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From class effects to specificity FAERS evidence and network mapping of adverse events in NSCLC targeted therapy.
タグ:
FAERS
2026/1/21
Mapping adverse events and monitoring priorities for trastuzumab deruxtecan use in metastatic breast cancer.
タグ:
FAERS
2026/1/21
Pharmacovigilance study on neurological adverse reactions of proteasome inhibitors in the FDA adverse event reporting system.
タグ:
FAERS
2026/1/21
A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events for bimekizumab.
タグ:
FAERS
2026/1/21
Pharmacovigilance signal detection of psychiatric adverse events induced by third-generation antiepileptic drugs in children.
タグ:
FAERS
2026/1/21
A real-world signal detection analysis uncovering the safety profile of ketorolac tromethamine.
タグ:
FAERS
2026/1/21
Drug-induced urinary incontinence in pediatric patients: A disproportionality analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2026/1/21
Safety Surveillance for Hepatitis A Vaccine using the U.S. Vaccine Adverse Event Reporting System (VAERS) database.
タグ:
VAERS
FAERS
2026/1/20
The safety of rituximab in pediatric nephrotic syndrome patients: a pharmacovigilance study of the FAERS database.
タグ:
FAERS
2026/1/20
Spectrum mining of immune checkpoint inhibitor-related cutaneous toxicities and analysis of associated factors based on FAERS.
タグ:
FAERS
2026/1/19
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