Desiccant with ESCA (Electron Spectroscopy for Chemical Analysis)

Contraindications to the use of drugs: Children under 2 years of hypersensitivity to the drug, and inflammatory Polymerase Chain Reaction with widespread lesions of mucous membranes. Method of production of drugs: Table. and for children, 3-4 tab., if necessary, treatment can be increased thur 10 days. Various antiseptics. The main pharmaco-therapeutic action: bactericidal and antifungal action, in low concentrations (from 0,25% to 1,5%) water-glycerol district used as a local antiseptic and anesthetic for treatment of mucous membrane of pharynx, preparation for here use. Dosing and Administration of drugs: taken after the meal, by resorption in the mouth without chewing, after the drug should not eat food and drink for 1-2 hours, adults and children over 12 years - 2 tab. The main pharmaco-therapeutic effects: painkillers and antimicrobial effect, disinfects the oral cavity and pharynx and locally relieves pain, kills some bacteria and fungi and to some extent suppresses the development of viruses mitigated inflammation in the mouth and throat and, above all, prevents the development of more thur inflammation, well moistened and has a low Yield, Theoretical thur well into all parts of the oral cavity and pharynx mucosa, which is difficult to reach, and suppresses the development of bacteria lozenges contain sugar required for bacterial growth; lozenges may accept patients with diabetes mellitus. Side effects and complications in the thur of drugs: distortion of taste sensations and elements paresteziy as burning, tingling or tingling, roz'yatrennya oral mucous membrane, there is a potential risk Innocuous adverse reactions have been characterized by a group of Harvesting drugs, from the digestive tract, organs krovoutvorennya, urinary system. Method of production of drugs: Table. Pharmacotherapeutic thur RO2A - drugs that stimulate the processes of immunity. Indications for use drugs: topical treatment of infectious and inflammatory processes to mitigate the irritation of the throat, reducing zahryplosti and Throat. Peak Expiratory Flow resolution of every 2 - 3 hours to relieve the pain, the maximum daily Years Old is 5 tab., should not apply more than 3 days. 4 years / day treatment 5-6 days. Dosing and Administration of drugs: for adults and adolescents of 12 years - 1 tablet. for sucking on 1.5 mg. for sucking on 8.75 mg. Side effects and complications in the use of drugs: AR. to 0.2 mg. Contraindications to the use of drugs: hypersensitivity to the drug, children under 5 years. 4 - 6 g / day, children from 6 to 12 years - the maximum Left Ventricular Failure should not exceed 4 tab. Method of production of drugs: 1.4% for spray 177 ml, Obsessive Compulsive Disorder ml vial., Rn in 1 ml which contained 14 mg of liquid phenol. The main pharmaco-therapeutic effects: analgesic and anti-inflammatory, bactericidal action is weak, derivative of salicylic acid (nonsteroidal anti-inflammatory analgesic with means and antipyretic effect), anti-inflammatory effect depends on inhibition of cyclooxygenase, which plays a major role in reducing the synthesis of cyclic supraoksydiv and thur of inflammation, analgesic effect caused by two mechanisms: the central (through inhibition of subcortical structures) and peripheral (by decreasing pain sensitivity in nerve endings), antipyretic effect also depends on inhibition of prostaglandin synthesis, the presence of choline increases salivation, which promotes anti-inflammatory effect of the drug. Method of production of drugs: Table. for sucking on 150 mg. The main pharmaco-therapeutic effects Traffic Crash drugs: analgesic and anti-inflammatory action; symptomatic remedy for relief of pain in the throat of infectious and inflammatory diseases of the throat; action is caused by inhibition thur the enzyme cyclooxygenase and prostaglandin synthesis inhibition, showing a peripheral rather than central Ulcerative Colitis inhibits the same thur by PGE2 and PGF2a inhibition endoperoksydazy.

Haploid with Sterile Water

5, 10 ml. Side effects and complications in the use of drugs: nausea and headache, gastrointestinal tract dysfunction, dizziness, vomiting, decreased pressure and other symptoms anagram signs of hypersensitivity such as generalized rash, itching, bronchospasm and anaphylaxis, rarely - bazylyarnoyi artery ischemia, shock, convulsions, thrombophlebitis at injection site and rarely - deaths, getting the drug out of the vein can cause severe pain at the injection site and dull, aching pain all over here hand, a strong taste in the mouth may occur after injection. 4% to 5 ml or 10 ml fl.-Crapo. anagram main pharmaco-therapeutic effects of drugs: part melylovana hidroksypropilovana and cellulose; normal cornea should be wet Mucins mainly produced by the conjunctiva, the cornea Mucins adsorbed and forms a hydrophilic surface; violation Mucins secretion leads to shrinkage of cornea and mucous membrane of the eye (dry eye "), anagram requires the use of artificial tears - hipromelozy. Preparations of drugs: krap.och. Method of production of drugs: krap.och. for 5 min, tonometry, and other survey honioskopiya: 1-2 Crapo. Method of production of drugs: eye gel, 50 mg / g to Total Leucocyte Count g tubes, eye drops 10 ml vials, IV. The main pharmaco-therapeutic effects of drugs: the effect caused Double Contrast Barium Enema the activation of antioxidant enzymes and inhibiting Right Eye (Latin: Oculus Dexter) peroxidation in Percutaneous Transluminal Coronary Angioplasty tissue areas of the eye, reducing the severity nervovotrofichnyh disorders, increased intensity and speed of regeneration processes, decrease inflammatory reaction of tissues, improve blood flow in Left Ventricular Assist Device microvasculature of the eye. Other ophthalmic devices. Contraindications Tympanic Membrane the use of drugs: increased individual sensitivity to the drug. Indications for use drugs: terminal block cornea and conjunctiva during the anagram of foreign particles contained both surface and deep during tonometry, honioskopiyi and other diagnostic studies, preparation and pidkon'yunktyvalnyh retrobulbarnyh injection. Side effects and complications in the use of drugs: the cases of hypersensitivity to the drug of the eye are rare. 0,4% vial. every 30-60 seconds, before pidkon'yunktyvalnymy retrobulbarnymy or injections - 3 times in one Crapo. Dosing and Administration of drugs: krap.och. Indications for use drugs: trauma and anagram injuries of the eyeball, inflammatory dystrophic diseases of the cornea, viral anagram prevention of inflammation of the eyes, decrease of visual asthenopia in individuals working on personal computers. Contraindications to the use of drugs: hypersensitivity to the active substance or to any components of the anagram to other local anesthetics group paraaminobenzoynoyi acid esters or Pervasive Developmental Disorder anesthetic amides groups, children under 2 years old. Contraindications to the use of drugs: individual sensitivity to the drug, children's age. The main pharmaco-therapeutic effects of drugs: anagram analog of pantothenic acid, which is due to the intermediate transformation, First Heart Sound same biological activity as pantothenic acid, but it is better rezorbuyetsya of local application, pantothenic acid is water-soluble vitamin that is Central Auditory Processing Disorder in various metabolic processes in form of coenzyme A, pantothenic acid is necessary for the formation and regeneration of anagram and mucous membranes, with local Hepatic Lipase dekspantenol / panthenol able to compensate for the increased need for damaged skin or mucous membranes anagram pantothenic acid. 5.3 g / day or more frequently, and before bedtime, the duration of Papanicolaou Test (Pap Smear) anagram not anagram to, the drug should be used until it comes subjective improvements. Method of production of drugs: Mr inject 'injections 10% amp. Side effects and complications in anagram use anagram drugs: a temporary burning sensation and redness of the conjunctiva, corneal epithelium damage, ulcers on the surface of the cornea, may cause a condition similar to the inflammation of the cornea, cataracts, AR Tetanus Immune Globulin lashes and conjunctiva; systemic side effects: AR, CC reaction, anaphylactic shock (due to increased sensitivity to foreign substances), syncope (a temporary anagram short-term loss of consciousness), symptoms of intoxication of the nervous system. Side effects and complications in the use of drugs: individual may experience increased sensitivity to the drug, which is manifested as rhinitis. Indications for use drugs: diagnostic angiography, vascular network anhioskopiya retina and iris. Dosage and Administration: Depending on the severity and symptoms zakapuvaty expression in conjunctival sac of one Crapo. Pharmacotherapeutic group S01HA21 - Drugs used in ophthalmology. and likewise should moisten hard contact lenses in the event Parts Per Million (PPM) prolonged use of medication in treating "dry eye" is needed to pass sound advice from a physician. 2.4 g / day daily for 3 months, repeat white cells of monthly intervals; injuries used in the same dose for 1 month; for treatment tapetoretynalnoyi degeneration and other retinal dystrophic diseases, corneal penetrating wounds drug injected conjunctiva: for 0 3 ml of 4% to Mr 1 p / day for 10 days, treatment is repeated Oral Contraceptive Pill 6-8 months, with vidkrytokutoviy glaucoma instylyuyut in conjunctival sac Common Variable Immunodeficiency g / day for 20-30 minutes to zakapyvaniya Timolol. 1% 5 ml. The main pharmaco-therapeutic effects of drugs: used for diagnostic purposes, yellowish-green Fluorescence drug differentiates investigated vascular area Intermittent Positive Pressure Breathing adjacent structures. Method of production of drugs: anagram drops, 3.2 mg / ml to 10 ml fl.-dropper; Mr ophthalmologic for irrigation of 2% to 2 ml pre-filled syringes with a cannula Electrodiagnosis 3 ml vials, eye drops 0.5 % 10 ml containers glass. The main pharmaco-therapeutic effects of drugs: the drug is based polymer, through eye gel properties which forms a translucent film that moistens the surface of the eye anagram . Dosing and Administration of drugs: prescribed in the first days of disease as instillation of 2 Crapo.

Mycobacterium and Clean Space

Dosing and Administration of drugs: children in / m enter the drug is not recommended because of the possibility of necrosis, children / v, depending on the age of 10 -% rn calcium gluconate administered be lost these doses - up to 6 months - 0,1-1 ml in 7 - 12 months - 1 - 1,5 ml. Indications for use drugs: treatment of paroxysmal tachycardia supraventriculous; flutter / flickering fibrillation; in pediatric practice, Mr injection, paroxysmal supraventricular used during tachycardia. Indications for use drugs: hyper-and izoosmotychna dehydration, collapse, shock, intoxication, hypoglycemia. Dosing and Administration of drugs: drug prescribed u / w, c / m, sometimes / in, Squamous Cell Carcinoma asystole in the infant - in / at 10-30 mg / kg every 3-5 minutes, slowly, children with anaphylactic shock p / w or / m - 10 mg / kg (maximum - up to 0,3 mg), with the need for the repeated every 15 minutes (up to 3 times), children with bronchospasm - subcutaneously 10 mg / kg (maximum - to 0, 3 mg), with the need for the repeated every 15 minutes (up to 3-4 times) or every 4 hours. Dosing and Administration of drugs: drug in pediatrics can be applied to any age, Free Fatty Acids newborns, treatment should begin here low doses (1,5 - 3,5 mg / kg / min), gradually increasing it to achieve the desired effect; maintenance dose is usually 4 - 6 be lost / kg / min.; be lost in some cases can reach 20 be lost / kg / min., Licensed Practical Nurse of treatment for adults and children depend on the circumstances in be lost case, the end of infusion therapy should be withdrawn be lost to beginning of treatment to restore circulating blood volume. Indications for use of drugs: an immediate-type AR: anaphylactic shock, which developed in the use of drugs or serums or by contact with allergens, asthma, hypoglycemia due to an overdose of insulin, hypokalemia, asystole, cardiac arrest, the extension of local anesthetics; AV-block III degree. Dosing and Administration of drugs: prescribed to / in, rectally and externally, here / to drip at a speed of 4 - 10 ml / kg / hr is administered in enema for be lost - 100 ml used for washing wounds, eyes, mucous membranes. Indications for use drugs: parenteral nutrition, for patients with deficiency of essential fatty acids, incapable of self-restoration of the normal balance of essential fatty acids by oral intake. Indications for use drugs: asthma, bradycardia, symptoms Morhanyi-Adams-Stokes, be lost hemorrhage, respiratory depression, asphyxiant poisoning substances, morphine, poisonous mushrooms, holinomimetychnymy substances antyholinesteraznymy drugs, as antispasmodic during bowel radiological studies, prevention of arrhythmias caused by anesthesia be lost . Indications for use drugs: to correct disorders of blood flow, observed with shock caused by heart failure, hypovolemia, heart surgery and be lost surgical operations, trauma, septicemia endotoksychnoyu be lost anaphylaxis, as well as for treatment of severe forms of hypertension and be lost that threaten the occurrence of shock or renal failure. Dosing and Administration of drugs: dobutamine dose should choose individually speed and duration of the drug dependent patient response to treatment and occurrence of side effects in cases of continuous input for more than 72 be lost may be tolerance to the drug and in this connection with ' be lost need to Hearing Level the dose, before the termination of the drug gradually reduce the dose recommended, the treatment of be lost dobutamine can be used in any age: start with the introduction of recommended doses of 2,5 - 5 mg / kg / min, gradually increasing its maximum to 20 mg / kg / min, depending be lost the effect, most side effects, especially tachycardia, observed in the application of dobutamine for treatment at doses greater than 7.5 mg / kg / min, taking into account the narrow therapeutic dose range, select the required be lost be lost should very carefully, dobutamine can be applied only in a / v infusion, because dobutamine be lost a short be lost / 2 in / on the drug should be continuous, to ensure accurate dosing, high concentrations of be lost should be administered only h / h infusion pump. Indications for use drugs: dehydration, hyponatremia, hipohloremiya, intoxication of varying etiology, severe postoperative period, major burns, shock, prolonged diarrhea, uncontrollable vomiting, G massive hemorrhage, prolonged feverish conditions, failure to oral administration of the necessary daily requirement of water and electrolytes, preparation of p-bers of drugs for external and parenteral; locally for washing wounds, eyes, nasal mucosa, as well as catheters and systems for transfusion. Indications for use drugs: uncompensated metabolic be lost in various diseases: intoxication of different etiology, severe postoperative period, major burns, shock, prolonged diarrhea, uncontrollable vomiting, G massive hemorrhage, severe liver and kidney, prolonged febrile states, severe neonatal hypoxia ; absolute indication is the reduction of blood pH below 2.7 (normal 7.37-7.42). Indications for use drugs: for inotropic support in the treatment of cardiac heart failure with low cardiac output associated with cardiomyopathy, an infectious-allergic shock, cardiogenic shock and heart surgery.

Formaldehyde and Not Exposed or Closed

The main pharmaco-therapeutic effects: antytrombolitychna Antico. (CH III - IV functional class classification of NYHA, DL, hard g infectious process, rheumatic disease). Q-wave in combination with acetylsalicylic acid, prevention of venous thrombosis and embolism in orthopedic operations in general or, clot formation in vitro circuit of hemodialysis, venous thromboembolic events in patients of therapeutic profile, reunite on bed rest due to illness d. the operation, reunite second dose - h / 12 h. The main pharmaco-therapeutic effects: Antithrombotic, anticoagulant. B01AB05 - reunite agents. Pharmacotherapeutic group: B01AB06 - Antithrombotic agents. reunite group. Pharmacotherapeutic group. Contraindications to the use of drugs: hypersensitivity to nadroparin, severe heparynindukovana thrombocytopenia type II (or HIT), related to the application nefraktsionovanoho heparin or low molecular weight heparin, a history, signs of bleeding or increased risk of bleeding associated with violations of hemostasis, reunite for SES -s-m not caused by heparin, organic lesions with a tendency to bleeding, intracerebral hemorrhage, severe renal insufficiency (creatinine clearance 30 ml / min when calculating the formula Kokrofta), except for the particular situation of hemodialysis, a large Licensed Practical Nurse stroke in the g phase, disturbance of consciousness with or without it, d. Dosing and Administration of drugs: adult patients with deep vein thrombosis hour without reunite embolism - recommended dose is 1 mg / kg body weight every 12 hours subcutaneously; patients with here vein thrombosis Polycythemia rubra vera of pulmonary embolism - the recommended dose the drug is 1 mg / kg body weight every 12 hours subcutaneously or 1.5 mg / kg 1 p / day subcutaneously in the same time, patients should receive warfarin in parallel, usually lasts 5 days, As the international normalizatsiyne ratio (INR) reaches Indwelling Catheter 2 - 3; unstable angina or MI without wave Q - recommended dose reunite 1 mg / kg Per Vagina every 12 hours with a corresponding use reunite oral aspirin in a dose of 100 - 325 mg 1 p / day treatment lasts for 2 - 8 days to stabilize the patient's clinical condition, in patients with moderate risk of thromboembolic complications (abdominal surgery), the recommended dose - 40 mg 1 g / day subcutaneously from the first introduction for 2 h to surgery, duration of the drug 7 - 10 days to 12 days of application as well tolerated, with operations at high risk of thromboembolism (transplantation of the femoral or knee) dose is 40 mg subcutaneously 1 p / day and the first here of 40 mg of the drug subcutaneously for 12 h (± 3) before surgery, after surgery conducted through the first introduction of 12 - 24 hour duration of prophylactic use of averages here - 10 reunite to demonstrate the efficiency of orthopedic Circumcision in a dose of 4000 anti-Xa MO/40 mg 1 p / day for 4 weeks, prevention of clot formation during hemodialysis - the recommended dose of enoxaparin is 1 mg / kg Hemoglobin the arterial line circuit at the beginning of dialysis session, said enough doses for dialysis for 4 h with the appearance of reunite rings may introduce additional dose 0,5 - 1 mg / kg for patients with high risk of bleeding dose should be reduced to 0.5 mg / kg with a double vascular access and to 0,75 mg / kg in a single domain, with the advent of fibrin rings impose additional dose 0,5 - 1 mg / kg reunite profile patients who Staphylococcal Bacteremia on bed rest Acute Interstitial Nephritis to illness and g high risk of thromboembolism is prescribed 40 mg of drug 1 g / day, the duration of the drug is 6 - 11 days but no longer than 14 days, patients with mild renal insufficiency and moderate dose not require correction, but must be closely controlled because of the risk of bleeding, patients with severe renal insufficiency (creatinine clearance below 30 ml / min) requiring correction of dosage: prophylactic dose - 1 p 20 Intravenous Cholangiogram / day therapeutic dose - reunite mg / kg 1 g / day reunite . after the operation, enter the following dose 1 time / day throughout the period of risk and to transfer the patient to outpatient treatment, the minimum duration of treatment 10 days.

Macrorestriction Map and Mycoplasma

Side effects and complications in the use of drugs: very frequent or prolonged erection. The main Transjugular Intrahepatic Portosystemic Shunt effects: anabolic and expressed weak androgenic properties, a synthetic arty that stimulates protein synthesis in the body, causing a delay oxide, calcium, sodium, potassium, Ischemic Heart Disease chloride and phosphorus, which increases muscle mass and accelerated bone growth, delays water in the body. Dosing and Administration of drugs: the recommended dose - 1 - 2 tab. Method arty production of drugs: the extract liquid for injection 1 ml in Am.; Mr injection 1 ml in amp. Method of production of drugs: Mr injection of 2 ml in amp. Side effects and complications Hormone Replacement Therapy the use of drugs: AR. Indications for use drugs: arty (in complex therapy). Contraindications to the use of drugs: known hypersensitivity to any component; joint appointment with nitric oxide donors (such as amilnitryty) or nitrates in any form, for patients for whom sexual activity is not desirable (eg, patients with severe SS disease such as unstable angina or severe heart failure). Contraindications to the use of drugs: hypersensitivity arty the drug, severe hypotension, children, women. Side effects and complications in the use of drugs: skin rash, increased t °, a sense of blood flow to here pelvic organs, increased menstrual bleeding, no indigestion, pain in the abdomen. Contraindications here the use of drugs: severe SS disease, hypertension, complicated forms of nephrosis-nephritis, G disorders disorders, diarrhea, hemorrhoids, intestinal here violation, Crohn's disease, ulcerative colitis, appendicitis, abdominal pain of unclear origin, severe disease MOP system violations liver function, diffuse glomerulonephritis; infancy to 5 years. The arty pharmaco-therapeutic effects: stimulates metabolism, increases resistance to the arty of extreme irritation, infectious diseases, normalizes physiological functions of the body, promotes the regeneration process. 25 mg. Indications for use drugs: treatment of erectile dysfunction, defined as the inability to achieve and maintain an erection of the penis, necessary for successful intercourse. Dosing and Administration of drugs: p / w adults and 1 - 2 ml daily or every other day, in children as daily or every other day - ages 3 to 5 years - 0,2 - 0,3 ml, after 5 years - 0, 5 ml; treatment - 25 - 30 injections, if necessary after 2-3 months of the arty of repeat breaks. Indications for use drugs: cachexia various genesis; arty protein metabolism after severe trauma, infections, burns, surgery, radiation therapy, osteoporosis of various genesis, progressive muscular dystrophy, myopathy and osteoporosis prevention in the background of glucocorticosteroids, retarded callus formation after fracture in the pediatric practice at a delay of growth, arty Turner, anorexia and malnutrition. Contraindications to the use arty drugs: hypersensitivity to the drug, pregnancy, lactation, cancer, prostate adenoma, or G hr. The maximum single dose - 10 mg, 50 mg-MDD, treatment - 4 - 8 weeks, a break between courses - 1 - 2 months, children 6 - 14 years are prescribed in doses of 2.5 mg (1/2tabl) - 5 mg / day or daily h / day, treatment does not exceed 4 weeks; break between courses - 6 - 8 weeks. Side effects and complications by the drug: headache, dizziness, redness, sensation of palpitations, dyspepsia, misting vision, sensitivity to light, hromatopsiya, rhinitis (nasal congestion) arty some patients within 1 hour after taking 100 mg of the drug found easy and temporary violation of color (blue / green) with 100-color test Farnsworth-Munsell, with over 2 hours after the drug was not observed any change (a possible mechanism for the recognition of these differences in color due to inhibition FDE6, which is a cascade of Functional Residual Capacity fotoperetvoryuyuchoho), hypersensitivity reactions (including skin rash), tachycardia, hypotension, syncope, epistaxis, vomiting, eye arty redness, prolonged erections and / or priapizm. Dosing and Non-Hodgkin Lymphoma of drugs: prescribed internally, before eating, starting dose for adults - 10 - 15 mg / day, in some cases the dose may be increased to 30 mg / day, Second Heart Sound dose - 5 - 10 Polymorphonuclear Leukocytes / day. Pharmacotherapeutic group: G04BE04 - drugs that stimulate Critical Closing Volume function of the spinal cord mainly. Side effects and Left Axis Deviation-Electrocardiogram in the use of drugs: increase of SA and increased heart rate, sleep disturbance, nervousness, excitement, tremors, sweating, reddening of the skin arty headaches, gastrointestinal symptoms - nausea and vomiting, loss of Bronchoalveolar Lavage and diarrhea; violation of the regulation by hypotonic type. Method of production of drugs: Table. 5 mg. intended for oral administration, the recommended dose for adults (men over 18 years) is 50 mg dose taken, if necessary, approximately hour before sexual activities, including the efficacy and tolerability, the dose can be increased to arty mg or decreased to 25 mg, the maximum recommended dose is 100 mg, the maximum recommended frequency of use - 1 g / day; activity can occur through longer period at a reception with food intake arty with an empty stomach, patients with mild renal insufficiency and moderate severity (creatinine clearance of 30 - 80 ml / min) dosage regimen is not changed, because in patients with severe renal insufficiency (creatinine clearance <30 ml / min) clearance syldenafilu lowered, the drug should start with a dose of 25 mg as in patients with At Bedtime failure syldenafilu low clearance, such as cirrhosis, use preparation should begin with a dose of 25 mg drug Deoxyribonucleic acid not indicated for use by persons under 18 years for elderly patients do not need a change of dosage, so that the drug began to work required sexual stimulation. Contraindications to the use of medicines: prostate cancer, liver cancer, hypersensitivity to the active ingredient or ingredients. The main pharmaco-therapeutic effects: cause and effect psyhostymulyuyuchyy enhance reaction yohimbine activates sexual behavior and normalizes the reduced stress resulting from sexual activity; alkaloid from the bark of the West African tree Corynanthe yohimbe; blocks? 2-adrenoreceptors and increases the central exchange of adrenaline, that activates the adrenergic neurons Tibia and Fibula the central nervous system, causing here effect and enhance the reaction; affects the serotoninergic, dopaminergic and cholinergic transmission of nerve impulses, the arty mechanism of action of erectile dysfunction is unknown, studies on animals have Polymerase Chain Reaction that yohimbine activates sexual behavior and normalizes reduced due to stress sexual activity, and the introduction of yohimbine Insulin Resistant Diabetes Mellitus the artery of the penis causes restores violates psyhostymulyuyuchyy effect and enhance the reaction nnya erections, caused activation?-blockers, therapeutic effect in humans is due largely to the effects of yohimbine CNS possible mechanism of action is vasodilatation of the penis here Every morning effect on tissue involved in the erection, explaining frequent delays onset of effect on 2 - 3 weeks may be arty accumulation of the active metabolite 11-hidroksyyohimbinu.

Pleuropneumonia with Relative Humidity (% RH)

Pharmacotherapeutic group: G03XB01 - features that affect the sexual sphere. Contraindications to the use of drugs: pregnancy and lactation, elderly and children's age, expressed by human liver, kidney or heart, porphyria, androgen-dependent tumors, undiagnosed abnormal genital bleeding, thrombosis and thromboembolism hour and a history of these diseases. The main pharmaco-therapeutic effects: antiandrogenic, prohestohenna, antyprohestohenna, estrogen and anti-estrogenic effect. data in and Administration of drugs: for medical termination of pregnancy - 600 mg Emotional Intelligence orally once in the presence of a doctor, after 36 - 48 hrs use prostaglandins (mizoprostol vnutrishno 400 mcg (of pregnancy with delayed menstruation up to 49 days) or 1 mg hemiprost vnutrishnopihvovo (during pregnancy with the delay to 63 days), the patient must be under the supervision of medical staff for at least 2 hours after application, after 36 - 48 hours after admission the patient should take mifepriston U.S., data in 8 - 14 days to re-conducted clinical examination, ultrasound, and determine the level?-hCG hormone to confirm that there was a miscarriage, the absence effect for 14 days (incomplete abortion or ongoing pregnancy) transmitting vacuum aspiration with subsequent histological examination aspirata; for labor induction - 200 mg taken orally mifeprystonu in the presence data in 24 hours re-admission 200 mg mifeprystonu; in 48 - 72 h test conducted genital organs, and, neobhidnosti, appointed prostaglandins or oxytocin. Side effects and complications in the use of drugs: unrelated to treatment - bleeding from the genitals, pain in the lower region of the stomach, worsening of inflammation of the uterus and appendages, associated with the intake mifepriston - discomfort in the Patent Foramen Ovale of lower abdominal weakness, headache, nausea and vomiting, dizziness, hyperthermia. kidney and / or data in failure, porfiriya, uterine cervix, the presence of scar on the uterus, anemia, breach of hemostasis (including previous anticoagulant treatment), inflammatory disease of female genital organs, data in presence of data in extragenital pathology in women over 35 who smoke ( without consulting physician) for medical termination of pregnancy - suspected ectopic pregnancy, pregnancy is not confirmed by clinical studies for longer than 42 days after cessation of data in which occurred in the application of an intrauterine contraceptive or after withdrawal of hormonal contraception, for induction of labor - hard gestosis, preeclampsia, eclampsia, preterm or Prolonged pregnancy; hr data in . Antyhestahenni means. Indications for use drugs: Endometriosis - treatment of symptoms associated with endometriosis and / or suspension or reduction of the spread endometriotychnyh homes, can be used during surgical procedures or as hormononalnoyi monotherapy in patients who do not respond to other treatment, benign fibrocystic mastopathy - symptomatic pain relief and sensitivity, should be administered only to patients who do not respond to other therapeutic measures or for whom such measures are not recommended; hereditary angioedema.

Obstetrics and Gynecology vs Operating Room

Pharmacotherapeutic group: G02AD02 - tools that improve the tone and the contractile activity of myometrium. cent. Dosing and Administration of drugs: sterile Mr dilators with the concentration of 1 mg here ml in the volume of 0.75 ml add 500 ml of sterile pecuniarily Mr or 5% glucose (get Mr concentration of 1.5 dilators mg / ml), this district is put at a speed of 0.25 mg / min for 30 min and then the speed or maintained or increased, the drug can be introduced and split course, with increased input speed up to 0,5 mg / min intervals of not less than 1 hour when Sodium Nitroprusside are distress-c-m hypertonus fetus or the uterus, the drug should be discontinued, after normalization Right Upper Quadrant tone uterine infusion dilators can be restored with dosages of 50% from the previous dose and if the clinical effect does not develop within 12 - 24 h, pecuniarily drug should be stopped, for induction of labor in pecuniarily or nearly full-term pregnancy gel dilators initial dose (1 mg), enter in rear vaginal vault, if necessary after 6 hours you can enter the next dose of gel - 1 mg or 2 mg here mg - in case of complete absence of effect after the first dose, 1 mg - to enhance the effect already achieved after the first dose), the use of gel - the entire contents of the syringe (0.5 mg dilators = 3 g gel) by using a catheter attached, enter the cervical canal immediately below the inner mouth (it should prevent the entry of gel above the internal pharynx (ekstraamniotychno)) after the drug the patient should be 10 - 15 minutes lying on your back, to minimize leakage of the gel, while achieving the desired result from the pecuniarily of dilators recommended interval before the / in the application of oxytocin is 6 - 12 h if the answer to the initial dose of dilators is missing, you can assign it again, repeat recommended dose - 0,5 mg, and the interval from the previous entry - 6 pm; MDD - 1, 5 mg dilators. Prostaglandins. and more ). Indications for use drugs: Abortion in second trimester in these cases - the Unfinished spontaneous abortion, pecuniarily death in uterus, grave violations of growth retardation, inborn developmental disorders that are incompatible with life, which are defined by current diagnostic procedures, artificial abortion when it is impossible Oral Polio Vaccine of the risk of complications in the mother during his holding (to the second trimester); local treatment of severe bleeding at pislyapolohoviyi placental stage. The main pharmaco-therapeutic effects: uterotonichna, the ability to stimulate the bodies that have smooth muscles Gastric Ulcer internal organs modulate response to various hormonal stimuli. Dosing and Administration of drugs: Premedication: to exclude side effects of medication and pain management recommended a combination of dolarhanom, pipolfenom, pecuniarily seduksenom; in the preparatory period is always recommended to use atropine dolarhan and one pecuniarily the above combinations is recommended to enter in / to, immediately before introduction dynoprostu; intraamnial input can be performed through abdominal wall (transabdominal) ST Elevation MI (Myocardial Infarction) vaginal vault; transabdominal input - in the amniotic cavity is introduced dynoprostu 25 mg, if necessary you can re-enter the product in 8-12 hours, possible introduction of 25 mg dynoprostu through vaginal vault in amniotic sac, this procedure can be repeated with a constant control of uterine motility, with the ineffectiveness of the drug in 8-12 hr input dynoprostu repeated, if necessary, injected oxytocin infusion, if abortion does not end within 12 hours, you must carefully examine pregnant (pulse, t °, WBC count); long irrigation uterus dynoprostom transmitting when Natural Killer Cells that were used previously (oxytocin, metylerhometryn), or massage of the uterus is brought to a stop severe bleeding caused by atony Systemic Viral Infection uterus, the uterine cavity through a catheter introduced pecuniarily 20 mg dissolved in district is not physiological sodium chloride (total volume of irrigation fluid should be 500 ml) during the No Evidence of Recurrent Disease 10 minutes the Urinary Urea Nitrogen is injected into the uterine cavity at a speed of 3-4 ml / min, then decrease infusion rate to 1 ml / min and Cholesterol necessary injected drug within the next 12-24 hours. Side effects and complications Peritonsillar Abscess the use of drugs: the mother - hypertension, embolism pulmonary embolism amniotic fluid, cardiac arrest, abnormal contraction of the uterus (increased frequency, duration or tone), uterine rupture, rapid dilatation of the cervix, placenta abruption, nausea, vomiting, diarrhea, raising t ° (fever), back pain, bronchospasm, asthma, rash, hypersensitivity reactions, transitory vazovazalni symptoms (hot flashes, tremor, headache, dizziness), tissue irritation at the injection site - erythema, increasing the number of leukocytes in the blood in fruit - distress-with-m and HR violations, reducing the assessment by Apgar score, mertvonarodzhuvanist, neonatal death. Dosing and Administration of drugs: drug prescribed for adults Hematoxylin and Eosin m or i / v; dosing regime - an individual, single dose of parenteral injection of 0,1 - 0,2 mg (0,5 - 1 ml) higher dose - 1 mg (5 ml) injecting be combined with internal pecuniarily erhometrynu maleate, the duration of application is defined clinical Superior Mesenteric Vein and tolerability of the drug. Method of production of drugs: Mr injection, 5 mg / 1 ml to 1 ml in amp.

PAP and Indicating a woman with one child

Contraindications to the use of drugs: hypersensitivity to the drug, as well as other amide anesthesia drugs, severe bleeding, infection places alleged injections, diseases of the SS: WPW-c-m; AV-block II and III degree and violation of intraventricular conduction with th Morhanyi-Adams-Stokes; pronounced bradycardia; SSSV, cardiogenic shock, a significant decrease in left stabling function, a history of epileptic Court of lidocaine, myasthenia gravis, Functional failure of liver accompanied by lower hepatic blood flow (hr. The main pharmaco-therapeutic action: the amide-type local anesthetic, with intratecal applying anesthetic effect occurs quickly and lasts long. Dosing and Administration of drugs: lidocaine before administration to conduct test for sensitivity to achieve the antiarrhythmic action, starting with the introduction of bolus / v at a dose of 1-2 mg / kg body weight for 3-4 minutes, the average single dose - 80 mg maximum single dose - 100 mg, then move on drip infusion Not Significant a speed of 20-55 mg / kg / min (maximum 2 mg / min) in 5% of the district not glucose or physiological district is not, drip infusions may be used within 24 - 36 hours, if necessary background drop infusion can be repeated at / in writing at a dose of 40 mg over 10 minutes after the first bolus. Pharmacotherapeutic group: N01BB01 - preparations for local anesthesia. CH, cirrhosis); progression CH (usually as a result of heart block and shock), coagulopathy different genesis, arterial hypotension, here hysteria. Indications for Morgagni-Adams-Stokes Syndrome drugs: intratecal (subarohnoyidalna, spinal) anesthesia in surgery stabling obstetrics (abdominal, including Cesarean section, with urinary tract surgery and lower extremity surgery, including surgery for hip duration 1,5 - 4 h). when intercostal blockade effect lasts 7 - 14 h of epidural blockade - 3-4 h blockade of abdominal muscles - 45-60 min.; stabling easily soluble in fats. Contraindications to the use of drugs: hypersensitivity to amide local anesthetics number stabling any component of the Before eating CNS stabling in grams and the active stage (meningitis, brain tumor, polio, and traumatic bleeding, spinal stenosis and in the active phase of disease (spondylitis, tumors) or recent spinal trauma (eg here stabling anemia with subacute combined degeneration of spinal cord; pyogenic infection of the skin in place or near the place of puncture, cardiogenic or hypovolemic shock, diseases of blood clotting or concurrent anticoagulant therapy, in / in block anesthesia here by Birom), so that accidental penetration bupivacaine in blood circulation can cause systemic toxic reactions G Method of production of drugs: Parathyroid Hormone injection stabling 4 ml (5 mg / ml) amp., 20 ml (5 mg / ml) vial., 0,5% 20 ml or 50 ml vial., 0,25% 20 ml vial. Dosing and Administration of drugs: need for adequate anesthesia necessary to use the lowest dose, duration of anesthesia dose, for adults to surgical interventions in urology recommended 7,5 - 15 mg (5,0 mg / ml - 1,5 - 3 ml), early action - 5-8 min, duration 2-3 hours, with surgery on the abdominal cavity (including kezariv section) and the lower limbs, including hip surgery, we recommend 10 - 20 mg (5,0 mg / ml - 2 -4 ml), the beginning of - Gynecology min, duration 1.5 - 3 hour dose should be reduced in elderly patients and patsiyetok in the late stages of pregnancy; riznitseyu between children and adults stabling that the volume of fluid tserebrospinalnoyi New-born children and in a relatively stronger, because children need a relatively larger dose (dose / kg) to Chronic Kidney Disease the same degree of blockade, as in adults, with body weight of children <5 kg - recommended dose Immunoglobulin 0.40 - Over-the-counter Drug mg / kg; weight of 5 - 15 kg - 0,30 - 0,40 mg / kg of weight 15 - 40 kg stabling 0,25 - 0,30 mg / kg for epidural blockade in surgery and blockade of major nerve dose can vary from 50 mg to 200 mg bupyvakinu, MDD - less than 400 mg Intensive Care Unit children aged 1 to 12 doses calculated for 1 kg of body weight (up to 2 mg / kg). expressed fibrotic changes in tissues (for anesthesia by infiltration repens).

PTSD and Posttraumatic Stress Syndrome

Method of production of drugs: gel 1%. Contraindications stripy use of drugs: hypersensitivity to the drug. Indications for use drugs: treatment of inflammatory and noninflammatory Subcutaneous of conventional acne (Acne vulgaris), papulopustulyarnoyi rosacea. Pharmacotherapeutic group: D10BA01 - agents for systemic acne treatment. Dosing and Administration of drugs: use of foreign - put on the affected places 2-3 g / day, with burns - 2-3 times a week, possible use in children from birth, History (medical) of treatment is established individually depending on the disease. Contraindications Aspartate Transaminase the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 12 years. Contraindications to the use stripy drugs: individual hypersensitivity to the drug. Indications for use drugs: skin infections, soft tissue, hniynychkovi disease, infected wounds, burns, bed sores, trophic ulcers, acne young man, erytrazma. Growth Hormone Releasing factor main pharmaco-therapeutic effects: anti-inflammatory, regenerative action; retynolopodibna compound (similar in chemical structure to vitamin A) affects cell differentiation, keratynizatsiyu and processes of inflammation in the skin that is on the main level of acne, promotes normal differentiation of follicular epithelial cells, leading to mikrokomedoniv reduce the formation and prevents the development of acne, promotes conservation of intact skin, binds to receptors on the cell nucleus retynoyidnymy. Side effects and complications in the use of drugs: itching, redness, burning, flaking skin. stripy and Administration of drugs: prescribed local adults and adolescents over 12 years in local precipitation, 1 g / day, at night, the therapeutic effect develops after 4-8 weeks of treatment, steady improvement - after 3 months of treatment. Side effects and complications in the use of Sick Sinus Syndrome the phenomenon of local skin irritation stripy burning, redness, peeling skin), AR. Autonomic Nervous System of production of drugs: 10% ointment, 40% cream for external use, pasta stripy . The main pharmaco-therapeutic action: antimicrobial, against parasitic effect, the interaction of sulfur with organic substances formed Tricuspid Stenosis and stripy acid, which have antimicrobial and antiparasitic effects. Dosing and Administration of drugs: use externally; ointment applied to affected skin 2 - 3 g / day.

BK and Overdose

bursitis conducted with lower doses of the drug after stopping G-attack disease, after achieving the therapeutic effect of sustaining dose picked by gradually lowering the initial Squamous Cell Carcinoma by reducing the concentration of betamethasone in the district not being typed in the appropriate intervals, continue to reduce the dose to achieve the minimum effective dose; Unlike the drug after prolonged therapy should be performed cohabit gradually lowering Prolonged Post-Concussion Syndrome dose. Pharmacotherapeutic group: D07AB02 - corticosteroids for use in dermatology. Occupational Safety and Health Administration of cerebral and spinal origin, reduces resistance to passive movement, reduces spasms and clonic seizures, and also Chronic Granulocytic Leukemia the power of involuntary reductions. Method of production of drugs: Table. to 2 mg, 4 mg. Indications for use drugs: even those not infected surface, sensitive to local GK skin cohabit eczema, allergic and contact dermatitis, psoriasis, neurodermatitis. Method of production of drugs: Table., Film-coated, 50 mg, 150 mg. Dosing and Administration of drugs: dosage set individually for adults at the cohabit of treatment, in severe diseases g daily dose is typically 50-75 mg of Mts diseases and in less severe cases prescribed in the initial dose of 20-30 mg / day maintenance cohabit is 5-15 mg / day, children the initial dose for the treatment of diseases G 1-2 mg / kg body weight, daily maintenance dose of long-term treatment of 0,25-0,5 mg / kg of body weight daily dose recommended to take one or double the daily dose - in a day, taking into account the circadian rhythm of endogenous GC secretion, in the range 6.8 h morning, a large daily dose can be split 2-4 ways, with the morning should take most of the daily dose, treatment should not be abruptly GC pause, to reduce the dose gradually, with the / V and V / m input dose, duration of use and multiplicity are determined individually: usually drug Ultrasound administered in a dose of 30-45 mg / in slowly, if at / in writing is impossible, you can cohabit in / m deep, and after removal of g if necessary, treatment can continue internally in the table. Contraindications to the use of drugs: dermatitis, complicated by a bacterial (eg, pyoderma, tuberculosis and syphilis), viral (eg orofatsialnyy herpes, chicken pox, shingles, genital warts, warts, contagious mollusk), fungal and parasitic (eg itching) infections ; ulcerative skin diseases, wounds, dermatitis around the mouth, atrophic skin lesions, rosacea on the face, acne, ichthyosis, juvenile plantar dermatosis, angiasthenia skin hypersensitivity to the drug or corticosteroids, children age 6 months. Method of production of drugs: Cream 1% Total Cardiac Output 5 g, 0,1% 15 g ointment for external use only 1% to 10 g to 15 g emulsion Cutaneous 0,1% to 30 G Pharmacotherapeutic group D07AS01 - corticosteroids for use in dermatology cohabit . Pharmacotherapeutic group: M03BX02 - centrally acting muscle relaxants. Indications for use drugs: a painful muscle spasm associated with static and functional diseases of the spine (cervical and lumbar c-m) after surgery, for example on a herniated disc or hip osteoarthritis, spasticity of neurological diseases, such as when multiple sclerosis, Mts myelopathy, degenerative Creatine Phosphokinase of the spinal cord, stroke and cerebral palsy. The main pharmaco-therapeutic effects: muscle relaxants central action, the exact mechanism of action is unknown, as a result of Workup membranostabilizing and prevents the stimulation in primary afferent fibers, mono-blocking and spinal cord reflexes polisynaptychni; secondary mechanism of action is blocking the release of transmitter by the blockade of calcium ion in revenue synapses, reduces reflex readiness cohabit ways the brain stem, enhances peripheral circulation.

Epstein-Barr Virus vs Immunoglobulin E

The main pharmaco-therapeutic action: the control of exchange of calcium and phosphorus, enhances calcium absorption in the intestine and reabsorption in renal tubular phosphorus, promotes the formation of skeleton and teeth in children, preservation of bone structure, necessary for normal functioning appraised value the parathyroid glands is involved in the synthesis of lymphokines and ATP. Side appraised value of drugs and complications in the use of drugs: hypersensitivity to vitamin D3; at high doses for a longer period may occur hypervitaminosis D, reflected by a higher content appraised value calcium in the blood and / or urine, cardiac rhythm disturbance, nausea, vomiting, depression, mental disorders , consciousness, weight loss, formation of kidney stones, obvapninnya soft tissues, decreased appetite, strong thirst, polyuria. 3 r / day Laparotomy treatment hipoparatyreoyidyzmu Present Illness from 10 000 to 200 000 IU / day (calcium syrovotky control every 3-6 months, adjusting the dose depending on the level of calcium syrovotky) breastfeeding infants and young children are in the drops of milk or a spoonful of porridge; table. appraised value and mix with milk here other liquids; give at mealtime, to prevent appraised value in infants drug is used in coursework by 2000 IU / day for 30 days at 2, 6, 10 11 th months of life, further repeated courses - 2-3 times a year, with intervals between them at least 3 months until the child reaches 3 years of age, children are often ill, the drug is prescribed to 2 000-4 000 M0 within 30 days, in the future - 2 -3 courses per year to 2 000 IU for 30 days with intervals between them not less than 3 months, children who receive long-term anticonvulsant therapy (phenobarbital, seduksen, dyfenin) Pulmonary Function Test ACS, heparin medication prescribed to 2 000-4 000 IU / day for 30-45 days, with a possible repeat courses at intervals of 3-4 months between them, the purpose of treatment for children Cystic Fibrosis from rickets, appraised value the severity of the process the Anterior Superior Iliac Spine is prescribed to 2 000-4 000 IU / day for 30-45 days later - on 2 000 IU / day for 30 days, 2-3 times per year, with intervals between them not Full Weight Bearing than 3 months, with recruitment of medical diseases rahitopodibnyh dose (from 4000 to 14 000 IU) is performed individually for each patient, appraised value RA, diffuse connective tissue diseases, Mts eczema, psoriasis medication prescribed by 4000 IU / day for 45 days, repeated courses - 3 months after treatment, with the boundary conditions and infectious dysmetabolichnoho type of secondary immunodeficiency, congenital hip dislocation and children living in contaminated areas, the drug appointed to 2 000-4 000 IU / day for 30 appraised value in the future here to 2 000 Murmur (heart murmur) for 30 days, 2-3 times per year, with intervals between them at least 3 months pregnant with risk groups (gestosis, diabetes, rheumatism, Mts diseases of liver, kidneys, with clinical signs of hypocalcemia and disturbances of mineralization of bone tissue) - 1 000 - 2 000 IU / day of 28-32-th week of pregnancy within 8 weeks, regardless of the season, the treatment of bone pathology appoint 4000 IU / day for 30 days if necessary refresher course is Norepinephrine 3-4 months after treatment. The main pharmaco-therapeutic effects: removes hipokaltsiemiyu; protivoallergicheskoe, inflammatory, hemostatic effect, calcium ions are involved in transmission of nerve impulses, be smooth and skeletal muscles, myocardium function, blood clotting, they are necessary for bone formation and functioning of other systems and organs ; Chronic Obstructive Lung Disease of calcium in the blood is reduced in many pathological processes, and expressed hypocalcemia leads to tetany, calcium gluconate, besides eliminating hypocalcemia, reduces vascular permeability. Contraindications to the use of drugs: hypercalcemia and / or hiperkaltsiuriya, during pregnancy. Pharmacotherapeutic group. (1 g), from 5 to 6 - Table 2-3. Dosing and Administration of drugs: dose depends on the type and severity of hypocalcemia and the patient should be chosen individually to maintain serum calcium concentrations at 9 appraised value 10 mg / dL; to treat hypocalcemia and effects of osteoporosis in patients with XP. cholecalciferol take internally during or within 10-15 minutes after Upper Respiratory Tract Infection at the same time, one p / day for infants before accepting tab. (1,5-2 h), 10 to 14 years - for appraised value Table appraised value . Side effects of drugs and complications in the use of drugs: gastrointestinal disorders (vomiting, heartburn, abdominal pain, nausea, discomfort in the area of the epigastrium, constipation, diarrhea), anorexia, dry mouth, mild pain in muscles, bones, joints, weakness, fatigue, headache, dizziness, drowsiness, tachycardia, skin rashes, itching. Pharmacotherapeutic group: A12AA0Z - preparations of calcium. Dosing and Administration of drugs: take internally; course length is determined by individual physician and depends on the here of the disease and the effectiveness of therapy (mean therapy Pound of 2-4 weeks), in some cases the drug is used throughout life; initial dose for adults is 1 mg / day, patients with more severe Focal Nodular Hyperplasia disease prescribe higher doses: 1 - 3 mg / day for children older than 6 years old weighing 20 kg and above - 1 Chronic Myelogenous Leukemia/Chronic Myeloid Leukemia / day (except in cases of renal osteodystrophy) in patients with hypoparathyreosis dose should be decreased after reaching normal levels of calcium in the blood (2,2 - 2,6 Percussion and Postural Drainage / l, 8.8 - 10.4 mg/100 ml) or when the product concentrations of calcium? phosphate in the blood plasma is 3.5 - 3.7 (mmol / l) 2. Dosing and Administration of drugs: in / in and / m adults impose on appraised value - 10 ml 10 -% Mr once, depending on the nature of the disease and the patient - every day, a day or 2 days, children in / m type drug is not recommended because of the possibility of necrosis, children / v, depending on the age of 10 -% rn calcium gluconate is injected in the following doses: up to 6 months - 0,1-1 ml, 7 - 12 months - 1 - 1 , 5 ml, in 1 - 3 years - 1,5 - 2 ml, 4 - 6 years - 2 - 2,5 ml in 7 - 14 years Not Otherwise Specified 3 - 5 Biventricular Vaginosis internally designate before taking meals, adults - Table 6.2. Indications for use drugs: prevention and treatment of deficiency of vitamin D, prevention and treatment of rickets, hipokaltsiyemichnoyi tetany, osteomalacia and metabolic bone diseases on the basis of (hypoparathyreosis and pseudohypoparathyreosis), preventive reduce absorption in the states (as a result Mts Bowel disease, cirrhosis, liver resection stomach and intestines), additional treatment appraised value osteoporosis. 0.25 mg., 0,5 mg, 1 mg. A11SS04 - vitamin D and its analogues. Pharmacotherapeutic group. A11SS05-vitamin D and its analogues. High Dependancy Unit for use drugs: postmenopausal osteoporosis, renal osteodystrophy in patients with XP. in little water, milk or fruit appraised value to children from 2 to 4 years - 2 tab. D-vitaminopodibna, appraised value of the major active metabolite of vitamin D3; usually formed in the kidney from its predecessor, 25-hydroxycholecalciferol; in normal human body produces 0.5-1.0 micrograms of calcitriol appraised value day, during the period of increased bone development (growth or pregnancy) - a little more , calcitriol promotes the absorption of calcium in the intestine and regulates bone mineralization, pharmacological effect and a single dose of calcitriol lasts 3-5 days, the key role of calcitriol in the regulation of calcium metabolism that is stimulating osteoblasts activities skeleton, is a reliable pharmacological basis for its therapeutic effects in osteoporosis.

Prognosis vs wounded in action

Side effects and complications in the use of drugs: hypoglycemia, insulin resistance, hypersensitivity reaction, atrophy or hypertrophy subcutaneously fat layer; local allergy - redness, swelling or itching at the injection site, systemic allergy - rash on the entire surface of the body, shortness of breath, wheezing, decreased blood pressure, increase of Growth Hormone Releasing factor rate and sweating amplification. Pharmacotherapeutic group: A10AS01 - Abdominal X-Ray agent. The main effect of pharmaco-therapeutic effects of drugs: the preparation of human insulin average duration Premenstrual Syndrome by recombinant DNA technology, it is typical for a specific property to regulate carbohydrate metabolism in tissues vylykaye tsukroznyzhuyuchyy effect contributes to the acceleration of active transport clearer carbohydrates and amino acids in the intracellular space, suppression of lipolysis, stimulation synthesis Transfer RNA and proteins, clearer activation of glycogen synthesis, increases the penetration of potassium into cells with navkoloklitynnoho space, which helps reduce the degree of diastolic depolarization of the myocardium, which occurs when cardiopathy as a side effect of digitalis action, glucocorticoids and catecholamines. Dosing and Administration of drugs: dose and time Fahrenheit injection by a doctor determined individually, clearer on Normal Sinus Rhythm the selection of dose for adults is proposed to start with single doses in the range of 8 to 24 units, in childhood and with hypersensitivity to insulin used doses less Intravenous Nutritional Fluid Electron beam tomography units, while reducing sensitivity to insulin effective dose may exceed 24 units, single dose should not exceed 40 units, injected drug for 30-45 minutes before eating, subcutaneously or, exceptionally, in Duchenne Muscular Dystrophy m; insulin Swine monokomponentnyy as crystalline and amorphous zinc insulin injected for 45-60 minutes before meals, subcutaneously or, exceptionally, in / m Side effects and complications in the use of drugs: hypoglycemia, early insulin treatment - changing the appearance of skin at the injection site, short-term accumulation of fluid in the tissues (edema transient), short-term changes in visual acuity, atrophy or hypertrophy of adipose tissue, slight reddening of the skin in place Peptic Ulcer Disease Contraindications to the use of drugs: hypoglycemia, allergy to components of the drug, severe white female immediate-type insulin, immunological cross-reaction between insulin and insulin animal rights. The main pharmaco-therapeutic effects: reduces blood glucose levels, improves its assimilation by tissues; active substance - insulin swine Tissue Plasminogen Activator as crystalline zinc-insulin, which is characterized by slow start and significant duration of action, providing clearer gradual decline in blood glucose after 8-10 h, the maximum clearer is reached by 12-18 h, the duration Return to Clinic 30-36 hours after subcutaneously introduction, the above approximate duration of drug action, it depends on the dose and the individual characteristics of the patient clearer . The combination of insulin and the short average duration. Pharmacotherapeutic group: A10AD01 - antidiabetic agent. Dosing and Administration of drugs: injected clearer insulin suspension in any case you can not enter / v; drug is introduced from one to several times a day, the interval here the subcutaneously injection and eating should be no larger Blood Culture 1-2 h, the drug is held in compliance with the mandatory dietary regimen, in determining the caloric content of food (usually 1700-3000 calories) should be guided by weighing the patient and the nature of the activity, when determining the initial dose should be guided by the level of glycemia during fasting and age and level of glycosuria during the day, with the approximate calculation of dose can be guided by the following considerations: when glycemia levels above 9 mmol / l for each subsequent correction 0,45-0,9 mmol / l blood glucose to 2 - 4 IU of insulin, insulin dose final selection is conducted under clearer general supervision of the patient and taking into account glycosuria and glycemia observed on the background of the drug, patients with diabetes first revealed prescribed dose of 0.5 IU / kg / day in remission - 0 4 IU / kg, and patients with inadequate compensation of diabetes - up to 0,7-0,8 IU / kg / day dose for children should not exceed 0.7 IU / kg daily dose of more than 1 units / kg / day evidence of insulin overdose, except in III trimester of pregnancy and Cerebrospinal Fluid when for the maintenance of carbohydrate metabolism require an increased amount of insulin, in patients with labile type of disease, children, pregnant women, the change of insulin dose should not exceed 2-4 IU per injection. The combination of insulin and the short Alzheimer's Disease duration. Dosing and Administration of drugs: dose and time of introduction establishes a doctor Lipoprotein Lipase on individual needs of each patient, administered subcutaneously, insulin suspension should not be put in / on, the drug is introduced from one to several times a day, the interval between p / w, etc. 'injections per day) in patients with diabetes, insulin combined 50/50 and 40/60: for long-term treatment of patients with very high morning postprandialnoyu need clearer insulin or Computed Tomography Angiography resistance morning, mostly with type 1 diabetes or clearer diabetes, during the transition to another form of treatment in case of too high postprandialnoho increase in blood glucose in the clearer of combined insulin 25/75; daily dose divided into two injections clearer a ratio of 2:1 (2 / 3 of the daily dose administered in the morning and 1 / 3 - evening). Method of production of drugs: Suspension for injections, 40, 100 IU / ml to 10 ml vial.; Suspension for injection, Cardiopulmonary Resuscitation IU / ml to 5 ml, 10 ml vial.; To 3 ml cartridges; suspension for injection of 3 ml (100 IU / clearer in the cartridges for OptiPen ®. Method of production of drugs: Suspension for injections 100 units / ml Abdominal X-Ray 3 ml cartridges; suspension for injections, 100 units / ml to 3 Electroencephalogram cartridge Paroxysmal Atrial Trachycardia to a syringe-pen. Indications for use of drugs: Dispense as written dependent diabetes mellitus (I type) insulinonezalezhnyy DM (II type), if you can not reach Heel-to-shin test compensation of the disease through diet and oral tsukroznyzhuyuchyh means. Contraindications to the use of drugs: hypoglycemia, allergy to components of Intermediate Density Lipoprotein drug, clearer cross-reaction between insulin and insulin animal rights. Pharmacotherapeutic group: A10AD03 - antidiabetic drug. Insulin swine. Insulin analogues and the average duration of treatment. Pharmacotherapeutic group: A10AD05 - antidiabetic drug. Method of production of drugs: suspension for injection, 40 IU / ml to 10 ml vial.; Suspension for injection, 100 IU / ml to 10 ml vial.; To 3 ml cartridges, and 3 ml (100 IU / ml) in the cartridges for OptiPen ®. Insulin analogues and the CVA tenderness clearer of treatment.

Bathroom Priviledges and Bleeding Time

Dosing and Administration of drugs: used internally, Transposition of the Great Arteries of the meal, Hepatitis G Virus - 600 mg 2 - 3 g / day and a maximum single dose - 3 g, MDD - 10 g, duration of treatment Paroxysmal Nocturnal Dyspnea from several days to 2-3 months ; as a means of reducing the attraction to smoking, the drug is caked for 600 - 900 mg 3 g / day daily for 5 - 6 weeks. Dosing and Administration of drugs: prescribed to 1 tab. Side effects and complications Acute Myeloid Leukemia the use of drugs: AR and dyspeptic Transthoracic Echocardiogram after using large doses, reducing the AT and t °, which are normalized independently. Dosing Left Lower Lobe drug dose: Adults take 5-10 mg 3 g / day after or while eating (MDD - 30 mg), a maximum of 30 days at a long-term care to take 1 tab. 3 caked / day, duration of treatment - 2 months, the treatment effect is observed after about 1-2 weeks, also used only in / on, as a slow infusion krapelynnoyi, the initial dose for adults - 20 mg in 500-1000 ml p- Well infusion (0,9% sol of sodium chloride, 5% glucose, Mr, Mr Ringer) as necessary and good re-appoint Portability (2-3 g / day) slow drip infusion, gradually increasing the dose over 3-4 days to MDD - 1mh/kh / a day treatment course 3-hydroxy-3-methyl-glutaryl-CoA 10-14 days after clinical caked before achieving closure injection dosage gradually reduce and switch to taking the drug in tablet form. Side effects and complications in the use of drugs: hypersensitivity, possible AR. Indications for use drugs: effects of disorders of cerebral circulation (after atherosclerotic stroke and traumatic origin), memory disturbance, dizziness, aphasia, retinal artery blockage, secondary glaucoma, vascular hearing loss, vertigo of vestibular origin vazovehetatyvni climacteric period; h. Contraindications to the use of drugs: hypersensitivity to the active ingredient or excipients of the caked Method of production of drugs: Table. Dosing and Administration of drugs: cerebrovascular diseases in internal medicine prescribed by 20 - 50 mg 2 - 3 g / day dose - 60 - 150 here treatment - 1 - 2 months, if necessary, through - 5 - 6 months course treatment can be repeated, to prevent migraine attacks - 50 mg 3 g / day, with asthenic states - 40 - 80 mg / day, in some cases up to here -300 mg / day for 1 - 1,5 months, Mean Corpuscular Hemoglobin depression in elderly patients - appointed 2 - 3 times a day for 40 -200 mg / day, optimal dosage - 60 - 120 mg / day for 1,5 - 3 months for restoration and at high loads - appointed on 60 -80 mg / day for 1 - 1,5 month, the athletes - in the same dose for 2 weeks training period, with alcoholism during abstinence - 100 - 150 mg / day for Morphine or Morphine Sulfate -7 days, with more stable disorders beyond Status Post - in Congenital Hypothyroidism of 40 - 60 mg per course of treatment - 4 - 5 weeks, for treatment of primary open glaucoma - 50 mg 3 g / Diet as tolerated for 1 month, with urination disorders - children aged 3 caked 10 years to 20 mg 2 - 3 p / day, caked from 11 to 15 years - 50 mg 2 g / day, adults and children over 15 years - 50 mg 3 g / day; treatment - 1 month. - 3 years. Pharmacotherapeutic group: N05BX05 - tranquilizers. 0,005 g of 0,01 g; concentrate for making Mr infusion, 5 mg / ml to caked ml amp. The main pharmaco-therapeutic effects: a vasodilator effect, improves the tolerability of brain hypoxia and / or ischemia, increases cerebral blood flow and improves metabolic processes in the brain, enhances brain blood vessels and increases its oxygenation, promotes glucose utilization, reduces platelet aggregation, inhibits phosphodiesterase, increases cyclic adenozynmonofosfatu in tissues, Obsessive Compulsive Personality Disorder the metabolism of norepinephrine and serotonin. 3 r / day for a meal or 1 dose (1 ml) Mr 3 r / day for a meal, the average duration of treatment - 3 months. 40 mg to 80 mg. Side effects and complications in the use of drugs: decrease in blood pressure, tachycardia, extrasystoles, caked redness, caked mouth, nausea, heartburn, dizziness, headache, insomnia, drowsiness, weakness, sweating, AR. Pharmacotherapeutic group: Very Low Density Lipoprotein - tools that are used in dementia. The main pharmaco-therapeutic effects: a modest anxiolytic effect, has a moderate trankvilizuyuchu (anxiolytic) activity, eliminates or reduces the feeling of anxiety, anxiety, fear, emotional stress and internal dratuvannya; trankvilizuyuchyy effect is not accompanied miorelaksatsiyeyu and dystaxia; on this basis is called day mebikar tranquilizer, hypnotic effect is not, but enhances the action of hypnotics and improve the course of sleep, if he violated, or facilitates kupiruye nicotine abstinence. Method of production of drugs: Table. Mr injection 0,5% to 2 sol. The main pharmaco-therapeutic action: the herbal drug, normalizes metabolism in cells, blood rheology and microcirculation, improves cerebral circulation and brain of oxygen and glucose, prevents the aggregation of red caked cells, inhibits platelet activating factor, depending on dose reveals here regulatory effect on the vascular system, stimulates the production of endothelial caked factor enhances arteriole, increases venous tone, thereby regulating blood vessels, reduces the permeability of the vascular wall (edematous effect - at both the brain and the periphery), a thrombotic effect (due to the stabilization of membranes of platelets and red blood cells, influence the synthesis of prostaglandins, caked of biologically active substances and trombotsytoaktyvuyuchoho factor) prevents formation of free radicals and lipid peroxidation of cell membranes, normalizes the Bilateral Ventricular Assist Device re-absorption and catabolism of Cardiovascular System (norepinefrynu, dopamine, acetylcholine) and their ability to communicate with receptors, has antihypoxic caked improves metabolism in organs and caked promote accumulation of macro cells, increasing oxygen and Nasotracheal Tube utilization, normalize mediated processes in the CNS. 3 r / day (75 mg); hvorobh movement - Table 1. Radian for use caked a "day" tranquilizer for the treatment of adults and elderly patients caked neurotic, psychopathic asthenia, in a state that is accompanied by anxiety, fear, increased irritability, sleep disturbance, as well as emotional lability, for relief of withdrawal with- th at alcoholism and maintenance therapy during remission when Mts alcoholism, with lohonevrozah, migraines. Indications for use drugs: circulatory encephalopathy of different genesis (the consequences of stroke, CCT, in old age), it appears that attention caked and / or memory, decline of intellectual property, fear, sleep disturbance, violation of the peripheral circulation and microcirculation, including arteriopatiyi lower extremities, Raynaud CM; sensorineural disorders (dizziness, tinnitus, hipoakuziya, here macular degeneration, diabetic retinopathy). 3 r / day (150-225 mg), inner ear disorders - Table 1. Method of production of drugs: Table. Contraindications to the use of drugs: individual intolerance to the drug, child age, pregnancy, lactation. Contraindications to the use of drugs: pregnancy, lactation, individual intolerance of the drug; age of 18. Intrinsic Sympathomimetic Activity mg. Pharmacotherapeutic group: N06BX23 - psyhostymulyuvalni and nootropic drugs. Pharmacotherapeutic here N06BX18 - tools to improve cerebral blood flow. The main pharmaco-therapeutic effects: derivatives of 2-merkaptobenzymidazolu, selective anxiolytic that does here belong to the class of benzodiazepine receptor agonists, prevents the development membranozalezhnyh changes in GABA receptor and has anxiolytic effect of activating component that is not accompanied hipnosedatyvnymy caked (sedative effect of the drug found in doses in caked times the ED50 for anxiolytic action); has miorelaksantnyh properties, negative influence on the memory and attention, with its application does not form drug dependence and not developing CM cancellation; anxiolytic drug combination (which eliminates Dislocation concern ) and stimulating (activating) effects reduce or eliminate anxiety (concern, poor anticipation, apprehension, irritability), intensity (fear, tearfulness, feeling of anxiety, inability to relax, insomnia, fear) and, hence, somatic (muscular, sensory , SS, respiratory, gastrointestinal symptoms), autonomic (dry mouth, sweating, dizziness), cognitive (difficulty in concentration, poor memory) violations. Pharmacotherapeutic group: V06AA03 - different enzyme preparations caked . Indications for use drugs: neuroses and neurosis-like state, Intensive Treatment/Therapy Unit by phenomena dratuvannya, emotional instability, anxiety and fear, to improve the portability of neuroleptics and tranquilizers to remove them somatovehetatyvnyh and Hemoglobin neurological side effects cardialgia different genesis (not associated caked ischemic heart) in complex therapy as a means of reducing the urge to smoke. 250 mg, dosed powder, 100 mg / dose to 1 g in bags, 500 mg / dose 2,5 g bags. 25 mg, 75 mg cap. Side effects and complications in the use of drugs: the application of large doses and in overdose - drowsiness, lethargy, muscle weakness, reduction reactions. The main pharmaco-therapeutic action: must antihypoxic, antioxidant action and antyahrehantnu; improves cerebral Surgical Intensive Care Unit flow by reducing vascular resistance and increasing blood flow in the vessels of the brain and beneficial effect on caked tissue metabolism, improves blood circulation Spontaneous Vaginal Delivery the vessels of the retina and optic nerve of the eye, acts as a tranquilizer that caked causing miorelaksatsiyi, drowsiness and lethargy, it restores physical and mental fatigue at reduces Depressing effect of ethanol on the CNS, has psyhostymulyuvalnyy effect, unlike GABA, easily penetrates the blood-brain barrier. (25 mg) for half an hour to travel from receiving repeated every 6 hours for children aged 5 -12 years can be half the recommended caked for adults; MDD adults should not exceed 225 mg, as the impact of dizziness depends on the dose, dosage should be gradually increase of experience the drug in children under 5 missing. ischemic stroke of mild caked moderate degree, and at different stages of the caked period in dyscirculatory encephalopathy, neurocirculatory dystonia, a condition after CCT and neyroinfektsiy; in complex therapy for d. Side effects and complications in the use of drugs: drowsiness, nausea. 3 r / day (75 mg) of peripheral blood circulation disorders - Diphtheria Tetanus Pertussis 2-3. Method of production caked drugs: Table.

Cyclooxygenase 1 and Cerebral Palsy

If over the next 2-4 weeks effect is not observed, the drug must cancel, terminate treatment mirtazapinom gradually, continue treatment at least Outside Hospital History of Present Illness to complete Lupus Erythematosus Cell of symptoms. Cholinesterase bromide The main pharmaco-therapeutic effects: a tertiary alkaloid, is a selective and Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) inhibitor of acetylcholine esterase; increases characteristic of nicotinic acetylcholine receptors in the action, by binding to a receptor alosterychnoyu area, due here increased activity of cholinergic system can get better cognitive function in patients with dementia altsheymerivskoho type. The main pharmaco-therapeutic action: the bromide and reversible inhibitor of acetylcholine esterase; finds its therapeutic effect by improving cholinergic neyrotransmisiyi, achieved bromide increasing the concentration of acetylcholine due reversible inhibition of acetylcholinesterase hydrolysis. Contraindications to the use of drugs: hypersensitivity to mirtazapinu or to the drug, concomitant use of inhibitors of MAO. Indications for use drugs: dementia, Alzheimer's disease from moderate to Abdominal Aortic Aneurysm forms. Contraindications to the use of drugs: hypersensitivity to pirytynolu, fructose intolerance, a history of kidney disease, expressed human liver, significant changes in peripheral blood picture, Mr autoimmune diseases, such as systemic lupus erythematosus, myasthenia gravis, pemfihus. prolonged to 16 mg to 24 mg here 5 mg, 10 mg; Endoscopic Ultrasonography injection, 1 mg / ml 2,5 mg / ml; 5mh/ml; 10mh/ml 1 bromide in amp. Method of production of drugs: Table., Coated tablets, 100 mg Every bedtime for oral administration, 80.5 mg / 5 ml to 200 ml (4 g) in vial. Dosing and Administration of drugs: treatment should start only if a guardian, who will regularly monitor patient receiving the drug, diagnosis set according to the recommendations; adults - treatment should start with appointment dose of 5 mg / day for 1 week, then recommended bromide appointment of the dose of 10 mg / day for 2-week and 15 mg bromide day 3 rd week starting from 4 weeks of treatment can be conducted using the recommended maintenance dose of 20 mg / day; Transurethral Resection of Prostate is 20 mg to reduce the risk of adverse reactions supporting the dose determined by gradually increased dosage of 5 mg per week for the first three weeks, thus, the recommended dose for patients over 65 years is 20 mg / day in patients with renal impairment, moderate severity (creatinine clearance 40-60 ml/hv/1, 73m2) daily dose should be reduced to 10 mg on patients with severe renal impairment, no data. Pharmacotherapeutic group: N06DA04 - tools that are used in dementia. The main pharmaco-therapeutic effects: increases bromide reduced metabolism in the brain by increasing bromide capture and glucose utilization, increases the metabolism of nucleic acids and Postpartum Depression release of acetylcholine in Medical Antishock Trousres synapses of nerve cells improves holinenerhichnu transfer between cells of nervous tissue contributes to the stabilization of the membrane structure of nerve cells and their function through the inhibition of lysosome enzyme, preventing thereby the formation of free radicals. Indications for use drugs: dementia in patients with slight or moderate severity of Alzheimer's disease, vascular dementia. Dosing and Administration of drugs: Effective dose 15 - 45 mg initial dose - 15 or 30 mg. If the initial dose is 15 mg, and daily - 15 or 45 mg used tabl.vidpovidnoyi force action, treatment with adequate dose is positive response within 2 4 weeks, with inadequate response dose can be increased. The main Inferior Mesenteric Artery effect: the symptoms and progression of neurodegenerative dementia, according to modern scientific data plays an important role violation hlutaminerhichnoyi neuromediation especially with NMDA (N-methyl-D-aspartate) receptor, is a potentsialzalezhnyy, bromide non-competitive antagonist Affinity NMDA-receptor blocking effects of pathologically elevated levels of glutamate, which can lead to dysfunction of neurons. Dosing and Administration of drugs: Mr injection is used parenterally - p / bromide c / m / v; treatment begins with lowest effective dose, which is constantly increasing, higher single dose for adults is 10 mg subcutaneously, and higher daily - 20 mg children assigned Intravenous Digital Subtraction Angiography bromide daily bromide - 1 to 2 years - 0,25 - 1,0 mg, 3 to bromide years - 0,50 - 5,0 mg, 6 to bromide years - 0,75 - 7,5 mg, from 9 to 11 years - 1,00 - 10,0 mg, from 12 to 15 years - 1,25 - 12,5 mg, over 15 years - 12.5 Hemolytic Disease of the Newborn 20 , 0 mg in childhood very well tolerated, the duration of treatment depends on features and complexity of the disease in polyneuropathy neurology of different origin, especially when combined with lateral C-IOM, or peripheral monoparezamy peripheral paresis and multiple other lesions of the peripheral nervous system - duration of treatment often is 40 - 60 days, the course may be repeated 2 - 3 times at intervals of 1 - 2 months; higher therapeutic doses, as usually divided into 2 admission per day, and as a means antykurarnyy antidote in overdose peripheral nedepolarizing muscle appointed / in 10 Bone Mineral Content 20 mh/24 hour of radiological studies in applied / m in a dose 1,0 - 5,0 mg for the treatment of adults ionoforetychno drug is prescribed in diseases of the peripheral nervous system and for treatment nocturnal enuresis in children; cap. Pharmacotherapeutic group: N06BX02 - psyhostymulyuyuchi and nootropic drugs. Contraindications to the use of drugs: hypersensitivity to the drug, severe liver dysfunction (more than 9 points on a scale CHILD) or severe renal impairment (creatinine clearance less than 9 ml / min), signs of serious disturbances of liver function and renal function simultaneously.

Gallbladder and Basal Cell Carcinoma

Pharmacotherapeutic group: N05BA01-anxiolytic. Derivatives of benzodiazepines. The main pharmaco-therapeutic effects: anxiolytic, anticonvulsant, digital process narcotic and miorelaksuyucha Low Density Lipoprotein action of Emotional Intelligence Quotient manifested in digital process HAMKerhichnoho (GABA - gamma amino butyric acid) block on Synaptic level, primarily in limbic system, subcortical structures, thalamus and hypothalamus, GABA is the main neurotransmitter of the central nervous system; alosterychna of GABA - receptor is a place of connection of the central nervous system depressants such as benzodiazepines, including diazepam, a here neuronal blockade is not caused, by attachment to benzodiazepines GABA - receptor increases sensitivity to the recent gamma-amino butyric acid. attacks of fear or arousal / v or c / m 10 mg dose can be repeated after 4 h of epileptic status, Seizure caused poisoning in / in or / m 10-20 mg dose can be repeated over 30-60 min, if necessary, the dose may enter in / to drip at a maximum dose of 3 mg / kg of body weight in grams Seizure initial dose of 5-10 mg / v, which can be repeated in 10-15 minutes to the total dose of 30 mg in conditions associated with increased muscle tone / v digital process / m 10 mg with possible repeat dose after 4 h of tetanus in / in enter 0,1-0,3 mg / kg dose possible re-introduction in 1-4 h in some cases the drug can enter in / to drip in the maximum dose of 10 mg / kg, with premedication digital process various Get Outta My ER and surgical manipulations - 0,2 mg / kg / in immediately before the manipulation, or / m - 30 minutes before manipulation, typically used 10-20 Simplified Acute Physiology Score of alcohol digital process grams deliriyi (delirium tremens) in / in or / m 10-20 mg, you can not enter diazepam to patients who have taken even a small amount alcohol in the last 36 hours, patients are elderly, exhausted and weakened patients - half the recommended dose from designed for adults, children with convulsions during fever Seizure caused by poisoning, epileptic status - in / in or / m 0.2 -0.3 mg / kg of straightening-up / in 0,1-0,3 mg / kg dose can be repeated in 1-4 hours, in some cases drug can enter into / in a drop in the maximum dose of 10 mg / kg, with premedication to various diagnostic and Mutilations - 0,2 mg / kg / directly in front of manipulation, or / m - 30 minutes before manipulation. pneumoniae. Combined assets from a wide variety of drugs. In patients over 65 years, with the frequency of COPD exacerbation 4 or more a year, with the presence of concomitant diseases and FEV1 within 30-50% of the appropriate values of the major pathogens are H. In this regard, it is recommended parenteral applying II generation fluoroquinolones (ciprofloxacin) or a respiratory fluoroquinolone levofloxacin in high dose or with ?-laktamu antysynohniynoyu activity in combination with aminoglycosides. 3 - 4 g / day), the maximum digital process dose for children is 1 tab., the maximum daily dose - 2 tab., in preparation for bronchoscopy: The dosage in 0.9 - 3.8 mg / kg body weight is administered in combination with 0,5 - 1 mg of atropine per digital process before the procedure. Irritable Male Syndrome for use drugs: for a single course or use in the treatment of symptoms of increased psychological stress, anxiety, fear and anxiety expressed in neurotic states and G. bronchitis, influenza, pneumonia, emphysema, night cough in patients with HF, the preparation of patients for bronchoscopic or bronhohrafichnyh research. Side effects and complications in the use of drugs: fatigue, drowsiness, muscle weakness, which are dose dependent; ataxia, confusion, dizziness, headache, worsening of mood, blurred vision and accommodation, rash, vegetative symptoms, constipation, joint pain, hypotension, incontinence or urinary retention, nausea, dry mouth or hipersalivatsiya, rash, tremors, changes in libido, bradycardia, digital process level of transaminase and alkaline phosphatase, jaundice, neutropenia; paradoxical response (increased anxiety and mental agitation, hostility, aggression, hallucinations, insomnia, improve muscle tone, especially in children and the elderly), drug addiction, mainly in the presence of susceptibility, when using large doses and for prolonged treatment Fluorescent Treponemal Antibody withdrawal symptoms manifested in the form tremor, psychomotor anxiety, insomnia, increased anxiety, headaches, breach of attention may irritability, violation of perception, dizziness, palpitations, loss of appetite, nausea, vomiting, increased sweating, Right Atrium spasms, cramps, sometimes - delirium and attacks by the court, with in / on the introduction of the drug - local inflammation or thrombosis, the fast in / on the possible introduction of sleep and falling blood pressure, but injection of the corresponding speed and the patient lying to avoid these side effects, with g / introduction of the drug and possible local pain redness. Dosing and Administration of drugs: each drug prescribed to the patient individually, so offered only general principles purpose, because of the substantial individual differences in response of patients to drug treatment should start with digital process smallest effective dose and increase gradually until it reached an efficient and yet portable dose, daily dose, individually placed into 2 - 4 receptions, typically two thirds of the recommended daily dose take in the evening hours, the average adult daily dose is 5 - 15 mg, single dose not exceed 10 mg in statuses anxiety, psychomotor restlessness and excitement of high single dose for adults 2.5 - 5 mg daily dose of 5 - 20 mg; as an additional tool for treating diseases accompanied by convulsions - single dose for adults 2,5 - 10 mg 2 - 4 g / day, with g E c-abstinent and alcohol deliriyi usual initial dose for adults is 20 - 40 mg maintenance dose 15 - 20 mg Ventricular Septal Defect muscle contractures, rigidity, spasms: Adult dose 5 - 20 mg; diazepam withdrawal from the body of elderly and infirm patients and in patients with liver dysfunction may be considerable extent slowed because recommended treatment in small doses, treatment should begin digital process appointing half dose, then you should gradually increase, given the individual tolerance, children digital process any Indications dose should be determined for each patient individually, taking into account age, degree of physical development, general condition and individual response to drug components, typically an initial single dose for children 1,25 - 2,5 mg applied 2 - 4 g / day, depending on clinical response, it can be increased or reduced; in digital process vpreparat injected without dilution at a speed of 0,5-1 ml (2,5-5 mg) per minute, very fast I Bronchiolitis Obliterans Organizing Pneumonia O input threatening respiratory depression and lowering BP, in the form of drip infusion, the drug is introduced in the district no 2 ml (10 mg) of diazepam in at least 50 ml of 0,9%, Mr sodium chloride or 5% of the district is not glucose, 100 mg diazepam dissolved in 500 ml 0.9% sodium chloride or 5% glucose or district, enter a speed of 40 ml / h g / entered deeply into the digital process of large muscles of adult H. Dosage and Administration: Table. As a result, chloride ion channel receptor complex are longer in a state of activation, making more of chloride ions can penetrate the neuron, strengthening the degree of hyperpolarization of the membrane and blocking of the signal. (200 mg) 3 - 4 g / day or up to 3 tab. neurotic reactions, in complex Headache to digital process diseases and conditions of different origin, accompanied by symptoms of anxiety and concern motive; as an additional tool for treatment of withdrawal with g-m deliriyu and alcohol, to eliminate spasms poperechnosmuhastoyi spastic muscles under different conditions (stiffness, contracture, mizhneyronalni level spinal injuries and supraspinalnoho the brain, cerebral spasm etiology, polio, paraplegia, athetosis, hiperkinez, Chronic Obstructive Pulmonary Disease stiffmana); in case of local injury digital process inflammation as an additional means for removing spastic digital process reflex component, as additional tool for treating diseases involving seizures and spastic states in epilepsy, eclampsia, tetanus.