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702806008: Ruxolitinib (substance)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3006149011 Ruxolitinib en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3006175010 Ruxolitinib (substance) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1866021000195112 ruxolitinib it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
839091000172115 ruxolitinib fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ruxolitinib Is a Protein-tyrosine kinase inhibitor false Inferred relationship Some
Ruxolitinib Is a Antineoplastic agent (substance) true Inferred relationship Some
Ruxolitinib Is a Janus kinase inhibitor true Inferred relationship Some
Ruxolitinib This attribute specifies the behavior that a substance will exhibit or participate in, given the appropriate context. Janus kinase inhibitor (disposition) true Inferred relationship Some
Ruxolitinib Is a produit chimique catégorisé selon sa fonction false Inferred relationship Some
Ruxolitinib Is a Enzyme inhibitor false Inferred relationship Some
Ruxolitinib Is a Nitrile true Inferred relationship Some
Ruxolitinib Is a Pyrazole derivative true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Product containing ruxolitinib (medicinal product) The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. True Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 5 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some
Product containing precisely ruxolitinib 10 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some
Product containing precisely ruxolitinib 20 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some
Product containing precisely ruxolitinib 15 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some
Product containing precisely ruxolitinib 25 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some
Product containing precisely ruxolitinib 5 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 5 milligram/1 each conventional release oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 10 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 10 milligram/1 each conventional release oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 20 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 20 milligram/1 each conventional release oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 15 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 15 milligram/1 each conventional release oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 25 milligram/1 each conventional release oral tablet The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 25 milligram/1 each conventional release oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. False Ruxolitinib Inferred relationship Some 1
Ruxolitinib phosphate (substance) Is a False Ruxolitinib Inferred relationship Some
Product containing precisely ruxolitinib 5 milligram/1 each conventional release oral tablet The most specific description of a substance present in the manufactured dose form, before any dilution or transformation. It includes modifiers, such as salts, esters, polymers (e.g. pegylation), and/or solvates (including waters of hydration). False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 10 milligram/1 each conventional release oral tablet The most specific description of a substance present in the manufactured dose form, before any dilution or transformation. It includes modifiers, such as salts, esters, polymers (e.g. pegylation), and/or solvates (including waters of hydration). False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 20 milligram/1 each conventional release oral tablet The most specific description of a substance present in the manufactured dose form, before any dilution or transformation. It includes modifiers, such as salts, esters, polymers (e.g. pegylation), and/or solvates (including waters of hydration). False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 15 milligram/1 each conventional release oral tablet The most specific description of a substance present in the manufactured dose form, before any dilution or transformation. It includes modifiers, such as salts, esters, polymers (e.g. pegylation), and/or solvates (including waters of hydration). False Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib 25 milligram/1 each conventional release oral tablet The most specific description of a substance present in the manufactured dose form, before any dilution or transformation. It includes modifiers, such as salts, esters, polymers (e.g. pegylation), and/or solvates (including waters of hydration). False Ruxolitinib Inferred relationship Some 1
Ruxolitinib-containing product in oral dose form The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. True Ruxolitinib Inferred relationship Some 1
Ruxolitinib phosphate (substance) This attribute indicates that the concept is a structural modification of another concept, and that the substance's intrinsic physicochemical properties remain unchanged. True Ruxolitinib Inferred relationship Some
Ruxolitinib only product The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. True Ruxolitinib Inferred relationship Some 1
Ruxolitinib only product in oral dose form The clinically relevant part or whole of the substance that is intended to have a therapeutic action on or within the body. It excludes esters, salts or other non-covalent derivatives (such as a complex, chelate etc.), but may include secondary modifications. True Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib (as ruxolitinib phosphate) 5 milligram/1 each conventional release oral tablet (clinical drug) This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. True Ruxolitinib Inferred relationship Some 1
Ruxolitinib (as ruxolitinib phosphate) 10 mg oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. True Ruxolitinib Inferred relationship Some 1
Ruxolitinib (as ruxolitinib phosphate) 20 mg oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. True Ruxolitinib Inferred relationship Some 1
Product containing precisely ruxolitinib (as ruxolitinib phosphate) 15 milligram/1 each conventional release oral tablet (clinical drug) This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. True Ruxolitinib Inferred relationship Some 1
Ruxolitinib (as ruxolitinib phosphate) 25 mg oral tablet This attribute represents an ingredient that is the part of the active ingredient that the strength of a given product is based upon. True Ruxolitinib Inferred relationship Some 1
A characteristic ruxolitinib discontinuation syndrome includes an acute relapse of disease symptoms, splenomegaly, and occasional hemodynamic decompensation. Symptoms can appear from less than 24 hours to up to 3 weeks after the abrupt discontinuation of ruxolitinib. Associated with False Ruxolitinib Inferred relationship Some 1
A condition where a patient requires continuous administration of the drug ruxolitinib to manage their symptoms or disease effectively. This dependence can develop because stopping or reducing the dose of ruxolitinib may lead to a relapse or worsening of the condition it was treating, such as myelofibrosis or polycythemia vera. Causative agent (attribute) True Ruxolitinib Inferred relationship Some 1

This concept is not in any reference sets

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