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Unveiling Aducanumab’s safety profile: A comprehensive pharmacovigilance analysis.
タグ:
FAERS
2025/7/14
Adverse events following 9-valent human papillomavirus vaccine (GARDASIL(R) 9) reported to the Vaccine Adverse Event Reporting System (VAERS), 2015-2024.
タグ:
VAERS
FAERS
2025/7/15
Is the Safety of Finasteride Correlated With Its Route of Administration: Topical Versus Oral? A Pharmacovigilance Study With Data From the United States Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2025/7/15
Dupilumab adverse reactions in eosinophilic esophagitis treatment: a Food and Drug Administration Adverse Event Reporting System database analysis.
タグ:
FAERS
2025/7/15
Chloroquine and hydroxychloroquine-related ocular adverse events in SLE treatment: a real-world disproportionality analysis based on FDA adverse event reporting system (FAERS).
タグ:
FAERS
2025/7/15
Trimethoprim/sulfamethoxazole and risk of haemophagocytic lymphohistiocytosis (HLH): a literature review and disproportionality analysis using individual case safety reports from FAERS.
タグ:
FAERS
2025/7/15
Postmarketing adverse events of efgartigimod alfa: a real-world pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2025/7/15
Psychiatric safety associated with hormone replacement therapy for menopausal symptoms: a real-world study of the FDA adverse event reporting system.
タグ:
FAERS
2025/7/14
Case Report: Omalizumab-associated hair loss: a case of eyebrow alopecia areata, literature review and FAERS database analysis.
タグ:
FAERS
2025/7/14
Seasonal Variations in Drug-Related Erythema Multiforme: A Time Series Analysis Using the JADER Database.
タグ:
JADER
2025/7/17
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