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Corrigendum: Neurological adverse events associated with esketamine: A disproportionality analysis for signal detection leveraging the FDA adverse event reporting system.
タグ:
FAERS
2022/11/29
Data mining and safety analysis of BTK inhibitors: A pharmacovigilance investigation based on the FAERS database.
タグ:
FAERS
2022/11/29
Exploring the underlying mechanisms of drug-induced impulse control disorders: a pharmacovigilance-pharmacodynamic study.
タグ:
FAERS
2022/11/28
The Food and Drug Administration’s (FDA’s) Drug Safety Surveillance During the COVID-19 Pandemic.
タグ:
FAERS
2022/12/3
Immune checkpoint inhibitor-induced pure red cell aplasia: Case series and large-scale pharmacovigilance analysis.
タグ:
FAERS
2022/12/3
Characterization of Immune Checkpoint Inhibitor-Induced Myasthenia Gravis Using the US Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2022/12/2
The importance of renal function in anemic patients treated with edoxaban after orthopedic surgery in a real-world clinical setting: A retrospective study.
タグ:
JADER
FAERS
2022/12/2
Evaluation of Lung Toxicity With Lenalidomide Using the Pharmacovigilance Database.
タグ:
JADER
2022/12/2
Kikuchi-Fujimoto Disease and COVID-19 vaccination: pharmacovigilance approach.
タグ:
EudraVigilance
2022/12/3
Dilemma of belimumab therapy (dis)continuation during pregnancy: Results of a retrospective study in eudravigilance.
タグ:
EudraVigilance
2022/12/1
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