Mifepristone Complication Form

As drug-induced abortions increase across the country and are available via online and mail access, the impact on our patients is increasing significantly. Many of us are treating patients with complications of these abortions on a regular basis and yet the FDA continues to enable this dangerous dispensing regimen. It is imperative that the FDA hear not only from women who have been harmed by mifepristone and misoprostol abortions but also from those of us who are caring for them. We are collecting stories from our members to help the FDA understand the negative impact that these abortions are having on our patients. We encourage you to fill out this form anytime you manage a complication. This can be done anonymously and your answers should not include any patient identifying information.

If no to the above question, we encourage you to report it. That can be done here: https://www.accessdata.fda.gov/scripts/medwatch/index.cfm?action=reporting.home