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122 积分 2024-11-22 加入
Gastrointestinal adverse events associated with SNRIs: A FAERS-based pharmacovigilance study
2天前
已完结
Drug-associated hyperprolactinemia: A comprehensive disproportionality analysis based on the FAERS database
7天前
已完结
Tarlatamab-induced immune-related adverse events: Real-world pharmacovigilance study using the FAERS database
8天前
已完结
Relationship between Anaplastic Lymphoma Kinase Inhibitors and Epileptic Seizure Disorder: A Post-Marketing Surveillance Study
11天前
已完结
Disproportionality Analysis of Abemaciclib in the FDA Adverse Event Reporting System: A Real-World Post-Marketing Pharmacovigilance Assessment
15天前
已完结
The guanylate cyclase stimulator vericiguat: Insights and adverse events from a FAERS-based pharmacovigilance study
17天前
已关闭
Tumor Lysis Syndrome Associated with Monoclonal Antibodies in Patients with Multiple Myeloma: A Pharmacovigilance Study Based on the FAERS Database
22天前
已完结
Postmarketing Safety of Sacituzumab Govitecan: A Pharmacovigilance Study Based on the FDA Adverse Event Reporting System
28天前
已完结
Tumor Lysis Syndrome Associated with Monoclonal Antibodies in Patients with Multiple Myeloma: A Pharmacovigilance Study Based on the FAERS Database
28天前
已完结
An evaluation of the federal adverse events reporting system data on adverse effects of 5-alpha reductase inhibitors
29天前
已完结
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