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Adverse event profile of fondaparinux sodium: a disproportionality analysis based on FAERS, JADER, and VigiAccess databases.
タグ:
JADER
FAERS
2026/2/23
Adverse events associated with tirzepatide: a focus on subgroup-specific differences.
タグ:
JADER
FAERS
2026/2/26
Efficacy and safety of full-endoscopic sacroiliac joint denervation for the treatment of chronic low back pain: a systematic review.
タグ:
JADER
2026/2/26
Cardiovascular Adverse Events Associated With Carfilzomib, Bortezomib, and Ixazomib: A Disproportionality Analysis Using the Japanese Adverse Drug Event Report Database With Anticancer Agents as the Reference Group.
タグ:
JADER
2026/2/28
Drug-induced Aseptic Meningitis: Pharmacovigilance Analysis of Japanese Adverse Event Reporting Database.
タグ:
JADER
2026/2/28
Drug-induced vanishing bile duct syndrome: A real world pharmacovigilance study using the FDA adverse event reporting system.
タグ:
FAERS
2026/2/20
A pharmacovigilance analysis of carbapenem-related utilizing the FDA adverse event reporting system (FAERS) database from 2013 to 2025.
タグ:
FAERS
2026/2/20
A Real-World Pharmacovigilance Study of Cilostazol Based on the Food and Drug Administration Adverse Event Reporting System: A Cross-Sectional Disproportionality Analysis.
タグ:
FAERS
2026/2/20
Drug-associated paronychia: Pharmacovigilance signals from the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) and the Canada Vigilance Adverse Reaction Database (CVARD).
タグ:
CVAR
FAERS
2026/2/20
Prenatal exposure to antiseizure medications and risk of autism spectrum disorder in offspring: an integrated pharmacovigilance and two-sample mendelian randomization study.
タグ:
EudraVigilance
FAERS
2026/2/20
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