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Safety assessment of anti-B cell maturation antigen chimeric antigen receptor T cell therapy: a real-world study based on the FDA adverse event reporting system database.
タグ:
FAERS
2024/9/18
Drug-Related Keratitis: A Real-World FDA Adverse Event Reporting System Database Study.
タグ:
FAERS
2024/9/17
Adverse reactions associated with nivolumab and small molecule antiangiogenic drugs: A pharmacovigilance analysis.
タグ:
FAERS
2024/9/17
Exploring the top 30 drugs associated with drug-induced constipation based on the FDA adverse event reporting system.
タグ:
FAERS
2024/9/17
Sodium-glucose cotransporter 2 inhibitors and renal cancer in the US FDA adverse event reporting system.
タグ:
FAERS
2024/9/17
BAYESIAN LEARNING OF COVID-19 VACCINE SAFETY WHILE INCORPORATING ADVERSE EVENTS ONTOLOGY.
タグ:
VAERS
FAERS
2024/9/17
Safety profile of levonorgestrel intrauterine system: Analysis of spontaneous reports submitted to FAERS.
タグ:
FAERS
2024/9/17
Drug-Induced Gynecomastia: Data Mining and Analysis of the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2024/9/16
Postmarketing Analysis of Eosinophilic Adverse Reactions in the use of Biologic Therapies for Type 2 Inflammatory Conditions.
タグ:
FAERS
2024/9/16
Abemaciclib increases the risk of venous thromboembolism in breast cancer: Integrate meta-analysis, pharmacovigilance database analysis, and in vitro validation.
タグ:
FAERS
2024/9/16
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