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Drug-associated oropharyngeal infection: a real-world pharmacovigilance study using the FDA adverse event reporting system database.
タグ:
FAERS
2026/5/25
Real-world pharmacovigilance analysis of drug-induced liver injury in 18-65 years: Based on the FDA adverse event reporting system (FAERS).
タグ:
FAERS
2026/5/25
Safety analysis of long-acting dual bronchodilator after market approval: a real-world study from FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2026/5/25
Analysis of drug-induced pulmonary embolism risk based on the Food and Drug Administration Adverse Event Reporting System database.
タグ:
FAERS
2026/5/25
Cost-effectiveness analysis of 23-valent pneumococcal polysaccharide vaccine for adults in China.
タグ:
VAERS
FAERS
2026/5/25
Cardiovascular adverse events associated with bispecific antibodies in relapsed or refractory B-cell non-Hodgkin lymphomas.
タグ:
FAERS
2026/5/27
Adverse events associated with statin co-use in breast cancer patients: a disproportionality analysis based on the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/5/25
Predicting Serious Adverse Events, Medication Abuse, Misuse, and Risk of Dependence for Medications with High Dependence Potential: Role of Patient-Reported Factors and Machine Learning Approach.
タグ:
KAERS
FAERS
2026/5/27
Etiology Model of Kawasaki Disease and Multisystem Inflammatory Syndromes: Mast Cell Activation.
タグ:
VAERS
FAERS
2026/5/27
Signal Detection and Machine Learning-Based Prediction of Cytokine Release Syndrome in B-Cell Maturation Antigen-Targeting Immunotherapies Using FAERS Data.
タグ:
KAERS
FAERS
2026/5/27
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