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Immune-related adverse events in Hodgkin lymphoma treated with pembrolizumab or nivolumab: A disease-restricted US Food and Drug Administration Adverse Event Reporting System (FAERS) pharmacovigilance analysis.
タグ:
FAERS
2026/7/30
The Real-World Safety Profile of Immune Checkpoint Inhibitors in Melanoma: FAERS Pharmacovigilance Analysis Complemented by Randomized Trial Evidence.
タグ:
FAERS
2026/7/29
The real-world safety of ruxolitinib in graft-versus-host disease treatment: a pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2026/7/31
Thyroid Immune-related Adverse Events Following Immune Checkpoint Inhibitors in NSCLC: Insights From Pharmacovigilance Data, a Retrospective Case-control Study, and Single-cell RNA Sequencing Dataset.
タグ:
FAERS
2026/7/31
A real-world pharmacovigilance analysis of cardiac adverse events associated with newer antibody-drug conjugates for hematological malignancies in adults: A disproportionality analysis from FDA adverse event reporting system database.
タグ:
FAERS
2026/7/31
Sepsis reporting signals associated with endothelin receptor antagonists and IFITM3-Centered interferon-responsive monocyte features: a pharmacovigilance and transcriptomic study.
タグ:
FAERS
2026/7/31
Disproportionality analysis of off-label intravitreal bevacizumab in the FDA Adverse Event Reporting System database.
タグ:
FAERS
2026/7/31
Signal detection and analysis of adverse events associated with sevelamer post-marketing based on the FAERS database.
タグ:
FAERS
2026/7/31
Reported Characteristics of Anaphylaxis Associated With Glatiramer Acetate: A Pharmacovigilance Analysis of the FDA and Canadian Databases.
タグ:
FAERS
2026/8/1
Topical Cycling and Systemic Eligibility in Patients With Psoriasis in Japan.
タグ:
DeSC
2026/7/25
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