| DESCRIPTION OF ENHANCEMENTS |
This Build addresses the following problems:
known allergies or adverse reactions?" prompt and does not enter a
causative agent the software assesses the patient as having a reaction on
file in the database. It should not.
3) The GMRA PRINT-COMPLETE LISTING option does not distinguish between
patients who not in the ART database and those patients who are assessed
as NKA (No Known Allergies).
4) The ART package calls an Outpatient Pharmacy utility to get and display
any outpatient medications for a patient. The SIG code value for the
prescription return is changing in size from one line of text to one plus
lines of text. The ART package will store the first 30 characters of the
SIG code for its SUSPECT and CONCOMITANT drug entries in File 120.85.
5) Changes the description for the GMRA PRINT-FDA EXCEPT BY PT option so
that it accurately describes what that option does.
6) Changes the description for the GMRA PRINT-EXCEPT BY DATe option so
that it accurately describes what that option does.
1) Corrects a bug introduced by the GMRA*4.0*2 patch. Users are not being
For more detailed information please see the GMRA*4*5 patch description on
FORUM.
asked to sign-off on autoverified reactions in the enter/edit reaction
process if they answer YES to the "Enter another Causative Agent?" prompt,
but do not enter another causative agent. This results in the reaction not
be considered as autoverified.
2) When a user mistakenly answers YES to the "Does this patient have any
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