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Hemolytic anemia following alectinib reported to the U.S. Food and Drug Administration Adverse Event Reporting System.

Graça M DoresAfrouz NayernamaConnie ChengCharlotte MoureaudS Christopher Jones
Published in: American journal of hematology (2022)
Keyphrases
  • drug administration
  • adverse drug
  • iron deficiency
  • chronic kidney disease
  • human health
  • emergency department
  • electronic health record
  • risk assessment
  • drug induced
  • climate change