Novel adverse events of vortioxetine: A disproportionality analysis in USFDA adverse event reporting system database.
CONCLUSION: The present study suggests that vortioxetine may result in these adverse events. Further pharmacoepidemiologic studies are necessary to confirm this conclusion and to improve the precision of the prevalence and/or the risk factors of this ADRs.
PMID: 28942181 [PubMed - as supplied by publisher]
Source: Asian Journal of Psychiatry - Category: Psychiatry Tags: Asian J Psychiatr Source Type: research
More News: Clinical Trials | Databases & Libraries | Depression | Drugs & Pharmacology | Insomnia | Psychiatry | Study | Weight Loss