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検索結果

- Development of an Adverse Event Reporting Form for Herbal Medicine: A Delphi Expert Consensus Study.
  タグ:
  
  KAERS
  2025/2/22
- Disproportionality analysis of Raynaud’s phenomenon associated with calcitonin gene-related peptide inhibitors using the Food and Drug Administration adverse event reporting system.
  タグ:
  
  KAERS
  
  FAERS
  2025/2/16
- Enhancing Adverse Event Reporting With Clinical Language Models: Inpatient Falls.
  タグ:
  
  KAERS
  2025/2/14
- Sex Differences in Adverse Event Reporting Rates Following COVID-19 Vaccination in South Korea During the Pandemic.
  タグ:
  
  KAERS
  
  VAERS
  
  FAERS
  2025/10/9
- Adherence to Animal Research: Reporting of In Vivo Experiments Guidelines in Stem Cell Studies in Animal Models of Parkinson’s Disease: A Systematic Review.
  タグ:
  
  KAERS
  2025/10/28
- Adverse events of androgen receptor pathway inhibitors in prostate cancer from real world data.
  タグ:
  
  KAERS
  
  FAERS
  2025/10/24
- Characteristics and risk factors of serious adverse drug reactions in older patients using the Korea Adverse Event Reporting System data: a retrospective observational study.
  タグ:
  
  KAERS
  
  FAERS
  2025/10/24
- Systemic Drugs Associated With Maculopathy.
  タグ:
  
  FAERS
  
  KAERS
  2025/10/23
- Global Disproportionality Analysis of Adverse Event Reports on Interstitial Lung Diseases for Cancer-Targeted Therapies, 1968-2024.
  タグ:
  
  KAERS
  2025/10/22
- A Comprehensive 10-Year Nationwide Pharmacovigilance Surveillance on Antibacterial Agents in Korea: Data Mining for Signal Detection of Trends and Seriousness of Adverse Events.
  タグ:
  
  KAERS
  
  FAERS
  2025/1/25
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