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<CourseDefinition>
  <Schema>
    <Version>3.0</Version>
    <Date>20120717</Date>
  </Schema>
  <Details>
    <RegimId>NRB-1429</RegimId>
    <Name>Rituximab-Idelalisib</Name>
    <ShortName/>
    <MajorVersion>1</MajorVersion>
    <MinorVersion>3</MinorVersion>
    <DefinitionStatus>COMPLETED</DefinitionStatus>
    <PatientMaxSurface/>
    <CourseICDZCode>NONE</CourseICDZCode>
    <CourseAUC>0.00</CourseAUC>
    <MaxAge/>
    <CycleLength/>
    <ValidForAllDiagnoses/>
    <IsStudyDefinition>NO</IsStudyDefinition>
    <PhysicianComment>Villkor för start av regimen: Infektionsprofylax mot pneumocystis ges i 6 månader efter avslutad behandling.\nRisk för reaktivering av cytomegalovirus (CMV), CMV monitorering rekommenderas.\n\nAnvisningar för ordination: Hydrering och behandling med Allopurinol bör ges inför behandlingsstart.\nIdelalisib - Uppmärksamhet på infektion, kolit, pneumonit och leverpåverkan. \nInteraktion kan ske med ett flertal läkemedel, se FASS.\nRituximab - Premedicinering med Paracetamol 1000 mg peroralt och Klemastin 2 mg intravenöst eller Cetrizin 10 mg peroralt. Steroider kan övervägas vid tidigare reaktion eller enligt lokal rutin.\nFörsta infusion av Rituximab ges enligt FASS. Efter komplikationsfri infusion kan resterande kurer ges på 30 minuter.\nFrån andra dosen kan Rituximab ges subkutant i dosen 1600 mg.\n\nEmetogenicitet:Medel.\n\nBehandlingsöversikt: Idelalisib ges dagligen peroralt 150 mg x 2. Rituximab ges med dos 375 mg/m2 dag 1, följt av 500 mg/m2 givet varannan vecka, 4 doser, och därefter var fjärde vecka, 3 doser (totalt 8 doser)..\n\nDiagnoskod: C91.1.\n\nBehandlingsavsikt: Remissionssyftande.\n\nBiverkningar för substanser i regimen\nrituximab\nAkut infusionsreaktion/anafylaxi(Infusionsrelaterade reaktioner mycket vanliga (symtom så som; feber, frossa, stelhet, angioödem, utslag, illamående, trötthet). Premedicinering minskar risken. Högst risk vid första infusionen. Se FASS för rekommenderad infusionshastighet vid första behandlingen. I övrigt följ instruktion respektive regim, det finns studier som visat bra säkerhet även vid infusioner på 30 minuter, om tolererat tidigare infusion på 90 minuter bra. \nAllvarligt cytokinfrisättningssyndrom (svår dyspné, bronkospasm, hypoxi) har rapporterats.\nHematologisk toxicitet(Hematologisk toxicitet kan vara behandlingsmålet (antalet B celler sjunker). \nNeutropeni förekommer, anemi och trombocytopeni har rapporterats. Oftast milda och reversibla.\nInfektionsrisk(Viss ökad infektionsrisk. Hepatit B reaktivering fallrapporter. Screening av förekomst av Hepatit B  ska utföras före behandlingsstart, se FASS. Hepatit B virus profylax, se FASS.\nGastrointestinal påverkan(Illamående vanligt, oftast grad 1-2. Kräkningar, diarré och dyspepsi förekommer till ovanligt, grad 1-2. Illamående och kräkningar kan vara en del av infusionsreaktionen.\nHjärttoxicitet(Kärlkramp, hjärtinfarkt och arytmier (så som förmaksflimmer och takykardi) har rapporterats.\nTumörlyssyndrom(Hyperurikemi kan uppstå till följd av snabb lys av tumörceller vid vissa sjukdomar under vissa förutsättningar (exempelvis vanligast i uppstartsbehandling). Viktigt att patient är väl hydrerad och har god diures. Vid hög tumörbörda skall Allopurinol ges. Vid behov kan antidoten rasburikas (Fasturtec) ges.\nCNS påverkan(Fallrapporter med progressive multifokal leukoencefalopati (PML) finns. Risk kan vara relaterad till tidigare kemoterapi. PML kan misstänkas vid nya eller försämrade neurologiska, kognitiva eller beteendemässiga tecken hos patienter (exempelvis: förändrat humör, minne, kognition, koordination, motorisk svaghet/pares, tal eller synrubbning), utred vid misstanke, se FASS.\nHudtoxicitet(Alopeci finns rapporterat vid kombination med andra antitumorala läkemedel. Fallrapporter finns om svåra hudreaktioner så som toxisk epidermal nekrolys (Lyells syndrom) och Stevens-Johnsons syndrom.\nExtravasering(Klassas som ej vävnadsskadande (låg eller minimal risk för vävnadsskada vid extravasering).\n\nrituximab\nAkut infusionsreaktion/anafylaxi(Infusionsrelaterade reaktioner mycket vanliga (symtom så som; feber, frossa, stelhet, angioödem, utslag, illamående, trötthet). Premedicinering minskar risken. Högst risk vid första infusionen. Se FASS för rekommenderad infusionshastighet vid första behandlingen. I övrigt följ instruktion respektive regim, det finns studier som visat bra säkerhet även vid infusioner på 30 minuter, om tolererat tidigare infusion på 90 minuter bra. \nAllvarligt cytokinfrisättningssyndrom (svår dyspné, bronkospasm, hypoxi) har rapporterats.\nHematologisk toxicitet(Hematologisk toxicitet kan vara behandlingsmålet (antalet B celler sjunker). \nNeutropeni förekommer, anemi och trombocytopeni har rapporterats. Oftast milda och reversibla.\nInfektionsrisk(Viss ökad infektionsrisk. Hepatit B reaktivering fallrapporter. Screening av förekomst av Hepatit B  ska utföras före behandlingsstart, se FASS. Hepatit B virus profylax, se FASS.\nGastrointestinal påverkan(Illamående vanligt, oftast grad 1-2. Kräkningar, diarré och dyspepsi förekommer till ovanligt, grad 1-2. Illamående och kräkningar kan vara en del av infusionsreaktionen.\nHjärttoxicitet(Kärlkramp, hjärtinfarkt och arytmier (så som förmaksflimmer och takykardi) har rapporterats.\nTumörlyssyndrom(Hyperurikemi kan uppstå till följd av snabb lys av tumörceller vid vissa sjukdomar under vissa förutsättningar (exempelvis vanligast i uppstartsbehandling). Viktigt att patient är väl hydrerad och har god diures. Vid hög tumörbörda skall Allopurinol ges. Vid behov kan antidoten rasburikas (Fasturtec) ges.\nCNS påverkan(Fallrapporter med progressive multifokal leukoencefalopati (PML) finns. Risk kan vara relaterad till tidigare kemoterapi. PML kan misstänkas vid nya eller försämrade neurologiska, kognitiva eller beteendemässiga tecken hos patienter (exempelvis: förändrat humör, minne, kognition, koordination, motorisk svaghet/pares, tal eller synrubbning), utred vid misstanke, se FASS.\nHudtoxicitet(Alopeci finns rapporterat vid kombination med andra antitumorala läkemedel. Fallrapporter finns om svåra hudreaktioner så som toxisk epidermal nekrolys (Lyells syndrom) och Stevens-Johnsons syndrom.\nExtravasering(Klassas som ej vävnadsskadande (låg eller minimal risk för vävnadsskada vid extravasering).\n\nidelalisib\nHematologisk toxicitet(Såvida hematologisk toxicitet inte är behandlingsmålet, följ dosreduktionsinstruktioner och/eller skjut upp nästa dos enligt vårdprogram eller lokala instruktioner.\nGastrointestinal påverkan(Diarré, illamående, buksmärta, nedsatt aptit och kräkningar. Läkemedelsrelaterad kolit vanligt, allvarliga fall finns. Kan uppstå sent, efter flera månader.\nHudtoxicitet(Utslag vanligt, oftast av mild till måttlig grad. Allvarliga hudreaktioner, inklusive Stevens Johnsons syndrom, har rapporterats när Idelalisib givits i kombination med andra antitumorala preparat.\nLevertoxicitet(Transaminas förhöjningar vanligt, kan bli allvarliga, men är enligt uppgift oftast asymptomatiska och reversibla och utan återfall om återstart på lägre dos av preparatet efter ett uppehåll, se FASS.\nAndningsvägar(Hosta vanligt. Övre luftvägsinfektion förekommer. Lunginflammation. Fallrapporter om pneumonit förekommer, överväg diagnos om allvarlig lunghändelse ej svarar på konventionell antimikrobiell behandling.\nInfektionsrisk(Allvarliga infektioner finns rapporterade, inklusive Pneumocystis jiroveci pneumoni, varför profylax mot Pneumocystis jiroveci skall ges till alla patienter under hela behandlingen.\nInteraktionsbenägen substans(Samtidig behandling med CYP3A-substrat med allvarliga biverkningar bör undvikas (Alfuzosin, Amiodaron, Cisaprid, Pimozid, Kinidin, Ergotamin, Dihydroergotamin, Quetiapin, Lovastatin, Simvastatin, Sildenafil, Midazolam och Triazolam).\nSamtidig behandling med CYP3A-inducerare kan ge minskad effekt av Idelalisib och bör därför undvikas (Rifampicin, Fenytoin, Johannesört och Karbamazepin).\n</PhysicianComment>
    <NurseComment>Villkor och kontroller för administration: Idelalisib - Missad dos med mindre än 6 timmar - den missade dosen tas snarast möjligt.\nMissad dos med mer än 6 timmar - dosen hoppas över och därefter följs det vanliga doseringsschemat.\n\nInformation från basfakta för substanser i regimen\nidelalisib\nDosering i förhållande till måltid: Tas med eller utan mat vid ungefär samma tidpunkt varje dag\n\n</NurseComment>
    <PharmacistComment/>
    <PatientComment/>
    <ExternalDocumentation/>
    <ExternalPhysicianDoc>https://kunskapsbanken.cancercentrum.se/redirect/regim/1429</ExternalPhysicianDoc>
    <ExternalNurseDoc>https://kunskapsbanken.cancercentrum.se/redirect/regim/1429</ExternalNurseDoc>
    <ExternalPharmacistDoc/>
    <ExternalPatientDoc/>
    <Rounding/>
    <HasSteps/>
  </Details>
  <Miscellaneous>
    <OriginOfExport>Regimbiblioteket</OriginOfExport>
    <IsAuthorized/>
    <CommittedBy/>
    <CreatedBy/>
    <CreatedDate>20260211</CreatedDate>
  </Miscellaneous>
  <Sideeffects>
    <Substance Name="rituximab">
      <Observandum Name="Akut infusionsreaktion/anafylaxi" Tillagg="Infusionsrelaterade reaktioner mycket vanliga (symtom så som; feber, frossa, stelhet, angioödem, utslag, illamående, trötthet). Premedicinering minskar risken. Högst risk vid första infusionen. Se FASS för rekommenderad infusionshastighet vid första behandlingen. I övrigt följ instruktion respektive regim, det finns studier som visat bra säkerhet även vid infusioner på 30 minuter, om tolererat tidigare infusion på 90 minuter bra. \nAllvarligt cytokinfrisättningssyndrom (svår dyspné, bronkospasm, hypoxi) har rapporterats.">
        <Control Name="Puls">
          <SupportingTreatment Name="Paracetamol"/>
        </Control>
        <Control Name="Blodtryck">
          <SupportingTreatment Name="Antihistamin"/>
          <SupportingTreatment Name="Kortikosteroid"/>
        </Control>
      </Observandum>
      <Observandum Name="Hematologisk toxicitet" Tillagg="Hematologisk toxicitet kan vara behandlingsmålet (antalet B celler sjunker). \nNeutropeni förekommer, anemi och trombocytopeni har rapporterats. Oftast milda och reversibla.">
        <Control Name="Blodvärden">
          <SupportingTreatment Name="Enligt lokala riktlinjer"/>
        </Control>
      </Observandum>
      <Observandum Name="Infektionsrisk" Tillagg="Viss ökad infektionsrisk. Hepatit B reaktivering fallrapporter. Screening av förekomst av Hepatit B  ska utföras före behandlingsstart, se FASS. Hepatit B virus profylax, se FASS.">
        <SupportingTreatment Name="Infektionsbehandling/profylax"/>
      </Observandum>
      <Observandum Name="Gastrointestinal påverkan" Tillagg="Illamående vanligt, oftast grad 1-2. Kräkningar, diarré och dyspepsi förekommer till ovanligt, grad 1-2. Illamående och kräkningar kan vara en del av infusionsreaktionen."/>
      <Observandum Name="Hjärttoxicitet" Tillagg="Kärlkramp, hjärtinfarkt och arytmier (så som förmaksflimmer och takykardi) har rapporterats.">
        <Control Name="EKG"/>
      </Observandum>
      <Observandum Name="Tumörlyssyndrom" Tillagg="Hyperurikemi kan uppstå till följd av snabb lys av tumörceller vid vissa sjukdomar under vissa förutsättningar (exempelvis vanligast i uppstartsbehandling). Viktigt att patient är väl hydrerad och har god diures. Vid hög tumörbörda skall Allopurinol ges. Vid behov kan antidoten rasburikas (Fasturtec) ges.">
        <Control Name="Urat">
          <SupportingTreatment Name="Hydrering"/>
          <SupportingTreatment Name="Allopurinol"/>
        </Control>
      </Observandum>
      <Observandum Name="CNS påverkan" Tillagg="Fallrapporter med progressive multifokal leukoencefalopati (PML) finns. Risk kan vara relaterad till tidigare kemoterapi. PML kan misstänkas vid nya eller försämrade neurologiska, kognitiva eller beteendemässiga tecken hos patienter (exempelvis: förändrat humör, minne, kognition, koordination, motorisk svaghet/pares, tal eller synrubbning), utred vid misstanke, se FASS."/>
      <Observandum Name="Hudtoxicitet" Tillagg="Alopeci finns rapporterat vid kombination med andra antitumorala läkemedel. Fallrapporter finns om svåra hudreaktioner så som toxisk epidermal nekrolys (Lyells syndrom) och Stevens-Johnsons syndrom."/>
      <Observandum Name="Extravasering" Tillagg="Klassas som ej vävnadsskadande (låg eller minimal risk för vävnadsskada vid extravasering)."/>
    </Substance>
    <Substance Name="rituximab">
      <Observandum Name="Akut infusionsreaktion/anafylaxi" Tillagg="Infusionsrelaterade reaktioner mycket vanliga (symtom så som; feber, frossa, stelhet, angioödem, utslag, illamående, trötthet). Premedicinering minskar risken. Högst risk vid första infusionen. Se FASS för rekommenderad infusionshastighet vid första behandlingen. I övrigt följ instruktion respektive regim, det finns studier som visat bra säkerhet även vid infusioner på 30 minuter, om tolererat tidigare infusion på 90 minuter bra. \nAllvarligt cytokinfrisättningssyndrom (svår dyspné, bronkospasm, hypoxi) har rapporterats.">
        <Control Name="Puls">
          <SupportingTreatment Name="Paracetamol"/>
        </Control>
        <Control Name="Blodtryck">
          <SupportingTreatment Name="Antihistamin"/>
          <SupportingTreatment Name="Kortikosteroid"/>
        </Control>
      </Observandum>
      <Observandum Name="Hematologisk toxicitet" Tillagg="Hematologisk toxicitet kan vara behandlingsmålet (antalet B celler sjunker). \nNeutropeni förekommer, anemi och trombocytopeni har rapporterats. Oftast milda och reversibla.">
        <Control Name="Blodvärden">
          <SupportingTreatment Name="Enligt lokala riktlinjer"/>
        </Control>
      </Observandum>
      <Observandum Name="Infektionsrisk" Tillagg="Viss ökad infektionsrisk. Hepatit B reaktivering fallrapporter. Screening av förekomst av Hepatit B  ska utföras före behandlingsstart, se FASS. Hepatit B virus profylax, se FASS.">
        <SupportingTreatment Name="Infektionsbehandling/profylax"/>
      </Observandum>
      <Observandum Name="Gastrointestinal påverkan" Tillagg="Illamående vanligt, oftast grad 1-2. Kräkningar, diarré och dyspepsi förekommer till ovanligt, grad 1-2. Illamående och kräkningar kan vara en del av infusionsreaktionen."/>
      <Observandum Name="Hjärttoxicitet" Tillagg="Kärlkramp, hjärtinfarkt och arytmier (så som förmaksflimmer och takykardi) har rapporterats.">
        <Control Name="EKG"/>
      </Observandum>
      <Observandum Name="Tumörlyssyndrom" Tillagg="Hyperurikemi kan uppstå till följd av snabb lys av tumörceller vid vissa sjukdomar under vissa förutsättningar (exempelvis vanligast i uppstartsbehandling). Viktigt att patient är väl hydrerad och har god diures. Vid hög tumörbörda skall Allopurinol ges. Vid behov kan antidoten rasburikas (Fasturtec) ges.">
        <Control Name="Urat">
          <SupportingTreatment Name="Hydrering"/>
          <SupportingTreatment Name="Allopurinol"/>
        </Control>
      </Observandum>
      <Observandum Name="CNS påverkan" Tillagg="Fallrapporter med progressive multifokal leukoencefalopati (PML) finns. Risk kan vara relaterad till tidigare kemoterapi. PML kan misstänkas vid nya eller försämrade neurologiska, kognitiva eller beteendemässiga tecken hos patienter (exempelvis: förändrat humör, minne, kognition, koordination, motorisk svaghet/pares, tal eller synrubbning), utred vid misstanke, se FASS."/>
      <Observandum Name="Hudtoxicitet" Tillagg="Alopeci finns rapporterat vid kombination med andra antitumorala läkemedel. Fallrapporter finns om svåra hudreaktioner så som toxisk epidermal nekrolys (Lyells syndrom) och Stevens-Johnsons syndrom."/>
      <Observandum Name="Extravasering" Tillagg="Klassas som ej vävnadsskadande (låg eller minimal risk för vävnadsskada vid extravasering)."/>
    </Substance>
    <Substance Name="idelalisib">
      <Observandum Name="Hematologisk toxicitet" Tillagg="Såvida hematologisk toxicitet inte är behandlingsmålet, följ dosreduktionsinstruktioner och/eller skjut upp nästa dos enligt vårdprogram eller lokala instruktioner."/>
      <Observandum Name="Gastrointestinal påverkan" Tillagg="Diarré, illamående, buksmärta, nedsatt aptit och kräkningar. Läkemedelsrelaterad kolit vanligt, allvarliga fall finns. Kan uppstå sent, efter flera månader."/>
      <Observandum Name="Hudtoxicitet" Tillagg="Utslag vanligt, oftast av mild till måttlig grad. Allvarliga hudreaktioner, inklusive Stevens Johnsons syndrom, har rapporterats när Idelalisib givits i kombination med andra antitumorala preparat."/>
      <Observandum Name="Levertoxicitet" Tillagg="Transaminas förhöjningar vanligt, kan bli allvarliga, men är enligt uppgift oftast asymptomatiska och reversibla och utan återfall om återstart på lägre dos av preparatet efter ett uppehåll, se FASS."/>
      <Observandum Name="Andningsvägar" Tillagg="Hosta vanligt. Övre luftvägsinfektion förekommer. Lunginflammation. Fallrapporter om pneumonit förekommer, överväg diagnos om allvarlig lunghändelse ej svarar på konventionell antimikrobiell behandling."/>
      <Observandum Name="Infektionsrisk" Tillagg="Allvarliga infektioner finns rapporterade, inklusive Pneumocystis jiroveci pneumoni, varför profylax mot Pneumocystis jiroveci skall ges till alla patienter under hela behandlingen."/>
      <Observandum Name="Interaktionsbenägen substans" Tillagg="Samtidig behandling med CYP3A-substrat med allvarliga biverkningar bör undvikas (Alfuzosin, Amiodaron, Cisaprid, Pimozid, Kinidin, Ergotamin, Dihydroergotamin, Quetiapin, Lovastatin, Simvastatin, Sildenafil, Midazolam och Triazolam).\nSamtidig behandling med CYP3A-inducerare kan ge minskad effekt av Idelalisib och bör därför undvikas (Rifampicin, Fenytoin, Johannesört och Karbamazepin)."/>
    </Substance>
  </Sideeffects>
  <Diagnoses>
    <Diagnose Text="Kronisk lymfatisk leukemi (KLL)"/>
  </Diagnoses>
  <Protocols/>
  <AdditionalInformation/>
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        <ConfirmationMandatory>NO</ConfirmationMandatory>
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            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
          </Details>
          <Substance Name="idelalisib">
            <Dose Max="">150</Dose>
            <Steps>0</Steps>
            <Unit>MG</Unit>
            <Calculation>STANDARD</Calculation>
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            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
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            <Unit>MG</Unit>
            <Calculation>STANDARD</Calculation>
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            <Volume/>
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          <Comments>
            <Comment Text="Premedicinering för rituximab"/>
          </Comments>
        </Line>
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            <Type>FLUID</Type>
            <Route>IVINF</Route>
            <InfusionHours>0</InfusionHours>
            <InfusionMinutes>0</InfusionMinutes>
            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
          </Details>
          <Fluid Name="Natriumklorid 9 mg/ml">
            <Volume>250</Volume>
            <Steps>0</Steps>
            <Unit>ML</Unit>
            <Calculation/>
          </Fluid>
          <Comments>
            <Comment Text="Spoldropp att fördelas mellan och efter sista läkemedlet"/>
          </Comments>
        </Line>
        <Line Number="4">
          <Details>
            <Type>ANTIDOTE</Type>
            <Route>PO</Route>
            <InfusionHours>0</InfusionHours>
            <InfusionMinutes>0</InfusionMinutes>
            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
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          <Substance Name="Antiemetika">
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          <Comments>
            <Comment Text="Tablett/Injektion Antiemetika"/>
          </Comments>
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        <Line Number="5">
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            <Type>SUBSTANCE</Type>
            <Route>IVINF</Route>
            <InfusionHours>0</InfusionHours>
            <InfusionMinutes>30</InfusionMinutes>
            <ProductionBy>PHARMACY</ProductionBy>
            <RelationType>NONE</RelationType>
          </Details>
          <Substance Name="rituximab">
            <Dose Max="">375</Dose>
            <Steps>0</Steps>
            <Unit>MG</Unit>
            <Calculation>SURFACE</Calculation>
          </Substance>
          <Fluid Name="Natriumklorid 9 mg/ml">
            <Volume>500</Volume>
            <Steps>0</Steps>
            <Unit>ML</Unit>
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        <Line Number="6">
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            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
          </Details>
          <Substance Name="idelalisib">
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            <Unit>MG</Unit>
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    </Day>
    <Day Number="2">
      <Details>
        <Name/>
        <ConfirmationMandatory>NO</ConfirmationMandatory>
        <Comment/>
      </Details>
      <CriticalParameters/>
      <Lines>
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            <Type>ANTIDOTE</Type>
            <Route>PO</Route>
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            <InfusionMinutes>0</InfusionMinutes>
            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
          </Details>
          <Substance Name="Antiemetika">
            <Dose Max="">0</Dose>
            <Unit>MG</Unit>
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            <Type>SUBSTANCE</Type>
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    <Day Number="139">
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        <Name/>
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        <Comment/>
      </Details>
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          </Details>
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            <Volume/>
            <Unit/>
            <Calculation/>
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            <Unit>MG</Unit>
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            <Volume/>
            <Unit/>
            <Calculation/>
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          </Details>
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            <Unit>MG</Unit>
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            <Volume/>
            <Unit/>
            <Calculation/>
          </Fluid>
          <Comments/>
        </Line>
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        <Name/>
        <ConfirmationMandatory>NO</ConfirmationMandatory>
        <Comment/>
      </Details>
      <CriticalParameters/>
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          </Details>
          <Substance Name="Antiemetika">
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            <Volume/>
            <Unit/>
            <Calculation/>
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            <Unit/>
            <Calculation/>
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            <Volume/>
            <Unit/>
            <Calculation/>
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    <Day Number="141">
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        <Name/>
        <ConfirmationMandatory>NO</ConfirmationMandatory>
        <Comment/>
      </Details>
      <CriticalParameters/>
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          <Details>
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            <ProductionBy>WARD</ProductionBy>
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            <Volume/>
            <Unit/>
            <Calculation/>
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            <Unit>MG</Unit>
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            <Volume/>
            <Unit/>
            <Calculation/>
          </Fluid>
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            <Comment Text="Premedicinering för rituximab"/>
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          <Details>
            <Type>FLUID</Type>
            <Route>IVINF</Route>
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            <InfusionMinutes>0</InfusionMinutes>
            <ProductionBy>WARD</ProductionBy>
            <RelationType>NONE</RelationType>
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            <Steps>0</Steps>
            <Unit>ML</Unit>
            <Calculation/>
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            <Comment Text="Spoldropp att fördelas mellan och efter sista läkemedlet"/>
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            <Unit/>
            <Calculation/>
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            <ProductionBy>PHARMACY</ProductionBy>
            <RelationType>NONE</RelationType>
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            <Unit>MG</Unit>
            <Calculation>SURFACE</Calculation>
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          </Substance>
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            <Volume/>
            <Unit/>
            <Calculation/>
          </Fluid>
          <Comments/>
        </Line>
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</CourseDefinition>
