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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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Id | http://purl.obolibrary.org/obo/NCIT_C41332
http://purl.obolibrary.org/obo/NCIT_C41332
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Preferred Name | Adverse Reaction |
Definitions |
Any noxious and unintended response(s) to a medical product or procedure, for which a causal relationship with this product or procedure is at least a reasonable possibility i.e., the relationship cannot be ruled out.
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
definition | Any noxious and unintended response(s) to a medical product or procedure, for which a causal relationship with this product or procedure is at least a reasonable possibility i.e., the relationship cannot be ruled out. |
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label |
Adverse Reaction
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prefLabel |
Adverse Reaction
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Legacy Concept Name |
Adverse_Reaction
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in_subset | |
Preferred_Name |
Adverse Reaction
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DesignNote |
WHO Technical Report 498 definition the post-marketing setting: A response to a drug which is noxious and unintended and which occurs at doses normally used in man for prophylaxis, diagnosis, or therapy of disease or for modification of physiological function.
The old term Side Effect is retired and should not be used.
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UMLS_CUI |
C0559546
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prefixIRI |
NCIT:C41332
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Contributing_Source |
CDISC-GLOSS
FDA
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subClassOf | |
code |
C41332
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type | |
ALT_DEFINITION |
An unexpected medical problem that happens during treatment with a drug or other therapy. Adverse effects do not have to be caused by the drug or therapy, and they may be mild, moderate, or severe.
A response to a medicinal product, devices, or procedures, which is noxious and unintended. Response in this context means that a causal relationship between a medicinal product and an adverse event is at least a reasonable possibility. In the context of drug development, the term is used as a synonym of adverse drug reaction. (After ICH E2A)
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Semantic_Type |
Finding
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