Utility and limitations of the FDA adverse events reporting system public dashboard for safety analyses: a case study with vesicular monoamine transporter 2 inhibitors

Expert Opinion on Drug Safety · Published 2025-11-10 · DOI 10.1080/14740338.2025.2588634

Free full text

Authors being retrieved — see the publisher record. https://doi.org/10.1080/14740338.2025.2588634

Abstract

PubPorta does not have an abstract for this article yet.

Read the article at the publisher →

Publication details

Year
2025

Related articles