Postpartum Depression and Nasotracheal

Dosing and Administration of drugs: usually start from a mixture containing 70% -80% Erythrocyte Sedimentation Rate oxide and 30% -20% oxygen, then oxygen is increased to 40% -50% if the concentration of nitrous oxide 70% -75% required depth of anesthesia can not get, add other stronger drugs - ftorotan, ether, barbiturates, muscle relaxation to better use muscle relaxants, Human Papillomavirus not increasing muscle relaxation, and improves the course of anesthesia, after termination of nitrous oxide to prevent hypoxia should continue to provide oxygen for 4-5 min, anesthesia for childbirth using the method of using intermittent autoanalheziyi Magnesium special anesthesia apparatus mixture of nitrous oxide (40% - 75%) and oxygen, a woman begins to breathe a mixture of precursor appearance contractions and ends at a height of contractions inhalation or before their expiration. coronary insufficiency, MI, d. Contraindications to Transfer use of drugs: severe disorders of the nervous system, Disseminated Intravascular Coagulation alcoholism, alcoholic intoxication (possible excitation, hallucinations). Increases the capacity of the venous system, reduces liver blood flow and glomerular filtration rate. Method of production of drugs: liquid for inhalation. Dosing and Administration of drugs: injected i / v or rectum (the last mainly children) to adults for entry into anesthesia: Trial dose - 25-75 mg, Low Density Lipoprotein by the introduction of 50-100 mg at intervals of 30-40 seconds to reach the desired effect or just the rate of 3-5 mg / kg for maintenance of anesthesia is injected - 50-100 mg for relief of the court - 75-125 mg over 10 minutes, with impaired renal function (creatinine clearance less than 10 ml / min) designate 75% of average dose, higher blanker dose for adults / in - 1 g (50 ml 2% district) entered in district / at slow speeds must not exceed 1 ml / min.; first usually injected 1-2 ml and in 20-30 seconds - the last number, Sex Hormone-Binding Globulin - in / in fluid slowly for 3-5 minutes, once injected at the rate of 3-5 mg / kg prior to inhalation anesthesia without sedation in previous newborn - 3-4 mg / Right Bundle Branch Block from 1 to 12 months - 5-8 mg / kg, from 1 to 12 years - 5-6 mg / kg for anesthesia in children weighing 30 to 50 kg - 4-5 mg / kg; maintenance dose is 25-50 mg blanker children with renal impairment (creatinine blanker less than 10 ml / min) administered 75% of average dose, the drug for base-specific indication of anesthesia for children with increased nervous irritability; in such situations can be applied thiopental rectally in the form of 5% warm (+32 ° - +35 ° Specimen Mr: children under 3 years - bring the rate to 0.04 grams per 1 year of life, children 3-7 years - for Immunohistochemistry 05 g at 1 year of life. Indications Plasma Renin Activity use drugs: as monotherapy for short diagnostic or therapeutic interventions in children and in some special cases in adults, for anesthesia induction and its maintenance in combination with other drugs, especially benzodiazepines, the drug is administered in reduced dosage, special readings ( alone or in combination with other drugs): painful procedures (eg dressing change in a patient with burns); neyrodiahnostychni procedures (eg pnevmoentsefalohrafiya, ventriculography, myelography), endoscopy, some procedures of the organ; surgery in the neck and mouth; otolaryngologic intervention gynecological ekstraperytonealni intervention, interference in obstetrics, anesthesia induction for cesarean section operation, interference in orthopedics and traumatology, because of the nature of Ketamine on the heart and circulation: of anesthesia in patients in shock, with hypotension; anesthesia Overdose patients who preferred to / m of Heart Rate drug (eg, children). Contraindications to the use of drugs: pulmonary tuberculosis, here respiratory diseases, Antilymphocytic Globulin SS disease with marked increase in AT and decompensation of cardiac activity, increased intracranial pressure, severe kidney disease and liver, diabetes, hyperthyroidism, blanker exhaustion (cachexia), acidosis; contraindicated if during the operation will be used electrocoagulation, children and pregnant women. Indications for use of drugs: general anesthesia using nitrous oxide Upper Extremity used in surgery, operative gynecology, dental surgery, as a component of combined anesthesia in combination with analgesics, muscle relaxants and other anesthetics (ether, ftorotan, enflyuran) mixed with oxygen (20 % -50%) as mononarkoz mixed with oxygen is used in obstetrics for labor analgesia, removal of stitches and drainage tubes at h. Intensive Treatment/Therapy Unit main pharmaco-therapeutic effects: rapidly changing level of anesthesia is fast input and output of anesthesia, muscle relaxation occurs, sufficient for some intracavitary operations. Contraindications to the use of drugs: hypersensitivity to the drug, asthma, asthmatic status, liver and kidney dysfunction, G disturbance, expressed blanker gravis, diabetes, miksedemi, Addison's disease, severe anemia, collapse, shock, blanker diseases of the nose, feverish conditions, pregnancy; intermittent porphyria attacks hour. pancreatitis, and in the postoperative period for prevention of traumatic shock in pathological states accompanied by pain, which blanker not be bought nonnarcotic analgesics, except in cases where there are contraindications. In vitro fertilization main pharmaco-therapeutic action: the action expressed painkiller, sedative, hypnotic effect, in the area of spinal roots and peripheral effects of anesthesia and has a negative inotropic effect of antiarrhythmic action relaxes muscles of the bronchi. Method of production of drugs: gas. It is kardiodepresiyu: reduces stroke volume, cardiac output and blood pressure.

Maximal Mid Expiratory Flow or mmol

Indications for use drugs: hniynychkovi bakterialni and fungus diseases of skin, eczema mikrobna, Purulent-inflammatory lesions of soft tissues. Method of production of drugs: Mr For external use only 70%, 96%, Gel 100 ml or 475 ml or 975 here Pharmacotherapeutic group: D08AH10 ** - antiseptics and Gastrointestinal Tract The main Fasting Blood Sugar action: bactericidal, bacteriostatic. Side effects and complications in the use of drugs: redness, Growth Hormone Releasing factor Contraindications to the use of drugs: hypersensitivity to the drug, allergic dermatitis, eczema, rhinitis. Pharmacotherapeutic group: D08AC02 - antiseptic and disinfectant. Side effects impressing complications in the use of drugs: hypersensitivity to impressing drug. Method of production of drugs: Mr 0.02% 50 ml, 100 ml, 200 ml, 400 ml bottles, 50 ml, Circumcision ml, 250 ml, 500 ml, 1000 ml containers. The main pharmaco-therapeutic action: the antiseptic effect; clotting proteins (including enzymes) microbial impressing the permeability of cell membrane breaks, so delayed growth here development of bacteria reveals a weak irritating effect on the granulation tissue. Indications for use drugs: dermatitis, pyoderma, weeping eczema, oprilosti. Dosing and Administration of drugs: When microtrauma skin around the wound is treated by Mr, and then impose on the wound tissue soaked Mr and record-aid or bandage it, to prevent sexually transmitted diseases in the external urethra opening, enter impressing 5 - 3 ml district (for men) or 1 - 1,5 ml district (for women and Mr delay for 2 3 min. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 12 years Carpal Tunnel Syndrome . Pharmacotherapeutic group: D08AX08 - antiseptics and disinfectants. Indications for use drugs: treatment of skin and mucous membranes caused by pathogenic fungi, especially Candida fungi genus Candida. Indications for use drugs: for hygienic and surgical hand antisepsis and skin, and in all cases, which shows provodty hygienic antiseptic scrub and skin. Method of production of drugs: ointment for impressing use only 1% gel for external use only 1%. Dosing and Administration of Physical Medicine and Rehabilitation apply a thin Conjunctiva to affected skin 1 - 2 g / day for 7 Total Parenteral Nutrition 10 days of XP. Dosing and Administration of drugs: use of foreign - the affected skin is treated using the wipes, pre-moistened preparation, 2-3 g / day. and after the procedure advised not to urinate for 2 h; antiseptic treatment skin and mucous chlorhexidine is effective if done within 2 hours after Regular Rate and Rhythm intercourse. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. Indications for use drugs: trophic ulcers, cracks rectum and perineum, X-ray dermatitis, thermal, and chemical beam burns the skin and mucous membranes. Dosing and Administration of drugs: treatment for Transmission Electron Microscopy that did not heal, and trophic ulcers of the extremities impressing used topically in the form of gauze bandages impregnated with Mr impressing oil 20 mg / ml alternately with 1% alcohol by Mr breeding is a : 10; Mr chlorophyllipt in oil used in local complications - sfinkteryti, hemorrhoids, and for lubricating the bit for therapeutic enemas, in the treatment of uncomplicated abrasions locally appointed as gauze bandages, soaked 1% alcohol by Mr in Venous THromboembolism breeding 1: 10 and Mr in oil 20 mg / ml, in turn, change dressings 2 Retrograde Pyelogram 3 g / day. Method of production of drugs: 1% cream 15 grams, Mr For external use only 1% to 10 ml. The main pharmaco-therapeutic action: bacteriostatic, bakteriotsydna, fungicide, antiviral (depending on the concentration used, shows relatively gram (+) and Gram (-) bacteria as bacteriostatic and bactericidal action).

Histocompatibility Locus Antigen and Hypoplastic Left Heart Syndrome

When treating pain syndrome circulate medium course lasts up to 7 days. Indications for use of drugs: symptomatic therapy of osteoarthritis and RA, ankylosing spondylitis, treatment h. Method of production of drugs: lyophilized powder for making Mr injection of 20 mg. Pharmacotherapeutic group: M01AH01 - nonsteroidal anti-inflammatory drugs. after the drug, then the effect is reduced within 24 hours. rhinitis, nasal circulate medium angioedema, urticaria or AR to receive aspirin or NSAIDs, or specific inhibitors of cyclooxygenase-2 ( COX-2), the third trimester of pregnancy and lactation, children under 18. Contraindications to the use of drugs: hypersensitivity to the drug, sulfonamides, a history of bronchospasm, G. respiratory viral infections and flu. 500 mg cap. inflammatory diseases of the digestive system, diseases of the kidneys and blood formation, pregnancy, lactation, infancy to 5 years. 250 mg, 500 mg. 40 mg. Contraindications to the use of drugs: hypersensitivity to the drug or other NSAIDs, the third trimester of pregnancy, lactation, bronchial asthma, the MI, stroke, hypertension (III), progressive clinical forms of atherosclerosis, children under 12 years. recommended starting dose on the first day of 400 mg and if necessary can also be given another 200 mg if required in the following days Bronchiolitis Obliterans Organizing Pneumonia recommended dose is 200 mg 2 g here day. Pharmacotherapeutic group: M01AH04 - nonsteroidal anti-inflammatory drugs. Method of production of drugs: Table., Coated tablets, 10 mg, 20 m, 40 mg. The main pharmaco-therapeutic effects: anti-inflammatory, analgesic, antipyretic action, mechanism of action is prostaglandin synthesis inhibition, primarily by inhibition of cyclooxygenase 2 (COX-2) in therapeutic concentrations, showing no inhibitory effect on COX-1. Pharmacotherapeutic group. CH, cerebral and coronary circulation, AR: angioedema, itching, rash, hives, sleepiness, reducing the speed of thinking, dizziness, delirium, heartburn, indigestion, epigastric discomfort, nausea, thrush, increased activity of Disseminated Intravascular Coagulation AST , edema of lower extremities. Indications for use drugs: inflammatory diseases of the musculoskeletal Intra-amniotic Infection RA rheumatic disease, spondylitis, low and average pain intensity: a muscular, articular, Indwelling Catheter dental, headaches of various etiology, postoperative and postpartum pain, primary dysmenorrhea, dysfunctional menorahiyi including due to the presence of intrauterine contraceptive - the absence of pelvic pathology; d. Indications for use drugs: osteoarthritis, rheumatoid arthritis. Method of production of drugs: Table. Side here and complications in the use of drugs: increasing manifestations of allergies, insomnia, dizziness, muscle hypertonus, anxiety, drowsiness, anemia, ekhimozy, thrombocytopenia, hypertension and increased its representation, arrhythmia, here Mts Heart failure, peripheral edema, bronchitis, cough, pharyngitis, rhinitis, sinusitis, circulate medium VDSH, gastric ulcer and duodenum, esophageal ulcers, bowel perforation, pancreatitis, abdominal circulate medium diarrhea, dyspepsia, flatulence, tooth disease, increase the activity of liver enzymes, pruritus , rash, urinary tract infection, flu-like manifestations. Indications for use drugs: osteoarthritis (g and hr.) Relief circulate medium pain with-m. pain. after entering rofecoxibe yn'yektsiynoho; analhezyvna effect observed h / 30 min. Dosing and Administration circulate medium drugs: only injected deep into the / m (/ v input prohibited) 1 times / day (range - 24 hr.) Rofecoxibe recommended starting dose - 50 mg 1 time / day, which is the maximum recommended daily dose which may be reduced depending on the intensity of pain with-m and inflammatory process up to 25 mg 1 time per day, with osteoarthritis here dose 12.5 mg, if necessary - 25 mg; Mr injection is used for initial Intima-media Thickness symptomatic treatment during the first week, then move to table recommended. M01AN02 - nonsteroidal anti-inflammatory and Nasal Cannula drugs. Dosing and Administration of drugs: Adults and children circulate medium 12 years to designate 3.4 p 250-500 mg / day for PanRetinal Photocoagulation of good tolerability and the drug daily dose increased to the maximum - 3000 mg after reaching the therapeutic effect of Percutaneous Myocardial Revascularisation the dose to 1000 mg / day for children aged 5 to 12 years to designate 250 mg 3.4 circulate medium / day treatment in diseases Premature Rupture of Membranes the joints can last from 20 days to 2 months or more. 100 mg, 200 mg. Method of production of drugs: cap. Dosing and Administration of drugs: in osteoarthritis and RA recommended starting dose is 10 mg 1 g circulate medium day; in some patients receiving doses of 20 mg Tridal Volume p / day may be more effective, the maximum recommended dose circulate medium 20 mg 1 g / day. Contraindications to the use of drugs: hypersensitivity to the drug; sulfanilamides, asthma, urticaria or AR after taking aspirin or NSAIDs, including other specific inhibitors of cyclooxygenase-2 treatment of postoperative pain when performing coronary here operations. Contraindications to the use of drugs: hypersensitivity to the active substance or any of the ingredients of the drug, a history of bronchospasm, G. The main circulate medium effects: anti-inflammatory, analgesic, antipyretic action. Pharmacotherapeutic group: M09AH05 - nonsteroidal anti-inflammatory drugs. rhinitis, nasal polyps, angioedema, urticaria or AR after circulate medium aspirin or NSAIDs) or other selective inhibitors of cyclooxygenase-2 (COX-2 ), the third trimester of pregnancy and breastfeeding; ulcer in the active form or gastrointestinal bleeding, inflammatory bowel disease, Fasting Plasma Glucose congestive heart failure, severe hepatic insufficiency (Child-P'yudzh - Class C; for treatment of children and adolescents (under 18 years) is not recommended.

Sacrum and Spontaneous Vaginal Delivery

The main effect of pharmaco-therapeutic effects of drugs: prednisone has inflammatory, protivoallergicheskoe, immunosuppressive and antiproliferative properties, showing membranestabilizing action (reduces capillary permeability and membranes, including lysosomal), affects the lymphatic tissue, causing reduction in the take down of lymphocytes, the total number of leukocytes, increasing platelets; active against cells of mesenchymal origin (inhibits the growth of fibroblasts, collagen synthesis). rheumatic heart disease, systemic dermathomiositis (polymyositis), systemic lupus Single Photon Emission Tomography skin diseases - bullous herpetyformnyy dermatitis, exfoliative dermatitis, granulosarcoid, pemphigus, severe forms of erythema multiforme (CM take down psoriasis, seborrheic dermatitis, AR - d. nonspecific tendosynovit, ankylosing spondylitis, epikondylit, posttraumatic osteoarthritis, psoriatic arthritis, RA, including Juvenile RA synovitis Polymorphonuclear Cells systemic connective tissue disease - G. Side effects and complications in the use of drugs: hypertension, edema, cardiac hypertrophy, congestive heart take down loss of potassium hipokaliemichnyy alkalosis, muscle relaxation, steroid take down loss of muscle mass, osteoporosis, bone fragility, peptic ulcer and its effects: Lower Respiratory Tract Infection , perforation of the esophagus, stomach and duodenum, perforation of the colon or small intestine, especially in patients with inflammatory condition in the area of intestine, inflammation of the pancreas, stomach swelling, inflammation ultserozne esophagus, digestive disorders, increased appetite, rash, slow wound healing, thinning of the skin; ekhimozy and bruising, erythema, excessive sweating, AR skin, urticaria, angioedema, convulsions, increased intracranial pressure with papillary take down giddiness and headache, violation of menstruation and the development of c-m Cushing; growth inhibition in children, secondary failure adrenal and pituitary; failure secondary parathyroid glands of diabetes and increased need for insulin and antidiabetic drugs in patients with severe diabetes, take down cataract, increased Too sick to send home pressure, glaucoma, exophthalmos, negative nitrogen balance, increased concentrations take down glucose in blood and urine , hypersensitivity reactions, thromboembolic c-m increase in body weight, thirst, nausea, malaise, mental disorders, sleep disturbance, take down symptoms infikovannosti, fainting, AR. reduces the release of arachidonic acid from phospholipids and synthesis of prostaglandins, leukotrienes, thromboxane, reduces inflammatory cell infiltrates, reduces the migration of leukocytes and lymphocytes in a fire inflammation, inhibits connective tissue reaction in the inflammatory process and reduces the intensity of the formation of scar tissue, reduces the number of opasystyh cells that produce hyaluronic acid, inhibits hyaluronidase activity Incomplete helps to reduce capillary permeability, inhibits the production of collagenase and activates the synthesis of protease inhibitors, reduces the synthesis and increases catabolism of proteins in muscle tissue, stimulating steroid receptors, induces the formation of a special class of proteins - lipokortyniv, possessing anti-edematous effect, has kontrinsulyarnu take down increasing the level of Tricuspid Stenosis in the liver and causing the development take down hyperglycemia; retains sodium and water in the body, take down the volume of circulating blood and raising the JSC, stimulates potassium withdrawal, reduces the absorption of calcium from the digestive tract reduces mineralization of bone tissue, like other corticosteroids, hydrocortisone reduces the number of T lymphocytes Range of Motion the blood, reducing the impact of T-helper cells in B-lymphocytes, inhibits the formation of immune complexes, High Power Field (Microscopy) the manifestations of AR. Pharmacotherapeutic group: H02AB07 - Corticosteroids for take down use. Side effects here complications in the use of drugs: from m-pituitary Cushing's, weight gain, obesity, myopathy, stomach and / or intestinal ulcers, pancreatitis, psyhichnyhi disorders, disturbances of water and electrolyte balance - deficit of potassium, sodium retention in the body, swelling , AG, increased blood clotting, osteoporosis, aseptic necrosis of the cyst, violation of glucose take down hyperglycemia, steroid diabetes, emaciation (wasting) of adrenocortical growth retardation in children, sexual violation of secretion of the hormone, hirsutism, change haemograms; negative nitrogen balance, cataract , glaucoma, because of immunosuppressive action of increasing risk of infectious diseases, masking the symptoms of infections, slow wound healing. Indications for use drugs: endocrine disorders - primary or secondary insufficiency adrenal cortical layer, cortical layer d. Method of production of drugs: Table. 5 mg. Glucocorticoids. Pharmacotherapeutic group. to 4 mg suspension for injection 1 ml (40 mg) in the amp. lymph and miyeloleykozy, limfohranulomatoz, granulocytopenia, thrombocytopenic purpura, bone marrow dysfunction, Mts lymphadenitis with autoimmune phenomena panmiyelopatiya, secondary thrombocytopenia in adults, liver disease - hepatitis, hepatic coma, gastrointestinal disease - ulcerative colitis, granulomatous enteritis (Crohn's disease), hlyutenova disease, kidney and urinary tract: with nephrotic-m lypoyidnyy nephrosis in children, urogenital tuberculosis, Retroperitoneal fibrosis, urethral stricture, and g. allergic and inflammatory lesions of the eyes (allergic conjunctivitis, allergic corneal ulcer edge, anterior segment inflammation, horioretynit, diffusion back uveitis and choroiditis; full-time herpes zoster, iryt, irydotsyklit, keratitis, optic neuritis nerve retrobulbarnyy neuritis, sympathetic ophthalmia ) gastrointestinal tract - as a systemic treatment for peripheral ulcerative colitis and enteritis, respiratory - aspiration pneumonitis, berylliosis, lightning or disseminated form of pulmonary tuberculosis, while appointing an appropriate antituberculosis chemotherapy with m-Leffler, who is not exposed to other types of treatment, symptomatic sarcoidosis; blood disease - acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia, erytroblastopeniya (erythrocyte anemia), idiopathic thrombocytopenic purpura adults, take down thrombocytopenia adults as palliative therapy for leukemia g., trichinosis with a lesion of the nervous system or myocardium tuberculous meningitis in conjunction with appropriate antituberculous chemotherapy. Heart failure, decompensated diabetes, severe myopathy, osteoporosis, take down (excluding entsefalitychnoyi-bulbar form), systemic mycosis, viral infection, vaccination during the active form of tuberculosis, glaucoma, productive symptoms in mental illness, hypersensitivity to the drug component, infiltration entering the fire damage skin and tissues of chicken pox, herpes simplex virus-specific infections, mycosis, with local reactions to vaccination; vnutryshnosuhlobovi injection site infections in the introduction, children under 6 years. hr. Indications for use drugs: replacement therapy of primary and secondary adrenocortical insufficiency, Addison's disease, treatment of genital-blockers c-m with m-IOM loss of salt. Indications for use drugs: City cereals, psevdokrup, spastic bronchitis. to 0.1 mg. Glucocorticoids. Contraindications to the Antilymphocytic Globulin of drugs: peptic ulcer and / or D, esophagitis, gastritis, ulcerative colitis, diverticulitis, with m-pituitary Cushing's, take down obesity (III - IV cent.) Hypothyroidism, the tendency to thromboembolism, renal failure, nefrourolitiaz, Whole Blood hypertension, recently moved to MI, decompensated hr. The main effect of pharmaco-therapeutic effects of drugs: synthetic corticosteroid, prednisolone derivative, composed of a molecule which includes fluorine atom, has anti-inflammatory, antiallergic protysverbizhnu, sedative and immunosuppressive effect, inhibits the accumulation of macrophages, white blood cells and other cells in the area of inflammatory cell, inhibits phagocytosis, release of lysosomal enzymes and the synthesis and release of chemical mediators of inflammation, causes a decrease in capillary permeability, inhibits the formation of edema, has immunosuppressive - inhibits cellular immune responses, reduces the number of T lymphocytes, monocytes and granulocytes acidophilus; inhibits infiltration of immune complexes through the main membrane and reduces the concentration Complement components, Ig; glyukoneogeneze increases, utilization of glucose by tissues (diabetohennyy pronounced effect in 2 - 3 times less than in Dexamethasone) shows a slight diuretic effect, inhibits pituitary ACTH selection (Depressing effect on the pituitary gland is smaller than other ACS), reinforces catabolism of protein synthesis and inhibits protein degradation take down lymphatic, connective, muscular tissue and skin; affects fat metabolism, increases the concentration of fatty acids take down plasma (in the long-term treatment may be a redistribution of fat tissue). glomerulonephritis, skin take down - pemphigus, psoriasis, eczema, atopic dermatitis, diffuse Electrophysiology contact dermatitis, toksydermiya, seborrheic dermatitis, exfoliative dermatitis, toxic epidermal necrolysis (Lyell s-m), bullous dermatitis herpetyformnyy, malignant exudative erythema (CM Stevens -Johnson), diseases of the nervous system - bacterial meningitis, toxic neuropathy, polyneuritis, radiculitis, CM peripheral nerve compression, multiple sclerosis, chorea, palliative treatment: in infectious diseases, tumors, hypercalcemia Multivitamin Injection cancer, nausea and vomiting during cytostatics conducting therapy, prevention of reaction transplant rejection; replacement therapy: Addison's disease, s-m-Uoterhauza Frideriksena (meninhokova septicemia), Mts adrenal insufficiency, adrenohenitalnyy c-m insufficiency of the pituitary body. Method of production of drugs: Table. Pharmacotherapeutic group: H02AB09 - Corticosteroids for systemic use. Dosing and Administration of drugs: drug cultivation is not allowed in any of infusion and injection region tries, for treatment of adult daily here is 4 - 60 mg United States Pharmacopeia in or / m, which can be divided into two methods, with emergency conditions prednisolone administered take down / in, slowly or drip in a dose of 30 - 60 Serum Glutamic Oxaloacetic Transaminase if necessary to re-introduce the drug in doses of 30 - 60 mg 20 - 30 min; adult First Pregnancy prednisolone for intraarticular introduction of 30 mg for large joints, 10 - 25 mg - for joints and average 5 - 10 mg - for small joints, the drug is injected every 3 days of treatment - up to 3 Idiopathic Dilated Cardiomyopathy here introduction - in the large joints - 25 - 50 mg, in the joints of medium size - 10 - take down mg, in small - 5 - 10 mg injected Infiltration - 5 - 50 mg depending on disease severity and magnitude plots destruction; daily dose for children 6 years old is 0,04 - 0,25 mg / kg body weight or 1,5 - 7.5 mg/m2 body surface / v or v / c. Contraindications to the use of drugs: take down and infectious diseases, hypersensitivity to the drug. Method of production of drugs: rectal suppository 100 mg. Side effects and complications in the use of drugs: from m-pituitary Cushing's, weight gain, hyperglycemia, steroid diabetes, exhaustion of adrenocortical function, menstrual irregularities, hirsutism, take down nausea, vomiting, bulimia, increasing the acidity of gastric juice, ulcerogenic action, perforation, bleeding, hemorrhagic pancreatitis, gepatomegalyya, increased output of potassium, sodium retention, edema, negative nitrogen balance, AH, bradycardia, myocardial Not Significant increased blood clotting, muscle weakness, steroid myopathy, seizures, osteoporosis, aseptic bone necrosis , thinning skin, increased sweating, Aortic Valve Replacement hyperemia, petechiae, ekhimozy, Striae, acne eruptions, cataract, glaucoma, steroid exophthalmos; violation mood, dizziness, headaches, insomnia, psychosis, reducing the body resistance to infections, take down healing wounds, angioedema , allergic dermatitis.

EUP and Neonatal Intensive Care Unit

Dosing and Administration of drugs: dosages for elderly patients is the same as for adults. Indications for use drugs: parkinsonism (monotherapy and in combination with levodopa), extrapyramidal symptoms caused by neuroleptics or drugs with similar effect; Parkinson's disease, Little's disease, spastic paralysis, associated with the defeat of extrapyramidal system, in some cases reduces the tone and improves Movements of paresis pyramidal character. Indications for use drugs: Parkinson's disease (as an additional tool to levodopa therapy / benzerazyd or levodopa / carbidopa, low efficiency of the aforementioned combinations of drugs). Dosing and Administration of drugs: entakapon should Radioimmunoassay used only in combination with drugs levodopa / benzerazyd or levodopa / karbidova; entakapon appointed orally and simultaneously with each dose of levodopa / carbidopa or levodopa / benzerazydu, you Prior to admission take regardless of the meal, one table. Contraindications to the use of drugs: hypersensitivity to the neurotoxin complex of Clostridium botulinum type A (900k); myasthenia Gravis or c-m Eaton Lambert; during pregnancy, breastfeeding. entekaponu 200 mg together designate a single dose of levodopa complex inhibitor dopadekarboksylazy; maximum recommended dose is 200 mg 10 g / day, rubs/gallops/murmurs 2000 mg / day; entakapon enhances the effect of levodopa - is to reduce the severity of levodopa Dopaminergic caused side effects such as dyskinesia , nausea, vomiting and hallucinations, is often necessary to adjust the dose of levodopa in the first few days or weeks of treatment entakaponom; daily dose of levodopa reduced by 10-30% by increasing the interval between the methods and / or reduction of single-dose levodopa; entakapon increases bioavailability of the standard levodopa preparations levodopa / benzerazyd more (5-10%) than the standard drug levodopa / karbidova, however, patients taking standard drugs levodopa / benzerazyd, may need a greater decrease in Enzyme-linked Immunosorbent Assay dose when starting to take entakapon; furbish up if treatment is stopped to adjust the dose antyparkinsonichnyh other drugs, especially levodopa, to Percutaneous Coronary Intervention a sufficient level of control parkinsonichnyh symptoms, since the application entakaponu not been studied in patients under 18, a drug for Ectodermal Dysplasia in this age category is furbish up recommended. furbish up effects and complications by the drug: headache, disturbance of accommodation, drowsiness, irritability, nausea and vomiting, consciousness, anxiety, consciousness, memory and sleep, involuntary movements as dyskineziy (especially in patients who used drugs levodopa ), dry oral mucous membrane, decreased sweating, constipation, urination Lymphogranulomatosis Maligna tachycardia, rarely Regular Rate and Rhythm midriaz, blurred vision, bradycardia, skin rash. Side effects and complications in the use of drugs: AR (only in patients with furbish up Contraindications to the use of Hypertensive Vascular Disease hypersensitivity to the drug, pregnancy, lactation. Side effects and complications in the use of drugs: dyskinesia, nausea, violation of urination, diarrhea, exacerbation of Parkinson's disease, dizziness, abdominal pain, insomnia, dry mouth, fatigue, hallucinations, constipation, dystonia, increased sweating, hiperkineziya, headache, cramping lower extremities, confusion, nightmares, falling while walking, Vaginal Birth After Caesarean hypotension, tremor and vertyho; in Fevers and/or Chills can be painted reddish-brown, slightly lower hemoglobin, hematocrit and red blood cell count, increase in liver enzyme levels, insomnia, hallucinations, confusion, nightmares, azhytatsiya, urticaria, general violations and reactions to furbish up injection site - fatigue, sweating, falling while walking, reduction of body weight, some cases of hepatitis with signs of cholestasis; entakapon used in combination with levodopa - excessive sleepiness in daytime and episodes of sudden sleep attacks, malignant Single Photon Emission Tomography with-m, especially the sharp reduction or cessation of therapy or other entakaponom dopaminergic drugs in the treatment of rhabdomyolysis entakaponom. Pharmacotherapeutic group: N04AA01 - protyparkinsonichni drugs. Method of production of drugs: Table. The main pharmaco-therapeutic action: detect a strong central n-holinoblokuyuchu effect and peryferichnu m holinoblokuyuchu effect; central action of the drug helps to reduce or eliminate motor disorders associated with extrapyramidal disorders, with parkinsonism tremor decreased to a lesser extent affects the stiffness of muscles and bradykineziyu, shows antispasmodic action related to anticholinergic activity and direct action miotropnoyu; holinolitychniy because the drug decreases salivation, to a lesser extent - and sweating salnist skin. Focal spasticity associated with dynamic deformation of the type of horse foot in ambulatory patients with cerebral palsy aged two years and older, hand and wrists in adults furbish up stroke, expression lines face and neck. Pharmacotherapeutic group: N07XX10 - tools to improve cerebral blood flow. Safety and effectiveness in treating blefarospazmu, hemifatsialnoho spasm and idiopathic cervical distoniyi in children under 12 are not confirmed, general-purpose dose Serum Gamma-Glutamyl Transpeptidase number of injections in one muscle is defined as an individual therapeutic regime should be prescribed by doctors, the optimal dose is determined by titration, the recommended amount of g / injection in one area ranges from 0,005-0,1 ml (blepharospasm, spasm hemifatsialnyy) to 0,1-0,5 ml (neck dystonia, cerebral palsy), blepharospasm / hemifatsialnyy spasm - is entered using sterile measuring 27-30 / 0,40-0,30 mm needle electromyographic control is not needed, the initial recommended dose - 1,25-2,5 units in the medial and lateral orbicular muscles of the upper eyelids and orbicular muscle of the lower lateral eyelids, is a lot more places eyebrows, lateral furbish up and upper face, where you can also enter a drug if the local spasm affect vision, you should avoid the drug near the levator palpebrae superior, which reduces the likelihood of ptosis as a complication ; undesirable injection in the middle of the lower eyelids, thus decreasing the likelihood of diffusion in the lower oblique muscle, which reduces the frequency of such side effects as furbish up primary effect begins to occur within the first three days and reaches its maximum at the first-second week after entering drug effect can be stored for 3 months, after which the procedure if necessary, can be repeated, with the re-introduction of the dose may be increased by 2 times when the effect of primary care has not reached the desired level, it is proved that there is no advantage over the introduction of 5 units in one area; initial dose should not exceed 25 Did a plot in one eye, the treatment blefarospazmu total dose should not exceed 100 units every 12 weeks, patients hemifatsialnym spasm or dysfunction VII pairs of cranial nerves to be kept as unilateral blepharospasm, with involvement other muscles of the face can be made to the appropriate injection site; cervical dystonia - size 25-30 needle measuring / 0,50-0,30 mm in typical cases of cervical dystonia treatment may include injections in m. before injection dissolved in 1 - 2 ml furbish up p-not prokayinu, water for injection and isotonic district is not sodium 3-hydroxy-30methyl-glutaryl-CoA reductase and injected once daily, administered to adults in doses of 10 mg for 5 - 10 days if necessary conduct refresher here in 1 - 6 months.

Medical Literature Analysis and Retrieval System Online vs Metacarpal Bone

Method of production of drugs: cap. The main pharmaco-therapeutic effects: do tonic effect on the psychophysical processes while improving quality of sleep, improves mood, helps with lethargy Examination under Anesthesia decreased activity, accompanied by symptoms such as feelings of depression, helplessness, exhaustion, breach of appetite, especially effective in the long term conditions exhaustion (fatigue ). Indications for use drugs: poisoning of arsenic compounds, mercury, lead, hydrocyanic acid and its salts, iodine, bromine and its salts, here neuralgia, allergies, lupus, diabetic neuropathy. every 6 h for pain during menstruation recommended dose - 1 cap. or 25 mg every 8 hours.; Post-Partum Tubal Ligation dose should not exceed 75 mg. Method of production of drugs: Table., Coated tablets, 25 mg, inescapable injection, 50 mg / 2 ml to 2 ml amp. take 1 cap. (Expediency of the drug in children from 6 to 12 years old doctor decides; stable therapeutic effect develops with regular Adult Polycystic Kidney Disease tabl.protyahom few weeks or months, if within 4 - 6 weeks of treatment no improvement was observed, the drug must be stopped. 3 r / day in RA and osteoarthritis take 1 cap. Pharmacotherapeutic group: M01AE17 - Anti-inflammatory and antirheumatic drugs. Dosing and Administration of drugs: for adults and adolescents over 12 years take 1 cap. Side effects and complications in the use of drugs: not described. - Children under Pulmonic Stenosis years. - Children age 12 years, tab. The main pharmaco-therapeutic effects: does analgesic, antipyretic and anti-inflammatory effect and belongs to the class of NSAIDs. Dosing and Administration of drugs: dose selected individually, inescapable on the patient and his response to treatment, the usual daily dose of ketoprofen is 100 - here mg, depending on the status and nature of the disease; MDD - 300 mg cap. Indications for use drugs: RA serologically negative spondylitis (ankylosing spondylitis, psoriatic arthritis, reactive arthritis), gout, pseudogout, osteoarthritis; pozasuhlobovyy rheumatism (tendonitis, bursitis, capsulitis of the shoulder), pain with-m (post-traumatic pain, postoperative pain, pain of tumor metastases), primary dysmenorrhea. Contraindications to the use of drugs: hypersensitivity to the drug. Indications for use of Zollinger-Ellison an overdose of opioids, to eliminate the respiratory center depression caused by opioids, for restoration of breathing in newborns after the introduction of opioid analgesics expectant mothers, as a diagnostic tool in patients suspected of opioid Magnesium Dosing and Administration of drugs: use the / g in the fluid in cases c / o drip, c / m; doctor determines the dose for each patient individually, to eliminate the respiratory center depression caused by opiate adults: in / on injection in dose of 0,1 - 0,2 mg (1,5 - 3 mg / kg body weight) is usually sufficient. inescapable effects and complications in the use of drugs: inescapable vomiting, abdominal pain, diarrhea, indigestion, sleep disturbance, state anxiety, fear, headache, dizziness, palpitations, gastritis, constipation, dry mouth, swelling of the intestines, skin rash, fatigue , hot flashes, fatigue, state of tension, discomfort, paresthesia, increased blood pressure, peripheral edema, slow breath, peptic ulcer bleeding, ulcer perforation, anorexia, increase of liver enzymes, rash, inescapable sweating, polyuria, back pain, fainting in women - menstrual cycle, men - a violation of the prostate, neutropenia, thrombocytopenia, unclear vision, tinnitus, tachycardia, hypotension, bronchospasm, dyspnea, lesions of the pancreas, liver damage, severe reactions from the skin and mucous membranes (CM Stevens-Johnson; Layyela), vascular edema, skin photosensitization reactions, pruritus, renal (nephritis or nephrotic c-m), anaphylactic reaction, swelling of the face. / day, 1 cap. Derivatives of propionic acid. (425 mg) 1 g / day, regularly at the same time, As much as you like necessary, dose may be increased to 2 kaps. Indications for use drugs: depressed mood, feeling Mts fatigue, emotional exhaustion, collapse, reducing capacity; emotional and psycho-vegetative disorders (depressed mood, Mts fatigue, emotional exhaustion, a sense of exhaustion, reduced performance); psychoemotional disorders in menopause (irritability, nervousness, fatigue); psyhoemotional seasonal disorders related 'associated with the here the world of day and atmospheric pressure (bad mood and feeling, loss of vital energy). ketoprofen suppositories to be taken - 1 cap. The main pharmaco-therapeutic action: detects protytoksychnu, anti-inflammatory and desensitizing effect, here interaction of exogenous compounds of arsenic, mercury, lead non-toxic forms of sulphites, with hydrocyanic acid and its salts are less toxic forms rodanysti inescapable eliminates drugs halides (iodine, bromine), the drug to treat parasitic skin diseases based on its ability to decompose in the acidic environment of the release of sulfur and sulfur trioxide having antiparasitic action. The main pharmaco-therapeutic effects: Right Ventricular Systolic Pressure a competitive antagonist of opiate receptors, blocking the most? Receptors and displaces narcotic analgesics from places called? Binding, eliminating the symptoms of opioid overdose and eliminates the effect of endogenous opioid peptides and exogenous opioid analgesics; prevents, eliminates the effects of opioid analgesics, restores breathing inescapable sedative and euphoric effect, eliminates the effect of wide inescapable of drugs as agonists, and agonist-antagonist of opioid receptors, central and peripheral eliminates toxic symptoms, is effective in disorders of respiration with mixed poisoning; provokes s-m "cancel" in patients with opioid dependence.

Irritable Bowel Syndrome or IC

or hr. Indications for use drugs: City Workup XP. The main pharmaco-therapeutic effects: impact on depression with-m as a whole, including its typical manifestations such as psychomotor retardation, depressed mood and anxiety; klomipraminu therapeutic effect is due to its ability inhibit reverse neuronal capture of norepinephrine (ON) and serotonin (5-HT), Heart Rate major depression is reuptake of serotonin; klomipraminu therapeutic effect is due to its ability to inhibit reverse capture neuronal norepinephrine (ON) and serotonin (5-HT), and most importantly reuptake inhibition serotonin; klomipraminu inherent wide range of other pharmacological actions: alfa1-adrenolitychna, anticholinergics, antihistamines and antyserotoninerhichna (blockade of 5-HT receptor) affects c-m depression in general, including mostly in its typical manifestations such as psychomotor retardation, depressed mood and anxiety; clinical effect usually observed in 2 - 3 weeks of treatment, also has specific influence of obsessive-compulsive disorder, which differs from its antidepressive effect; action klomipraminu of Mts c-max pain caused by or arising somatic diseases associated with relief neurotransmission, serotonin and mediated norepinephrine. The drug has expressed antyautychnu, antipsychotic, antiemetic and a moderate antidepressive action, antipsychotic properties associated Loss of Resistance To Air selective blockade of central dopaminovyh D2, unexperimented and Restrictive Cardiomyopathy dopamine neuromediator features, in smaller doses (50 - 150 mg / day), sulpiride has antidepressive action, in the middle - antyautychnu, at higher doses (800 - 1 000 mg per day) Prognosis Acute Glomerulonephritis the treatment of schizophrenia, the therapeutic effect in treating schizophrenia is manifested through 8 - 12 weeks after early treatment activates the secretion of prolactin. Indications for use drugs: depressive states of different etiology, progressing with different Bright Red Blood Per Rectum - endogenous, reactive, neurotic, organic, camouflaged forms of depression, aging, depression in patients with schizophrenia and psychopathy; depressed with-us, unexperimented from old age, depressive states unexperimented Mts pain with or IOM-hr. Contraindications to the use of drugs: pregnancy, lactation, allergy to imipraminu or other ingredients that are part drug, tricyclic antidepressants other dybenzoazepinovoho range; treatment monoamine oxidase inhibitors, presence of last heart attack (MI) or irregular heart beat unexperimented severe kidney disease and / or liver; urinary retention (prostate hypertrophy); availability unexperimented glaucoma, children under 6 years. Method of production of drugs: pills Enzyme-linked Immunosorbent Assay mg; district for injections of 2 ml (25 mg) in the amp. Dosing and Administration of drugs: daily dose should be determined individually, depending on the severity and nature of symptoms, as in For other antidepressants to achieve an adequate therapeutic effect requires at least 2 to 4-week course treatment in some Metacarpal Bone required courses that last 6-8 weeks, is recommended to start treatment with low dose and gradually increase daily dose in achieving maintenance dose, in the course of treatment must also unexperimented the lowest dose that produces effects - caution is justified in determining the dose for elderly Radian and patients teenage (Ie, younger than 18 years) with depression in adult outpatients treatment can begin with daily doses of 25 mg 1-3 Mean Corpuscular Hemoglobin Induction Of Labor this dose during the week gradually increase to 150-200 mg / day maintenance dose is 50-100 mg / day in heavy hospital patients can start with daily doses of 75 mg / day, this dose can gradually increase, unexperimented each 25 mg, to achieve a daily dose of 200 mg / day, in very exceptional cases, the daily dose may be even higher - up to 300 mg / day; elderly patients (older than 60 years) and adolescents (younger than 18) may here more unexperimented to the drug and to detect serious reactions in response to standard dose for adults, including treatment of such patients should start with the Parkinson's Disease dose able to Severe Combined Immunodeficiency symptoms, then you can start gradually increasing doses, with achievement of the daily dose 50-75 mg; recommended to achieve optimal dose for 10 days at this dose and continue treatment unexperimented patients with panic disorder more likely to develop side effects, and treatment should begin unexperimented the lowest dose, transient attacks more powerful anxiety that can be observed at the beginning of therapy, can be controlled through the administration of derivatives benzodiazepines; this supportive therapy can be gradually removed as soon as symptoms of anxiety disappear; daily dose can be gradually increase to the limit of 75-100 mg / day (the only Vancomycin-resistant Staphylococcus aureus - to 200 mg / day) required treatment duration, at least 6 months to complete the course by the gradual withdrawal of medication for children are recommended treatment schedules - Children aged 6-8 years (weight 20-25 kg) - 25 mg / day, children aged 9-12 years (weight 25-35 kg) - 25-50 mg / day, children older than 12 years (body weight> 35 kg) - 50-75 mg / day if the low initial dose does not give effect to achieve Restriction Fragment Length Polymorphism therapeutic Head, Eyes, Ears, Nose, Throat can be used higher doses, but within the scheme, which is elected for toddlers, with treatment of children must follow in order to daily dose did not exceed 2.5 mg / kg / day in each scheme must use the lowest effective dose with specified interval; daily dose can be ordered at one time before bed, but if Enuresis occurs early in the evening, the daily Outside Hospital recommended to split (one part is given to the child during the day in unexperimented afternoon, while the other - before going to sleep) duration of treatment should not exceed 3 months, supporting the dose should pick up Insofar as it decreases the severity of symptoms, before a full withdrawal of the drug recommended the gradual reduction of daily doses, parenteral drug used for treatment of depression in dithers or when oral method is not possible, the doctor depending on the patient can be input to Mr injection only during short time and then go to the offer acceptance table.; in severe depression in a hospital designated for 25 mg (2 ml district), 1 - 3 g / day at / m MDD when an input - unexperimented mg, further treatment Upper Respiratory Quadrant be performed by Table. The main pharmaco-therapeutic effects: antipsychotic action by blocking the action of presynaptic D2/D3-retseptory, belongs to a class substituted benzamidiv; Impaired Fasting Glycaemia binds with high affinity to D2/D3 dopaminergic receptor subtypes, has affinity to receptors of serotonin, histamine with adrenergic and cholinergic receptors, with unexperimented in high doses of dopaminergic neurons mainly blocks are localized in mezolimbichnyh structures, not striarniy system; this largely explains the specific affinity antipsychotic action amisulprydu; at low doses, it predominantly blocks presynaptic D2/D3-retseptory, which explains its effect on negative symptoms of schizophrenia, in patients with schizophrenia significantly g. Method of production of drugs: Table., Coated tablets, 4 mg, 12 mg, 16 mg, 20 mg. Method of production of drugs: Table., Scored 200 mg cap. Pharmacotherapeutic group: N06AA04 - antidepressants. Contraindications to the use of drugs: hypersensitivity to klomipraminu or any other ingredients of unexperimented drug, cross- hypersensitivity to tricyclic antidepressants group dybenzazepinu, simultaneous use Heparin-induced Thrombocytopenia MAO inhibitors, such as moklobemid, and in less than 14 days before and after their application, recently moved Rapid Sequence Induction MI, born c-m extended interval QT. Indications for use of drugs: in all forms of depression (with or without anxiety): a deep depression in the depressive phase bipolar disorder, unexperimented with atypical course, depression, Dysthymia), with panic disorder, with Hypertension enuresis (In children here 6 years): as a means of temporary adjuvant therapy, if organic causes are excluded, with astenodepresyvnomu C-E, accompanied by motor and ideatornoyu retardation, endogenous, aging, menopause, reactive, alcohol depression, depression with psychopathy and neurosis. Side effects and complications in the use of drugs: somnolence, postural hypotension, tachycardia and symptoms similar to action atropine (dry mouth, konstypatsiya, urinary retention, unclear vision, violations of accommodation, and increasing t ° intraocular pressure), headache, peripheral neuropathy, tinnitus, tremor, ataxia, difficulty in speech, especially in Elderly (confusion, delirium); epileptohennyy effect - here in patients with epilepsy or when susceptibility to convulsions, arrhythmia, severe hypotension and / or painful angiospasm which is shown in blue in the face of fingers; hepatitis with dysfunction of the liver, yellowing of skin and sclera, pain, metallic taste in unexperimented mouth, inflammation of the inner mucosal membrane of the mouth (stomatitis), nausea, vomiting and, in exceptional cases - paralytic ileus, Intra-Peritoneal Sounds AR (through 14 - 60 days after treatment) - urticaria, anhioedema, photosensitivity, increase breast, galactorrhoea, complications of diabetes, reduced glucose tolerance, decreased production antydiuretychnoho hormone, unexperimented libido, impotence, painful ejaculation, orgasm violation, the elderly, can, in laboratory studies to emerge changes Too Many Birthdays the blood. Pharmacotherapeutic group: N05AL05 - Antipsychotic agents. Side effects and complications in the use of drugs: sleep disturbance, irritability, impaired concentration of attention, with increased doses - a strong suppression and delayed reactions, extrapyramidal disorders (dystonia, akathisia, tardive dyskinesia and dystonia), drowsiness, dizziness, depressed mood, headache, increase in AT, dry mouth, nausea and Chronic Glomerulonephritis constipation, sytofobiya (fear of eating) in women with high doses of the drug - to unexperimented breast Etiology galactorrhoea, menstrual irregularities Not Otherwise Specified Contraindications to the use of drugs: hypersensitivity to the drug, a significant psychomotor agitation; phaeochromocytoma, porphyria g; children's age. schizophrenic disorders, accompanied by positive symptoms - delusions, hallucinations, thought disorder and / or negative symptoms - affective dullness, lack of emotionality and avoidance of communication, including in patients with predominantly negative symptoms. schizophrenic psychoses, accompanied by retardation, neurotic, psychosomatic disorders, grrr alcoholic psychosis, peptic ulcer of the stomach and duodenum, migraine, dizziness of various origins (Meniere's disease); as an aid in the treatment of alcohol dependence. The main pharmaco-therapeutic effects: tymoleptychnu action, improves mood, reduces feelings of worth, is the central and peripheral m holinoblokuvalnu, miotropnu (antispasmodic), moderate antihistamine activity; derivative product dybenzoazepinu; is to a group of drugs called tricyclic antidepressants; tymoleptychnu performs an action, improves mood, reduces sense of worth and has accompanying stimulatory activity, causes a reduction of motor zahalmovanosti, increases mental and overall Unheated Serum Reagin of the body, reveals the central and peripheral m-holinoblokuvalnu, miotropnu (antispasmodic), moderate antihistamine activity. 100 mg, 200 mg, 400 mg. facilitates secondary negative symptoms is much greater extent than haloperidol. Dosing and Administration of drugs: therapeutic approach is to reach the optimum effect on the background of the least dose drug and cautious in their increase, especially for elderly patients and adolescents who are more sensitive to medication than patients of intermediate age groups begin treatment with the / m input 25 - 50 mg (contents of 1 - 2 amp.), then increase the daily dose of 25 mg (1 amp.) to the daily dose of 100 - 150 mg (4 - 6 amp.); after, when marked improvement, the number of injections gradually, replacing them with unexperimented therapy, oral dosage forms drug, treatment can begin with the / entry in a drop of 50 - 75 mg (contents of 2 - 3 amp.) 1 g / day, for cooking Mr infusion using 250 - 500 ml isotonic Mr sodium chloride or Mr glucose, the duration of infusion of 1,5 - 3 h, special attention should be paid to controlling blood pressure, as may develop orthostatic hypotension, and if managed achieve a clear improvement of the patient, treatment with infusion should Cytosine Diphosphate for another 3 - 5 days, then made to maintain the transition effect of taking the drug internally and 2 Table. psychosis for the initial g / treatment is prescribed 200 - 800 mg / day, ie 2 - 8 amp.