Table des matières

Tags explanation

DateOfGeneration

FullPrescription

Prescription

Drug

DrugForm

DrugRoute

DrugStrength

DrugName

Composition

Dose

MealTime: meal time relation with intakes

Period:

Duration

Intake params

Textual drugs

Prints

When user selected the PDF cache printing function, the prescription file will contains all the session printed documents.

Tags/attributes are:

XML code

Version 0.6.0

<?xml version='1.0' encoding='UTF-8'?>
<!DOCTYPE FreeMedForms>
<FreeDiams>
  <DateOfGeneration version="2011-11-15T15:35:32"/>
 
    <Printed file="/abs/path/to/" 
             docName="file_uid.pdf" 
             dateTime="2010-11-03T10:31:42" 
             userUid="FreeDiamsUserUid"/>
    <Printed file="/abs/path/to/" 
             docName="file_uid.pdf" 
             dateTime="2010-11-03T10:46:23" 
             userUid="FreeDiamsUserUid"/>
 
  <FullPrescription version="0.6.0">
    <Prescription>
      <Drug u1="68166740" u2="" old="68166740" u3="" db="FR_AFSSAPS">
        <DrugForm>gélule à libération prolongée</DrugForm>
        <DrugRoute>orale</DrugRoute>
        <DrugStrength/>
        <DrugName>5-MONONITRATE D'ISOSORBIDE ETHYPHARM LP 40 mg, gélule à libération prolongée</DrugName>
        <Composition inn="ISOSORBIDE MONONITRATE" route="orale" form="gélule à libération prolongée" strength="40 mg/une gélule" nature="SA" natureLink="1" atc="C01DA14" molecularName="ISOSORBIDE (MONONITRATE D')"/>
      </Drug>
      <Dose MealTime="0" Period="1" DurationFromTo="false" RefDosage="7f553b43c98d470185181bbe1ffb3f3d" Daily="&lt;Distribute/>" DurationScheme="mois" INN="false" DurationFrom="1" IntakeIntervalScheme="3" IntakeFrom="1" IntakeIntervalTime="0" PeriodScheme="jour(s)" RouteId="48" IntakeScheme="gélule à libération prolongée" IntakeFromTo="false"/>
    </Prescription>
    <Prescription>
      <Drug u1="69422961" u2="" old="69422961" u3="" db="FR_AFSSAPS">
        <DrugForm>comprimé</DrugForm>
        <DrugRoute>orale</DrugRoute>
        <DrugStrength/>
        <DrugName>ACIDE ALENDRONIQUE ALMUS 70 mg, comprimé</DrugName>
        <Composition inn="ACIDE ALENDRONIQUE" route="orale" form="comprimé" strength="70 mg/un comprimé" nature="FT" natureLink="1" atc="M05BA04" molecularName="ACIDE ALENDRONIQUE"/>
        <Composition inn="ACIDE ALENDRONIQUE" route="orale" form="comprimé" strength="91,36 mg/un comprimé" nature="SA" natureLink="1" atc="M05BA04" molecularName="ALENDRONATE MONOSODIQUE TRIHYDRATÉ"/>
      </Drug>
      <Dose MealTime="0" Period="1" DurationFromTo="false" RefDosage="10c47af66d9041f8a80c988d8d0dcd10" Daily="&lt;Distribute/>" DurationScheme="mois" INN="false" DurationFrom="1" IntakeIntervalScheme="3" IntakeFrom="1" IntakeIntervalTime="0" PeriodScheme="jour(s)" RouteId="48" IntakeScheme="comprimé" IntakeFromTo="false"/>
    </Prescription>
    <Prescription>
      <Drug u1="61634827" u2="" old="61634827" u3="" db="FR_AFSSAPS">
        <DrugForm>poudre pour suspension buvable</DrugForm>
        <DrugRoute>orale</DrugRoute>
        <DrugStrength/>
        <DrugName>AMOXICILLINE ACIDE CLAVULANIQUE SANDOZ 100 mg/12,5 mg par ml ENFANTS, poudre pour suspension buvable en flacon (rapport amoxicilline/acide clavulanique : 8/1)</DrugName>
        <Composition inn="AMOXICILLINE" route="orale" form="poudre pour suspension buvable" strength="100 mg/1 ml de suspension reconstituée" nature="FT" natureLink="1" atc="J01CA04" molecularName="AMOXICILLINE BASE"/>
        <Composition inn="AMOXICILLINE" route="orale" form="poudre pour suspension buvable" strength="" nature="SA" natureLink="1" atc="J01CA04" molecularName="AMOXICILLINE TRIHYDRATÉE"/>
        <Composition inn="" route="orale" form="poudre pour suspension buvable" strength="12,50 mg/1 ml de suspension reconstituée" nature="FT" natureLink="2" atc="" molecularName="CLAVULANIQUE (ACIDE)"/>
        <Composition inn="" route="orale" form="poudre pour suspension buvable" strength="" nature="SA" natureLink="2" atc="" molecularName="CLAVULANATE DE POTASSIUM"/>
      </Drug>
      <Dose MealTime="0" Period="1" DurationFromTo="false" RefDosage="dfdd5947e63241e6a9d31e3018177f36" Daily="&lt;Distribute/>" DurationScheme="mois" INN="false" DurationFrom="1" IntakeIntervalScheme="3" IntakeFrom="1" IntakeIntervalTime="0" PeriodScheme="jour(s)" RouteId="48" IntakeScheme="poudre pour suspension buvable" IntakeFromTo="false"/>
    </Prescription>
  </FullPrescription>
</FreeDiams>

Version 0.4.x and 0.5.x

<?xml version='1.0' encoding='UTF-8'?>
<FreeDiams>
    <DateOfGeneration>2010-11-03T10:55:54</DateOfGeneration>
    <DrugsDatabaseName 
        version="versionOfDatabase"
        provider="databaseProvider"
        complementaryWebSite="webLink" 
        webLink="webLink" 
        packUidName="nameOfPack_UID" 
        compatWithFreeDiamsVersion="FreeDiamsVersion" 
        drugUidName="NameOfDrugs_UID" 
        date="DatabaseDate">FDA_US</DrugsDatabaseName>
 
    <Printed file="/abs/path/to/" 
             docName="file_uid.pdf" 
             dateTime="2010-11-03T10:31:42" 
             userUid="FreeDiamsUserUid"/>
    <Printed file="/abs/path/to/" 
             docName="file_uid.pdf" 
             dateTime="2010-11-03T10:46:23" 
             userUid="FreeDiamsUserUid"/>
 
    <FullPrescription version="0.4.0">
        <Prescription>
            <SpecifyPresentation/>
            <Drug_UID>40145001</Drug_UID>
            <DrugRoute>ORAL</DrugRoute>
            <OnlyForTest/>
            <IntakeIntervalTime>0</IntakeIntervalTime>
            <DurationFrom>1</DurationFrom>
            <DurationFromTo>false</DurationFromTo>
            <Pack_UID/>
            <Daily>&lt;Distribute/></Daily>
            <MealTime>0</MealTime>
            <SpecifyForm/>
            <Period>1</Period>
            <DrugForm>TABLET</DrugForm>
            <IsTextual>false</IsTextual>
            <IntakeIntervalScheme>3</IntakeIntervalScheme>
            <DrugStrength>1MG</DrugStrength>
            <IntakeFrom>1</IntakeFrom>
            <IntakeFullString/>
            <IntakeTo/>
            <DurationTo/>
            <IntakeFromTo>false</IntakeFromTo>
            <Note/>
            <IsAld/>
            <DurationScheme>mois</DurationScheme>
            <RefDosage>{c1bdad6d-5f1e-41cb-9fe8-43af4dc940fe}</RefDosage>
            <IntakeScheme>TABLET</IntakeScheme>
            <PeriodScheme>jour(s)</PeriodScheme>
            <DrugName>WARFARIN SODIUM (TABLET, 1MG)</DrugName>
            <INN>false</INN>
            <Composition inn="WARFARINE" route="ORAL" form="TABLET" 
                         strenght="1MG" nature="SA" natureLink="1"
                         molecularName="WARFARIN SODIUM"/>
        </Prescription>
        <Prescription>
            <Drug_UID>70575001</Drug_UID>
            <DrugRoute>INHALATION, ORAL</DrugRoute>
            <DrugName>MUCOSIL-10 (SOLUTION, 10%)</DrugName>
            <OnlyForTest>true</OnlyForTest>
            <DrugForm>SOLUTION</DrugForm>
            <DrugStrength>10%</DrugStrength>
            <Composition inn="ACETYLCYSTEINE" route="INHALATION, ORAL" form="SOLUTION" strenght="10%" nature="SA" natureLink="1" molecularName="ACETYLCYSTEINE"/>
        </Prescription>
    </FullPrescription>
    <ExtraDatas>
        <PatientDatas>
            <Lastnames>data</Lastnames>
            <HeightUnit>data</HeightUnit>
            <Height>data</Height>
            <Firstnames>data</Firstnames>
            <WeightUnit>data</WeightUnit>
            <UID>data</UID>
            <Creatinine>data</Creatinine>
            <Weight>data</Weight>
            <CreatinClearance>data</CreatinClearance>
            <DateOfbirth>data</DateOfbirth>
            <CreatinineUnit>data</CreatinineUnit>
            <Gender>data</Gender>
            <DrugsInnAllergies>data;data;data</DrugsInnAllergies>
            <DrugsUidAllergies>data;data;data</DrugsUidAllergies>
            <DrugsAtcAllergies>data;data;data</DrugsAtcAllergies>
            <DrugsUidIntolerances>data;data;data</DrugsUidIntolerances>
            <DrugsAtcIntolerances>data;data;data</DrugsAtcIntolerances>
        </PatientDatas>
        <EMR uid="SessionUIDWillBeReturnedInOutputFile" name="EMRName"/>
    </ExtraDatas>
</FreeDiams>
2010/09/27 12:09