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Cardiac disorders associated with compound long-acting bronchodilators for inhalation: a pharmacovigilance analysis of the FDA adverse event reporting system database.
タグ:
FAERS
2026/3/25
Comparative pharmacovigilance of non-benzodiazepine receptor agonists versus dual orexin receptor antagonists for insomnia in older adults.
タグ:
FAERS
2026/3/26
Sexual Safety Signals of Common Antidiabetic Drugs: Insights From FAERS Disproportionality Analysis.
タグ:
FAERS
2026/3/26
Hydrochlorothiazide and chlorthalidone use and glaucoma risk: pharmacovigilance analysis and nationwide cohort study.
タグ:
FAERS
KAERS
2026/3/26
Risk factors for drug-related gastrointestinal ulcer:a retrospective pharmacovigilance study.
タグ:
FAERS
2026/3/26
Not All GLP-1 Receptor Agonists Are Alike: Real-World Evidence of Differential Endocrine and Dermatologic Safety.
タグ:
KAERS
FAERS
2026/3/26
Vigilance for drug safety of darolutamide in the cancer therapies: a disproportionality analysis from the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/3/26
Disproportionality analysis of adverse events associated with endothelin receptor antagonists based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2026/3/26
Machine Learning Model for Predicting Severe Adverse Events in Oncology Patients Using the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2026/3/27
Chronic Kidney Disease Amplifies Gabapentin-Associated Dementia Risk: Evidence for a Renal Pharmacokinetic Mechanism.
タグ:
FAERS
2026/3/27
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