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

Benzer Materyaller

• Assessment of factors associated with completeness of spontaneous adverse event reporting in the United States: A comparison between consumer reports and healthcare professional reports
  Yazar:: Toki, Tadashi, ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• Retrospective analysis of adverse events with spironolactone in females reported to the United States Food and Drug Administration
  Yazar:: Wang, Yu, ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• Hyperglycemic adverse events following antipsychotic drug administration in spontaneous adverse event reports
  Yazar:: Kato, Yamato, ve diğerleri
  Baskı/Yayın Bilgisi: (2015)
• Review of Reported Clinical Information System Adverse Events in US Food and Drug Administration Databases
  Yazar:: Myers, R.B., ve diğerleri
  Baskı/Yayın Bilgisi: (2011)
• Miscategorization of Deaths in the US Food and Drug Administration Adverse Events Database
  Yazar:: Meier, Lily, ve diğerleri
  Baskı/Yayın Bilgisi: (2019)