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I have essential thrombocytemia and have been on Hydrea for more than 5 years. The dosage differs from time to time, according to my blood tests. Actually I undergo blood tests every months since the time I was diagnosed with the disease. This is not the first thrombocytemia medication I am on, but this is by far the best one. With Hydrea I have least side effects and it provides excellent results on my platelets level. However I have some nausea and occasional headaches I feel much better with Hydrea than with any other med. I do hope that one day I will be able to find a more effective treatment that will help me conquer the illness but in general I am happy with Hydrea as it makes my quality of life so much higher. My doctor is also satisfied with the results we achieve when on Hydrea and he plans to continue this treatment course. I wish him lots of luck!)
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I have been taking varying doses of Hydrea for over 9 years to control Essential Thrombocythemia following a thrombotic event directly related to the ET. At the time of diagnosis, my platelet count was over 1,000,000 however under regular monitoring and occasional dose adjustment, I have been able to maintain a stable and normal ranged platelet count. Side effects have been negligible to date.
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These results also confirm that the benefits of hydroxyurea persist.
First, education of healthcare providers must be emphasized to ensure that accurate information is available to patients and families.
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Using this medicine for a long time may increase your risk of developing cancer of the blood (leukemia).
there were 21 episodes of laboratory toxicities leading to hydroxyurea withdrawal
hydroxyurea was restarted at lower doses if patients had a good response
An abbreviation for a chemotherapy combination used to treat some types of acute lymphoblastic leukemia (ALL) and non-Hodgkin lymphoma (NHL).
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Images were recorded using a charge-coupled video camera device (Hamamatsu) and a Sony SVHS SVO-9500 video recorder.
Given this, we agreed to include evidence obtained from expert testimony and studies analyzing barriers to the delivery of quality health care to patients with sickle cell disease.
An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell disease.
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One concern about this practice of designated donations from African-Americans donors to patients with SCD is that it may increase the incidence of transfusion-related graft versus host disease unless such blood is routinely irradiated.
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Patients in the new study were originally participants in the NHLBI's Multicenter Study of Hydroxyurea (MSH) in Sickle Cell Anemia.
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Subjects for this study will receive hydroxyurea therapy for accepted clinical indications, and will be treated per best clinical management using treatment algorithms established at St.
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