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Increasing Trends in the Pancreatitis Risk With Tumor Necrosis Factor Inhibitor Use.
タグ:
FAERS
2024/12/23
Drug-induced nephrolithiasis: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/12/23
Detection of risk signals for ustekinumab in the real world using the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/12/23
Risk of congenital anomalies associated with psychotropic medications: a review of neonatal reports in the FDA adverse event reporting System (FAERS).
タグ:
FAERS
2024/12/23
Metoprolol adverse events and literature analyses: case/non-case analyses using the FDA Adverse Event Reporting System (FAERS).
タグ:
FAERS
2024/12/24
Systematic analysis of sugammadex-related adverse drug reaction signals using FAERS database.
タグ:
FAERS
2024/12/23
Adverse reactions associated with SSRIs and PD-1/PD-L1 inhibitors: a disproportionality analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/12/23
Fulminant type 1 diabetes mellitus: a neglected but high-risk adverse event associated with immune checkpoint inhibitors.
タグ:
FAERS
2024/12/23
Pharmacologically induced autoimmune encephalitis-disproportionality analysis utilizing FAERS database.
タグ:
FAERS
2024/12/23
Severe cutaneous adverse reactions associated with antifungal agents: a pharmacovigilance analysis based on the FDA Adverse Event Reporting System (FAERS) database.
タグ:
FAERS
2024/12/26
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