Intended Effect/Comorbidity Attributes
You can use the attributes to describe the intended effect/comorbidity associated to a product.
| Attribute | Description |
| Application Code | The code of the application with which the PDS is associated. |
| Application Name | The name of the application with which the PDS is associated. |
| Countries | The name of the country (countries) for which the intended effect/comorbidity is created. The countries available for selection are all countries associated with the Application. This attribute defines the values included in the XML output during XEVMPD Submission wizard execution. |
| Family Code | The code of the product family with which the PDS is associated. |
| Family Name | The name of the product family with which the PDS is associated. |
| Comorbidity | Any comorbidity (concurrent condition) or co-infection described as part of the indication as is referenced in the regulated product information. |
| Intended Effect | The intended effect as part of the indication describes the result/type of outcome intended for the target condition. |
|
Indication/Intended Effect/Comorbidity Last Update Date |
The date the Indication was set from Pending Add to Approved. This attribute is updated automatically by the system. |
|
Product Detail Set Name |
The name of the PDS with which the intended effect/comorbidity is associated. The Product Details Set name is the concatenation of PDS Name + PDS Code. |
| Product Name | The name of the product with which the PDS/template is associated including Product Name, Product Strength, Product Dosage Form, Product Code. |
