2026-05-04T11:05:41-0400 / 哥伦比亚广播公司新闻
作者:梅利莎·奎因
梅利莎·奎因是CBSNews.com的资深记者,负责报道美国政治,重点关注最高法院和联邦法院。
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梅利莎·奎因
2026年5月4日 / 美国东部时间上午11:05 / 哥伦比亚广播公司新闻
华盛顿讯——大法官塞缪尔·阿利托周一暂时叫停了一项上诉法院命令,该命令此前阻断了美国食品药品监督管理局(FDA)允许在线开具堕胎药米非司酮处方并通过邮寄方式配发的规定。
阿利托向米非司酮制造商丹科实验室(Danco Laboratories)以及该药物的仿制药生产商GenBioPro授予了临时救济。他的行政暂缓令将持续至5月11日下午5点。此举为最高法院留出更多时间,以便在诉讼程序推进期间,考虑两家制药公司提出的撤销上诉法院命令的请求。
丹科实验室和GenBioPro同时请求最高法院接手此案并就法律实质问题作出裁决。阿利托设定了周四的截止期限,要求路易斯安那州官员就制药公司的紧急上诉作出回应。
此次上诉使米非司酮的可获得性问题第二次提交至最高法院。自2022年最高法院推翻“罗伊诉韦德案”以来,反堕胎组织一直试图限制这种广泛使用的堕胎药的获取渠道,他们声称FDA在2000年首次批准米非司酮时,未充分考虑该药物的安全性和有效性,并在过去十年中放宽了其使用规定。
2024年,最高法院一致驳回了一组反堕胎医生和医疗团体提出的挑战,这些团体针对米非司酮的可获得性提起诉讼,最终裁定原告没有起诉FDA的法律权利。
当时的案件涉及FDA自2016年以来采取的一系列简化堕胎药获取流程的措施。这些措施包括允许在妊娠更晚阶段服用米非司酮、扩大可开具该药物处方的医护人员范围,以及取消面对面配发药品的要求,允许通过邮寄方式递送药物。
根据此前的规定,患者必须亲自从医护人员处获取该药物。但在新冠疫情期间,FDA暂停了面对面配发药品规定的执行,并认定该药物“无需面对面配发即可安全使用”。FDA于2023年正式允许通过远程医疗会诊开具米非司酮处方,并通过邮寄方式配发该药物。
在最高法院维持米非司酮的获取渠道后,路易斯安那州提起诉讼,挑战FDA允许通过邮寄方式递送米非司酮的举措。不过该州的一家联邦地区法院在4月份暂停了诉讼程序,在FDA审查该药物安全性期间,维持了米非司酮的宽松使用条件。
路易斯安那州官员向美国第五巡回上诉法院提起上诉,该法院于周五同意暂时阻断2023年的规定,该规定允许医疗保健提供者远程开具米非司酮处方并通过邮寄方式递送药物。
第五巡回上诉法院的一致裁决小组认定,路易斯安那州拥有起诉的法律资格,因为该州的医疗补助计划为两名在从州外医护人员处获取堕胎药后出现并发症的女性支付了急诊护理费用。
法官们表示,2023年的这项规定“通过破坏路易斯安那州保护未出生人类生命的法律,同时导致该州将医疗补助资金用于治疗因米非司酮受到伤害的女性,从而对路易斯安那州造成损害”。
第五巡回上诉法院的裁决小组指出:“FDA的行动所促成的每一例堕胎,都抵消了路易斯安那州对药物堕胎的禁令,并破坏了其‘每一个未出生的孩子从受孕那一刻起就是人类,因此是法律上的人’的政策。”
在“罗伊诉韦德案”被推翻后,路易斯安那州禁止堕胎,仅存在少数例外情况。该州还在2024年通过一项法律,将米非司酮和米索前列醇——药物堕胎中使用的第二种药物——列为受控物质,并将无处方持有该药物定为刑事犯罪。
在第五巡回上诉法院作出裁决后,丹科实验室和GenBioPro向最高法院寻求紧急救济,丹科实验室称该裁决“给高度依赖时间的决策带来了即时的混乱和动荡”。
这家制药公司在其请求中写道:“第五巡回法院前所未有的命令迫使患者、医护人员和药店立即陷入不确定性,没有过渡期,也没有实际的指导方针。那些预约(最早就在今天上午)的患者陷入了困境。已经完成筛查、咨询并为治疗做好准备的医护人员可能不得不中途停止,可能无法完成数天前就已启动的治疗计划。”
GenBioPro在其自身的紧急上诉中表示,第五巡回法院的裁决“引发了监管混乱”,并威胁要突然切断全国患者获取米非司酮的渠道,包括在堕胎合法的州。
该公司表示:“多年来,患者和临床医生一直依赖无需到诊所就诊即可配发米非司酮的方式,尤其是对于来自农村地区以及因交通、育儿或工作限制而难以亲自就医的女性而言。第五巡回法院的裁决直接导致全国患者可能面临紧急医疗护理的延误或无法获得、供应链中断以及随之而来的健康风险。”
Alito temporarily restores FDA rule allowing abortion pill mifepristone to be sent by mail
2026-05-04T11:05:41-0400 / CBS News
By Melissa Quinn
Melissa Quinn is a senior reporter for CBSNews.com, where she covers U.S. politics, with a focus on the Supreme Court and federal courts.
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Melissa Quinn
May 4, 2026 / 11:05 AM EDT / CBS News
Washington — Justice Samuel Alito on Monday temporarily halted an appellate court order that blocked a Food and Drug Administration rule allowing the abortion pill mifepristone to be prescribed online and dispensed through the mail.
Alito granted temporary relief to the maker of mifepristone, Danco Laboratories, and the manufacturer of a generic version of the drug, GenBioPro. His administrative stay will remain in place until 5 p.m. on May 11. The move gives the Supreme Court more time to consider the drug companies’ requests to set aside the appellate court’s order while litigation proceeds.
Danco and GenBioPro also asked the high court to take up the case and decide the legal merits. Alito set a Thursday deadline for Louisiana officials to respond to the drugmakers’ emergency appeals.
The appeals put the issue of mifepristone’s availability before the Supreme Court for a second time. Anti-abortion rights groups have sought to restrict access to the widely used abortion pill since the high court overturned Roe v. Wade in 2022, claiming that the FDA failed to adequately consider the drug’s safety and effectiveness when it first approved mifepristone in 2000 and relaxed the rules for its use over the past decade.
In 2024, the high court unanimously rejected a challenge from a group of anti-abortion rights doctors and medical groups that targeted mifepristone’s availability, ruling that the plaintiffs did not have the legal right to sue the FDA.
That case involved a series of steps taken by the drug agency since 2016 that made the abortion pill easier to obtain. Those actions included allowing mifepristone to be taken later into a pregnancy, expanding the healthcare workers who can prescribe it and lifting an in-person dispensing requirement to allow the drug to be sent through the mail.
Under the prior rules, patients were required to obtain the drug from healthcare providers in person. But the agency suspended enforcement of the in-person dispensing rule during the COVID-19 pandemic and found that the drug “may be safely used without in-person dispensing.” The FDA formally allowed mifepristone to be prescribed through telehealth appointments and dispensed through the mail in 2023.
Following the Supreme Court’s decision preserving access to mifepristone, the state of Louisiana filed a lawsuit challenging the FDA’s move to let mifepristone be delivered by mail. A federal district court in the state, however, paused the litigation in April, which maintained the eased conditions for use of mifepristone while the FDA reviewed its safety.
Louisiana officials appealed to the U.S. Court of Appeals for the 5th Circuit, which agreed on Friday to temporarily block the 2023 rule allowing healthcare providers to prescribe mifepristone remotely and send the drug through the mail.
The unanimous 5th Circuit panel found that the state had legal standing to sue because its Medicaid program covered emergency-room care for two women who experienced complications after receiving the abortion pill from an out-of-state provider.
The 2023 regulation, the judges said, “injures Louisiana by undermining its laws protecting unborn human life and also by causing it to spend Medicaid funds on emergency care for women harmed by mifepristone.”
“Every abortion facilitated by FDA’s action cancels Louisiana’s ban on medical abortions and undermines its policy that ‘every unborn child is a human being from the moment of conception and is, therefore, a legal person,’” the 5th Circuit panel found.
Louisiana banned abortion, with narrow exceptions, after Roe’s reversal. The state in 2024 also enacted a law that designates mifepristone and misoprostol — the second drug used in a medication abortion — as controlled substances and criminalizes possession without a prescription.
Danco and GenBioPro came to the Supreme Court for emergency relief on the heels of the 5th Circuit’s decision, which Danco said “injects immediate confusion and upheaval into highly time-sensitive decisions.”
“The Fifth Circuit’s unprecedented order forces patients, providers, and pharmacies into immediate uncertainty, with no transition period and no practical guidance,” the drug company wrote in its request. “Patients who have appointments — as soon as this morning — are in limbo. Providers who have already screened, counseled, and prepared patients for care may have to stop midstream, potentially unable to complete treatment plans that were set in motion days earlier.”
In its own emergency appeal, GenBioPro said the 5th Circuit’s decision has “unleashed regulatory chaos” and threatened to abruptly cut off access to mifepristone for patients nationwide, including in states where abortion is legal.
“Patients and clinicians have, for years, relied on dispensing mifepristone without an in-clinic visit, particularly for women from rural areas and those for whom transportation, childcare, or occupational constraints make it difficult to see providers in person,” the company said. “As a direct result of the Fifth Circuit’s order, patients nationwide may face delay or denial of access to time-sensitive medical care, supply-chain disruptions, and attendant health risks.”
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