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Comprehensive Post-marketing safety analysis of Tildrakizumab: insights from the FDA adverse event Reporting system.
タグ:
FAERS
2025/6/13
Carpal Tunnel Syndrome Attributed to Medication Use: A Pharmacovigilance Study.
タグ:
FAERS
2025/6/13
Cardiovascular Safety Profile of BRAF and MEK Inhibitors in Melanoma: FAERS Data Through a Retrospective Disproportionality Analysis (2014-2023).
タグ:
FAERS
2025/6/13
Gender and age disparities in cardiac immune-related adverse events associated with immune checkpoint inhibitors: a pharmacovigilance analysis of the FAERS database.
タグ:
FAERS
2025/6/13
A real-world population-based study on the association between cataracts and antipsychotics.
タグ:
FAERS
2025/6/13
Constipation-predominant irritable bowel syndrome treatment options Linaclotide, Lubiprostone, plecanatide, and Tenapanor: analysis of the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2025/6/12
Comparative pharmacological analysis of fam-trastuzumab deruxtecan-nxki and sacituzumab govitecan-hziy: Two recently developed chemotherapies in the crucial battle against breast cancer.
タグ:
FAERS
2025/6/12
Pharmacovigilance Analysis of Lifitegrast-Associated Adverse Events Using the FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2025/6/12
Analysis of the relationship between histamine H1 receptor antagonists and broad dementia events using the FAERS, JADER, and CVAR databases.
タグ:
CVAR
JADER
FAERS
2025/6/12
Adverse event profile differences between maribavir and valganciclovir: findings from the FDA adverse event reporting system.
タグ:
FAERS
2025/6/10
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