Issue Briefs
Date of this Version
9-10-2020
Abstract
Mifepristone, a drug used to manage early miscarriage or end an early pregnancy, carries unique restrictions imposed by the U.S. Food and Drug Administration (FDA). Patients are required to pick up the drug in person from a doctor or a clinic, even though they can take the drug at home. In July, a federal court ruled that the FDA must suspend these restrictions during the COVID-19 pandemic, for patients seeking an early abortion, although the ruling did not apply to women with an early pregnancy loss. But the challenges to FDA restrictions on mifepristone predate the pandemic. This Issue Brief provides the context for this ongoing controversy, and reviews recent evidence on the clinical and cost effectiveness of mifepristone for the medical management of first trimester miscarriage.
Document Type
Brief
Volume
24
Number
1
License
This work is licensed under a Creative Commons Attribution-No Derivative Works 4.0 License.
Keywords
miscarriage, mifepristone, fda, pregnancy, pregnant, trimester
View On LDI Website
https://ldi.upenn.edu/brief/fda-restrictions-mifepristone-time-change
Included in
Health Economics Commons, Health Policy Commons, Maternal and Child Health Commons, Obstetrics and Gynecology Commons, Women's Health Commons
Date Posted: 03 February 2021