CORRECTION article
Front. Cardiovasc. Med.
Sec. Cardiovascular Pharmacology and Drug Discovery
Volume 12 - 2025 | doi: 10.3389/fcvm.2025.1636315
Adverse Events Associated with Amlodipine: A Pharmacovigilance Study Using the FDA Adverse Event Reporting System
Provisionally accepted- 1Department of Cardiovascular Medicine, First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
- 2The First Clinical Medical School, Guangzhou University of Chinese Medicine, Guangzhou, China
- 3Department of Cardiovascular Medicine, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China
- 4Clinical Medical College of Acupuncture, Moxibustion and Rehabilitation, Guangzhou University of Chinese Medicine, Guangzhou, China
- 5The Fifth Clinical College, Guangzhou University of Chinese Medicine, Guangzhou, China
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Keywords: Amlodipine, adverse drug reactions, FDA Adverse Event Reporting System, Risk signal detection, Logistic regression
Received: 27 May 2025; Accepted: 11 Jun 2025.
Copyright: © 2025 Di, Jiang, Zhong, Zhou, Zhou, Zheng and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Xingwei Di, Department of Cardiovascular Medicine, First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China
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