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A Drug Similarity-Based Bayesian Method for Early Adverse Drug Event Detection.
タグ:
FAERS
2025/4/22
Identifying signals of disproportionate reporting for calcitonin gene-related peptide inhibitors: real-world evidence from the FDA adverse event reporting system.
タグ:
KAERS
FAERS
2025/4/22
A real-world pharmacovigilance study of netarsudil based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2025/4/22
Immune Checkpoint Inhibitor-induced Uveitis: Disproportionality and Timing Analyses of the Japanese Pharmacovigilance Database.
タグ:
JADER
2025/4/29
HIF-PHIs associated with embolic and thrombotic events: a real-world pharmacovigilance study based on the Japan Adverse Drug Event Report database.
タグ:
JADER
2025/4/23
H1 antihistamine-induced adverse events and time to onset: A retrospective analysis using the Japanese Adverse Drug Event Report Database.
タグ:
JADER
2025/4/22
Disproportionality analysis of European safety reports on autoimmune and rheumatic diseases following COVID-19 vaccination.
タグ:
EudraVigilance
2025/4/28
Comparison Study of the Safety Profile of Olaparib Versus Niraparib: Analysis of Real-World Data from EudraVigilance.
タグ:
EudraVigilance
2025/4/26
Bevacizumab-Insights from EudraVigilance Database on the Assessments of the Safety Profile of Monoclonal Antibodies Used as Targeted Cancer Treatment.
タグ:
EudraVigilance
2025/4/26
Oral Adverse Effects of Antipsychotic Medications: A Case/Noncase Analysis of EudraVigilance Data.
タグ:
EudraVigilance
2025/4/22
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