R interface for FDA Adverse Event Reporting System
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Updated
Sep 18, 2024 - R
R interface for FDA Adverse Event Reporting System
Datasets and source code for reproducing the paper 'Integrating multiple evidence sources to predict adverse drug reactions based on systems pharmacology model'.
Population-scale patient safety data reveal inequalities in adverse events before and during COVID-19 pandemic
The Shakespeare-Method repository contains the code we used to develop a new method to identify attributed and unattributed potential adverse events using the unstructured notes portion of electronic health records.
IEEE BIBM 2021: Bayesian optimization-guided topic modeling for automatic detection of sepsis-related events from free text
OAE: Ontology of Adverse Events
OVAE is the Ontology of Vaccine Adverse Events
Risk Prediction of COVID-19 Vaccine Adverse Event by using Bayesian Network
Drug Side Effect Checker - The Pharmacovigilance Dashboard Prototype build with FDA (FAERS) data
This is Loan Robinson Github Page, which includes all tutorials for education purpose.
Reportable clinic events, reference ranges, grading
Author: Cong Zhu. Purpose: code for paper "Investigating safety profiles of human papillomavirus vaccine across group differences using VAERS data and MedDRA."
Adverse Events models and handling
Your Doctor's Guide to Vaccine Adverse Events
Adverse Event classes
Suspected adverse drug reaction (sADR) data for Librela.
Safety and Efficacy Figures based on ADaM datasets using SAS version 9.4
Metformin treatment for diabetes prevention in Africa: META Trial
Reportable clinic events, reference ranges, grading
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