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Education article ISSN 23349492 (Online) UDC: 81374:61Hospital Pharmacology. 2015; 2(2):266271doi:10.5937/hpimj1502266MMedical Dictionary Media used in over 60 countries, among which is Montenegro
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To fill out the medical dictionary MedDRA, follow these steps:
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Start by collecting all relevant information for each term you want to include in the dictionary.
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Create a new entry for each term in the MedDRA format, following the specified hierarchy and coding rules.
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Include the term's preferred term, synonyms, and related terms, if applicable.
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Assign appropriate codes to each term based on the MedDRA coding system.
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Provide detailed descriptions and characteristics for each term to ensure accuracy and clarity.
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Who needs medical dictionary meddra?

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Medical professionals, researchers, and regulatory agencies utilize the medical dictionary MedDRA.
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Pharmaceutical companies also use MedDRA to classify and analyze adverse drug reactions in clinical trials and pharmacovigilance.
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Health authorities and drug regulatory bodies rely on MedDRA for proper drug classification, adverse event reporting, and drug safety monitoring.
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MedDRA is essential for standardizing medical terminologies and facilitating efficient communication and analysis of medical data across different healthcare systems and organizations.
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MedDRA is a standardized medical terminology used for the classification of adverse event information related to medical products.
Health authorities, pharmaceutical companies, CROs, and other organizations involved in drug development and regulatory activities are required to file medical dictionary MedDRA.
Medical professionals can fill out MedDRA by selecting relevant terms that best describe the adverse events associated with a medical product.
The purpose of MedDRA is to provide a common language for reporting and analyzing adverse events associated with medical products.
Information such as the medical product involved, the adverse event, its severity, outcome, and any relevant medical history must be reported on MedDRA.
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