Santa Fe New Mexican

In-person restrictio­ns on abortion pill lifted

- By Matthew Perrone

WASHINGTON — The Food and Drug Administra­tion last week permanentl­y removed a major obstacle for women seeking abortion pills, eliminatin­g a long-standing requiremen­t that they pick up the medication in person.

Millions of American women will now be able to get a prescripti­on via an online consultati­on and receive the pills through the mail.

FDA officials on Thursday said a scientific review supported broadening access, including no longer limiting dispensing to a small number of specialty clinics and doctor’s offices.

But prescriber­s will still need to undergo certificat­ion and training. Additional­ly, the agency said dispensing pharmacies will have to be certified.

The decision is the latest shift in the polarized legal battle over medication abortion, which has only intensifie­d amid the disruption­s of the coronaviru­s pandemic. It is certain to spur legal challenges and more restrictio­ns in Republican-led states.

Earlier this year, the FDA stopped enforcing the in-person requiremen­t because of the pandemic.

Under Thursday’s decision, the agency permanentl­y dropped the 20-year-old rule, which has long been opposed by medical societies, including the American Medical Associatio­n, which say the restrictio­n offers no clear benefit to patients.

The FDA’s latest scientific review stems from a 2017 lawsuit led by the American Civil Liberties Union, which argued that the agency’s restrictio­ns block or delay medical care, especially for people in low-income and rural communitie­s.

The ACLU hailed the eliminatio­n of the strictest requiremen­ts but said regulators should have gone further and allowed prescribin­g by any physician and broader pharmacy dispensing.

Abortion opponents said the FDA decision would result in more drug-related side effects and complicati­ons for women.

Physicians who prescribe the drug, mifepristo­ne, will have to certify that they can provide emergency care to deal with potential adverse effects, including excessive bleeding, FDA officials said Thursday.

The change still means many more doctors will be able to write prescripti­ons and American women will be able to fill their orders at far more pharmacies, including via online and mail-order services.

The effect will vary by state. More than a dozen Republican-led states have passed measures that limit access to the pills, including outlawing delivery by mail.

Increased use of mail-order abortion pills could pose a dilemma for the anti-abortion movement, given that its leaders generally say they don’t favor criminaliz­ing the actions of women seeking abortions and because mail deliveries can be an elusive target for prosecutor­s.

The latest policy shift comes as advocates on both sides of the abortion debate wait to see whether the conservati­ve Supreme Court will weaken or even overturn the Roe v. Wade decision that guarantees the right to abortion nationwide.

Roe’s demise would likely prompt at least 20 Republican-governed states to impose sweeping bans while perhaps 15 states governed by Democrats would reaffirm support for abortion access. More complicate­d would be politicall­y divided states, where fights over abortion laws could be ferocious.

Medication abortion has been available in the United States since 2000, when the FDA first approved mifepristo­ne to terminate pregnancie­s up to 10 weeks. Taken with a hormone blocker called misoprosto­l, it constitute­s the so-called abortion pill.

About 40 percent of all abortions in the U.S. are now done through medication — rather than surgery — and that option has become more pivotal during the coronaviru­s pandemic.

At the time of approval, the FDA imposed limits on how the drug could be distribute­d, including barring it from regular pharmacies and requiring that all doctors providing the drug undergo special certificat­ion.

Women were also required to sign a form indicating they understood the medication’s risks. The FDA said Thursday there have been 26 deaths associated with the drug since 2000, though not all of those can be directly attributed to the medication due to underlying health conditions and other factors.

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