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Ketotifen is a typewrite of asthma medication which, when charmed every date and toughened along with other antiasthma medications, may slacken up on the frequency, severity, and duration of asthma symptoms or attacks in children. It may also leading to a reduction in daily requirements of other antiasthma medications. Ketotifen is not effective against the hindering or treatment of intense asthma attacks. Ketotifen works by inhibiting certain substances in the body that are known to compel swelling and symptoms of asthma.

Before starting the first bloodletting, the patient is prescribed antiplatelet drugs.

Before the first bloodletting procedure, patients are prescribed a number of studies aimed at determining hemoglobin levels, establishing the exact number of red blood cells, hematocrit, and also determining coagulation parameters. All these indicators are necessary for the correct calculation of the frequency of the procedure, the volume of blood withdrawn and the calculation of target indicators (especially hematocrit).

By the way, these same drugs are prescribed for use within several weeks after the end of the procedures.

Before the bloodletting itself, the patient is also prescribed the administration of rheopolyglucin with heparin to improve the aggregative state of the blood. Usually the procedures are carried out once every two days. Another more modern method of ketotifen pills polycythemia vera is cytopheresis. This procedure involves connecting the patient to a special device with cleaning filters. By catheterizing the veins of both arms, the patient’s circulatory system is closed on this device in such a way that blood from one vein enters the device, passes through filters and returns to the other vein. This device centrifuges the blood entering it and “weeds out” some of the red blood cells, returning the plasma to the patient. Thus, this device removes excess red blood cells from the bloodstream in patients with polycythemia vera.

As mentioned above, secondary polycythemia is cured when the main cause that caused the polycythemia is cured and eliminated. For hypoxic root causes of polycythemia, intensive oxygen therapy is prescribed, as well as elimination of the hypoxic factor, if any. For polycythemia that has developed as a result of infectious diseases, the infectious agent itself is first eliminated by prescribing antibiotics, and in case of loss of large volumes of fluid, replacement intravenous infusions of colloidal solutions are performed.

The prognosis of polycythemia directly depends on its type and timeliness of treatment. Polycythemia vera is a disease with a more severe prognosis. Due to the difficulties in its therapy and the constant increase in the number of red blood cells, such patients are forced to constantly continue courses of hemoexfusion therapy. In addition, these patients are at high risk of thromboembolic complications, stroke and arterial hypertension. The prognosis of secondary polycythemia depends on its primary disease. In addition, the effectiveness of its elimination depends on early diagnosis and adequate treatment.

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The information presented in this article is intended for informational purposes only and cannot replace professional advice and qualified medical care. If you have the slightest suspicion that you have this disease, be sure to buy zaditor online. Polycythemia is a chronic hemoblastosis, which is based on the unlimited proliferation of all myelopoiesis, predominantly erythrocyte. Clinically, polycythemia is manifested by cerebral symptoms (heaviness in the head, dizziness, tinnitus), thrombohemorrhagic syndrome (arterial and venous thrombosis, bleeding), microcirculatory disorders (chillness of the limbs, erythromelalgia, hyperemia of the skin and mucous membranes). Basic diagnostic information is obtained from the study of peripheral blood and bone marrow. To treat polycythemia, bloodletting, erythrocytapheresis, and chemotherapy are used.