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Drug-induced fever: a pharmacovigilance analysis based on the FDA adverse event reporting system.
タグ:
FAERS
2026/4/1
Pharmacovigilance analysis of iodinated contrast media related respiratory adverse effects based on the FDA adverse event reporting system.
タグ:
FAERS
2026/4/1
Orphan drug propranolol for infantile hemangioma: ten-year real-world safety data from the FAERS database.
タグ:
FAERS
2026/4/2
Arterial hypertension: A safety risk of calcitonin gene-related peptide ligand and receptor blocker class.
タグ:
FAERS
2026/4/2
Reporting patterns of renal failure associated with immunosuppressant combinations following liver transplantation: a retrospective analysis.
タグ:
FAERS
2026/4/2
Immune-Related Adverse Events in Bladder Cancer Patients Treated With Immune Checkpoint Inhibitors: Insights From a FAERS Disproportionality Analysis.
タグ:
FAERS
2026/4/2
Comparative Safety of Long-Acting Versus Short-Acting Erythropoiesis-Stimulating Agents (ESA): Disproportionality Analysis Using the FDA Adverse Event Reporting System.
タグ:
KAERS
FAERS
2026/4/2
A FAERS database study on visual impairment adverse events associated with three long-acting insulin analogues.
タグ:
FAERS
2026/4/2
Post-marketing safety profile of meningococcal group B vaccines: a real-world disproportionality analysis of the VAERS database, 2015Q1-2025Q3.
タグ:
VAERS
FAERS
2026/4/3
Identifying Risk Factors for Fall-Related Injuries Among Inpatients at a Tertiary Hospital in China: A Retrospective Cohort Study.
タグ:
FAERS
2026/4/3
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