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Gastrointestinal Safety Assessment of GLP-1 Receptor Agonists in the US: A Real-World Adverse Events Analysis from the FAERS Database.
タグ:
FAERS
2025/1/8
Safety assessment of deutetrabenazine: real-world adverse event analysis from the FAERS database.
タグ:
FAERS
2025/1/7
Safety evaluation of medroxyprogesterone acetate: a pharmacovigilance analysis using FDA adverse event reporting system data.
タグ:
FAERS
2025/1/7
An exploratory study evaluated the 30 most commonly reported medications in the United States food and drug administration’s adverse event reporting system that are associated with the occurrence of kidney stones.
タグ:
FAERS
2025/1/7
Urotoxicity of Cyclophosphamide: A Comparison Across Neoplastic, Autoimmune, and Transplant Indications.
タグ:
FAERS
2025/1/7
Autoimmune hepatitis associated with statins: a retrospective study of pharmacovigilance databases and review of the literature.
タグ:
FAERS
2025/1/6
Evaluation of link between COVID-19 adjacent spike in hydroxychloroquine use and increased reports of pemphigus: a disproportionality analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/1/6
Age-stratified analysis of adverse event signals for clarithromycin: a disproportionality analysis using the FDA Adverse Event Reporting System.
タグ:
FAERS
2025/1/6
Association of antidepressants with cataracts and glaucoma: a disproportionality analysis using the reports to the United States Food and Drug Administration Adverse Event Reporting System (FAERS) pharmacovigilance database.
タグ:
FAERS
2025/1/6
Exploration and evaluation of adverse event signals of droxidopa based on the FAERS database.
タグ:
FAERS
2025/1/6
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