| DESCRIPTION OF ENHANCEMENTS |
This patch addresses Remedy ticket, HD67403. The site reported
This patch will also correct a problem with the bulletin generation during
entry of Adverse Reactions described in Remedy ticket HD85125.
The problem occurs when the user answers "No" to verify an observed/drug
adverse reaction when it is first entered. If the user skips the
verification step but then uses the GMRA PATIENT A/AR EDIT option and
edits the existing observed/drug allergy and then verifies it (with or
without making changes) an additional NOTIFICATION OF OBSERVED DRUG
REACTION bulletin is triggered.
that test patients entered in production are appearing on the
This patch will modify the logic in the code so that, if the user
re-enters the adverse reaction and then verifies it, a second
NOTIFICATION OF OBSERVED DRUG REACTION bulletin will not be triggered.
Adverse Reaction Tracking reports, and are also being included in
report counts.
This patch will update the Adverse Reaction Tracking reports that
display the patient name and/or SSN, and reports that produce counts
of reaction data so that they all exclude test patients.
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