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2024-03-21 加入
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Bevacizumab and gastrointestinal perforations: a review from the FDA Adverse Event Reporting System (FAERS) database
3小时前
待确认
Ginkgo biloba Extract Safety: Insights from a Real-world Pharmacovigilance Study of FDA Adverse Event Reporting System (FAERS) Events
1天前
已完结
Comparing adverse events of tenecteplase and alteplase: a real-world analysis of the FDA adverse event reporting system (FAERS)
3天前
已完结
Exploring the correlation between cardiovascular adverse events and antidepressant use: A retrospective pharmacovigilance analysis based on the FDA Adverse Event Reporting System database
6天前
已完结
Risk of angioedema and thrombolytic therapy among stroke patients: An analysis of data from the FDA Adverse Event Reporting System database
10天前
已完结
Risk of angioedema and thrombolytic therapy among stroke patients: An analysis of data from the FDA Adverse Event Reporting System database
10天前
已完结
Risk of angioedema and thrombolytic therapy among stroke patients: An analysis of data from the FDA Adverse Event Reporting System database
10天前
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A pharmacovigilance study of association between proton‐pump inhibitors and rhabdomyolysis event based on FAERS database
10天前
已完结
Risk of angioedema and thrombolytic therapy among stroke patients: An analysis of data from the FDA Adverse Event Reporting System database
18天前
已完结
The real-world safety of ticagrelor among older adults (above 75 years): a pharmacovigilance study from the FDA data
20天前
已完结
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