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Analysis of diroximel fumarate data for patients with relapsing forms of multiple sclerosis using related adverse events from the FDA adverse reporting system.
タグ:
FAERS
2025/4/2
Adverse events reporting of Etelcalcetide: a real-word analysis from FAERS database.
タグ:
FAERS
2025/4/2
A real-world safety surveillance study of aducanumab through the FDA adverse event reporting system.
タグ:
FAERS
2025/4/2
A real-world disproportionality analysis of ripretinib data mining of the public version of FDA adverse event reporting system.
タグ:
FAERS
2025/4/2
Exploring the Relationship Between Antipsychotic Drug Target Genes and Epilepsy: Evidence From Food and Drug Administration Adverse Event Reporting System Database and Mendelian Randomization.
タグ:
FAERS
2025/4/2
Analysis of Adverse Events Associated With Dental Local Anaesthetics Using Food and Drug Administration Adverse Event Reporting System Data.
タグ:
FAERS
2025/4/2
Sedatives and Opioids Best Practices: An Approach to the Use of Technological Tools.
タグ:
FAERS
2025/4/1
Disproportionality analysis of interstitial lung disease associated with novel antineoplastic agents during breast cancer treatment: a pharmacovigilance study.
タグ:
JADER
FAERS
2025/4/1
Enhancing Relation Extraction for COVID-19 Vaccine Shot-Adverse Event Associations with Large Language Models.
タグ:
VAERS
FAERS
2025/4/1
Melasma secondary to drugs: a real-world pharmacovigilance study of the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2025/4/1
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