Lindsay Clancy

The Lindsay Clancy Case Isn’t A ‘Who-Dun-It.’ Why Are TikTok Moms Pretending It Is?

anti-depressants

Big Pharma

Feminism

postpartum depression

Social Media

TikTok

When the Food and Drug Administration announced that the agency would be removing the black-box warning from hormone replacement therapy, or HRT, women everywhere threw their hands up in celebration.
And rightly so. America’s health agencies are finally acknowledging that women are not simply “little men,” and that research and clinical care must account for a woman’s unique biology and hormonal fluctuations across every stage of life.
But amid the cheering, some important nuance is being overlooked. The FDA’s decision to remove the black-box warning from HRT is just one example of how recommendations offered without adequate context or distinction may do more harm than good.
The idea that estrogen supplementation is a cure-all for the symptoms women commonly experience during perimenopause and menopause — hot flashes, disrupted sleep, fatigue, muscle aches, inflammation, weight gain, bloating, and mood swings — is a myth.
Often, women are not suffering from a lack of estrogen, but from what <a href="https://www.healthygutgirl.com/">Kitty Martone</a>, a holistic health educator who works with women to <a href="https://www.facebook.com/groups/1426024567689906">navigate perimenopause and menopause</a>, refers to as <a href="https://www.amenclinics.com/blog/what-is-estrogen-dominance/">estrogen dominance</a> — a state in which estrogen outweighs progesterone, producing symptoms that look identical to low estrogen.
Estrogen does not act in isolation, but the details are rarely explained to women. To be tolerated well, estrogen must be balanced by adequate progesterone and supported by a healthy metabolic rate. For many women, progesterone is the first hormone to decline — often years before estrogen meaningfully drops — due to chronic stress, under-eating, thyroid suppression, and blood sugar instability.
This creates a common paradox: estrogen may appear “normal,” or even low, on a lab test, yet functionally feel excessive in the body because there is not enough progesterone to counterbalance its effects. Women are then told they are estrogen-deficient and prescribed more estrogen, while symptoms such as anxiety, insomnia, migraines, heavy or irregular bleeding, bloating, and inflammation intensify rather than improve.
In these cases, simply prescribing more estrogen does not resolve symptoms. In fact, it can make them worse.
These mechanisms were not understood properly during the Women’s Health Initiative study, which was abruptly halted in the early 2000s upon a suggested correlation between HRT and breast cancer as well as heart disease. In an effort to recover from the fallout of the highly <a href="https://pmc.ncbi.nlm.nih.gov/articles/PMC10758198/">flawed study</a>, which caused millions of women to abandon hormone therapy altogether, the pendulum has swung in the opposite direction.
Cue the pharmaceutical ads: dancing women in sunflower meadows, singing about how wonderful life is with the latest HRT option. The fine print instructs women to “ask your doctor if it’s right for you,” but many doctors may not be properly equipped to offer nuanced guidance.
Over the past few decades, medical visits have been reduced to 15–20 minute symptom reviews that are translated into billing codes entered into a computer. While this system serves insurance and data collection, it fails to treat women as whole individuals. It leaves little room to explore how diet, stress, thyroid function, gut health, or metabolic status influence hormonal symptoms — particularly in perimenopausal women.
Martone argues that this system has created an environment where estrogen is prescribed casually, without sufficient context. “Doctors now essentially have carte blanche to prescribe estrogen for any hormone complaint — without evaluating detox pathways, metabolism, liver function, or estrogen clearance.”
Some clinicians have been cautioning against this oversimplification for decades. <a href="https://raypeat.com/">Dr. Ray Peat</a>, who studied hormones, metabolism, and stress physiology extensively, <a href="https://raypeat.com/articles/aging/aging-estrogen-progesterone.shtml">wrote about</a> how estrogen tends to accumulate under conditions of chronic stress and low thyroid function, while progesterone plays a stabilizing, protective role for both the nervous system and bodily tissues.
In plain terms, how a woman feels on hormones can have less to do with hormone levels and more to do with improper functioning of the liver, metabolism, and stress load at the time therapy is introduced. Two women can take the same prescription and have completely different outcomes — not because one is “doing it wrong,” but because their internal terrain is different.
This helps explain why so many women feel dismissed when HRT is presented as a simple solution. When symptoms worsen, they are often told to increase the dose or switch brands, rather than step back and ask whether the body is prepared to handle additional estrogen.
Martone emphasizes that women often need to experiment with hormones to discover individualized therapies that are right for them. Even low doses may require careful adjustment, alternative delivery methods, and significant trial and error — an experience that can be costly, frustrating, and far from straightforward.
Meanwhile, big pharmaceutical companies are circling middle-aged women like sharks around blood. With the FDA’s decision, they’ve gained an expanded customer base — one encouraged to start hormone therapy earlier and remain on it for decades.
The truth is no one — not even a doctor — can predict exactly how a woman will respond to HRT. Hormones are powerful biological signals, not cosmetic fixes. Their effects depend heavily on the body’s metabolic health, stress physiology, and ability to process and clear them.
The renewed interest in hormone therapy reflects a real and valid desire for relief for women. But before removing warning labels and declaring HRT a universal solution, it’s worth asking why those cautions existed in the first place.
Hormone replacement therapy is not a magic bullet. Women deserve care that honors complexity, not just convenience.
* * *
Jennifer Galardi is a Senior Policy Analyst for Restoring American Wellness in Heritage’s DeVos Center.
The views expressed in this piece are those of the author and do not necessarily represent those of The Daily Wire.

Nurse talks with female patient about prescription medication

What The FDA Doesn’t Tell Women About Hormone Replacement Therapy

Doctors

Health Care

Heritage Foundation

Pharmaceuticals

Women

On Thursday, the U.S. Food and Drug Administration (FDA) <a href="https://www.fda.gov/news-events/press-announcements/fda-approves-novel-non-opioid-treatment-moderate-severe-acute-pain">approved</a> Journavx (suzetrigine) 50 mg oral tablets, a first-in-class non-opioid analgesic for the treatment of moderate to severe acute pain in adults.
Developed by Vertex Pharmaceuticals, Journavx represents a novel approach to pain management, targeting sodium channels in the peripheral nervous system to block pain signals before they reach the brain, offering an alternative to addictive opioids for post-surgical pain.
The FDA highlighted this approval as a major public health milestone, providing patients with a safer pain management option while addressing the opioid crisis. The agency has long promoted the development of non-opioid therapies through its Overdose Prevention Framework, issuing guidance to encourage innovative analgesics and supporting clinical practice guidelines for acute pain management. Journavx’s application received Breakthrough Therapy, Fast Track, and Priority Review designations, reflecting its therapeutic significance.
Efficacy was demonstrated in two randomized, double-blind, placebo- and active-controlled clinical trials involving patients recovering from abdominoplasty and bunionectomy. Both trials showed that Journavx significantly reduced pain compared to placebo, with participants allowed to use ibuprofen as “rescue” medication if needed. Safety data from 874 participants in these trials, along with supportive data from 256 patients in a separate open-label study, showed that common adverse effects included itching, muscle spasms, rash, and elevated creatine phosphokinase. Journavx is contraindicated with strong CYP3A inhibitors and should not be taken with grapefruit-containing foods or drinks.
Journavx joins the broader category of non-opioid analgesics, which includes acetaminophen, NSAIDs, COX-2 inhibitors, topical agents, and adjuvant therapies. Unlike opioids, these drugs relieve pain without binding to central opioid receptors, avoiding risks of dependence, tolerance, and respiratory depression. Journavx distinguishes itself as the first approved drug to block pain at peripheral nerves without affecting the brain, offering a promising new option for acute pain management while reducing reliance on opioid medications.
Most side effects in clinical trials were rated as mild to moderate and resolved without long-term issues. While no serious adverse events were directly linked to the drug in primary trials, the FDA and medical guides list several precautions:
<ul style="font-weight: 400;">
<li>Liver Function: Patients with moderate hepatic impairment require a lower dose. The drug is not recommended for those with severe liver disease (Child-Pugh Class C).</li>
<li>Kidney Function: It should be avoided in patients with severe renal impairment (eGFR &lt;15 mL/min).</li>
<li>Fertility &amp; Pregnancy: It may temporarily reduce the chance of becoming pregnant while on treatment. There is currently no human data on its safety during pregnancy or breastfeeding.</li>
</ul>

Peripheral Neuropathy pain in elderly patient on foot, hand, fingers, sensory nerves with numbness, muscle cramps, weakness from chronic inflammatory demyelinating polyneuropathy

Breakthrough In Acute Pain Management: FDA Approves First-In-Class Non-Opioid

Health

U.S.

A famed doctor with tens of millions of followers on social media was recently schooled on the issues plaguing public health by a supporter of the &#8220;Make America Healthy Again&#8221; agenda.
Mikhail Varshavski, known online as Dr. Mike, argued on a recent episode of Jubilee&#8217;s &#8220;<a href="https://www.youtube.com/watch?v=y90R8BPc8Ag">Surrounded</a>&#8221; that Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. should step down from his position, citing cuts to bureaucracy within the department.
A supporter of the MAHA movement named Brian needed under two minutes to decimate Dr. Mike&#8217;s argument.
&#8220;So considering all of that &#8230; where did that get us?&#8221; the MAHA supporter asked Dr. Mike, responding to specific HHS cuts cited by the online personality.
Notably, Secretary Kennedy has defended cuts to HHS, citing absurd bureaucracy and overlapping offices that he contends are wasteful and not helping improve public health.
&#8220;Look at the state of America, of Americans&#8217; health, and you tell me that the public is actually healthy,&#8221; Brian dared Dr. Mike. &#8220;What RFK is doing is he is saying, &#8216;enough is enough, something has to change.&#8217; And I will say this very politely &#8212; I think that you have to be f***ing insane to say &#8216;more&#8217; is somehow going to get us out of the current public health crisis that we have right now.&#8221;
&#8220;Americans are fat and they are sick and it is not getting better, and taking more and more money and continuing to flush it down the toilet is not going to solve the problem,&#8221; he continued.
&#8220;We know what will stop cancer dead in its tracks. We know what will stop all chronic disease dead in its tracks. Do you know what it is?&#8221; Brian asked.
&#8220;Lifestyle changes,&#8221; Dr. Mike responded.
&#8220;Lifestyle changes,&#8221; the MAHA supporter agreed. &#8220;The American Heart Association has known about this for years, that the most important predictor of longevity, risk of chronic disease, all-cause mortality is <a href="https://www.ahajournals.org/doi/pdf/10.1161/cir.0000000000000461">VO2 max</a>. So why aren&#8217;t doctors &#8212; why isn&#8217;t the government creating a public health system that says, &#8216;you know what, we&#8217;re gonna focus on VO2 max because even if we stopped every dollar we had [going] into cancer research right now, and we took that money and we said, let&#8217;s get people moving, let&#8217;s increase their VO2 max.'&#8221;
&#8220;The question is, when is enough enough to admit that the system you are a part of has drastically failed Americans?&#8221; Brian posed.
The supporter added that Secretary Kennedy, &#8220;by the very fact of how he looks in his 70s, does more to encourage people to live a healthy lifestyle and truly make America healthy again.&#8221;
WATCH:
<blockquote class="twitter-tweet" data-media-max-width="560">
🔥 Dr. Mike Claims RFK Jr is ‘Decimating Public Health’, Gets Lit Up by a MAHA Supporter
“Look at the state of America and you tell me that the public is actually healthy. What RFK is doing is he is saying enough is enough, something has to change. I will say this very politely,… <a href="https://t.co/3yAeFCB0b9">pic.twitter.com/3yAeFCB0b9</a>
— Chief Nerd (@TheChiefNerd) <a href="https://twitter.com/TheChiefNerd/status/1997734282479988779?ref_src=twsrc%5Etfw">December 7, 2025</a></blockquote>
Related: <a href="https://www.dailywire.com/news/rfk-jr-shakes-up-childhood-vax-schedule-with-hep-b-decision?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=2&amp;row=0&amp;rowType=Vertical+List&amp;title=RFK+Jr.+Shakes+Up+Childhood+Vax+Schedule+With+Hep+B+Decision">RFK Jr. Shakes Up Childhood Vax Schedule With Hep B Decision</a>

MAHA supporter

MAHA Supporter Destroys Famed Doctor Attacking RFK Jr. In Under 2 Minutes

Disease

Robert F. Kennedy Jr.

Texas Attorney General Ken Paxton is suing the makers of Tylenol for marketing the drug to pregnant mothers despite allegedly knowing that early exposure to the drug leads to an increased risk of autism, The Daily Wire can exclusively report.
Paxton has filed suit against Johnson &amp; Johnson and its former subsidiary, Kenvue, &#8220;deceptively marketing Tylenol to pregnant mothers despite knowing that early exposure to acetaminophen, Tylenol’s only active ingredient, leads to a significantly increased risk of autism and other disorders,&#8221; a statement from Paxton&#8217;s office reads.
“Big Pharma betrayed America by profiting off of pain and pushing pills regardless of the risks,&#8221; Paxton said. &#8220;These corporations lied for decades, knowingly endangering millions to line their pockets.&#8221;
Paxton&#8217;s office accused Johnson &amp; Johnson of attempting to &#8220;silence the science&#8221; about the apparent association between prenatal and early childhood exposure to their acetaminophen products and autism and ADHD. It also said the company marketed Tylenol as a &#8220;completely safe pain medication for pregnant women,&#8221; while knowing about the association, which the office said is in violation of Texas’ consumer protection laws.
Texas is the first state to sue the makers of Tylenol after the Department of Health and Human Services trumpeted a link between prenatal acetaminophen consumption and the incidence of autism and ADHD in newborns.
“Taking Tylenol is not good. I’ll say it. It’s not good,” President Donald Trump said last month at a press conference with Health and Human Services Secretary Robert F. Kennedy Jr.
Join us now during our exclusive Deal of the Decade. Get everything for $7 a month. Not as fans. As fighters. Go to <a href="https://get.dailywire.com/subscribe/plus/" target="_blank" rel="noopener">DailyWire.com/Subscribe</a> to join now.
In the lawsuit, Paxton accuses Johnson &amp; Johnson of trying to &#8220;escape responsibility&#8221; for its actions by breaking off Kenvue as a separate entity after becoming aware of the Trump administration&#8217;s impending announcement.
“Seeing that the day of reckoning was coming, Johnson &amp; Johnson attempted to escape responsibility by illegally offloading their liability onto a different company,&#8221; Paxton writes. &#8220;By holding Big Pharma accountable for poisoning our people, we will help Make America Healthy Again.”
Paxton&#8217;s office says the pharmaceutical company &#8220;violated the Texas Uniform Fraudulent Transfer Act by fraudulently transferring liabilities arising from Tylenol to a separate company, Kenvue, in order to shield their assets against lawsuits arising from the harmful impact Tylenol had on children.&#8221;
“We believe independent, sound science clearly shows that taking acetaminophen does not cause autism,&#8221; Kenvue <a href="https://www.axios.com/2025/09/22/trump-tylenol-autism-announcement-kenvue" target="_blank" rel="noopener">said</a> in a statement last month. &#8220;We strongly disagree with any suggestion otherwise and are deeply concerned with the health risk this poses for expecting mothers.”
Paxton has taken on other large pharmaceutical companies, suing Pfizer over the COVID vaccine and Eli Lilly for allegedly bribing providers to prescribe its medications.
In 2024, Paxton — along with dozens of other states — secured a $700 million settlement with Johnson &amp; Johnson for misleading and deceptive claims related to its baby powder products that contained talc.
Related: <a href="https://www.dailywire.com/news/potential-cause-treatment-of-autism-revealed-by-trump-rfk-jr?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=0&amp;row=0&amp;rowType=Vertical+List&amp;title=Potential+Cause%2C+Treatment+Of+Autism+Revealed+By+Trump%2C+RFK+Jr.">Potential Cause, Treatment Of Autism Revealed By Trump, RFK Jr.</a>

A photo illustration of Tylenol packing,

We Have Our First Major Tylenol Lawsuit

Courts

Texas

Tylenol

Flanked by Secretary of Health and Human Services Robert F. Kennedy Jr. and other leaders of the free world, President Trump announced on Tuesday a new <a href="https://www.dailywire.com/news/i-think-weve-found-an-answer-to-autism-what-to-know-about-trumps-major-announcement?author=Amanda+Prestigiacomo&amp;category=undefined&amp;elementPosition=105&amp;row=3&amp;rowHeadline=Latest+News&amp;rowType=Vertical+Carousel&amp;title=%E2%80%98I+Think+We%E2%80%99ve+Found+An+Answer+To+Autism%E2%80%99%3A+What+To+Know+About+Trump%E2%80%99s+Major+Announcement">investigation</a> into a potential link between a popular pain medication and autism.
During the briefing, the president pointed out that the Amish are a good example of a people with <a href="https://www.dailywire.com/news/potential-cause-treatment-of-autism-revealed-by-trump-rfk-jr?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=5&amp;row=0&amp;rowType=Vertical+List&amp;title=Potential+Cause%2C+Treatment+Of+Autism+Revealed+By+Trump%2C+RFK+Jr.">essentially</a> no autism.
What’s so special about the Amish? That’s easy: clean living and a high tolerance for pain. Plus, the Amish have never even heard of acetaminophen.
Underneath those broad-brimmed straw hats, plain shirts, and suspenders, however, lies a rugged, hard-working people with smooth skin and wavy hair. Amish men may have rough hands from doing rough work, but their muscular upper arms are notoriously smooth. World famous.
And who doesn&#8217;t want to be like the Amish?
Thanks to <a href="https://www.jeremysrazors.com/collections/bestselling-essentials/products/all-day-set?selling_plan=3028484309">Jeremy’s Hair &amp; Body Bundle</a>, your hair and skin can also look and feel like the Amish.
<a href="https://www.jeremysrazors.com/collections/bestselling-essentials/products/all-day-set?selling_plan=3028484309"><img loading="lazy" decoding="async" class="size-large wp-image-976453 aligncenter" src="https://dw-wp-production.imgix.net/2025/09/JR-Hair-Body-Bundle-dark-4x5-1-461x576.jpg" alt="" width="461" height="576" srcset="https://dw-wp-production.imgix.net/2025/09/JR-Hair-Body-Bundle-dark-4x5-1-461x576.jpg 461w, https://dw-wp-production.imgix.net/2025/09/JR-Hair-Body-Bundle-dark-4x5-1-240x300.jpg 240w, https://dw-wp-production.imgix.net/2025/09/JR-Hair-Body-Bundle-dark-4x5-1-768x960.jpg 768w, https://dw-wp-production.imgix.net/2025/09/JR-Hair-Body-Bundle-dark-4x5-1.jpg 1230w" sizes=" (max-width: 461px) 100vw, 461px" /></a>
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Jeremy’s bath and body products are all about freedom, just like you. They’re paraben-free, sulfate-free, and even woke-free.
Former guest host of The Oprah Winfrey Show and current Administrator for the Centers for Medicare &amp; Medicaid Services, Dr. Mehmet Oz, also had something to say about taking acetaminophen.
“Make sure there’s an important reason to take it. Don’t take it willy-nilly,” said Dr. Oz.
<div id="attachment_976455" style="width: 875px" class="wp-caption aligncenter"><img loading="lazy" decoding="async" aria-describedby="caption-attachment-976455" class="size-large wp-image-976455" src="https://dw-wp-production.imgix.net/2025/09/dea60e29-a11e-4e96-8a5e-3a6f3ffdaef8-865x576.jpg" alt="US President Donald Trump, left, and Mehmet Oz, administrator of the Centers for Medicare &amp; Medicaid Services, in the Roosevelt Room of the White House in Washington, DC, US, on Monday, Sept. 22, 2025. Trump said his administration was linking acetaminophen, the active ingredient in Tylenol, to autism and urging pregnant women to largely avoid the medication. Photographer: Francis Chung/Politico/Bloomberg via Getty Images" width="865" height="576" srcset="https://dw-wp-production.imgix.net/2025/09/dea60e29-a11e-4e96-8a5e-3a6f3ffdaef8-865x576.jpg 865w, https://dw-wp-production.imgix.net/2025/09/dea60e29-a11e-4e96-8a5e-3a6f3ffdaef8-300x200.jpg 300w, https://dw-wp-production.imgix.net/2025/09/dea60e29-a11e-4e96-8a5e-3a6f3ffdaef8-768x512.jpg 768w, https://dw-wp-production.imgix.net/2025/09/dea60e29-a11e-4e96-8a5e-3a6f3ffdaef8.jpg 1024w" sizes=" (max-width: 865px) 100vw, 865px" />Francis Chung/Politico/Bloomberg via Getty Images</div>
Dr. Oz, of course, does not have to tell the Amish not to do anything willy-nilly. The &#8220;Plain People&#8221; are among the most disciplined subcultures on the continent. Have you ever seen a willy-nilly Amish barn? We didn’t think so.
The president ended the briefing by telling the crowd that acetaminophen does cause harm.
To which Big Pharma quickly responded by saying, “Does not.”
To which Trump replied, saying, “Does too.”
Big Pharma: “Does not.”
Trump: “Does too.”
Big Pharma: “Does not.”
Trump: “Does too.”
The exchange went on for so long that the Legacy Media were forced to turn off their cameras and break for dinner before an agreement could be reached. Thankfully, the Amish in attendance had already prepared a hearty spread of meat and potatoes for all to enjoy.
The good news is, when it comes to quality shampoos and lotions that are good for your skin, you don’t have to wait for government officials to agree. 
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f6f34234-bcb3-448d-983d-96a16866283f

HHS Explores Link Between The Amish And Smooth Skin And Wavy Hair

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Drugmaker Bristol Myers Squibb is set to release a new schizophrenia treatment in the United Kingdom for the same price it’s listed for in the United States, a decision that will certainly please those in the White House who have fought to get Americans the same prices offered overseas.
The announcement, made by Bristol on Monday, follows a push from President Donald Trump for U.S. drugmakers to lower prescription drugs for Americans to the greatest extent possible. Bristol’s approach to the United Kingdom market aligns with the White House’s strategy to secure lower drug prices in the United States.
The pharmaceutical company has never before brought its price for a drug to parity across the United States and the United Kingdom. Adam Lenkowsky, chief commercialization officer at Bristol, said that the drug company is prepared to pull its drug, Cobenfy, from the European nation&#8217;s market if the relevant government authorities do not agree to the price listed in the United States, at $1,850 a month.
“Our intention is to work with NICE and NHS to make this medicine available, but we are prepared to make the difficult decision to walk away if they cannot better recognize the value our medicine brings to patients and society,” Lenkowsky said in a statement.
“We agree with the Trump Administration that other countries need to pay their fair share,” he added.
Cobenfy has not yet been approved for sale in the United Kingdom. Bristol plans to file for approval in the coming weeks and expects to receive approval sometime next year, according to the <a href="https://www.ft.com/content/0913ee5f-1631-4e1b-8bd8-99ce2c9dd64f">Financial Times</a>.
Last year, the research group RAND <a href="https://www.rand.org/news/press/2024/02/01.html">found</a> that Americans pay significantly more for prescription drugs than other countries. The research pegged the inflated price at 2.78 times what is charged in other countries.
The Trump administration is determined to end that trend, and has pointed to drug manufacturers.
“The United States has less than five percent of the world’s population and yet funds around three quarters of global pharmaceutical profits,” a May 12 White House <a href="https://www.whitehouse.gov/presidential-actions/2025/05/delivering-most-favored-nation-prescription-drug-pricing-to-american-patients/">executive order</a> on drug prices says. “This egregious imbalance is orchestrated through a purposeful scheme in which drug manufacturers deeply discount their products to access foreign markets, and subsidize that decrease through enormously high prices in the United States.”
The order aims to pressure drugmakers to push for parity between prices for its drugs in the United States and elsewhere in the world. The president last week said that other countries have treated Americans unfairly when it comes to drug prices.
“For years, we&#8217;ve been paying for a pill $100 and they&#8217;re paying $10,” the president said on Fox News last week. Trump suggested he intends to pressure other countries into raising drug prices to offset the costs of making new drugs for Americans.
“The drug companies agree that I&#8217;m right, and the countries, if they don’t agree, I’ll use tariffs to get them to agree,” Trump said. “We&#8217;re going to be reducing drug costs over the next year, year and a half by not 50% or 60%, by 1,000% … You&#8217;re talking about a monumental change in health care that&#8217;s going to affect Medicare, Medicaid, even Social Security.”
<blockquote class="twitter-tweet">
.<a href="https://twitter.com/POTUS?ref_src=twsrc%5Etfw">@POTUS</a>: &#8220;For years, we&#8217;ve been paying sometimes for a pill, $100, and [other countries] are paying $10&#8230; We&#8217;re going to be reducing drug costs over the next year, year and a half&#8230; You&#8217;re talking about a monumental change in healthcare.&#8221; <a href="https://t.co/Pxnj8vU1hc">pic.twitter.com/Pxnj8vU1hc</a>
— Rapid Response 47 (@RapidResponse47) <a href="https://twitter.com/RapidResponse47/status/1968758480476528710?ref_src=twsrc%5Etfw">September 18, 2025</a></blockquote>

UK Hosts President Trump And First Lady Melania Trump For State Visit – Day Three

Trump Push Pays Off: Pharma Giant Says Brits Must Pay Same Price As Americans For New Drug

Donald Trump

United Kingdom

United States

World

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;

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Monopolies have been rigging the system for decades. They cozy up to Washington, throw cash around, hire armies of lobbyists, and manipulate rules so that everyday Americans always lose.
Thankfully, President Trump isn’t playing by their rules. He’s standing up for Main Street, not corporate boardrooms.
We first saw this with Big Tech. Mark Zuckerberg <a href="https://www.nytimes.com/2025/04/02/technology/mark-zuckerberg-trump-meta-antitrust.html">thought</a> he could cut a favorable deal to get Facebook off the hook, possibly even counting on Trump to back him. Instead, the Trump administration <a href="https://www.reuters.com/sustainability/boards-policy-regulation/facebook-privacy-practices-focus-8-billion-trial-targeting-zuckerberg-2025-07-16/">allowed</a> the case to go to trial, and Zuckerberg found himself sweating it out on the witness stand. 
Google attempted a similar stunt, <a href="https://www.cnbc.com/2025/04/21/google-argues-doj-breakup-could-hurt-us-economy-in-battle-with-china.html">claiming</a> national security would be at risk if it faced a breakup. Trump’s DOJ wasn’t buying it. 
 
“You know what is dangerous?” Antitrust chief Gail Slater <a href="https://nypost.com/2025/04/30/business/google-ceo-sundar-pichai-testifies-extraordinary-doj-remedies-would-cause-many-unintended-consequences/">asked</a> outside the courthouse. “The threat Google presents to our freedom of speech, to our freedom of thought, to free American digital markets.” That case has now <a href="https://www.breitbart.com/tech/2025/08/20/google-will-soon-learn-its-fate-as-judge-prepares-to-reveal-antitrust-remedies/">reached</a> the remedies stage, and for the first time since AT&amp;T in the 1980s, we could see a Big Tech monopoly actually broken apart. That’s how monopolies should be treated.
Now Ticketmaster is running the same playbook. 
Controlling <a href="https://insights.som.yale.edu/insights/did-ticketmasters-market-dominance-fuel-the-chaos-for-swifties">80% of the market</a>, the ticket marketplace is infamous for outrageous fees and predatory practices, such as charging junk fees and allowing scalping bots to buy up most of its inventory, leaving regular fans at the mercy of price gougers. Yet now the monopoly wants Trump to think it’s the solution, not the problem. 
Ticketmaster’s owner, Live Nation, <a href="https://thehill.com/homenews/administration/5311464-ric-grenell-live-nation-board-trump-doj-ticketmaster-antitrust/">added</a> a MAGA-friendly face to its board and is now floating “reform” ideas, like capping resale prices. Such caps would <a href="https://www.whiskeyriff.com/2025/07/09/live-nation-asks-the-trump-administration-to-cap-ticket-resale-prices-which-would-conveniently-put-their-competition-out-of-business/">bankrupt</a> almost all of Ticketmaster’s rivals, leaving the company even more dominant while pretending to “fix” the market.
It’s a double scam: they make the mess, then turn around and sell the “solution” as regulation.
It’s like an arsonist showing up with a bucket of water after lighting the fire.
Fortunately, the Trump administration is not paying any attention to Ticketmaster’s desperate attempt to protect itself from the White House’s wrath. It is already <a href="https://www.claimsjournal.com/news/national/2025/03/14/329490.htm">continuing</a> the antitrust suit against Ticketmaster, and a <a href="https://www.whitehouse.gov/fact-sheets/2025/03/fact-sheet-president-donald-j-trump-will-end-price-gouging-by-middlemen-in-the-entertainment-industry/">ticketing reform plan</a> set to drop in September could put the company’s “business as usual” to an end.
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Big Tech and Ticketmaster aren’t alone.
In June, the Trump administration hit Mexican bank CIBanco with the <a href="https://www.foley.com/insights/publications/2025/07/fincen-new-authority-targeting-mexico-based-financial-institutions-cartel/">toughest sanctions possible</a>, accusing it of aiding the fentanyl trade. A few weeks later, CIBanco — never before a client of Washington lobbyists — <a href="https://lda.senate.gov/filings/public/filing/ab337cdd-495b-4498-a1f9-4f3b0ec83631/print/">hired</a> the MAGA-connected Rubin, Turnbull &amp; Associates. The sanctions haven’t moved, and Trump has stood firm.
Amazon has also tried its usual political maneuvering on the president. When Trump won the White House, executives <a href="https://lda.senate.gov/filings/public/filing/b22dc7d6-7900-40e4-9f3f-985bbbb32579/print/">hired</a> Brian Ballard — Trump’s former lawyer and Florida finance director — to lobby on Amazon’s behalf. They even contributed <a href="https://docquery.fec.gov/pdf/286/201704180300150286/201704180300150286.pdf">over $50,000</a> to the president’s inauguration. Did it work? No. Trump didn’t blink, and Amazon lost its effort to dodge federal antitrust charges.
Hardworking Americans are tired of being taken advantage of. Insider games, where a board seat or a lobbyist equals immunity, have gone on for too long. Trump sees it, and he’s the one president actually saying “No” loud enough for all of us to hear.
Trump is different from most politicians. He doesn’t feel he owes these corporations anything, and he isn’t inclined to give them a free pass. His administration is pushing back against any monopoly that harms consumers or breaks the law.
The bottom line? Corporate America needs to clean up its act or face the consequences. Because the Trump administration isn’t standing up for special interests, it’s standing up for everyday Americans like you and me.
* * *
Haley Kennington (@LadyKennington) is an investigative journalist and conservative commentator. She served as the Research Director &amp; Story Editor for The Daily Wire’s “2020:The Plot Against the President” and the Research/Archive Editor for “What Is a Woman?“
The views expressed in this piece are those of the author and do not necessarily represent those of The Daily Wire.

In Trump’s White House, It’s Main Street Over Monopolies

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President Donald Trump sent letters to drug company CEOs demanding that they lower prices.
The letters, which Trump <a href="https://truthsocial.com/@realDonaldTrump/posts/114949049238065269">posted</a> to social media, say name-brand drug prices &#8220;are up to three times higher on average than anywhere else for identical medicines.&#8221;
&#8220;This unacceptable burden on hardworking American families ends with my Administration,&#8221; Trump said.
The letters were sent to 17 companies and are identical. They give companies 60 days to lower drug prices through most-favored-nation (MFN) pricing as explained in an executive order <a href="https://www.whitehouse.gov/presidential-actions/2025/05/delivering-most-favored-nation-prescription-drug-pricing-to-american-patients/">titled</a> &#8220;Delivering Most-Favored-Nation Prescription Drug Pricing to American Patients.&#8221;
The executive order, signed in May, orders companies to sell drugs in the United States for the same price charged in foreign countries, The Daily Wire previously <a href="https://www.dailywire.com/news/trump-signs-order-to-reduce-drug-prices-tells-rest-of-world-to-pay-up">reported</a>. The order says companies charge Americans more for drugs because &#8220;drug manufacturers deeply discount their products to access foreign markets, and subsidize that decrease through enormously high prices in the United States.&#8221;
Both the order and the letters direct companies to charge MFN prices in America.
Some of the companies that received letters include AbbVie, Eli Lilly and Company, Johnson and Johnson, Novartis, and Pfizer.
The letters tell companies to provide their &#8220;full portfolios&#8221; of drugs at MFN prices for Medicaid patients, guarantee MFN prices for new drugs, negotiate with &#8220;freeloading&#8221; nations to &#8220;return increased revenues&#8221; to American patients, and allow direct purchasing of drugs at MFN prices.
&#8220;Moving forward, the only thing I will accept from drug manufacturers is a commitment that provides American families immediate relief from the vastly inflated drug prices and an end to the free ride of American innovation by European and other developed nations,&#8221; Trump said in the letters.
Companies have until September 29 to implement Trump&#8217;s terms.
In May, Health and Human Services Secretary Robert F. Kennedy Jr. said other nations should chip in for research and development. He said raising prices in other nations by 20% would drastically reduce costs in the U.S.
Trump signed another executive order earlier in May to reduce the regulatory burden on the domestic production of critical medicines.
&#8220;[If] you refuse to step up, we will deploy every tool in our arsenal to protect American families from continued abusive drug pricing practices,&#8221; Trump said.
The other companies that received letters were Amgen, AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb, EMD Serono, Genentech, Gilead Sciences, GSK, Merck, Novo Nordisk, Regeneron Pharmaceuticals, and Sanofi.

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‘Unacceptable Burden’: Trump Gives Drug Companies 60 Days To Lower Prices

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