Примери за използване на High cumulative на Английски и техните преводи на Български
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Cardiac function must be carefully monitored in patients receiving high cumulative doses and in those with risk factors.
Additionally, bycatch in many areas causes high cumulative effects on seahorses, with an estimated 37 million individuals being removed annually over 21 countries.
The Agency had been asked to arbitrate on the removal of the contraindication for children andadolescents treated with high cumulative doses of cancer medicines called anthracyclines.
Heart function monitoring should be particularly severe in patients receiving high cumulative doses of the drug and in patients with risk factors for increased cardiotoxicity.
The Committee considered the data submitted by the MAH in relation to the objections raised on the lifting of the contraindication for Cardioxane in children andadolescents receiving high cumulative doses of anthracycline.
Monitoring of cardiac function must be particularly strict in patients receiving high cumulative doses and in patients with risk factors for increased cardiotoxicity.
However ANSM and the concerned Member States were unable to reach agreement on whether the contraindication could be removed just for children andadolescents treated with high cumulative doses of anthracyclines, and, on 31 January 2017.
Use sorafenib with caution in patients who have, or may develop prolongation of QTc, such as patients with a congenital long QT syndrome,patients treated with a high cumulative dose of anthracycline therapy, patients taking certain anti-arrhythmic medicines or other medicinal products that lead to QT prolongation, and those with electrolyte disturbances such as hypokalaemia, hypocalcaemia, or hypomagnesaemia.
The CHMP considers that the presented data support the removal of the contraindication for Cardioxane for the subset of paediatric population receiving high cumulative anthracycline doses(above 300mg/m2 of doxorubicin or equivalent).
Caution should be exercised with escalation of EPREX doses in patients with chronic renal failure since high cumulative epoetin doses may be associated with an increased risk of mortality, serious cardiovascular and cerebrovascular events.
Caution should be exercised with escalation of Aranesp doses in patients with chronic renal failure, since high cumulative epoetin doses may be associated with an increased risk of mortality, serious cardiovascular and cerebrovascular events.
Caution should be exercised with escalation of Silapo doses in patients with chronic renal failure, since high cumulative epoetin doses may be associated with an increased risk of mortality, serious cardiovascular and cerebrovascular events.
Caution should be exercised with escalation of Abseamed doses in patients with chronic renal failure since high cumulative epoetin doses may be associated with an increased risk of mortality, serious cardiovascular and cerebrovascular events.
Caution should be exercised with escalation of Retacrit doses in patients with chronic renal failure since high cumulative epoetin doses may be associated with an increased risk of mortality, serious cardiovascular and cerebrovascular events.
The grounds for the referral were the concerns of the UK that removing the contraindication in patients less than 18 years old receiving a high cumulative dose of anthracyclines was not justified given the remaining uncertainties regarding the safety and effectiveness of Cardioxane in this population, particularly given the previous decision of the CHMP regarding dexrazoxane medicines.
The risk is stronger in patients who have higher cumulative doses from multiple scans.
In patients receiving trastuzumab after completion of adjuvant chemotherapy,the risk of cardiac dysfunction was associated with a higher cumulative dose of anthracycline given prior to initiation of trastuzumab and a body mass index(BMI)> 25 kg/m2.
A tendency towards increased risk estimates for all-cause mortality, cardiovascular andcerebrovascular events associated with higher cumulative ESA doses independent of the diabetes or dialysis status was observed(see sections 4.2 and 4.4).
A tendency towards increased risk estimates for all-cause mortality, cardiovascular andcerebrovascular events associated with higher cumulative ESA doses independent of the diabetes or dialysis status was observed(see section 4.2 and section 4.4).
With higher cumulative doses of anthracyclines, studies(including several RCTS and non-randomised studies) have showed that DRZ could improve the surrogate cardiac markers and therefore reduce subclinical acute cardiotoxicity.
A tendency towards increased risk estimates for all-cause mortality, cardiovascular andcerebrovascular events associated with higher cumulative ESA doses independent of the diabetes or dialysis status was observed(see sections 4.2 and 4.4).
A tendency towards increased risk estimates for all-cause mortality, cardiovascular andcerebrovascular events associated with higher cumulative ESA doses independent of the diabetes or dialysis status was observed(see section 4.2 and section 4.4).
A tendency towards increased risk estimates for all-cause mortality, cardiovascular andcerebrovascular events associated with higher cumulative ESA doses independent of the diabetes or dialysis status was observed(see sections 4.2 and 4.4).
In patients receiving Herceptin after completion of adjuvant chemotherapy,the risk of cardiac dysfunction was associated with a higher cumulative dose of anthracycline given prior to initiation of Herceptin and a body mass index(BMI)> 25 kg/m2.
Although studies suggest there is nosafe dose of anthracycline, it is known that the risk of anthracycline induced cardiotoxicity increases with higher cumulative dosing; guidelines imply that above 250 mg/m2 there is sufficient cardiac risk to provide recommendations on lifelong surveillance1.
A tendency towards increased risk estimates for all-cause mortality, cardiovascular andcerebrovascular events associated with higher cumulative epoetin doses independent of the diabetes or dialysis status was observed(see sections 4.2 and section 4.4).