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Friday, October 3, 2025

'UK: Early At-Home Abortion: As Safe As in the Hospital?'

 'COVID changed UK laws to allow more early abortions to occur at home'

[Self-reported??]

  • Gestational cutoff for early medication abortion at home varies across countries in Great Britain.
  • Both at-home and in-hospital early medication abortion groups had 97% complete abortion rates.
  • Authors call for changed laws to expand access to at-home early medication abortion across the U.K. to up to 12 weeks' gestation.

Early medication abortion outcomes were similar when performed at home as when in a hospital for women between 10 and 12 weeks' gestation, a retrospective review of U.K. data found.

Among 371 women who had an early medication abortion, complete abortion rates didn't differ significantly between at-home versus hospital medication abortion (97% [251/258], 95% CI 94-99% and 97% [110/113], 95% CI 92-99%), reported researchers led by Jacqueline Quinn, MBChB, of the University of Edinburgh Medical Research Council Centre for Reproductive Health and Chalmers Sexual Health Centre in Edinburgh, Scotland.

Neither did significant differences emerge between the home and hospital groups in incomplete abortion rates (1.6% vs 2.6%), nor in ongoing pregnancy rates (1.2% vs 0%), they wrote in BMJ Sexual and Reproductive Health.

Only four total cases of serious complications occurred -- one hemorrhage requiring transfusion and three cases of infection receiving intravenous antibiotics, all within the at-home group.

"This study demonstrates that early medical abortion at home should be extended to allow women across the U.K. to access this up to 12 weeks if they wish to," Quinn told MedPage Today. "Therefore, the law and regulations in other parts of the U.K. need to be changed to allow women access to this procedure between 10 and 12 weeks."

Since the COVID-19 pandemic, Britain has allowed early medication abortion at home, though England and Wales allow this option up to 9 weeks 6 days' gestation and Scotland permits it through 11 weeks 6 days' gestation. The WHO endorses both medication abortion at home up to 12 weeks' gestation as well as telemedicine and hybrid models of care for medication abortion.

Rates of follow-up visits were low but more likely in the at-home medication abortion group (7% vs 2%, P=0.03) and with telephone advice (11% vs 4%, P=0.04). The at-home group was also more likely to make unscheduled contact with the hospital or abortion clinic (23% vs 9%, P≤0.01).

Ashley Brant, DO, MPH, an ob/gyn and complex family planning subspecialist at the Cleveland Clinic who was not involved in the research, told MedPage Today that these findings suggest "that providing instructions on how and when to seek additional care or medical advice is an important part of pre-abortion counseling."

She also noted that this study "supports the safety and efficacy of medication abortion via telemedicine at 10 to 11 weeks" and that "regulations, policies, and protocols that restrict access to medication abortion or require in-person evaluation do not improve the safety of abortion and are not grounded in medical evidence."

Researchers reviewed 5 years (April 2020 through March 2025) of routinely collected audit data from a health center in Edinburgh. Specifically, they compared outcomes of at home versus hospital cases of early medication abortion for patients between 10 weeks 0 days' and 11 weeks 6 days' gestation. In total, 258 had an at-home abortion and 113 had one in the hospital.

Both groups followed the same early medication abortion regimen: 200 mg of mifepristone, taken orally, followed 24 to 28 hours later with 800 µg of misoprostol (Cytotec), taken sublingually or vaginally. Patients were also provided with three additional 400-µg doses of misoprostol to take at 4 hour intervals, if necessary, until the abortion was complete. They were also given dihydrocodeine for analgesia and cyclizine as an antiemetic. A self-performed low-sensitivity urinary pregnancy test taken 2 weeks after the medication provided confirmation of a successful early medication abortion.

Complete abortion rate, defined by Medical Abortion Reporting of Efficacy guidelines as complete expulsion without requiring surgical intervention, was the primary outcome. Secondary outcomes included incomplete abortion, ongoing pregnancy, unscheduled contact with a hospital or abortion services due to an abortion-related concern within 6 weeks, and serious complications, like hemorrhage requiring transfusion or an infection receiving intravenous antibiotics.

Authors noted some limitations, including the small number of cases of abortion presenting this early. More patients in the at-home group didn't have a pre-abortion ultrasound to confirm gestational age, which means gestation could have been earlier or more advanced than predicted, though past research has determined that last menstrual period is accurate enough in most cases.

Quinn said the group plans to interview patients who have had at-home early medication abortion about their experience.

Disclosures

Quinn is a trainee editor of BMJ Sexual and Reproductive Health.

Co-authors reported being an an editor-in-chief and associate editor of BMJ Sexual and Reproductive Health; receiving research funding from Perrigo (HRA Pharma) and Nordic Pharma (Exelgyn) and grants from Gedeon Richter; being a European scientific advisory board member for Exelgyn on early medical abortion; and being principal investigator for a progestogen-­only injectable study.

Brant had no disclosures.

Hegseth Announces 4th Deadly Strike On 'Narco-Terrorist' Boat Off Venezuela

 Pentagon chief Pete Hegseth announced Friday another military strike on an alleged drug-smuggling boat off Venezuela which killed four people.

This marks at least the fourth such attack, and after President Trump formally notified Congress this week that the US was entering a "non-international armed conflict" with drug cartels. Hegseth made clear on social media, "These strikes will continue until the attacks on the American people are over!!!!"

USS Sampson (DDG 102), a U.S. Navy missile destroyer. via Anadolu Agency

Hegseth affirmed in a social media post that he had directed the latest strike on Trump's orders, and released overhead drone video of the attack.

"The strike was conducted in international waters just off the coast of Venezuela while the vessel was transporting substantial amounts of narcotics – headed to America to poison our people," Hegseth said on X.

"Our intelligence, without a doubt, confirmed that this vessel was trafficking narcotics, the people onboard were narco-terrorists, and they were operating on a known narco-trafficking transit route," he added.

Trump's rationale for the attacks in the aforementioned memo states the cartels are "non-state armed groups" whose actions smuggling drugs "constitute an armed attack against the United States".

As for Hegseth, his post claimed the boat was "affiliated with Designated Terrorist Organizations" - however there remains a legal dispute as to whether merely labeling a cartel as an FTO automatically warrants military action, and without warning or attempt to intercept the vessel.

In particular the administration has essentially declared war on the Tren de Aragua cartel, and says it is cooperating with the Maduro government, which Caracas has rejected, and so the presence of the cartel's members in the US is a "predatory incursion" by a foreign nation.

The new footage of the Friday (presumably) drone attack...

The Washington Examiner on Thursday said that war could be on the horizon. The publication "understands that military planners believe the assembled forces are now sufficient to seize and hold key strategic facilities such as ports and airfields on Venezuelan territory (the Washington Examiner is withholding some details for national security reasons)." And for now it appears the occasional attack on small alleged drug boats will continue.

https://www.zerohedge.com/geopolitical/hegseth-announces-4th-deadly-strike-narco-terrorist-boat-venezuela

Texas Stock Exchange Trading Expected to Begin in First Quarter

 


The Texas Stock Exchange is expected to begin trading during the first quarter, according to a key adviser to the new marketplace.

“I believe that we will be in a position to begin trading in Q1 of next year,” said Jeb Hensarling, a former member of Congress who is providing strategic advisory services to the Dallas-based TXSE. “A world-class trading engine has been created. It’s been beta tested.” Hensarling’s comments came during a Bloomberg Television interview on Friday.

https://www.bloomberg.com/news/articles/2025-10-03/texas-stock-exchange-trading-expected-to-begin-in-first-quarter

Esperion Therapeutics Blocks Dr. Reddy's Generic Version of Cholesterol Drugs Until 2040

 Dr. Reddy's Laboratories won't market a generic version of Esperion Therapeutics' cholesterol drugs after a reaching a settlement.

Esperion Therapeutics, a pharmaceutical company, said Friday that it has settled with India-based pharmaceutical company Dr. Reddy's which was seeking approval to market its own generic versions of its Nexletol and Nexlizet.

Nexletol and Nexlizet are prescription medications used to lower LDL cholesterol, known as the bad cholesterol, and reduce the risk of heart-related issues in adults.

Dr. Reddy's had made an abbreviated new drug application for its generic version of the drugs, but following the settlement, Dr. Reddy's Laboratories has agreed not to market a generic version of either in the U.S. before 2040.

Dr. Reddy's wasn't readily available for comment.

Earlier this year, Esperion said it had reached settlement agreements with a number of other pharmaceuticals regarding generic versions of Nexletol.

https://www.morningstar.com/news/dow-jones/202510032705/esperion-therapeutics-blocks-dr-reddys-generic-version-of-cholesterol-drugs-until-2040

The FDIC to vote on a new debanking proposal as Trump criticizes practice

 The Federal Deposit Insurance Corp. is expected to unveil a proposal next week to prohibit officials from forcing bank lenders to close customers’ accounts on political, social, cultural or religious grounds, according to a Bloomberg report.

This rule would focus on the government’s supervision powers, targeting how officials scrutinize banks’ risk as President Trump has repeatedly criticized the practice of depriving some individuals and businesses of banking services, known as debanking.

Trump has also said that bank giants such as JPMorgan Chase & Co. (JPM) and Bank of America (BAC) refused his money based on ideological grounds.

Trump signed the Guaranteeing Fair Banking for All Americans (the Executive Order or Debanking Order) executive order, which seeks to scrutinize bank practices related to debanking in order to address this practice “on the basis of political or religious beliefs or lawful business activities.”

This proposal will not require banks to assume any additional burdens.

The Office of the Comptroller of the Currency (or OCC) is to vote next week to propose a measure to ban the use of reputation risk – the idea that a bank’s negative public perception, such as misconduct events, poor service, or data breaches, can erode trust and negatively impact the bank's business.

Both the FDIC and the OCC have inquired big banks if they had closed customer accounts or denied people service on political or religious grounds, according to the report.

Top banks: JPMorgan Chase (JPM), Bank of America (BAC), Wells Fargo (WFC), Citigroup (C), Morgan Stanley (MS), Goldman Sachs (GS), U.S. Bancorp (USB)

https://www.msn.com/en-us/money/markets/the-fdic-to-vote-on-a-new-debanking-proposal-as-trump-criticizes-practice/ar-AA1NOO1f

FDA introduces program to expedite review of domestic generic drugs

 Today, the U.S. Food and Drug Administration (FDA) is announcing a new pilot prioritization program for the review of abbreviated new drug applications (ANDAs) that aims to spur and reward investment in U.S. drug manufacturing and research and development and strengthen the domestic pharmaceutical supply chain by providing faster reviews for generic companies who test and manufacture their products in the U.S. 

More than half of pharmaceuticals distributed in the U.S. are manufactured overseas. Further, the U.S. is reliant on overseas sources for active pharmaceutical ingredients (APIs). As of 2025, only 9% of API manufacturers are in the U.S., compared to 22% in China and 44% in India. In addition, pivotal studies for drugs, including bioequivalence testing for generic drugs, are increasingly conducted outside the U.S., weakening the U.S.’s pharmaceutical research and development infrastructure.

“Ensuring that Americans have access to high-quality, safe and effective generic medicines is critical to public health. Overreliance on foreign drug manufacturing and testing creates risks both to national security and patient access, and undermines investments in U.S. research, manufacturing and production,” said Dr. George Tidmarsh, M.D., Ph.D., Director of FDA’s Center for Drug Evaluation and Research. “It also slows down reviews and costs taxpayers more money, as these foreign research and testing sites must be inspected by FDA, and foreign inspections take more time to prepare for and are more expensive to conduct than domestic inspections. This pilot prioritization program can help ensure that Americans have a strong and resilient domestic drug supply, and also reflects the Trump Administration’s unwavering commitment to revitalizing American industry and providing American consumers affordable access to needed medications.”

Earlier this week, FDA hosted a public meeting titled “Onshoring Manufacturing of Drugs and Biological Products” on FDA’s PreCheck program, which introduces an innovative two-phase approach to accelerate the establishment of high priority new pharmaceutical manufacturing facilities in the U.S. and strengthen the domestic pharmaceutical supply chain. At that meeting, FDA heard from stakeholders about how incentives such as faster reviews could spur additional investment in U.S. manufacturing and research and development.

This ANDA prioritization pilot represents a further step FDA is taking to incentivize U.S. generic drug manufacturing and testing. Under this pilot, ANDA applicants who conduct any required bioequivalence testing in the United States and whose products are made in the U.S. using exclusively domestic sources for APIs are eligible for priority review. Applicants can request this priority review by following the procedures outlined in FDA’s Manual of Policies and Procedures (MAPP) 5240.3, Prioritization of the Review of Original ANDAs, Amendments, and Supplements (“Prioritization MAPP”) and referencing this pilot program as the basis for prioritization. Applicants should provide information with their priority review request to demonstrate that their ANDA qualifies for the pilot (i.e., (1) that either the pivotal bioequivalence testing was conducted in the U.S. or that the ANDA qualifies for a waiver of bioequivalence testing, (2) that the finished dosage form manufacturer is located in the U.S., and (3) that the API supplier is located in the U.S.). Prioritizing this additional category of ANDAs is expected to expedite the availability of high-quality, U.S.-made generics for American consumers. 

Related Information

Counter-flotilla leaves Tel Aviv in solidarity with hostages

 The Israeli Foreign Ministry bid farewell and blessings on Friday to a flotilla that set sail from Tel Aviv in support of the 48 hostages still held by Hamas.

"As Shabbat begins, we lift our prayers — for their safe return, for peace in Israel, and for strength for Jewish communities worldwide," the ministry tweeted. "Our hearts are especially with the community of Manchester, after the terror attack on a synagogue over Yom Kippur."

The journey of the Israeli boats came in response to the Global Sumud Flotilla's attempt to dock in Gaza and deliver humanitarian aid. However, the flotilla was intercepted by Israel, and the passengers were detained, now awaiting deportation.

https://breakingthenews.net/Article/Counter-flotilla-leaves-Tel-Aviv-in-solidarity-with-hostages/64923943