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Disproportionality analysis of drug-induced dry mouth using data from the United States food and drug administration adverse event reporting system database.
タグ:
FAERS
2024/10/15
Safety study on adverse events of zanubrutinib based on WHO-VigiAccess and FAERS databases.
タグ:
FAERS
2024/10/15
Drug-induced myocarditis: a real-world pharmacovigilance study using the FDA adverse event reporting system database.
タグ:
FAERS
2024/10/14
A real-world adverse events study of rimegepant from the FAERS database.
タグ:
FAERS
2024/10/16
Diabetic adverse events associated with three commonly used statins: a disproportionality analysis based on the FDA adverse event reporting system database.
タグ:
FAERS
2024/10/16
Thromboembolism adverse event profiles of thrombopoietin receptor agonists: a real-world, pharmacovigilance study.
タグ:
FAERS
2024/10/16
Neurotoxicity associated with chimeric antigen receptor T-cell therapy: a real-world study leveraging the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/10/16
Comparison of adverse events of poly adenosine diphosphate ribose polymerase inhibitors in patients with ovarian cancer using the United States Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2024/10/18
Drug-induced liver injury associated with pretomanid, bedaquiline, and linezolid: Insights from FAERS database analysis.
タグ:
FAERS
2024/10/18
Keratoconus Cases Associated with Medication Use: A Population-Based Pharmacovigilance Study.
タグ:
FAERS
2024/10/17
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