CDE ID | CDE Description | * 1063 | Site Participant ID (Go To: 1097) |
* 1899 | Adverse Event onset date (MM/DD/YYYY): (Go To: 422) |
* 422 | EDRN Site ID (Go To: 423) |
* 423 | EDRN Protocol ID (Go To: 929) |
* 929 | EDRN Staff ID of the person who collected the data: (Go To: 4644) |
* 4644 | Age at date of visit, procedure, or data abstraction: (Go To: 1897) |
* 1897 | Adverse Event: (Go To: 1898) |
* 1898 | Is this a Serious AE? (Go To: 1901) |
| Permissible Values (value): | No (0) |
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* 1901 | Adverse Event Status: (Go To: 1902) |
| Permissible Values (value): | Ongoing (1) |
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* 1900 | Adverse Event stop date (MM/DD/YYYY): (Go To: 1902) |
* 1902 | Adverse Event action(s) taken: Check all that apply. (Go To: 1904) |
| Permissible Values (value): | None (4) |
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| | Permanently Discontinued (7) |
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* 1904 | Adverse Event relationship to study treatment. (Go To: 1905) |
| Permissible Values (value): | Related (1) |
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* 1905 | Adverse Event Grade: (Go To: 1097) |
1097 | Comments (do not include any participant identifiers) (Go To: End of Form) |