Smart Adverse Drug Reaction Assessment Tools.
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Updated
Dec 8, 2022 - Jupyter Notebook
Smart Adverse Drug Reaction Assessment Tools.
A collection of signal detection methods used in the field of pharmacovigilance
For this problem, we proposed the use of bidirectional-LSTM’s(Long Short Term Memory) with 1-D CNN layer to classify patient notes at character level and at word level. The 1-D CNN is employed to scale back the training time. In order to improve the performance, we will also feed the network combined word embedding consisting of Pre-trained word…
BioDEX: Large-Scale Biomedical Adverse Drug Event Extraction for Real-World Pharmacovigilance.
FAERS Adverse Reaction Events database and OpenFDA API
Rank aggregated signal detection for VAERS data
This repository contains the code of Mining archive.org’s Twitter stream grab for Pharmacovigilance research gold paper.
Regional ADR event detection using Deep Learning
Functions to extract drug records from the FAERS (FDA Adverse Event Reporting System) database
Safety signal detection in pharmacological data (pharmacovigilance)
The PVClinical project aims to build a web-based platform, built to support Active Pharmacovigilance processes via the integration of several heterogeneous data sources.
An R package containing functions for quantifying drug exposure using routinely collected prescribing databases
Code and Datasets for the paper "Towards early detection of adverse drug reactions: combining pre-clinical drug structures and post-market safety reports", published on BMC Medical Informatics and Decision Making in 2019.
R interface for FDA Adverse Event Reporting System
Signal detection for the adverse reaction of pyoderma gangrenosum in rituximab use
Structured lists (csv, xml, sql) for PV apps configuration & localization.
Bog Cảnh giác Dược Việt Nam-Chia sẻ kinh nghiệm nghiên cứu khoa học và thông tin thuốc
GPADRlex: Grouped Phrasal Adverse Drug Reaction lexicon
This project uses data from the OpenFDA API to understand the impact of certain ingredients in drugs on adverse events reported over a period of five years. We quantify this impact, identify the most influential ingredients, and develop a predictive model for adverse events based on these ingredients.
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