A pharmacovigilance study of vortioxetine based on data from the FDA adverse event reporting system
Crossref DOI link: https://doi.org/10.1038/s41598-025-13786-7
Published Online: 2025-08-07
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Liu, Miao
Xia, Yang
Long, Wenwen
Han, Xiaowen
Xiong, Yu
Text and Data Mining valid from 2025-08-07
Version of Record valid from 2025-08-07
Article History
Received: 6 April 2025
Accepted: 28 July 2025
First Online: 7 August 2025
Declarations
:
: The authors declare no competing interests.