US Food and Drug Administration Sentinel Initiative and Postmarket Drug Safety Surveillance
JAMA Health Forum 10.1001/jamahealthforum.2026.0754April 17, 2026 at 11:00 AM EDT
This review observed that as FDA considers modernizing the Sentinel Initiative as part of forthcoming PDUFA reauthorization, opportunities exist to strengthen the use and impact of the ARIA system by creating a publicly available, centralized, and regularly updated database of safety concerns, establishing a complete record of ARIA system information, adopting standardized terminology, and further expanding data linkages beyond claims data.
Link to the article in your story
We encourage you to link out to this article in your story using the link below. It includes an access token that will give free access to the article for your readers up to one year after publication. (The link will be live after the article publishes and embargo is lifted.)
Please see the article for additional information, including full author list, author contributions and affiliations, conflict of interest and financial disclosures, and funding and support.
Need more information? Contact us.