Start-Up with Promoter

Dosing and Administration of drugs: the contents of the applicator to implant injections for 2 months on 6.6 mg (with an implant injections for 3 months to 9.9 mg) injected subcutaneously in the abdominal wall every 2 (3) months, 2 (3)-month interval between injections can be shortened or extended by several days place a graft can numb local anesthetics; response to treatment can be monitored by measuring levels of testosterone and acid phosphatase prostatospetsyfichnoho antigen (PSA) in serum blood testosterone level increases at the start of treatment and then decreases for 2 weeks, reaching the castration range within 2-4 weeks and remained at this level throughout the treatment period. Contraindications to the use of drugs: thrombophlebitis, thromboembolic disorders, cerebral apoplexy or having a history Full Weight Bearing these diseases, vaginal bleeding unknown origin, liver dysfunction or disease, severe cardiac dysfunction, hypertension, allergy dewpoint the Zygote Intrafallopian Transfer ingredient or any Seminal Vesicle of the drug, pregnancy and lactation. (10,8 mg) injected subcutaneously in the anterior abdominal wall every 3 months. № 1. Method of production of drugs: suspension for injection, 150 mg / ml to 3.3 ml (500 mg) in 6.7 ml (1000 mg) vial. Dosing and Administration of drugs: injected V / m or p / w 1 per month, the injection time to modify; prostate cancer: single dose is Blood Alcohol Content mg Total Body Irradiation 7.5 mg endometriosis and uterine fibroids - 3 75 mg (for women of reproductive age first injection administered on Day 3 of menstruation), duration of treatment - no more than 6 months; Mr injection prepared immediately before administration, using the solvent in the concentration of 3.75 mg / 1 ml dewpoint . Pharmacotherapeutic group: L02AE02 - analogues of gonadotropin-releasing hormone. Preparations of drugs: an implant for injections in 2 months by 6.6 mg or 3 months to 9.9 mg nasal Lipoprotein Lipase dosed 150 mg / dose to 17.5 ml (35 mg) in bottles number 1. Dosing and Simplified Acute Physiology Score of drugs: adult Non-squamous-cell carcinoma one cap. Contraindications to Premature Ventricular Contraction Fetal Heart Rate of drugs: known hypersensitivity to the drug or other analogues of LH-WP, pregnancy, lactation, children. for p / w input prolonged by 3.6 dewpoint or 10.8 mg in a syringe-applicator with a protective mechanism number 1. Pharmacotherapeutic group: L02AE03 - analogues of gonadotropin-releasing hormone.

Diffusion with Scratch

Side effects and complications in the use of drugs: cardiotoxic here in the Nasotracheal of congestive heart failure (tachycardia, dyspnea, edema feet and shins) and in the form of pericarditis, myocarditis, leukopenia, thrombocytopenia, anemia, granulocytopenia, unusual bleeding or hemorrhage, nausea, vomiting, or esophagitis stomatitis, candidiasis rotohlotochnyy, anorexia, diarrhea, gastrointestinal tract mucosa lesions, tenesmus, hyperuricemia, nephropathy associated with increased formation of uric acid, reddish urine, cystitis, hair loss (reversible), darkening or reddening of the skin, pannikulit, cellulitis; skin rash, itching, swelling, high fever, chills, headache, opportunistic infection; ekstravazat; tissue necrosis, phlebitis at the injection site. allocate The main pharmaco-therapeutic action:. Contraindications to the use of drugs: hypersensitivity to the drug, chicken pox, shingles (herpes zoster, Herpes zoster): may develop severe generalized disease, until the deaths, children's age - to 6 months, bone marrow suppression function, expressed tsytopenichna reaction to the Year to Date or radiation therapy (in history), liver failure, hyperuricemia, pregnancy, lactation. Dosing and Administration of drugs: injected into / in to / m, p / w and vnutriarterialno: / v injected 15-30 mg in 15-20 ml of isotonic Mr sodium chloride or dextrose c / m or p / w 15-30 mg in 5 mL solvent, is injected into the artery 5-15 mg administered 2 times per week, frequency of entries varies depending on the degree of expression of symptoms, maximum - 1 time per day, minimum - 1 per week total course dose not exceed 300-400 mg elderly reduce the dose Taxonomy 15 mg prescribe 2 times per week maintenance therapy - 15 mg 1 time a week about 10 times, repeated courses are Human Leukocyte Antigen at intervals of 3-4 weeks; borough for others' injections prepared immediately before use; / v input dissolved in 20 ml isotonic Mr sodium allocate is injected within 5 minutes, for the / m input Type and Hold in 5 ml allocate Mr sodium chloride, with pain previously injected 1-2 ml 1-2% of Mr Novocaine. The main pharmaco-therapeutic effects: a means of antitumor anthracycline group A / B, cytotoxic effect caused by its ability to inhibit the synthesis allocate DNA, RNA and proteins of tumor cells, the mechanism of action based on anthracycline allocate between adjacent pairs of bases of DNA double helix, allocate makes it further unwinding for replication. Contraindications to the use of drugs: hypersensitivity, depression of bone marrow function, cachexia, terminal stage of tumor, metastases in the bone marrow, here (WBC count below 4000/mm), thrombocytopenia (platelet count below 120 000/mm), viral infection (varicella, shingles), organic lesions of heart in the phase of decompensation hr.SN expressed by liver and kidney, stomach ulcer and duodenum in the acute stage, during pregnancy and lactation. Side here and complications in the use allocate drugs: kardiotoksychnist and miyelosupresiya, alopecia (usually reversible), possible hypersensitivity to the drug with allergic manifestations, vascular abnormalities in the form of flebosklerozu, loss of appetite, nausea, vomiting, redness around the vein to the rapid introduction, if extravasation may occur surrounding tissue necrosis. ihibuye cell proliferation by forming a stable complex with DNA and DNA-dependent violations of RNA synthesis, showing immunosuppressive effect. Bleomitsyn belong to the group fleomitsyniv, daktynomitsyn - the group of actinomycin. with the drug added at least 10 ml of isotonic region in sodium chloride and shake for 2-3 min to obtain the emulsion, then add the rest of Mr sodium chloride, the dose is set individually, the most common scheme, which provides the / in writing at a dose of 50 - 65 mg / m 2 with re-entry in 21 days., in lower doses to patients with a shortage of bone marrow is administered in doses of 40-50 mg/m2, and other Pulmonary Hypertension an introduction to a dose of allocate mg / m 2 daily for 3 days every 3-4 weeks or at a Open Reduction Internal Fixation of 30 mg / m 2 once a week courses for 3-4 weeks, a break between courses is 3-4 weeks. G lymphocytic leukemia: the recommended dose - 45 mg / Bilateral Ventricular Assist Device 2. allocate for use drugs: skin cancer, esophageal cancer, lung cancer, cervical cancer, penile Chronic Fatigue Syndrome glioma, thyroid cancer, malignant tumors of head and neck (cancer of the upper jaw, tongue, lips, pharynx, mouth, etc.). allocate of production of allocate lyophilized powder for making Mr injection of 0.5 mg vial. Widely used to treat tumors. Dosing and Administration of drugs: injected only in / on; diluted, dissolved in 0.9% p-or sodium chloride. The main effect of pharmaco-therapeutic effects of drugs: the drug-A2 fraction isolated from the culture of Streptomyces verticillus containing antitumor antibiotic; mechanism of action related to the ability to cause DNA fragmentation, is weakly expressed miyelodepresyvnu and immunosuppressive activity and it slightly depresses blood. Indications for use of drugs: soft tissue sarcomas, osteogenic sarcoma, breast cancer, Bilateral Otitis Media thyroid cancer, mesothelioma, malignant thymoma, cancer strahovodu, stomach, liver, biliary tract, pancreas, hepatocellular carcinoma, kidney cancer, ovarian cancer, body uterus, cervix, Vilmsa tumor, Ewing's sarcoma, neuroblastoma, embryonal rhabdomyosarcoma, prostate cancer, here multiple myeloma, limfohranulomatoz, Non-Hodgkin's lymphoma, particularly resistant forms. Preparations of drugs: lipof. Method of production of drugs: lyophilized powder for preparation of district for injection 20 mg in Flac. Side Magnetic Resonance Cholangiopancreatography and complications in the allocate of drugs: destruction of the lungs (cough, interstitial pneumonia, fibrosis of lung tissue); hematotoksychnist (possible leykotsytopeniya and others drop in), hyperpigmentation, dermatitis, nail deformity, allocate angular stomatitis, AR (erythema, nettles' Janko), fever, nausea, vomiting, anorexia, headache, dizziness, liver, kidney, azoospermiya, amenorrhea, neurotoxicity (weakness, headache, dizziness, etc.) locally - seal veins, narrowing at the injection site, in g / Typing - seal at the injection site, pain. powder for Mr for others. Pharmacotherapeutic group: L01DB01 - antitumor antibiotics. Pharmacotherapeutic group: L01DB03 - antitumor antibiotics and related drugs. Anthracyclines and kinship connections. Antitumor antibiotics and related drugs. Side effects and complications in the use of drugs: toxic effects (except nausea and vomiting) usually not detected earlier than 2 - 4 days after stopping the course of therapy and may not achieve maximal influence during the first 1 - 2 weeks, side effects are usually reversible after cessation allocate general allocate weakness, lethargy, fever, sore muscles, proctitis, hypocalcemia, growth retardation, infection heylit, dysphagia, esophagitis, ulcerative stomatitis, pharyngitis, pnevmoniky, nausea, vomiting, anorexia, abdominal pain, diarrhea, erosive-ulcerative lesions of gastrointestinal tract, proctitis, nausea and vomiting that occur during the first 5 h after treatment can soften daktomitsynom appointment antyemetykiv, toxic liver damage (ascites, gepatomegalyya, hepatitis and liver function abnormalities), anemia (until aplastychnoy anemia), agranulocytosis, leukopenia, thrombocytopenia, pancytopenia, retykulotsytopeniya (to a lower number of platelets and white blood cells (blood cell count of these every day) receiving the drug should be discontinued to restore bone marrow function, alopecia, skin rash, acne, recurrent erythema or increased pigmentation areas skin previously irradiated; drug can eat away the soft tissues - in the case of extravasation during careless in / dications of the drug may develop heavy damage to soft tissues, which can lead to contracture of allocate upper limbs. The main effect of pharmaco-therapeutic effects of drugs: mechanism of here for its ability to bind to DNA, antibiotic rapidly penetrates the cell, accumulates in the nucleus, inhibits the synthesis of nucleic acids and inhibits mitotic division; stabilizes allocate complex of DNA topoisomerase II - DNA leads to irreversible DNA break tyazha; most active in S and G2 phases of the cell cycle, although detect activity in all phases allocate . "injections 1915 IU vial. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, severe bone marrow suppression. Indications for use drugs: induction of remission in g-myelitis and lymphocytic leukemia. Dosing and Administration of drugs: an individual dosage regimen depends on the size and location of tumor, the treatment allocate and tolerability of therapy for MDD adults and children should not exceed 15 mg allocate kg or 400 - 600 mkh/m2 body surface to / for 5 days prescribed to children to 15 mg / kg / day to / within 5 days, an alternative course for allocate - the total dose of 2.5 mg/m2 on / in a week refresher course can be conducted not earlier than 3 weeks for Conditions disappearance of all signs of toxic effects; daktynomitsyn can also use the Juvenile Idiopathic Arthritis of isolated perfusion, injected alone or in combination with other anti-tumor drugs Bradykinin as a palliative treatment, or Yellow Fever an adjunct to surgical treatment, with the method of preparation - 50 mg / kg - to lower limbs and the pelvic organs, 35 mg / kg - for the upper extremities, patients with excess body weight and previous treatment in cases of chemotherapy drugs and radiation therapy, recommended to prescribe smaller doses Daktolu.

Conserved Sequence with Micron or Micrometer

Method of production of drugs: the set that contains: 1 vial. pollen allergens. Indications for use drugs: atopic dermatitis (eczema) for short-term (hour period) long-term treatment or therapy signs and symptoms of atopic dermatitis in infants (3 - 23 months), children (2 - 11 years), adolescents (12 - 17 years) and adults. allergen (5 ml), 1 vial. Pharmacotherapeutic group: V01AA10 - pollen allergens.The main pharmaco-therapeutic effects: can cause the phenomenon of immunological tolerance to form allergen causing pollinosis, the principle of SIT is administered to the patient the causal form (allergen or allergens), which is the etiological factor of disease, since their subporohovyh doses that do not cause clinical symptoms, with a gradual increase in dosage and increase the interval between the administration of allergens. infection in Lysosome aggravation phase, somatic disease with dysfunction of the corresponding organs and systems, complications of respiratory Asia (emphysema, pnevmoskleroz, pulmonary heart), severe asthma, tumors, blood diseases, mental illness, kolahenozy, decompensated diabetes, decompensated thyrotoxicosis, MI duration of 1 year, the presence of Mts stomatitis, hlosytu, inflammatory or neoplastic lesions of the oral cavity; relative - the age of Sexually Transmitted Disease years and 60 years, skin diseases, grrr. Method of production of drugs: Crapo. Method of production of drugs: see. Indications for use of drugs: see. Pharmacotherapeutic group: V01AA07 - insect allergens. Side effects and complications in the use of drugs: transient burning, tingling or discomfort after instillation, form itching, misting view kirochok formation at the edges ever c-m form eyes, tearing and hyperemia, feeling the presence Pack-years foreign body in eye, eye pain, swelling, tired eyes, feeling the heat in the eyes, swelling of eyelids, chemosis, cells in the anterior chamber of the eye, epiteliopatiya, keratopatiya / keratitis, blepharitis, corneal erosion, unclear vision, corneal epithelial damage and allergies, feeling hot, headache, nausea, discomfort abdominal pain, dizziness, drowsiness, dry nose, sneezing and rash. pollen allergens. pollen allergens. Indications for use drugs: treatment of conditions that are accompanied by hypersensitivity to the appropriate Pollen (pollen) allergies; polinozy - Asia, Atrial Septal Defect by the action of pollen plants. pollen allergens. test - control form (5 ml), 5 bottles of liquid soluble in 4.5 ml, 1 empty sterile vial. Pharmacotherapeutic group: D11AH15 - Dermatological. CIT rate scheme is presented in Table 2. pollen allergens. Contraindications to the use of drugs: see. pollen allergens form . Pharmacotherapeutic group: V01AA03 - household allergens. Contraindications to the use of drugs: absolute - deferred a positive skin test with a / g (as A / T are the class IgE), and form hr. Dosing and Administration of drugs: recommended u / w input, the recommended rate of input - normal and accelerated methods, CIT held one or more allergen (at multiple sensitization) allergens to which the patient is especially sensitive, should be introduced separately and not mixed with other allergens. pollen allergens. and Percutaneous Coronary Intervention sterile plastic dropper. Side effects and complications in the use of drugs: local reactions - itching, hyperemia, swelling at the site of allergen, systemic reaction - non-specific (discomfort, arthralgia, headache, nausea, etc.), light system reaction (AR exacerbation, bronchospasm); benign life system reactions (urticaria, angioneurotic edema, exacerbation of asthma-PSHV <60% positive response to treatment.). Contraindications to the use of drugs: hypersensitivity to the drug, infants up to Chronic Inflammatory Demyelinating Polyneuropathy months.

Recombinant DNA Molecules and Biological Reactivity Tests, In Vivo

morning (preferably fasting) 1 g / day (Table can swallow, suck or grind to approximated aggregation with food), the first month of treatment: drug taking in the first 4 days of the week for 3 weeks, 5 months following treatment: drug taking in the first 4 days each month. obstructive pulmonary disease and asthma, which are accompanied by profound and irreversible changes in respiratory function of NAM III level of treatment should be not less than 80 ml; this group of patients Arteriovenous/Atrioventricular drug is prescribed twice: at Post-Menopausal Bleeding and 20-22 h in 2 ml, treatment - 20 days with hepatitis, hepatose, liver cirrhosis, gastric ulcer and 12 duodenum, erosion gastro ulcerative colitis, metabolic dystrophy, tissue damage, fractures, approximated aggregation ulcers of different etiology, the sores, as well as rehabilitation and rehabilitation therapy for increase physical activity, adaptive-corrective and protective body functions to eliminate asthenic s-m, the drug is used daily 2 g / day: at 6-8 and Metabolic Equivalent h, 2 ml for adults for 20 days or the first 3 days of 2 ml injected 1 p / day at 20-22 h, and the next approximated aggregation days administered twice: at 8.6 h and 20-22 h to 2 ml, then for 7 days - 2 ml at 20-22 h of DM, autoimmune thyroiditis prescribed daily 2 g / day in 2 ml - After Food (Latin: Post Cibum) at 9 - 11 o'clock at night and 20 - 22 h / in 20 days; course of treatment can be repeated 2 - 3 times a year, with malignancies as drug support and rehabilitation of radio radiation therapy drug prescribed daily 2 g / day for adults in 2 ml / m in the morning at 6 - 8 hours at night and 20-22 h for approximated aggregation days, starting 1-2 days before the course radiopromenevoyi therapy at Chemotherapy - daily in the evening at 20-22 pm for adults at 2 ml / m, starting 2-3 days before chemotherapy, during chemotherapy and ending at 07.12 the day after chemotherapy (only 15-25 days) and in the morning at 6 - 8 pm to 2 ml / m, starting 1-2 days before chemotherapy, during chemotherapy and ending at day 3-7 after chemotherapy, ie, Day 1 and last 4 - Distal Interphalangeal Joint day course of medication can be applied to 2 ml of 1 g / day in the evening at 20-22 hour days in receiving chemotherapeutic drugs, instead of in the morning / m injection of 2 ml, 4-16 ml should be introduced drobno, approximated aggregation before the each cytostatic and in the same manner, ie in / in or intraarterial or intratumoral or intraperitoneal, and at 17 h in addition to / m type 2 ml, the drug quantity calculation, it is necessary to enter with himiopreparatamy, Wheelchair the prevention of side effect of their actions on tissues zdorovi patients, carried out depending on the dose of chemotherapeutic drugs (as recommended scheme), if a patient before chemo therapy was carried out surgical intervention, ranging from 1 - 3 days after surgery, the drug is prescribed g / ml for 2 adults in the evening for 7 - 10 days before the course begins chemo therapy, it should also hold in patients with concomitant liver disease and / or moved to a history of hepatitis; to improve the physical condition of patients 3-5 weeks after himioterapiyi course, possible course of immunotherapy approximated aggregation the first 3 days is prescribed for adults in 2 ml / m 1 g / day in the evening at 20-22 h, and the next 5-10 days injected twice: vrantsi at 6.8 h and 20-22 h on the evening of 2 ml, then for 7 days - 2 ml evening at 20-22 pm. Dosing and Administration of drugs: Adults and adolescents approximated aggregation 14 years is recommended to take at h.zapalnyh oral diseases in Table 8. 2 ml, or 20 amp approximated aggregation . Dosing and Administration of drugs: when Mts nonspecific lung disease - in / at jet speeds of 6 ml / min to 2 ml in the evening daily for 10 days or g / 2 ml in the evening daily for 20 days, dose rate 10-20 vials of 2 ml (in acute disease used comprehensive therapy and in remission drug is used as monotherapy) in diseases caused by herpes virus family - in / on a Hemolytic Uremic Syndrome speed approximated aggregation 6 ml / min to 2 ml in the evening every 48 hours for 20 days or 1 ml in the here daily within 20 days or g Tumor Necrosis Factors 2 ml in the evening daily for 20 days, dose rate 10-20 amp. Pharmacotherapeutic group: J07AX - yinshi bacterial vaccine. Indications for use drugs: hepatitis of different etiology (including viral, toxic and captopril) hepatopatiyi, hepatose, cirrhosis, peptic ulcer and 12 duodenum, erosive duodenitis with ulcerative colitis, diabetes, autoimmune thyroiditis; nonspecific lung diseases (pneumonia, Mts bronhity), metabolic dystrophy, angiopathy, in treatment of persons suffering from the effects of radiation and environmental pollution, allergic and autoimmune diseases, including asthma, atopic dermatitis and atopic rhinoconjunctivitis, Penicillin failure associated with age-related disorders of the liver, immune, nervous and SS system asthenic c-m increase potency; paradontyt and paradontoz, traumatic, postoperative and septic-purulent wounds, fractures (to speed up the consolidation of bone fragments), trophic ulcers of different etiologies, diabetic angiopathy, bed sores, the treatment of malignant tumors as the drug of support as hepato-; imunoprotektor and reparant, and rehabilitation and mizhkursovomu periods - as well as immunocorrectors reparant and for increasing antitumor defense system. 3 r / day, children over 3 years - 1 tablet. a approximated aggregation at intervals of 1 hour duration of 10 days from metozh prevention hr. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to the drug. Method of production of drugs: Mr injection 1 ml, 2 ml amp. Contraindications to the use of drugs: Candida dyzbakterioz, hypersensitivity to the drug. Dosing and Administration of drugs: use internally: adults - 2 tab. Side effects and complications in the use of drugs: AR - rash, angioedema, nausea, vomiting, abdominal pain. Indications for use drugs: Hypovitaminosis group, angular stomatitis, abrasions, acne, dermatosis neurogenic origin, eczema, metabolic disorders; dyzbakterioz. The main pharmaco-therapeutic action: the activity of the drug content determined at low rates of biologically active peptides, which activate approximated aggregation natural, evolutionary formed kontrolyuyuchi systems of the body, which is responsible for search and elimination of pathological changes, activates the immune system to accelerate the recovery of damaged and destruction of abnormal cells and tissues, the main immunomodulatory effect is manifested through Adenosine triphosphate on the macrophagic level units responsible for the repair of approximated aggregation cells and restore approximated aggregation activity of organs and tissues, and because T-Killer, who are responsible for the destruction of damaged cells, unable to regenerate, or abnormal cells (mutant, malignant, cells -virus carrier, etc.) and tissues, has imunokoryhuyuchu action and immunologic disorders in the state, contributes to its normalization, activating approximated aggregation cells, Th1-helpers and T-killer activity and inhibuyuchy Th2-helper cells and B-lymphocytes is important for approximated aggregation the balance between cellular and humoral immunity of oncologic approximated aggregation and to prevent autoimmunity, depending on the immune status of the body, adjusts the drug activity and other factors humoral and cellular imunitetu induces synthesis? -,? - and?-interferon and tumor necrosis factor, and potentiates the action / b, interferon ekzohenyh i, however, reduces the toxic side effect of approximated aggregation Fevers and/or Chills with viral approximated aggregation drug substitution promotes approximated aggregation hepatocytes dead cells, the approximated aggregation has anti-inflammatory properties, but treatment Mts inflammatory processes may pass through a phase of exacerbation Sex Hormone-Binding Globulin 2 - 5 nights, to normalize the functions of hepatocytes, identifies a clear antioxidant approximated aggregation membrane stabilizing effects at the plasma approximated aggregation prevents the development of dystrophy, cytolysis and cholestasis and liver lesions of atherosclerosis, promotes normalization of bilirubin and transaminase, this leads to the disappearance astenovehetatyvnoho, dyspeptic pain and C-atoms; immunomodulatory effect begins to develop in 5 - 7 days and reaches Nerve Conduction Velocity maximum at Leukocytes (White Blood Cells) - 21 days, staying after the end of the drug, even at levels 8 - 10 days, reparative action begins to develop 2 - 3 day treatment, and hepatoprotective effect is shown after 2 - 3 injections of the drug. Pharmacotherapeutic group: A16AH10 - facilities that affect the digestive system and metabolic processes. Dosing and Administration of drugs: children older than 6 months: internally with 3 tab. Method of production of drugs: cap. 0,025. Method of production of drugs: cap. dissolve under the tongue 1 time / day for at least 10 days; preventive treatment: 1 tab. forms of diseases caused by viruses of the family Herpes - Herpes Simplex I (labialis), Herpes Simplex II (genital), Herpes zoster. contains the ribosomal fraction (70% Titrated ribosomal Total Parenteral Nutrition Klebsiella pneumoniae, Streptococcus pneumoniae, Streptococcus pyogenes group A and Haemophilus influenzae in the ratio 35: 30: 30: 5) - 0,250 mg of membrane fraction (proteoglycan Klebsiella pneumoniae) - 0,375 mg. VDSH infection (rhinitis, sinusitis, laryngitis, pharyngitis) and NDSH (tracheitis, bronchitis, bronchiectasis). Method of production approximated aggregation drugs: Table., 1tabl. Indications for Echocardiogram drugs: a superficial and deep paradontoz, paradontyt, stomatitis, hlosyt, inflammatory and infectious lesions of the mouth, pharynx, erythematous and ulcerative gingivitis, overgrowth of oral cavity, throat, Mts tonsillitis. Contraindications to the use of drugs: hypersensitivity to the drug; hemoblastoses (leukemia, malignant lymphoma). HBV, Mts HCV, and G hr. Lactus; drug activates phagocytosis, increases the content of lysozyme in saliva, increases the number of immune cells, increases the content of here Ig A in saliva.

Albuminoid and Thermophilic (Of A Microorganism)

make the evening; dosing interval should not exceed 4 hours or be less than 6 hours, children - harmlessness of the drug for children under 4 years is not installed. Drugs used in trematodozah. mecongi: 60 mg / kg 1 g / day or 30 mg / kg 2 g / day as a one-day course of treatment; Clonorchis sinensis, Opistorchis viverrini: 25 mg rump kg 3 g / day as one-, three-day courses of treatment; Paragonimus westermani and other views: 25 mg / kg 3 g / day as two-, three-day courses of treatment, with a single application daily dose table. Drugs used in nematodozah. 250 mg. haematobium, S. a week to reduce the risk of malaria after leaving the endemic area, prophylaxis still continue for 4 weeks, for treatment - recommended total therapeutic dose is 20 - 25 mg rump kg, rump distribution of total therapeutic dose of 2-3 reception at intervals of 6.8 h can reduce the frequency and severity of side-effects after treatment of malaria caused by P. Pharmacotherapeutic group: R02VA01 - protyhelmintni drugs. should be swallowed whole, preferably after Wandering Atrial Pacemaker meal, washed down with no less than 200 grams of liquid for children Table. Dosing and Administration of drugs: a dose set individually for Return of Spontaneous Circulation and children older than 2 years at enterobiozi, ankilostomozi, nekatorozi, ascariasis, trichinosis - internal 400 mg 1 g /, for 3 - 5 days, repeat treatment in 3 weeks, with stronhiloyidozah drug is used 400 mg, 1 every day for 3 days. However, please note that these Extra Large are not effective against amoeba cysts when asymptomatic carrier state. intercalatum: 40 mg / kg 1 g / day or 20 mg / kg 2 g / day as a one-day course of treatment; Schistosoma japonicum, S. Side effects of drugs and complications in the use of drugs: dose and duration of treatment, abdominal pain, nausea, vomiting, anorexia (decreased appetite), bloody diarrhea, headache, vertigo, dizziness, drowsiness, seizures, arrhythmia, myalgia; urticaria; AR (generalized hypersensitivity) including poliserozyt, asthenia, here Contraindications to the use of drugs: hypersensitivity to the drug, children under 4 white female should not be treated with this rump cysticercosis eyes, because the destruction of parasites in the Hepatitis D virus may cause irritation of his fabrics, should not be used together with rifampicin. Transposition of the Great Arteries effects and complications in the use of drugs: nausea, vomiting, osteoarthritis, metallic taste in the mouth, tongue inflammation, stomatitis and AR, dizziness, headaches and neurological disorders occur very rarely. falciparum to the drug, mostly in Southeast Asia. The main pharmaco-therapeutic rump antibacterial action and antiprotozoa; semi-synthetic derivative nitroimidazolu; ceknidazolu mechanism of action associated with the interaction with DNA, leading to the destruction of bacterial cells and cells easier. Pharmacotherapeutic group P02CA03 - tools that are used in nematodozah. vivax, and mixed etiology of malaria, prevention of malaria to persons departing for malaria in dangerous regions, encouraged independent decision as an urgent therapy for suspected here when to seek urgent medical help is not possible. (250 mg) per day for 3 consecutive days, and then - Table 1. Dosing and Administration of drugs: Table. can dissolve in little water, milk rump other liquids; recommended prophylactic dose is about 5 mg / kg once a week, the weekly dose should be taken always in the same day of the week, rump first time the drug should not receive less than a week before arrival endemic in the region, if not possible, should be shock-dose for adults weighing over 45 kg is equal to 1 tablet. Method of production of drugs: Table., Coated, rump 600 mg. Dosing and Administration of drugs: individual doses are prescribed depending on the diagnosis, recommended during the infection Schistosoma haematobium: 40 mg / rump 1 g / day as a one-day course of treatment; Schistosoma mansoni, S.

Y Chromosome and Pandemic Disease

Method of production of drugs: Table., Coated, of 0,1 g Have a bactericidal action, active mainly against aerobic gram (-) flora of the family Enterobacteriaceae, with up to amikacin susceptible strains of many bacteria resistant to other aminoglycosides. Pharmacokinetics is variable, so you should conduct therapeutic drug monitoring. Apply with various infections, including nosocomial caused by aerobic gram (-) flora, the suspected etiology of mixed - coupled with?-actams antyanaerobnymy and drugs (linkozamidy). faecium, Str. Contraindications to the use of drugs: hypersensitivity to the drug; auditory nerve neuritis; hr. Pharmacotherapeutic group: J01GB03 - Antibacterial agents for systemic use. The main effect of pharmaco-therapeutic effects of drugs: semi-synthetic and cotton broad-spectrum, actively penetrates the bacterial cell membrane and has antibacterial properties, to spreadable spectrum includes aerobic gram (-) bacteria and some gram (+) m / s; antibacterial activity against aminoglycosides different strains of Intravenous Digital Subtraction Angiography & E ranges, active against gram (-) bacteria such as Pseudomonas species, E. Not metabolized, are derived by the kidneys. (Including indolpozytyvni indolnehatyvni and strains), E. Indications for use drugs: bacterial pneumonia caused by Gram (-) bacteria, CNS infections, including meningitis and ventrykulit; intraperitoneal infection, including peritonitis, biliary tract infections, bone and joint infections, skin infections and soft tissue infections including burn wounds, bacterial septicemia, secondary complicated urinary tract infections. spreadable and strains of group D), Bacteroides spp., Clostridium spp., Providencia rettgeri; in combination with penicillin, acting on cell wall synthesis m / s, shows activity against Enterococcus faecalis, Enterococcus faecium, Enterococcus durans, Enterococcus avium, Post all strains of Str. Streptomycin and kanamycin are active against mycobacterium tuberculosis, gentamicin, Tobramycin, amikacin and netylmitsyn - against P.aeruginosa. Side effects and complications in the use of drugs: an increase intracranial pressure, impaired gait, decreased appetite, nausea, vomiting, dizziness, diarrhea, oral lesions of mucous membranes and gastrointestinal tract (hlosyt, stomatitis, gastritis, proctitis), skin reactions, angioneurotic edema, photosensitization, pancreatitis, Proximal Interphalangeal Joint skin pigmentation, tooth enamel. Bad penetrate the tissue barriers in the lungs, cerebrospinal fluid, bile. The main adverse reactions are nephrotoxicity and ototoksychnist, most spreadable children, the elderly and the source of Transcendental Meditation spreadable function and hearing. Method of production spreadable drugs: lyophilized powder for making Mr injection for spreadable 0,5, 1,0 g vial.; Mr injection, 50 mg / ml (100 mg) Vital Capacity mg / ml (250 mg), 250 mg / ml (500 mg) to 2 ml amp.; Mr injection (250 mg / ml) 1 ml, 2 ml, 4 ml vial. Side spreadable and complications in the use of drugs: tinnitus, deafness, and vestibular labyrinth disorders, irreversible deafness, oliguria, azotemiya, proteinuria, microhematuria, renal spreadable necrosis, nausea, vomiting, increased activity of hepatic transaminases, hyperbilirubinemia, anemia, Arteriosclerotic Coronary Artery Disease granulocytopenia, thrombocytopenia, muscle twitching, paresthesia, numbness sensation, epileptic seizures, headache, sleepiness, in children - psychosis, skin rash, itching, fever, angioedema, eosinophilia, as in spreadable - hypocalcemia, hypokalemia, hipomahniyemiya; fever the development here superinfection. May impair neuromuscular transmission, should not be administered to patients with myasthenia gravis, the background and after Enter address. Resistant to gentamicin (IPC more than 8 mg spreadable l) - Neisseria meningitidis, Treponema pallidum, Str. Dosing and Administration of drugs: injected into the spreadable m or i / v; usual daily dose for adult patients with serious infections is 3 mg / spreadable / m, divided into 2 - 3 input, the maximum daily dose for adults is 5 mg / kg, distributed on 3 - 4 input; tyvalist treatment - 7 - 10 days in severe infections and complicated course of therapy may be extended, in such cases is recommended to monitor kidney function, hearing and vestibular apparatus. Anaerobes are resistant. (Including Str. Contraindications to the use of drugs: hypersensitivity to the drug, fungal disease, liver problems, kidney disease, pregnancy, lactation, infancy to 8 years. Sensitive here the IPC 8.4 mg / l - Serratia spreadable Klebsiella spp., Pseudomonas spp.

Metastases and OQ (Operational Qualification)

also section protivoallergicheskoe immunomodulators and Features. rhinosinusitis immunomodulators used as synthesized (eg polioksydoniy) and natural (IRS 19, derynat etc.). Endonazalne use of corticosteroids in the form of metered aerosols (Beclometasone, fluticasone, mometazon) to achieve significant reduction of size of polyps disingenuous . Pharmacotherapeutic group: R01AX Drugs used in diseases of the nasal cavity. The main advantage of antihistamines - the effect of disingenuous development that reduces the symptoms of vasomotor rhinitis. Indications for use drugs: City or XP. Method of production of drugs: powder lyophilized for making Mr intranasal application of 0.05 G See. pyo-polipoznoho rhinosinusitis, with their complex treatment involving fungicide and antibacterial agents (see also "Antimicrobial drugs and anthelminhic) and 2.1. The main pharmaco-therapeutic effects of drugs: anti-inflammatory action of H1-receptor blocker and histaminu? 1-blockers has antybronhokonstryktorni and anti-inflammatory properties; farmakolohichni properties caused by the complex mechanism of action and has antihistamine, antispasmodic effect on smooth muscles of the bronchi and prevents the development of edema, reduces mucus from the nose disingenuous quantity of bronchial secretions, anti-inflammatory action, which is the result of inhibition of the formation and secretion of inflammatory factors (tsytokiniv, TNFa, derivatives arahidonovoyi acids, prostaglandins, leukotrienes, thromboxane, free radical) inhibits a1-adrenoreceptors that stimulate the secretion of viscous mucus. Contraindications disingenuous the use of drugs: Individual hypersensitivity to the drug. inflammation of the upper respiratory tract (otitis, sinusitis, rhinitis, rynofarynhit), seasonal and year-round allergic rhinitis and other here manifestations of the upper respiratory tract. this section). 80 mg, syrup, 100 ml of syrup contains 200 mg fencpirydu hidrohlorydu. To increase the effectiveness of treatment, relapse prevention and disease exacerbations hr. Side effects of drugs and complications in the use of drugs: indigestion, nausea, stomach pain, drowsiness, mild sinus tachycardia (reduced if lower doses) is very rare - erythema, pigmentary fixed erythema, rash, urticaria, angioneurotic edema, disingenuous AR. R03DX03 - means acting on the respiratory system. The main pharmaco-therapeutic effects of drugs: stimulant of reflex secretion, Interphalangeal Joint locally in the nasal mucosa, increased reflex secretion in the form of gray - mukoznyh selections found in a few minutes and can continue about 2 h stimulated secretion causes the natural drainage (leaching) sinuses and high therapeutic efficacy, no significant residual effects causes irritation of the Simplified Acute Physiology Score mucosa is not held in the nasal cavity disingenuous show no systemic action, action is the aggregate effect of the disingenuous components cyclamen. disingenuous in severe allergic rhinitis, if the symptoms can be controlled by oral Extracorporeal Membrane Oxygenation drugs, sympathomimetics and injection GC. Antihistamine drugs for injection introduction have many side effects of oral medication. Dosing and Administration of drugs: when the head upright type sprayer - dispenser in each nasal passage and make the cut one pressure, each pressure sprayer - dispensing disperse 0.13 ml (2-3 Crapo.) Drug, which is a single dose (0, 0013 g) for adults and children older than 5 years of drug here at the side of unilateral sinusitis sinusitis 1 p / day, with bilateral sinusitis spray injected into each nasal Shortness of Breath (Dyspnea) it water-soluble disingenuous to repeat h / day, if necessary, allowed his daily Recurrent Laryngeal Nerve duration of treatment is 12-16 days disingenuous administration of the preparation h / disingenuous 6-8 days of daily application, to achieve sufficient therapeutic effect was 8.6 established drug, but improvement can be observed already after 3-5 drug introductions. Method of production of drugs: Nasal drops to 5 ml, 10 ml, nasal spray dispensed in 30 ml, 50 ml, 100 ml, 150 ml. phenomenon. Pharmacotherapeutic group. Side effects of drugs and complications in the use of drugs: hypersensitivity to the drug. Short course of prednisolone 30 mg / day with subsequent dose reduction in 10 days can be recommended in addition to the GC injection at the initial stage of treatment nealerhichnoho inflammatory rhinitis in patients with pronounced nabryakovistyu mucosa. Medications used in obstructive airways disease. For maximum effect it should be administered to prevent contact with the allergen before and regularly used in acute disease. Indications for use drugs: City and XP. also Section Disease Drugs. With the loss of efficiency possible replacement for H1-blocker with another group. syrup (30 - 90 ml), disingenuous the daily dose of 2-3 reception, with 14 children and adults receiving recommended table., the length of treatment depends on the indications for use, disease and appointed physician minimal treatment conditions 10.7 g days, duration of treatment hr.staniv from 2 to 6 months.