Donor Adverse Reaction
Donor reactions are captured to fulfill AABB Biovigilance reporting requirements.
The Add Reaction module allows the User to collect donor reaction information during the donation process and report follow-up data post-donation
- Donors are available for reaction reports as soon as their registration is complete.
- The User has the ability to record donation data, enter donor vitals, add free-form comments, and report reaction and treatment details, as required.
- Specific reaction data entry fields may be configured to display to collection site staff or central location staff, as needed.
- Information reported is configurable by the blood center.
- Data can be captured using a wireless handheld device.
The Reaction Report Selection module allows the User to view all donor reaction data that was entered at the donation site and/or enter new reaction data after the drive has ended
- Donor reaction reports can be updated and reviewed at any time.
- New donor reactions that occur after the donation date can be reported.
- Information reported is configurable by the blood center.
- Reports can be approved and printed.
- Report reviewers are tracked by the system.
- Files are archived after report completion, and can be uploaded directly to AABB.
Cost Savings
- Simplifies the reaction reporting procedure, resulting in less man hours spent managing it
- Reduces entry errors
- Eliminates the need for time consuming manual entries
- Formats files for upload to AABB Donor Hemovigilance Site
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