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A pharmacovigilance study of adverse events associated with polymyxins based on the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2024/4/28
Unveiling potential adverse events associated with escitalopram oxalate: A real-world analysis based FDA adverse event reporting system database.
タグ:
FAERS
2024/4/28
Blind Spots in Therapy: Unveiling Drug-Induced Angle-Closure Glaucoma Through a National Analysis.
タグ:
FAERS
2024/4/29
Phosphodiesterase type 5 inhibitors related hearing impairment: a real world study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/4/29
Rising cases of drug-induced pulmonary fibrosis: Analysis of the Food and Drug Administration Adverse Event Reporting System (FAERS) database, 2000-2022.
タグ:
FAERS
2024/4/29
Safety of marketed biosimilar monoclonal antibody cancer treatments in the US: a disproportionality analysis using the food and drug administration adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/4/29
Signal detection of adverse reactions for bendamustine based on FDA adverse event reporting system.
タグ:
FAERS
2024/4/29
A real-world disproportionality analysis of the FDA adverse event reporting system events for ibuprofen.
タグ:
FAERS
2024/4/30
Comparison of safety of acetaminophen and ibuprofen in minors: based on the FAERS database.
タグ:
FAERS
2024/4/30
Timing Matters: A Machine Learning Method for the Prioritization of Drug-Drug Interactions Through Signal Detection in the FDA Adverse Event Reporting System and Their Relationship with Time of Co-exposure.
タグ:
FAERS
2024/4/30
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