On
May 9, 1960–64 years ago today - the FDA approved the world's first
commercially produced birth-control pill. Timed to that anniversary,
nonpartisan public radio show Open to Debate is releasing a mock trial
on the question "Should Courts Restrict Access to the Abortion Pill?"
The Open To Debate podcast plays a critical role in our society today.The mission of Open to Debate is to
restore critical thinking, facts, reason, and civility to America’s
public square. Open to Debate is a platform for intellectually curious
and open-minded people to engage with others holding opposing views on
complex issues.
The full episode was released on May 9th (look for it here, on NPR stations, or via the Open to Debate podcast). Below are three clips on YouTube:
In
a post-Roe v. Wade world, mifepristone, a medication that 63% of women
undergoing an abortion use, is under consideration by the Supreme Court.
Mifepristone was approved as a two-drug regimen for use up to seven
weeks of pregnancy and initially required in-person clinical visits, but
changes by the FDA were made in 2016 and 2021 to expand accessibility
via telehealth and the length of its administration. FDA v. Alliance for
Hippocratic Medicine seeks to address whether the FDA's approval
process was thorough and whether the drug should continue to be
available.
Those
in favor of restrictions argue that the FDA approved mifepristone
without adequate consideration of long-term health impacts, failing to
adhere to stringent regulatory standards. They also consider restricting
access to abortion pills a moral imperative, forcing some doctors to
treat patients for a procedure against their beliefs.
Arguing in favor of restrictions is Catherine Glenn Foster,
Senior Fellow in Legal Policy at the Charlotte Lozier Institute. She
has worked on topics from euthanasia and assisted suicide to abortion
and maternal health, health and safety regulations, conscience
protections, and constitutional aspects of the right to life and has
authored and testified on numerous domestic, foreign, and international
legislation and initiatives, appearing on multiple occasions before the
Senate, the House, and other federal and state bodies.
Those
against restrictions point out the approval was based on extensive
research and clinical trials, which should not be undermined without
substantial scientific evidence. They also argue access to mifepristone
is essential for women's health, providing a safer alternative to
surgical abortion and enabling privacy and autonomy in healthcare
decisions.
Arguing against restrictions is Julia Kaye,
Senior Staff Attorney at the ACLU Reproductive Freedom Project. She was
lead counsel in two lawsuits that led the FDA to allow patients to
obtain mifepristone through telehealth and pharmacy dispensing. She has
also led or co-counseled litigation in numerous states challenging
abortion bans, mandatory abortion delay requirements, laws preventing
qualified nurse practitioners and midwives from providing abortion or
birthing care, and other political interference with patients’ health
and autonomy.
Listen to Open to Debate wherever you get podcasts, or watch the video version at opentodebate.org.
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