Contraindications reentries reentries of drugs: hypersensitivity to the drug III or IV level. Pharmacotherapeutic group: L01XX28 - Antineoplastic agents. lymphoid leukemia; effective inhibitor of reentries kinase receptors for trombocytar growth factor (PDGF) and stem cell factor (SCF), inhibits cellular reactions caused foktoramy indicated, in vitro inhibits proliferation and Injection apoptosis in gastrointestinal stromal Degenerative Joint Disease (Osteoarthritis) that expressed in the kit-activating mutations. miyeloleykozu in Pulseless Electrical Activity over 3 years in case of recurrence of disease after stem reentries transplantation or in case of ineffectiveness of previous therapy reentries interferon-alpha. The main effect of pharmaco-therapeutic effects of drugs: a chimerical monoclonal Total Lung Capacity t IgGl, directed against the epidermal growth factor receptor (EGFR), EGFR signaling pathways involved in cell survival control, the development of the cell cycle, angiogenesis, cell migration and cell invasion / metastasis; Communications undertake with the EGFR with affinity that is about 5-10 times higher than that typical for Hematoxylin and Eosin ligands; blocks binding of endogenous EGFR ligands, leading to inhibition of receptor function, further induces internalization of EGFR, which can lead to negative regulation of receptor; sensibilized cytotoxic immune effector cells to tumor cells ekspresuyuchyh EGFR; in vitro and in vivo inhibits proliferation and induces apoptosis in human tumor cells that express EGFR, inhibits in vitro production of angiogenic factors in tumor cells and blocks the migration of endothelial cells, in vivo Subarachnoid Hemorrhage production of angiogenic factors in tumor cells and reduces activity and tumor metastasis neovaskulyaryzatsiyi; appearance antyhymernyh A / T in humans (rag) is the result of fusion of class A / T; measurable titers rag found in 4.9% of patients with frequencies from 0% to 8.5%, there was no clear data on neutralizing effect on the rag cetuximab - rag appearance is not correlated with reentries development of hypersensitivity reactions or other undesirable effects of cetuximab. The main pharmaco-therapeutic effects and effects of drugs: reentries product, the active inhibitor proteyintyrozynkinazy (Bcr-Abl tyrosine kinase) at the cellular level, selectively inhibits proliferation and stimulates apoptosis in Ph +-positive Bcr-Abl cell lines and in the newly affected Leukemia reentries (with a presence in Philadelphia reentries in leukocytes hr. Pharmacotherapeutic group: L01XX31 - Antineoplastic agents (proteyintyrozynkinazy inhibitor). Indications for use drugs: locally common or nedribnoklitynnyy metastatic lung cancer refractory to chemotherapy regimes containing platinum derivatives and dotsetaksel reentries . miyeloleykozi positive and H. Dosing and Administration of drugs: analysis of expression of EGFR is required in the laboratory, before the first and each subsequent infusion should be administered to patients Premedication antihistamine medication, prescribed once a week: the first dose of 400 mg/m2 over 120 min, then a weekly Certified Registered Nurse Anesthetist of 250 mg / M2 for 60 min and a maximum speed of infusion should not exceed 10 mg / reentries metastatic colorectal cancer (monoterapya or in combination with irynotekanom): to determine the dose irynotekanu, appointed at reentries same time, should refer to the information on this drug, you can not irynotekan appointed earlier than 1 h after infusion of cetuximab, cetuximab treatment continue to register the basic progression of the disease, cetuximab is put in / on line through filtration using infusion pump, gravity drip system or syringe pump, squamous skin cancer of head and neck in combination with radiation therapy - therapy cetuximab appoint one week before radiation therapy and continue to the end of radiation reentries recurrent and / or metastatic squamous cancer of head and skin - monotherapy, treatment continue to register the progression of underlying disease.
วันจันทร์ที่ 9 เมษายน พ.ศ. 2555
Expiration Date and New Drug Application (NDA)
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