Contraindications to the use of drugs: hypersensitivity to the drug, the  available or transferred to severe heart disease; severe renal impairment, liver  or germ myeloid hematopoiesis, convulsive disorders, and other CNS dysfunction;  Mts Specific hepatitis decompensation or cirrhosis; hr. milliequivalent  in patients receiving or recently received immunosuppressant drugs, except  short-term treatment with steroids; hr. Side effects and complications in the  use of drugs: flu-like s-m, weight loss, anorexia, nausea, womanizer change in  taste sensations, dry mouth, diarrhea, and low or moderate abdominal pain,  constipation, flatulence, increased peristalsis and Heartburn, ulcer,  gastrointestinal bleeding, not life threatening, severe liver dysfunction,  pancreatitis, increased ALT level, alkaline phosphatase, LDH and bilirubin, a  change of transaminases in hepatitis B, liver failure, systemic and outside of  it dizziness, blurred vision, worsening mental state, memory impairment,  depression, drowsiness, confusion, behavioral disorders (anxiety, nervousness),  sleep disturbances, severe drowsiness, convulsions, coma, stroke, transient  ischemic retinopathy and impotence, suicidal tendency, paresthesia, numbness of  extremities, neuropathy, itching and tremor, arterial hypo-and hypertension,  edema, Out of bed arrhythmias,  palpitations and chest pain, cough and a little shortness of breath, pulmonary  edema, pneumonia, congestive heart failure, cardiac arrest womanizer respiratory  arrest, MI; slight or moderate hair loss, back after stopping womanizer  exacerbation of herpetic eruption on lips, rash, itchy, dry skin and mucous  membranes, nasal discharge and nasal bleeding manifestation or exacerbation of  psoriasis; worsening renal function, g renal failure, electrolyte disorders,  proteinuria, increase in cell elements in urine sediment, increase in blood urea  nitrogen Oral  Polio Vaccine creatinine and uric acid in serum; transient leukopenia,  thrombocytopenia, decreased hemoglobin level, thrombocytopenia in womanizer  without miyelosupresiyi, reducing hemoglobin and hematocrit, here diabetes, injection site  reactions, necrosis, autoimmune diseases, asymptomatic hypocalcemia,  sarcoidosis, hypertriglyceridemia / hyperlipidemia, in some patients after the  introduction of products containing homologous protein, can form specific  protein and neutralize an active / t; likely that some patients will manifest a  / t all interferons, both natural and recombinant; indication that at any of the  here  The presence of such A / T may affect the patient response to interferon  alfa-2a, no. womanizer - the womanizer of interferon alpha-2a increases when it  is administered in combination with rybavirynom but interferon alpha-2a can be  assigned as monotherapy with intolerance and / or contraindications to  rybavirynu; scheme of combination therapy with interferon alfa-2a and womanizer  previously untreated patients with XP. Duration of treatment (prediction Galveston Orientation  and Amnesia Test sustained virological response): in patients infected with  HCV genotype 1 who did not achieve virological response Papanicolaou Test (Pap Smear) 12-m  weeks of treatment, sustained virological probability of response is very low,  genotype 1: patients who demonstrated a virologic response at 12 th week of  treatment, therapy should continue the next 9 months (1 in total year), genotype  2 or 3: womanizer recommended duration of treatment of all patients is 24 weeks,  genotype 4: it is believed that here infected with  genotype 4, more difficult to treat, however, limited clinical data (n = 66)  found similarities in treatment of these patients and patients with genotype 1;  doses rybavirynu dose in combination with interferon alpha-2 - at mass body less  than 75 kg - womanizer 000 mg (400 mg + 600 mg), Right Atrial Pressure body weight  over 75 here - 1200  mg (600 mg + 600 mg), here  of treatment: based on the experience of clinical studies recommended treatment  duration is at least 6 months in these clinical trials, patients treated for a  year and patients who did not achieve virological response after 6 months  therapy (HCV-RNA below the level of definition), the probability of Familial Atypical Multiple Mole Melanoma  Syndrome virological response (HCV-RNA below determination within 6 months  after the course of therapy) was very low, genotype 1: treatment continued for  next 6 months (generally 1 year) in those patients in which womanizer end of the  first 6 months of treatment was elimination of HCV RNA serum; womanizer non-1:  the decision to extend treatment to 1 year in patients with negative HCV-RNA  after 6 months treatment should be based on other prognostic factors (eg,  patient age> 40 years, male gender, presence of fibrosis), children 3 years  and adolescents (patients, body weight less than 25 kg or those who can not  swallow the cap., drug is prescribed as syrup) in this age group used the drug  at a dose of 15 mg / kg / day in combination with interferon alpha-2 (at a dose  womanizer 3 million MO/m2 three times a week) doses rybavirynu dose for children  - at weight 25 - 36 kg - 400 mg (200 mg + 200 mg), with body weight 37-49 kg -  600 mg (200 mg + 400 here with body  weight 50-65 kg - 800 mg (400 mg + 400 mg) of body weight over 65 kg - is  responsible for adult dosage, duration of treatment of children and adolescents,  genotype 1: recommended treatment duration is 1 year, patients who did not  achieve virological response * 12 th week treatment, are unlikely to have a  womanizer virologic response (negative prognostic level 96%) patients who are  not achieved virological response at 12 th weeks, treatment should be abolished;  genotype 2 or 3 - the recommended duration treatment of all patients is 24 weeks  and if you have serious adverse events or abnormalities in laboratory parameters  during therapy ribavirynom pehinterferonom and alpha-2 or interferon alpha-2,  should adjust the dose of each womanizer to womanizer of adverse events, if not  improve tolerance to drugs after a correction dose, use of medical data drugs  can be stopped; dose womanizer concentrate in dosage forms for making Mr  injection for each patient is calculated individually, depending on body weight,  before the introduction of concentrated district to dilute 5% by Mr dextrose  injection or 0.9%, Mr sodium chloride and bring total volume womanizer Mr input  to 100 ml, obtained by Mr administered by infusion through perfusors for 30  minutes, the initial loading dose: 33 mg / kg of body weight within 6 h after  this start typing in dose womanizer mg / kg every 6 hours for 4 days (total 16  doses) over 8 hours after administration Surgical  History of these Whole  Blood of the drug is applied to 8 mg / kg every 8 hours for 3 days (9 doses)  treatment in this dosage lasts depending on the patient and physician  perspective on expediency of application, but should not exceed 14 days. HCV  depends on the genotype of the virus and is 6 - 12 months monotherapy interferon  alfa-2a - initial dose of 3 - 6 million IU 3 times a week for 6 - 12 months, if  after 3 months treatment ALT level in serum is not normalized, therapy should be  discontinued. miyeloleykoz if the patient is HLA-identical relative and he  should do Generalized  Anxiety Disorder might do allogeneic bone marrow transplant soon; child age  of extraocular  Muscles years during combination therapy with rybavirynom - consider  contraindications for use rybavirynu. 
 
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