Supreme Court temporarily restores full access to abortion pill

Catch up with NBC News Clone on today's hot topic: Supreme Court Access Abortion Pill Mifepristone Rcna343445 - Politics and Government | NBC News Clone. Our editorial team reformatted this story for clarity and speed.

The decision means mifepristone remains available nationwide without an in-person meeting required while litigation continues.
Get more newsSupreme Court Access Abortion Pill Mifepristone Rcna343445 - Politics and Government | NBC News Cloneon

WASHINGTON — The Supreme Court on Monday provisionally blocked a lower court decision that would have limited availability nationwide of the abortion pill mifepristone.

In two brief orders, Justice Samuel Alito, one of the court's conservatives, said the decision by the New Orleans-based 5th U.S. Circuit Court of Appeals would remain on hold until at least May 11. Alito issued the order because he is the justice who handles emergency issues arising from that appeals court, which covers Texas, Louisiana and Mississippi.

The temporary pause gives the high court time to consider next steps in the case as it weighs separate emergency requests filed by drugmakers Danco and GenBioPro.

The nationwide availability of mifepristone was cast into jeopardy Friday when the appeals court granted Louisiana's request to void Biden administration rules that allowed the drug to be administered without an in-person meeting, meaning it can in theory be mailed anywhere in the country, even in states with strict abortion bans.

Alexis McGill Johnson, president of abortion rights group Planned Parenthood Action Fund, welcomed the decision.

"While mifepristone access returns to where it was on Friday morning, the whiplash and chaos that patients and providers are navigating have already had real consequences for real peoples’ lives and futures," she said in a statement.

Anti-abortion groups have been pushing for years to reinstate the in-person dispensing requirement, alleging that taking mifepristone at home can be dangerous — despite studies that have found it to be safe and effective.

Danco makes Mifeprex, the brand-name version of mifepristone, while GenBioPro makes a generic version.

Alito ordered Louisiana to file its response to the companies' request by the end of the day Thursday.

In 2024, the Supreme Court rejected an earlier attempt to overturn the Food and Drug Administration's approvals for mifepristone. The court said then that those challenging the approvals did not have legal standing.

The new case focuses more narrowly on the Biden administration's decision the previous year to make permanent Covid-era rules that made it easier to obtain the drug during the pandemic.

That move came after the Supreme Court's 2022 ruling that overturned abortion rights landmark Roe v. Wade, giving conservative states a green light to heavily restrict, if not ban, abortion.

Medication abortion is harder for states to regulate than surgical procedures, especially if pills are available through the mail.

The drugmakers say that, like in the earlier case, Louisiana does not have legal standing to bring the claims.

In their lawsuit against the FDA, Louisiana Attorney General Liz Murrill and the Alliance Defending Freedom, a conservative Christian legal group that opposes abortion, alleged that data did not support lifting the in-person dispensing requirement.

"Big abortion pharma claims they need an emergency stay because they will lose massive amounts of money if they can’t kill more babies quickly and efficiently by mail without medical oversight," Murrill said in a statement after Monday's Supreme Court action. "The administrative stay is temporary, and I am confident life and the law will win in the end."

In January, the FDA requested the case be paused until the agency finished conducting its own safety review of mifepristone. Health Secretary Robert F. Kennedy Jr. commissioned the review last year in response to a report that claimed to find a higher rate of serious complications from mifepristone than reported by the FDA.

But researchers who study reproductive health said the report amounted to junk science and exaggerated the risks of the medication. The report was released online by the Ethics and Public Policy Center, a conservative think tank. It was not peer-reviewed nor published in a medical journal.

A district judge in Louisiana agreed to the FDA’s request to pause the case last month before the appeals court stepped in.

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