| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Product containing human insulin zinc suspension crystalline (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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Product containing precisely human insulin (as human insulin zinc suspension crystalline) 1000 unit/10 milliliter conventional release suspension for injection vial |
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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Product containing human insulin zinc suspension crystalline in parenteral dose form (medicinal product 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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Human insulin zinc suspension crystalline 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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Human insulin zinc suspension crystalline only product in parenteral 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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Product containing precisely human insulin (as human insulin zinc suspension crystalline) 100 unit/1 milliliter conventional release suspension for injection (clinical drug) |
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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Product containing precisely human insulin zinc suspension crystalline 100 unit/1 milliliter conventional release suspension for injection (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 |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
| Product containing precisely human insulin zinc suspension crystalline 100 unit/1 milliliter conventional release suspension for injection (clinical drug) |
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). |
True |
Human insulin zinc suspension crystalline (substance) |
Inferred relationship |
Some |
1 |
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