| Name | Steward Organization | Suggested Domain | Suggested Domain Description | Cde Group | Classification |
|---|---|---|---|---|---|
| 3. Has the participant ever experienced amyloid related imaging abnormalities-edema (ARIA-E), amyloid related imaging abnormalities-hemorrhage (ARIA-H), or other major adverse events associated with treatments expected to modify ADRD biomarkers? | NACC | Treatment |
Treatment for all conditions |
Other NIA-funded studies |
|
| # | Datatype |
|---|---|
|
|
Value List |
| # | Permissible value | Value meaning name |
|---|---|---|
|
|
0 | No |
|
|
1 | Yes |
|
|
9 | Unknown |
| # | Identifier | Origin | Version |
|---|---|---|---|
|
|
UDS_a4a_Initial Visit Packet_advevent | NACC-source_dataset+form_name+packet+var_name | NACC_uds-v4-ivp-ded-11122025 |