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Identifying Drug-Drug Interactions in Spontaneous Reports Utilizing Signal Detection and Biological Plausibility Aspects.
タグ:
FAERS
2024/4/9
Evaluating cardiac disorders associated with triazole antifungal agents based on the US Food and Drug Administration Adverse Event reporting system database.
タグ:
FAERS
2024/4/8
Discovering clinical drug-drug interactions with known pharmacokinetics mechanisms using spontaneous reporting systems and electronic health records.
タグ:
FAERS
2024/4/8
Severe cutaneous adverse reactions associated with the immune checkpoint inhibitors: A case/non-case analysis using the Food and Drug Administration Adverse Event Reporting System.
タグ:
FAERS
2024/4/4
Investigating bleeding adverse events associated with BTK inhibitors in the food and drug administration adverse event reporting system (FAERS).
タグ:
FAERS
2024/4/3
Detection and analysis of signals of adverse events of memantine based on the US food and drug administration adverse event reporting system.
タグ:
FAERS
2024/4/3
Exploring the association between weight loss-inducing medications and multiple sclerosis: insights from the FDA adverse event reporting system database.
タグ:
FAERS
2024/4/3
Drug Repurposing Using FDA Adverse Event Reporting System (FAERS) Database.
タグ:
FAERS
2024/4/3
Post-marketing safety concerns with palbociclib: a disproportionality analysis of the FDA adverse event reporting system.
タグ:
FAERS
2024/4/2
Examining the safety of mirabegron: an analysis of real-world pharmacovigilance data from the US FDA adverse event reporting system (FAERS) database.
タグ:
FAERS
2024/4/2
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