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Sexual dysfunctions associated with antipsychotic drug intake: a retrospective analysis of the FDA adverse events reporting system (FAERS).
タグ:
FAERS
2025/1/11
A UK population-based case-control study of blood tests before cancer diagnosis in patients with non-specific abdominal symptoms.
タグ:
CPRD
2025/1/12
Lactic acidosis with metformin accumulation in the intensive care units of the Nord Pas de Calais region: A known serious adverse event that can be better prevented.
タグ:
FPVD
2025/1/12
Drugs associated with tachyphylaxis: results from a retrospective pharmacovigilance study using disproportionality analysis.
タグ:
FAERS
2025/1/10
Post-marketing safety of antiseizure medications: Focus on serious adverse effects including drug reaction with eosinophilia and systemic symptoms (DRESS).
タグ:
FAERS
2025/1/10
Post-marketing safety concerns with lecanemab: a pharmacovigilance study based on the FDA Adverse Event Reporting System database.
タグ:
FAERS
2025/1/9
Pharmacovigilance study of the association between progestogen and depression based on the FDA adverse event reporting System (FAERS).
タグ:
FAERS
2025/1/9
A Real-World Pharmacovigilance Study of FDA Adverse Event Reporting System Events for Obeticholic Acid.
タグ:
FAERS
2025/1/8
Real world pharmacovigilance assessment of drug related macular degeneration risks.
タグ:
FAERS
2025/1/8
Interaction between dipeptidyl-peptidase-4 inhibitors and drugs acting on renin angiotensin aldosterone system for the risk of angioedema: a pharmacovigilance assessment using disproportionality and interaction analyses.
タグ:
FAERS
2025/1/8
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