WASHINGTON—Republicans are calling on the Department of Health and Human Services to take &#8220;immediate action&#8221; to reinstate safety requirements on abortion drugs, highlighting a growing body of evidence showing that the drugs are causing severe and underreported harm to women.
In a letter first obtained by The Daily Wire, New Jersey Rep. Christopher Smith and Tennessee Rep. Diana Harshbarger call on Health and Human Services Secretary Robert F. Kennedy Jr. and FDA Commissioner Marty Makary to &#8220;at a minimum, reinstate the in-person dispensing requirement for mifepristone.&#8221; Until 2023, the FDA required abortion drugs to be administered to women under a doctor&#8217;s supervision.
&#8220;The need for urgent investigation and review of this drug comes in the wake of the Biden-Harris administration’s egregious action to remove critical safeguards that once applied to abortion drugs, and the FDA’s approval of a new abortion drug generic in September 2025,&#8221; write the 175 lawmakers, including House Speaker Mike Johnson (R-LA), Majority Leader Steve Scalise (R-LA), and Majority Whip Tom Emmer (R-MN).
&#8220;Under your leadership, HHS and FDA can reverse this wrong,&#8221; they conclude. &#8220;We urge you to immediately reinstate the REMS requiring in-person dispensing of mifepristone and to expedite the promised review by the FDA into the dangers of abortion drugs.&#8221;
The move is significant since President Joe Biden&#8217;s administration green-lit the removal of safety standards on the drugs during the COVID-19 pandemic, allowing women to easily obtain the drugs at home. Pro-life advocates have long argued that women are being put in danger simply from taking the abortion drugs, but they are even more anxious about women taking the drugs on their own.
New studies are showing that complications are &#8220;astonishingly higher than what is reported on the drug’s label,&#8221; the lawmakers say: &#8220;Even the current Obama FDA-approved label for mifepristone — which the data show understates the dangers to women — says that roughly 1 in 25 women who use mifepristone as directed will end up in the emergency room.&#8221;
“We join House and Senate Republicans in calling on the FDA to – at a minimum – immediately end Joe Biden’s legacy of mail-order abortion and restore the in-person doctor requirement that existed during President Trump’s first administration,&#8221; said SBA Pro-Life America&#8217;s head, Marjorie Dannenfelser. &#8220;<a href="https://sbaprolife.org/newsroom/press-releases/breaking-7-in-10-voters-want-to-roll-back-biden-covid-abortion-drug-policy-reinstate-in-person-doctor-visits">Seven in 10</a> voters agree. We are deeply grateful to Reps. Chris Smith and Diana Harshbarger for leading this important letter, and to House leadership and every member of Congress who joined in standing for women and their unborn children.&#8221;
Meanwhile, abortion proponents and legacy media insist the drugs are safer than Tylenol. President Donald Trump&#8217;s administration has weighed the issue carefully, cognizant of how electorally delicate abortion is. And in early October, the FDA approved a new abortion pill, shocking the president&#8217;s <a href="https://www.dailywire.com/news/pro-lifers-demand-answers-from-trump-admin-after-shocking-abortion-pill-approval">pro-life supporters.</a>
At the time, Kennedy put out a statement clarifying that he understood that the Biden administration had removed mifepristone&#8217;s safety standards &#8220;without studying the safety risks.&#8221;
&#8220;We are filling that gap,&#8221; he promised, sharing that he and Makary wrote to state attorneys general and promised to &#8220;review all the evidence — including real-world outcomes — on the safety of this drug.&#8221;
<blockquote class="twitter-tweet">
The Biden administration removed mifepristone’s in-person dispensing rule without studying the safety risks. We are filling that gap. Last month, I joined <a href="https://twitter.com/DrMakaryFDA?ref_src=twsrc%5Etfw">@DrMakaryFDA</a> in writing to state attorneys general, pledging to review all the evidence — including real-world outcomes — on… <a href="https://t.co/G0eE4H4y42">pic.twitter.com/G0eE4H4y42</a>
— Secretary Kennedy (@SecKennedy) <a href="https://twitter.com/SecKennedy/status/1973866621245567344?ref_src=twsrc%5Etfw">October 2, 2025</a></blockquote>
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&#8220;Recent studies already point to serious risks when mifepristone is used without proper medical oversight,&#8221; he said, and he clarified of the new abortion pill that that the FDA just approved: &#8220;[The FDA] only approved a second generic mifepristone tablet because federal law requires approval when an application proves the generic is identical to the brand-name drug.&#8221;
In their appeal, the Republican lawmakers express gratitude to Kennedy and Makary for serving the most pro-life president in American history, saying that Trump has &#8220;done more to advance a culture of life and the protection of women and children from the violence of abortion than any president before him.&#8221; But they also cite polling from McLaughlin and Associates that found that 7 in 10 voters agree that it &#8220;makes sense&#8221; to bring the former FDA safety standards back, arguing that &#8220;clear majorities of Americans recognize the extreme overreach of the previous administration’s actions.&#8221;
The lawmakers also dive into how the abortion drugs affect mothers, citing an Ethics and Public Policy Center study showing the adverse events from mifepristone are about 22 times more frequent than the FDA recognizes. That study found that almost 11% of women experience sepsis, infection, hemorrhaging, or other life-threatening events after aborting their unborn baby with mifepristone.
&#8220;While we have long known that mifepristone causes the death by starvation of children alive in the womb — it is baby poison — we now know with greater certitude that their mothers are also being seriously harmed. Despite the mainstream media and the Biden-Harris administration perpetuating the lie that these drugs are &#8216;safer than taking a Tylenol,&#8217; science and women’s lived experiences clearly say otherwise.&#8221;
And while the Biden administration claimed that the removal of safety standards was in response to the COVID pandemic, to help women receive &#8220;medically necessary&#8221; care, the lawmakers argue that the former administration was really just using COVID as a &#8220;smokescreen&#8221; to &#8220;accomplish its radical abortion agenda, which even now wreaks havoc across the nation.&#8221;
&#8220;Even the current Obama FDA-approved label for mifepristone — which the data show understates the dangers to women — says that roughly 1 in 25 women who use mifepristone as directed will end up in the emergency room,&#8221; they write.
They also say that the Biden FDA ignored warning signs from the studies on which it had already relied, including data showing that 3% of the women who took the drugs need to be hospitalized, &#8220;a 330% increase over the rate on the approved drug label,&#8221; data showing that 6% of participants had unplanned visits to emergency rooms, surgery was required to complete the abortions for 4.1% of the women, and, in the telemedicine group, 5.8% of women had emergency room visits.
&#8220;Beyond the studies, women tell us how they have suffered harm from mifepristone, and stories of coercion and abuse involving abortion drugs now run rampant,&#8221; they continue. &#8220;Real women like Rosalie Markezich — who is just one example of many — felt coerced by her boyfriend to take abortion drugs that he ordered from an out-of-state prescriber in her name and had delivered to her home through the U.S. Postal Service.&#8221;
&#8220;Rosalie did not want to have an abortion, but Biden’s egregious weakening of mifepristone’s safety standards let her boyfriend obtain abortion drugs and force her to take them,&#8221; they argue. &#8220;The dangerous Biden mail-order scheme was designed to give abortion activists license to mail drugs everywhere, even into states like Markezich’s home state of Louisiana that have pro-life protections for pregnant mothers and their unborn babies.&#8221;
&#8220;Today, abortion drugs account for nearly two-thirds of all abortions in the United States; there are over six hundred thousand abortions committed using these drugs each year,&#8221; the lawmakers write. &#8220;The Biden FDA’s reckless, no-contact, mail-order abortion scheme is to blame. Abortion providers are reaping increased profits, while women and their unborn children suffer irreparable harm.&#8221;

Illustrated by Daily Wire

‘Reverse This Wrong’: Republicans Push RFK To Fix Biden’s Abortion Drug Mistakes

Abortion

Robert F. Kennedy Jr.

White House

The Centers for Disease Control and Prevention (CDC) has updated its website to suggest that autism could be caused by infant vaccinations &#8212; a major agency shift from past administrations.
&#8220;The claim &#8216;vaccines do not cause autism&#8217; is not an evidence-based claim because studies have not ruled out the possibility that infant vaccines cause autism,&#8221; the site now reads.
The CDC also now says that studies &#8220;supporting a link have been ignored by health authorities,&#8221; and Health and Human Services (HHS) &#8220;has launched a comprehensive assessment of the causes of autism, including investigations on plausible biologic mechanisms and potential causal links.&#8221;
The site was updated on Wednesday.
<div id="attachment_1003207" style="width: 979px" class="wp-caption alignnone"><img loading="lazy" decoding="async" aria-describedby="caption-attachment-1003207" class="wp-image-1003207 size-large" src="https://dw-wp-production.imgix.net/2025/11/Screenshot-2025-11-20-at-8.31.15-AM-969x576.png" alt="" width="969" height="576" srcset="https://dw-wp-production.imgix.net/2025/11/Screenshot-2025-11-20-at-8.31.15-AM-969x576.png 969w, https://dw-wp-production.imgix.net/2025/11/Screenshot-2025-11-20-at-8.31.15-AM-300x178.png 300w, https://dw-wp-production.imgix.net/2025/11/Screenshot-2025-11-20-at-8.31.15-AM-768x457.png 768w, https://dw-wp-production.imgix.net/2025/11/Screenshot-2025-11-20-at-8.31.15-AM-1536x913.png 1536w, https://dw-wp-production.imgix.net/2025/11/Screenshot-2025-11-20-at-8.31.15-AM-2048x1218.png 2048w" sizes=" (max-width: 969px) 100vw, 969px" />CDC.gov</div>
Before HHS Secretary Robert F. Kennedy Jr. was sworn into office, the CDC firmly stated that autism does not have any links to vaccination. The CDC website, for example, previously said, &#8220;Studies have shown that there is no link between receiving vaccines and developing autism spectrum disorder (ASD).”
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The CDC also previously stated that &#8220;no links have been found between any vaccine ingredients&#8221; and autism.
The current site stresses the HHS investigation into autism causes and notes that many parents believe their child&#8217;s autism was in some way related to vaccination (emphasis added):
<blockquote>It is critical to address questions the American people have about the cause of autism to ensure public health guidance is adequately responsive to their concerns. Approximately <a class="tp-link-policy" href="https://pubmed.ncbi.nlm.nih.gov/16685182/" target="_blank" rel="noopener noreferrer" data-domain-ext="gov">one in two surveyed parents</a> of autistic children believe vaccines played a role in their child&#8217;s autism, often pointing to the vaccines their child received in the first six months of life (Diphtheria, tetanus, pertussis (DTaP), Hepatitis B (HepB), Haemophilus influenzae type B (Hib), Poliovirus, inactivated (IPV), and Pneumococcal conjugate (PCV)) and one given at or after the first year of life (Measles, mumps, rubella (MMR)). This connection has not been properly and thoroughly studied by the scientific community.</blockquote>
As part of his investigation into the massive spike in autism cases, Kennedy <a href="https://www.dailywire.com/news/potential-cause-treatment-of-autism-revealed-by-trump-rfk-jr">announced</a> back in September that acetaminophen use during pregnancy is tied to an increased risk of autism. Acetaminophen is the active ingredient in Tylenol, one of the most widely used medications globally for pain relief and fever reduction. But in late October, Kennedy <a href="https://www.reuters.com/business/healthcare-pharmaceuticals/us-health-chief-says-not-enough-data-show-tylenol-causes-autism-still-advises-2025-10-29/">said</a> he did not have sufficient evidence to back up a definitive link.
&#8220;The causative association between Tylenol given in pregnancy and perinatal periods is not sufficient to say it definitely causes autism, but it is very suggestive,&#8221; he <a href="https://x.com/atrupar/status/1983591905385390220">said</a>.
At the time, FDA Commissioner Dr. Marty Makary told <a href="https://www.dailywire.com/news/potential-cause-treatment-of-autism-revealed-by-trump-rfk-jr">The Daily Wire</a> he had already sent out a “Dear doctor” letter to all U.S. physicians about the association.
“We have an epidemic of autism that has increased 400% in the recent decades and we don’t have a known cause,” he said. “Now this may be a cause, but when you have enough evidence to suggest an association and you have no other plausible cause, we have a duty to notify parents and doctors.”
&nbsp;

Donald Trump

Trump’s CDC Suggests Autism Could Be Caused By Vaccines In Major Website Update

CDC Suggests Autism Could Be Caused By Vaccines In Major Website Update 

Autism

Health

Politics

Tylenol

Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. announced on Monday that the Food and Drug Administration (FDA) has removed broad &#8220;black box&#8221; warnings from hormone replacement therapy (HRT) for menopause.
The move reverses FDA action to apply the warning more than two decades ago. It&#8217;s been praised by some medical professionals as &#8220;far overdue&#8221; and a reversal of the &#8220;greatest single failure of the modern medical system.&#8221;
<div>
&#8220;Women have used HRT products for decades to relieve menopausal symptoms,&#8221; an HHS press release sent to The Daily Wire said. &#8220;However, their use plummeted in the early 2000s when the FDA applied boxed warnings following a Women’s Health Initiative study that found a statistically non-significant increase in the risk of breast cancer diagnosis. The average age of women in the study was 63 years — over a decade past the average age of a woman experiencing menopause — and study participants were given a hormone formulation no longer in common use.&#8221;
</div>
<div>
&#8220;The FDA is initiating removal of the boxed warnings following a comprehensive review of the scientific literature, an <a href="https://cisionone-email.hhs.gov/c/eJxszD1u5SAUQOHVmO4-8WugoEjzthFdw30xGmMYYOxk96OMpkz7HemkIFEpySgIu0rr-Sos24NMJkWlvbI6KuNE5Na_nNYoKG24CZbD6oXkMaJGEuZdCBu36KTxUmxu0XzkRL_ybyiYD-oDVqM3o-PLObg-9ys9vgM7wj5nG4t6W-Rzkc_7vh-vhI-Pei3y2XBmOudY5POVEOizUZ_Q8KTjJ4NCZ234ZxDgmWCvvdSToFM7MFKhc8LcqWP7grsWOoFbYSWXhhVKGaHTQTgIcgr_4P0_LOpNOK69YT1g6zRm_sgYa6mL5gnz8XXnTo9YCxuzE5Xvg7U-knIO9Bo1aCU1-E0TGMtt5CJZHhW7gvwbAAD__6XJezs" target="_blank" rel="noopener" data-saferedirecturl="https://www.google.com/url?q=https://cisionone-email.hhs.gov/c/eJxszD1u5SAUQOHVmO4-8WugoEjzthFdw30xGmMYYOxk96OMpkz7HemkIFEpySgIu0rr-Sos24NMJkWlvbI6KuNE5Na_nNYoKG24CZbD6oXkMaJGEuZdCBu36KTxUmxu0XzkRL_ybyiYD-oDVqM3o-PLObg-9ys9vgM7wj5nG4t6W-Rzkc_7vh-vhI-Pei3y2XBmOudY5POVEOizUZ_Q8KTjJ4NCZ234ZxDgmWCvvdSToFM7MFKhc8LcqWP7grsWOoFbYSWXhhVKGaHTQTgIcgr_4P0_LOpNOK69YT1g6zRm_sgYa6mL5gnz8XXnTo9YCxuzE5Xvg7U-knIO9Bo1aCU1-E0TGMtt5CJZHhW7gvwbAAD__6XJezs&amp;source=gmail&amp;ust=1762889361534000&amp;usg=AOvVaw26tCOXcCnlNCDZHVl-UfgA">expert panel</a> in July, and a public comment period,&#8221; HHS said. &#8220;The agency is working with companies to update language in product labeling to remove references to risks of cardiovascular disease, breast cancer, and probable dementia. The FDA is not seeking to remove the boxed warning for endometrial cancer for systemic estrogen-alone products.&#8221;
FDA Commissioner Dr. Marty Makary said the FDA has moved away from harmful &#8220;groupthink&#8221; with this decision, and stressed that HRT has &#8220;profound long term health benefits&#8221; for women.
According to HHS, randomized studies show that women who start HRT within 10 years of the onset of menopause have a reduction in all-cause mortality and fractures. They also may reduce their risk of cardiovascular diseases by as much as <a href="https://cisionone-email.hhs.gov/c/eJwszE1u5CAQQOHTwA6rKP4XLHrja7SgqGmjMe0e2-Mkt486yvZ70msZizEoOevgMSTwOsglB0iQqivGtOIiuJAcmWKJOflqdJI9-6QRiIotrN1d60CVIrqEukZh4eiN__Z_apS-8n4o72x1lv7EqK7P5WrTO8g1L-f5OoS5CZwFzq__dXCbnlT79FzH9OzL9NgugTMCuGC8wFkObr2onVcuB6ve8g_cf0GYm45gk5N7Lq-dj7M_eqFtbMJCK339-ug7T7QNeZw783gfQkjEJkZlPVllDVqVqmXlAgQC3QKQkVfG7wAAAP__zBpbaA" target="_blank" rel="noopener" data-saferedirecturl="https://www.google.com/url?q=https://cisionone-email.hhs.gov/c/eJwszE1u5CAQQOHTwA6rKP4XLHrja7SgqGmjMe0e2-Mkt486yvZ70msZizEoOevgMSTwOsglB0iQqivGtOIiuJAcmWKJOflqdJI9-6QRiIotrN1d60CVIrqEukZh4eiN__Z_apS-8n4o72x1lv7EqK7P5WrTO8g1L-f5OoS5CZwFzq__dXCbnlT79FzH9OzL9NgugTMCuGC8wFkObr2onVcuB6ve8g_cf0GYm45gk5N7Lq-dj7M_eqFtbMJCK339-ug7T7QNeZw783gfQkjEJkZlPVllDVqVqmXlAgQC3QKQkVfG7wAAAP__zBpbaA&amp;source=gmail&amp;ust=1762889361535000&amp;usg=AOvVaw241IAG8RoXHXhkKV1qLnXc">50%</a>, Alzheimer’s disease by <a href="https://cisionone-email.hhs.gov/c/eJwszMFuhCAQgOGngRsGBpDhwGEvvsYGhulKKqtVa9u3b7bp9fuTvybI1oLkZMIIIerRBDknxoDZB6sN6BotR7AVjbYj5YqARbY0RgOaKLvMxt-NCVQIwUcwBYXTR6v83j5Uz23h_VCjd8U7ekNU1_d81eEV5JLm89wOYW8CJgHT9lk61-FJpQ3PpQ_PNg-P9RIwIaJH0AIm2bm2rHZeOB-sWk1_cP8HYW8GtYte7ilvOx9ne7RMa1-F0zW35eer7TzQ2uVx7sz9dQghEltE5UZyyllwKhbHygcdSJsaNFl5JfgNAAD__54gW0M" target="_blank" rel="noopener" data-saferedirecturl="https://www.google.com/url?q=https://cisionone-email.hhs.gov/c/eJwszMFuhCAQgOGngRsGBpDhwGEvvsYGhulKKqtVa9u3b7bp9fuTvybI1oLkZMIIIerRBDknxoDZB6sN6BotR7AVjbYj5YqARbY0RgOaKLvMxt-NCVQIwUcwBYXTR6v83j5Uz23h_VCjd8U7ekNU1_d81eEV5JLm89wOYW8CJgHT9lk61-FJpQ3PpQ_PNg-P9RIwIaJH0AIm2bm2rHZeOB-sWk1_cP8HYW8GtYte7ilvOx9ne7RMa1-F0zW35eer7TzQ2uVx7sz9dQghEltE5UZyyllwKhbHygcdSJsaNFl5JfgNAAD__54gW0M&amp;source=gmail&amp;ust=1762889361535000&amp;usg=AOvVaw3ubq3rbutdcX2Ek1SyxLWC">35%,</a> and bone fractures by <a href="https://cisionone-email.hhs.gov/c/eJws0Ltu4zAQheGnITsKM0OKl4KFi1WxwO4rGLyMbSZS5FCKlbx94CDtd4BT_DVS0pokR3SWXACLTt4ik8VcMkO9UHUFMBuwnFNxwXtTs2zRBiQoJZnEOJ4RXcnF0xgIsxcGtlb5tb2rJbWZ-6bsaPJoysV79fi8PerwHOQcb_t-34Q-CZoETcdxDG_8sgxrvwqa6toETZePeRY0IQwIoxU0_f_z9x8GD4gEGjQhkFy4tqQ6z5w2Vq3GHzj_gtAn9GDCKHtM987b3q4tlXVZhYGa2vx1tM5DWRe57Z15eT44Fwpr75WxxSijyaiQDavRwTNJdVC0fET6DgAA__94-mC9" target="_blank" rel="noopener" data-saferedirecturl="https://www.google.com/url?q=https://cisionone-email.hhs.gov/c/eJws0Ltu4zAQheGnITsKM0OKl4KFi1WxwO4rGLyMbSZS5FCKlbx94CDtd4BT_DVS0pokR3SWXACLTt4ik8VcMkO9UHUFMBuwnFNxwXtTs2zRBiQoJZnEOJ4RXcnF0xgIsxcGtlb5tb2rJbWZ-6bsaPJoysV79fi8PerwHOQcb_t-34Q-CZoETcdxDG_8sgxrvwqa6toETZePeRY0IQwIoxU0_f_z9x8GD4gEGjQhkFy4tqQ6z5w2Vq3GHzj_gtAn9GDCKHtM987b3q4tlXVZhYGa2vx1tM5DWRe57Z15eT44Fwpr75WxxSijyaiQDavRwTNJdVC0fET6DgAA__94-mC9&amp;source=gmail&amp;ust=1762889361535000&amp;usg=AOvVaw1C6UyQvuh4jiJqaycENCqb">50 to 60%</a>.
“Tragically, tens of millions of women have been denied the life-changing and long-term health benefits of hormone replacement therapy because of a medical dogma rooted in a distortion of risk,” Makary said. “For too long, issues of women’s health have been underrecognized. Women and their physicians should make decisions based on data, not fear.”
</div>
<div>
<div>
<blockquote class="twitter-tweet" data-media-max-width="560">
NEW: HHS advances women’s health by removing misleading FDA warnings on hormone replacement therapy to help women through menopause.
FDA COMMISSIONER MAKARY: “By a large body of evidence, there are now recognized to be profound long-term health benefits that few people — even… <a href="https://t.co/c4yrRiYXrG">pic.twitter.com/c4yrRiYXrG</a>
— Fox News (@FoxNews) <a href="https://twitter.com/FoxNews/status/1987937746841669924?ref_src=twsrc%5Etfw">November 10, 2025</a></blockquote>
</div>
</div>
Secretary Kennedy said his department was &#8220;standing up for every woman who has symptoms of menopause and is looking to know her options and receive potentially life-changing treatment.&#8221;
&#8220;We are returning to evidence-based medicine and giving women control over their health again,&#8221; RFK Jr. added.
<div>
In addition to the removal of &#8220;black box&#8221; warnings, the FDA is approving two new drugs to expand treatment options for menopausal symptoms. 
Physician, podcast host, and author Dr. Peter Attia said in a pre-recorded interview released Monday that the warnings on HRT were &#8220;the greatest single failure of the modern medical system,&#8221; and noted the FDA&#8217;s plans to reverse the error.
</div>
<blockquote class="twitter-tweet" data-media-max-width="560">
“It&#8217;s very hard not to argue that this is the greatest single failure of the modern medical system,” says Dr. Peter Attia, referring to the hesitancy to prescribe hormone replacement therapy for perimenopausal and menopausal women. <a href="https://t.co/g7LbhIrY5f">https://t.co/g7LbhIrY5f</a> <a href="https://t.co/NoFfGWlwR1">pic.twitter.com/NoFfGWlwR1</a>
— 60 Minutes (@60Minutes) <a href="https://twitter.com/60Minutes/status/1987923135023255783?ref_src=twsrc%5Etfw">November 10, 2025</a></blockquote>
&#8220;FDA removes black box warning on HRT for women, FAR OVERDUE!&#8221; Dr. Nicole Saphier posted to X. &#8220;These absurd 2002-based fears scared millions from safe relief based on antiquated data and mislabeled products. The entire FDA should be EMBARRASSED it took 20+ years to fix this blunder. Ladies, talk to your doc.&#8221;
<blockquote class="twitter-tweet">
FDA removes black box warning on HRT for women, FAR OVERDUE!
These absurd 2002-based fears scared millions from safe relief based on antiquated data and mislabeled products.
The entire FDA should be EMBARRASSED it took 20+ years to fix this blunder.
Ladies, talk to your doc.
— Nicole Saphier, MD (@NBSaphierMD) <a href="https://twitter.com/NBSaphierMD/status/1987897868296782115?ref_src=twsrc%5Etfw">November 10, 2025</a></blockquote>
Related: <a href="https://www.dailywire.com/news/trumprx-trump-scores-significantly-lower-prices-for-popular-weight-loss-drugs?author=Amanda+Prestigiacomo&amp;category=News&amp;elementPosition=4&amp;row=0&amp;rowType=Vertical+List&amp;title=TrumpRx%3A+Trump+Scores+Significantly+Lower+Prices+For+Popular+Weight+Loss+Drugs">TrumpRx: Trump Scores Significantly Lower Prices For Popular Weight Loss Drugs</a>

HHS Secretary Kennedy Holds News Conference On Synthetic Dyes In Food Supply

‘Far Overdue!’: RFK Jr. Makes Major Women’s Health Announcement To High Praise

Pharmaceuticals

Women

President Donald Trump announced on Thursday that he&#8217;s reached deals with major pharmaceutical companies to lower the costs of popular weight loss drugs known as GLP-1s.
Pharma companies Eli Lilly, which makes Zepbound, and Novo Nordisk, which makes Wegovy and Ozempic, have agreed to lower prices of their drugs to the tune of hundreds of dollars, Trump said. Notably, Ozempic is primarily a type 2 diabetes medication, but is often prescribed off-label for weight loss.
Now, monthly out-of-pocket costs of the drugs will range from $50 to around $350, depending on a person&#8217;s dosage and insurance coverage. The drugs currently cost at least $1,000 a month.
Medicare patients will cover a $50 copay each month for the injectable drugs, no matter if the medications are used for obesity or diabetes.
Through Trump&#8217;s direct-to-consumer government website, called TrumpRx, Americans will pay $350-a-month for Wegovy, Zepbound, or Ozempic. Moreover, the cost is expected to soon drop to $245 a month, according to the administration.
<blockquote class="twitter-tweet">
🇺🇸 President Trump announces another HISTORIC PRICE SLASH on top drugs that help Americans struggling with diabetes, heart disease, obesity, and more.
💉Ozempic: $1,000 → $350/mo via TrumpRx 
💉Wegovy: $1,350 → $350/mo
MAKE AMERICA HEALTHY AGAIN! <a href="https://t.co/9lezvtZ6q0">pic.twitter.com/9lezvtZ6q0</a>
— The White House (@WhiteHouse) <a href="https://twitter.com/WhiteHouse/status/1986517540500115548?ref_src=twsrc%5Etfw">November 6, 2025</a></blockquote>
Additionally, both Eli Lilly and Novo Nordisk are working on oral GLP-1 medications for the public. The companies plan to make those available on TrumpRx for <a href="https://www.whitehouse.gov/fact-sheets/2025/11/fact-sheet-president-donald-j-trump-announces-major-developments-in-bringing-most-favored-nation-pricing-to-american-patients/">$150</a> per month, the White House said.
<blockquote class="twitter-tweet" data-media-max-width="560">
🚨 BREAKING: <a href="https://twitter.com/POTUS?ref_src=twsrc%5Etfw">@POTUS</a> announces that pharmaceutical companies Eli Lilly and Novo Nordisk have agreed to offer their most popular GLP-1 drugs &#8220;at drastic discounts.&#8221; <a href="https://t.co/PG9ffacUJf">pic.twitter.com/PG9ffacUJf</a>
— Rapid Response 47 (@RapidResponse47) <a href="https://twitter.com/RapidResponse47/status/1986481440482087010?ref_src=twsrc%5Etfw">November 6, 2025</a></blockquote>
Health and Human Services Secretary Robert F. Kennedy Jr. praised the deal.
“This is the biggest drug in our country, and that’s why this is the most important of all the announcements we’ve made,&#8221; he said. &#8220;This is going to have the biggest impact on the American people. All Americans, even those who are not on Medicaid, Medicare, are going to be able to get the same price for their drugs, for their GLP-1s.”
&#8220;The American public, because of this agreement, will lose 125 million pounds by this time next year — so it is going to have dramatic effects on human health in this country,&#8221; RFK added.
<blockquote class="twitter-tweet" data-media-max-width="560">
.<a href="https://twitter.com/SecKennedy?ref_src=twsrc%5Etfw">@SecKennedy</a>: &#8220;The American public, because of this agreement, will lose 125 million pounds by this time next year — so it is going to have dramatic effects on human health in this country.&#8221; <a href="https://t.co/Wq2nrKUdUG">https://t.co/Wq2nrKUdUG</a> <a href="https://t.co/GTKc0vjfdi">pic.twitter.com/GTKc0vjfdi</a>
— Rapid Response 47 (@RapidResponse47) <a href="https://twitter.com/RapidResponse47/status/1986485104135295203?ref_src=twsrc%5Etfw">November 6, 2025</a></blockquote>
Eli Lilly will also provide Emgality, a treatment for migraines, for $299 per pen, which is $443 lower than the current list price. Also, a diabetes medicine from Eli Lilly called Trulicity will be discounted by $598, now costing $389 per month.
NovoLog and Tresiba, popular insulin products from Novo Nordisk, will now cost $35 per month.
The president has also secured a $10 billion investment from Novo Nordisk to &#8220;to strengthen its domestic footprint&#8221; in the U.S. and $27 billion from Eli Lilly in new U.S. manufacturing investments.

Trump Tells Pregnant Women To Avoid Tylenol Over Autism Fear

TrumpRx: Trump Scores Significantly Lower Prices For Popular Weight Loss Drugs

Executive

Ozempic

Cheryl Hines is calling out the hosts of “The View” for using her entire time on the show to ask about her husband, HHS Secretary Robert F. Kennedy Jr., rather than to discuss her life or ask about her book.
The “Curb Your Enthusiasm” actress shared her thoughts during a Tuesday episode of Billy Bush’s “Hot Mics” podcast.
&#8220;Were they what you expected? The women of ‘The View?’&#8221; Bush asked Hines, prompting her to say, &#8220;Mhmm&#8221; with tight smile.
“You know, I was actually hoping that it was going to be more personal on ‘The View,’ but it was what it was. They just wanted to grill me about Bobby,” Hines continued. “I mean, I don’t think the ladies on ‘The View’ asked me one question about my book. But, you know, that’s OK.”
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Hines had initially joined the host of “The View” to promote her memoir, “Cheryl Hines Unscripted,” but host Sunny Hostin used the time to criticize comments RFK Jr. made and policies he promoted.
“Respectfully, your husband is the least qualified Department of Health and Human Services head that we’ve had in history. I think that’s very, very dangerous,” Hostin opened with. 
“Why is he less qualified than an economist? How is that possible?” Hines replied, referencing former President Barack Obama’s choice for the position, economist Sylvia Burwell.
“I think he is less qualified,” Hostin insisted, as The Daily Wire previously <a href="https://www.dailywire.com/news/sunny-hostin-scolds-rfk-jrs-wife-during-heated-segment-your-husband-is-the-least-qualified?author=Virginia+Kruta&amp;category=News&amp;elementPosition=undefined&amp;row=0&amp;rowType=Vertical+List&amp;title=Sunny+Hostin+Scolds+RFK+Jr%E2%80%99s+Wife+During+Heated+Segment%3A+%E2%80%98Your+Husband+Is+The+Least+Qualified%E2%80%99">reported</a>.
“He has spent his career studying toxins, studying people’s health, fighting for one guy who was using Roundup for his job,” Hines defended her husband.
“He has also spread a lot of misinformation, a lot of chaos, a lot of confusion. And I think it’s just a very dangerous thing,” Hostin said before claiming, “I say it with the utmost respect.”
“Some of it’s good and some of it is not. That’s the point,” Joy Behar interrupted.
“Listen, we all have different views here. Yes. And when you say misinformation, disinformation, we could go back to COVID when —” Hines said. 
“He’s connecting circumcision to autism,” Hostin interrupted.
“May I finish?” Hines asked.
“Please,” co-host Whoopi Goldberg chimed in.
“When people, Fauci, people were saying when you get the vaccine, you cannot transmit COVID, it will stop COVID. And that was disinformation, misinformation,” Hines reminded the panelists.
At the end of the interview, Goldberg said it was important to have guests with different viewpoints and invited Hines to come back. 
“We don’t often get people on this show who we can ask these questions to, and I appreciate that you came on,” Goldberg said. “Because you know what, if we can have the discussion back and forth, it then becomes people’s — then they can decide what they believe, and they don’t just hear one side.”

Cheryl Hines

Cheryl Hines Unloads On ‘The View’ Hosts: They ‘Just Wanted to Grill Me’ On RFK Jr.

Cheryl Hines Unloads On 'The View' Hosts: They 'Just Wanted to Grill Me' On RFK Jr.

Entertainment

Media

Television

The View

President Donald Trump lambasts Democrats as the shutdown grinds on, blue state governors form a “shadow” public health alliance, and one of the boldest heists of the century leaves the Louvre missing priceless jewels.
It’s Wednesday, October 22, 2025, and this is the news you need to know to start your day.
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<h2 style="text-align: center;">Brennan Referred And Shutdown Drags On</h2>
<img loading="lazy" decoding="async" class="alignnone size-medium wp-image-989357" src="https://dw-wp-production.imgix.net/2025/10/Rose-Garden-Pep-Rally-300x169.jpg" alt="" width="300" height="169" srcset="https://dw-wp-production.imgix.net/2025/10/Rose-Garden-Pep-Rally-300x169.jpg 300w, https://dw-wp-production.imgix.net/2025/10/Rose-Garden-Pep-Rally-1024x576.jpg 1024w, https://dw-wp-production.imgix.net/2025/10/Rose-Garden-Pep-Rally-768x432.jpg 768w, https://dw-wp-production.imgix.net/2025/10/Rose-Garden-Pep-Rally-1536x864.jpg 1536w, https://dw-wp-production.imgix.net/2025/10/Rose-Garden-Pep-Rally.jpg 1920w" sizes=" (max-width: 300px) 100vw, 300px" />
Topline: President Trump is applying more pressure on Democrats as the government shutdown stretches on. Meanwhile, a major political opponent of Trump is referred for charges.
Former CIA Director John Brennan has been referred for charges from the Justice Department. Similar to former FBI Director James Comey, he is in hot water over statements he made during the probe into Trump-Russia collusion.
House Judiciary Chair Jim Jordan (R-OH) announced that his committee was recommending the charges on Tuesday. Jordan said that Brennan “knowingly made false statements” during sworn testimony last year. The Judiciary Committee says Brennan lied when he denied using the discredited Steele Dossier in drafting an intelligence assessment in 2017 – specifically, the Intelligence Community Assessment on Russian interference.
Rose Garden lunch: Trump – in typical Trump fashion – surprised lawmakers on Tuesday with a Rose Garden lunch. No one really knew what the lunch was about, not even Republicans.
A reporter asked Senator John Kennedy of Louisiana what the purpose of the lunch was, and he said, “I have no idea.” But Chuck Schumer and the Democrats saw things through a more sinister lens, <a href="https://x.com/AmberJoCooper/status/1980656632246988850">calling</a> the event a “Rose Garden pep rally” for the shutdown.
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There was a pep rally element to the lunch. The president had just redone the Rose Garden and spoke excitedly about how it looks. YMCA blared over the speaker system prior to the president’s remarks.
Despite the festive atmosphere, Trump and Senate Republicans were clear that they were there for business: the business of reopening the government.
“From the beginning, our message has been very simple: we will not be extorted on this crazy plot of theirs. They’ve never done this before. Nobody has!” <a href="https://x.com/EricLDaugh/status/1980681699529752893">said</a> Trump. “Chuck Schumer and the Senate Democrats need to vote for the clean, bipartisan CR and reopen our government. It’s gotta be reopened, right now. We’re not doing that. They are the obstructionists. The reason they’re doing that is because we’re doing so well.”
Senate Majority Leader John Thune (R-SD) spoke with the press after the lunch concluded. He stressed that Republicans are united on Trump&#8217;s team.
Senate Republicans are planning to hold a separate vote on paying troops and law enforcement agents for the remainder of the shutdown. It’s not clear if Democrats will join them. But there’s a chance that, if they manage to get those essential workers paid, it may empower both sides to dig in and keep the shutdown fight going even longer.
<h2 style="text-align: center;">Democrats’ ‘Shadow Public-Health Alliance’</h2>
<img loading="lazy" decoding="async" class="alignnone size-medium wp-image-989359" src="https://dw-wp-production.imgix.net/2025/10/Health-Defiance-Alliance-300x169.jpg" alt="" width="300" height="169" srcset="https://dw-wp-production.imgix.net/2025/10/Health-Defiance-Alliance-300x169.jpg 300w, https://dw-wp-production.imgix.net/2025/10/Health-Defiance-Alliance-1024x576.jpg 1024w, https://dw-wp-production.imgix.net/2025/10/Health-Defiance-Alliance-768x432.jpg 768w, https://dw-wp-production.imgix.net/2025/10/Health-Defiance-Alliance-1536x864.jpg 1536w, https://dw-wp-production.imgix.net/2025/10/Health-Defiance-Alliance.jpg 1920w" sizes=" (max-width: 300px) 100vw, 300px" />
Topline: More than a dozen Democrat governors have signed on to a new health alliance, in a direct challenge to the Trump administration&#8217;s federal health agencies. 
The Governors&#8217; Public Health Alliance is being pitched as “non-partisan” and “all about the science.” The claim is that the Trump administration, and HHS Secretary Robert F. Kennedy, Jr., in particular, is anti-science. Therefore, this organization is necessary to protect Americans. However, so far, the Governors’ Public Health Alliance is strictly partisan: only Democrat governors have signed on. 
The alliance will dole out medical guidance that will likely challenge federal agencies such as the CDC and FDA, or at least lobby the federal government on these matters. It will make public health guidelines or offer “best practices&#8221; on vaccines and other measures. The allied states will share medical statistics, data, and advice on preventive care, and buy vaccines and supplies in bulk. 
The Wall Street Journal <a href="https://www.hcinnovationgroup.com/policy-value-based-care/article/55323774/fifteen-governors-create-new-public-health-alliance?utm_source=chatgpt.com">called</a> the alliance a “shadow public-health alliance” and said it’s the “largest move” so far “to create an alternative public-health universe outside the federal government.”
Governor JB Pritzker of Illinois, a Democrat, signed on to this association and <a href="https://gov-pritzker-newsroom.prezly.com/gov-pritzker-joins-launch-of-governors-public-health-alliance-to-protect-illinoisians-from-trumps-attack-on-science?utm_source=chatgpt.com">claimed</a> that Trump and Kennedy have turned the CDC “into a misinformation machine.”
California Democratic Governor Gavin Newsom also signed on. He said “extremists” in the Trump administration are trying to “weaponize the CDC and spread misinformation.”
Other states include Colorado, Connecticut, Delaware, Hawaii, Maryland, Massachusetts, New Jersey, New York, North Carolina, Oregon, Rhode Island, Washington, and the territory of Guam. The residents in these states make up about one-third of the U.S. population.
The Democrat health effort has to do mostly with vaccines. The governors who have signed on have highlighted vaccine “access” and attacked Kennedy for challenging orthodoxy. There was also mention of abortion “access.”
The association is primarily funded by a nonprofit called Governors Action Alliance, known as GovAct. The nonprofit claims to be nonpartisan, but supports Democrat causes and generally teams up with Democrats to expand Medicaid and bolster abortion and voting rights.
GovAct is behind the “Reproductive Freedom Alliance,” a coalition of 23 Democrat governors working to expand abortion. GovAct is also behind the “Governors Safeguarding Democracy” alliance that is like a Resist Trump 2.0 effort launched just days after Trump won the 2024 election.
Trump admin’s response: HHS spokesman Andrew Nixon <a href="https://apnews.com/article/governors-public-health-alliance-kennedy-7d5f277178697bbdfc228567c6d9f616">called</a> out Democrat governors for “destroy[ing] public trust in public health.” He noted that Democrat-led states “imposed unscientific school closures, toddler mask mandates, and vaccine passports during the COVID era.” He said the Trump administration is rebuilding trust by “grounding every policy in rigorous evidence and Gold Standard Science – not the failed politics of the pandemic.” 
<h2 style="text-align: center;">Louvre Heist</h2>
<img loading="lazy" decoding="async" class="alignnone size-medium wp-image-989361" src="https://dw-wp-production.imgix.net/2025/10/Louvre-Heist-Whodunit-300x169.jpg" alt="" width="300" height="169" srcset="https://dw-wp-production.imgix.net/2025/10/Louvre-Heist-Whodunit-300x169.jpg 300w, https://dw-wp-production.imgix.net/2025/10/Louvre-Heist-Whodunit-1024x576.jpg 1024w, https://dw-wp-production.imgix.net/2025/10/Louvre-Heist-Whodunit-768x432.jpg 768w, https://dw-wp-production.imgix.net/2025/10/Louvre-Heist-Whodunit-1536x864.jpg 1536w, https://dw-wp-production.imgix.net/2025/10/Louvre-Heist-Whodunit.jpg 1920w" sizes=" (max-width: 300px) 100vw, 300px" />
Topline: Investigators are still scrambling for clues after priceless jewels were stolen from the world’s most famous museum during a daring, broad-daylight heist.
On Sunday morning, a half-hour after the Louvre Museum in Paris had opened its doors, four thieves arrived in a construction truck with an electric ladder mounted on top. Two men, posing as construction workers, then ascended to a second-floor facade, where they used special disc cutters to slice holes through the windows.
The thieves entered through the windows to the famed Galerie d’Apollon, home to some of France’s most priceless Crown Jewels. With stunned patrons watching, they smashed two display cases. They removed nine objects, including a large brooch, a pair of emerald earrings, a necklace, and other jewelry belonging to Empress Marie-Louise, the second wife of Napoleon Bonaparte.
The thieves then joined their accomplices on the street, where they escaped on motorbikes, fleeing along the banks of the Seine River. The operation lasted no more than seven minutes.
As the heist went on, museum visitors were ordered to evacuate immediately. Many said they thought the building was on fire or had been struck by terrorists.
French President Emmanuel Macron called the heist an “attack on a heritage that we cherish.” The biggest concern now is that the jewels may never be recovered. Experts say the thieves certainly know they’d likely get caught if they tried to sell them on the black market, so it’s a real possibility they could remove the stones and melt down the precious metals to sell piece by piece. One of the tiaras alone had more than 1,000 diamonds and dozens of sapphires.
One official said the heist wasn’t an art crime, but a “commodity theft.” The jewels they took are of “inestimable worth,” according to the museum.
The haul could have been even larger. In their haste to get away, the thieves abandoned efforts to take the crown of Empress Eugénie, which contained nearly 2,500 diamonds and more than 50 emeralds, though it was damaged during the robbery.
The investigation: Interior Minister Laurent Nuñez said the robbery was “a major, highly organized operation” carried out by a team that had clearly done scouting. But at the moment, if they have any leads, they aren’t letting the public know.
Speculation has been rampant. Many people wonder if this could’ve been part of an inside job – they want to know if someone on staff at the Louvre could have offered aid. The country’s foreign minister said they weren’t ruling out an inside job.
Others have questioned why these specific jewels were targeted. In the same room they hit lies a display case housing the famous Regent Diamond, a $60 million stone. Even some French officials have expressed confusion over why the thieves, who clearly had done their research, seemingly ignored such a prime target just a few feet away.
Heist hysteria: Just last week, a group of thieves stole a number of collectible clocks from the President Jacques Chirac Museum in the French town of Corrèze. Then last month, a separate heist saw thieves lift $700,000 worth of gold from the French Museum of Natural History. Weeks before that, $11 million worth of porcelain was stolen from yet another museum in the city of Limoges.
This is only the latest heist to hit the Louvre. A diamond-studded sword was stolen back in 1976. Most famous of all, the Mona Lisa was lifted back in 1911. Ultimately, the world-famous portrait painting was located two years later.

MRN_251022_V1

Morning Brief: Govt Gridlock Persists, Dem ‘Shadow’ Health Alliance, & Louvre Heist Intrigue

Morning Brief: Govt Gridlock Persists, Dem ‘Shadow’ Health Agency, And Louvre Heist Intrigue

Department of Health and Human Services

Emmanuel Macron

France

Gavin Newsom

Government Shutdown

JB Pritzker

John Brennan

John Thune

Morning Wire

Paris

More than a dozen Democrat governors have signed on to a new health alliance that is effectively meant to challenge the Trump administration&#8217;s health agencies.
The Governors&#8217; Public Health Association, which was created last week, seeks to dole out medical guidance that will likely be at odds with the Trump administration&#8217;s Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA). It will make recommendations on vaccines and other public health measures, and work with allied states to share medical statistics and data. 
It&#8217;s been pitched as “non-partisan” and science- and health-backed, and a way to restore public trust. However, only Democrat governors have signed on to the initiative. So far, those states include California, Illinois, Colorado, Connecticut, Delaware, Hawaii, Maryland, Massachusetts, New Jersey, New York, North Carolina, Oregon, Rhode Island, Washington, and the territory of Guam.
Health and Human Services (HHS) spokesman Andrew Nixon has <a href="https://apnews.com/article/governors-public-health-alliance-kennedy-7d5f277178697bbdfc228567c6d9f616">called</a> out the allied Democrat governors for imposing school closures and mask mandates, even for toddlers, during the pandemic. He asserted that they are the ones who “destroyed public trust in public health&#8221; &#8212; not the Trump administration.
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 Nixon added that Trump and HHS Secretary Robert F. Kennedy Jr. are rebuilding that trust &#8220;by grounding every policy in rigorous evidence and Gold Standard Science – not the failed politics of the pandemic.”
Illinois Gov. JB Pritzker (D) unsurprisingly signed on to the Governors&#8217; Public Health Association, and has <a href="https://gov-pritzker-newsroom.prezly.com/gov-pritzker-joins-launch-of-governors-public-health-alliance-to-protect-illinoisians-from-trumps-attack-on-science?">claimed</a> it’s a necessary body since &#8220;public health should never be politicized.” Trump and RFK, he claims, have turned the CDC “into a misinformation machine.”
Fellow Democrat, California Gov. Gavin Newsom, similarly emphasized that science should be put before politics. Newsom, who <a href="https://sd11.senate.ca.gov/news/senator-wieners-historic-bill-provide-refuge-trans-kids-and-their-families-signed-law">supports</a> sex changes for minors based on &#8220;gender identity,&#8221; added that “extremists” are trying to “weaponize the CDC and spread misinformation.”
The association is primarily funded by a nonprofit called Governors Action Alliance, known as GovAct. The nonprofit claims to be nonpartisan, but supports Democrat causes and generally teams up with Democrats to expand Medicaid and bolster so-called abortion and voting rights.
Notably, GovAct is behind the “Reproductive Freedom Alliance,&#8221; which is a coalition of Democrat governors working to expand abortion. The nonprofit dumped more than half a billion dollars into the initiative. It’s also behind the “Governors Safeguarding Democracy” alliance, which was launched to resist Trump shortly after he won the 2024 election.
The goal of the Governors&#8217; Public Health Association is seemingly to undermine the FDA and CDC with heavy focus on vaccine and abortion “access.&#8221; 
This will, however, come with complications for Democrats. States have to comply with certain federal health guidance or standards if they want federal funding. Additionally, health insurers generally follow federal guidance for their coverage, and large health insurers operate in multiple states if not nationwide. It would be chaotic and impractical to implement different sets of standards in different states.
Opposing guidance could also trigger legal battles. For example, the FDA is currently reviewing the safety of a controversial abortion pill called mifepristone. If there were some determination that the governors&#8217; alliance disagreed with, that could potentially set up a legal challenge.

Pritzker/RFK Jr.

Dem Govs Create Association To Challenge CDC, FDA In Name Of ‘Science’ And Health

Democrats

&#8220;The View&#8221; host Sunny Hostin used some of her time during Tuesday&#8217;s broadcast to scold guest Cheryl Hines about how &#8220;unqualified&#8221; her husband — Health and Human Services Secretary Robert F. Kennedy Jr. — is for the job he holds in President Donald Trump&#8217;s administration.
Hines had initially joined the ABC midday program to promote her own memoir, &#8220;Cheryl Hines Unscripted,&#8221; but Hostin quickly dropped all pretense as she unloaded on Hines, criticizing comments made and policies promoted by her husband.
WATCH:
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Cheryl Hines put Sunny Hostin in her place on The View after she attacked her husband RFK Jr.
Hostin used her airtime to smear Kennedy, claiming he was spreading “misinformation”, but Hines exposed how those labels were weaponized against him, even when he was right.
HOSTIN:… <a href="https://t.co/rC3TDLr1EY">pic.twitter.com/rC3TDLr1EY</a>
— Overton (@overton_news) <a href="https://twitter.com/overton_news/status/1978135662239891458?ref_src=twsrc%5Etfw">October 14, 2025</a></blockquote>
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&#8220;Respectfully, your husband is the least qualified Department of Health and Human Services head that we’ve had in history. I think that’s very, very dangerous,&#8221; Hostin came out of the gate swinging.
&#8220;Why is he less qualified than an economist? How is that possible?&#8221; Hines referenced former President Barack Obama&#8217;s choice for that post, economist Sylvia Burwell.
&#8220;I think he is less qualified,&#8221; Hostin protested.
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&#8220;He has spent his career studying toxins, studying people’s health, fighting for one guy who was using Roundup for his job,&#8221; Hines defended her husband.
&#8220;He has also spread a lot of misinformation, a lot of chaos, a lot of confusion. And I think it’s just a very dangerous thing,&#8221; Hostin said before claiming, &#8220;I say it with the utmost respect.&#8221;
&#8220;Some of it’s good and some of it is not. That’s the point,&#8221; Joy Behar interrupted.
&#8220;Listen, we all have different views here. Yes. And when you say misinformation, disinformation, we could go back to COVID when —&#8221; Hines attempted to bring the conversation back to reality.
&#8220;He’s connecting circumcision to autism,&#8221; Hostin interrupted.
&#8220;May I finish?&#8221; Hines asked.
&#8220;Please,&#8221; cohost Whoopi Goldberg encouraged Hines to continue.
&#8220;When people, Fauci, people were saying when you get the vaccine, you cannot transmit COVID, it will stop COVID. And that was disinformation, misinformation,&#8221; Hines reminded them.
Cohost Alyssa Farah Griffin attempted damage control, saying, &#8220;We were also still learning about it. It was a novel virus we’ve never encountered before. Because now the doctors will acknowledge that it can.&#8221;
&#8220;And Dr. Fauci has a medical degree,&#8221; Hostin interjected.
But Hines was not finished: &#8220;At the time, they were censoring Bobby, because Bobby said, where’s the science to show us this? And there wasn’t any. But people attacked him and said, you’re wrong. So it’s like, let’s take a step back. I know that’s your opinion, and that’s okay.&#8221;

US-POLITICS-HEALTH-KENNEDY

Sunny Hostin Scolds RFK Jr’s Wife During Heated Segment: ‘Your Husband Is The Least Qualified’

Sunny Hostin

Last month marked 25 years since the Food and Drug Administration approved the abortion drug mifepristone, then called RU-486, for use in the United States.
On September 19, Health and Human Services Secretary Robert F. Kennedy, Jr., and the FDA Commissioner Marty Makary, sent a letter to 22 pro-life state attorneys general informing them that the agencies will perform a review of the drug’s safety.
Such a review is long overdue and should result in the revocation of the FDA’s approval of mifepristone or, at minimum, the restoration of important protections around the drug’s prescription.
Since sending that letter, the FDA unexpectedly approved a generic form of the chemical abortion drug. RFK, Jr., and Dr. Makary have regulatory tools at their disposal that could begin the process of removing these dangerous drugs from the market. It is time for them to take decisive action.
The FDA first approved mifepristone in 2000 under a regulation known as Subpart H which allows for the expedited approval of drugs that treat “serious or life-threatening illnesses” and that provide a “meaningful therapeutic benefit to patients over existing treatments.” Mifepristone meets neither of these requirements.
First, mifepristone does not “treat” a “serious or life-threatening illness.” Pregnancy is not an illness and killing an unborn child is not treatment.
Second, chemical abortion does not now, and certainly did not then, provide a “meaningful therapeutic benefit . . . over existing treatments.” As a 2006 <a href="https://advancingamericanfreedom.com/mifepristone-resource-congressional-staff-report-the-fda-and-ru-486-lowering-the-standard-for-womens-health/" target="_blank" rel="noopener">congressional report</a> on mifepristone’s approval explained, “it appears that no concurrently-controlled trials comparing medical and surgical abortion were required by FDA, because the Agency already knew that medical abortion—i.e., abortion by RU-486—is unambiguously inferior to surgical abortion with respect to safety and effectiveness.”
Nor, as the same report lays out in detail, did the FDA rely on studies of sufficient rigor to meet Subpart H’s requirements.
How could the FDA so blatantly disregard its own rules? Because the approval of chemical  abortion was <a href="https://humanlifereview.com/playing-politics-with-the-abortion-pill-a-quarter-century-of-abuse-of-power-at-the-fda/" target="_blank" rel="noopener">political from the start</a>.
In his <a href="https://url.avanan.click/v2/r01/___https:/advancingamericanfreedom.com/mifepristone-resource-judicial-watch-special-report-the-clinton-ru-486-files/___.YXAzOmFhZjphOm86YmM2NTQ4Zjk3MDAzZTY4MjA0NDM5NzQyZjdmNzQ4NGU6Nzo4ZDhkOjI3ZDY5MjU2MWJkOTU4OTZlNjNjYmUwMDI3ZmZjODA5NGMzNmZjYzNiYWU2NDk5MGYxZDE0MmIzNGE0Y2JiNjA6aDpUOk4" target="_blank" rel="noopener">first official act</a> as President, Bill Clinton directed HHS to promote the introduction of the abortion drug into the American market. Over the next seven years, the Clinton administration worked to have the patent rights transferred to the Population Council, which then sought the FDA’s approval.  That transfer of patent rights was necessitated by the fact that the French company that owned the patent was unwilling to introduce the drug to the American market without indemnification of liability for the harms it would foreseeably cause.
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Upon approval of mifepristone, the FDA implemented certain limitations on the drug’s prescription to provide at least some protection to women. <a href="https://url.avanan.click/v2/r01/___https:/storage.courtlistener.com/recap/gov.uscourts.txnd.370067/gov.uscourts.txnd.370067.137.0_20.pdf___.YXAzOmFhZjphOm86YmM2NTQ4Zjk3MDAzZTY4MjA0NDM5NzQyZjdmNzQ4NGU6Nzo3MWI3OjEzNTE0ZGZhZjY0OTJkZGEwMzg2NmU3ZDRhYjFjYjlhZjQ2MDZiMzc2MzEyMDEzZjNkMmQ4NzgyYTJhOTEwNDY6aDpUOk4" target="_blank" rel="noopener">Specifically,</a> the abortion drug could only be prescribed to women who were less than seven weeks pregnant, women were required to visit the doctor three times, and abortionists were required to report all adverse events.
These restrictions did not make mifepristone safe, but they did reduce the risk of harm to women. For example, in-person consultations provided women with necessary procedures, such as ultrasounds, critical for recognizing ectopic pregnancies, which, if left untreated, are deadly.
In March 2016, the Obama FDA significantly <a href="https://url.avanan.click/v2/r01/___https:/storage.courtlistener.com/recap/gov.uscourts.txnd.370067/gov.uscourts.txnd.370067.137.0_20.pdf___.YXAzOmFhZjphOm86YmM2NTQ4Zjk3MDAzZTY4MjA0NDM5NzQyZjdmNzQ4NGU6NzozMzQ4OjU0ZDdkY2E2NzEzOWExMDlmZTU0NzVjM2QwMTdkZmFjOGE1YzcxNzc3NTU2OWI3OTg4NzIxOGFlMjJhNjViYTc6aDpUOk4" target="_blank" rel="noopener">reduced</a> these protections, now referred to as a Risk Evaluation and Mitigation Strategy (REMS). Under the updated REMS, women could be prescribed mifepristone for abortions up to 10 weeks’ gestation and only needed to visit a doctor once, non-doctors were allowed to prescribe chemical abortions, and abortionists were only required to report fatal adverse events.
In 2021, the FDA “<a href="https://url.avanan.click/v2/r01/___https:/storage.courtlistener.com/recap/gov.uscourts.txnd.370067/gov.uscourts.txnd.370067.137.0_20.pdf___.YXAzOmFhZjphOm86YmM2NTQ4Zjk3MDAzZTY4MjA0NDM5NzQyZjdmNzQ4NGU6Nzo2ZGViOmVkNjQ0OWNmMjVmNWFiNzUyNDhjYzZkNGE2NzAxODU0ZTkyNjcwNGIzMDIzOWQyMGI0YWY5YjY2NjJkMDdlMzI6aDpUOk4" target="_blank" rel="noopener">removed</a> the ‘in-person dispensing requirement’” altogether.
In 2023, <a href="https://url.avanan.click/v2/r01/___https:/nrlc.org/nrlnewstoday/2024/03/guttmacher-says-abortions-increased-after-dobbs/___.YXAzOmFhZjphOm86YmM2NTQ4Zjk3MDAzZTY4MjA0NDM5NzQyZjdmNzQ4NGU6NzpjZjQ2OmNhNDQ5Mzc5ZWY2OGZhYjg5MjYyMDNlM2RhZGU5NGU3MDU2YjE3M2YwMzlhNjQwMGYwMmYzNmI2MTkyMWIyMDg6aDpUOk4" target="_blank" rel="noopener">63%</a> of abortions were chemical rather than surgical, and <a href="https://url.avanan.click/v2/r01/___https:/www.guttmacher.org/report/stability-number-abortions-2023-2024-us-states-without-total-bans-masks-major-shifts-access___.YXAzOmFhZjphOm86YmM2NTQ4Zjk3MDAzZTY4MjA0NDM5NzQyZjdmNzQ4NGU6Nzo0N2Q2OjFlMjhlNWE0NzQxODVlNWZiZDQ4YThmZWE5ODIzNTFkZTNlOWM3NWM5MGY4ZjJlOWI2NzY2YmM3ZGJmNDM4ZjI6aDpUOk4" target="_blank" rel="noopener">tens of thousands</a> of chemical abortions were shipped into pro-life states in 2024.
The FDA’s review of the dangers of mifepristone to women’s health is long overdue. A recent study by the Ethics and Public Policy Center suggesting that the adverse event rate for chemical abortion is much higher than FDA data suggests, is only the most recent in two and a half decades of evidence that the FDA’s approval of the drug is dangerous for women.
Armed with this and other data, the heads of HHS and the FDA have legal authority to <a href="https://www.ecfr.gov/current/title-21/chapter-I/subchapter-D/part-314/subpart-D/section-314.150" target="_blank" rel="noopener">call for a hearing</a> to determine whether the FDA’s initial approval of mifepristone should be withdrawn. This would be an important step toward removing dangerous chemical abortion drugs from the market, and allow the agency to delay approval of any other generic forms of mifepristone currently being considered.
For the past 25 years, mifepristone has been used to terminate innocent human life while injuring and harming women for life. The abortion drug’s reckoning is long overdue. The FDA’s recently announced review is a good first step, but pro-life Americans cannot rest until the dangerous chemical abortion pill is taken off the market and pre-born Americans are safe from its harms.
Marc Wheat is general counsel for Advancing American Freedom.
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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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The FDA’s Review Of Abortion Drugs Is Long Overdue

Abortion Drug

WASHINGTON—The Department of Health and Human Services is taking steps to ensure that federal HIV/AIDS funds cannot be used for so-called gender-affirming care, as they were under President Joe Biden’s administration, The Daily Wire has learned.
Under the Biden administration, states were using federal funding for HIV/AIDS treatment to cover transgender surgeries, hormones, and puberty blockers. For example, the Biden administration <a href="https://ryanwhite.hrsa.gov/sites/default/files/ryanwhite/hiv-care/gender-affirming-care-rwhap.pdf">allowed the Ryan White HIV/AIDS Drug Assistance Program</a> to provide “access to gender-affirming hormone therapy.”
The Department of Health and Human Services declared its intent to block the funds from being misused in April. Now, it is taking further steps to make sure that fund recipients are aware.
“The Ryan White HIV/AIDS Program is a lifeline for thousands of Americans living with HIV, and HRSA will not allow funds to be diverted from their true purpose,” HRSA Administrator Tom Engels explained to The Daily Wire on Friday. “Every dollar of the AIDS Drug Assistance Program must support HIV/AIDS-related treatment — not sex trait modification medications unrelated to HIV care.”
HHS will post a “Notice of Funding Opportunity” on Friday through its Health Resources and Services Administration, adding language that clarifies funding — specifically the AIDS Drug Assistance Program (ADAP) Emergency Relief Funds — are strictly limited to HIV/AIDS treatments. If medications such as hormones are medically necessary for HIV/AIDS care, they will be covered, but not if they are for “sex-trait modification purposes,” the notice says, and any funds received through drug rebates will have to remain within the HIV/AIDS program and can’t be redirected for other unrelated health purposes.
“This Notice of Funding Opportunity makes clear that HRSA is safeguarding program integrity and cracking down to ensure that people living with HIV get the care they need,” Engels added.
Some states were using the funds to pay for hormonal treatments for gender transitions, even when they weren’t medically necessary for HIV treatment — raising questions about whether drug rebate funds were being redirected to other health services.
The District of Columbia Department of Health AIDS Drug Assistance Program, for example, <a href="https://nastad.org/sites/default/files/2022-11/PDF-Success-Stories-DC-2019-ADAP.pdf">openly covered</a> transgender hormone treatments and used the federal 340B program to subsidize those hormones.
“The initial funding will be appropriated from the DC Ryan White Part B ADAP grant award, and any other cost for pharmacy provider education will be supplemented by DC ADAP rebates,” the explanation of the program explains.
In New Jersey, the Department of Medicine at Rutgers University <a href="https://njms.rutgers.edu/departments/medicine/infectious_diseases/cc_rwp.php">states that it</a> “offers gender-affirming hormone therapy for transgender persons” in line with the disgraced “World Professional Association of Transgender Health,” describing the transgender procedures as “an important part of a holistic approach to wellness and preventative medicine.”
This week, HHS added language to the notice of funding opportunity that reminds states that “therapeutics funded under the ADAP may only be provided ‘to treat HIV/AIDS or prevent the serious deterioration of health arising from HIV/AIDS in eligible individuals, including measures for the prevention and treatment of opportunistic infections.’”
For example, HHS notes, if an ADAP provides trans hormones, it can only allow those hormones to be dispensed to “treat HIV/AIDS or prevent the serious deterioration of health arising from HIV/AIDS, rather than for non-statutory purposes such as specified sex-trait modification procedures.”
The language will also remind states that the Ryan White HIV/Aids Program legislation states: “A State shall ensure that any drug rebates received on drugs purchased from funds provided pursuant to this section [ADAP] are applied to activities supported under this subpart [RWHAP Part B], with priority given to activities described under this section [ADAP].”
“As such,” the language notes, “all 340B rebates directly generated by a federal dollar are subject to HRSA HAB’s rebate policies and rules for expenditure. All rebates generated through ADAP must be used for RWHAP Part B activities, with priority given to ADAP, rather than diverted for unsupported activities that exceed the RWHAP’s limited statutory purpose, such as for specified sex-trait modification procedures.”

Pfizer Gets Three-Year Reprieve From Trump Pharma Tariffs

HHS Reverses Biden Policy, Ensures HIV Funds Cannot Be Diverted For Trans Procedures

Transgenders

A coalition of pro-life advocates led by Live Action President Lila Rose on Friday urged Health and Human Services Secretary Robert F. Kennedy Jr. and FDA Commissioner Marty Makary to reverse the recent approval of an abortion drug. 
Over two dozen pro-life advocates petitioned the FDA following the agency&#8217;s Tuesday approval of Evita Solutions’ generic version of mifepristone, the drug used in over 60% of all abortions. The signatories say that instead of approving new life-ending drugs, the FDA should completely remove mifepristone from the market. 
“We urge you, in the strongest possible terms, to reverse this dangerous approval immediately,&#8221; the coalition wrote, according to a <a href="https://dw-wp-production.imgix.net/2025/10/FDA-Coalition-Letter_-Abortion-Pill-10.3.2025-1.pdf">copy of the letter</a> obtained by The Daily Wire. &#8220;Rather than expanding the license for these drugs, the FDA should acknowledge the clear evidence of harm and withdraw mifepristone from the market.&#8221;
“Every abortion is a violation of human rights, and every life lost is an irreplaceable son or daughter. The federal government must stop enabling this violence under the false banner of ‘healthcare,’” they added. 
Signers of the letter included Ethics and Public Policy Center President Ryan Anderson, Students for Life President Kristan Hawkins, and Concerned Women for America CEO Penny Nance.
On Friday, White House Press Secretary Karoline Leavitt said that the administration did not endorse the drug, but was required by law to approve Evita’s application because it was a generic offering of a drug already offered by two other pharmaceutical companies. 
The letter to Kennedy also laid out the brutal process that takes place after a mother takes a chemical abortion pill. 
“A chemical abortion consists of a two-step process. First, a pregnant mother will take mifepristone to starve her preborn child to death. Next, she will take misoprostol to induce labor contractions and deliver the baby&#8217;s dead body. At this stage in the first trimester, children developing in the womb already have a detectable heartbeat and brainwaves, and are beginning to move their arms and legs,” the coalition wrote. 
The coalition said that the approval contradicted a recent commitment from Kennedy to study the dangers of mifepristone. 
“Yet rather than pausing to examine the mounting evidence showing the harmful effects of mifepristone, the FDA has chosen to expand access to a drug that has already killed millions of preborn children and harmed countless women, undermining the very commitment that the Secretary publicly made to protect patients,” they wrote. 
Chemical abortions account for about two-thirds of all abortions in the United States and have ended the lives of at least 7.5 million unborn babies. At the same time, the mothers who take the pills often experience additional medical complications like hemorrhaging and sepsis. Studies showing the dangers of the drug have been manipulated to hide the harm, the coalition said. 
The decision has already triggered outrage from many Republican lawmakers. Senator Josh Hawley (R-MO) said he had completely lost faith in the FDA over the move, while over a dozen Republican representatives <a href="https://www.dailywire.com/news/republicans-demand-rfk-fire-rogue-actors-at-fda-who-approved-abortion-drug?author=Leif+Le+Mahieu&amp;category=News&amp;elementPosition=1&amp;row=0&amp;rowType=Vertical+List&amp;title=Republicans+Demand+RFK+Fire+%E2%80%98Rogue+Actors%E2%80%99+At+FDA+Who+Approved+Abortion+Drug">sent a letter</a> on Friday telling Kennedy to fire the “rogue actors” at the agency who approved the lethal drug.

Great American Farmers Market 2025

‘Every Abortion Is A Violation Of Human Rights’: Pro-Life Advocates Demand FDA Yank Abortion Drug

Live Action

Pro-Life Movement

A group of 13 House Republicans led by North Carolina Congressman Mark Harris demanded Friday that Health and Human Services Secretary Robert F. Kennedy Jr. fire the bureaucrats responsible for the FDA’s “alarming” approval of a new abortion pill, according to a letter obtained by The Daily Wire. 
Harris told Kennedy that the FDA’s <a href="https://www.dailywire.com/news/pro-lifers-demand-answers-from-trump-admin-after-shocking-abortion-pill-approval?author=Leif+Le+Mahieu&amp;category=News&amp;elementPosition=2&amp;row=0&amp;rowType=Vertical+List&amp;title=Pro-Lifers+Demand+Answers+From+Trump+Admin+After+%E2%80%98Shocking%E2%80%99+Abortion+Pill+Approval">approval</a> of Evita Solutions’ generic mifepristone, the drug used in over 60% of all abortions, ran contrary to the Trump administration’s pro-life record. Harris and his co-signers suggested that “rogue actors” in the FDA were responsible for the decision. 
“The approval of a generic version of this dangerous drug not only contradicts the announced review but also runs directly counter to this Administration’s stated pro-life agenda,” the lawmakers <a href="https://dw-wp-production.imgix.net/2025/10/10.3.25-Letter-to-Sec-Kennedy-on-Abortion-Pill-Approval.pdf">wrote</a>. “It is clear that rogue actors within the FDA are working to undermine both the sanctity of life and the Administration’s commitment to protecting it.”
They said that Kennedy should look at removing the officials responsible for the decision. 
“For this reason, we respectfully urge that you consider the director of the Office of Generic Drugs, the director of the Center for Drug Evaluation and Research, and other bureaucrats responsible for this reckless decision as part of your reduction-in-force evaluations,” he wrote. 
Signing onto the letter were Reps. Josh Brecheen (OK), Keith Self (Texas), Eli Crane (AZ), Paul Gosar (AZ), Chip Roy (Texas), Mary Miller (IL), Andy Biggs (AZ), Barry Moore (AL), Scott Perry (PA), Ralph Norman (SC), Sheri Biggs (SC), and Ben Cline (VA). 
Mifepristone works by starving an unborn child to death by cutting it off from the necessary nutrients provided by its mother. A different drug is then taken to induce labor and expel the deceased baby from the mother. 
Harris said that removing the officials responsible for the decision would send a message that the administration still believes in defending innocent life. 
“As stewards of the taxpayers’ trust and defenders of the unborn, we must ensure that no federal office operates in open defiance of our values or the administration’s pro-life commitments. This is a critical moment to send a clear message that the lives of the unborn and the health of women will not be compromised by bureaucratic mismanagement or ideological activism.
Commenting on the approval, Health and Human Services Communications Director Andrew Nixon told The Daily Wire that the FDA “has very limited discretion in deciding whether to approve a generic drug. By law, the Secretary of Health and Human Services must approve an application if it demonstrates that the generic drug is identical to the brand-name drug.”
Nixon added that applicants for generic drugs do not need to submit independent evidence proving safety and efficacy. He also noted that HHS is conducting a review of the “reported adverse effects” of mifepristone.
Only two other drug companies, Danco Labs and Genbiopro, were previously approved to distribute the life-ending drug. The FDA wrote to Evita Solutions on September 30 that it had “concluded that adequate information has been presented to demonstrate that the drug meets the requirements for approval.”
The announcement shocked pro-life advocates, who have continued to press for action to crack down on the widespread distribution of abortion pills across the country.

MixCollage-03-Oct-2025-09-31-AM-5086

Republicans Demand RFK Fire ‘Rogue Actors’ At FDA Who Approved Abortion Drug

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