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Spontaneous adverse event reporting

Spontaneous adverse event reporting

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(341) Development and Evaluation of Python Language Processed Automated Disproportionality Analysis System for FAERS Database

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(342) Exploration of Novel Adverse Drug Reactions of Trifluoperazine using FAERS database and Identification of Associated Genes and Proteins

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(343) Identifying the Safety Signals for Adverse Events Causing Mortality Due to Ferric Carboxymaltose: A Disproportionality Analysis of Spontaneous Reports and Extensive Systematic Review

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(344) Interpreting Vedolizumab: Uncovering Cachexia Signal in U.S Food and Drug Administration Adverse Event Reporting System (FAERS) Database.

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(345) Medication Errors in EudraVigilance: Signals of Disproportionate Reporting Among Age Groups

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(346) Novel Adverse Event of Atezolizumab: A Disproportionality Analysis in US Food and Drug Administration Adverse Event Reporting System (FAERS) Database

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(347) Post-marketing safety of ALK inhibitors: an analysis of EudraVigilance reports between 2012 and 2022

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(348) Recent Trends in Global Adverse Event Reporting: A Descriptive Analysis of VigiBase

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(349) Safety Analysis of Adverse Drug Reactions in United States: A 21-Year descriptive Study of FDA Adverse Event Reporting System

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(350) Transverse Myelitis Associated with Tozinameran Use: Adverse Events- Signal

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(351) Unveiling the Hidden Toll of Drug-Induced Impulsivity: A Network Analysis of the FDA Adverse Event Reporting System.

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(352) Views on The Development and Use of a New Digital Health Platform to Improve Adverse Drug Event Detection, Management and Reporting in Australia: A Qualitative Study

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