Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

Lignende værker

• Assessment of factors associated with completeness of spontaneous adverse event reporting in the United States: A comparison between consumer reports and healthcare professional reports
  af: Toki, Tadashi, et al.
  Udgivet: (2019)
• Retrospective analysis of adverse events with spironolactone in females reported to the United States Food and Drug Administration
  af: Wang, Yu, et al.
  Udgivet: (2020)
• Risk of medication-induced lactic acidosis and hyperlactatemia: a pharmacovigilance study of the United States Food and Drug Administration’s Adverse Event Reporting System database
  af: Houci Yang, et al.
  Udgivet: (2025-04-01)
• Hyperglycemic adverse events following antipsychotic drug administration in spontaneous adverse event reports
  af: Kato, Yamato, et al.
  Udgivet: (2015)
• Review of Reported Clinical Information System Adverse Events in US Food and Drug Administration Databases
  af: Myers, R.B., et al.
  Udgivet: (2011)