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Tofacitinib safety in inflammatory bowel disease: a disproportionality analysis of the FDA adverse event reporting system.
タグ:
FAERS
2026/4/8
Safety Analysis of Oxymetazoline Eye Drops for Blepharoptosis Using the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/4/8
Infections Post-CAR-T Therapy: A Real-World Pharmacovigilance Analysis of the FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2026/4/9
Bisphosphonate use and pregnancy complications: Insights from the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2026/4/9
Safety recommendations for ALK tyrosine kinase inhibitors in non-small cell lung cancer: evidence from FAERS and CVARDD real-world databases.
タグ:
FAERS
2026/4/10
Pharmacovigilance analysis of infliximab in inflammatory bowel disease: novel safety signals and sex-specific adverse event profiles from the FAERS database (2004-2024).
タグ:
FAERS
2026/4/9
Adverse events of proton pump inhibitor-associated parathyroid dysfunction: a real-world study based on the FDA adverse event reporting system.
タグ:
FAERS
2026/4/9
Pharmacovigilance analysis of vaccination errors during pregnancy using VAERS data.
タグ:
VAERS
FAERS
2026/4/11
Real-world safety profile of anifrolumab: An observational disproportionality analysis of the FAERS database.
タグ:
FAERS
2026/4/10
Indications and Adverse Events of Toradol: Based on FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2026/4/11
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