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Characterization and corroboration of safety signals identified from the US Food and Drug Administration Adverse Event Reporting System, 2008-19: cross sectional study.
タグ:
FAERS
2022/10/6
Acute Cholecystitis Associated With the Use of Glucagon-Like Peptide-1 Receptor Agonists Reported to the US Food and Drug Administration.
タグ:
FAERS
2022/8/30
Analysis of adverse drug events in patients with bipolar disorders using the Japanese Adverse Drug Event Report database.
タグ:
JADER
2022/10/7
A Data-Driven Reference Standard for Adverse Drug Reaction (RS-ADR) Signal Assessment: Development and Validation.
タグ:
FAERS
2022/10/7
Safety of trastuzumab deruxtecan: A meta-analysis and pharmacovigilance study.
タグ:
FAERS
2022/10/7
Adverse event profiles of hypomagnesemia caused by proton pump inhibitors using the Japanese Adverse Drug Event Report (JADER) Database.
タグ:
JADER
2022/10/7
Development of Pharmacovigilance System in India and Paradigm of Pharmacovigilance Research: An Overview.
タグ:
VigiBase
2022/10/7
Changing paradigms in detecting rare adverse drug reactions: from disproportionality analysis, old and new, to machine learning.
タグ:
VigiBase
2022/10/2
Sodium-Glucose Cotransporter 2 Inhibitors and the Short-term Risk of Bladder Cancer: An International Multisite Cohort Study.
タグ:
CPRD
2022/9/29
Liver blood marker testing in UK primary care: a UK wide cohort study, 2004-2016.
タグ:
CPRD
2022/9/28
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