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Drug-induced osteoporosis/osteopenia: a pharmacovigilance analysis using the FDA Adverse Event Reporting System database.
タグ:
FAERS
2025/11/6
Drug-associated serotonin syndrome in elderly patients: a comprehensive disproportionality analysis based on the FAERS database.
タグ:
FAERS
2025/11/6
Pegylated liposomal doxorubicin-induced hand-foot syndrome in a patient with breast cancer: Case report and FAERS database analysis.
タグ:
FAERS
2025/11/5
Oral anticoagulants and gastrointestinal bleeding: pharmacovigilance insights from the FDA adverse event reporting system database.
タグ:
FAERS
2025/11/5
Risk of pulmonary fungal infections associated with biologics: a FAERS database disproportionality analysis.
タグ:
FAERS
2025/11/5
Real-world feasibility of co-administration of RSV, COVID-19, and influenza vaccines in older adults: a VAERS-based analysis.
タグ:
VAERS
FAERS
2025/11/5
Post-marketing safety assessment of Tyrvaya: A real-world pharmacovigilance analysis based on the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/11/5
Exploration of adverse event profiles for glofitamab: A disproportionality analysis using the FDA adverse event reporting system.
タグ:
FAERS
2025/11/4
Comparative Analysis of Adverse Drug Reactions Between Oritavancin Diphosphate and Oritavancin-HPbetaCD Using FAERS Data.
タグ:
FAERS
2025/11/4
Post-market surveillance data demonstrate high mortality associated with enfortumab vedotin skin toxicity, not worsened by immune checkpoint inhibitors or corticosteroids.
タグ:
FAERS
2025/11/4
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