Showing 1 - 3 results of 3 for search 'Xingwei Di', query time: 0.01s Refine Results
  1. 1
    Drug-induced pulmonary edema: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System (FAERS)

    Drug-induced pulmonary edema: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System (FAERS) by Zilan Zhong, Manting Liu, Qian Zhong, Miao Zhou, Xingwei Di

    Published 2025-08-01
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  2. 2
    Adverse events associated with amlodipine: a pharmacovigilance study using the FDA adverse event reporting system

    Adverse events associated with amlodipine: a pharmacovigilance study using the FDA adverse event reporting system by Jiazhen Jiang, Qian Zhong, Xinyu Zhou, Lisi Zhou, Jiyuan Zheng, Bingshuo Liu, Xingwei Di

    Published 2025-05-01
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  3. 3
    Correction: Adverse events associated with amlodipine: a pharmacovigilance study using the FDA adverse event reporting system

    Correction: Adverse events associated with amlodipine: a pharmacovigilance study using the FDA adverse event reporting system by Jiazhen Jiang, Qian Zhong, Xinyu Zhou, Lisi Zhou, Jiyuan Zheng, Bingshuo Liu, Xingwei Di

    Published 2025-06-01
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