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Safety Profile of Amantadine: A Comprehensive Analysis of Real-World Adverse Events from the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2025/5/15
Drug-Associated Pemphigus Reported by Physicians: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/5/15
Multidimensional Assessment of Psychiatric Adverse Events Related to Proton Pump Inhibitors: A Real-World, Pharmacovigilance Study.
タグ:
FAERS
2025/5/14
Proton pump inhibitors use and risk of type 2 diabetes mellitus: correlation analysis, prediction model construction, and key genes identification.
タグ:
FAERS
2025/5/14
A pharmacovigilance analysis of post-marketing safety of durvalumab.
タグ:
FAERS
2025/5/14
Nephrotoxicity of direct factor Xa inhibitors: a pharmacovigilance study using real-world data from the Federal Adverse Event Reporting System database.
タグ:
FAERS
2025/5/13
Antiplatelet-Proton Pump Inhibitor Interactions and Arterial Thrombotic Events: A Pharmacovigilance Assessment using Disproportionality and Interaction Analysis.
タグ:
FAERS
2025/5/13
Adverse drug events associated with insulin glargine: a real-world pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2025/5/13
Post-marketing safety concerns with pirfenidone and nintedanib: an analysis of individual case safety reports from the FDA adverse event reporting system database and the Japanese adverse drug event report databases.
タグ:
JADER
FAERS
2025/5/13
Age-related adverse effects of Tamoxifen in female breast cancer patients: Insights from the FDA’s adverse event reporting system.
タグ:
FAERS
2025/5/13
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