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A real-world disproportionality analysis of mepolizumab based on the FDA adverse event reporting system.
タグ:
FAERS
2023/12/25
The Possible Role of Prescribing Medications, Including Central Nervous System Drugs, in Contributing to Male-Factor Infertility (MFI): Assessment of the Food and Drug Administration (FDA) Pharmacovigilance Database.
タグ:
FAERS
2023/12/23
Safety of daratumumab in the real-world: a pharmacovigilance study based on FAERS database.
タグ:
FAERS
2023/12/18
Liver injury due to endothelin receptor antagonists: a real-world study based on post-marketing drug monitoring data.
タグ:
FAERS
2024/1/5
Effect of acid suppressant medications on the laxative action of magnesium preparations in patients with opioid-induced constipation: A pharmacovigilance analysis of the FDA Adverse Event Reporting System.
タグ:
FAERS
2024/1/5
Enhancing Transparency in Defining Studied Drugs: The Open-Source Living DiAna Dictionary for Standardizing Drug Names in the FAERS.
タグ:
FAERS
2024/1/4
Is pitolisant safe for clinical use? A retrospective pharmacovigilance study focus on the post-marketing safety.
タグ:
FAERS
2024/1/4
Exploring the incidence and etiopathogenesis of pathological yawning as adverse side effect of psychotropic drugs.
タグ:
CVAR
FAERS
2024/1/4
Five years of safety profile of bevacizumab: an analysis of real-world pharmacovigilance and randomized clinical trials.
タグ:
FAERS
2024/1/4
Sex-biased gene expression and gene-regulatory networks of sex-biased adverse event drug targets and drug metabolism genes.
タグ:
FAERS
2024/1/4
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