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Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), MedDRA or Medical Dictionary for Regulatory Activities is a clinically validated

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

needed] The MedDRA Management Committee (MC) is responsible for direction of MedDRA, ICH's standardised medical terminology. The MedDRA MC has the role

SNOMED CT

overlap between MedDRA and SNOMED CT that is not beneficial for pharmaceutical industry. In 2021, two maps map between SNOMED CT and MedDRA were jointly

Common Terminology Criteria for Adverse Events

Reference" form) as a PDF document. The classification of events uses the MedDRA at its granular (Lowest Level Terms: LLTs) level. For each term, specific

Pharmacovigilance

65–75. doi:10.1093/oxfordjournals.aje.a115125. PMID 2910073. "MedDRA MSSO | MedDRA". www.meddra.org. Retrieved March 16, 2020. "Common Terminology Criteria

Uppsala Monitoring Centre

in drug safety, including the WHO Drug Dictionary – with a bridge to the MedDRA terminology and WHO ICD – tools for searching in the database, and a program

electronic design System organ class, an organizational division in the MedDRA dictionary Society (abbr.: "soc.") Scottish Ornithologists' Club Scouts

VigiBase

of Diseases (ICD), and the Medical Dictionary for Regulatory Activities (MedDRA). Type of reports: Most preferred data includes post-marketing spontaneous

Pfizer–BioNTech COVID-19 vaccine

videos have been debunked. According to the British National Formulary and MedDRA conventions, side effects are "very common" when they occur in more than

Nosology

Headings), COSTART (Coding Symbols for Thesaurus of Adverse Reaction Terms) or MedDRA (Medical Dictionary for Regulatory Activities) Other systems like Current