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Adverse Event Reporting Ontology
The Adverse Event Reporting Ontology (AERO) is an ontology aimed at supporting clinicians at the time of data entry, increasing quality and accuracy of reported adverse events.
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1 |
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Adverse Drug Reaction Markup Language
The Adverse Drug Reaction Markup Language (EU-ADR ML) was created to as part of the EU-ADR project. The ultimate aim of this project was to develop an innovative approach to the early detection of adverse drug reactions. The status of this format is
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2 |
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Adverse Childhood Experiences Ontology
An ontology to help describe data about Adverse Childhood Experiences.
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3 |
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Ontology of Adverse Events
The Ontology of Adverse Events (OAE) is a community-driven ontology that is developed to standardize and integrate data on biomedical adverse events (e.g., vaccine and drug adverse events) and support computer-assisted reasoning. As a result of a med
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4 |
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Ontology of Drug Adverse Events
The Ontology of Drug Adverse Events (ODAE) is a biomedical ontology in the area of drug adverse events, developed by following OBO Foundry principles (e.g., openness, collaboration).
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5 |
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WHO Adverse Reaction Terminology
WHO Adverse Reaction Terminology is a standardization of the vocabulary for adverse reactions.
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6 |
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Ontology of Vaccine Adverse Events
The Ontology of Vaccine Adverse Events (OVAE) is a biomedical ontology in the area of vaccine adverse events. While they are extremely useful in decreasing infection prevalence in human populations, vaccines may also induce some unintended adverse ev
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7 |
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FDA's Adverse Event Reporting System
The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA.
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8 |
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DART - Drug Adverse Reaction Targets
A database for facilitating the search for drug adverse reaction target. It contains information about known drug adverse rection targets, functions and properties. Associated references are also included.
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9 |
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COVID-19 Vaccination Adverse Reaction
Data relating to any adverse reactions which occur within the first fifteen minutes after administration of the coronavirus (COVID-19) vaccination.
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10 |
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Ontology of Drug Neuropathy Adverse Events
The Ontology of Drug Neuropathy Adverse Events (ODNAE) is an extension of OAE which serves as a knowledge base comprising drug components, chemical entities of active drug ingredients, drug mechanisms, and drug-inducing neuropathy AEs. ODNAE is a pla
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11 |
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Vaccine Adverse Reactions data for QResearch
Adverse reactions occurring shortly after COVID_19 vaccination.
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12 |
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Ontology of Cardiovascular Drug Adverse Events
With increased usage of cardiovascular drugs (CVDs) for treating cardiovascular diseases, it is important to analyze CVD-associated adverse events (AEs). The Ontology of Cardiovascular Drug Adverse Events (OCVDAE) is an ontology of adverse events ass
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13 |
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Common Terminology Criteria for Adverse Events
A coding system for reporting adverse events that occur in the course of cancer therapy. It was derived from the Common Toxicity Criteria (CTC) v2.0 and is maintained by the Cancer Therapy Evaluation Program (CTEP) at the National Cancer Institution
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14 |
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Canada Vigilance Adverse Reaction Online Database
The Canada Vigilance Adverse Reaction Online Database contains information about suspected adverse reactions (also known as side effects) to health products. Adverse reaction reports are submitted by: consumers and health professionals, who submit re
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15 |
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Coping Strategies for Adverse Drug Events Ontology
This is an ontology of possible coping strategies that patients advise for managing side effects they experience. It was created based on a forum for patients with a GastroIntestinal Stromal Tumor (GIST) . This ontology can be found here: https://git
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16 |
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Coding Symbols for a Thesaurus of Adverse Reaction Terms
Coding Symbols for Thesaurus of Adverse Reaction Terms (COSTART). 5th ed. Rockville (MD). COSTART is used for coding, filing, and retrieving post-marketing adverse drug and biologic experience reports. COSTART is organized in body system and pathophy
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17 |
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MetaADEDB
A comprehensive database on adverse drug events.
MetaADEDB is an online database we developed to integrate comprehensive information of adverse drug events (ADEs).
The new version consists of 744,709 drug-ADE associations between 8,498 compounds (i
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18 |
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Side Effect Resource
SIDER contains information on marketed medicines and their recorded adverse drug reactions. The information is extracted from public documents and package inserts. The available information include side effect frequency, drug and side effect classifi
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19 |
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T-ARDIS
Mining drug-target and drug-adverse drug reaction databases to identify target-adverse drug reaction relationships.
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20 |
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ADReCS
Adverse Drug Reaction Classification System
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21 |
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SuperTarget
Drug-related information: medical indications, adverse drug effects, drug metabolism and Gene Ontology terms of the target proteins.
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22 |
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Ontology for Genetic Susceptibility Factor
Ontology for Genetic Susceptibility Factor (OGSF) is an application ontology to model/represent the notion of genetic susceptibility to a specific disease or an adverse event or a pathological biological process. It is developed using BFO 2.0's frame
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23 |
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Common Evidence Model
The CommonEvidenceModel (CEM) provides an evidence base of a wide variety of sources with information relevant for assessing associations between drugs and health outcomes of interest.
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24 |
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Surgical Secondary Events
Memorial Sloan-Kettering Cancer Center Surgical Secondary Events Ontology (Adverse Events)
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25 |
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COVID-19 CVD Registry
As physicians, scientists and researchers worldwide struggle to understand the novel coronavirus (COVID-19) pandemic, the American Heart Association (AHA) is developing a novel registry to aggregate data and aid research on the disease, treatment pro
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26 |
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STIFDB2
Various genes get upregulated in plants during adverse environmental conditions, which alter the metabolic functions to mitigate the stress effects for adaptation. Therefore, it is important to know the regulatory motifs of stress-induced genes for g
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27 |
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Placental Maternal Health Conditions
Physical and psychological disorders in the mother that occur during pregnancy, childbirth, and the postpartum period. These include both pre-existing and gestational maternal health conditions that may result in adverse pregnancy outcomes. The Mater
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28 |
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The Drug-Drug Interactions Ontology
DINTO is an OWL ontology that systematically organizes all drug-drug interaction (DDI) related information. Drug-drug interactions (DDIs) form a significant risk group for adverse effects associated with pharmaceutical treatment. These interactions a
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29 |
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Biomedical Research Integrated Domain Group Model
BRIDG is a domain analysis model that represents the realm of protocol-driven clinical, pre-clinical, translational and basic research. This breadth includes concepts from Common (i.e., concepts shared by all research protocols), Protocol Representat
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30 |
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EK-DRD
A Comprehensive Database for Drug Repositioning Inspired by Experimental Knowledge | Drug Repositioning Drug repositioning, or the identification of new indications for approved therapeutic drugs, has gained substantial traction with both academics a
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31 |
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Ontology for Systems Chemical Biology and Chemogenomics
Chem2Bio2RDF has been created by aggregating data from multiple chemogenomics repositories and is cross-linked into Bio2RDF and LODD. There is also a linked-path generation tool to facilitate SPARQL query generation, and have created extended SPARQL
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32 |
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Minimum Information Required for a Drug Metabolism Enzymes and Transporters Experiment
Pharmacogenomics studies are expanding exponentially, both in terms of number and amount of data generated. To facilitate future research and diagnostic applications, Affymetrix has developed a microarray targeting known genetic variations in absorpt
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33 |
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DrugCentral
DrugCentral is online drug information that provides information on active ingredients, chemical entities, pharmaceutical products, drug mode of action, indications, and pharmacologic mode of action. DrugCentral monitors FDA, EMA, and PMDA for new dr
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34 |
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National Unified Renal Translational Research Enterprise (NURTuRE)
Collection of samples and data across the following diseases: Chronic kidney disease (disorder), Nephrotic syndrome (disorder). The NURTuRE project was devised to create a national kidney biobank as recommended in the UK Renal Research Strategy 2016.
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35 |
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SuperDRUG2 - A One Stop Resource for Approved/Marketed Drugs
SuperDRUG2, an update of the previous SuperDrug database, is a unique, one-stop resource for approved/marketed drugs, containing more than 4,600 active pharmaceutical ingredients. Drugs are annotated with regulatory details, chemical structures (2D a
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36 |
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aBiofilm
Biofilms play an important role in the antibiotic drug resistance, which is threatening public health globally. Almost, all microbes mimic multicellular lifestyle to form biofilm by undergoing phenotypic changes to adapt adverse environmental conditi
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37 |
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Comparative Toxicogenomics Database
Database that aims to advance understanding about how environmental exposures affect human health. It provides manually curated information about chemical–gene/protein interactions, chemical–disease and gene–disease relationships. These data are inte
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38 |
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UHB Linked Diabetic Eye Disease and Cardiac Outcomes
Vision and systemic cardiac outcome data for those identified by having a diabetic screening eye test and an acute episode at Queen Elizabeth Hospital, Birmingham. Key data include demographics, longitudinal cardiac outcomes, visual data, and eye gra
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39 |
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Medical Dictionary for Regulatory Activities Terminology
MedDRA is a multilingual terminology allowing most users to operate in their native languages. MedDRA can be used to analyse individual medical events (e.g., “Influenza”) or issues involving a system, organ or etiology (e.g., infections) using its hi
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40 |
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Immunology Database and Analysis Portal
The Immunology Database and Analysis Portal (ImmPort) data repository was created for the exploration of clinical and basic research data on immunology and associated findings. ImmPort intends to promote effective data sharing across the basic, clini
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41 |
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Early Pandemic Evaluation and Enhanced Surveillance of COVID-19 (EAVE II)
Population-level surveillance and rapid assessment of the effectiveness of therapeutic or preventive interventions are required to ensure that interventions are targeted to those at highest risk of serious illness or death from COVID-19. Introduction
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42 |
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PLANT-PIs
Plant protease inhibitors (PIs) can be counted among the defensive proteins that plants display to minimize the adverse effects deriving from the attack of phytophagous insects. They are usually present in seeds and storage tissues, but are also expr
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43 |
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*ReputationScore indicates how established a given datasource is. Find out more.