Примери за използване на Polycythaemia vera на Английски и техните преводи на Български
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The recommended starting dose in polycythaemia vera is 10 mg twice daily.
In polycythaemia vera, the recommended starting dose is 10 mg twice a day.
Besremi is used as monotherapy for the treatment of polycythaemia vera in adults.
In polycythaemia vera treatment should also be stopped when haemoglobin levels are very low.
These actions may be involved in the therapeutic effects of interferon alfa in polycythaemia vera.
Polycythaemia vera in adults who are resistant or intolerant to treatment with the medicine hydroxyurea.
The recommended starting dose in polycythaemia vera is 10 mg twice daily, depending on your blood cell count.
Polycythaemia vera is a disorder of the bone marrow, in which the marrow produce too many red blood cells.
Besremi is indicated as monotherapy in adults for the treatment of polycythaemia vera without symptomatic splenomegaly.
In myelofibrosis and polycythaemia vera, there is too much JAK activity, leading to the abnormal production of blood cells.
A main study of 257 patients showed that Besremi is effective at reducing levels of red blood cells in patients with polycythaemia vera.
Besremi is a medicine used to treat polycythaemia vera in adults who do not have symptoms of an enlarged spleen.
In polycythaemia vera, the company will extend the main study to provide long-term data on the safety and effectiveness of Jakavi.
Jakavi is also used to treat patients with polycythaemia vera who are resistant to or intolerant of hydroxyurea.
Polycythaemia vera is rare, and Besremi was designated an‘orphan medicine'(a medicine used in rare diseases) on 9 December 2011.
Jakavi is indicated for the treatment of adult patients with polycythaemia vera who are resistant to or intolerant of hydroxyurea.
In patients with polycythaemia vera, the body produces too many red blood cells, which can cause the blood to thicken and reduce blood flow to the organs.
Following treatment-related adverse reactions were reported with ropeginterferon alfa-2b in clinical studies in 178 polycythaemia vera adult patients.
Polycythaemia vera is a type of cancer in which the bone marrow produces too many red blood cells, white blood cells and platelets(cells that help the blood to clot).
Besremi can only be obtained with a prescription andtreatment should only be started under the supervision of a doctor experienced in managing polycythaemia vera.
Besremi is effective at reducing the excessive number of blood cells in patients with polycythaemia vera, and the proportion of patients improving increased with longer treatment.
In polycythaemia vera the CHMP considered that Jakavi is of benefit to patients who do not respond or are intolerant to treatment with hydroxyurea, while the safety profile is acceptable.
An open label, randomised phase III study(PROUD-PV) evaluated the efficacy andsafety of ropeginterferon alfa-2b in comparison to hydroxycarbamide in 254 adult polycythaemia vera patients(randomisation 1:1).
In polycythaemia vera, 21%(23 out of 110) of patients given Jakavi showed an improvement after 8 months of treatment, compared with 1%(1 out of 112) of patients given the best available treatment.
An open-label, phase IIIb extension study(CONTINUATION-PV) enrolled 171 adult polycythaemia vera patients who previously completed the PROUD-PV Study to evaluate the long-term efficacy and safety of ropeginterferon alfa-2b.
Polycythaemia vera is a disease that mainly causes too many red blood cells to be produced, which can cause reduced blood flow to the organs due to‘thickening' of the blood and occasionally the formation of blood clots.
The European Medicines Agency has waived the obligation to submit the results of studies with Besremi in all subsets of the paediatric population in the treatment of polycythaemia vera(see section 4.2 for information on paediatric use).
In a clinical study in polycythaemia vera, the end of the mean individual titration phase for ropeginterferon alfa-2b was reached after approximately 3.7 months, for hydroxycarbamide after approximately 2.6 months of treatment.
Jakavi is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with primary myelofibrosis(also known as chronic idiopathic myelofibrosis),post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis.
In polycythaemia vera, the most common side effects with Jakavi(seen in more than 1 patient in 10) are thrombocytopenia(low blood platelet counts), anaemia(low red blood cell counts), bleeding, bruising, hypercholesterolaemia(high blood cholesterol levels), hypertriglyceridemia(high blood fat levels), dizziness, raised liver enzyme levels and high blood pressure.