- Associated Press - Wednesday, October 19, 2011

OKLAHOMA CITY — An Oklahoma judge Wednesday temporarily blocked from taking effect a new law designed to reduce the number of abortions performed in the state by restricting the ways in which doctors can treat women with abortion-inducing drugs.

Oklahoma County District Judge Daniel Owens issued the ruling after a conference call with attorneys for both sides. The temporary injunction prevents the bill from going into effect Nov. 1.

Passed earlier this year by the GOP-controlled Legislature and signed by Gov. Mary Fallin, the measure requires doctors to follow the strict guidelines and protocols authorized by the U.S. Food and Drug Administration, and prohibits off-label uses of the drugs. It also requires doctors to examine the woman, document certain medical conditions and schedule a follow-up appointment.

Opponents of the measure say the off-label use of drugs - such as changing a recommended dosage or prescribing it for different symptoms than the drug was initially approved for - is common, and that the measure would prevent doctors from using their best medical judgment.

“We’re thrilled that women in Oklahoma will continue to be able to access medical care that accounts for scientific evidence, sound medical judgment and advancements in medicine,” said Michelle Movahed, an attorney for the New York-based Center for Reproductive Rights, which challenged the law on behalf of Nova Health Systems, a Tulsa-based abortion provider, and the Oklahoma Coalition for Reproductive Justice, a nonprofit pro-choice group.

Similar laws approved in North Dakota and Ohio have been delayed pending legal challenges, Ms. Movahed said. The North Dakota lawsuit says that state’s law would prevent doctors from using the drug misoprostol because it’s labeled for treatment of stomach ulcers. It’s one of two drugs that are administered in combination to induce abortions.

Attorneys for Oklahoma contend the drugs are dangerous and should be used only in strict accordance with FDA guidelines.

“To date, at least eight American women have died from mifepristone abortions,” Assistant Attorney General Victoria Tindall wrote in the state’s response to the center’s lawsuit. “The dangerous risks of mifepristone demand strict adherence to the FDA-approved protocol.”

Attorney General Scott Pruitt said in a statement Wednesday that the judge’s decision “is unfortunate for the state and our public health, but it is not a surprise with new legislative provisions being tested.”

Ms. Movahed said as many as 21 percent of all drugs are prescribed for off-label use. In the case of drug-induced abortions, she said a common regimen is to use one-third of the FDA-recommended amount of the abortion drug mifepristone in conjunction with misoprostol, which has been determined to be effective for a variety of purposes in addition to gastric ulcers.

She said in the decade since the mifepristone FDA label was approved, numerous studies have shown the combination is safe and effective.

“The evidence supporting these alternative regimens are of such high quality that the American College of Obstetricians and Gynecologists gave these alternative regiments their highest possible recommendation,” Ms. Movahed said.

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