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A retrospective analysis of gastrointestinal adverse events associated with nicorandil using the FDA Adverse Event Reporting System (FAERS) following STROBE guidelines.
タグ:
FAERS
2026/5/23
Comparative adverse event reporting patterns of desogestrel versus norethisterone in third-generation combined oral contraceptives: A disproportionality analysis of the FAERS satabase.
タグ:
FAERS
2026/5/23
Cerebral venous sinus thrombosis risk across various oral contraceptives: a disproportionality analysis of the FDA adverse event reporting system.
タグ:
FAERS
2026/5/16
Association between ranitidine use and thyroid cancer based on FAERS and VigiAccess databases.
タグ:
FAERS
2026/5/16
Exploring risk signals of association between drugs and suicide: a retrospective investigation from 2004 to 2024.
タグ:
FAERS
2026/5/15
Comparative Analysis of Reported Adverse Events with Nirsevimab and Palivizumab: A FAERS Observational Study.
タグ:
FAERS
2026/5/15
Factors associated with serious adverse event following immunization: a real-world analysis of the vaccine adverse event reporting system 2025.
タグ:
VAERS
FAERS
2026/5/15
A comprehensive analysis of the adverse drug events of metastatic and unresectable gastrointestinal stromal tumor treatment options: avapritinib, imatinib, regorafenib, ripretinib, and sunitinib safety insights and implications.
タグ:
FAERS
2026/5/15
Atypical Shoulder Pain and Dysfunction After Vaccinations Reported to the Vaccine Adverse Event Reporting System (VAERS) January 1, 2018, Through October 31, 2022.
タグ:
VAERS
FAERS
2026/5/15
A Feasibility Assessment of the FDA Adverse Event Reporting System for the Detection of Cannabis-Related Safety Signals.
タグ:
CVAR
FAERS
2026/5/14
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