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Safety assessment of Edaravone: A real-world adverse event analysis based on the FAERS Database.
タグ:
FAERS
2025/10/23
Systemic Drugs Associated With Maculopathy.
タグ:
KAERS
FAERS
2025/10/23
A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events for cabazitaxel.
タグ:
FAERS
2025/10/23
Comparative evaluation of pregnancy-related adverse events associated with proton pump inhibitors using the FDA adverse event reporting system database.
タグ:
FAERS
2025/10/23
Association between incretin-related drugs and fractures in patients treated with pioglitazone: A pharmacovigilance study using the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/10/22
Real-world safety assessment of tamsulosin based on adverse event analysis from the FAERS database.
タグ:
FAERS
2025/10/22
Safety evaluation of etrasimod for ulcerative colitis based on the FAERS database.
タグ:
FAERS
2025/10/22
Real-world safety assessment of ublituximab: a pharmacovigilance analysis based on the FDA adverse event reporting system.
タグ:
FAERS
2025/10/21
Real-world safety profile of opicapone: a comprehensive pharmacovigilance analysis of the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2025/10/21
Immune checkpoint inhibitor-associated aseptic meningitis: a pharmacovigilance study using the FDA adverse event reporting system (2011-2024).
タグ:
FAERS
2025/10/20
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