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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An adverse trend in stability may result in a significant decrease in the adjustment slopes (down to 0.7) and a negative shift in patient values of 20-25% at concentrations > approx. 300 ng/ml.