ADVERSE REACTION TRACKING (71)    PACKAGE (9.4)

Name Value
NAME ADVERSE REACTION TRACKING
PREFIX GMRA
DEVELOPER (PERSON/SITE) RFM-WAA/HISC
DEVELOPMENT ISC HISC
CLASS National
CURRENT VERSION 4.0
ADDITIONAL PREFIXES
  • GMA
SHORT DESCRIPTION Adverse Reaction Tracking package
AFFECTS RECORD MERGE
VERSION
  • 4.0
    DATE DISTRIBUTED:   2005-11-19 00:00:00
    PATCH APPLICATION HISTORY:
    • 2
      DATE APPLIED:   1996-08-12 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This Build:
         array in the routine GMRAPTB.
       
      4) fixes the problem reported in NOIS NOP-0596-12146. A user presses
         RETURN or enters an up-arrow at the Causative Agent prompt and is
         prompted to enter another causative agent.
       
      5) fixes the problem reported in NOIS ISH-0596-42277. Under certain
         instances the 'Sign-off' event point is not being executed.
       
      6) modifies the field description for the REQUIRE ORIGINATOR COMMENTS
       
         field (#4) in the GMR ALLERGY SITE PARAMETERS file (#120.84).
         NOIS CLA-0696-20854.
       
      7) fixes a problem where the REACTION ASSESSMENT field (#1) in the ADVERSE
         REACTION ASSESSMENT file (#120.86) is marked 1 (yes), but the patient
         does not have any active entries (i.e., entries that have not been
         entered-in-error) in the PATIENT ALLERGIES file (#120.8).
         NOIS: CMO-0696-40833.
       
      8) identifies the patient (e.g., T1234), suspect medication and event date
      1) deletes the Soundex cross-reference from the NAME field (#.01) of the
         on the Attachment page of the MedWatch form. NOIS: BRX-0696-11081.
       
      9) modifies the GMRADPT utility to return "unsigned" reactions in the
         GMRAL array.
       
      10) changes the ORCHK^GMRAOR utility call. If the calling routine is
          checking for Contrast Media Reactions and the patient is not in the
          ART database, then the utility will return a null value instead of a
          0 (zero).
       
         GMR ALLERGIES file (#120.82).
      11) fixes a bug in the GMRADPT utility which returns a GMRAL array node
          stating the person has No Known Allergies if the person is not in the
          ART database.
       
      12) fixes a bug in the GMRANKA routine which may enter the wrong value in
          the ADVERSE REACTION ASSESSMENT file (#120.86), REACTION ASSESSMENT
          field (#1). NOIS: MAR-0696-21799.
       
      2) fixes a possible undefined variable error (GMRAREC) in the routine
         GMRASIG1.
       
      3) fixes a FOR loop which uses the wrong variable to loop through an
      
    • 12
      DATE APPLIED:   1998-11-04 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Allergies entered via CPRS were being entered into the ART database as
      unverified even if they met the criteria to be auto-verified in the ART
      site parameters. This patch will auto-verify those allergies entered via
      CPRS that meet the criteria as defined at the site.
      
    • 13
      DATE APPLIED:   1998-11-12 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch will make the ARTS software compatible with the National Drug
      File regardless of version.
      
    • 14
      DATE APPLIED:   1999-01-21 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      The METHOD OF NOTIFICATION field in file 120.84 is used to determine the
       
      DBIA #1471 has been retired which allowed ART to call ALLERGY^RAUTL3 in
      This patch corrects this error by changing the reference to use file 12d
      RADIOLOGY/NUCLEAR MEDICINE v 4.5 to retrieve and store information
      relating to allergies to radiologic contrast media. This reference is
      being removed from the ART software.
      users that should receive the chart and ID band marking bulletin. If this
      field is set to OE/RR TEAMS, the code made reference to PCMM team lists.
      CPRS has ceased use of PCMM teams for list functionality.   The errant
      reference to PCMM caused an error when a patient with data in the ADVERSE
      REACTION TRACKING (ART) database was admitted. The same error can be
      generated when a new adverse reaction is entered and the charts and/or ID
      bands have not been marked. patch corrects this error by changing the
      reference to use the OE/RR LIST (#100.21) file.
      
    • 16
      DATE APPLIED:   2001-01-03 00:00:00
      APPLIED BY:   USER,ONE
    • 17 SEQ #16
      DATE APPLIED:   2003-12-31 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch includes a utility for updating free text entries.  Please see
      the FORUM patch description for a detailed explanation of this patch.
      
    • 19 SEQ #17
      DATE APPLIED:   2004-07-02 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Update to allergy tracking package consisting of changes to the free text 
      utility distributed in patch GMRA*4*17 as well as updates to send 
      bulletins from CPRS GUI upon new allergy entry.  Please see the FORUM 
      module for complete details.
      
    • 18 SEQ #18
      DATE APPLIED:   2005-01-18 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch will install new cross-references on files 120.8, 120.85
      and 120.86 in support of the health data repository.  See the
      patch description on FORUM for complete details.
      
    • 22 SEQ #19
      DATE APPLIED:   2005-01-18 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      HDR related changes.  Please see FORUM patch description
      for details regarding this patch.
      
    • 21 SEQ #20
      DATE APPLIED:   2005-02-12 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Allergy updates required to support the removal of allergies
      as orders.  After installation of this patch and CPRS GUI v25,
      allergies will no longer be treated as orders.
       
      Please see the FORUM patch module for a complete description.
      
    • 23 SEQ #21
      DATE APPLIED:   2005-08-13 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch includes changes required for continued support
      of the Health Data Repository project.  Please see the national
      patch module for a full description of this patch.
      
    • 5
      DATE APPLIED:   1996-10-09 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      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
      
    • 24 SEQ #22
      DATE APPLIED:   2005-08-13 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      See FORUM patch module for a full description.  Updates HDR related
      trigger code.
      
    • 25 SEQ #23
      DATE APPLIED:   2005-09-05 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Update to fix blank sign/symptom issue.  Please see FORUM for the
      complete description of this patch.
      
    • 27 SEQ #24
      DATE APPLIED:   2005-09-05 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch will correct the reported problem of the allergy bulletin
      not being fired if the contrast media has a VA DRUG CLASS of DX109.
      
    • 30 SEQ #26
      DATE APPLIED:   2005-11-15 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Remedy ticket HD67463 was logged because the site noticed that deceased 
      patients were appearing on the [GMRA PRINT-PATIENT NOT ASKED] report.  
      This report lists patients who have not been given an allergy/adverse 
      reaction assessment.  The sites then use this list and contact the 
      patients in an attempt to get the assessment information from them.  It 
      is not desirable for the VA to inadvertently contact the family of a 
      deceased individual in an attempt to get the allergy/adverse reaction 
      information for that person.
      
    • 34 SEQ #29
      DATE APPLIED:   2006-04-10 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Updates to HL7 messaging for HDR.  See FORUM for a complete
      description.
      
    • 35 SEQ #30
      DATE APPLIED:   2006-08-07 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      POSSIBLE PROBLEM WITH LIST BY LOCATION UNASSESSED ALLERGIES.
      
    • 20 SEQ #31
      DATE APPLIED:   2006-09-23 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch updates the clean up utility to include ingredient based
      and drug class based allergies.  Please see FORUM for the complete
      description of this patch.
      
    • 36 SEQ #32
      DATE APPLIED:   2007-09-04 22:38:44
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Removes ability to delete existing allergy entries from the
      roll and scroll environment.
      Please see the FORUM patch module for a complete description.
      
    • 26 SEQ #33
      DATE APPLIED:   2007-09-04 23:07:28
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Remote Data Interoperability updates.  Please see FORUM for a full 
      description of the updates.
      
    • 37 SEQ #34
      DATE APPLIED:   2007-09-04 23:12:30
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Updates for RDI and contrast media
      Please see the FORUM patch description for full details.
      
    • 7 SEQ #5
      DATE APPLIED:   1997-06-02 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      GMRA*4.0*7  See National patch module for a description of the changes
      incorporated in this patch.
      
    • 29
      DATE APPLIED:   2007-09-04 23:47:20
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      Provides an auto-update for existing free text allergies
      
    • 40 SEQ #36
      DATE APPLIED:   2007-12-12 22:04:07
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch reviews updates made in patch GMRA*4*29 related
      to terms that begin with the text ANGIOTEN and assures that
      they were correctly updated.  A few ANGIOTEN entries were
      incorrectly updated to the wrong drug class and need to be
      updated to the correct drug class.
      
    • 33 SEQ #37
      DATE APPLIED:   2008-07-22 08:06:57
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      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.
         
      
    • 38
      DATE APPLIED:   2009-04-21 15:49:38
      APPLIED BY:   USER,SEVENTEEN
    • 41 SEQ #39
      DATE APPLIED:   2009-04-22 12:22:54
      APPLIED BY:   USER,SEVENTEEN
      DESCRIPTION:   
      See GMRA*4*41 in the National Patch Module
      
    • 42 SEQ #40
      DATE APPLIED:   2009-06-24 14:41:02
      APPLIED BY:   USER,SEVENTEEN
      DESCRIPTION:   
      Fixes issue with historical allergy entries being associated with
      a progress note when the historical entry follows the entry of
      an observed drug reaction.
      Also, fixes issue with 0 node not being set correctly on XTMP node
      and provides failsafe for sending data to HDR.
      
    • 44 SEQ #41
      DATE APPLIED:   2011-03-03 11:30:43
      APPLIED BY:   USER,SEVENTEEN
    • 45
      DATE APPLIED:   2011-03-08 13:52:03
      APPLIED BY:   USER,SEVENTEEN
    • 47
      DATE APPLIED:   2014-04-07 17:24:03
      APPLIED BY:   USER,SEVENTEEN
      DESCRIPTION:   
      This is a companion patch to the Order Entry/Results Reporting (OE/RR) 
      version 3.0 software patch number 345 (OR*3.0*345). See the patch message
      for a full listing of issues addressed and installation instructions.
      
    • 43 SEQ #44
      DATE APPLIED:   2014-06-05 13:17:44
      APPLIED BY:   USER,SEVENTEEN
      DESCRIPTION:   
      The patch is to create a merge routine to check for allergy assessments 
      in Patients before the merge occurs.
      
    • 4
      DATE APPLIED:   1997-09-22 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This build fixes several problems in the ART portion of the ART-CPRS
       GMRAOR4
         The ART EP asked the CPRS developers to include the OBSERVER field
         value for all new reactions CPRS sends to the ART package. This routine
         was changed to recognize this piece of data when it is passed to ART.
       
       GMRAOR5
         Fixes a syntax error.
       
         Simplifies some code used to check for duplicate patient reactions.
       
      interface.
         Fixes a bug where the reaction was not completely filed if the reaction
         value pointer and file was not recognized as one of the five pointed-to
         files used by the ART package.
       
         Modifies the code to call GMRAOR9 to store any drug ingredients or drug
         classes if the reaction was of a drug type.
       
         Modifies the code to add an entry to File 120.85 only if the patient
         reaction was an observed drug reaction.
         
       
         Sends the reaction as unverified so it will appear on the
         list of reactions to be verified.
       
       GMRAOR7
         The sign/symptom data was not being stored in File 120.85 because a
         call to SIGN^GMRAOR6 was passing the variable GMRAL when it should send
         the array GMRAL.
       
       GMRAOR8
         This routine was modified to correct subfile numbers being set
      Routine changes:
         in fileman.
       
       GMRAOR9 
         This is a new routine which stores drug ingredients and/or drug classes
         for a patient drug reaction.
       
       GMRAOR0
         The DUPCHK entry point was quitting prematurely and therefore not
         accurately checking for duplicate entries.
       
      
    • 48 SEQ #45
      DATE APPLIED:   2016-05-26 15:47:43
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      This patch installs a tool that will assist sites in ensuring that the 
      ADVERSE REACTION ASSESSMENT file (#120.86) is synced with the PATIENT 
      ALLERGIES file (#120.8).  See the associated patch description for 
      additional details and installation instructions.
      
    • 46
      DATE APPLIED:   2016-05-26 15:49:10
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      UPDATES ADVERSE REACTION TRACKING TO RETURN SIGN/SYMPTOM DATA WITH 
      COMPUTERIZED PATIENT RECORD SYSTEM (CPRS) ORDER CHECK MESSAGES AND TO 
      INLUCDE HEALTH DATA REPOSITORY (HDR) DATA WITH THE EN1^GMRADPT 
      APPLICATION PROGRAMMING INTERFACE (API). REFER TO THE PATCH DESCRIPTION 
      FOR ADDITIONAL INFORMATION.
      
    • 52 SEQ #47
      DATE APPLIED:   2016-07-13 12:59:07
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      This patch is a follow-up patch to GMRA*4*46. See the associated patch 
      description for details on this patch.
      
    • 49 SEQ #48
      DATE APPLIED:   2016-08-15 12:39:08
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      Patch GMRA*4.0*49 addresses the following two issues:
       
      1. Excessive number of entries in the PATIENT ALLERGIES file (#120.8)
         causes issues with the allergy HL7 messages.
       
      2. Embedded carriage returns in some old allergy HL7 messages prevented 
         the messages from being sent.
      
    • 50 SEQ #49
      DATE APPLIED:   2016-12-01 15:48:04
      APPLIED BY:   USER,FIFTYFOUR
    • 55 SEQ #50
      DATE APPLIED:   2017-05-30 16:08:55
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      See National Patch Module for details.
      
    • 54 SEQ #51
      DATE APPLIED:   2017-12-27 13:46:40
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      Patch GMRA*4.0*54 addresses the following three issues:
       
      1. FDA report SUBSCRIPT error with non-VA drugs 
       
      2. Adverse Reaction Assessment update when no previous Reaction 
         Assessment value
       
      3. Allergy file allows MECHANISM to be null
      
    • 58 SEQ #52
      DATE APPLIED:   2018-11-02 15:31:07
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      This patch has the following enhancements for Clinical Ancillary Services
         the Drug code of "D", as no action was needed to be taken for this
         scenario.
      (CAS) Enhancements (RXSU2).
       
      1. Suppress Non-Drug Ingredient-Level Alert
       
         Previously released patch GMRA*4*50 added a new alert when the DRUG 
         CLASSES field (#3) in the PATIENT ALLERGIES file (#120.8) is empty.  
         This patch will add a filter, to ignore those alerts, where ALLERGY
         TYPE field (#3.1) in PATIENT ALLERGIES file (#120.8), does not contain
      
    • 59 SEQ #53
      DATE APPLIED:   2018-12-04 15:44:22
      APPLIED BY:   USER,FIFTYFOUR
      DESCRIPTION:   
      This patch addresses NSR 20171203. See the Forum patch description for
      additional details.
      
    • 60 SEQ #54
      DATE APPLIED:   2019-10-03 15:50:37
      APPLIED BY:   USER,SIXTYFIVE
      DESCRIPTION:   
      IEN MISMATCH ISSUE
      
    • 6 SEQ #7
      DATE APPLIED:   1997-10-06 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      The Description of this build can be found in the Nation Patch Module
      under patch GMRA*4.0*6
      
    • 53
      DATE APPLIED:   2020-06-24 12:14:43
      APPLIED BY:   USER,SIXTYFIVE
      DESCRIPTION:   
      This patch resolves issues identified during the testing of CPRS v31 as 
      well as post-release issues with recently released patches. See the patch 
      description for the list of issues resolved.
      
    • 62 SEQ #56
      DATE APPLIED:   2020-07-21 13:51:02
      APPLIED BY:   USER,SIXTYFIVE
      DESCRIPTION:   
      This patch addresses the following issue:
       
      1.      INC9435820 - WRONG URL IN AN ALLERGY OPTION
              When utilizing Menu Option GMRA ALLERGY FILE EDIT the user is
              presented with an incorrect URL (Uniform Resource Locator) or Web
              Page to be used when making their request.
      
    • 61 SEQ #57
      DATE APPLIED:   2020-09-23 15:42:24
      APPLIED BY:   USER,SIXTYFIVE
      DESCRIPTION:   
      This patch will resolve the following issue in the Clinical Procedures 
       
       
      Patient Safety Issues (PSIs):
      -----------------------------
      N/A
       
        
      Defect Tracking System Ticket(s) & Overview:
      --------------------------------------------
      1. INC8167520 - Cannot enter NKDA into the patient's allergy assessment.
      (CP) Flowsheet application.
       
      Problem 1:
      ----------
      If the user "up carats out" of the GMRA assessment utility prior to the 
      report running, the next time a user enters the utility it will appears 
      as though the report ran, even though it did not.
       
      Resolution 1:
      -------------
      Routine GMRAFA was modified to kill the ^XTMP("GMRAFAL") global if the 
       
      user exits before running the report. This will reset the option, 
      allowing the user to run the report.
      1.  INC8167520 - Cannot enter NKDA into the patient's allergy assessment.
       
       
      New Service Requests (NSRs):
      ----------------------------  
      N/A
      
    • 64 SEQ #58
      DATE APPLIED:   2021-01-29 09:22:28
      APPLIED BY:   USER,SEVENTEEN
      DESCRIPTION:   
      This patch addresses a post-release issue identified with patch 
      GMRA*4*53, part of the CPRS v31b release. See the patch description for a 
      full explanation of the issue.
      
    • 63
      DATE APPLIED:   2021-07-01 11:28:00
      APPLIED BY:   USER,SEVENTEEN
    • 66b
      DATE APPLIED:   2021-07-01 00:00:00
      DESCRIPTION:   
      Backup of GMRA*4.0*66 on Jul 01, 2021
       
      Warning:  Installing this backup patch message will install older versions
      of routines and Build Components (options, protocols, templates, etc.).
      Please verify with the Development Team that it is safe to install.
      
    • 66 SEQ #60
      DATE APPLIED:   2021-07-01 11:30:22
      APPLIED BY:   USER,SEVENTEEN
      DESCRIPTION:   
      This patch will resolve the following issue:
                       that cannot be resolved with the Modify Assessment tool.
         INC17041569 - CPRS ERROR_unable to update allergies for ONE patient
         INC17069709 - Adverse Reaction Tracking - Allergy Assessment
         INC17072229 - Adverse Reaction Tracking - Allergy Assessment
        
      Defect Tracking System Ticket(s) & Overview:
      --------------------------------------------
      1) INC11926924 - MAD: GMRA*#*### not resolve: order appeared verified by nurse
                       in BCMA but CPRS it was found not to be.     
      Problem: 
        
      -------
      The Captain James A. Lovell Federal Health Care Center reported that they were
      unable to modify an allergy assessment for a specific patient using the
      Assessment clean up utility option [GMRA ASSESSMENT UTILITY]. After some 
      research it was discovered that when two patients were merged and the 'TO'
      patient (remaining patient after them merge) had not Allergy assessment while
      'FROM' patient (deleted after the merge) a corrupt record was being created
      for the 'TO' patient. These records could not be fixed using the Assessment
      clean utility option [GMRA ASSESSMENT UTILITY].
           
      1) INC17497887 - UNABLE TO MODIFY AN ALLERGY ASSESSMENT USING THE VISTA
      Resolution:
      ----------
      The root of the problem is within the Kernel Patient Merge module. However we
      were able to address the problem by modifying GMR code specifically designed
      to run right before two patients are merged. The solution applied consisted of
      copying the 'FROM' Allergy assessment information to 'TO' before the patient
      merge were performed by the Kernel Patient Merge utility. In addition to
      fixing this problem so no new entries are affected this patch also fixes the
      existing entries with the problem through a post-install routine that is
      described below.
         (HITPS-7808)  ASSESSMENT CLEANUP UTILITY ECN 74075
        
      Technical Resolution:
      --------------------
      Modified the routine XMRAMRG by adding right at the beginning of the ASSESS
      tag code to identify whether the 'FROM' patient had an allergy assessment in
      the ADVERSE REACTION ASSESSMENT file (#120.86) and the 'TO' patient did not.
      If that's the case for the patient par being merged the new code will copy the
      'FROM' patient allergy assessment and create an identical assessment for the
      'TO' patient in the ADVERSE REACTION ASSESSMENT file (#120.86). This will
      effectively prevent the Kernel Patient Merge Utility from creating a corrupt
         Duplicate:
      entry for the 'TO' patient. 
         -----------
         INC16946767 - allergy info being displayed differently (incorrectly) in
                       different areas of Vista/CPRS
         INC17041102 - Adverse Reaction Tracking-Allergy Assessment; 3 Discrepancies
      
    • 51
      DATE APPLIED:   2022-10-05 14:55:07
      APPLIED BY:   USER,EIGHTYNINE
      DESCRIPTION:   
      Please refer to the patch description for contents and detailed 
      information.
      
    • 70 SEQ #63
      DATE APPLIED:   2023-12-15 13:21:09
      APPLIED BY:   USER,EIGHTYNINE
      DESCRIPTION:   
      This patch will resolve the following issue:
       
      <SUBSCRIPT>DRUG+95^GMRAOR *ITEMS() Subscript 1 > 511
        
      It was reported that a hard error was encountered when the reporting 
      site, using CPRS, placed an inpatient medication order for hydroxyzine 
      for a patient that has noted severe allergic reactions to hydroxyzine. 
      The error caused CPRS to shut down and prevented the user from further 
      processing the order. 
       
      The error encountered is as follows: 
      
    • 68 SEQ #64
      DATE APPLIED:   2024-01-25 11:57:42
      APPLIED BY:   USER,EIGHTYNINE
      DESCRIPTION:   
      Please see forum for a complete description of patch GMRA*4.0*68.
      
    • 8
      DATE APPLIED:   1998-01-09 00:00:00
      APPLIED BY:   USER,ONE
    • 9
      DATE APPLIED:   1998-05-11 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      This patch will update the mark chart/id band option to use
      the new ACRP APIs that become available with patch SD*5.3*131.
      Please see the national patch module for a full description of
      this patch as well as patch 131.
      
    • 10 SEQ #10
      DATE APPLIED:   1998-10-26 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      See Description in the National Patch Module for Patch GMRA*4*10.
      
    • 11
      DATE APPLIED:   1998-10-26 00:00:00
      APPLIED BY:   USER,ONE
      DESCRIPTION:   
      The description of this build can be found in the National Patch Module 
      within the patch description of GMRA*4*11.
      
    DATE INSTALLED AT THIS SITE:   1996-07-15 00:00:00
    INSTALLED BY:   USER,ONE
    DESCRIPTION OF ENHANCEMENTS:   
    The Adverse Reaction Tracking package tracks patient allergies/adverse
    reactions.
    
DESCRIPTION
This package permits clinical users to track and report patient allergies
and adverse reactions. The intended users are physicians, nurses, other
clinicians and clerks.