Reporter’s occupation and source of adverse device event reports contained in the FDA’s MAUDE database

Ítems similars

• The Dangers of Dental Devices as reported in the FDA MAUDE Database
  per: Hebballi, Nutan B, et al.
  Publicat: (2015)
• A Primer to the Structure, Content and Linkage of the FDA’s Manufacturer and User Facility Device Experience (MAUDE) Files
  per: Ensign, Lisa Garnsey, et al.
  Publicat: (2017)
• Biclustering of Adverse Drug Events in FDA’s Spontaneous Reporting System
  per: Harpaz, Rave, et al.
  Publicat: (2010)
• Reducing Glucose Meter Adverse Events by Using Reliability Growth With the FDA MAUDE Database
  per: Krouwer, Jan S.
  Publicat: (2018)
• Adverse events associated with Implantable Collamer Lens: insights from the FDA MAUDE database
  per: Qing Chen, et al.
  Publicat: (2025-07-01)