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Comment on “Evaluation of anticancer therapy-related dermatologic adverse events: Insights from Food and Drug Administration’s adverse event reporting system dataset”.
タグ:
FAERS
2024/12/12
Thromboembolic events associated with combined oral contraceptives: a real-world study based on the FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/12/6
Association between cyclin-dependent kinase 4/6 inhibitors and nephrotoxicity in patients with breast cancer: A Systematic Review and meta-analysis.
タグ:
FAERS
2024/12/6
Signal detection and analysis of sulfasalazine adverse reaction events based on the US FDA adverse event reporting database.
タグ:
FAERS
2024/12/6
Pulmonary adverse events associated with amiodarone: a real-world pharmacovigilance study based on the FDA adverse event reporting system.
タグ:
FAERS
2024/12/6
Sex-differences in reporting of statin-associated diabetes mellitus to the US Food and Drug Administration.
タグ:
FAERS
2024/12/6
Real-world safety evaluation of atorvastatin: insights from the US FDA adverse event reporting system (FAERS).
タグ:
FAERS
2024/12/5
Safety assessment of tafamidis: a real-world adverse event analysis from the FAERS database.
タグ:
FAERS
2024/12/5
The drug risks of cilostazol: A pharmacovigilance study of FDA Adverse Event Reporting System database.
タグ:
FAERS
2024/12/4
Precision Adverse Drug Reactions Prediction with Heterogeneous Graph Neural Network.
タグ:
FAERS
2024/12/4
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