POST-MARKETING ADVERSE EVENTS (AES) ASSOCIATED WITH TETRABENAZINE (TBZ): FINDINGS USING FDA'S ADVERSE EVENT REPORTING SYSTEM (FAERS)

被引:0
|
作者
Claassen, Daniel O. [1 ]
Iyer, Ravi [2 ]
Dimbil, Mo [3 ]
Giron, Abril [3 ]
De Boer, Lisa [4 ]
Gandhi, Sanjay [2 ]
Hoffman, Keith B. [3 ]
机构
[1] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[2] Teva Pharmaceut Ind, Frazer, PA USA
[3] Advera Hlth Analyt, Santa Rosa, CA USA
[4] Teva Pharmaceut, La Jolla, CA USA
关键词
D O I
10.1136/jnnp-2016-314597.206
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
I41
引用
收藏
页码:A73 / A73
页数:1
相关论文
共 50 条
  • [41] Reports of adverse events related with second generation antipsychotics in children in the FDA adverse event reporting system (FAERS)
    Zapata, Lorenzo Villa
    Bibbs, Janese
    Crapps, Mariah
    Lumbreras, Ainhoa Gomez
    Malone, Daniel
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2022, 31 : 579 - 580
  • [42] Alpelisib-related adverse events: The FDA Adverse Event Reporting System Database (FAERS) pharmacovigilance study
    Li, Yun
    Li, Hang
    Xiang, Zhongyuan
    [J]. HELIYON, 2024, 10 (06)
  • [43] Assessing taxane-associated adverse events using the FDA adverse event reporting system database
    Lao, Dong-Hui
    Chen, Ye
    Fan, Jun
    Zhang, Jian-Zhong
    [J]. CHINESE MEDICAL JOURNAL, 2021, 134 (12) : 1471 - 1476
  • [44] Contact dermatitis adverse events: A review of contact dermatitis-associated reports from the FDA adverse event reporting system (FAERS)
    Taylor, J. S.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2022, 142 (08) : S42 - S42
  • [45] Vedolizumab Adverse Events: Analysis of the FDA Adverse Event Reporting System
    Jow, Steven
    Hutfless, Susan
    [J]. INFLAMMATORY BOWEL DISEASES, 2017, 23 : S35 - S36
  • [46] A REALWORLD PHARMACOVIGILANCE STUDY OF FDA ADVERSE EVENT REPORTING SYSTEM (FAERS) EVENTS FOR EMPAGLIFLOZIN AND DAPAGLIFLOZIN
    Milutinovic, Stefan
    Petrovic, Marija
    Jancic, Predrag
    Trajkovic, Hristina
    Alarcon, Ricardo Orlando Escarcega
    Chazal, Richard A.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2024, 83 (13) : 319 - 319
  • [47] Post-marketing safety of lorlatinib: a real-world study based on the FDA adverse event reporting system
    Li, Huqun
    Wang, Chongshu
    Guo, Cuilian
    [J]. FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [48] Post-Marketing Safety of Vemurafenib: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System
    Liu, Yan-xin
    Dong, Chang-jiang
    He, Xu-cheng
    Shu, Ya-min
    Wu, Pan
    Zou, Jian
    [J]. JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, 2022, 25 : 377 - 390
  • [49] A disproportionality analysis of sunitinib in the FDA adverse event reporting system (FAERS)
    Zou, Wenbin
    Yang, Han
    Xi, Yu
    Zeng, Chenxi
    Chen, Wei
    Fu, Xiangning
    [J]. HELIYON, 2024, 10 (17)
  • [50] Comparing the difference of adverse events with HER2 inhibitors: a study of the FDA adverse event reporting system (FAERS)
    Bao, Yiwen
    Chen, Jiaju
    Duan, Luting
    Wang, Fujue
    Lai, Han
    Mo, Zeming
    Zhu, Weiliang
    [J]. FRONTIERS IN PHARMACOLOGY, 2024, 15