Evaluating the process of standardizing investigational drug substance names reported to the United States Food and Drug Administration adverse event reporting system

被引:0
|
作者
Fung, Maggie [1 ]
Brajovic, Sonja [1 ]
Patel, Nitin [1 ]
Chang, Sherry [1 ]
机构
[1] US FDA, Silver Spring, MD USA
关键词
D O I
暂无
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
383
引用
收藏
页码:189 / 190
页数:2
相关论文
共 50 条
  • [1] Suspected adverse drug reactions of rivaroxaban reported in the United States food and drug administration adverse event reporting system database: a pharmacovigilance study
    Wu, Jingying
    Wu, Jianru
    Tang, Biyu
    Wang, Xinru
    Wei, Fenfang
    Zhang, Yi
    Li, Limin
    Li, Hongqiao
    Wang, Bei
    Wu, Wenyu
    Hong, Xiang
    FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [2] Drug Associated Toxic Nephropathy Identified in the United States Food and Drug Administration Adverse Event Reporting System Database
    Balaha, Mohamed F.
    Ahmed, Nehad J.
    Khafagy, El Sayed A.
    LATIN AMERICAN JOURNAL OF PHARMACY, 2022, 41 (11):
  • [3] Adverse events reported to the US Food and Drug Administration Adverse Event Reporting System for tisagenlecleucel
    Dores, Graca M.
    Jason, Christopher
    Niu, Manette T.
    Perez-Vilar, Silvia
    AMERICAN JOURNAL OF HEMATOLOGY, 2021, 96 (09) : 1087 - 1100
  • [4] Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database
    Toki T.
    Ono S.
    Drugs - Real World Outcomes, 2018, 5 (2) : 117 - 128
  • [5] Osteonecrosis of the Jaw in the United States Food and Drug Administration's Adverse Event Reporting System (FAERS)
    Zhang, Xiaoyan
    Hamadeh, Issam S.
    Song, Shuang
    Katz, Joseph
    Moreb, Jan S.
    Langaee, Taimour Y.
    Lesko, Lawrence J.
    Gong, Yan
    JOURNAL OF BONE AND MINERAL RESEARCH, 2016, 31 (02) : 336 - 340
  • [6] Adverse drug events of denosumab: Data-mining based on the United States Food and Drug Administration Adverse Event Reporting System database
    Liu, Shaohua
    Jiang, Wangyan
    Guo, Jieru
    Zhou, Xinrong
    Liu, Zhelong
    JOURNAL OF RESEARCH IN PHARMACY, 2024, 28 (04): : 1220 - 1230
  • [7] Reporting of pancreatitis with tocilizumab use: A disproportionality analysis using the United States Food and Drug Administration adverse event reporting system
    Kamath, Ashwin
    Acharya, Sahana
    Rao, Rashmi
    Ullal, Sheetal
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2021, 30 : 324 - 324
  • [8] Fatal neutropenic enterocolitis associated with docetaxel use: A review of cases reported to the United States Food and Drug Administration Adverse Event Reporting System
    Singh, Pritpal
    Nayernama, Afrouz
    Jones, S. Christopher
    Kordestani, Laleh Amiri
    Fedenko, Katherine
    Prowell, Tatiana
    Bersoff-Matcha, Susan J.
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2020, 26 (04) : 923 - 928
  • [9] Drug-induced torsades de pointes: Disproportionality analysis of the United States Food and Drug Administration adverse event reporting system
    Wu, Ziyang
    Zhou, Pengxiang
    He, Na
    Zhai, Suodi
    FRONTIERS IN CARDIOVASCULAR MEDICINE, 2022, 9
  • [10] Drug-Associated Acute Kidney Injury Identified in the United States Food and Drug Administration Adverse Event Reporting System Database
    Welch, Hanna K.
    Kellum, John A.
    Kane-Gill, Sandra L.
    PHARMACOTHERAPY, 2018, 38 (08): : 785 - 793