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VigiBase, the Glossary

Index VigiBase

VigiBase is a World Health Organization's (WHO) global Individual Case Safety Report (ICSR) database that contains ICSRs submitted by the participating member states enrolled under WHO's international drug monitoring programme.[1]

Table of Contents

  1. 27 relations: Adverse drug reaction, Allopathic medicine, Clinical trial, Competent authority, Council for International Organizations of Medical Sciences, Drug development, EudraVigilance, Geneva, Health authority, International Classification of Diseases, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use, International Society of Pharmacovigilance, MedDRA, Medical device, Open Database Connectivity, Pharmacovigilance, Relational database, Society of Pharmacovigilance, India, SQL, Sweden, Thalidomide, Uppsala, Uppsala Monitoring Centre, Vaccine, WHOART, World Health Organization, Yellow Card Scheme.

  2. Pharmacological classification systems
  3. Pharmacovigilance databases

Adverse drug reaction

An adverse drug reaction (ADR) is a harmful, unintended result caused by taking medication.

See VigiBase and Adverse drug reaction

Allopathic medicine

Allopathic medicine, or allopathy, is an archaic and derogatory label originally used by 19th-century homeopaths to describe heroic medicine, the precursor of modern evidence-based medicine.

See VigiBase and Allopathic medicine

Clinical trial

Clinical trials are prospective biomedical or behavioral research studies on human participants designed to answer specific questions about biomedical or behavioral interventions, including new treatments (such as novel vaccines, drugs, dietary choices, dietary supplements, and medical devices) and known interventions that warrant further study and comparison.

See VigiBase and Clinical trial

A competent authority is any person or organization that has the legally delegated or invested authority, capacity, or power to perform a designated function.

See VigiBase and Competent authority

Council for International Organizations of Medical Sciences

The Council for International Organizations of Medical Sciences (CIOMS) is an international non-governmental organization of 40 international, national, and associate member groups representing the biomedical science community. VigiBase and Council for International Organizations of Medical Sciences are pharmaceuticals policy.

See VigiBase and Council for International Organizations of Medical Sciences

Drug development

Drug development is the process of bringing a new pharmaceutical drug to the market once a lead compound has been identified through the process of drug discovery.

See VigiBase and Drug development

EudraVigilance

EudraVigilance (European Union Drug Regulating Authorities Pharmacovigilance) is the European data processing network and management system for reporting and evaluation of suspected adverse reactions to medicines which have been authorised or being studied in clinical trials in the European Economic Area (EEA). VigiBase and EudraVigilance are pharmaceuticals policy and pharmacovigilance databases.

See VigiBase and EudraVigilance

Geneva

Geneva (Genève)Genf; Ginevra; Genevra.

See VigiBase and Geneva

Health authority

Between 1996 and 2002, the National Health Service in England and Wales was organised under health authorities (HAs).

See VigiBase and Health authority

International Classification of Diseases

The International Classification of Diseases (ICD) is a globally used medical classification used in epidemiology, health management and for clinical purposes. VigiBase and International Classification of Diseases are World Health Organization.

See VigiBase and International Classification of Diseases

International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use

The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is an initiative that brings together regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of pharmaceutical product development and registration. VigiBase and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use are pharmaceuticals policy.

See VigiBase and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use

International Society of Pharmacovigilance

The International Society of Pharmacovigilance (ISoP), previously the European Society of Pharmacovigilance (ESOP), is an international non-profit scientific organisation, which aims to foster pharmacovigilance both scientifically and educationally, and enhance all aspects of the safe and proper use of medicines, in all countries. VigiBase and international Society of Pharmacovigilance are pharmaceuticals policy.

See VigiBase and International Society of Pharmacovigilance

MedDRA

A subscription-based product of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), MedDRA or Medical Dictionary for Regulatory Activities is a clinically validated international medical terminology dictionary-thesaurus used by regulatory authorities and the biopharmaceutical industry during the regulatory process, from pre-marketing (clinical research phase 0 to phase 3) to post-marketing activities (pharmacovigilance or clinical research phase 4), and for safety information data entry, retrieval, evaluation, and presentation. VigiBase and MedDRA are Pharmacological classification systems.

See VigiBase and MedDRA

Medical device

A medical device is any device intended to be used for medical purposes.

See VigiBase and Medical device

Open Database Connectivity

In computing, Open Database Connectivity (ODBC) is a standard application programming interface (API) for accessing database management systems (DBMS).

See VigiBase and Open Database Connectivity

Pharmacovigilance

Pharmacovigilance (PV, or PhV), also known as drug safety, is the pharmaceutical science relating to the "collection, detection, assessment, monitoring, and prevention" of adverse effects with pharmaceutical products. VigiBase and Pharmacovigilance are pharmaceuticals policy.

See VigiBase and Pharmacovigilance

Relational database

A relational database (RDB) is a database based on the relational model of data, as proposed by E. F. Codd in 1970.

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Society of Pharmacovigilance, India

The Society of Pharmacovigilance, India (SoPI), is an Indian national non-profit scientific organisation, which aims at organizing training programmes and providing expertise in pharmacovigilance and enhance all aspects of the safe and proper use of medicines The International Society of Pharmacovigilance (ISoP) granted status of 'associated society' to Society of Pharmacovigilance India (SoPI). VigiBase and society of Pharmacovigilance, India are pharmaceuticals policy and Pharmacological classification systems.

See VigiBase and Society of Pharmacovigilance, India

SQL

Structured Query Language (SQL) (pronounced S-Q-L; historically "sequel") is a domain-specific language used to manage data, especially in a relational database management system (RDBMS).

See VigiBase and SQL

Sweden

Sweden, formally the Kingdom of Sweden, is a Nordic country located on the Scandinavian Peninsula in Northern Europe.

See VigiBase and Sweden

Thalidomide

Thalidomide, sold under the brand names Contergan and Thalomid among others, is an oral medication used to treat a number of cancers (e.g., multiple myeloma), graft-versus-host disease, and many skin disorders (e.g., complications of leprosy such as skin lesions).

See VigiBase and Thalidomide

Uppsala

Uppsala (archaically spelled Upsala) is the county seat of Uppsala County and the fourth-largest city in Sweden, after Stockholm, Gothenburg, and Malmö.

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Uppsala Monitoring Centre

Uppsala Monitoring Centre (UMC), located in Uppsala, Sweden, is the field name for the World Health Organization Collaborating Centre for International Drug Monitoring. VigiBase and Uppsala Monitoring Centre are international medical and health organizations, organizations established in 1978, pharmaceuticals policy and World Health Organization.

See VigiBase and Uppsala Monitoring Centre

Vaccine

A vaccine is a biological preparation that provides active acquired immunity to a particular infectious or malignant disease.

See VigiBase and Vaccine

WHOART

The WHO Adverse Reactions Terminology (WHOART) was a dictionary meant to serve as a basis for rational coding of adverse reaction terms. VigiBase and WHOART are Pharmacological classification systems.

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World Health Organization

The World Health Organization (WHO) is a specialized agency of the United Nations responsible for international public health. VigiBase and World Health Organization are international medical and health organizations.

See VigiBase and World Health Organization

Yellow Card Scheme

The Yellow Card Scheme is the United Kingdom's system for collecting information on suspected adverse drug reactions (ADRs) to medicines. VigiBase and Yellow Card Scheme are pharmaceuticals policy.

See VigiBase and Yellow Card Scheme

See also

Pharmacological classification systems

Pharmacovigilance databases

References

[1] https://en.wikipedia.org/wiki/VigiBase