Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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The drug fulvestrant cross react with antibodies used in immunoassays on the market. this is due to the fact that the fulvestrant molecule has a similar chemical structure to estradiol which leads to an overestimation of estradiol level.