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Drug-related pulmonary fibrosis: A real-world pharmacovigilance study of the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/6/9
Evaluating adverse reaction signals of vancomycin in pediatric patients: A FAERS database analysis.
タグ:
FAERS
2026/6/9
Optic Ischaemic Neuropathy in Incretin-Based Therapy: A Comparative Analysis of Real-World Safety Data.
タグ:
FAERS
2026/6/9
Assessing drug-associated adverse events of spontaneous abortion or fetal death: A disproportionality analysis based on FDA adverse event reporting system.
タグ:
FAERS
2026/6/9
Adverse event mining for Breztri and Trelegy Ellipta based on the three international pharmacovigilance databases.
タグ:
CVAR
JADER
FAERS
2026/6/9
Fluoxetine-associated adverse event signals with a focus on seizure: A study based on the FAERS database, network pharmacology, and molecular docking.
タグ:
FAERS
2026/6/10
Reporting of atrial fibrillation with bispecific T-cell engagers in the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2026/6/9
The Safety Profile of Ticagrelor Among Older Adults (age >/= 75 years): A Pharmacovigilance Analysis.
タグ:
FAERS
2026/6/9
A Retrospective Pharmacovigilance Disproportionality Analysis of Possible Nephrotoxicity and Natural Products Using Data from the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/6/11
Real-world safety profile of mosunetuzumab: a pharmacovigilance study based on the food and drug administration adverse event reporting system.
タグ:
FAERS
2026/6/11
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