[604] | 1 | English French Notes Complete/Exclude
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| 2 | patients found.
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| 3 | Select STATUS:
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| 4 | To list only those patients with this problem in a specific status, select:
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| 5 | BOTH ACTIVE & INACTIVE
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| 6 | Someone else is currently editing this file.
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| 7 | Missing problem narrative
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| 8 | Invalid patient
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| 9 | Invalid provider
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| 10 | Invalid problem
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| 11 | Patient does not match for this problem
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| 12 | Date Recorded is not editable
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| 13 | Cannot delete problem status
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| 14 | Date Resolved cannot be prior to Date of Onset
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| 15 | Date Recorded cannot be prior to Date of Onset
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| 16 | data item
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| 17 | Invalid ICD Diagnosis
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| 18 | Invalid Lexicon term
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| 19 | Duplicate problem
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| 20 | Invalid hospital location
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| 21 | Invalid problem status
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| 22 | Invalid Date of Onset
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| 23 | Invalid Date Resolved
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| 24 | Active problems cannot have a Date Resolved
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| 25 | Invalid Date Recorded
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| 26 | Invalid SC flag
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| 27 | Invalid AO flag
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| 28 | Invalid IR flag
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| 29 | Invalid EC flag
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| 30 | Invalid HNC flag
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| 31 | Invalid MST flag
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| 32 | DATA NAME
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| 33 | HEAD AND/OR NECK CANCER
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| 34 | No problems available.
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| 35 | OR WORKSTATION
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| 36 | PRN|
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| 37 | OR WINDOWS HFS
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| 38 | ICD-
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| 39 | AI/RHEUM
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| 40 | MeSH
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| 41 | TITLE 38
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| 42 | Select Problem(s)
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| 43 | Enter the problems you wish to
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| 44 | act on
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| 45 | , as a range or list of numbers
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| 46 | Select Problem
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| 47 | Enter the number of the problem you wish to
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| 48 | Are you sure you want to continue?
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| 49 | Enter YES if you want to duplicate this problem on this patient's list;
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| 50 | press <return> to re-enter the problem name.
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| 51 | is already an
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| 52 | ACTIVE problem on this patient's list!
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| 53 | Onset:
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| 54 | Resolved:
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| 55 | This problem is currently being edited by another user!
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| 56 | Enter YES to remove this value or NO to leave it unchanged.
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| 57 | Are you sure you want to remove this value?
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| 58 | + Next Screen - Prev Screen ?? More actions
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| 59 | ERROR -- Please check your Patient Files #2 and #9000001 for inconsistencies.
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| 60 | AO/IR/EC/HNC/MST
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| 61 | Enter YES to continue and add new problem(s) for this patient:
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| 62 | press <return> to select another action.
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| 63 | DATE OF DEATH:
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| 64 | Lastname,F
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| 65 | Enter the clinic to be associated with these problems, if available
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| 66 | Only clinics are allowed!
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| 67 | Select Specialty Subset:
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| 68 | GENERAL PROBLEM
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| 69 | Because many discipline-specific terms are synonyms to other terms,
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| 70 | they are not accessible unless you specify the appropriate subset of the
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| 71 | Clinical Lexicon to select from. Choose from: Nursing
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| 72 | Immunologic
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| 73 | Dental
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| 74 | Social Work
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| 75 | General Problem
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| 76 | GMRA*4.0*2
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| 77 | GMRA*4.0*2 has not been installed on your system. Done.
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| 78 | It does not appear that GMRA*4.0*2 was installed.
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| 79 | Please contact your IRM Field Office Customer Support Representative.
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| 80 | GMRA*4.0*5
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| 81 | GMRA*4.0*2 was installed on
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| 82 | Your current AUTOVERIFY site parameters are:
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| 83 | Site Parameter Name:
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| 84 | Autoverify Food/Drug/Other:
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| 85 | NO AUTOVERIFY
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| 86 | AUTOVERIFY DRUG ONLY
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| 87 | AUTOVERIFY FOOD ONLY
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| 88 | AUTOVERIFY DRUG/FOOD
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| 89 | AUTOVERIFY OTHER ONLY
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| 90 | AUTOVERIFY DRUG/OTHER
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| 91 | AUTOVERIFY FOOD/OTHER
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| 92 | AUTOVERIFY ALL
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| 93 | <none specified>
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| 94 | Autoverify Logical Operator:
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| 95 | Autoverify Observed/Historical:
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| 96 | AUTOVERIFY HISTORICAL ONLY
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| 97 | AUTOVERIFY OBSERVED ONLY
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| 98 | AUTOVERIFY BOTH
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| 99 | Want to stop (Y/N)
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| 100 | Answer YES to continue or NO to halt.
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| 101 | Since your site does not autoverify any reactions you can halt now.
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| 102 | Autoverify this reaction (Y/N)
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| 103 | Answer YES to mark this reaction as autoverified or NO to leave it unchanged.
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| 104 | Answering YES will change the ORIGINATOR SIGN OFF and VERIFIED fields to YES
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| 105 | and enter a date/time into the VERIFICATION DATE/TIME field (i.e., this will
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| 106 | mark the record as autoverified).
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| 107 | Answering NO will not change the record.
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| 108 | No unsigned reactions were found for the time period between the
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| 109 | installation of GMRA*4.0*2 and GMRA*4.0*5.
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| 110 | DO NOT USE DECIMAL VALUES.
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| 111 | 1 Current Inpatients
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| 112 | 2 Outpatients over Date/Time range
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| 113 | 3 New Admissions over Date/Time range
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| 114 | 4 All of the above
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| 115 | Enter the number(s) for those groups to be used in this report: (1-4):
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| 116 | ENTER THE NUMBER(S) FOR THOSE GROUPS TO BE INCLUDED IN THIS REPORT.
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| 117 | THIS RESPONSE MUST BE A LIST OR RANGE, E.G., 1,3 OR 2-3
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| 118 | Enter date/time range in which patients were
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| 119 | admitted into the hospital
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| 120 | seen at an outpatient clinic
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| 121 | Enter START Date (time optional):
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| 122 | ENTER THE START DATE/TIME OF RANGE TO SEE PATIENTS THAT WERE
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| 123 | ADMITTED TO THE HOSPITAL
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| 124 | SEEN AT AN OUTPATIENT CLINIC
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| 125 | Enter END Date (time optional): T//
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| 126 | ENTER THE END DATE/TIME OF RANGE TO SEE PATIENTS THAT WERE
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| 127 | Another
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| 128 | Do you mean ALL Locations
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| 129 | Enter Y for yes you mean ALL or N for no.
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| 130 | YOU HAVE ALREADY SELECTED:
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| 131 | TO STOP:
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| 132 | You may deselect from the list by typing a '-' followed by location name.
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| 133 | E.g. -3E would delete 3E from the list of locations already selected.
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| 134 | You may enter the word ALL to select all appropriate locations.
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| 135 | GMRA*
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| 136 | List of patients without ID band or Chart marked
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| 137 | Request queued...
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| 138 | Request NOT queued please try later...
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| 139 | ID BAND/CHART
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| 140 | ID BAND
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| 141 | PATIENTS WITH UNMARKED ID BAND/CHART
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| 142 | CURRENT INPATIENTS
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| 143 | NEW ADMISSIONS
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| 144 | / NEW ADMISSIONS
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| 145 | PLEASE ENTER 'Y' TO DELETE THE CAUSATIVE AGENT
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| 146 | 'N' NOT TO DELETE THE DATA
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| 147 | Do you wish to delete
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| 148 | Causative Agent
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| 149 | One moment please deleting data...
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| 150 | Fire Bulletin to Mark Patient Allergy DFN=
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| 151 | Allergy
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| 152 | Adverse Reaction
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| 153 | ALLERGY;0
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| 154 | PHARMACOLOGIC;2
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| 155 | UNKNOWN;U
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| 156 | ALLERGY;A
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| 157 | PHARMACOLOGIC;P
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| 158 | OTHER REACTION
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| 159 | PHARM
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| 160 | UNKNOWN
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| 161 | CAUSATIVE AGENT:
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| 162 | AGENT:
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| 163 | INGREDIENTS:
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| 164 | VA DRUG CLASSES:
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| 165 | ORIGINATOR:
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| 166 | ORIGINATED:
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| 167 | SIGN OFF:
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| 168 | OBS/HIST:
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| 169 | ID BAND MARKED:
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| 170 | CHART MARKED:
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| 171 | SIGNS/SYMPTOMS:
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| 172 | MECHANISM:
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| 173 | VERIFIER:
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| 174 | VERIFIED:
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| 175 | USER ENTERING
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| 176 | IN ERROR:
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| 177 | ALLERGY/ADVERSE REACTION DATA EXISTS FOR THIS PATIENT
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| 178 | HOWEVER, THERE IS DATA ENTERED IN ERROR ON FILE
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| 179 | PATIENT HAS ANSWERED NKA
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| 180 | BUT HAS
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| 181 | DATA ON FILE
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| 182 | ALLERGY/ADVERSE REACTION REPORTS
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| 183 | Select 1:DRUG, 2:FOOD, 3:OTHER
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| 184 | Type of allergy
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| 185 | Select 1:ACTIVE, 2:ENTERED IN ERROR
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| 186 | Which would you like to see?
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| 187 | This patient has No Known Allergies.
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| 188 | THERE IS NO DATA FOR THIS REPORT.
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| 189 | TYPE:
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| 190 | GMRA Print Complete List of Patient's Reactions
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| 191 | ALLERGY/ADVERSE REACTIONS TO BE SIGNED OFF
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| 192 | ORIGINATION DATE/TIME
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| 193 | GMRA-ALLERGY VERIFY
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| 194 | NO DATA FOR THIS REPORT
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| 195 | Patient reactions not signed off
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| 196 | ACTIVE ALLERGY/ADVERSE REACTION LISTING
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| 197 | OBS/
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| 198 | ADVERSE REACTION
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| 199 | NO ALLERGY/ADVERSE REACTION DATA EXISTS FOR THIS PATIENT
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| 200 | Patient has answered NKA.
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| 201 | No Data Found
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| 202 | Reactions:
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| 203 | This a print out of the allergies signed off for the patient
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| 204 | VER.
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| 205 | Press RETURN to continue or '^' to stop listing
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| 206 | Press RETURN to continue, '^' stop reactant listing.
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| 207 | OUT PATIENT
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| 208 | GMRA ENTERED IN ERROR
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| 209 | G.GMRA VERIFY
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| 210 | G.GMRA MARK CHART
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| 211 | No data for this REPORT.
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| 212 | PLEASE TRY LATER
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| 213 | Print FDA Exception Report
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| 214 | FDA EXCEPTION REPORT (
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| 215 | Starting at
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| 216 | ORIGINATION D/T
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| 217 | CAUSATIVE AGENT
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| 218 | This patient has No Known Allergies
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| 219 | This patient has no allergies on file
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| 220 | Enter the Date to start search (Time optional)
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| 221 | ENTER THE DATE YOU WANT THE SYSTEM TO START IT'S SEARCH
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| 222 | Select Start Date
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| 223 | Select End Date
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| 224 | YOU CAN ONLY EDIT DRUG REACTIONS
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| 225 | Indicate which FDA Report Sections to be completed:
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| 226 | 1. Reaction Information
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| 227 | 2. Suspect Drug(s) Information
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| 228 | 3. Concomitant Drugs and History
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| 229 | 4. Manufacturer Information
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| 230 | 5. Initial Reporter
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| 231 | Choose number(s) of sections to be edited
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| 232 | ENTER THE NUMBER SECTION OR SECTIONS YOU WISH TO COMPLETE.
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| 233 | YOU CAN ENTER: YOU TYPE SYSTEM WILL DO
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| 234 | THIS REPORT SHOULD BE SENT TO A 132 COLUMN PRINTER.
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| 235 | PLEASE TRY AGAIN LATER
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| 236 | Produce FDA Report for
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| 237 | ATTACHMENT PAGE
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| 238 | PATIENT ID:
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| 239 | SUSPECT MEDICATION:
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| 240 | DATE OF EVENT:
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| 241 | Section B. Part 5. Describe event Continued
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| 242 | Section B. Part 6. Relevant Test/Laboratory Data Continued:
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| 243 | TEST:
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| 244 | COLLECTION DATE:
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| 245 | Section B. Part 7. Other Relevant History Continued
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| 246 | Section C. Part 10. Concomitant Drugs Continued
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| 247 | Select Start Date/Time
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| 248 | Select End Date/Time
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| 249 | Do you want an Abbreviated report
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| 250 | ENTER
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| 251 | FOR YES OR
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| 252 | FOR NO
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| 253 | Print FDA Report by Date/Time
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| 254 | (SENT TO FDA:
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| 255 | FDA ABBREVIATED REPORT
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| 256 | SUSPECTED AGENT
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| 257 | D/T OF EVENT
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| 258 | MEDWatch
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| 259 | Approved by FDA on 10/20/93
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| 260 | THE FDA MEDICAL PRODUCTS REPORTING PROGRAM
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| 261 | | Triage unit sequence #
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| 262 | A. Patient Information
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| 263 | | C. Suspect Medication(s)
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| 264 | 1. Patient Indentifier|2. DOB:
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| 265 | B. Adverse Event or Product Problem
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| 266 | 1. [X]Adverse Event [ ]Product problem
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| 267 | |2. Dose,frequency & route used
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| 268 | | 3. Therapy dates
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| 269 | 2. Outcomes attributed to adverse event
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| 270 | ] congenital anomaly
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| 271 | ] congenital anomaly
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| 272 | ] required intervention to
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| 273 | |4. Diagnosis for use(indication)|5. Event abated after use
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| 274 | initial or prolonged prevent impairment/damage
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| 275 | | stopped or dose reduced?
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| 276 | 3. Date of event
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| 277 | |4. Date of this report
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| 278 | |6. Lot # (if known) |7. Exp. date|8. Event reappeared after
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| 279 | 5. Describe event or problem
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| 280 | SEE ATTACHED
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| 281 | |9. (Not applicable to adverse drug event reports)
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| 282 | 6. Relevant test/laboratory data. including dates
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| 283 | |10. Concomitant medical products/therapy dates(exclude treatment)
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| 284 | PLEASE SEE ATTACHED
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| 285 | |D. Suspect Medical Devices
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| 286 | 7. Other relevant History, including preexisting medical
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| 287 | | Note: Please use the actual MedWatch form if the event
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| 288 | | involves a suspected device as well as a suspect drug
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| 289 | Mail to: MedWatch or FAX to:
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| 290 | 5600 Fishers Lane 1-800-FDA-0178
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| 291 | |2. Health professional? |3. Occupation |4. Reported to Mfr.
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| 292 | |5. If you don't want your identity disclosed to the Manufacturer,
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| 293 | | place an
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| 294 | in the box.[
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| 295 | FDA Form 3500
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| 296 | 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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| 297 | Select a LOCAL ALLERGY/ADVERSE REACTION:
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| 298 | THIS ENTRY IS BEING EDITED BY SOMEONE ELSE
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| 299 | CANNOT EDIT NAME FIELD OF A NATIONAL ALLERGY.
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| 300 | Select a LOCAL SIGN/SYMPTOM:
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| 301 | (no editing)
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| 302 | NAME: HOSPITAL// (No editing)
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| 303 | #################### #################### ####################
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| 304 | #################### #################### ####################
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| 305 | #################### #################### ####################
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| 306 | #################### #################### ####################
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| 307 | #################### #################### ####################
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