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検索結果

- Drug-associated postpartum hemorrhage: a comprehensive disproportionality analysis based on the FAERS database.
  タグ:
  
  FAERS
  2025/9/9
- Real-world pharmacovigilance assessment of drug-induced male hypogonadism risks: An analysis of FDA adverse drug event data.
  タグ:
  
  FAERS
  2025/9/9
- Drug-induced vitiligo: a real-world pharmacovigilance analysis of the FAERS database.
  タグ:
  
  FAERS
  2025/9/8
- A real-world pharmacovigilance study of FDA Adverse Event Reporting System events for gefitinib and docetaxel.
  タグ:
  
  FAERS
  2025/9/6
- Olmesartan-Induced Enteropathy: Case Reports and Insights From FDA Adverse Event Reporting System (FAERS).
  タグ:
  
  FAERS
  2025/9/6
- Stacking the Risks: Fatal Consequences of Anabolic Steroid Misuse and Stacked Substance Use in FAERS Data.
  タグ:
  
  KAERS
  
  FAERS
  2025/9/5
- Safety assessment of laronidase: real-world adverse event analysis based on the FDA adverse event reporting system (FAERS).
  タグ:
  
  FAERS
  2025/9/5
- Aioli: Standardising Drugs in the FDA Adverse Event Reporting System (FAERS) to RxNorm and Anatomical Therapeutic Chemical (ATC) Codes.
  タグ:
  
  FAERS
  2025/9/5
- Pharmacovigilance study of ramucirumab: A safety analysis based on the FDA adverse event reporting system.
  タグ:
  
  FAERS
  2025/9/4
- Characterizing the Real-World Risks of Kidney Injuries Associated with Chimeric Antigen Receptor T Cell Therapies-Evidence and Safety.
  タグ:
  
  FAERS
  2025/9/4
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