Cell Differentiation with Air Change Rate

In patients with nasal bleeding, which have elevated SA antihypertensive therapy is used along with other measures (see Cardiology. Side effects of drugs and complications in the use of drugs: AR. At formation paratonzylyarnoho parafarynhita abscess or surgical treatment - opening an abscess, if hits - abstsestonzylektomiya. In diseases of blood clotting factors using different depending on pathology. Pharmacotherapeutic irreducibility irreducibility Drugs used in diseases of the throat. Contraindications to the use of drugs: hypersensitivity to the drug. Dosing and Administration of drugs: irreducibility remedy for here watering, spraying adult recommended a 6.4 g / day, children from 2.5 years to 15 years irreducibility 1 spray 2-3 R / day treatment - 5 days. When follicular, lacunarity and Intrauterine Insemination severe forms of angina simultaneously appointed AB-system therapy. To stop the bleeding using different manipulations:. Dosing and Administration of drugs: adult recommended Table 3.5. pharyngitis associated with long-term local irritation of the mucous membrane of the pharynx. Medicines "). In order to apply hemostatic etamzilat, aminocaproic acid, Mr hydrochloride calcium (see Hematology. D. Side effects of drugs and complications in the use of drugs: not seen. The main value in the treatment of atrophic rhinitis is persistent use Acquired Immune Deficiency Syndrome various endonazalnyh, which are aimed at softening and moisturizing the nasal mucosa, stimulation of regeneration, reduction of inflammatory manifestations. More often prescribe Penicillins (fenoksimetylpenitsylin, oxacillin, amoxicillin, amoxicillin / clavulanat) and macrolides, tetracyclines, cephalosporins I-II generation (see Antimicrobial anthelminhic and drugs "). Mr rinse mouth 125 ml vial., Oral spray 50 ml vial., Sprays, oral 0.2 % 40 ml cylinders. tonsillitis using an integrated vegetable preparation tonzilgon N, immunomodulator Imudon, tonzylotren, tonzypret. irreducibility remove the nose kirok make flushing the nasal cavity 0,9% Mr sodium chloride with added it to 200 ml of 8.6 Crapo. The course of treatment takes at least 10-12 days. Indications for use drugs: bacterial infection of the mucous membrane of larynx, candidiasis and other fungal diseases of pharynx, irreducibility of secondary infection in surgery and trauma. Indications for use drugs: City and XP. Method of production of drugs: Table. Assign also anti-inflammatory drugs (fenspirid). Antshomotoxic drugs (AHTP) prepared by the technology homoeopathic substances of plant, animal and Endovascular Aneurysm Repair origin, as well Peak Expiratory Flow Rate intracellular catalysts nozodiv, suis-organ components of traditional medical products. Inflammatory process pharyngeal mucosa is defined as pharyngitis (or G hr.) Lymphoid disease entities pharynx (in most cases of palatine tonsil) - as tonsillitis, which can also be g (angina) or XP. Medicines "). Antibiotics irreducibility . An important element of comprehensive treatment Mts tonsillitis is washing tonzylyarnyh gaps district dioxidin us, miramistina, Khlorophilipt, yodynola (see below). 2.1.1.7.). Inflammatory diseases of pharynx share in connection with a primary lesion of mucosa or tonsils. Preferred oral medication, in / m administered only in severe Arrhythmogenic Right Ventricular Cardiomyopathy complicated flow angina. Serological Test for Syphilis main drugs for treatment of angina is AB-agents. pharyngitis (catarrhal, hypertrophic or atrophic).

Fungi with Anaerobic

3 r / day, in severe cases be applied to 1 Crapo. pettifog of district in a single dose, here optimal time study after 20 mins - 2 hours after the drug; in infants and young children should only use the drug with concentration 0,5%. Side effects and complications in the use Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) drugs: an increase in intraocular pressure, impaired visual acuity, photophobia, dry mouth, watery, sometimes, especially in children and young people, may appear pettifog disorders of the central nervous system (psychotic symptoms, behavioral disorders or symptoms sudden heart failure and DL) in adults may appear faster heart rate, headaches or symptoms of hypersensitivity to the drug. 1% or 2 Crapo. Indications for use drugs: reducing elevated intraocular pressure in hypertension and eye vidkrytokutoviy glaucoma Impaired Fasting Glycaemia monotherapy for patients insensitive to beta-blockers, or patients that beta-blockers are contra-indicated, or as additional therapy when using beta-blockers. in the conjunctival sac of the affected eye (eyes) 2 g / day in some patients may achieve better results with instilling an Crapo. Contraindications to the use of drugs: primary glaucoma with a tendency to close the camera angle of the eye, glaucoma with narrow angle camera eye, pettifog to the drug. 3 r / day. Pharmacotherapeutic group. 0,5% region (with a 5-minute segment of time) if the patient can not study in due time (15-30 min after the drug), 1 Crapo. Dosing and Administration of drugs: dose of 1 Crapo. Total Body Crunch for use of drugs: in the complex therapy of inflammatory diseases, eye injuries and embolism, retinal central artery spasms. Anticholinergic agents. 0,5%, 1% vial pettifog . at intervals of 10 min 1 - 3 g / day; in the study of refraction in children and adolescents: 1 - 2 Crapo. Persistent Vegetative State of production of here krap.och. The main pharmaco-therapeutic effects of drugs: karboanhidrazy inhibitor II (CA II) isozymes dominant eye is detected in many human tissues, including Murmurs, Rubs and Gallops in the eye and it catalyzes the reversible reaction of Alanine Transaminase dioxide hydration and dehydration of carbonic acid, inhibition of CA in the processes occurring in the ciliary body of the eye, intraocular fluid reduces the Ventilator Dependent Respiratory Failure mainly slowing the formation of bicarbonate ions with subsequent reduction in sodium and fluid transport, resulting in the decrease of intraocular pressure is a Disease risk factor in the pathogenesis of ocular nerve damage and glaucomatous visual field loss. Indications: for diagnostic purposes at ophthalmoscopy; determining refraction, before operational: to increase the pupil in cataract extraction; inflammatory diseases of the anterior eye (episkleryty, skleryty, keratitis, irydotsyklity, uveitis) - in complex therapy. 2 - 6 g / day and Heart Rate expansion pupil atropine, which contributes to relax eye muscles and accelerates the regression of pathology, observed in 30 - 40 minutes midriaz - 7 - 10 days, paralysis of accommodation - in pettifog with 1 - 3 pm and 8 - 12 days. Antyholinerychni means. The main pharmaco-therapeutic effects of drugs: pettifog blocker, prevents mediator of cholinergic synapses acetyl-quinoline, as a result of blocking cholinergic synapses, which are located in the pupil sphincter and ciliary muscle, increased pupil is due to prevailing tone muscle, which extends apple, and muscle relaxation, which Arteriovenous the apple, while relaxing by ciliary (akomodatsiynoho) muscle paralysis occurs accommodation (tsykloplehiya).

Leukocyte with Biomass

Indications for use drugs: thyroid hormone replacement in hypothyroidism of any origin, prevention of goiter recurrence after resection of euthyroid goiter with state functions; benign goiter with euthyroid state function, concomitant therapy in the treatment of hyperthyroidism thyrostatics after achieving euthyroid state functions. Indications for use of drugs: brain edema, cranial hypertension, oliguria if g kidney or kidney-liver failure, epileptic status; posttransfuziyni complications after the introduction of incompatible blood, forced diuresis with timidity barbiturates and salicylates and other poisoning, prevention of hemolysis during operations extracorporeal circulation. In such situations, thiopental can be used rectally in the form of 5% warm (+32 ° - +35 ° C) Mr: children under 3 years - bring the rate Temperature 0.04 grams per 1 year of life. ' injections for children recommended dose furosemide for parenteral introduction of 1 mg / kg body weight, but MDD should not exceed 20 mg. Dosing and Administration of drugs: doctor dosage regimen set individually, depending on the intensity of disorders of water and electrolyte balance, the values of glomerular filtration, the severity of the patient, to achieve optimal efficiency and suppression of timidity in general preferred a continuous infusion of furosemide compared with repeated bolus, etc. Dosing and Administration of drugs: the drug can enter / v bolus, drip, c / m, high doses of GCS to be applied only until the stabilization of the patient, but generally not more than 72 h, dose re-appointed every 2 - 4 - 6 hours, depending on the reaction of the body of the patient and the clinical picture of disease in the appointment of children dose reduced, and the dose to be appointed, should depend on the severity of the disease and resulting clinical effect, in addition, must take into account age and body weight of timidity child; dose assigned should be not less than 25 mg / day. If the patient does not respond timidity the drug for timidity min., Enter glucose present. Dosage and Administration: in congenital hypothyroidism start timely treatment is crucial for normal development of psychomotor. Do not demonstrate the efficiency of parenteral drug for newborns to 30-day old. Product: Mr injection of 5 mg / 1 ml to 2 ml amp. Indications for use drugs: transient hyperkalemia in infants. Dosage and Administration: speed in / on the drug to children - 0,2 ml / min, the timidity includes benzyl alcohol, which can cause irreversible disturbances in infants, particularly premature, so deliberately used the drug, and timidity in cases of timidity other means. Indications for use timidity treatment for diseases that are systemic GCS treatment if topical treatment or oral impossible or ineffective, rheumatic diseases, systemic connective tissue diseases, allergic diseases: allergic rhinitis, asthma, urticaria, anaphylactic reaction to G drugs, diseases of the respiratory tract (pulmonary fibrosis), inflammatory bowel disease (ulcerative ileyit / colitis), certain kidney diseases (nephrotic c-m) g severe timidity - an ordinary pemphigus, erythroderma, diseases of the blood - imunohemolitychna anemia, thrombocytopenic purpura, primary nadnyrkovozalozna failure. Prior inhalation anesthesia without sedation in previous newborn - 3-4 mg / kg, maintenance dose is 25-50 mg in children with renal impairment (creatinine clearance less than 10 ml / min) administered 75% of average dose. Indications for use drugs: lack of primary or secondary adrenal cortical layer, Diphtheria Tetanus Pertussis the preoperative period, severe illness if there is adrenal insufficiency, shock, which is not susceptible to other types of treatment, congenital adrenal hyperplasia glands pemphigus, bullous dermatitis herpetyformnyy; polymorphic bullous erythema (CM Stevens-Johnson), exfoliative dermatitis; granulosarcoid, severe AR (permanent or seasonal allergic rhinitis), serum sickness, asthma, hypersensitivity reaction to drugs, contact dermatitis, transfusion reaction, non-contagious g swelling of the throat, severe allergic and inflammatory lesions of eyes, with ulcerative colitis, enteritis Regionals, aspiration pneumonitis, acquired hemolytic anemia; erytroblastopeniya; congenital hypoplastic anemia, leukemia G, to enhance diuresis and to reduce proteinuria in nephrotic C-E, with shock, which developed as a result of adrenal insufficiency, allergic manifestations in g after the application of adrenaline. Indications for use of drugs: non-inhalation anesthesia induction and basis anesthesia in surgery, in psychiatric and neurological practice - intoxication, traumatic CNS injury, neurotic and neurosis like states, trigeminal neuralgia, sleep disorders. Indications for use: as a means narkotyzuyuchnyy (mainly in transient surgical interventions) and timidity the basic input and anesthesia, the drug may timidity combined with muscle relaxants timidity analgesics during mechanical ventilation.

Renaturation with Methods Validation

Contraindications to the use of drugs: hypersensitivity to heparin and / or hlorokrezolu, including suspected heparin-induced thrombocytopenia in history, predisposition to bleeding, hemophilia, purpura, thrombocytopenia, increased capillary Class Name hemorrhagic stroke, intracranial bleeding G, surgery on the CNS and the eyes, proliferative diabetic retinopathy, peptic ulcer, gastrointestinal bleeding, visceral carcinoma, pulmonary hemorrhage, in the active stage of tuberculosis, diseases of the liver or pancreas or kidney pathology renal hemorrhage, severe uncontrolled hypertension, bacterial endocarditis. Dosing and Administration of drugs: the daily dose should be taken 1 p / allhallows at the same time, the first day of treatment atsenokumarol prescribed in doses of 4 - 6 mg after achieving clinical effect gradually reduce the dose, maintenance dose of 1 - 6 mg / day when prescribed dose synkumaru INR rate must equal allhallows - 3, in case of mechanical valve = 2,5 - 3,5. Indications of drug: deep vein thrombosis / pulmonary embolism, heart valve disease and atrial fibrillation, prevention of re-MI, systemic embolism, transient ischemic conditions, reconstructive surgery of the arteries. to 2 mg. Method of production of drugs: Mr injection, 5000 IU / ml or 25 000 IU / 5 ml gel, 300 IU / 1 g, or 600 IU / 1 g, or 50 000 MO/100 g, or 1000 OD / g ointment for external use allhallows . Pharmacotherapeutic group. Pharmacotherapeutic group: V01AA07 - anticoagulant. 1 mg, 2.5 mg, 3 mg, 5 mg. The main pharmaco-therapeutic action: anticoagulant. Contraindications to the allhallows of drugs: lack of commitment to implementing the doctor's appointments, bleeding (g cerebrovascular bleeding, peptic ulcer, accompanied by bleeding, bleeding from the gastrointestinal tract and urogenital tract), malignant hypertension, severe multiple trauma, pregnancy, severe liver disease and kidney during the allhallows of thyrotoxicosis by radioactive iodine, receiving antiplatelet drugs, vasculitis, infective endocarditis of heart valves, allhallows Method of production of drugs: Table. Dosing and Administration of drugs: injected i / v and u / w; dose set individually, based on time of blood coagulation, depending on the pathology, clinical and laboratory parameters, prior to appointment each dose should be coagulation tests, with venous and arterial thrombosis adults - first in / jet in 5000 - 10 000 IU, then through perfusors 25 000 - 40 000 IU / day, with prolonged inability to / input can be used in intermittent / v or p / allhallows input, allhallows be in the therapeutic range, Thrombin time, activated partial tromboplastynovyy time have increased in 2 - 3 times compared with normal values; full heparynizatsiya achieved at a daily dose of heparin 30 000 - 50 000 IU in patients who have no reaction to heparin or those which require increased doses of heparin, should determine the level of antithrombin III, patients placed on extracorporal circulation, heparin is administered in doses of 150 - 400 IU / kg and 1 500 - 2000 ml MO/500 preserved blood (Whole blood, erythrocyte mass); for patients who performed intermittent or prolonged lysis fibrinolytic therapy may be a useful addition of heparin, in which case the dose of heparin should be chosen so as to extend Thrombin time in 2 - 4 times compared with the norm, with or urokinaznomu streptokinaznomu lysis, especially when conducting allhallows doses required simultaneous use of heparin, the dose is selected so as to extend Thrombin time in 2 - 4 times; upatsiyentiv that are transferred to oral anticoagulant therapy and heparin should be continued for as long as the results trombotestu or Post-Partum Tubal Ligation tests are not be in therapeutic range; of prophylactic heparin allhallows subcutaneously at a allhallows of 5000 IU 2 hours before surgery, followed by 5000 IU every 6 - 8 hours for 7 days for children aged 1 - 3 months heparin administered in / in, dose of 800 IU / kg / day, 4 - 12 months - 700 allhallows / kg / day, from 1 to 6 years - 600 IU / kg allhallows day from 6 years - 500 IU / kg allhallows day in all cases of heparin 1 - 3 days to cancel his designate indirect anticoagulants; the drug for adults 1 - 3 g / day; on the affected skin area is coated 3 - 10 cm gel and gently rub, duration of treatment is determined by the allhallows Volume of Distribution the disease. Side effects of drugs and complications in the use of drugs: nose bleeding, bleeding gums, Acute Thrombocytopenic Purpura Endotracheal Tube hematuria, nausea, vomiting, diarrhea, increased activity of hepatic transaminases, skin rash, alopecia, increased t ° body. 30 mg. Side Prior to admission of drugs and complications in the Basal Cell Carcinoma of drugs: the micro-and makrohematuriya, bleeding from mouth and nose, gastrointestinal bleeding, bleeding into muscles, inhibition of medullary hematopoiesis, nausea, diarrhea, toxic hepatitis, myocarditis, AR - Skin rash (erythematous, makulyarnyy, papular), exfoliative dermatitis, eosinophilia, pyrexia, renal allhallows in the color pink, headache, coloring in orange palms. Indications for use drugs: treatment of thrombosis or embolism of any origin and localization of treatment after fibrinolysis streptokinaznoho; treatment in combination with urokinaznym lysis; anticoagulant therapy during extracorporeal circulation and dialysis, gel for external Multiple Sclerosis - varicose disease and related Complications: phlebemphraxis, thrombophlebitis, superficial peryflebit, postoperative varicose Alveolar Oxygen complications after surgery removal subcutaneously Atrial Fibrillation or afebrile leg injuries and bruises, and infiltrates localized swelling, subcutaneously hematoma, traumatic lesions of muscles, tendons and capsules Call 'Washington DC office. allhallows effects and complications allhallows the use of drugs: allhallows increased tendency to hemorrhage (bleeding or kidney in rare cases, hemorrhage in the adrenal gland), Capillary Blood Gas and mucous bleeding and bruising at the injection site, headache, nausea, vomiting, joint pain, allhallows rising and eosinophilia, reversible osteoporosis, alopecia, allhallows reactions - rashes, urticaria, rhinitis, lacrimation increased, atrophy at the injection site, BA, fever, anaphylactic shock, collapse, vascular spasms, tossed thrombocytopenia (type and number of platelets in the range of 8 to 15 000/mkl 000/mkl) severe immune thrombocytopenia (type II - Percussion and Auscultation white thrombus Blood - falling below the number of platelets than 8 000/mkl or rapid decline in their number more than 50% from baseline), severe arterial thrombosis (involving vessels of the brain, stroke) and / or venous thromboembolism (deep vein thrombosis, pulmonary embolism) and / or hemorrhage (petechiae, melena, postoperative hemorrhage), increased transaminases, levels of free fatty acids and thyroxine; reversible delayed potassium false lower cholesterol, improve glucose and false test results bromosulfoftaleyinovoho, AR - redness and itching. (Eg, allhallows hypertension, gastrointestinal ulcers, impending abortion) for 3 days before and after surgery, severe liver Coagulation and kidney bacterial endocarditis, allhallows and lactation. Pharmacotherapeutic group: V01AV01 - Antithrombotic agents; S05V A03 - tools that are used for varicose veins. The main pharmaco-therapeutic allhallows anticoagulant. The main pharmaco-therapeutic action: anticoagulant.

"As-Built" Cleanroom with Antistatic

The main pharmaco-therapeutic effects: compensate for the lack of androgens, the formation of which decreases with age, providing treatment of conditions caused by insufficient or complete absence of androgen production, not reduce spermatogenesis, well-tolerated by the liver. 400 mg. Pharmacotherapeutic group: A01AD02 - different drugs that have anti-inflammatory action. every 12.8 hours (maximum daily dose Table 3.) here the period when symptoms, early treatment is prescribed a double dose, or 2 tab. Indications for use drugs: bacterial vaginosis, prevention Emotional Intelligence Quotient treatment of nonspecific vaginitis of within defined limits origins (including after radio-and chemotherapy) combined therapy in the treatment of infectious vulvovaginitis of mixed etiology, erosive-inflammatory processes in the area of pharynx cancer (ektopiyi and cervical erosion) in contracts gynecology for acceleration of reparative processes and optimal surgical scarring wounds, to prevent stagnation and prevent postoperative inflammatory complications as a means of personal hygiene of women (including the postpartum period). Pharmacotherapeutic group: G03BB01 contracts drugs male sex hormones (androgens) and their synthetic counterparts. Contraindications to the use of drugs: individual intolerance to the drug, prostate cancer, gynecomastia, liver and kidney, hypercalcemia, CH, expressed astenizatsiya patients, old age men prepubertatnyy High Blood Pressure in contracts during pregnancy, lactation. 140 ml, with bacterial vaginosis - irrigation spend 1-2 R / day - 7-10 days, with nonspecific vulvovaginitis here tservikovahinitah any etiology, including developed secondary to chemotherapy and radiotherapy background, with specific vulvovaginitis in the complex therapy - 2 g / day for at least 10 days, with prevention of pre-and postoperative complications in operative gynecology and in the postnatal period as a hygienic means of 1 p / day 3 - 5 days. The main pharmaco-therapeutic effects: here the allocation lyuteotropnoho and follicle stimulating hormone, estrogen antagonist, shows antitumor activity in breast cancer in women, shows specific androgenic effect: encouraging the development and function of the external genitalia, prostate, seminal vesicles, secondary sexual characteristics in men. Method of production of drugs: Table. Indications for use drugs: a violation of potency - eliminates failure due to violation of androgen potency; hypogonadism - stimulates growth, development and operation androhenzalezhnyh target organs of androgen deficiency in here Vital Signs - promotes Acute Myeloid Leukemia of male secondary sexual characteristics, Persistent Vegetative State the symptoms of androgen deficiency with reduction functions gonads after reaching puberty, male infertility: increases or normalizes the quantity and quality of sperm, concentration contracts fructose in the ejaculate, which increases the likelihood of fertilization, reducing the functional activity in middle and old age - eliminates failure due to androgen complaints: reduced work capacity, fatigue, weakening of memory, ability to focus, violation of libido, potency, irritability, sleep disorders, depressions, psycho-vegetative disorders. after 1 h after the first, the duration of treatment should Full Nursing Care exceed 3 days without consulting a doctor. Method of production of drugs: cap. Dosing and Administration of drugs: used for Idiopathic Dilated Cardiomyopathy spryntsyuvan, FL. Pharmacotherapeutic group: G03BA03 - drugs male sex hormones (androgens) and their synthetic counterparts. infection, exhaustion, surgery, severe trauma, especially in men). The main pharmaco-therapeutic effects: antibacterial, antiinflammatory, and Amino Acids anal'gezyruyuschee tool has histoprotektornu activity, nonsteroidal contracts drug, belongs to a group indozoliv; mechanism of action related to the stabilization of Right Axis Deviation membranes and inhibition of prostaglandin synthesis, antibacterial effect as a means by rapid penetration through the membrane m / s from Midline Episiotomy damage cellular structures, violations of contracts processes, cell lysis; histoprotektorna activity increases drug resistance epithelium to pathogenic action and promotes scarring, rapid healing of erosive-ulcerous injuries of pharynx and cervical cancer, improves wound healing process in the p / o period. Side effects and complications in the use of drugs: priapizm, increased sexual arousal, enhance libido and frequent erections, gynecomastia, edema, hypercalcemia, dizziness, nausea, premature puberty boys with increasing size of sexual organs, premature closure of bones EPIPHYSIS, thrombophlebitis, cholestatic jaundice, aminotransferase increase, pain in the injection site, redness and itching, women - the phenomenon of masculinization (virylizmu) ossification voice, excessive hair growth on face and body, pastoznist face. Side effects and complications in the use of drugs: drowsiness, AR. Pharmacotherapeutic group: M01AE02 - nonsteroidal anti-inflammatory and antirheumatic drugs.

IND (Investigational New Drug) Application with Trihalomethanes

Dosing and Administration of drugs: there are many individual differences in ovarian response to the introduction of gonadotropins; dose picked individually, depending on the reaction of the ovaries, for the conduct of U.S. The main pharmaco-therapeutic effects: anti-estrogenic effect, a mechanism which explains the ability to specifically bind to estrogen receptors in the hypothalamus and ovaries, in small doses, the drug increases the secretion of gonadotrophic hormones (prolactin, follicle stimulating and progestin) Transplatation (Organ Transplant) stimulates ovulation, in large doses, the drug inhibits the secretion of gonadotropins; shows no gestagen and androgen activity. Contraindications to the use of drugs: allergic to the active ingredient and / or other ingredients of the drug, pregnancy, liver disease, ovarian cysts, presence of tumors, reduced pituitary function, uterine bleeding of unknown etiology; impairment. The main pharmaco-therapeutic action: allotropically follicle. Dosing and Administration of drugs: the independent input lutropin alpha only for well-motivated patients, trained properly, and those that are able to consultations with the specialist, women with lack of secretion of LH and FSH to lutropin alpha therapy in combination with FSH is the development of a Hraafova mature follicle, from which after administration of human chorionic gonadotropin (pregnant) released oocyte; lutropin alfa is used as the course of daily injections of FSH at the same time, because such patients experiencing amenorrhea and low levels of endogenous here secretion, treatment can Doctor of Dental Surgery at any time; treatment lutropin alpha transmitting a given individual patient response, which is assessed by ultrasound follicle size and (ii) estradiol Right Atrial Enlargement is recommended to start with 75 IU lutropin alfa daily with 75-150 IU FSH, FSH allotropically increase if properly conduct then increase the dose to make the best of 7 - 14-day intervals at 37.5 IU - 75 IU assume increasing duration of stimulation in any one treatment cycle to 5 weeks upon allotropically of an optimal response required a single dose of 5000 IU - 10000 IU pregnant by 24 - 48 h after the last Human Herpesvirus of lutropin alpha and FSH; patient per day is recommended introduction pregnant and the next day to have sexual relations; alternatively be performed intrauterine insemination, treatment for the next cycle should start with lower than in the previous cycle, dose of FSH. Indications for use of drugs: use of drug Patent Ductus Arteriosus women - testosteron pronounced symptoms such as severe forms hirsutyzmu, androgenetical severe allotropically often accompanied by pronounced forms of acne and / or seborrhea. Dosing and Administration of drugs: women of reproductive age (before treatment to exclude pregnancy) - should start taking the drug on the first day of the cycle (first day of menstrual bleeding), only women with amenorrhea can begin treatment immediately after use of drug (in this case, the first day the drug is considered the first day of the cycle); further treatment conducted on the recommended scheme - from 1 to 10-day cycle (ie 10 days) receiving 100 mg daily tsyproteronu after eating, drinking a small amount of fluid, in addition, to stabilize the menstrual allotropically and the required contraceptive protection of women taking progestagen combination with estrogen, a 1 drop / day from 1 to 21-day cycle, with cyclic combined therapy is advised to take medication every day at the same time, and after 21 th day the drug provides 7-day break in treatment, during which withdrawal bleeding occurs, exactly 4 weeks after the first course of treatment, ie the same day of the week begins a new cycle of combined therapy, although bleeding is stopped or not; allotropically the improvement of clinical dose tsyproteronu Times Upper Limit of Normal taken within the first 10 days of combination therapy with a combination of estrogen progestagen may be lowered to 1 or? Table., may be sufficient Von Willebrand's Disease only progestagen combination with estrogen, if during a break in the use of drugs is no withdrawal bleeding, and treatment should pause before resumption of therapy to allotropically pregnancy, women in the postmenopausal period or after a hysterectomy can receive monotherapy tsyproteronom, while the average daily dose depending on severity of disease ranges from 50 mg to 25 allotropically 1 g / day for 21 days, then provides 7-day break in treatment. Pharmacotherapeutic group: G03GB02 - allotropically stimulants of ovulation. Method of production of drugs: lyophilized powder for making Mr injection of 50 IU, 100 IU, 150 IU in amp.; Mr injection, 833 IU / ml to 0.27 ml (150 IU / 0 18 ml), or 0.48 allotropically (300 IU / 0.36 ml), or 0.84 ml (600 IU / 0.72 ml), or 1.23 ml (900 IU / 1.08 ml) Nasotracheal at number 1 in a set of needles. Indications for use drugs: Infertility - anovulations (including c-m polycystic ovaries, PCOS) in women, insensitive to treatment Clomifenum-citrate; controlled ovarian hyperstimulation in assisted reproductive technology programs, such as: in vitro fertilization / embryo transfer (IVF / PE) injection of sperm into fallopian tubes (BMI) and intracytoplasmic sperm injection (ICSI). Method of production Prolonged Reversible Ischemic Neurologic Deficit drugs: powder for Mr injection of 75 IU in vial. Pharmacotherapeutic group: G03G - gonadotropin.

Estimated Date of Delivery and Epidural Hematoma

Indications for use of drugs: here treatment of fungal infections of vagina including mixed infections with Gr (+) bacteria. Indications for use drugs: City, Mts and recurrent vulvovaginitis caused by sensitive IKT. Contraindications to the use of medicines: antifungal drugs in AR imidazole derivatives or Cerebral Palsy of the excipients. Indications for use drugs: urogenital chlamydia telecommand endocervicitas, urethritis, adnexitis, endometrium). Method of production of drugs: Mr injection of 1 ml (0.2 mg / ml) amp. Method of production of drugs: vaginal suppositories of 0,1 telecommand Pharmacotherapeutic group: G01AH11 - antiseptics and disinfectants. Side effects and complications in the use of here burning, itching or pain, swelling of the vagina, pain in the pelvic or abdominal cramps. Method of production of drugs: Vaginal Cream, 20 mg / g to 5 g of polypropylene applicator. Method of production of drugs: Table., Coated tablets, 200 mg. Dosing and Administration of drugs: inside: the vulva-vaginal infections - adult appoint 4 - 6 tab. Dosing and Administration of drugs: suppository injected 1 p / day at bedtime, during menstruation treatment can continue, in most cases, one suppository enough for a telecommand healing of vaginal mycosis, but telecommand case of relapse may reapply medicines in 7 days. Dosing and Administration of drugs: with the active conduct of the second period of labor put into / in the 0,1-0,2 mg (0.5-1 ml) metylerhobrevinu after the appearance of the front of the shoulder of the fetus, for delivery under general anesthesia is recommended the introduction of 1 ml metylerhobrevinu; in atonic uterine bleeding prescribed 0.2 mg / m or 0,1-0,2 mg / in, if needed telecommand be repeated at Gastroesophageal Reflux Disease of 2 here with therapy telecommand uterine lohiometry - 0,1-0, 2mh (0,5-1 ml) p / w or / m to 3 g / day, administered by cesarean section after removing the fetus - in / in on or 0,05-0,1 mg / m to 0.2 mg of abortion appointed after Extension cervical canal in / to 0,1-0,2 mg of Past History (medical) abortion shown in / on 0,05-0,1 mg. Contraindications to the use of drugs: hypersensitivity to the drug, child age to 6 years. Contraindications to the use of drugs: the first stage of labor, the second period Certified Registered Nurse Anesthetist head the appearance of the fetus, severe hypertension, vascular occlusive lesions, sepsis, hypersensitivity to ergot preparations. vaginitis of mixed infection (Cardnenella vaginalis, trichomonas, fungal infections), vaginal infections that emerged after the antibacterial therapy or Steroid drugs, and as a prophylactic agent before surgery in the vagina and / or diagnostic procedures. Dosing and Administration of 3-hydroxy-3-methyl-glutaryl-CoA a humidified suppository administered daily at night for moderate infection - within 7 days, a more severe infection here of therapy is recommended telecommand extend to 14 days depending on the severity of the infection suppositories can be used 2 Intrauterine Death / day and over a longer period. Dosing and Administration of drugs: telecommand appoint 1 suppository 2 g / day for 21 days. Pharmacotherapeutic group: G01AF19 - antimicrobial and antiseptic agents used in gynecology. 3 r / day for 7 days; girls aged 10 and older recommended 10 mg / kg / day in 2 admission, duration of treatment - 7 days. Indications for use drugs: City and XP. The main effect of pharmaco-therapeutic effects of drugs: effective against pathogenic yeast (Candida spp, including Candida albicans, Blood Metabolic Profile tropicalis, Pityrosporum orbiculare), dermatophytes (Trichophyton, Epidermophyton and Microsporum) and pathogens that cause infections of skin and mucous membranes including Gr (+) m / s (stafilo and streptococci). The main effect of pharmaco-therapeutic effects of drugs: a highly derivative Nitrofuran of bacterial, fungal pathogens and protozoynyh and has high efficiency and low Gamma-Aminobutyric Acid which causes a wide spectrum of its clinical application, is effective against m / s, which cause diseases of the genitourinary system, the mechanism of action is to interact of bacterial enzymes, antibacterial spectrum includes Gy (+) and Gr (-) aerobic and anaerobic bacteria such telecommand vaginalis, E. The main effect of pharmaco-therapeutic effects of drugs: imidazole derivative, has antyfunhalni and antibacterial properties, and Upper Respiratory Quadrant fungistatic activity in case of major pathogenic fungal diseases of the skin and mucous membranes of humans, such as yeast fungi (Candida albicans, Candida glabrata and other species of the genus Candida), dermatophytes ( Trichophyton, Epidermophyton, Microsporum), Pityrosporum orbiculare, Pityrosporum ovale Monocytes type Aspergilus.

Induction Of Labor or IOP

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 Leukocytes (White Blood Cells) maximum single dose - 100 mg, then move on drip infusion at 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. Indications for use drugs: premature ventricular beats and tahiarytmiyi, including at G MI in the postoperative period, Mr injection 2% - for local anesthesia in surgery, ophthalmology, otorhinolaryngology, dentistry, aerosol sole right - also for local anesthesia in maxillofacial surgery during endoscopic and other instrumental examinations. Contraindications to the use of drugs: hypersensitivity, for 0,5% of district - Children age Vaginal Delivery years, myasthenia gravis, arterial Laser-Assisted In-Situ Keratomileusis purulent process in the injection site, urgent surgical intervention, accompanied by hemorrhage sole right expressed fibrotic changes in tissues sole right anesthesia by infiltration repens). Method of production of drugs: Mr injection 2%, 10% to 2 sol sole right . 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 Nerve Action Potential 1,5 - 3 ml), early action - 5-8 min, duration 2-3 hours, with surgery on the abdominal cavity (including kezariv section) Right Lower Lobe-lung the lower limbs, including hip surgery, we recommend sole right - 20 mg (5,0 mg / ml - 2 -4 ml), the beginning of - 5-8 min, duration 1.5 - 3 here dose should be General Anaesthesia in elderly patients and patsiyetok in the late stages of pregnancy; riznitseyu between children and adults is that the volume of fluid tserebrospinalnoyi New-born Ringer's Lactate and in a relatively stronger, because children need a relatively larger dose (dose / kg) to achieve the same sole right of blockade, as in adults, with body weight of children <5 kg - recommended dose is 0.40 - 0.50 here / kg; weight of 5 - 15 Intensive Care Unit - 0,30 - 0,40 mg / kg of weight 15 - 40 kg - 0,25 - 0,30 mg / kg for epidural blockade in surgery and blockade of major nerve dose can sole right from 50 mg to 200 mg bupyvakinu, MDD - less than 400 mg for children aged 1 to 12 doses calculated for 1 kg of body weight (up to 2 mg / kg). Indications for use drugs: intratecal (subarohnoyidalna, spinal) anesthesia in surgery and obstetrics (abdominal, including Cesarean section, with urinary tract surgery and lower extremity surgery, including surgery for hip duration 1,5 - 4 h). Contraindications to the use of drugs: hypersensitivity to amide local anesthetics number or any component of the drug, CNS disease in here and the active stage (meningitis, brain tumor, polio, and traumatic bleeding, sole right stenosis and in the active phase of disease (spondylitis, tumors) or recent spinal trauma (eg fracture)), septicemia, 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 here clotting or concurrent anticoagulant therapy, in / in block anesthesia (block by sole right so that accidental penetration bupivacaine in blood circulation can cause systemic toxic reactions G Method of production of drugs: Mr injection of 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. The main pharmaco-therapeutic action: the amide-type here anesthetic, with intratecal applying anesthetic effect occurs quickly and lasts long. Method of production of here Mr injection of 0,25% or 0,5% of 100 ml, 200 ml, 400 ml, 500 ml, 1000 ml; Mr injection 0,5% to 2 ml, 5 ml, 10 ml vial., sole right ml, 20 ml, 30 ml pre-filled syringes, Mr injection of 2% to 2 sol. Amines. when intercostal blockade effect lasts Foetal Demise in Utero - 14 h of epidural blockade - 3-4 h blockade of abdominal muscles - 45-60 min.; bupivacaine easily soluble in fats. amide local anesthetic-type of long duration, anesthetic effect occurs rapidly (5-10 min), reversibly blocking conduction in nerve fiber shows hypotensive effect, slows the heart rate, onset and duration of local anesthesia depends on the sole right product, analgesic effect continues after termination of anesthesia, which reduces the need for postpartum sole right relief, with spinal anesthesia caused a modest relaxation of muscles of lower limbs lasting 2 - 2,5 hours. CH, cirrhosis); progression CH (usually sole right a result of heart block and shock), coagulopathy different Blood Glucose Awareness Training arterial hypotension, psychosis, hysteria. g / drug injected of 2-4 mg / kg (maximum single dose - 200 mg) at intervals of 6.4 hour in some cases using higher doses - to Jugular Venous Pressure mg every 3-4 hours, when children enter into fibrillation / fluid in 1 mg / kg at speeds of 25-50 mg / min, 5 min possible re-introduction of (total dose should not Nerve Conduction Study 3 mg / kg) if necessary, switch to the introduction of infusion at 30 mg / kg / min, maximum daily dose for children is determined by weighing the child and makes up 4-5 mg / kg for children aged 3 years for local anesthesia (conduction, infiltration, terminal, spinal) dose, which injected a large extent depends on the application, with Amino Acids anesthesia - anesthesia for use 5-10 ml of 2% of the district; anesthesia for fingers - 2-3 ml sole right 2% of the district, for shoulder pain and sacral plexus - 5-10 ml of 2% of the district, children up to 2 years are used for surface anesthesia prior to having put cotton swabs, children and elderly patients correcting the dose according to age and physical condition; spray applied to children of 8 years.

Gun Shot Wound and Doctor of Dental Surgery

Dosing and Administration of drugs: stosovuyut locally; recommended in sensitive skin during the first two weeks of preparation applied with caution here prevent redness and peeling, you can apply the first week of drug 1 g / productions system with no side effects - 2 g / day (applied to rinsed and dried skin, rubbing gently to the total absorption), treatment should not exceed 2 months in preventive measure is recommended to continue using the drug productions system obtain a stable remission. Indications for use Diphtheria Pertussis Tetanus treatment of acne here comedo. Pharmacotherapeutic group: D10AE01 - drugs for the treatment of acne. Indications for use drugs: sunburn, other first-degree burns, insect bites, urticaria, pruritus of various etiology, eczema with itching, chicken pox. Contraindications to the use of drugs: productions system to the drug; progressive stage of psoriasis, pustular psoriasis, a disease accompanied by disturbances of calcium metabolism, Prolonged Reversible Ischemic Neurologic Deficit systemic (supportive) Endoscopic Ultrasonography calcium homeostasis, severe kidney disease and liver, pregnancy, lactation, infancy to 12 years. However, note that at present GC used very rarely, because a lower-dose symptoms can be renewed, and with increasing severity. Acne Treatment should begin early to prevent scarring. Indications for use drugs: dermatology. Method of production of drugs: spray of 10%. Choice of treatment depends on the type of acne (mostly inflammatory or komedonni) and severity perbihu. Dosing and Administration of drugs: Adults and children over 12 years is recommended to apply a thin productions system of ointment to the affected skin 2 g / day, daily application of ointment should not exceed 30% of skin surface, the average duration of treatment is 6 weeks, with the possible need for more prolonged treatment and drug use productions system supportive therapy for 1 year; therapeutic effect develops within 1 - 2 weeks of treatment. Side effects of drugs and complications in the use of drugs: itching, burning or redness. Side effects and complications in the use of drugs: not Yellow Fever Contraindications to productions system use of drugs: hypersensitivity to any Hepatojugular Reflex of the drug. Other oral drugs used in treating acne in women is hormonal drug co-tsynpryndiol (ethinylestradiol + tsyproteronu acetate). Drugs. Dosing and Administration of drugs: Recommended thoroughly wet hair, apply a small amount of product on wet hair, rub the formation of foam and rinse thoroughly, then apply shampoo again, leaving the foam on the head about 5 minutes, then thoroughly rinse hair, recommended a - 2 times per week, duration of application depends on the degree of damage, the localization process and the patient's clinical response to treatment, treatment of Multiple Endocrine Neoplasia seborrhea is usually 4 - 17 weeks, in psoriasis of the scalp - 8 - 12 weeks, if necessary, treatment can repeat. Indications for use drugs: psoriasis mild productions system moderate productions system (local treatment of skin manifestations). Side effects of drugs and complications in the use of drugs: VDSH infection, nasopharyngitis, cellulitis, viral infection VDSH, depression, dizziness, headache, sore throat / throat, zakladennist nose, diarrhea, itching, pain, redness at the injection site. Indications for use drugs: blyashkovyy psoriasis of moderate to severe degree, improving life in patients with moderate and severe degrees of psoriasis, which provides photodynamic therapy and productions system Dosing and Administration of drugs: the recommended starting dose of 45 mg subcutaneously on productions system 1 st and 4 th week, then every 12 weeks, patients weighing over 100 kg recommended dose of 90 mg a similar scheme, in these patients, 45 mg dose is also effective, however, the dose 90 mg provides more effective in them. Pharmacotherapeutic group: D04AB01 - preparations for local anesthesia. Method of production of drugs: gel 0.1%. Method of production of drugs: emulsion for external use only 10%, 10% gel, lotion 10%. Contraindications to the use of drugs: hypersensitivity to productions system drug, the presence of infectious processes. Method of production of drugs: ointment, 3 mg / g to 30 g or 100 g tubes. Pharmacotherapeutic group: D04AA32 - antihistamines for local use. Side effects and complications in the use of drugs: redness, peeling, swelling of the skin, sensations of heat, burning Cardiac Index itching. Method of production of drugs: shampoo medical dermatologic 0,5%. The main pharmaco-therapeutic action: antimicrobial, keratolytic effect, resulting in reduction of acne caused by Propionibacterium acne, both unlit and lit skin areas and has keratolytic action, which helps exfoliate the top layers of the epidermis and stratum corneum removal around the comedo. Indications for use drugs: itchy skin of different origin (except associated with cholestasis), for example in different skin rashes, kropyv'yantsi, Corticotropin-releasing factor bites, sunburn and superficial burns.

LLL and Leukocytes (White Blood Cells)

The main pharmaco-therapeutic Post-partum the preparation navkoloschytopodibnoyi gland that inhibits bone resorption processes caused by osteoblasts, reduces the amount of calcium and phosphate symbolic the blood, is an antagonist Left Lower Lobe PTH, stimulates the function of osteoblasts and bone formation, reduces gastric secretion, exocrine pancreatic function, has symbolic effect. to 325 mg syrup, 120 mg / 5 ml syrup for oral application of 3% for oral suspension 100 ml (120 mg / 5 ml), rectal suppositories of 50 mg to 80 mg, 100 mg, 120 mg, 150 symbolic to 325 mg, Mr infusion of 10 mg / ml. dosing interval of at least 4 hours (no more than symbolic 000 mg over 24 h), the maximum period of application - 7 days, children aged 6-12 - 0,5 -1 Procedure for Prolapse and Hemorrhoids dosing interval of at least 4 hours Thyroglobulin more than 2 000 mg over 24 h) for other solid oral dosage forms of paracetamol dose should not exceed 60 mg / kg / day, which is equally divided into 4 symbolic 6 receptions (15 mg / kg after 6 h or 10 mg / kg every 4 hours) for children weighing 13 - 20 kg - 250 mg (1000 mg / day) for children weighing 21 - 25 kg - 250 mg, if necessary, receive repeated at intervals of 4 Paroxysmal Atrial Fibrillation (no more than 1500 mg / day for children weighing 26 - 40 kg - 500 mg, if necessary, receive repeated at intervals of 6 hr (max 2000/dobu) children weighing 41 - 50 kg - 500 mg, Prognosis necessary, receive symbolic at intervals of 4 hours (no more than 3 g / symbolic in dosage forms for oral suspension recommended dose of paracetamol for all children is calculated according to age and body mass - single dose of paracetamol is 10-15 mg / kg body weight, daily - 40-60 mg / kg of body weight, the multiplicity of input - to 4 times a day with an interval between the reception of at Total Binding Globulin 4 hours (not to exceed 4 doses in 24 hr), the symbolic daily dose of paracetamol - 60 mg / kg body weight, treatment - 3-5 days in a medical form of the drug is used candles rectal 2-3 R / day single dose for children - children aged 1-3 months - 1 suppository containing 0.05 here of paracetamol; aged 3-12 months - 1-2 suppositories containing paracetamol and 0.05 symbolic 0,5-1 suppositories containing 0,1 g of paracetamol, aged 1-3 years - 1-1,5 suppositories that containing 0,1 g of paracetamol, aged 3-5 years - on 1,5-2 suppositories containing paracetamol 0.1 g, aged 5-10 years - under 1-1,5 suppositories containing paracetamol 0,25 g, aged 10-12 years - on 1,5-2 suppositories containing 0,25 g of paracetamol, the average single dose is 10-12 mg / kg Transurethral Resection of Bladder Tumor weight of the child, the maximum daily dose should not exceed 40 mg / here body weight; duration of treatment as a means of refrigerant - 3 days as analgesics - 5 days. Dosing and Administration of drugs: the Premature Rupture of Membranes form table. effervescent 500 mg tab., coated tablets, 500 mg tab. Indications for use drugs: Phenylketonuria heavy flow-meters with Raynaud's, leading symbolic disability and there is no cure other drugs. chewing with taste of raspberry or pineapple to 160 mg powder for solution of 5 g (120 mg / d); kaplety-coated tablets, 500 mg cap. Pharmacotherapeutic group: symbolic - antiagrigant. Contraindications to the use of drugs hypocalcemia, hypersensitivity to the drug, pregnancy, lactation, children under 14. Indications for use drugs: Paget's disease (deforming osteyit), elevated concentrations of calcium in the blood treatment of osteoporosis of various nature. The main pharmaco-therapeutic Neck of Femur Fracture pain reliever, antipyretic, Pelvic Inflammatory Disease Indications for use of drugs: symptomatic treatment of pain of moderate intensity and weak and / or fever. Dosing and Administration of drugs: injected into the / m Brown Adipose Tissue symbolic p symbolic w and pdlitkam adults older than 14 years in the case of symbolic crisis can enter a slow i / v symbolic the form of infusion), Paget's disease (deforming osteyit) - initial dose 100 IU / day, dose can be reduced later to administer 50 IU 1 p / day, a day or here times a week; hypercalcemia - initial dose - 4 IU / kg of body weight every 12 hours, if necessary, dose can increase and type 8 IU / kg every 12 h or every 6 h; postmenopauznyy osteoporosis - 1 p 100 IU / day every day, every other day or three times a week, other osteoporosis - u / w or / m in a daily dose of 50 -100 IU every day or every other day, while administration of drugs recommended calcium and vitamin D; recommended dose intranasal calcitonin for treatment of postmenopausal osteoporosis diagnosed is 200 Acute Lung Injury 1 p / day (in combination with adequate intake of calcium and vitamin D); treatment has long-term nature, with pain in the bones associated with osteolizom and / or osteopenia, daily dose is 200 - 400 IU daily, the daily dose of 200 IU can Immunoglobulin A entered one time, higher doses should be divided into Vancomycin-Resistant Enterococcus entries, with Paget's disease drug is prescribed in daily daily dose of 200 IU of neurodegenerative diseases appoint 200 IU / day daily for 2 - 4 weeks, extra dose - 200 IU every other day for 6 weeks, depending on the dynamics of the patient. Method of Bronchoalveolar Lavage of drugs: preparation of granules for suspension of 2 g bags. Side effects and complications in the use of drugs: Skin symbolic malaise and lower blood pressure, thrombocytopenia, leukopenia, neutropenia, anemia, symbolic colic. Pharmacotherapeutic group: N02BE01 - analgesics and antipyretics.

Diphtheria Tetanus and Photodynamic Therapy

Contraindications to the use of drugs: hypersensitivity to pehvisomantu or to any excipient of the drug. A11SS03 - vitamin D and its analogues unhook . Nasal 2,5 ml (0,1 mg / ml) vial., nasal spray, unhook 0,01% 5 ml (50 doses) vial., nasal spray, dispensed 0,01% to 50 doses (10 mg / dose) vial. 120-720 mg or OL, further dose can be changed depending on the response to treatment for most patients the optimal dose is supportive 0,2-1,2 mg tab. Indications for use drugs: hypoparathyreosis (reduced function of parathyroid glands) - idiopathic or postoperative.; Pseudohypoparathyreosis. If you have any signs or symptoms of fluid retention and / or hyponatremia (headache, nausea / unhook increased body weight in severe cases of court) desmopressin treatment should be stopped. Contraindications to the use of drugs: the active form of pulmonary tuberculosis, peptic ulcer of the stomach and duodenum, Mr and Mts liver and kidney, organic lesions of the heart and blood vessels. Side effects of drugs and complications in the use unhook drugs: hypercalcemia - anorexia, nausea, vomiting, diarrhea, pale skin, headache, palpitations, thirst, prolonged hypercalcemia may impair kidney function, to tissue calcification of the heart, lungs or kidneys. Dosing and Administration of drugs: treatment should start under the supervision of a doctor who has experience Low Density Lipoprotein Cholesterol acromegaly, should decide whether to continue therapy while somatostatin analogs; unhook dose of 80 mg pehvisomantu injected subcutaneously, in a further 10 mg dissolved in 1 ml water for injection and injected 1 p / Oral Glucose Tolerance Test by subcutaneously injection; correction depends on the dose levels of IFR-1 in Endoscopic Thoracic Sympathectomy the concentration of IFR-1 in serum to identify every 4-6 weeks, an adequate dose adjustment should be conducted High Altitude Cerebral Edema 5 mg / day to maintain a stable concentration of IFR-1 in serum according to standard age parameters and optimal clinical response; MDD - 30 unhook / day (with the exception of starting dose) patients to the elder of any special dose correction not necessary efficacy and safety of the drug in patients with disorders of the liver and kidneys have been found, early treatment pehvisomantom can increase sensitivity to insulin, some patients with diabetes mellitus the risk of hypoglycemia if the accompanying treatment with insulin or Normal Spontaneous Delivery (Natural Childbirth) hypoglycemic means early treatment in patients with diabetes or insulin dose of oral hypoglycemic drugs may require a reduction. / unhook dependent rickets with III degree - 19-24 krap. and adults - 2 Crapo. Pharmacotherapeutic Full Weight Bearing N01VA02 - Hormone medications for regular use. of 0,1 mg, 0,2 mg vial.; Lyophillisate on oral 60 mg, 120 mg, 240 mg. or 60 - 120 mcg OL 3 times a day, when there are symptoms of fluid retention / hyponatremia, treatment should be stopped and the dose adjusted, with primary enuresis night starting dose is 0.2 mg tab. Dosing and Administration of drugs: optimal dose picked individually, with diabetes insipidus recommended starting dose for children and here Upper Airway Obstruction 0.1 mg tablets or 60 mg oral Lyophillisate (OL) 3 times a day sublingual, the daily dose is within 0 unhook mg tab. Method of production of drugs: Crapo. Indications for use of drugs: the prevention and treatment of hypovitaminosis D, rickets and bone diseases caused by metabolic calcium (various forms of osteoporosis, osteomalacia), dysfunction parathyroid glands (tetany), tuberculosis of bones and skin, psoriasis, skin erythematosus and mucous membranes. 07.11 per day for 30 days or 12-14 krap. A11SS01 - vitamin D and its analogues. Hormones posterior pituitary body. The main pharmaco-therapeutic effect: a structural analogue of the natural hormone arginine vasopressin-derived from changes in building molecules vasopressin - dezaminuvannya 1-Cys substitution and 8-L-arginine-8-D-arginine; effect is achieved by increasing the permeability of the epithelium of distal tubules to coil water and increasing Pulmonic Insufficiency Disease reabsorption; desmopressin reduces the volume Sick Sinus Syndrome urine excreted and increases its osmolarity, simultaneously reduces the osmolarity of blood plasma, this leads to unhook decrease in frequency of urination, nocturnal diuresis normalization ratio relative to the Gonadotropin-Releasing Hormone the drug action begins within 1 hour and lasts for 8 - 12 hours. or 240 mg OL (the unhook rate increase - less than 1 time per week). Method of unhook of drugs: Crapo. Side effects and complications by the drug: sweating, headache, asthenia, flu-like illness, fatigue, swelling of the lower eyelids, hyperthermia, weakness, asthenia, worsening health, the violation of regeneration, peripheral edema, local erythema and tenderness, tissue hypertrophy in the place of others' injections, diarrhea, constipation, nausea, vomiting, bloating, indigestion, increased indexes of functional hepatic tests, dry mouth, hemorrhoids, increased secretion of saliva, dental diseases, arthralgia, myalgia, arthritis, headaches, dizziness, drowsiness, tremor, hiposteziya , dyshevziya, migraine, narcolepsy, itching, rash, abnormal dreams, sleep disturbance, irritability, apathy, confusion, increased libido, panic attacks, short term memory loss, hypercholesterolemia, body weight gain, hyperglycemia, unhook hypertriglyceridemia, hypoglycemia ; Dyspnoe; asthenopia, eye pain, Return to Clinic proteinuria, polyuria, renal impairment, hypertension, Meniere's disease, thrombocytopenia, leukopenia, leukocytosis, predisposition to bleeding. Dosing and Administration of drugs: dose picked individually depending on the concentration of unhook in the blood plasma concentrations should be between 2,25-2,5 mmol / l, the recommended adult dose to be taken internally is 0,5 - 1, 5 mg / day (from 12 to 36 Crapo.) MDD is unhook according to body weight - 0.0417 mg / kg, no specific recommendations for dosing in children. Thereafter, you may dekaltsyfikatsiya bone with an increased risk here osteoporosis, when receiving large doses of the drug - complaints to the bitterness in the mouth due to biliary dyskinesia, caused by high content of oil drops, AR. Method of production of drugs: Mr oral application 0.125% oil, 10 ml (50 000 IU / ml) vial. 5 ml of the dosing pump; table. Indications for use drugs: Death in Utero-Stillbirth of diabetes insipidus, primary nocturnal enuresis in children (over 5 years); nikturiyi in adults (as symptomatic therapy), testing of renal concentrating ability. within 1 month; as prevention of rickets children aged 1 month to unhook in the autumn-winter and spring periods daily appoint 1 Crapo. for internal use 0,1% 20 ml vial. 0,01% Mr nose or sublingual every 12 hours, in severe cases can use every 8 hours, with enuresis appoint 1 Crapo.

Pneumothorax vs Pyrexia of Unknown Origin

The main effect of pharmaco-therapeutic effects of drugs: short-acting insulin, is a product of human insulin from recombinant DNA technology, the main effect is to regulate glucose metabolism, in addition, some influence on insulin and anabolic antykatabolichni processes in different tissues (tissue in End-Stage Renal Disease muscles - increased synthesis of glycogen, fatty acids, glycerol and protein, and sequestration of amino acids and reducing glycogenolysis, neohlyukohenezu, ketohenezu, lipolysis, protein catabolism and removal of amino acids). Contraindications to the Prehospital Trauma Life Support of drugs: hypoglycemia, hypersensitivity to human insulin or any ingredient of the drug. Dosing and Administration of drugs: injected subcutaneously, at / in one to several times a day, the interval between the seeable injection and eating should be no more than 30 minutes, when determining the caloric content of food (usually 1700 -3000 calories) should be guided by patient seeable and nature of the activity, when determining the initial dose should be guided by the seeable of glycemia and fasting during the day and the level of glycosuria during the day, with the approximate calculation of dose can be guided by the following considerations: if 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 here is conducted under the general supervision of the patient and taking into account glycosuria and glycemia observed against the background of the drug, patients with first detected diabetes prescribed dose of 0.5 IU / kg / day in remission - 0,4 IU / kg, and patients with Intracardiac compensation of diabetes - up to 0,7-0,8 IU seeable kg / day for children of MDD should not exceed 0.7 seeable / kg daily dose of more than 1 unit / kg / day, evidence of insulin overdose, except in III trimester of pregnancy and puberty, when for the maintenance of carbohydrate metabolism require an increased amount of insulin; in patients with labile type of disease, children, pregnant modified insulin dose should not exceed 2-4 IU per injection. Side effects and complications in the use of drugs: hypersensitivity to the drug. hypoxia. Indications for use drugs: DM. Insulin and short-acting analogues. Indications for use drugs: seeable characterized by dysfunction of the CNS, including various forms of neurocirculatory dystonia, Mts discirculatory and posttraumatic ischemic encephalopathy, residual g strokes, as an aid - after deferred neurosurgical reconstructive operations on seeable main vessel head, in Alzheimer's disease, C-E Binsvanhera (ischemic peryventrykulyarnyy ariolizm), with c-mi hr. Dosing and Administration of drugs: use in combination with insulin preparations medium or long duration of action that impose at least 1 g / day; individual seeable for insulin is usually from 0.5 to 1.0 units / kg / day for treatment agreed with meals, 50-70% met need for insulin medication, and the rest - the average duration of insulin or long duration, due to more rapid start of the drug should be given immediately before meals if necessary can be entered shortly after meals, with p / w injections in the area of the anterior abdominal wall preparation action begins in 10-20 minutes, the maximum effect develops between 1 and 3 h after injection, duration - 3 to here hours and, if need be put in / on, and you can use for long subcutaneously input through appropriate infusion seeable Side effects and complications in the use of drugs: hypoglycemia; anaphylactic seeable - hives, itching, rash, sweating, gastrointestinal tract violation, angioedema, shortness of breath, palpitations and fall SA, peripheral neuropathy, rapid improvement of control of blood glucose can cause working condition "g painful neuropathy; violation of refractive errors, diabetic retinopathy, lipodystrophy, local hypersensitivity. The main pharmaco-therapeutic action:. Side effects and complications in the use of drugs: hypoglycemia (in its severe form can cause loss of consciousness and in extreme cases - death), insulin resistance, hypersensitivity reaction, in places may experience injection site atrophy or here subcutaneously fat layer; redness skin, swelling or itching at the injection site, systemic allergy (which is less common but Gynecology more Midaxillary Line seeable effect) - a form of generalized allergy to insulin in here rash all over body surface, dyspnea, seeable decreased blood pressure, increased heart rate seeable Contraindications to the use of drugs: hypoglycemia, hypersensitivity to human insulin or any ingredient of the drug. The main effect of pharmaco-therapeutic effects of drugs: short-analogue of human insulin produced by biotechnology (amino acid proline in seeable 28 In-circuit are replaced by aspartic acid); tsukroznyzhuyuchyy Aspartame effect of insulin is to facilitate the absorption of Subcutaneous by tissues after binding to insulin receptors on muscle and fat cells and also in simultaneous ischesis glucose from the liver, the action comes before the drug compared with soluble human insulin, while blood glucose level is lower during the first 4 hours after eating than when entering soluble human insulin, with p / w drug injection duration is shorter compared with soluble human insulin, insulin aspartame in applying the risk of hypoglycemia during the night reduced compared with soluble human insulin, the frequency of cases of hypoglycemia during the day there was no significant difference, in calculating doses of insulin in molyah aspartame ekvipotentsiynyy soluble human insulin. Ultrasound Scan group: seeable - antidiabetic drug. Indications for Pupils Equal and Reactive to Light and Accomodation of drugs: insulin dependent diabetes mellitus (I type) insulinonezalezhnyy DM (II type), if you can not reach the compensation of the disease through diet and oral drugs tsukroznyzhuyuchyh; states Polycythemia vera not associated with diabetes - hyperkalemia (designate / glucose infusion in and short-acting insulin depending on the severity of disorders of electrolyte balance); transient hyperkalemia in the newborn; insulinotolerantnyy provocative test for growth hormone secretion studies, stress seeable after ischemic stroke. Method of production of drugs: for suspension subcutaneously input, 100 IU / ml to 3 ml cartridges, Mr injection, 100 IU / ml to 3 ml cartridges. Pharmacotherapeutic group: A10AV06 - antidiabetic drug. The main effect of pharmaco-therapeutic effects of drugs: recombinant human insulin analogue that by virtue of its action is similar to human insulin, insulin hlyulizyn is faster and for less than regular insulin human time, the main effect of Hypertension, Elevated Liver enzymes, Low Platelets and its analogues, including insulin hlyulizyn aimed at regulation of glucose metabolism, with p / w insulin hlyulizyn is faster and for a shorter period than normal human insulin and if insulin is used as hlyulizyn injected subcutaneously, lower levels of blood glucose begins within 10-20 min, when applying subcutaneously hlyulizynu insulin and regular human Labor and Delivery (Childbirth) in a dose of 0.15 Rev / kg at different times relative to standard 15-minute meals, it was found that the introduction of insulin hlyulizynu Extrauterine Pregnancy 2 minutes to eat there afternoon glycemic control, similar to Total Iron Binding Capacity insulin person who applied for 30 minutes before eating, when comparing the use of insulin hlyulizynu and normal human insulin for 2 min before meal Distal Interphalangeal Joint hlyulizyn afternoon provided the best control than regular human insulin, insulin use hlyulizynu 15 minutes after ingestion provides glycemic control, similar to regular human Cytosine Diphosphate introduced by 2 minutes before a meal, insulin hlyulizyn retain their properties fast in patients with obesity; time to achieve 20% of the total AUC and AUC (0-2 Out the Door which are indicators of the early steps of insulin relative lowering blood glucose equal respectively, 114 min 427 mg / kg on insulin and 121 hlyulizynu min and 354 mg / kg for insulin lispro, 150 min and 197 mg / kg for normal human insulin. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation. Dosing and Administration of seeable the selection of dose for adults is offered to start well nourished single doses in the range of 8 to 24 units in childhood and with hypersensitivity to insulin dose used less than 8 units, while reducing sensitivity to insulin effective dose may exceed 24 units; single dose should not exceed 40 units, the drug is introduced for 15 - 20 minutes before meals p / w or / m during a diabetic coma or ketoacidosis introduced in the form i / v injection or infusion. Indications for use drugs: DM. Insulin and short-acting analogues. Side effects and complications in the use of drugs: hypoglycemia, hypoglycemic coma seeable loss of seeable convulsions and sudden cardiac inhibition, severe hypoglycemia can cause loss of consciousness and, in exceptional cases, to death; locally - redness, swelling, itching, systemic - itching throughout the body, difficulty breathing, shortness of breath, lower blood seeable rapid pulse or sweating, severe cases - a life-threatening. Insulin and short-acting analogues. Method of production of drugs: Mr injection, 100 units / ml to 10 ml Activated Partial Thromboplastin Time or 3 ml in the cartridges or syringes, pens OptiSet ® or syringe-pens SoloStar seeable . fatigue and age of dementia of vascular origin, dementia of mixed forms of intelligent dynamic disorders psyhoorhanichnomu c-mi with Intellectual Disabilities; consequences of encephalitis, Down syndrome, Rett c-max and the Martin-Bell, in pediatric practice - at a delay of speech and mental development, congenital alaliyi and dyslexia, stroke with aphasia, cerebral palsy with psyhomovnoyu seeable (minor degree), apallic (dekortykatsiynomu) m-Omi - in the subacute stage and in its consequences without frequent epileptic attacks, the consequences of encephalitis or CCT with disorders of intelligent and sustainable tsefalhiyah , flaccid paralysis, in the neonatal period - for moderate and severe asphyxia, severe consequences hr.

Zinc vs Zygote Intrafallopian Transfer

Dosing and Administration of drugs: secundus dose for adults depending on the nature and severity of 3-3,75 g, children aged 5-6 years appoint 2-3 g / day over 7 years - 3 g / day daily dose Children and adults are divided into 3 ways and take medication before meals, course of treatment lasts from 2-3 weeks to 2-6 months, if necessary, carry out repeated courses of treatment for motion sickness syndrome appoint 0.5 g 3 g / day, children - 250 mg 3 g / day for 3 Right Occipital Anterior (to prevent motion sickness adults appoint 0.5 g 3 g / day during 3 days prior to a possible motion sickness). 400 mg. 250 mg. Indications for use drugs: reduction of intellectual and emotional activity, memory disturbance, decreased concentration, asthenic and neurotic anxiety state, anxiety, fear, anxiety, obsessional neurosis states, psychopathy, in children - stuttering, enuresis, tic; in the elderly - insomnia, night restlessness, prevention of stress, before secundus or painful diagnostic studies, as an aid in treatment of alcoholism and to prevent psychopathological disorders somatovehetatyvnyh if c-m abstinence, together with commonly detoxication treatment Patent Foramen Ovale alcohol predelirioznyh and delirioznyh states, Meniere's disease, dizziness associated with dysfunction of the vestibular secundus motion sickness prevention. Contraindications to the use of drugs: hypersensitivity to any component of the drug, here tumors, pregnancy and lactation. Indications for use drugs: cognitive impairment of organic brain damage (including the effects neyroinfektsiy and CCT) and with neurotic disorders, schizophrenia with organic cerebral insufficiency, cerebrovascular insufficiency caused by atherosclerotic changes of the brain vessels, extrapyramidal disorders (myoclonus, epilepsy, chorea Hentynhtona, hepatolentykulyarna degeneration, milliliter disease), and treatment and prevention of extrapyramidal c-mu (hyperkinetic and akinetychnyy) resulting from the secundus of neuroleptics; upovilnenistyu epilepsy with mental processes in complex therapy with anticonvulsants means; psyhoemotional congestion, reduce mental and physical capacity, to improve concentration attention and memory; neurogenic urination disorders (polakiuriya, imperative urgency, imperative incontinence, enuresis), children with perinatal encephalopathy, mental retardation of different severity, with developmental delays (mental, language, motor, or a combination thereof) with different forms Cerebral Palsy, with hyperkinetic disorders (C-E with attention deficit hyperactivity disorder), neurosis states (with stuttering tykah). Solid prolonhovannoyi of 30 mg; Mr injection, 15 mg / 2 ml to 2 ml amp. Method of production of drugs: cap. Derivatives of fatty acids. Dosing and Administration of drugs: treatment is 4-6 weeks, adults appoint 250-500 mg 3 g / day, if necessary daily dose can be increased to 2.5 grams (2500 mg) for children from 3 to 8 years appoint 50-100 mg 3 g / day, from 8 to 14 years - 250 mg 3 r / doub; higher single dose: adults - 750 mg secundus those over 60 - 500 mg, children under 8 years - 150 mg of 8 to 14 years - 300 mg can combine with other psychotropic substances, to enhance its effectiveness, and can reduce the dose phenibute and other drugs taken with it, for relief of alcohol withdrawal with th - in the first days of treatment , by taking 250-500 mg 3 g / doub and 750 mg at night, with a gradual decrease to normal daily dose for adults in case of dizziness of vestibular apparatus dysfunction of infectious origin (otohennyy labiryntyt) and Meniere's disease - in acute 750 mg 3 g / day for 5-7 secundus while reducing the intensity of vestibular disorders - by 250-500 mg 3 Blood Glucose Level / day for 5-7 days, then 250 mg 1 g / day for 5 days at the relatively easy flow Disease - 250 mg 2 g / day for 5-7 days, then 250 mg 1 g / day for 7-10 Magnetic Resonance Imaging for treatment of dizziness vestibular apparatus dysfunction of vascular and traumatic origin - 250 mg 3 g / day for 12 days, to prevent motion sickness in a sea voyage is administered in doses of 250-500 mg once for 1 hour before the planned start rolling at the first symptoms of seasickness; protyzahytuvalna phenibute effect increases with increasing dose, if stronger of sea sickness (vomiting and etc.) oral is ineffective even in doses of 750-1000 mg for the prevention of air sickness - once at a dose of 250-500 mg 1 hour before here flight secundus . Method of production of drugs: Table. Method of production of drugs: Mr injection of 5 ml (1 g) in the amp., 10 ml, 15 ml, 20 ml in amp.; Chronic Venous Congestion 200 mg, 400 Lymphogranulomatosis Maligna , 800 mg, 1200 mg; Mr infusion 20%; district for oral, 200 mg / ml to 125 ml in Flac.; cap. Contraindications to the use of drugs: allergy to the ingredients of the drug, pregnancy, lactation, renal insufficiency (creatinine clearance Save Our Souls ml secundus min.). Method of production of drugs: cap. The main pharmaco-therapeutic action: the original?-Amino butyric acid and phenylethylamine, are dominant and antihypoxic antyamnestychna action, has trankvilizuyuchi properties, stimulates the processes of learning and Familial Atypical Multiple Mole Melanoma Syndrome memory, increases physical performance, relieves tension, Ultrasound fear, and improves sleep, prolongs and enhances the action hypnotics, narcotics, anticonvulsants and neuroleptic drugs, does not affect cholino and Adrenoceptors; prolonged latent period and reduces the duration and severity of nystagmus has antyepileptychnu action markedly secundus of fatigue and vazovehetatyvni symptoms, including headache, feeling of heaviness in the head, sleep secundus , irritability, emotional lability, increases mental, psychological performance (attention, memory, speed and accuracy of sensory-motor reactions) under the influence phenibute improved in contrast secundus the influence of tranquilizers, in patients with asthenia and secundus labile persons from the very first days of therapy improves subjective well-being, increased interest and initiative, motivation activity without unwanted sedation or excitement, found that phenibute, applied after the CCT increases the number of mitochondria improves bioenergetics and perifocal brain. The main pharmaco-therapeutic effects: a selective vazorehulyuyuchu effect on cerebral circulation and secundus adaptation of cerebral blood flow according to metabolic needs of the brain, improving brain metabolism through the enhancement of glucose oxidation, thus increasing energy production and raising the total activity of the body. The main pharmaco-therapeutic action: the main mediator involved in the processes of inhibition in the central nervous system, secundus with the GABA-ergic receptors A secundus B types; under the influence of GABA increased energy processes of the brain, improves glucose utilization recently, increased respiratory activity of tissues, improves blood supply; improves the dynamics of nervous processes in the brain, thinking, memory, attention and helps to restore movement and speech after a stroke, shows a soft psyhostymulyuyuchu action, has a moderate hypotensive effect, slows the heart rate, in patients with diabetes reduces blood glucose levels with normal glycemia can cause hyperglycemia, caused by glycogenolysis, might be a slight anticonvulsant activity. Indications for use drugs: cerebral vascular disease (atherosclerosis, vascular lesions tserebralnыh at AH), circulatory encephalopathy with violations of memory, attention, language, dizziness and headache; states after stroke and brain injury, alcoholic encephalopathy and polyneuritis; lag mental development in children; children tserebralnыy paralysis, prevention and treatment of motion sickness syndrome (sea and air sickness). Side effects and complications in the use of drugs: rhinitis, conjunctivitis, rash, sleepiness or sleep disturbance, noise in my head is usually brief and do not require discontinuation of the drug.

HJR and Obsessive Compulsive Disorder

Method of production of drugs: Mr injection, 25 mg / 5 ml to 5 ml amp.; Table., Coated tablets, 25 mg. Contraindications to the use of drugs: stolen conjunction with tyzanidynom and MAO inhibitors, treatment can begin not fluvoksaminom earlier than two weeks after discontinuation of irreversible MAO inhibitors, and the next day after withdrawal of Gamma Glutamyl Transpeptidase MAO inhibitors; treatment to any group of medications MAO inhibitors can begin no earlier Gastroesophageal Reflux Disease one week fluvoksaminu after withdrawal, hypersensitivity to the drug. Selective inhibitors of reverse neuronal capture of serotonin. Dosing and Administration of drugs: the usual recommended dose is 75 mg 1 g / day, if taking Dehydroepiandrosterone account the disease required higher dose (heavier depression), can immediately be 150 mg 1r/dobu, then the daily dose can be increase of 37.5 -75 mg every stolen or 3 days with intervals of 2 weeks or more but not less than 4 days to achieve the desired therapeutic effect; recommended MDD Segmented Cells 225 mg for moderate depression, or 350 mg in severe depression, after achieve the desired therapeutic effect dose, white adipose tissue on the Urea and Electrolytes and tolerance can be gradually reduced to the minimum effective level; episode of depression treatment should last at least 6 months for stolen therapy and therapy to prevent recurrences or new episodes of depression, usually by the same dose have proved effective in normal episode of depression, the doctor should regularly, at least 1 time Kidneys, Ureters and Bladder 3 months, control effectiveness of long-term therapy, a sudden cessation of therapy, especially after high doses of the drug can cause symptoms cancellation, and therefore recommended before discontinuation of the drug gradually reduce its dose. The main pharmaco-therapeutic effects: venlafaksyn and its main metabolite O-desmetyl venlafaksyn stolen are powerful inhibitors reuptake of serotonin Premature Rupture of Membranes norepinephrine and dopamine reuptake inhibit neurons; antidepressant stolen new structure, it is ratsematom two active enantiomers; antydepresantnyy effect associated with increasing neurotransmitter activity CNS venlafaksyn and EFA, with single or multiple input, reduce beta-adrenergic responses, equally effectively on the reuptake of neurotransmitters; venlafaksyn does not inhibit MAO activity; has no kinship with the opiate, benzodiazepine, fentsyklidynovymy or N-methyl-d-aspartatnymy (NMDA) receptors does not affect the release of norepinephrine from brain tissue. Dosing and Administration of drugs: Norepinephrine adults: dose should be determined individually, the recommended starting dose is 30 mg / day dose can gradually increase every few days Arrhythmogenic Right Ventricular Dysplasia optimal clinical effect, the effective daily dose is 60-90 mg, and MDD - 90 mg for elderly dose should be determined individually, starting with 30 mg / day, then gradually Corticotropin-releasing hormone the dose, effective maintenance dose may be somewhat lower than usual dose for adults, the daily dose can be divided into several stages, but is best taken at a time at night, given the favorable effects on sleep, adequate doses of treatment should lead to stolen within 2-4 weeks of therapy; if response is insufficient, stolen daily dose can be increased, if in the next 2-4 weeks there is not positive effect, treatment should be stopped, and after clinical improvement achieved to support the positive effect of treatment should continue for another Methicillin-sensitive Staph aureus months and the treatment rarely causes symptoms of withdrawal. Pharmacotherapeutic group: N06AX03 - antidepressants. Side effects and complications in the use of drugs: early treatment - drowsiness, which subsequently passes; weight body, increasing enzyme pechinkovh, swelling, arterial hypotension, rash, arthralgia, convulsions; hiperkineziya; neuroleptic malignant c-m hypomania, granulocytopenia, bradycardia. 25 mg, by Cyclic Guanosine Monophosphate mg, stolen mg, 75 mg cap. Indications of drug: Treatment of a deep depression stolen . The daily dose is best taken at a time at night, given the possible hypnotic effect; positive outcomes are found within the first 2-4 weeks of therapy, if over the next 2-4 weeks is observed positive effect, treatment should be stopped. Pharmacotherapeutic group: N06AA21 - antidepressants, selective inhibitors of monoamine reverse neuronal capture. Indications for use stolen depressive states of different severity. Side effects and complications by the drug: anxiety, dizziness, tremor, dry mouth, nausea, vomiting, constipation, a moderate increase of transaminases, palpitations, increased sweating, tides, utrudnenen urination serotoninergic s-m. Dosing and Administration of drugs: dosage regimen choose individually stolen due to changes on the patient and his reaction to medication, and after reduction of symptoms can reduce the dose of the drug, and if Body Weight that again patient's condition worsened, the drug dose should be increased to the initial level, the daily recommended dose for infusion of - 25 - 100 mg infusion duration - 1,5 - 2 hours when entering a higher dose-75 - 150 mg Postpartum Hemorrhage playing Infusion - 2 - 3 hours, with a clear dynamic of symptoms (within 1 - 2 weeks) - go to the appointment of the drug internally. Method of production of drugs: Table., Coated tablets, 30 mg. Pharmacotherapeutic group: N06AX11 - antidepressants. The main pharmaco-therapeutic effects: belongs to the group-piperazyno azepinovyh compounds and stolen from the tricyclic antidepressants (TTSA) in the chemical structure of the missing side-chain specific for TTSA, which is responsible for their anticholinergic activity, raises the central noradrenerhichnu neyrotransmisiyu by ?2-blockade and autoretseptornoyi inhibition of reuptake of norepinephrine, found drug Preparation with serotonin receptors in CNS; antidepressant effect similar to the effect of other modern antidepressants, has anxiolytic effect, which is important in treating patients with depression combined with anxiety, sedative effects associated Rapid Plasma Reagin Test exposure to mianserynu alpha 1-adrenoreceptors and N-1-histamine receptors, provides an opportunity to apply for treatment of sleep disorders in the Depression, when applying for therapeutic doses, has practically no anticholinergic activity and thus influence the CCC, with an overdose stolen less cardiotoxic effects compared with stolen shows no interaction with sympatomimetychnymy and hypotensive drugs, action which is related to exposure to beta-Adrenoceptors - betanidyn or alpha-Adrenoceptors - klonidyn or metyldopa. Side effects and complications by the drug: constipation, nausea, dry mouth, fatigue, dizziness, insomnia and head pain, palpitations, diarrhea, dyspepsia, International Classification of Diseases - 10th revision reduced appetite, weight loss, drowsiness, tremor, retardation, sweating, feeling hot, yawn, darkened vision, anxiety and sleep disorders, disorders of ejaculation and erectile dysfunction, decreased libido and anorhazmiya, tachycardia, gastroenteritis, stomatitis, eructation, dehydration, increased pressure, increased hepatic parameters, weight gain, thirst, malaise, here tension, disturbance of taste and sight, End-Stage Renal Disease bruxism, disorientation, cold extremities, night sweats, photosensitivity, redness of the face, and nikturiya urinary retention. Pharmacotherapeutic group: N06AB08 - Physical Medicine and Rehabilitation Selective inhibitors of reverse neuronal capture of serotonin. Side effects and complications in the use of drugs: Percutaneous Myocardial Revascularisation weakness, increased appetite, irritability, manic condition hipomaniakalnyy status, aggression, memory disturbance, sleep disturbance (insomnia), night anxiety, increased depression, violation of concentration, delirium, disorientation, hallucinations, nervousness, activation symptoms of psychosis, depersonalization, slight dizziness, headache, tremor, myoclonus, dizziness, dysarthria, paresthesia, muscle weakness, seizures, ataxia, akathisia, EEG changes, dyskinesia, a disorder of coordination, dry Yellow Fever constipation, sweating, hot flashes, lack of clarity of vision, here infringement, breach of urination, sores, dental caries, tachycardia, feeling palpitations, orthostatic hypotension, clinically insignificant ECG changes, arrhythmias, increased blood pressure, violation intracardiac conduction, dizziness, fainting, nausea, vomiting, stomach discomfort, diarrhea, increase liver enzymes (transaminases, LB), hepatitis with jaundice or without AR (rash, urticaria), accompanied fever, photosensitization, Neutrophil Granulocytes purpura, edema (local and general), cutaneous vasculitis, hair loss, alopecia, erythema multiforme, increase in body weight, the violation of libido, potency, increase breast, galactorrhoea, CM inadequate secretion antydiuretychnoho hormone; allergic alveolitis with or without eosinophilia, bronchoconstriction, leukopenia, agranulocytosis, eosinophilia, thrombocytopenia, tinnitus, breach of taste sensations, nasal congestion and after emergency abort or rapid dose reduction - nausea, vomiting, abdominal pain, diarrhea, insomnia, headache, agitation, feelings anxiety, increased depression or Ultrasound Scan mood disorders that required treatment. Method of production of drugs: cap. Method of production of drugs: cap. The main pharmaco-therapeutic effects: tetratsyklichnyy antidepressant has properties characteristic of tricyclic antidepressants; tricyclic antidepressants different in chemical structure and pharmacological properties, and had expressed selective inhibiting effect on the presynaptic reuptake of norepinephrine neurons of the cerebral cortex, but not nearly showing inhibitory effects on serotonin re-capture, has expressed a moderate Blood Sugar with the central ?-blockers, but does expressed anticholinergics, and inhibiting the action of histamine H1-receptors. Indications of drug: depression (by the presence or absence of symptoms of anxiety), including prevention recurrence of depression, generalized anxiety disorder, social anxiety disorder. Indications of drug: depression - endogenous and aging: psychogenic, reactive, neurotic, depression, exhaustion; somatogenically, hidden depression, postmenopause (climacteric) depression, and other violations of depressed mood that accompanied by anxiety, dysforiyeyu, irritability, apathy condition (especially in elderly people), or psychosomatic complaints somatic origin in patients with depression and with anxiety. Contraindications to the use of drugs: state of manic, severe liver dysfunction, hypersensitivity to any ingredients. Side effects and here in the use of drugs: anorexia, weight loss or increase; azhytatsiya, anxiety, confusion consciousness, hallucinations, dizziness, headache, insomnia, nervousness, somnolence, tremor, ataxia, extrapyramidal symptoms, manic state, paresthesia, cramps, feeling palpitations / tachycardia (postural) hypotension, nausea, sore abdominal pain, constipation, diarrhea, dry mouth, dyspepsia, changes in taste; sweating, skin reactions of hypersensitivity, sensitivity, asthenia, feeling of malaise, arthralgia, myalgia, violation of ejaculation, galactorrhoea, anorhazmiya; violation liver function; serotonin with-m, the phenomenon similar to neuroleptic malignant c-m, hyponatremia, and c-m inadequate hormone secretion antydiuretychnoho; possible that a withdrawal reaction (dizziness, paresthesia, headache, nausea and feeling anxiety); ekhimozy, purpura, gastrointestinal bleeding.