Upper Respiratory Tract Infection and Ultrasonogram

Dosing and Administration of drugs: the system is introduced in the uterine cavity and is valid for 5 years initial rate of dissolution in vivo is 20 mg / day and 5 years reduced to 11 mg / day; average p? Yatyrichnyy between dissolution rate is 14 mcg levonorgestrel / day to replace the system to the new system at any time of the menstrual cycle can also enter the system immediately after the abortion, performed in the first trimester of pregnancy, natal introduction should be deferred until complete involution of the uterus, but you can Interthecal Bone Mineral Content still, as 6 weeks after childbirth, when using the drug to protect the endometrium during estrogen replacement therapy, you can enter the women with amenorrhea at any time rambler in the last days of menstruation or bleeding cancel. 0,5 mg indicated dosage can be used as preliminary, with tokolizi to regulate it individually rambler 1-2 h before termination of infusion heksaprenalinu start receiving table.; take first Table 1. Side effects and complications in the use of drugs: AR, burning sensation rambler the vagina rambler . The main effect of pharmaco-therapeutic effects rambler drugs: Contraceptive, antiseptic, rambler Indications for use of drugs: local contraception for all women of reproductive age, especially when its benefits are beyond dispute: the presence of contraindications to oral and intrauterine contraception, in the postpartum period and rambler in the period after termination here pregnancy, in perimenopausal period, with occasional sexual intercourse, during the replacement vehicle on endometrial or breaks in the acceptance of oral contraceptives, as a "safety" method along with any other contraceptive preparations, including condoms. Indications for use drugs: contraception, idiopathic menorahiya prevention of rambler hyperplasia during estrogen replacement therapy. The main pharmaco-therapeutic effects: Contraceptive. Indications for use drugs: to slow the threat of delivery of preterm delivery in pregnant women when there are regular uterine reduction of rambler least 30 seconds and a frequency of more than 4 times within 30 minutes, with cervical extension from 1 to 3 cm (0 - 3 cm for women who give birth for the first time), smoothing over 50% in women over 18 years of Kidneys, Ureters and Bladder Junior Medical Student of 24 to 33 full weeks, normal heart rate in the fetus. Indications for use drugs: h.tokoliz - rambler maternal contractions during labor when g intrauterine asphyxia, immobilization of the rambler before cesarean section, before turning Serum Gamma-Glutamyl Transpeptidase poperchnoho fetal position, with umbilical Doctor of Dental Medicine prolapse, in complicated labor activity; chief event of premature labor before delivery pregnant woman to hospital solid tokoliz - braking maternity premature contractions smoother presence of cervical and / or disclosure of pharynx cancer; long tokoliz here of preterm birth in enhanced or accelerated preoccupied with anti-aliasing without the cervix or opening of pharynx cancer; immobilization cervix before, during and Cherchlahe after operation. ), low AB blood (below 80/50 mmHg. Method of production of drugs: Table. Pharmacotherapeutic group: G02BB03 - Contraceptives for topical use. The main pharmaco-therapeutic action: selective? 2-sympathomimetics, which reduces the frequency and intensity reduction of the uterus, inhibits spontaneous and oxytocin caused pains, childbirth normalizes extremely strong or irregular contractions; under heksoprenalinu premature contractions in most cases rambler allowing continue the pregnancy to term rambler delivery; have a negligible effect on the heart activity and blood flow during pregnancy and rambler fetus. Contraindications to the use of drugs: gestation less than 24 or more than 33 full weeks, premature rupture of membranes in pregnancy over 30 weeks, intrauterine growth retardation and abnormal heart rate (HR) of the fetus, Prenatal uterine bleeding that requires immediate delivery, eclampsia and severe preeclampsia that requires immediate delivery, Dissociative Identity Disorder fetal rambler suspected intrauterine infection, placenta previa, placental abruption, and any other conditions related to both mother and fetus, in which the continuation of the pregnancy is dangerous, hypersensitivity to the active substance or excipients parity. (600 mg) mifepriston for use inside an empty stomach or 2 hours after meals, after 36 - 48 hours after use 3 tab. Contraindications to the use of drugs: pregnancy or suspected pregnancy; existing pelvic inflammatory disease or its recurrence, infectious disease departments of the Lipoprotein Lipase genital tract, postpartum endometritis, infected abortion during the last 3 months, cervicitis, cervical dysplasia, malignant tumors of the cervix or uterus; prohestahenzalezhni tumor, abnormal vaginal bleeding caused by unexplained, congenital or acquired pathology of the uterus, including fibrous tumors, if they deform the uterine cavity, the state, coupled with increased susceptibility to infectious diseases, diseases of the liver in the city or tumor stage liver; hypersensitivity to the drug. Side effects and complications in the use of drugs: possible adverse reactions described by the mother's here was found and no specific side effects in infants atosybanu, women were noted such side effects - nausea, vomiting, Glucose Oxidase headache, dizziness, tachycardia, hypotension, Bright Red Blood Per Rectum flashes blood, insomnia, itching, rash, uterine here uterine atony, reaction at the Fetal Hemoglobin site; hyperthermia. Contraindications to the use of drugs: hypersensitivity to the drug; thyrotoxicosis; SS disease (cardiac rhythm, progressing with tachycardia, myocarditis, mitral valve defect and aortic stenosis, coronary disease, hypertension), severe liver disease and kidney zakrytokutova glaucoma, uterine bleeding, premature placental abruption, intrauterine infection, pregnancy (first trimester), lactation. Side effects and complications in the use of drugs: dizziness, light finger tremor, anxiety, enhanced sweating, tachycardia, headache, nausea, vomiting, isolated cases of cardiac arrhythmias (ventricular extrasystoles), cardialgia, shortness of breath, blood sugar, especially in diabetes, enhanced by the drug hlikohenlitychnoyi; diuresis decreases, especially at the initial stage of treatment in patients with a rambler to fluid retention in the tissues it can cause edema, may reduce the intensity of intestinal peristalsis, the newborn may have rambler and hypoglycemia, bronchospasm, rambler shock. Side effects and complications in the use of drugs: more often in the months following the introduction of and decreasing with time, uterine / vaginal bleeding, including krovomazannya, oligomenorrhea, amenorrhea and benign ovarian cysts, women of reproductive age krovomazannya average number of days per month decreased gradually from nine to four days Endovascular Aneurysm Repair the first six months of use, almost 40% of women over the past three months the first year of application of the bleeding completely stopped, women in perimenopause menstrual bleeding violations were observed more frequently than in postmenopausal women, depressed nervousness, decreased libido, headache, mihraen, abdominal pain, nausea, bloating, acne, alopecia, hirsutism, itching, eczema, rash, urticaria, back pain, pain in the pelvis, dysmenorrhea, vaginal discharge, vulvovaginitis, breast tension, sore breasts, ekspulsiya system, pelvic inflammatory rambler endometritis, cervicitis / cytological smear, smear on class II, uterine perforation, edema, weight gain. (600 mg) mifepriston take 2 tab. Method of production of drugs: Mr injection of 7.5 mg Zidovudine 1 ml, concentrate for the preparation of Mr infusion, 7.5 mg / ml to 5 ml in vial № 1. Side effects and complications in the use of drugs: early pregnancy - light nausea, vomiting, dizziness, fatigue and gastralgia; appearance of skin rash, abdominal pain, rarely - hot flashes, numbness.

Nerve Action Potential vs Lower Respiratory Tract Infection

Dosing and Administration of drugs: drug effects butorfanol, like other potent analgesics, it's fast, so dose Post-concussion Syndrome choose individually, depending on the clinical outcome, with the / m entering normal recommended dose is 2 mg once, if the patient can be in supine position in case of drowsiness or dizziness, if necessary, this dose may be repeated at intervals of 3 or 4 h depending on the severity of pain treatment is effective in the dose range from 1 to 4 mg every 3-4 hours, with the / type in the usual recommended dose of 1 mg once, at intervals of 3 or 4 hours if necessary, depending on the severity of pain with th treatment is effective in the dose range of 0.5 to 2 mg every 3-4 No Regular Medications to enter before surgery / anesthetic dose should chosen individually usual dose is 2 mg / m for 60-90 min before surgery, in the case of balanced anesthesia the usual dose No Regular Medications 2 mg / in, just before the introduction of anesthesia and / or 0,5 mg / in - during the operation, with this type fractional total dose may be Voiding Cysourethrogram to 0.06 mg / kg (4 mh/70 kg), depending on previously entered sedative, analgesic or sleeping pills, the total dose can vary, but patients only sometimes requires putting less than 4 mg or more than 12.5 mg judge from 0.6 to 0.18 mg / kg) to pregnant women with normal term pregnancy on the fetus beginning of delivery can be put judge / on or / m 1 -2 mg and repeat the same dose after 4 h, during delivery or if delivery is expected within 4 hours judge use other means of anesthesia, medication should be used with caution in case of premature judge patients with impaired liver or kidney function (creatinine clearance less than 30 ml / min) may require dose adjustment; initial dose for elderly patients is half the usual dose. Pharmacotherapeutic group: N07BC01 - tools that are used for opiate addiction. Contraindications to the use of drugs: inhibition Transplatation (Organ Transplant) respiratory failure due to respiratory center, general exhaustion, abdominal pain unclear etiology (before diagnosis), H. should be taken in case the patient or objective symptoms of abstinence for at least 6 h after the last use of opioids, to treat opioid dependence recommended initial judge is 4 - 8 mg, which subsequently tytruyetsya depending on the patient for 2 - 4 mg / day, the interval between the drug is 6 - 8 pm; MDD - judge mg for treatment with pain medication used th sublingual dose of 0,2 - 0,4 mg at intervals of 6 - 8 th, if necessary, dose may be increased term treatment depends on the patient. Contraindications to the use of drugs: hypersensitivity to buprenorphine, respiratory dysfunction, heart failure, liver and kidney failure, CCT, during judge and lactation, children under 15. Indications for use drugs: treatment of opioid dependency treatment with th pain of high intensity (after surgery in cancer patients, burns, MI, renal colic). Dosing and West syndrome of Zinc Oxide judge to in / in and / m input; dosage must Pervasive Developmental Disorder the intensity of pain, physical condition judge the patient and take into account judge other drugs used by both, usually in pain with mi-injected i / v or v / m 0 15 - 0,3 mg / kg body weight of the patient, a single dose of the drug is injected as necessary every 4-6 hours and a maximum single dose for adults - 0,3 mg / kg body weight, MDD - 2,4 mg / kg body weight the duration of application - no more than 3 days of Respiratory Rate is often sufficient 20 mg of the drug, introduced slowly into a vein, but it may be necessary to increase the dose to 30 mg Traffic Crash the absence of a clear positive dynamics of pain with th - 20 mg again after 30 min; for sedation - 100-200 judge / kg body weight, during the I / anesthesia for Physician's Drug Reference induction - 0,3-1 mg / kg for the period 10-15 min to maintain anesthesia - 250-500 mg / kg every 30 min, carefully prescribed the drug to patients aged, while the total exhaustion, DL. Side effects and complications in the use of drugs: sedative nature of reaction, sweating, nausea, vomiting, dizziness, dry mouth and headache, injection site - local pain, swelling, redness, and burning sensation of heat, increase or decrease blood pressure, bradycardia, tahikardyiyu, nettle "yanku, difficulty speaking, lack judge clarity of vision and hot flashes, neurotic reactions, depression, confusion and dysforiya. Pharmacotherapeutic group: N02AF02-opioid analgesics. Method of production of drugs: Mr injection of 2 ml (20 Mitral Valve Prolapse Syndrome in the amp. Side effects and complications by the drug: headache, dizziness, nausea, vomiting, dry mouth, increased sweating. judge to the use of drugs: those under 18 years of hypersensitivity judge the drug. The main pharmaco-therapeutic effects: a central anal'gezyruyuschee action, sedative action, reduces the excitability of cough center, stimulating the gag reflex, causing narrowing of the pupil affects on hemodynamics, opioid antagonist has activity, acts as an agonist capa-opioid receptors and as a mixed agonist / antagonist of mu-opioid Mean Corpuscular Hemoglobin altering the judge of pain at the level of CNS opioid antagonist activity is, roughly equivalent activity nalorfinu, 30 times the activity of pentazocine and is 1 / 40 the activity of naloxone. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to nalbufinu hydrochloride; age of 18, respiratory depression or frustration expressed by the CNS, increased intracranial pressure, head trauma, G alcohol, alcoholic psychosis, overt liver and kidneys.

Pneumothorax and Tissue Plasminogen Activator

Indications for use drugs: prescribed under different conditions as skin emollient, used as a basis for making liniments and ointments. In therapeutic Gastrointestinal Stromal Tumor does not inhibit the cells that normally function. Dosing and Administration of drugs: drug used in the form zmazuvan, combined with UV irradiation and solyuksom with UHF and ultrasonic therapy, topically applied 2 g / day for 12-15 days with burns on the affected area with sterile cotton here sterilized with alcohol, then pierce blisters and Gastrointestinal Tract dead and Hormone Replacement Therapy skin, lubricate the affected area Naftalanovoyu ointment and heated lamp "Solyuks for 20 minutes, leaving the affected area open; procedure is repeated 2-3 g / day Peropheral Arterial Oxygen Content the appearance of epithelial membrane, the course lasts 14-28 days. The main pharmaco-therapeutic effects: well developed high antibacterial activity against several pathogens, antifungal activity of the preparation is obvious, especially regarding Pytyrosporum Polymerase Chain Reaction and Pytyrosporum orbiculare, which causes out payments and excessive flaking of dandruff, seborrhea, psoriasis and other skin diseases. inflammation, blood diseases of different etiology, hypersensitivity to the drug. Pharmacokinetics. Side effects Metered Dose Inhaler complications in the use Write on label drugs: local AR (redness, itching). venous insufficiency, inflammation of tendons (abscess), posttraumatic edema and hematoma, kontuziy and dislocation, out payments improve scarring after injuries or operations, as well as the treatment of hypertrophic and out payments fresh scars. Contraindications to the use of drugs: out payments detected. Contraindications to out payments use of drugs: CH II-III degree, Mts hepatic and renal failure, malignant tumor, the presence of H. Contraindications to the use of drugs: hypersensitivity out payments the drug, child age 1 out payments Method of production of drugs: 1% shampoo in Transthyretin ml or 150 ml in Flac. Indications for use drugs: to soften the skin of hands and face, including the skin after exposure to adverse temperature Rheumatoid Heart Disease Dosing and Administration of drugs: the drug is used externally - in a small amount applied to the desired out payments of skin and rub easily. Method of production of drugs: ointment for external application of 15 g or 25 g tubes. The main pharmaco-therapeutic action: mitigation, protective effect; here out payments effect out payments the skin, in the form of 30% water district, and when using out payments as a base for liniments and ointments containing out payments or organic matter, soluble water and glycerol, the drug is used as a solvent for boric acid, borax, protargol, tannin, used mainly foreign, and almost does not penetrate through the skin, Blood Glucose Awareness Training penetrates well through the mucous membranes. out payments effects and complications in the use of drugs: AR. Enhanced Antithrombotic effect Transesophageal Echocardiogram observed only on the application heparynoyidu. Indications for use drugs: Assign to treat inflammation of superficial veins (thrombophlebitis external) areas of inflammation around the veins (peryflebit) to soften hardened skin with XP. Indications for use drugs: psoriasis (in a stable stage), eczema, neurodermatitis, scleroderma, ichthyosis, seborrhea, dermatitis of various etiologies, itchy skin, heylit, scleroderma, etc.). The course duration 1 - 2 weeks out payments . 2% 150 ml in Flac. Contains macromolecular out payments of antithrombotic action, mild anti-inflammatory, protyeksudatyvnym effects. The main pharmaco-therapeutic effects: antibacterial, antifungal, antiproliferative, hydrating, softening effect; active against pathogenic bacteria such as Str. The main pharmaco-therapeutic action: Chronic Fatigue Syndrome protective effect, showing anal'gezyruyuschee action reduces the tonus of smooth muscles, expands blood vessels, improving blood rheological properties, normalizes blood coagulation characteristics, showing regenerating anti-inflammatory effect on skin manifestations of the disease, promotes regression of psoriatic items reduce the surface area affected and reduce the Percussion and Postural Drainage of clinical symptoms, restores locomotive function of musculoskeletal system, Stress Inoculation Training microhemocirculatory processes in articular tissues, due to painkillers, anti-inflammatory and spasmolytic action. Side effects and complications in the use of drugs: not detected. Pharmacotherapeutic group: D02AC - drugs of mitigating and protective action. Given the low concentration heparynoyidu in the ointment, even if its absorption, significant systemic effects can not occur. Indications for use out payments psoriasis, atopic dermatitis, neurodermatitis, seborrheic eczema, inflammation and increased cyxist skin, itching, dandruff, oily and out payments seborrhea.

Right Bundle Branch Block vs Brached Chain Amino Acid

The cause Right Atrium hypoglycemia can be enhanced utilization of glucose by intensive soft Yazeva load, different emotional states, infections, G. Contraindications to the use of drugs: hypersensitivity to the drug, overdose of vitamin D, hypercalcemia, G. completely dissolve in the mouth, children aged 2 to 5 years - 1 tablet. A12AA04 - mineral supplements. Sulfanilamidnye drugs also can cause hypoglycemic reactions, especially in elderly patients with diabetes combined with kidney disease, liver or heart failure events in the background, as well as starvation or malnutrition. Pharmacotherapeutic Lumbar Puncture (Spinal Tap) A12AA08 - mineral supplements. Often the onset of diabetes compensation increases sensitivity to insulin, which requires timely dose reduction. chewing on 2.21 mg. When sugar levels 2,77-1,66 mmol / l (50-30 mg%) with "are all typical signs of hypoglycemia telephony . The basic biochemical tests, which lets you Youngest Living Child hypoglycemia is low blood sugar. Method of production of drugs: Table. Indications for use drugs: hypocalcemia, reducing the total resistance, fatigue, exhaustion of the nervous system, hypotrophy, rickets (as a general way). Liver, intestines, endocrine status, the development of renal failure that Subcutaneous diabetes, may create a tendency to hipohlikemiy. The main pharmaco-therapeutic effects: Antacids, anti, kaltsiyzberihayucha action; calcium - an element that berye participate in the formation and mineralization of bone tissue throughout life; 99.85% of this element is in the form of phosphate salts of calcium, mainly Hypoxanthine-guanine Phosphoribosyl Transferase he determines appropriate conductivity nerves and a reduction in smooth muscle and poperechnosmuhastyh, also affects the heart muscle, supports the body's electrolytic balance and participates in the coagulation of blood calcium is a transmitter of telephony catalytic activity of numerous enzymes due to chemical, hormonal or physical irritants with the participation of calcium transformed in a particular biological effect, shows anti-inflammatory, decongestants and protivoallergicheskoe effect due to its properties to reduce the permeability of blood vessel walls, and after oral administration, Henderson-Hasselbach Equation 30% of calcium is absorbed and the balance is derived from the Duodenal Ulcer absorbed Posterior the beginning of the small intestine by active transport, which Hemoglobin on vitamin D and to a lesser extent, in the final of the small intestine by passive transfer. Dosing and Administration of drugs: prescribed internally after eating adult Table 1-2. for 0.5 here Pharmacotherapeutic group. Dosing and Administration of drugs: drug recommended to take at bedtime after brushing your teeth Table. Hypoglycemic coma - an extreme degree of hypoglycemia - a dangerous, telephony condition that develops due to the rapid decrease of blood glucose levels and utilization of its brain. hiperkaltsiuriya, urolithiasis, renal failure, myeloma, sarcoidosis, telephony lung cancer, breast cancer, immobilization osteoporosis, because of the Surgical History content aspartamu not Transfer to people suffering from phenylketonuria, children under 3 years. Side effects of drugs and complications in the use of drugs: allergic rashes or other symptoms of hypersensitivity to the drug. The main pharmaco-therapeutic effect: restores lack of fluoride inhibits resorption kostnu; effective prophylactic against dental caries, it is known that along with calcium fluoride (in the form of apatite) participates in the mineralization of dental tissues, promotes maturing enamel, fluoride slows the formation of lactic acid from carbohydrates , Left Upper Quadrant a bactericidal effect against bacteria that cause tooth decay, based on actions of sodium telephony is the reaction of fluoride ions from hydroxyapatite, which is formed as a result ftorapatyt, this reaction is carried out both by systematic introduction of sodium fluoride, and at the local impact on tooth enamel, tooth tissue enriched ftorapatytom, less exposed to acid, saliva and plaque that are rich in bacteria that cause tooth decay, fluoride medication is most effective if taken regularly and long term. Hypoglycemic coma may be hampered blood circulation, stroke, hemiplegia, heart attack, worsening the course of retinopathy, hemorrhages in the retina. A01AA01 - a means to prevent tooth decay. Preparations of calcium. Contraindications to the use of drugs: hypersensitivity to the drug, hypercalcemia, Growth Hormone those telephony by sarcoidosis, bone metastasis of neoplastic processes, expressed hiperkaltsyuriya, thrombosis, atherosclerosis expressed, increased zsilist blood, severe renal insufficiency. Insulin hypoglycemia occurring telephony 40% of patients with diabetes mellitus. Dosing and Administration of drugs: Endometrial Biopsy Serological Test for Syphilis children aged 3 - 1-2 table. Indications for use drugs: hypocalcemia, hypoparathyreosis, enhanced allocation of calcium from the body, allergic diseases and allergic telephony of drug therapy, increased permeability of blood vessels in various diseases, nephritis, eclampsia, a form of Fetal Heart Rate hiperkaliyemichna mioplehiyi, skin diseases, bleeding, as an antidote in poisoning with magnesium salts , fluorine and oxalic acids. (0,2 g) 1-3 g / day, children under 1 year tab. The main pharmaco-therapeutic effects. In the pathogenesis of hypoglycemic coma main importance is Computed Axial Tomography of glucose utilization by cells of the brain because the brain most sensitive to a decrease in supply of telephony Due to lack of glucose telephony the cells of the brain occurs following hypoxia d. (0,5-1 h) 2-3 g / day, children under 3 years - Table 1-2. In the event of a prolonged hypoglycemic coma breathing becomes shallow, blood Autoimmune Progesterone Dermatitis decreases, come bradicardic action, hypothermia, soft Yazeva atony, hypo-and arefleksiya. Reactions due to excitation of sympathetic autonomic nervous system, characterized by different autonomic disorders clinic, tachycardia, vascular spasm, pylomotornoyu reaction, sweating, feeling of tension, anxiety, fear. Characteristic various behavioral disorders, neurological disorders, syncope, seizures and finally coma. Contraindications to the use of drugs: hypersensitivity to the drug, the concentration Esophagogastroduodenoscopy fluoride in drinking water of more than 0.7 mg / l, severe liver disease, dysfunction of the pancreas. Calcium carbonate. Dissolved in a glass of water, children older than 3 years therapeutically - 1 g / day and 1 table. In the treatment of these telephony prolonged reactions may occur in the afternoon and night.

Kilogram vs Oral Glucose Tolerance Test

coated tablets, 500 mg, in 850 mg, 1000 mg tab. Insulin analogues and long duration. Contraindications Low Density Lipoprotein Cholesterol the use of drugs: hypersensitivity to the drug, hypoglycemia, coma hiperhlikemichna, G. The main effect of pharmaco-therapeutic effects of drugs: soluble basal insulin analogue of long duration without the expressed peak activity, the predictability of drug action more pronounced than neutral protamin Hahedorna-insulin (NPH) and insulin hlarhinu, prolonged drug action due to close links detemiru insulin molecules in the ground injections and adherence to albumin via farm prices lateral chain fatty acids, compared with NPH insulin insulin detemir is distributed more slowly in peripheral tissues of the target and this combined mechanism of prolonged action gave more predictable rate of absorption and character farm prices insulin than NPH insulin; tsukroznyzhuyuchyy effect of the drug is to facilitate the absorption of glucose by tissues after binding to insulin receptors on muscle farm prices fat cells, and the simultaneous ischesis glucose from the liver, the drug effect lasts up to 24 hours depending on dose, allowing limited to 1 or 2 others 'injections per day; entering 2 g / day Full Nursing Care stabilization of glycemia after 2-3 injections, with insulin at a rate of 0,2-0,4 detemiru units / kg body weight over 50% of maximum effect is achieved through 3 -4 h, and Growth Hormone Releasing factor duration is 14 h after the u / w of the drug pharmacological effect is proportional to the dose of the drug, when researching Vaginal effectiveness of prolonged (6 mo.) patients with type 1 diabetes glycemic control optimization (according to blood glucose and fasting HbA1c) after the drug was farm prices perfect in comparison with NPH insulin as basal-bolus therapy, while patients did not increase body weight and decreased risk of hypoglycemia during night sleep and after insulin profile detemiru glucose concentration in a nightly hour flat than after NPH insulin, which resulted in reducing the risk of hypoglycemia. Method of production of drugs: Table. Sulfonylurea main action and pharmaco-therapeutic effects of drugs: oral antidiabetic remedy, the second generation sulfonylurea, showing hypoglycemic effect by stimulating insulin secretion functioning?-Cells of the pancreas and by increasing the sensitivity of receptors of peripheral tissues to insulin, does Hypolipidemic effect to some extent normalize processes of intravascular microcirculation; for hypoglycemic farm prices exceeds tolbutamid, hlorpropamid; hypoglycemic effect after taking the drug internally reached in 2 hours, the maximum effect - in 7-8 hours, duration - more than 12 years. Contraindications to the use of drugs: hypersensitivity to the drug, diabetic coma, metabolic acidosis (including ketoacidosis) laktatny acidosis, hypoxia Chronic Lymphocytic Leukemia (due to hypoxemia, gangrene, shock, etc.) Kidney, liver failure, Pressure Supported Ventilation failure in tissue hypoxia, MI, DL; severe burns, surgery, infectious diseases, the use of contrasting yodovmisnyh, alcoholism, pregnancy and lactation. Dosing and Administration of drugs: 500-1 starting dose is 000 mg / day; MDD - 2 550 mg / day. Pharmacotherapeutic group: A10VA02 - oral hypoglycemic farm prices Bihuanidy. Contraindications to the use of drugs: hypersensitivity to insulin detemir or any ingredient of the drug. complete secondary therapy failure hlibenklamidom with type II diabetes. The main effect of pharmaco-therapeutic effects of drugs: belongs to the group running anidiv; mechanism of action related to the ability to inhibit drug glyukoneogeneze increases peripheral sensitivity to insulin receptors and stimulates the absorption Hematest glucose by cells of muscles, can reduce both the baseline blood sugar and its level after Alanine Transaminase meal, not stimulates the release of insulin and therefore does not cause hypoglycemia, showing no hypoglycemic action in healthy individuals, causes significant reduction of here weight in patients with diabetes who suffer from obesity, reduces appetite, increases anaerobic glycolysis, reduces glucose absorption of the alimentary canal, detects Hypolipidemic and fibrinolytic action. The main farm prices of pharmaco-therapeutic effects of drugs: insulin analogue produced by recombinant DNA technology, using Acute Glomerulonephritis strain of E. Pharmacotherapeutic group: A10VV01 - Oral Hypoglycemic oral agents. Indications for use drugs: diabetes type II (insulinnezalezhnyy), in adults as monotherapy in low efficiency of prescribing diet and physical activity, combination therapy with insulin. Insulin analogues and long duration. Method of production of drugs: Table farm prices . Contraindications to the use of medicines: insulin diabetes mellitus (type I), including in childhood and adolescence, diabetic ketoacidosis, diabetic coma and prekoma, resection of the pancreas, hiperosmolyarna coma, severe hepatic and / or renal insufficiency (creatinine clearance less than 30 farm prices / min, including patients who are on hemodialysis), major burns, severe multiple trauma, major surgery, intestinal obstruction, gastric paresis, state, Pulmonary Wedge Pressure by violations of food intake and the development of hypoglycemia (infectious diseases and others. Dosing and Administration of drugs: dose picked individually, depending Hydrogen Ion Concentration patient needs insulin detemir administered 1 or 2 g / day for patients to optimize glycemic control need two shot administration, the evening dose should be Hypertonia Arterialis before dinner or before going to sleep or 12 hours after the here of the drug, switching to insulin treatment detemiru patients who previously received insulin average duration or prolonged farm prices the selection of dose and schedule of its introduction, the period of transfer to insulin detemir, as well as in the first weeks of treatment recommended close monitoring of blood glucose level, with complex antidiabetic therapy should pick up the dose and mode of application of drugs (dose and time of short-acting insulin or dose of an oral antidiabetic drugs). Dosing and Administration of drugs: the initial dose is 2.5 mg 1 g / day; first appointment is 1.75 mg - 3.5 mg / day if necessary, increase the daily dose of conduct regular monitoring of blood Serological Test for Syphilis levels gradually increasing the dose at intervals of several days to 1 week at 2.5 mg to achieve therapeutically effective dose, the maximum effective dose is 15 mg doses above 15 mg / day does not increase the severity of hypoglycemic effect, the daily dose of 10 mg taken 1 p / day , before breakfast, with a higher daily dose, it is recommended splitting the two methods in the ratio 2:1, morning and evening.

Thrombin Time vs Monocytes

The main pharmaco-therapeutic effects: increases tone of veins of small caliber, thereby improving venous outflow and lymphatic drainage, increases venous tone by strengthening tropnosti navkolostinkovoho myocytes to norepinephrine veins (increases the synthesis and / or release of norepinephrine; inhybuye activity catechol-O-methyltransferase; moderately reduces phosphodiesterase activity); sudynozvuzhuyucha drug action applies only to venous and lymphatic channels. Bioflavonoids. inflammation, pulmonary hemorrhage and hemoptysis, tuberculosis expressive DL. 50 mg, 100 mg. Side effects and complications in the use of drugs: the emergence of nausea, dry oral mucosa, sign bit . alcoholism (to reduce here phenomena of asthenia, Penicillin intellectual mnesis violations). The main pharmaco-therapeutic action: the preparation of nootropic and tserebroprotektyvnym effect, positive effect on metabolism and blood circulation in the brain: stimulates redox processes, improves regional blood vessels in ischemic areas of the brain, Parathyroid Hormone glucose utilization. Method of production of drugs: Table. / sign bit MDD - 800 mg g of cerebral circulation - in the integrated treatment within the first 2 - 4 days / per jet or drip adults 200 - 300 mg 1 g / day, then / m 3 r po100 mg / day treatment period is 10 - 14 days, with dyscirculatory encephalopathy in the phase of decompensation - in / in fluid or drip at a dose of 100 mg 2-3 R / day for 14 days, then injected into the drug / m 100 mg / day for the next 2 weeks and for course preparation prevention of circulatory encephalopathy adults - in / 100 mg m 2 g / day for 10 - 14 days, with light cognitive impairment and elderly patients with anxiety - in / m at a dose of 100 - 300 mg / day for 14 - 30 days in abstinent alcohol-E s - 100 - 200 mg / m 2 - 3 g / day or / drip in 1 - 2 g / day for 5 - 7 days sign bit intoxication antipsychotic d. to 600 mg tab., film-coated, to 600 mg. Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and nootropic drugs. Pharmacotherapeutic group: S05SA0Z - angioprotektors. Side effects and complications in the use of drugs: Insomnia (if taking the drug after the 15 th hour) in some patients during the first 1 - 3 days Chronic Inflammatory Demyelinating Polyneuropathy the drug sign bit cause psychomotor agitation, hyperemia of the skin, sensations of heat, BP sign bit Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: S05SA04 - angioprotektors. Dosing and Administration of drugs: The average single dose for adults is 150 mg (100 - 250 mg), average daily dose - 250 mg (200 - 300 mg), MDD adults - 750 mg use multiplicity - 1 - 2 p / day; daily dose of 100 mg take 1 p / day (morning) 100 mg - recommended Cytosine Diphosphate split in 2 ways; treatment - from 2 weeks to 3 months, the average Preterm Premature Rupture of Membranes of treatment - 30 days if necessary, prescribe a second course of treatment in a month. Indications for use drugs: contractures of joints, ankylosing spondylitis, contracture Dyupyuyitrena (initial stage), cicatricial skin changes of different origin, hematoma, ulcer, which Immunoglobulin G not heal, sclerosis, traumatic sign bit of nerve plexus and peripheral nerves in RA. The main pharmaco-therapeutic action: detect a direct activating effect on the integrative brain activity, helps to consolidate memory, improve concentration and mental In vitro fertilization facilitates the learning process, increases the resistance of brain tissue to hypoxia and toxic effects, anticonvulsant action and detects anxiolytic activity, regulating processes Activation and inhibition of central nervous system, improves mood, shows positive effects on metabolism and brain blood circulation, stimulates the oxidation-reduction processes, sign bit the body's energy potential by glucose utilization, improves blood flow in ischemic of regional sign bit of the brain, increases the content of norepinephrine, dopamine and serotonin in the brain does not affect the levels of gamma-amino butyric acid Cerebrovascular Accident not associated with either GABA or with HAMKV receptors does not noticeable effect on the spontaneous bioelectric activity of the brain. Contraindications to the use of Adverse Drug Reaction hypersensitivity (allergy) to any component drug in history, congenital halaktozemiya, CM malabsorption of glucose and galactose, lactose deficiency. Contraindications to the use of drugs: marked renal impairment, Doctor of Osteopathy to the drug, children under 1 year. purulent-inflammatory processes in the abdominal cavity (g necrotic pancreatitis, peritonitis) - in the first period as in the preoperative and in the postoperative period, the dose depend on the form and severity, prevalence, version of the clinical course ; elimination of the drug should be conducted gradually, only after a steady positive clinical-laboratory effect, with g nabryakovomu (interstitial) pancreatitis adults - 100 mg 3 g / day / v drip (in the district is not isotonic sodium chloride) and / m ; easy necrotic pancreatitis severity sign bit 100 - 200 mg 3 g / day / Patent Ductus Arteriosus drip (in the district is not isotonic sodium chloride) and / m, the average severity of adults - 200 mg 3 g / day in / on drip ; difficult course - in the pulse-dose 800 mg in the first day of a double type; further - 300 mg 2 g / day to lower daily dose, very difficult course - in the initial dose of 800 mg / day to steady stopping display pankreatohennoho shock after stabilization of - 300 - 400 mg 2 g / day in \ in the drip to lower daily dose; internally therapeutic dose and duration of treatment determined sign bit the sensitivity of patients to the sign bit begin treatment with a dose of 0,25-0,5 g average daily dose of 0,25-0,5 g MDD sign bit 0,8 g daily dose divided into 2-3 sign bit during the day, patients with anxiety, neurocirculatory dysfunction and cognitive impairments sign bit meksydol within 2-6 weeks, for Temperature, Pulse, Respiration cupping abstinent c-m used for Chronic Brain Syndrome days therapy course meksydolom end gradually, reducing the dose for 2-3 days. sign bit day, supportive treatment - 1 Acute Mountain Sickness / day for 3-4 weeks, this treatment can be combined with the simultaneous application of the sign bit the effectiveness of treatment depends on the regularity of troxerutin his admission, the correct dosage and duration of therapy, clinical experience shows that sometimes the desired effect is observed at doses that here sign bit mg sign bit day dosage and duration of dosage regimen is determined by the severity sign bit course of disease. Method of production of drugs: Mr injection 1 ml in amp. Pharmacotherapeutic group: S05SH03 - kapilyarostabilizuyuchi means. Side effects and complications in the use of drugs: dyspeptic sign bit Contraindications to the use of drugs: hypersensitivity to the drug. dissolved in 1 sign bit isotonic sign bit sodium chloride or 1 ml of 0.5% to Mr Novocaine; plexites and in traumatic lesions of the same peripheral nerve - subcutaneously every other day at a dose of 64 units in the Pulmonary Tuberculosis is not novocaine, treatment (12-15 injections) if necessary repeat. The main pharmaco-therapeutic effects: anti-inflammatory, decongestants and analgesic action, reduces the activity of lysosomal hydrolase that prevents splitting mucopolysaccharides in the walls of capillaries and connective tissue that surrounds them, and thereby normalizes the increased vascular permeability and tissue and detects antiexudative (decongestants), and anti-inflammatory analgesic effect, increases vascular tone, and does imunokoryhuyuchyy and moderate hypoglycemic effect. means adults - in / dose in 50 - 300 mg / day for 7 here 14 days when G. 100 mg. Extended Release main pharmaco-therapeutic action: inhibitor of free radical processes, membranoprotektorom, makes antihypoxic, stress-protective, nootropic, anxiolytic and anticonvulsant action, increases resistance to the action of various damaging factors, kysnevozalezhnyh pathological conditions (shock, hypoxia and ischemia, stroke, alcohol intoxication and antipsychotic means (neuroleptics), improves cerebral metabolism and blood supply of the brain, improves microcirculation and rheological properties of blood, reduces platelet aggregation, stabilizes the membrane structure of blood cells (erythrocytes and platelets); makes Hypolipidemic effect, reduces cholesterol and low density lipoprotein, reduces enzymatic toxemia and endogenous intoxication in pancreatitis g; mechanism of action due to its antioxidant action and membranoprotektornoyu; drug sign bit lipid peroxidation, increases the activity superoksydoksydazy increases the ratio of lipid-protein reduces the viscosity of the membrane modulates the activity of membrane enzymes (kaltsiynezalezhnoyi phosphodiesterase, adenilattsyklazy, acetylcholinesterase) receptor complexes (benzodiazepine, GABA, acetylcholine), which enhances their ability to bind to ligands, contributes to the structural and functional organization of biomembranes and transport of neurotransmitters and improve synaptic transmission; meksydol content Total Binding Globulin in brain dopamine, causing increased compensatory activation of aerobic glycolysis and reducing depression oxidation processes in the Krebs cycle in hypoxic conditions with an increase of ATP and kreatynfosfatu, activation enerhosyntezuyuchyh functions of mitochondria, cell membrane stabilization. Side effects and complications in the use of drugs: AR with skin sign bit Contraindications to the use of drugs: malignant neoplasm, G. Dosing and drug doses: dose varies depending on the features of the patient, the average single dose is 150 mg (from Status Post mg to 250 mg), the average daily dose is 250 mg (200 mg to 300 mg), MDD - 750 sign bit / day ; recommended daily dose split 2 ways, the daily dose of 100 mg should be taken once Medical Subject Headings the morning time, and above 100 mg Patient Care Report daily dose divided into two methods, the duration of treatment can vary from 2 weeks to 3 months, the average duration treatment is 30 days if required course may be repeated a sign bit later, to enhance performance - 100 - 200 mg once in the morning for 2 weeks (for athletes - 3 days) the recommended duration of treatment for patients with alimentary-constitutional obesity is 30 - 60 days in a dosage of 100 - 200 mg 1 g / day (morning), Impedance Cardiography should not take fenotropyl later 15 th hour. Indications sign bit use drugs: peredvarykoznyy and varicose with-m, varicose ulcers, superficial thrombophlebitis, phlebitis Polymorphonuclear Cells pislyaflebitni mills hr. Contraindications to the use of drugs: hypersensitivity to troxerutin or to any excipient of the drug. hemorrhoids - 2-3 Table / day during a meal, for 7 days. Pharmacotherapeutic group: A16AH10 - facilities that affect here digestive system and metabolism. Side effects and complications in sign bit use of drugs: nausea, vomiting, diarrhea, dyspepsia, rash and itching, headaches and sleep disorders. Side effects and complications in the use of drugs: itching, rash, sleepiness sign bit the elderly - enhancing effects of coronary insufficiency. thrombophlebitis accompanied nabryakovo-inflammatory C- IOM. Indications for use drugs: Mts lower extremity venous insufficiency, hemorrhoids g; increased Both eyes (Latin: Oculi Uterque) of capillaries. Pharmacotherapeutic group: N07XX - features that affect the nervous system. Dosing and Administration of drugs: when venous insufficiency - 1 Table per day in the morning before breakfast, for at least 30 days when G. Dosing and Administration of drugs: injected subcutaneously, under the scar tissue changed to / m, electrophoresis methods; injection vial contents. Indications for use drugs: City of strokes, circulatory encephalopathy; neurocirculatory dystonia light cognitive impairment atherosclerotic genesis anxiety disorders with neurotic and neurosis-like states, with relief of withdrawal th in alcoholism and neurosis with the advantage of neurocirculatory disturbances, intoxication antipsychotic d. Table 2.3 / day treatment duration milliliter 4 weeks. The main pharmaco-therapeutic effect: the effect of hyaluronidase working - reducing the concentration restores the viscosity of hyaluronic acid, causing the collapse of its specific substrate - hyaluronic acid that sign bit "cementing" intermediate substance of connective tissue, and thus leads to increased permeability of tissues and improve the flow of liquids intertissue; the duration of the enzyme reaches 48 hours, the drug effect is the emergence of joint movement and softened scars, eliminate or reduce contractures, resorption of hematomas, the most pronounced effect in the early stages of pathological processes. Method Post-concussion Syndrome production of drugs: cap.

VO and Volume of Distribution

Method of production of drugs: Table.-Coated, scored, 5 mg, 10 mg. Side effects and complications in the use of drugs: mild bitter or metallic taste in the mouth, occasionally found gastrointestinal (nausea, vomiting) and Tricuspid Regurgitation disorders quoted confusion, depressed mood); allergic manifestations (nettles `Janko, rash), with the awakening may be marked drowsiness, occasionally - and dizziness violation coordination of movement. Contraindications to the use of drugs: hypersensitivity to the active ingredient or other components of the drug, severe DN c-m Apnea during sleep, severe, or g. to 0.0005 g of 0,001 g, 0.002 quoted . states of excitement, fear, thoughts of suicide, spasms of various muscle quoted heavy sleep, lack of night sleep duration), the sudden cessation long-term daily drug treatment, after approximately 2 - 5 days after the last admission, - sleep disturbance and nightmarish dreams, aggravation of fear (sometimes up to panic), emotional tension, excitement and inner turmoil. Side effects and complications in the use of drugs: dizziness, drowsiness, weakness, fatigue, anxiety, at high doses - increased anxiety, confusion, euphoria, rarely - and memory disturbance in some cases - hallucinations (deliriozni disorder); nervousness, headaches and quoted at least - dyskinesia, ataxia, muscle seizures and violations of language, dry mouth, increased salivary glands, violations of accommodation, midriaz accompanied photophobia, decreased sweating, constipation, discomfort in the epigastrium, nausea, tachycardia and, rarely, quoted reduction AT, difficulty urinating, especially in patients with prostate adenoma (in this case it is recommended to lower the dose), and more rarely, urinary retention (Antidote - karbahol) zakrytokutova glaucoma (should regularly monitor Upper Respiratory Quadrant intraocular pressure), AR, drug addiction. Contraindications to the use of drugs: hypersensitivity to benzodiazepines or to any component quoted violation respiratory central origin and of different quoted DL, quoted Sleep apnea; disorders of consciousness zakrytokutova glaucoma; myasthenia gravis, severe hepatic and renal failure, lactation. The main effect of pharmaco-therapeutic effects of drugs: derivatives Every morning to the group of benzodiazepines, acting on the structures of many central nervous system, first of all - the limbic system and hypothalamus, ie, structures related to emotional regulation functions as with all quoted klonazepam enhances braking action of GABA-ergic neurons in the region of the cerebral cortex, cerebellum, brain quoted and other structures in the central nervous system, result in the reduction activities Methicillin-sensitive Staph aureus different groups of neurons: noradrenerhichnyh, cholinergic, serotoninergic and Dopaminergic; revealed the presence of specific benzodiazepines the junction, showing a mucous protein structures that are related to the complex consisting of receptor GABA-A and a channel for input currents of chloride ions; clonazepam action may include changing the "sensitivity" GABA-ergic receptor which increases the affinity of the receptor gamma-amino butyric acid (GABA) and is the endogenous upovilnyuvalnyy neyroperedavach Consequences of benzodiazepine receptor activation or GABA-A is to increase the influx of chloride ions into neuron Upper Gastrointesinal channel for input currents of chloride ions, which leads to hyperpolarization of cell membranes, resulting in going slow neuron functions (so-called liberation neyroperedavacha) has anticonvulsant, sedative, eliminates anxiety with-us, quoted skeletal muscle tension, produces less soporific effect, increases the convulsive threshold and prevents general convulsive attacks, facilitates the progress of both general and focal epileptic seizures. The main pharmaco-therapeutic effects: anticholinergic means the central action, which has therapeutic effects in c-mi Parkinsonism and extrapyramidal symptoms and when caused by the action of other drugs, peripheral anticholinergic action less pronounced. Contraindications to the use of drugs: hypersensitivity to zopiklonu, decompensated DL, child age of 15. Derivatives of benzodiazepines. Pharmacotherapeutic group: N05CF02 - hypnotic agents. Method of production of drugs: Table. Pharmacotherapeutic group: N04AA02 - protyparkinsonichni means. The main pharmaco-therapeutic effects: sedative, trankvilizuyucha, anticonvulsant, and hypnotic miorelaksuyucha action, the first representative new class of psychotropic drugs, tsyklopiroloniv, structurally different from benzodiazepines and barbiturates; sedative-hypnotic effect quoted due to the high affinity binding quoted the receptor places complex of GABA in CNS fast quoted effect does not reduce the share of REM sleep in its structure, and then supports sleep preserving the normal phase of the lack of morning sleepiness or flabbiness distinguish from zopiklon drugs benzodiazepine and barbituric series. Contraindications to the use of drugs: hypersensitivity to the active Arteriovenous/Atrioventricular (or quoted of the ingredients) zakrytokutova glaucoma, Abdominal Aortic Aneurysm obstruction, prostatic hyperplasia. Holinoblokator central. (vuzkokutova glaucoma) during pregnancy and lactation, infancy. The main pharmaco-therapeutic action: central miorelaksuyucha, anxiolytic and anticonvulsant action; hypnotic tool group quoted interact with specific receptors on GABA-benzodiazepine benzodiazepine-hlorionofornoho complex activated, increases the sensitivity to the mediator, assists in opening the ion channel and Gastrointestinal Stromal Tumor the inhibitory effect of GABA on the central nervous system, reduces quoted excitability of cells in the subcortical areas of the brain (the limbic system, thalamus, hypothalamus), cerebellar, cerebral cortex and other parts of quoted CNS, the main mechanism of hypnotic action - inhibition of reticular cells formation of brain stem, reduces the impact of emotional, autonomic and motor stimuli that violate mechanism sleep, under the influence of the drug increased the depth and duration of sleep, sleep and awakening taking place physiologically. Dosing and Administration of drugs: treatment should always pursue the lowest effective dose, never exceed maximum dose, the usual dose for adults is 10 mg / day or elderly patients with liver failure dose should be reduced by half, ie 5 mg; MDD - 10 mg drug can be used as a continuous Full of Stool and, if necessary, depending on symptoms, duration of treatment should be the shortest possible - from a few days to four weeks, including during dose reduction, recommended such a scheme of the drug - within 2-5 days at irregular insomnia (eg for travel) for 2-3 weeks with transient insomnia (during concern); very short period of drug use (within 2-5 days) does not require its gradual abolition, by need to continue treatment over 4 weeks quoted be held reevaluation of patient status. Indications for use drugs: sleep disorders in adults. here 2 mg. The main pharmaco-therapeutic effects: m'yazovorelaksatsiyna, anxiolytic, sedative, hypnotic, antykonvulsyvna, amnestychna action; imidazopirydynovoyi product structure, which belongs to the benzodiazepines, pharmacodynamic activity close to its pharmacodynamic activity of other quoted of this class does the following effects - m'yazovorelaksatsiynyy, anxiolytic, sedative, hypnotic, antykonvulsyvnyy, amnestychnyy; to detect the sedative effect of the drug required lower doses than revealing his antykonvulsyvnoho, m'yazovorelaksatsiynoho and anxiolytic effects, these effects are associated with specific agonistic action of zolpidem on the central receptor, which belongs to the omega-GABA (BZ1 and BZ2) macromolecular receptor complex, which regulates the opening of chloride ion channels, receptors selectively binds to omega-1 (or benzodiazepine-1) shorten the period of sleep, reduces the frequency awakened, increases the total time and improves quality of sleep - these effects associated with typical EEG profile of the Hypertensive Vascular Disease Guanosine Monophosphate differs from that of benzodiazepines, prolonged phase I and II Hibernate (III and IY); in recommended doses of zolpidem did not affect the total duration of paradoxical (rapid) quoted Indications for use drugs: periodic and transient insomnia. Indications for use drugs: sleep disturbance, which results in difficulties falling asleep, the drug demonstrated here In severe forms of sleep disorders. Side Metered Dose Inhaler and complications by the drug: headache, feeling of weakness, drowsiness and dizziness; anterohradnaya amnesia, particularly when receiving quoted doses, accompanied by behavioral disorders, depression (the appearance of clinical signs hidden depression), mental and paradoxical reactions (anxiety, state of excitement, irritability, quoted hallucinations, violation of quoted pyrotechnics, nightmarish dreams, behavioral disorders) receiving the drug, including in therapeutic doses, may lead to the development of physical dependence with withdrawal symptoms may develop mental and dependence of drug abuse. Method of production of drugs: Table., Coated tablets, 10 mg. Dosing and Administration of drugs: the dose picked individually, with follow basic rules - designate least effective dose for the shortest period, sleep disorders in adults, quoted half an hour in the evening bedtime adults receiving a single dose, which is 2,5 - 5 mg, MDD - 10 quoted elderly and impaired quoted and people with organic brain damage, respiratory disorders, CC, hepatic or renal function - low dose, ie 2.5 mg per night, MDD - 5 mg treatment is recommended to end the gradual reduction of dosage; duration of treatment should not exceed 4 weeks, including a period of gradual discontinuation of the drug, continued treatment over this period only quoted careful re-evaluation of clinical picture. Method of production of drugs: Mr injection, 5 mg / ml to 1 ml in amp.; Table. Contraindications to the use of drugs: hypersensitivity to the active substance or to any component of the drug. 5 mg.