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Comprehensive Study of Drug-Associated Severe Allergic Reactions: An Analysis of High-Risk Medications and Epidemiological Trends Based on the FAERS Database.
タグ:
KAERS
FAERS
2026/3/31
A Disproportionality Analysis of Immune Checkpoint Inhibitors in Combination With Platinum-Based Agents Using the FDA Adverse Event Reporting System Database.
タグ:
FAERS
2026/3/31
Post-marketing safety signals of four JAK inhibitors for alopecia areata: an indication-restricted FAERS pharmacovigilance study.
タグ:
FAERS
2026/4/1
A real-world pharmacovigilance analysis of uveitis from systemic medications.
タグ:
FAERS
2026/4/1
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:
KAERS
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
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