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Increased reporting of accidental overdose with glucagon-like peptide-1 receptor agonists: a population-based study.
タグ:
FAERS
2024/11/18
Pharmacovigilance insights into drug-induced cystitis: analysis of FDA data from 2004 to 2024.
タグ:
FAERS
2024/11/16
Fracture events associated with GLP-1 receptor agonists in FDA adverse events reporting system.
タグ:
FAERS
2024/11/18
Comparison of Adverse Event Profiles of Amphotericin B Formulations Using Real-World Data.
タグ:
FAERS
2024/11/18
Fibroblast growth factor receptor inhibitor-induced hyperphosphatemia: Lessons for the nephrologist.
タグ:
FAERS
2024/11/19
Unveiling the Hidden Risks: An Update Decade-Long Analysis of Abraxane-Related Adverse Events from the FAERS Database.
タグ:
FAERS
2024/11/19
Examining the safety of belimumab, especially in children: an analysis of real-world pharmacovigilance data from the US FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/11/19
Real-World Pharmacovigilance Study Identifies Drugs Linked to Hepatitis B Virus Reactivation.
タグ:
JADER
FAERS
2024/11/19
A real-world disproportionality analysis of FDA adverse event reporting system (FAERS) events for avatrombopag.
タグ:
FAERS
2024/11/19
Predictors and implications of renal injury after CD19 chimeric antigen receptor T-cell therapy.
タグ:
FAERS
2024/11/21
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