Summary

Thomas Owen Rice Washington v. U.S. Food and Drug Administration (2023)

I. Preliminary Injunction Standard Plaintiffs, on behalf of themselves and as parens patriae in protecting the health and well-being of its residents, moves for a preliminary injunction “affirming FDA’s original conclusion that mifepristone is safe and effective, preserving the status quo by enjoining any actions by Defendants to remove this critical drug from the market, and enjoining the unnecessary and burdensome January 2023 restrictions.”
Source: Wikisource

Thomas Owen Rice Washington v. U.S. Food and Drug Administration (2023)

The public’s interest in health care favors a preliminary injunction where the agency’s action likely “results in worse health outcomes.” New York v. U.S. Dep’t of Homeland Sec., 969 F.3d 42, 87 (2d Cir. 2020) .
Plaintiffs contend the public has an interest in access to safe and effective medicine for those who terminate their pregnancies. ECF No. 3 at 36. Defendants contend the public interest is “best served by deferring to FDA’s judgments about what restrictions are necessary to ensure drugs are safe.”
Source: Wikisource

Thomas Owen Rice Washington v. U.S. Food and Drug Administration (2023)

A court may imply a lack of irreparable harm where there is no “speedy action” and a plaintiff sleeps on its rights. Lydo Enters. v. City of Las Vegas, 745 F.2d 1211, 1213 (9th Cir. 1984) .
Plaintiffs assert that the Mifepristone REMS Program imposes costs that are not compensable where the restriction of access to mifepristone causes patients to miss the window for medication abortion, leaving patients with procedural abortion or carrying a pregnancy to term, options that impose higher costs on Plaintiffs’ state-run health care programs.
Source: Wikisource

Get perspective with Kwize: daily news enlightened by great literature