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Pharmacovigilance study on the reporting frequency of atrial fibrillation with immune checkpoint inhibitors: insights from FDA Adverse Event Reporting System.
タグ:
FAERS
2025/4/28
Two first-generation KRAS inhibitor safety profiles: a disproportionality analysis of individual reports from the FDA adverse event reporting system.
タグ:
FAERS
2025/4/28
Association between various dosage forms of semaglutide and ocular adverse events in a real-world setting.
タグ:
FAERS
2025/4/28
Ocular Adverse Events Associated with Pegcetacoplan and Avacincaptad Pegol for Geographic Atrophy: A Population-Based Pharmacovigilance Study.
タグ:
FAERS
2025/4/28
Postmarketing safety analysis of upadacitinib in atopic dermatitis: A Food and Drug Administration adverse reporting system review of boxed warning-related adverse events.
タグ:
FAERS
2025/4/28
Association of antibiotics with Stevens-Johnson syndrome and toxic epidermal necrolysis: A real-world pharmacovigilance study.
タグ:
FAERS
2025/4/28
Selective Serotonin Reuptake Inhibitors and Risk of Serotonin Syndrome as Consequence of Drug-Drug Interactions: Analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/4/28
Tacrolimus-Related Fanconi Syndrome: A Real World Pharmacovigilance Study based on FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2025/4/27
A Real-World Pharmacovigilance Analysis of Lorlatinib-Associated Metabolic Effects Using the FDA Adverse Events Reporting System (FAERS) Database From 2013 to 2024.
タグ:
FAERS
2025/4/27
Post-marketing safety of pralsetinib: a real-world disproportionality analysis based on the FDA adverse event reporting system database.
タグ:
FAERS
2025/4/26
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