%0 Journal Article
%T Reporter¡¯s occupation and source of adverse device event reports contained in the FDA¡¯s MAUDE database
%A Kevin T Kavanagh
%A Lindsay E Calderon
%A Raeford E Brown
%A Jr
%A Sean P Kavanagh
%A Steve S Kraman
%J Archive of "Patient Related Outcome Measures".
%D 2019
%R 10.2147/PROM.S212991
%X A review of the medical device adverse events submitted to the United States Food & Drug Administration (FDA) Manufacturer and User Facility Device Experience (MAUDE) database was undertaken to determine the major sources of the information
%K FDA
%K MAUDE
%K reporter
%K occupation
%K medical device
%K adverse events
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612978/