308 lines
10 KiB
Plaintext
308 lines
10 KiB
Plaintext
English French Notes Complete/Exclude
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patients found.
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Select STATUS:
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To list only those patients with this problem in a specific status, select:
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BOTH ACTIVE & INACTIVE
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Someone else is currently editing this file.
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Missing problem narrative
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Invalid patient
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Invalid provider
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Invalid problem
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Patient does not match for this problem
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Date Recorded is not editable
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Cannot delete problem status
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Date Resolved cannot be prior to Date of Onset
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Date Recorded cannot be prior to Date of Onset
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data item
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Invalid ICD Diagnosis
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Invalid Lexicon term
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Duplicate problem
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Invalid hospital location
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Invalid problem status
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Invalid Date of Onset
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Invalid Date Resolved
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Active problems cannot have a Date Resolved
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Invalid Date Recorded
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Invalid SC flag
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Invalid AO flag
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Invalid IR flag
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Invalid EC flag
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Invalid HNC flag
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Invalid MST flag
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DATA NAME
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HEAD AND/OR NECK CANCER
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No problems available.
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OR WORKSTATION
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PRN|
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OR WINDOWS HFS
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ICD-
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AI/RHEUM
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MeSH
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TITLE 38
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Select Problem(s)
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Enter the problems you wish to
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act on
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, as a range or list of numbers
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Select Problem
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Enter the number of the problem you wish to
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Are you sure you want to continue?
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Enter YES if you want to duplicate this problem on this patient's list;
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press <return> to re-enter the problem name.
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is already an
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ACTIVE problem on this patient's list!
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Onset:
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Resolved:
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This problem is currently being edited by another user!
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Enter YES to remove this value or NO to leave it unchanged.
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Are you sure you want to remove this value?
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+ Next Screen - Prev Screen ?? More actions
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ERROR -- Please check your Patient Files #2 and #9000001 for inconsistencies.
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AO/IR/EC/HNC/MST
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Enter YES to continue and add new problem(s) for this patient:
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press <return> to select another action.
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DATE OF DEATH:
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Lastname,F
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Enter the clinic to be associated with these problems, if available
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Only clinics are allowed!
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Select Specialty Subset:
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GENERAL PROBLEM
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Because many discipline-specific terms are synonyms to other terms,
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they are not accessible unless you specify the appropriate subset of the
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Clinical Lexicon to select from. Choose from: Nursing
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Immunologic
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Dental
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Social Work
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General Problem
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GMRA*4.0*2
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GMRA*4.0*2 has not been installed on your system. Done.
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It does not appear that GMRA*4.0*2 was installed.
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Please contact your IRM Field Office Customer Support Representative.
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GMRA*4.0*5
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GMRA*4.0*2 was installed on
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Your current AUTOVERIFY site parameters are:
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Site Parameter Name:
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Autoverify Food/Drug/Other:
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NO AUTOVERIFY
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AUTOVERIFY DRUG ONLY
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AUTOVERIFY FOOD ONLY
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AUTOVERIFY DRUG/FOOD
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AUTOVERIFY OTHER ONLY
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AUTOVERIFY DRUG/OTHER
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AUTOVERIFY FOOD/OTHER
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AUTOVERIFY ALL
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<none specified>
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Autoverify Logical Operator:
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Autoverify Observed/Historical:
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AUTOVERIFY HISTORICAL ONLY
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AUTOVERIFY OBSERVED ONLY
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AUTOVERIFY BOTH
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Want to stop (Y/N)
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Answer YES to continue or NO to halt.
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Since your site does not autoverify any reactions you can halt now.
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Autoverify this reaction (Y/N)
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Answer YES to mark this reaction as autoverified or NO to leave it unchanged.
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Answering YES will change the ORIGINATOR SIGN OFF and VERIFIED fields to YES
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and enter a date/time into the VERIFICATION DATE/TIME field (i.e., this will
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mark the record as autoverified).
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Answering NO will not change the record.
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No unsigned reactions were found for the time period between the
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installation of GMRA*4.0*2 and GMRA*4.0*5.
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DO NOT USE DECIMAL VALUES.
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1 Current Inpatients
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2 Outpatients over Date/Time range
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3 New Admissions over Date/Time range
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4 All of the above
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Enter the number(s) for those groups to be used in this report: (1-4):
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ENTER THE NUMBER(S) FOR THOSE GROUPS TO BE INCLUDED IN THIS REPORT.
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THIS RESPONSE MUST BE A LIST OR RANGE, E.G., 1,3 OR 2-3
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Enter date/time range in which patients were
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admitted into the hospital
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seen at an outpatient clinic
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Enter START Date (time optional):
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ENTER THE START DATE/TIME OF RANGE TO SEE PATIENTS THAT WERE
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ADMITTED TO THE HOSPITAL
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SEEN AT AN OUTPATIENT CLINIC
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Enter END Date (time optional): T//
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ENTER THE END DATE/TIME OF RANGE TO SEE PATIENTS THAT WERE
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Another
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Do you mean ALL Locations
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Enter Y for yes you mean ALL or N for no.
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YOU HAVE ALREADY SELECTED:
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TO STOP:
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You may deselect from the list by typing a '-' followed by location name.
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E.g. -3E would delete 3E from the list of locations already selected.
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You may enter the word ALL to select all appropriate locations.
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GMRA*
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List of patients without ID band or Chart marked
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Request queued...
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Request NOT queued please try later...
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ID BAND/CHART
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ID BAND
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PATIENTS WITH UNMARKED ID BAND/CHART
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CURRENT INPATIENTS
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NEW ADMISSIONS
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/ NEW ADMISSIONS
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PLEASE ENTER 'Y' TO DELETE THE CAUSATIVE AGENT
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'N' NOT TO DELETE THE DATA
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Do you wish to delete
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Causative Agent
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One moment please deleting data...
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Fire Bulletin to Mark Patient Allergy DFN=
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Allergy
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Adverse Reaction
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ALLERGY;0
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PHARMACOLOGIC;2
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UNKNOWN;U
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ALLERGY;A
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PHARMACOLOGIC;P
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OTHER REACTION
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PHARM
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UNKNOWN
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CAUSATIVE AGENT:
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AGENT:
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INGREDIENTS:
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VA DRUG CLASSES:
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ORIGINATOR:
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ORIGINATED:
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SIGN OFF:
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OBS/HIST:
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ID BAND MARKED:
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CHART MARKED:
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SIGNS/SYMPTOMS:
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MECHANISM:
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VERIFIER:
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VERIFIED:
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USER ENTERING
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IN ERROR:
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ALLERGY/ADVERSE REACTION DATA EXISTS FOR THIS PATIENT
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HOWEVER, THERE IS DATA ENTERED IN ERROR ON FILE
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PATIENT HAS ANSWERED NKA
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BUT HAS
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DATA ON FILE
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ALLERGY/ADVERSE REACTION REPORTS
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Select 1:DRUG, 2:FOOD, 3:OTHER
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Type of allergy
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Select 1:ACTIVE, 2:ENTERED IN ERROR
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Which would you like to see?
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This patient has No Known Allergies.
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THERE IS NO DATA FOR THIS REPORT.
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TYPE:
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GMRA Print Complete List of Patient's Reactions
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ALLERGY/ADVERSE REACTIONS TO BE SIGNED OFF
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ORIGINATION DATE/TIME
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GMRA-ALLERGY VERIFY
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NO DATA FOR THIS REPORT
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Patient reactions not signed off
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ACTIVE ALLERGY/ADVERSE REACTION LISTING
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OBS/
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ADVERSE REACTION
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NO ALLERGY/ADVERSE REACTION DATA EXISTS FOR THIS PATIENT
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Patient has answered NKA.
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No Data Found
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Reactions:
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This a print out of the allergies signed off for the patient
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VER.
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Press RETURN to continue or '^' to stop listing
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Press RETURN to continue, '^' stop reactant listing.
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OUT PATIENT
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GMRA ENTERED IN ERROR
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G.GMRA VERIFY
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G.GMRA MARK CHART
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No data for this REPORT.
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PLEASE TRY LATER
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Print FDA Exception Report
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FDA EXCEPTION REPORT (
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Starting at
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ORIGINATION D/T
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CAUSATIVE AGENT
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This patient has No Known Allergies
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This patient has no allergies on file
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Enter the Date to start search (Time optional)
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ENTER THE DATE YOU WANT THE SYSTEM TO START IT'S SEARCH
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Select Start Date
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Select End Date
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YOU CAN ONLY EDIT DRUG REACTIONS
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Indicate which FDA Report Sections to be completed:
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1. Reaction Information
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2. Suspect Drug(s) Information
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3. Concomitant Drugs and History
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4. Manufacturer Information
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5. Initial Reporter
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Choose number(s) of sections to be edited
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ENTER THE NUMBER SECTION OR SECTIONS YOU WISH TO COMPLETE.
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YOU CAN ENTER: YOU TYPE SYSTEM WILL DO
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THIS REPORT SHOULD BE SENT TO A 132 COLUMN PRINTER.
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PLEASE TRY AGAIN LATER
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Produce FDA Report for
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ATTACHMENT PAGE
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PATIENT ID:
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SUSPECT MEDICATION:
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DATE OF EVENT:
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Section B. Part 5. Describe event Continued
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Section B. Part 6. Relevant Test/Laboratory Data Continued:
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TEST:
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COLLECTION DATE:
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Section B. Part 7. Other Relevant History Continued
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Section C. Part 10. Concomitant Drugs Continued
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Select Start Date/Time
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Select End Date/Time
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Do you want an Abbreviated report
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ENTER
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FOR YES OR
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FOR NO
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Print FDA Report by Date/Time
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(SENT TO FDA:
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FDA ABBREVIATED REPORT
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SUSPECTED AGENT
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D/T OF EVENT
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MEDWatch
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Approved by FDA on 10/20/93
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THE FDA MEDICAL PRODUCTS REPORTING PROGRAM
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| Triage unit sequence #
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A. Patient Information
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| C. Suspect Medication(s)
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1. Patient Indentifier|2. DOB:
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B. Adverse Event or Product Problem
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1. [X]Adverse Event [ ]Product problem
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|2. Dose,frequency & route used
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| 3. Therapy dates
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2. Outcomes attributed to adverse event
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] congenital anomaly
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] congenital anomaly
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] required intervention to
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|4. Diagnosis for use(indication)|5. Event abated after use
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initial or prolonged prevent impairment/damage
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| stopped or dose reduced?
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3. Date of event
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|4. Date of this report
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|6. Lot # (if known) |7. Exp. date|8. Event reappeared after
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5. Describe event or problem
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SEE ATTACHED
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|9. (Not applicable to adverse drug event reports)
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6. Relevant test/laboratory data. including dates
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|10. Concomitant medical products/therapy dates(exclude treatment)
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PLEASE SEE ATTACHED
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|D. Suspect Medical Devices
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7. Other relevant History, including preexisting medical
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| Note: Please use the actual MedWatch form if the event
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| involves a suspected device as well as a suspect drug
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Mail to: MedWatch or FAX to:
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5600 Fishers Lane 1-800-FDA-0178
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|2. Health professional? |3. Occupation |4. Reported to Mfr.
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|5. If you don't want your identity disclosed to the Manufacturer,
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| place an
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in the box.[
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FDA Form 3500
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Submission of a report does not constitute an admission that medical personnel or the product caused or contributed to the event.
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Select a LOCAL ALLERGY/ADVERSE REACTION:
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THIS ENTRY IS BEING EDITED BY SOMEONE ELSE
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CANNOT EDIT NAME FIELD OF A NATIONAL ALLERGY.
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Select a LOCAL SIGN/SYMPTOM:
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(no editing)
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NAME: HOSPITAL// (No editing)
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#################### #################### ####################
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#################### #################### ####################
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#################### #################### ####################
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#################### #################### ####################
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#################### #################### ####################
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