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haematological monitoring
asins ainas kontrole
Ultimo aggiornamento 2024-04-14
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cytotoxicity and haematological monitoring
citotoksicitāte un hematoloģiskā kontrole
Ultimo aggiornamento 2024-04-14
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therefore, haematological monitoring of patients is indicated.
tādēļ nepieciešama pacientu hematoloģiska novērošana.
Ultimo aggiornamento 2024-04-14
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haematological monitoring should therefore be undertaken regularly.
tādēļ regulāri jāveic hematoloģiska uzraudzība.
Ultimo aggiornamento 2024-04-14
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the dose of siklos may then be increased again under close haematological monitoring.
tad siklos devu var atkal palielināt, vienlaikus veicot rūpīgu hematoloģisko rādītāju kontroli.
Ultimo aggiornamento 2024-04-14
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Attenzione: Questo allineamento potrebbe essere errato.
Eliminalo se ritieni che sia così.
haematological monitoring rosiglitazone treatment is associated with a dose-related reduction of haemoglobin levels.
asins ainas kontrole rosiglitazona terapija ir saistīta ar hemoglobīna līmeņa pazemināšanos kas atkarīga no devas.
Ultimo aggiornamento 2012-04-10
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treatment with tandemact therefore requires regular haematological monitoring (especially leucocytes and platelets).
tādēļ tandemact terapijas laikā ir regulāri jāpārbauda hematoloģiskie rādītāji (īpaši leikocītu un trombocītu skaits).
Ultimo aggiornamento 2024-04-14
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periodic haematological monitoring (especially leucocytes and thrombocytes) are required during treatment with avaglim.
avaglim terapijas laikā nepieciešams regulāri kontrolēt asins ainu (it īpaši leikocītus un trombocītus).
Ultimo aggiornamento 2017-04-26
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careful haematological monitoring (including white blood cell and platelet count, and haemoglobin) should be performed during therapy with myocet.
myocet terapijas laikā jāveic rūpīga hematoloģisko rādītāju kontrole (ieskaitot leikocītu un trombocītu skaitu, un hemoglobīna lielumu).
Ultimo aggiornamento 2017-04-26
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following routine haematological monitoring, the transdermal patch should only be applied to patients whose chemotherapy treatment is unlikely to be delayed in order to reduce the possibility of unnecessary exposure to granisetron.
pēc parastās hematoloģiskās kontroles transdermālo plāksteri drīkst uzlikt tikai tiem pacientiem, kam nav paredzama ķīmijterapijas atlikšana, lai samazinātu nevajadzīgas granisetrona iedarbības iespējamību.
Ultimo aggiornamento 2017-04-26
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under exceptional circumstances a maximum dose of 35 mg/ kg b. w. / day might be justified under close haematological monitoring (see section 4.4).
izņēmuma gadījumos, pieļaujama maksimālā deva, tas ir, 35 mg/ kg ķermeņa masas, vienlaikus veicot rūpīgu hematoloģisko rādītāju kontroli (skatīt apakšpunktu 4. 4.).
Ultimo aggiornamento 2012-04-10
Frequenza di utilizzo: 2
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