHi</a>
— HHS.gov (@HHSGov) <a href="https://twitter.com/HHSGov/status/1973065918897881436?ref_src=twsrc%5Etfw">September 30, 2025</a></blockquote>
Trump announced his &#8220;most favored nation&#8221; pricing plans at the end of July, promising to end &#8220;global freeloading&#8221; by other developed nations. The president suggested he would use tariffs and all other &#8220;tools&#8221; available to make sure all companies provide Americans with most-favored-nation prices.
Related: <a href="https://www.dailywire.com/news/trump-signs-order-to-reduce-drug-prices-tells-rest-of-world-to-pay-up">Trump Signs Order To Reduce Drug Prices, Tells Rest Of World To Pay Up</a>

‘End Of Great American Ripoff’: Trump Makes Major Drug Price Announcement

The U.S. Food and Drug Administration (FDA) announced on Tuesday evening that it&#8217;s cracking down on deceptive pharmaceutical ads, issuing thousands of warning letters and about 100 cease-and-desist notifications.
“For far too long, the FDA has permitted misleading drug advertisements, distorting the doctor-patient relationship and creating increased demand for medications regardless of clinical appropriateness,” FDA Commissioner Dr. Marty Makary said in a statement. “Drug companies spend up to 25% of their budget on advertising. Those billions of dollars would be better spent on lowering drug prices for everyday Americans.”
A press release from the agency said current law requires pharma ads to &#8220;present a fair balance between a product’s risks and benefits; avoid exaggerating benefits; not create a misleading overall impression; properly disclose financial relationships; and include information regarding major side effects and contraindications.&#8221;
That rule, which the FDA did not adequately enforce during the Biden years, will be &#8220;aggressively&#8221; enforced now, the release says. Additionally, the FDA is closing the “adequate provision” loophole created in 1997, which companies have used to &#8220;conceal critical safety risks in broadcast and digital ads, fueling inappropriate drug use and eroding public trust.&#8221;
Television ads are not the only promotional content being scrutinized and regulated. Social media posts, which often feature an influencer talking up the drug, rarely mention &#8220;potential harms,&#8221; or they fail to disclose that the influencers are being paid.
&#8220;[W]hile 100% of pharmaceutical social media posts highlight drug benefits, only 33% mention potential harms,&#8221; the FDA said, citing a 2024 review in the Journal of Pharmaceutical Health Services Research. &#8220;Moreover, 88% of advertisements for top-selling drugs are posted by individuals and organizations that fail to adhere to the FDA fair balance guidelines.&#8221;
In the thousands of letters sent to drug companies, the FDA warns, &#8220;You are hereby directed to remove any noncompliant advertising and bring all promotional communications into compliance.&#8221;
&#8220;This notice also serves to demand compliance with the [Federal Food, Drug, and Cosmetic] Act and FDA implementing regulations and requires companies to remove any and all DTC (direct-to-consumer) prescription drug advertising that violates the law,&#8221; the letter adds.
Robert F. Kennedy Jr. &#8212; the head of Health and Human Services (HHS), which oversees the FDA &#8212; has long been a critic of Big Pharma ads. He said in a statement issued Tuesday that &#8220;pharmaceutical ads hooked this country on prescription drugs.&#8221;
&#8220;We will shut down that pipeline of deception and require drug companies to disclose all critical safety facts in their advertising,&#8221; he continued. &#8220;Only radical transparency will break the cycle of overmedicalization that drives America’s chronic disease epidemic.”
While Kennedy was running for president in 2024, before he endorsed President Donald Trump, he said he would &#8220;issue an executive order banning pharmaceutical advertising on television.&#8221;
&#8220;We are one of only two countries in the world that allow pharmaceutical companies to advertise directly to consumers on television,&#8221; RFK Jr. said on X in 2024. &#8220;Not surprisingly, Americans consume more pharmaceutical products than anyone else on the planet.&#8221;

Great American Farmers Market 2025

Trump FDA Announces Major Crackdown On ‘Misleading’ Pharma Ads

Big Pharma

U.S. Health Secretary Robert F. Kennedy Jr. plans to announce that use of Kenvue&#8217;s popular over-the-counter pain medication Tylenol in pregnant women is potentially linked to autism, The Wall Street Journal reported on Friday, citing people familiar with the matter, without including evidence for the claims.
Kennedy, in the report, will also suggest a medicine derived from folate called folinic acid can be used to treat symptoms of autism in some people, the WSJ reported.
Shares of Kenvue fell 14% after the report. Tylenol, whose active ingredient is acetaminophen, is a widely used pain reliever, including by pregnant women.
Kenvue said in a statement that it believes there is no causal link between Tylenol use during pregnancy and autism. The company advises expecting mothers to speak to healthcare professionals before taking OTC medications, including Tylenol.
The U.S. Food and Drug Administration and leading medical organizations agree on the safety of acetaminophen, its use during pregnancy, and the information provided on the label, the company said.
Kennedy has promised to find the cause of autism and has long suggested it is related to vaccines. He has also said it must be related to an &#8220;environmental toxin.&#8221; Decades of science have yet to establish a definitive cause.
Under Kennedy, the National Institutes of Health is running an Autism Data Science Initiative that aims to mine large datasets to investigate possible contributors to autism and evaluate the outcomes of existing treatments. Researchers have submitted more than 100 proposals to participate in the $50 million study, with a list of up to 25 grant winners expected to be announced by the end of September, people with knowledge of the plans told Reuters.
The WSJ said that a report is likely to highlight how low levels of folate, an important vitamin, and Tylenol taken during pregnancy, could be a potential cause of autism.
&#8220;What&#8217;s striking to me is that this report is supposed to uncover all these new causes, and so far, all we&#8217;re learning is that they&#8217;re rehashing existing research,&#8221; said Dr. David Mandell, a professor of psychiatry and autism expert at the University of Pennsylvania.
&#8220;We have no understanding of why there might be a biological reason that Tylenol would cause autism.&#8221;
In December 2023, a U.S. federal judge struck a blow to hundreds of lawsuits claiming Tylenol can cause autism if mothers take it during pregnancy, barring expert witnesses from testifying after finding they lacked scientific evidence for their claims.
Last August, citing that ruling, the judge dismissed all the cases in federal court. A U.S. appeals court is slated to hear arguments next month in an appeal of that ruling, court records show.
&#8220;We are using gold-standard science to get to the bottom of America’s unprecedented rise in autism rates. Until we release the final report, any claims about its contents are nothing more than speculation,&#8221; said an HHS Spokesperson.
Children&#8217;s Health Defense, the anti-vaccine group formerly headed by Kennedy, has posted several times in recent weeks on social media site X about the potential link between Tylenol and autism.
Brian Hooker, chief scientific officer of CHD, said in a recent video posted on X that he expects Kennedy&#8217;s autism report to hit on Tylenol, but also vaccines and vaccine components.
CHD has cited a study published in August that found evidence of an association between use of acetaminophen by pregnant women and neurodevelopmental disorders such as autism in their offspring.
The scientists recommended medical guidelines advise that pregnant women use the lowest possible dose for the shortest time needed.
They noted that more studies were required to confirm any association and that failure to treat fever in pregnant women could lead to other fetal problems, such as neural tube defects.
Other studies have not found a link. A 2024 study published in the Journal of the American Medical Association involving 2.4 million children born in Sweden found no evidence to support a causal link.
&#8220;There is no clear evidence that proves a direct relationship between the prudent use of acetaminophen during pregnancy and fetal developmental issues,&#8221; said Christopher Zahn, chief of clinical practice for the American College of Obstetricians and Gynecologists.
(Reporting by Michael Erman in New Jersey and Julie Steenhuysen in Chicago, Additional reporting by Puyaan Singh in Bengaluru and Nancy Lapid in Tucson; Editing by Vijay Kishore and Aurora Ellis)

RFK Jr. To Link Tylenol Use In Pregnancy To Autism, Says Wall Street Journal

Department of Health and Human Services

Wall Street Journal

Following the <a href="https://www.dailywire.com/news/gavin-newsom-mocks-prayer-after-catholic-school-shooting?author=Zach+Jewell&amp;category=News&amp;elementPosition=undefined&amp;row=0&amp;rowType=Vertical+List&amp;title=Gavin+Newsom+Mocks+Prayer+After+Catholic+School+Shooting">deadly shooting</a> at Annunciation Catholic Church by a transgender-identifying 23-year-old, Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. dismissed rabid gun control calls and focused on the &#8220;health crisis&#8221; behind mass shootings.
&#8220;I certainly consider mass shootings a health crisis,&#8221; Kennedy <a href="https://x.com/nicksortor/status/1961159049866846589">said</a> on Thursday. &#8220;And we are doing, for the first time, real studies on what the ideology of that is, and we&#8217;re looking, for the first time, at psychiatric drugs.&#8221;
&#8220;People have had guns in this country forever,&#8221; the secretary continued. &#8220;When I was a kid, we had shooting clubs at our school. Kids, my classmates, and other people would bring a .22 rifle with their guns to school and park in the parking lot. Nobody was shooting up schools.&#8221;
&#8220;There&#8217;s never been a time in the history of humanity where people walked into a crowd, or a church, or a movie theater, or a school, or a crowd of strangers and just started randomly shooting,&#8221; he said. &#8220;It&#8217;s happening in our country, it&#8217;s not happening around the world. And there are many other countries that have comparable levels [of] guns that we have in this country &#8212; we had comparable levels in the &#8217;40s, &#8217;50s, and &#8217;60s and people weren&#8217;t doing that. Something changed, and it dramatically changed human behavior.&#8221;
&#8220;One of the culprits we need to examine is the fact that we&#8217;re the most overmedicated nation in the world, and a lot of those are psychiatric drugs that have blackbox warnings on them that warn of suicidal and homicidal ideation,&#8221; Kennedy added. &#8220;We are doing those studies right now for the first time, and we will have an answer.&#8221;
<blockquote class="twitter-tweet" data-media-max-width="560">
🚨 JUST IN: RFK Jr. launched a FULL INVESTIGATION into the meds the trans Minneapolis shooter was using
“There’s never been a time in America… where people walk into a crowd or a church or a movie theater or a school and just start randomly shooting.”
“SOMETHING changed, and… <a href="https://t.co/GSSPMfhTpr">pic.twitter.com/GSSPMfhTpr</a>
— Nick Sortor (@nicksortor) <a href="https://twitter.com/nicksortor/status/1961159049866846589?ref_src=twsrc%5Etfw">August 28, 2025</a></blockquote>
Kennedy has previously noted that HHS will look into the effects of psychiatric drugs and how they are being prescribed. Back in February, the secretary listed SSRI (Selective Serotonin Reuptake Inhibitor) and other psychiatric drugs as a potential contributor to our national health crisis.
<a href="https://get.dailywire.com/subscribe/plus/?utm_campaign=summer&amp;utm_content=editorialsummersale&amp;utm_medium=website&amp;utm_source=editorial" target="_blank" rel="noopener">End of Summer Sale – Get 40% off New DailyWire+ Annual Memberships</a>
“Whatever belief or suspicion I have expressed in the past, I’m willing to subject them all to the scrutiny of unbiased science,&#8221; RFK said at the time. “That is gonna be our template: unbiased science.”
<blockquote class="twitter-tweet" data-media-max-width="560">
HHS Secretary RFK Jr. pledges “NOTHING is gonna be off limits” in chronic disease investigation
“The childhood vaccine schedule, electromagnetic radiation, glyphosate, other pesticides, ultra processed foods, artificial food additives, SSRI and other psychiatric drugs, PFAs,… <a href="https://t.co/kWV2LHuqTG">pic.twitter.com/kWV2LHuqTG</a>
— Holden Culotta (@Holden_Culotta) <a href="https://twitter.com/Holden_Culotta/status/1891888695185375248?ref_src=twsrc%5Etfw">February 18, 2025</a></blockquote>
The use of SSRI drugs among teenagers and adults in the U.S. has increased by almost 400% from the early 1990s to 2006, <a href="https://www.dailywire.com/news/democrats-enter-panic-mode-as-rfk-sets-out-to-make-america-healthy-again">The Daily Wire</a> previously noted. By 2014, one in ten adults had an SSRI prescription, before there was another 35% increase from 2015 to 2021, totaling tens of millions of prescriptions.
Still, the number of Americans suffering from depression has continued to spike. “The percentage of U.S. adults who report having been diagnosed with depression at some point in their lifetime reached 29.0%, nearly 10 percentage points higher than in 2015,&#8221; a 2023 Gallup poll found.
Related: <a href="https://www.dailywire.com/news/new-research-finds-antidepressants-may-cause-emotional-blunting">New Research Finds Antidepressants May Cause ‘Emotional Blunting’</a>

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