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The Medical Dictionary for Regulatory Activities (MedDRA) - external site is an internationally used set of terms relating to medical conditions, medicines and medical devices.
It was created to assist regulators with sharing information. It is also used by industry, academics, health professionals and other organisations that communicate medical information.
MedDRA terms in the Database of Adverse Event Notifications - medicines
The TGA uses MedDRA terms for coding the reports it receives about adverse events.
Before a report is entered into the Database of Adverse Event Notifications - medicines - external site, the relevant MedDRA terms are assigned to describe the adverse event and other medical terms as necessary. This results in a consistent terminology, which enables related adverse events in DAEN - medicines to be grouped together in the medicine summary.
MedDRA terms
MedDRA includes standardised terms for:
- symptoms, signs, diseases, syndromes and diagnoses
- medical device malfunctions
- medication errors
- medical, social and family history information
- sites (e.g. application, implant and injection sites)
- medical and surgical procedures
- approved uses for medications and medical devices
- types of investigations (e.g. liver function analyses, metabolism tests).
MedDRA system organ classes
The MedDRA system organ class is defined as the highest level of the MedDRA terminology, distinguished by anatomical or physiological system, aetiology (disease origin) or purpose. Most of these describe disorders of a specific part of the body. For example:
- Cardiac disorders describe heart problems
- Renal and urinary disorders describe kidney and bladder problems
- Some of the system organ classes are not related to a particular part of the body. For example:
- investigations describes laboratory tests and other medical investigations that gave an unusual reading
- neoplasms describes any type of growth, including cancer, no matter where it appears in the body.
The 27 MedDRA system organ classes
MedDRA reaction terms
The term used to describe an adverse event in the Database of Adverse Event Notifications - medicines is the MedDRA 'preferred term', which describes a single medical concept.
Each MedDRA system organ class has a number of MedDRA preferred terms associated with it. For example, the system organ class 'cardiac disorders' includes (among others) the following preferred terms:
- angina
- cardiac arrest
- myocardial infarction
- palpitations.
The MedDRA Maintenance and Support Services Organization
The MedDRA Maintenance and Support Services Organization (MSSO) - external site maintains and distributes MedDRA information. The MSSO releases updated versions of MedDRA twice a year to subscribers.
MedDRA was developed by the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) - external site to assist regulatory authorities to easily and accurately share information on therapeutic goods, including about adverse events to medicines.
MedDRA terminology incorporates terminology from the:
- Medicines and Healthcare products Regulatory Agency (MHRA)
- World Health Organization Adverse Reaction Terminology (WHO-ART)
- International Classification of Diseases (ICD)
- International Classification of Diseases and Clinical Modification (ICD-CM)
- Coding Symbols for a Thesaurus of Adverse Reaction Terms (COSTART)
- Japanese Adverse Reaction Terminology (J-ART).