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Drug-induced intestinal obstruction: insights from the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/1/29
Pancreatitis induced by Peg-aspargase in children: a real-world pharmacovigilance analysis based on FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2026/1/29
Real-world adverse event profile and signal characteristics of bevacizumab in glioma: a FAERS-based disproportionality analysis.
タグ:
FAERS
2026/1/29
Safety analysis of gepants for migraine treatment: A pharmacovigilance study using the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2026/1/29
Profiling of Potential Postmarket Risk Tracking and Pharmacovigilance Data for Avacopan.
タグ:
FAERS
2026/1/29
Real-world database evaluation of drug-associated vitreous opacities and machine learning for clinical interpretability.
タグ:
FAERS
2026/1/28
Real-world safety profile of roflumilast: a pharmacovigilance analysis using FDA adverse event reporting system and Canada vigilance database.
タグ:
CVAR
FAERS
2026/1/28
Comparative safety profiles of baricitinib and tofacitinib in the treatment of adult alopecia areata: a pharmacovigilance study based on the FAERS database.
タグ:
FAERS
2026/1/28
Real-world safety profile and mechanistic insights into regorafenib-induced liver failure: a pharmacovigilance study integrated with network toxicology.
タグ:
FAERS
2026/1/28
Risk of neutropenia associated with Sacituzumab govitecan: a systematic review combined with the FAERS database and meta-analysis.
タグ:
FAERS
2026/1/28
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