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Profiling Immune-Related Adverse Events Associated with Imatinib: A Two-Decade Real-World Safety Study Based on FDA Adverse Event Reporting System.
タグ:
FAERS
2026/7/6
Flibanserin safety in real-world use: a decade of US Food and Drug Administration Adverse Event Reporting System pharmacovigilance evidence.
タグ:
FAERS
2026/7/6
Pharmacovigilance Analysis of Bleeding Events Associated With Selective Serotonin Reuptake Inhibitors (SSRIs) Using the US Food and Drug Administration Adverse Event Reporting System (FAERS).
タグ:
FAERS
2026/7/6
Real-world pharmacovigilance of drug-related bone metabolism disorders: integrating FAERS and VigiAccess with a Bradford Hill-based causal plausibility assessment.
タグ:
FAERS
2026/7/6
Bone-related adverse events of hormonal therapy: A pharmacovigilance study based on the Food & Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2026/7/6
Pharmacovigilance assessment of vinorelbine-associated adverse events using FAERS and VigiBase.
タグ:
VigiBase
FAERS
2026/7/7
Response to Li et al, “Comment on Nie et al (2026) ‘Suicidality reports in acne patients treated with isotretinoin and concomitant antidepressants: A descriptive analysis of FDA Adverse Event Reporting System data'”.
タグ:
FAERS
2026/7/7
Drug-induced paronychia: a disproportionality and time-to-onset pharmacovigilance study using FAERS and JADER.
タグ:
JADER
FAERS
2026/7/8
Multi-method statistical signal aggregation with machine learning for severity classification of neonatal adverse drug reactions.
タグ:
FAERS
2026/7/7
Postmarketing Safety Concerns With Caplacizumab: A Real-World Pharmacovigilance Study Based on the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2026/7/7
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