In ibrutinib therapy, clinicians usually decide what dose of ibrutinib to use and the treatment cycle based on factors such as the patient's condition and constitution. When using ibrutinib, you should follow the doctor's advice and do not adjust the dose or stop the drug without authorization. At the same time, since ibrutinib may cause certain adverse reactions, such as rash and nausea, please pay close attention to the patient's physical condition, be aware of any abnormal reactions in the patient at any time, and contact the doctor in time for guidance.

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Gleevec is a medicine that contains an active substance called imatinib. This medication works by inhibiting the growth of abnormal cells in the diseases described below. These include some types of cancer.
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Imatinib is taken orally. The bioavailability of Gleevec when taken orally is more than 97% and is independent of age and food intake. Pharmacological studies have not found an effect of body weight on the concentration of Imatinib in plasma, so the drug is dosed regardless of this indicator. Imatinib is characterized by rapid absorption with maximum plasma concentrations 1-2 hours after administration. The half-life of the drug ranges from 18 to 22 hours, which allows it to be taken once a day. Approximately 96% of the drug is bound to plasma proteins, especially albumin and glycoproteins and, to a very small extent, lipoproteins.
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Enzalutamide was jointly developed by Pfizer and Astellas. It was approved by the US FDA on August 31, 2012 for the treatment of metastatic adenocarcinoma. For resistant prostate cancer, the drug is branded as XTANDI. The drug is an oral preparation and does not require genetic testing before use. It is available on doctor prescription. Visit us to know Enzalutamide cost- https://www.medixocentre.com/xtandi-cost

Ibrutinib is an antineoplastic drug used to treat chronic lymphocytic leukemia, mantle cell lymphoma. Ibrutinib is a small molecule that acts as an irreversible and potent inhibitor of Burton's tyrosine kinase. It is designated as a targeted covalent drug and has shown potential activity against B-cell malignancies in clinical trials.
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