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Amid so much discouraging news about reproductive health access in the wake of Roe v. Wade's demise, the announcement by the Food and Drug Administration last week that it was approving Opill, a daily oral contraceptive, for over-the-counter sale to people of all ages, felt like a breath of fresh air. The evidence is clear that removing the prescription requirement for birth control pills — Opill was the first such medication to be approved but surely won't be the last — will improve access to a highly effective form of contraception for millions of Americans.
I've been involved in efforts to make oral contraceptives available over the counter for almost two decades, working alongside fellow doctors, nurses, lawyers, public health scientists, pharmacists, reproductive justice advocates and youth activists to make the case for this regulatory change, long before any pharmaceutical company expressed interest in submitting an application to the FDA. Like many of my colleagues, I've been holding my breath for the last year, since HRA Pharma, which manufactures Opill, submitted its application to the FDA.
But to my surprise, the Opill approval process went relatively smoothly. My colleagues and I were heartened to see that the conversation around Opill was generally grounded in evidence, rather than politics. We now have hope that other advances could be coming to help offset restrictions on minors' access to contraception and state-level abortion bans.
A lot could have gone wrong with the Opill process. Remember the fight over Plan B emergency contraception, sometimes referred to as the "morning-after pill?" In 2006, after a highly politicized battle that ran for more than three years, the FDA under President George W. Bush approved Plan B for over-the-counter sale, but only for people 18 or older. Because of the age restriction, the product was shunted behind the pharmacy counter, where the consumer's age could be confirmed. The FDA asked Plan B's sponsor for additional data on people 17 and younger to show the product could be used safely and effectively by adolescents. In response, researchers submitted additional research with several hundred young women, age 17 and under, demonstrating that adolescents understood the key concepts in Plan B's label and used the product appropriately in an over-the-counter simulation study.
It took a change in presidential administration before the FDA recommended approval of Plan B for people of all ages in 2011, five years after the original over-the-counter approval for adults only.
In a move that tarnished his record on reproductive rights, President Barack Obama endorsed a decision by his secretary of health and human services to override the FDA's decision and block over-the-counter access for anyone under 17. Ignoring the scientific evidence, Obama expressed concern about 10- or 11-year-olds who might encounter Plan B in drugstores "alongside bubble gum or batteries" and be harmed. It took a lawsuit and almost two more years before emergency contraception was actually available over the counter for people of all ages in 2013.