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- Myocarditis following the use of different immune checkpoint inhibitor regimens: A real-world analysis of post-marketing surveillance data.
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  FAERS
  2019/9/7
- Impact of a New Consumer Form on the Quantity and Quality of Adverse Event Reports Submitted to the United States Food and Drug Administration.
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  FAERS
  2019/9/4
- Combined SNA and LDA methods to understand adverse medical events.
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  FAERS
  2019/9/3
- Radioimmunotherapy in Non-Hodgkin’s Lymphoma: Retrospective Adverse Event Profiling of Zevalin and Bexxar.
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  FAERS
  
  VigiBase
  2019/9/25
- Adverse event profiles of ifosfamide-induced encephalopathy analyzed using the Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases.
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  FAERS
  
  JADER
  2019/9/11
- Comparing drug safety of hepatitis C therapies using post-market data.
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  FAERS
  2019/8/9
- Serious Cutaneous Toxicities with Immune Checkpoint Inhibitors in the U.S. Food and Drug Administration Adverse Event Reporting System.
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  FAERS
  2019/8/8
- Angioedema Risk Associated With Central Vascular Access Device Declotting.
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  FAERS
  2019/8/30
- Retrospective analysis reveals significant association of hypoglycemia with tramadol and methadone in contrast to other opioids.
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  FAERS
  2019/8/30
- Postpartum Bleeding in Pregnant Women Receiving SSRIs/SNRIs: New Insights From a Descriptive Observational Study and an Analysis of Data from the FAERS Database.
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  FAERS
  2019/8/3
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