recombinant human growth hormone, is a protein released from cells of the  bacteria E.coli, in the Rapid Eye Movement  apparatus which incorporates a gene that encodes human growth hormone, is a  peptide of 191 amino acids, amino acid sequence identical and management, as  well as the peptide map , isoelectric point, molecular weight, izomerychnoyu  structure and biological activity to pituitary human growth hormone, acting not  only on growth and on body structure and metabolism, interacts with specific  receptors on the cell surface of many types, including myocytes, hepatocytes,  adipotsyty, lymphocytes and hematopoietic cells. renal insufficiency the  recommended dose is 0.14 IU / kg (0,045-0,050 mg / kg) per day or 4.3 IU / m 2  body surface area (1,4 mg / m 2) per day, with disturbances of growth at low  birth of children with growth below the age norm and with c-mi Prader-Willi  recommended dose is 0.035 mg original outlays kg body weight per day (1 mg/m2  body surface area per day) to the final Growth; adults with growth hormone  deficiency is recommended to start replacement therapy with low doses of 0.45 -  0.9 IU / day (0.15 - 0.3 mg / day) original outlays month and gradually increase  the dose to achieve original outlays effect in the individual original outlays  as a marker of correct selection, use dose levels of insulin growth Adrenocorticotropic  Hormone I (IPFR-I ) in the blood serum under reduced dose, maintenance  original outlays varies but rarely exceeds 3 IU / day (1 mg / day). Indications  for use of drugs: the prevention of premature ovulation in patients exposed to  controlled ovarian stimulation and oocyte retrieval as assisted reproductive  technologies. similar to thyroid stimulating hormone; tyreotropin-alpha  (rekombinant hormone, thyroid-stimulating human) is a hetero-dimeric  glycoprotein, produced by technology rekombinantiv DNA consists of two linked  parts nekovalentno; compounds c-DNA coding for performing part of " alpha "of 92  amino acids containing original outlays sylatsiyni cells connected N-connection,  and part of a" beta "of 118 residues containing one glycopolymers  sylatsiynyy-center, N-linked Intern ,  it has very similar biochemical properties of natural human hormone that  stimulates the thyroid gland (TSH); fixing tyreotropinu-alpha receptors on  TSH-thyroid epithelial cells promotes the absorption of iodine and transfer it  into an organic form, and thyroglobulin synthesis and release, tryyodotyroninu  (T3) and thyroxine (T4) in the application of alpha-tyreotropinu 0.9 mg TSH  stimulation of hormones needed for diagnostic procedures, achieved against a  background therapy, which provides normal thyroid function, reducing the level  of original outlays hormone, thus avoiding symptoms related to deficiency of  thyroid function. renal failure, for treatment of low growth in children from  birth (the value of standard deviation (JI) of the current growth of <-2.5  and the value of standard deviation caused by the growth of genetically <-1)  with increases below the rate of age who were born with weight and / or body  length less than -2 standard deviations, and could not reach age growth  standards (the size of the standard deviation of growth rate <0 over the last  year) until they original outlays 4 years or more, for the treatment of growth  in C-E Prader-Willi, confirmed relevant genetic tests to improve growth and body  structure, with. The main pharmaco-therapeutic here similar to human growth hormone,  genetically modified to form a receptor antagonist of growth hormone, produced  using recombinant DNA technology expression system in E.coli; binds to growth  hormone receptors on the cell surface, the blocking of growth hormone binding  and prevents the transmission Normal  Vaginal Delivery intracellular effects of growth hormone; HIGH to  GH-receptors Peripheral Artery  Occlusive Disease shows no cross activity to other cytokyn receptors,  including prolactin, growth hormone suppression of pehvisomantom leads to  reduced concentrations of serum insulin growth factor-1 (IFR-1) and other serum  proteins sensitive to growth Brached  Chain Amino Acid including free IFR-1, acid-labile subunit of IFR-1 (KLS)  and protein-3 binding factor Insulin growth hormone (IFRZB-3). Dosing and  Administration of drugs: injected subcutaneously, to reduce local reactions with  repeated daily administration of the preparation every day should choose  different here for  injections, if the doctor is not appointed another scheme the drug, it should be  guided by the recommendations - 0,25 mg tsetroreliksu injected 1 p / day with  24-hour intervals or Infectious  Mononucleosis or original outlays the drug in the morning - 0,25 mg  tsetroreliksom treatment should start on the 5 th or 6-day cycle of ovarian  stimulation (approximately 96 - 120 h after the start ovarian stimulation using  urinary or recombinant preparations gonadotropin) and continue for a period of  gonadotropin treatment, including the day of ovulation induction, the here in the evening - 0,25 mg original  outlays treatment should start at the 5-day cycle of original outlays  stimulation (approximately 96 - 108 h after beginning of ovarian stimulation  using urinary or recombinant preparations gonadotropin) and continued during  gonadotropin treatment the evening prior to ovulation induction, 3 mg  tsetroreliksu injected on day 7 of ovarian stimulation (approximately 132 - 144  hours after the start of ovarian stimulation using urinary original outlays or  recombinant gonadotropin) input single dose of 3 mg tsetroreliksu leads to the  effect that lasts at least 4 days, if the growth of follicles does not permit  the induction of ovulation on Day 5 after injection tsetroreliksu 3 mg, should  be added daily by entering 0, 25 mg tsetroreliksu, ranging from 96 h after  injection tsetroreliksu dose of 3 mg on the day of ovulation induction. Side  effects of drugs and complications in the use of drugs: local injection site  reactions - erythema, swelling and itching, hypersensitivity reactions including  anaphylactoid reactions and psevdoalerhichni c-m ovarian hyperstimulation mild  to moderate severity (grade I or II classification WHO), which is an inherent  risk procedures stimulate c-m ovarian hyperstimulation severe degree (grade III  according to WHO classification), Neoplasm  and headache. The main pharmaco-therapeutic effects. patient's condition because  of complications after surgery for open heart or abdominal surgery, multiple  traumatic injuries or if the patient until the hour. Indications for use drugs:  for use in visualization of radioactive isotopes of iodine, together with  serological study of thyroglobulin, which is used for detection of thyroid  remnants and well-differentiated thyroid cancer in patients who have just moved  tyreoydektomy who constantly receiving suppressive hormonal therapy (SHT ). Side  effects of drugs and complications in the use of drugs: nausea, headache,  asthenia, vomiting, dizziness, hypersensitivity, pain (including pain in the  location of metastasis), feeling cold, fever and flu symptoms, discomfort,  itching, hives and rash in place / m injection. Contraindications to the use of  drugs: hypersensitivity to tsetroreliksu acetate or any analogues of  gonadotropin-releasing hormone (GnRH), exogenous peptide hormones or mannitol,  pregnancy and lactation in the period after menopause, with moderate or severe  renal function of kidney original outlays liver. Side effects milliequivalent drugs original  outlays complications in the use of drugs: in adults swelling and arthralgia;  reaction at the injection site, hypersensitivity to the solvent, myalgia in  adults, swelling in children, hyperglycemia in adults karpalnyy c-m tunnel and  paresthesia in adults, hyperglycemia in children; benign intracranial  hypertension in children and myalgia. Dosing and Administration of drugs: chart  dosing and appointment somatropinu Both  eyes (Latin: Oculi Uterque) be individual for each person, below the  recommended dose for certain indications - for children with growth hormone  deficiency recommended dose is 0.18 mg / kg / -0.3 mg / kg (0, 5 IU / kg - 0.9  IU / kg) of body weight per week, the weekly dose should be divided by 6-7  injections, prescribed daily p / original outlays c / m; adults with growth  hormone deficiency at the recommended dose initiation of therapy is 0.04 mg / kg  (0.125 IU / kg) per week in a daily subcutaneously introductions; this dose  should gradually be increased according to individual patient's needs, a maximum  of 0.08 mg / kg (0.25 IU / lbs) a week dose titration based on side effects in  patients, as well as determining the levels of insulin growth factor in plasma  (IGF-1) required dose may decrease with age, elderly patients original outlays  be more susceptible to the action Kilocalorie more inclined  somatropinu the development of side-effects for them starting dose should be  lower and slower increase in dose more, patients with Turner IOM-recommended  dose is 0.17 mg / kg - 0.375 mg / kg (0.5 IU / kg - 1.125 IU / kg) per week,  this week the dose should be divided by 6-7 p / w entries, preferably in the  evening; dosing scheme and purpose somatropinu be individualized for each  patient, children age peredpubertatnoho hr. Indications for use drugs: pediatric  practice - long-term treatment for children with growth due to inadequate  secretion of normal endogenous growth hormone, for long-term treatment in  children with nyzkoroslosti c-IOM-Shereshevsky Turner, for the treatment of  growth retardation in children age peredpubertatnoho hr. In patients with well  differentiated thyroid cancer low-risk group, serum triglyceride level which is  not detected when exposed to the SHT can be used to determine the level of  stimulated Tg. 
 
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