FDA requires overdose risk on opioid prescription labels

Published



The Food and Drug Administration announced on Thursday significant labeling changes that will affect all opioid pain medications, including clear information about the risk of addiction, misuse, and overdose in the long term. 

The change comes following two recent observational studies finding a high risk of serious adverse outcomes for patients prescribed opioid pain medications long-term, adding quantitative data to the decades of lived experience of the opioid epidemic across the United States. 

Trusted reporting.Unlimited access.

Subscribe for full access to Washington Examiner coverage, expert political analysis, and subscriber-only journalism.

Get Unlimited Access

Already a member? Log in

Cancel anytime.