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 weight-based drug dosage calculation may deliver incorrect recommendation values if the patient's body weight is not entered via the admin-/demographics screen but entered via the drug dosage application screen. one hospital in germany also reported a misalignment of ecg and art waveforms delivered from this product.