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Postmarketing safety of bimekizumab for hidradenitis suppurativa: An early pharmacovigilance analysis using the United States Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2026/4/13
Comparative neuropsychiatric safety signals of tacrolimus versus cyclosporine in solid organ transplantation: ten-year FAERS pharmacovigilance study.
タグ:
FAERS
2026/4/13
Serotonin syndrome risk with concomitant opioid and serotonergic antidepressant use: a multinational pharmacovigilance study.
タグ:
JADER
FAERS
2026/4/13
Updated profiling of COVID-19 vaccine adverse events using VAERS case reports.
タグ:
VAERS
FAERS
2026/4/13
Adverse events in different administration routes of Edaravone: A pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2026/4/13
Signals of Drug-Related Retinal Fibrosis: Findings From a 20-Year Disproportionality Analysis of Global Spontaneous Reports.
タグ:
FAERS
2026/4/13
Neurotoxicity of immune checkpoint inhibitors: a retrospective pharmacovigilance study using FAERS database.
タグ:
FAERS
2026/4/13
Post-marketing pharmacovigilance of tedizolid: emerging safety signals.
タグ:
FAERS
2026/4/14
Hemophagocytic Lymphohistiocytosis Associated with Immune Checkpoint Inhibitors: A Pharmacovigilance Analysis of Spontaneous Reports.
タグ:
FAERS
2026/4/14
Adverse event profiles of fenofibrate and gemfibrozil: a retrospective comparative study and literature synthesis.
タグ:
FAERS
2026/4/15
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