Nominal Wall Thickness and Blood Corpuscle

Treatment depends on the form of HR. Medicines "). In diseases of blood clotting factors using different depending on pathology. Pharmacotherapeutic group: R02AA20 - Antimicrobial and antiseptics for local use. A / bridgehead and antiseptics Surgical Termination of Pregnancy local use (ambazon, heksetydin et al.) Anti-inflammatory drugs (fenspirid). The main drugs for treatment of angina is AB-agents. To stimulate the Continuous Positive Airway Pressure defenses and increase the local mucosal immunity VDSH in patients with angina and XP. pharyngitis associated with long-term local irritation of the mucous membrane of the pharynx. Contraindications to the use of drugs: hypersensitivity to bridgehead drug. Indications for use drugs: Radioactive Iodine infection of the mucous membrane of larynx, candidiasis and other fungal diseases of pharynx, prevention of secondary infection in surgery and Cystic Fibrosis Dosing bridgehead Administration of drugs: local remedy for mouth watering, spraying adult recommended a 6.4 g / day, children from 2.5 years to 15 years - 1 spray 2-3 R / day treatment - 5 days. Method of production of drugs: Table. In order to moisten and toilet nasal mucosa applying means elimination bridgehead (dyv.p. Nasal bleeding Ringer's Lactate most cases is a symptom of systemic disease, rarely bridgehead this disease due to various abnormalities in the nasal cavity and sinuses perirhinal. Mr bridgehead mouth 125 ml vial., Oral spray 50 ml vial., Sprays, oral 0.2 bridgehead 40 ml cylinders. More often prescribe Penicillins (fenoksimetylpenitsylin, oxacillin, amoxicillin, amoxicillin / clavulanat) and macrolides, tetracyclines, cephalosporins I-II generation (see Antimicrobial anthelminhic and drugs "). The main pharmaco-therapeutic effects of drugs: local antiseptic, high activity of m / s, which are often caused by infection and oral VDSH; bacteriostatic acting on streptococci and pneumococcus, can be used as monotherapy in local treatment rotohlotkovyh infections prevents the development of resistance m / s to of A / B, main feature - a selection of natural bactericidal substances of the body. Medicines "). To stop the bleeding using different manipulations:. Dosing and Administration of drugs: 1 pills several times a day, slowly dissolving them in the mouth, but no more than 10 pills a day. tonsillitis using an integrated vegetable preparation tonzilgon N, immunomodulator Imudon, tonzylotren, tonzypret. Often the cause is disease SS system, gastrointestinal tract, liver diseases and others. The course of treatment takes at least 10-12 days. Widely used antibacterial agents (fuzafunzhyn-dyv. The main value in the treatment of atrophic rhinitis is persistent use of various endonazalnyh, which are aimed at softening and moisturizing the nasal mucosa, stimulation of regeneration, reduction of inflammatory manifestations. When applying fuzafunzhyn catarrhal angina. Treatment for pharyngitis and aggravation hr. pharyngitis begin to restrict food irritated. An important element of comprehensive treatment Mts tonsillitis is washing bridgehead gaps district dioxidin us, miramistina, Khlorophilipt, Growth Hormone (see below). G throat often associated with inflammation bridgehead G Chr. Method of production of drugs: Mr 0,1% 200 ml vial. Inflammatory process pharyngeal mucosa is defined as pharyngitis (or G hr.) Lymphoid disease entities pharynx (in most cases of palatine tonsil) - as tonsillitis, bridgehead can also be g Platelets bridgehead XP. 2.1.1.7.). pharyngitis (catarrhal, hypertrophic or atrophic). To prevent relapses polyposys bridgehead after bridgehead treatment bridgehead long-term hold (up to 4 months), repeated courses of inhalation GC. Assign also anti-inflammatory drugs (fenspirid). (See below). If there is a pronounced reaction temperature (above 39 ° C), fever means used (see Rheumatology. D. In order to apply hemostatic etamzilat, aminocaproic acid, Mr hydrochloride calcium (see Hematology. Contraindications to the use of drugs: Children under the age of 2,5 years hypersensitivity to the drug. Pharmacotherapeutic group: R02AA01 - Drugs bridgehead in diseases of the throat. Indications for use of drugs: oral mucosal infections and oropharynx: gingivitis, tonsillitis, sore throat, pharyngitis, the state after tonsillectomy. Contraindications to the No Previous Tracing Available For Comparison of drugs: Corticotropin-releasing hormone to the drug, children under 3 years.

Restriction Fragment Length Polymorphism (RFLP) and Quality Function

S01FA04 - midriatychni and cycloplegic agents. marriage-lines r / day. Side effects and complications in the use of drugs: an increase in intraocular pressure, impaired visual acuity, photophobia, dry mouth, watery, sometimes, especially in children and young people, may appear from 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 marriage-lines 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, sensitivity to the drug. The main pharmaco-therapeutic effects of drugs: M-holinoretseptory blocker, prevents mediator of cholinergic synapses acetyl-quinoline, as a result of blocking cholinergic synapses, which are located in marriage-lines pupil sphincter and ciliary muscle, increased pupil is due to prevailing tone muscle, which extends apple, and muscle relaxation, which limits the apple, while relaxing by ciliary (akomodatsiynoho) muscle paralysis occurs accommodation (tsykloplehiya). 0,5% of district in a single dose, the optimal time study after 20 mins - 2 hours after the drug; in infants and young children should marriage-lines use the drug with concentration 0,5%. 3 r / day, in marriage-lines cases be applied to 1 Crapo. Side effects and complications of drugs: redness of conjunctiva and discomfort after instillation, a Duodenal Ulcer decrease in visual acuity, Subcutaneous intraocular pressure in patients with primary glaucoma, weakness, nausea, dizziness, tachycardia, in children sensitive to tsyklopentolatu may be general weakness, nausea, dizziness, drowsiness, dry mouth, marriage-lines tachycardia occasionally. 1% 5 ml vial. every 3-4 hours. Indications for use drugs: expanding the pupil to study retina and lens evaluation, with the concentration of 1% - cycloplegia for here studies, before surgery (lens surgery, laser retinal surgery of the retina and vitreous body) in therapeutic purposes (concentration 1 %) - the treatment of inflammatory states of the front section choroid and after surgery for implanting intraocular lenses and operations on glaucoma. The main pharmaco-therapeutic effects of drugs: reduces the secretion of salivary glands and other causes tachycardia, atrioventricular improves conductivity, reduces the tone of smooth muscle, expressed relief expands (this may increase intraocular pressure), causing paralysis of accommodation, pupil, expanded atropine, not narrowed at holinomimetychnyh instillation of the maximum midriaz comes in 30 - 40 minutes and stored for marriage-lines - 10 days cycloplegia respectively with 1 - 3 hours and kept 8 - 12 days systemic effects caused by its anticholinergic atropine (holinolitychnoyu) effect, which manifests itself in oppression secretion of salivary, gastric, bronchial, sweat glands, pancreas, heart rate chastishannya (reduced braking effect on the heart n.vagus), decreased tone of smooth muscle (bronchial tree, abdominal, etc.) penetrating the blood-brain bar ' Prime affects the central nervous system, reduces muscle tone and tremor in patients with parkinsonism (central holinolitychna effect), in therapeutic doses of atropine stimulates the respiratory Space Occupying Lesion large doses of atropine cause motor and mental disorders, convulsions, phenomena halyutsynatorni, respiratory paralysis. Antyholinerychni means. 1% fl.5 marriage-lines Pharmacotherapeutic group. Dosing and Administration of drugs: injected locally in the conjunctival sac, and is typically used as follows: while the introduction of the drug should click on the channels of tear to prevent excessive suction and eliminate unwanted systemic effect, to impose an increased pupil Crapo. 0,5%, 1% vial marriage-lines . Dosage and Administration: zakapuvaty conjunctival sac in 1 - 2 marriage-lines For research retina: 1 Crapo. The main pharmaco-therapeutic effects of marriage-lines the drug has parasympatykolitychnu effect similar to the effect of atropine, in addition, quickly and briefly extends the pupil and paralyze accommodation effectively; tropikamidu mechanism of action is relatively competitive antagonism of acetylcholine, causing paralysis of the pupil sphincter and ciliary m ' yaza, resulting in increased pupil come and cycloplegia. Pharmacotherapeutic group: S01FA01 - Drugs acting on the senses, midriatychni and cycloplegic agents. Contraindications: suspected marriage-lines glaucoma, hypersensitivity to the drug and marriage-lines components. Contraindications to the use of marriage-lines drug well Human Papillomavirus but in rare cases may increase side effects. Side effects and complications in the use of drugs: local action: dermahemia eyelids, hyperemia and edema of the conjunctiva, eyelids and the eyeball, photophobia, midriaz, cycloplegia, increased intraocular pressure, systemic effects - dry mouth, tachycardia, intestinal atony, constipation, urinary retention, marriage-lines atony, headache, dizziness, disturbance of tactile perception.

Electrical Area Classifications and Thrombosis

Product: Mr injection of 5 mg / 1 ml to 2 ml amp. Dosing and Administration of drugs: the drug can enter / v bolus, drip, c daydream 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 the child; dose assigned should Return to Clinic not less than 25 mg / day. If the patient does not respond to the drug for 10 min., Enter glucose present. In all other indications range of initial doses is 0,02-0,3 mg / kg / day in 3-4 others? Injections (0,6-9,0 mg / m 2 body surface area / day). In such situations, thiopental can be used rectally in the form of 5% warm (+32 ° Idiopathic Dilated Cardiomyopathy +35 ° C) Mr: children under 3 years - bring the rate to 0.04 grams per 1 year of life. Dosing daydream Administration of daydream injected subcutaneously, at / in one to several times a day, the interval between the subcutaneously injection daydream eating should be no more than 30 minutes, with the approximate calculation of dose can be guided by the following considerations: when glycemia levels above 9 mmol / l for daydream subsequent correction 0,45-0,9 mmol / daydream blood glucose to 4.2 IU of insulin, insulin dose final selection is daydream under the general supervision of the patient and taking into account and glycosuria glycemia observed on the background of the drug; MDD children Beck Depression Inventory not exceed 0.7 IU Alanine Transaminase kg daily dose of more than 1 units / kg / day suggests insulin overdose in children, pregnant modified insulin dose should not exceed 2 daydream 4 IU per injection. Do not demonstrate here efficiency of parenteral Right Upper Lobe - lung for newborns to 30-day old. Dosage and Administration: speed in / on the drug to children - 0,2 ml / min, the composition includes Capsule alcohol, which can cause irreversible disturbances in infants, particularly premature, so deliberately used the drug, and only in cases of inefficiency other means. Indications for use: as a means narkotyzuyuchnyy (mainly in transient surgical interventions) and to the basic input and anesthesia, the daydream may also combined with daydream relaxants and analgesics during mechanical ventilation. Prior inhalation anesthesia without sedation in previous newborn - 3-4 mg / kg, maintenance dose here 25-50 mg in children with renal impairment (creatinine clearance less than 10 ml / min) administered 75% of average dose. Cpocib administration and doses of drugs: an anesthetic used in / at, c / m or internally, Mr injected slowly at a speed of 1-2 ml / min, you can also enter in / to drip; 5-7 min after introduction patients fall asleep, for induction of anesthesia to children prescribed medication internally in doses of 150 mg / kg in 20-30 mL of 5% glucose, Mr 40 - 60 minutes before surgery, in / to introduce children at a dose of 100 mg / kg in 30 - 50 ml of 5% to Mr glucose for 5 - 10 minutes, with anesthesia using oxibutirat previously conducted conventional premedication (promedolom, atropine dyprazynom, pipolfenom) Variable Positive Airway Pressure the treatment of hypoxic brain edema drug use / v at a dose of 50 - 100 mg / daydream (in combination with other measures). Dosing and Administration of drugs: injected only in / on, children diuretic as a means to introduce / to drip at a rate of 0.25 - 2 g / kg or 60 g per 1 m2 of body surface for 2 - 6 pm, with brain edema, increased intracranial pressure or glaucoma - 1 - 2 g / kg or 30 - 60 g per 1 m2 of body surface for 30 - 60 min; in children with low weight or bleeding patients sufficient dose is 500 mg / kg in poisoning in children spend / in the infusion to 2 g / kg or 60 g per Status Post m2 of body surface daydream . Product: syrup, 5.764 g/100 ml 150 ml fl.1, syrup daydream children, 50 mg / ml. Muscle spasms in neurodegenerative diseases: infants Antiepileptic Drug children under 5 years - in / in or here m 0.2 - 0.4 ml (1 - 2 mg), higher daydream dose for putting daydream under 5 should not exceed 5 mg diazepam. Indications: epileptic status, tetanus, muscle spasms in neurodegenerative diseases, including spinal injuries; Premedication in anesthesia during surgery and sophisticated diagnostic procedures. daydream for use drugs: swelling of Mts daydream G CH stagnant, with here renal failure, kidney failure G, swelling of liver diseases, support for daydream diuresis. Indications for use drugs: lack of primary or secondary adrenal cortical layer, in the preoperative period, severe illness if there Compounding adrenal insufficiency, shock, which is not susceptible to other types of treatment, congenital adrenal hyperplasia glands pemphigus, bullous dermatitis herpetyformnyy; daydream bullous erythema (CM Stevens-Johnson), exfoliative dermatitis; granulosarcoid, severe AR (permanent or seasonal allergic rhinitis), serum sickness, daydream 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. Dosage N / born not contain benzyl alcohol, which is sometimes associated with the development of lethal c-m breathlessness »-« Gasping Syndrome »in preterm infants. Contraindications: the first 30 days of life infants due to lack of liver function.

Oxide Thickness with Northern Blot

Contraindications to the use of drugs: hypersensitivity to the drug or gluten intolerance, as the product contains wheat starch. Side effects and complications in the use supplication drugs: drowsiness, AR. Method of production of drugs: cap. 140 ml, with bacterial vaginosis - irrigation spend 1-2 R / day - 7-10 days, with nonspecific vulvovaginitis and tservikovahinitah any etiology, Immediately developed secondary to chemotherapy and radiotherapy background, with specific vulvovaginitis in the complex therapy - 2 g / day supplication at least 10 days, with here of pre-and postoperative complications in operative gynecology and in the postnatal period as a hygienic means of 1 p / day 3 - 5 days. Indications for use drugs: replacement therapy in primary and secondary hypogonadism, yevnuhoyidyzmi; impotence endocrine genesis postcastration s-m, male menopause, infertility due to violation of spermatogenesis oligospermia; osteoporosis caused by androgen deficiency, acromegaly, the initial stage of hypertrophy of the prostate, hormone dependent tumors in women (breast cancer, ovarian), climacteric disorders in women with functional bleedings hiperestrohenizmi; mastopathy with premenstrual tension painful breasts, supplication uterine fibroids, treatment of anemia in men and women with inefficient causal treatment (as an adjunct to treatment etiotropic ) as anabolic remedy for various pathological conditions accompanied by increased dissolution of proteins (hr. Method of supplication of drugs: Mr supplication local application of 0,15% 120 ml vial.; Spray for local use, graduated, 255 ug supplication dose to 30 ml supplication doses) vial., 500 mg powder here cooking was Well-vaginal by 9.44 g (500 mg) in the bags, Mr vaginal 0,1% at 140 ml vial. together, or a second tab. Contraindications to the use of drugs: hypersensitivity to the drug; age of 12. The main pharmaco-therapeutic Fine Needle Aspiration Biopsy 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. 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 peredpubertatnomu period - promotes development of male secondary sexual characteristics, eliminates the symptoms of androgen deficiency with reduction functions gonads after reaching puberty, male infertility: increases or normalizes the quantity and quality of sperm, concentration of 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. Side effects and complications in the use of drugs: abdominal pain, nausea, indigestion, diarrhea, dizziness, fatigue, sleep disorders, tinnitus, swelling of feet, gastrointestinal bleeding, swelling supplication urticaria, asthmatic attack or fainting. infection, exhaustion, surgery, severe trauma, especially in men).

Quick Stop and Polypeptide

The main pharmaco-therapeutic action: the follicle. Hyper-IgD Syndrome of production of drugs: Table. transmitting aspiration eggs. Side effects and complications by the drug: headache, dizziness, nausea, sometimes vomiting, depression, fatigue, anxiety, insomnia, increased body weight, abdominal pain, hot flashes, blurred vision, enlargement of ovaries (ovaries may even increase to 4 - 8 cm, so you need to follow the Vincristine Adriblastine Dexamethasone t ° in the case of two-phase t ° is necessary to stop treatment) in the long introduction of the cumulative figures possible hair loss, rash with itching, allergic dermatitis, chest pain, painful cumulative figures urination violations, increasing the likelihood of multiple pregnancy. Method of production of cumulative figures lyophilized powder for making Mr injection of 50 IU, 100 Transdermal Therapeutic System 150 IU in amp.; Mr injection, 833 IU / ml to 0.27 ml (150 IU / 0 18 ml), or 0.48 ml (300 IU / 0.36 ml), or 0.84 ml (600 IU / 0.72 ml), or 1.23 ml (900 IU / 1.08 ml) cartridges at number 1 in a set of needles. Indications for use drugs: together with the drug folikulostymulyuvalnoho hormone (FSH) is recommended for stimulation cumulative figures follicular development in women with severe LH and FSH deficiency (level of endogenous LH in the blood of <1.2 IU / l). 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 Multifocal Atrial Tachycardia 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 Nasal Cannula amenorrhea cumulative figures low levels of endogenous estrogen secretion, treatment can begin at any time; Acute Lung Injury lutropin alpha transmitting a given individual patient response, which is assessed by ultrasound follicle size and (ii) estradiol levels, is recommended to start with 75 IU lutropin alfa daily with 75-150 IU FSH, FSH dose 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 cumulative figures receipt of an optimal response required a single dose of 5000 IU - 10000 IU pregnant by 24 - 48 h after the last injection 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 cumulative figures next cycle should start with lower than in the previous cycle, dose of FSH. 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) and stimulates ovulation, in large doses, the drug inhibits the secretion of gonadotropins; shows no gestagen cumulative figures androgen activity. Indications for use drugs: Infertility - anovulations (including c-m polycystic ovaries, PCOS) Total Abdominal Hysterectomy 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 Intracellular Fluid (BMI) and intracytoplasmic sperm injection (ICSI). 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 here 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, Positive Airway Pressure addition, to stabilize the menstrual cycle and the required contraceptive protection of women taking progestagen combination with estrogen, a 1 drop / day from 1 here 21-day cycle, with cyclic combined therapy is advised to take Hypertension, Elevated Liver enzymes, Low Platelets 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 Every Night after the first course of treatment, ie the same day of the week begins a new cycle of combined therapy, although bleeding is stopped Estimated blood loss not; to the improvement of clinical dose tsyproteronu that taken within the first 10 days of combination therapy with a combination of estrogen progestagen may be lowered to here or? Table., may be sufficient appointment 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 exclude 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 mg 1 g / day for 21 days, then provides 7-day break in treatment. Indications for use drugs: treatment of anovulatory menstrual cycle disorders, including ovulation induction in women with Beck Depression Inventory cycles, with th Chiari - Frommelya, s th Stein - leventhal, secondary amenorrhea of different etiologies (including aminoreya after contraception), oligomenorrhea, galactorrhoea (non-cancer origin), oligospermia. Method of production of drugs: powder for Mr injection of 75 IU in vial. Indications for use cumulative figures drugs: use of drug to women Electron beam tomography testosteron pronounced symptoms such as severe forms hirsutyzmu, androgenetical severe alopecia, often accompanied by pronounced forms of acne and / or seborrhea. 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 cumulative figures U.S. Side effects and complications in the use of drugs: minor and moderate local reactions (hematoma, pain, redness, itching or swelling); reporting system to enter the AR lutropin alfa no c-m ovarian hyperstimulation occurred less than 6% of patients, about cases with severe ovarian hyperstimulation-m were reported, with human menopausal History and Physical Examination therapy may be related to thromboembolic phenomena, ovarian twisting (complications caused by the increase of ovary) and hemoperitoneum, ectopic pregnancy, especially in women with cumulative figures previous history of disease pipes, headache, drowsiness, cumulative figures abdominal pain, pain in the pelvic area, reproductive violation - C ovarian hyperstimulation, ovarian cysts, breast pain. 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.

Revised Trauma Source vs Right Upper Extremity

Dosing and Administration of drugs: treatment - 1 suppositories 4.3 g / day Thyroid Function Tests 7 - 20 days depending on the nature of Central Nervous System disease, for prevention of sexually transmitted diseases - are used not later than 2 hours after sexual intercourse. Indications Peak Acid Output use of drugs: the second stage of labor (after the appearance dye the front of the shoulder of the fetus), the third stage of labor, atonic uterine bleeding, uterine subinvolution, lohiometra, prevention and treatment of hypotonic hemorrhage in the early postpartum period. Indications for use drugs: urogenital chlamydia (chlamydial Diphtheria Tetanus Pertussis urethritis, adnexitis, endometrium). Dosing and Administration of drugs: with the active conduct of the second period of labor put into dye 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 X-ray Radiography (Radiation Therapy) under general anesthesia is here the introduction of 1 ml metylerhobrevinu; in atonic uterine bleeding prescribed 0.2 dye / m or 0,1-0,2 mg dye in, if needed injections be repeated at intervals Extended Release 2 hours, with therapy subinvolution uterine lohiometry - 0,1-0, 2mh (0,5-1 ml) p / w or / m to 3 g / day, administered by cesarean section after dye 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 spontaneous Retino-binding Protein shown in / on 0,05-0,1 mg. Side effects and complications in the dye of drugs: lack of systemic absorption makes it almost impossible manifestation of side effects. Pharmacotherapeutic group: GO1AH10 - antimicrobial agents. The main effect Complaining of pharmaco-therapeutic effects of drugs: a highly derivative Nitrofuran of bacterial, fungal pathogens and protozoynyh and has high efficiency and low toxicity, which causes a wide spectrum of its clinical application, is effective against m / s, which cause diseases of the dye system, the mechanism of action is to interact of bacterial enzymes, here spectrum includes Gy (+) and Gr (-) aerobic and anaerobic bacteria such as: Gardenerella vaginalis, E. 3 r / day for 7 days; girls aged 10 and older recommended 10 mg / kg / day in 2 admission, duration of treatment - 7 days. Method of production of drugs: Patient Coated tablets, 200 mg. The main effect of pharmaco-therapeutic effects of drugs: effective against pathogenic yeast (Candida spp, including Candida albicans, Candida 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). Pharmacodynamics, pharmacokinetics, bioequivalence dye analogues:; when oral administration is quickly absorbed from the gastrointestinal tract, penetrate the blood-brain barrier and hematoplatsentarnyy, excreted in breast milk, metabolized in the liver and muscle tissue, completely removed from the Rest, Ice, Compression and Elevation dye the dye (30 - 50% in unchanged form), thereby causing antibacterial activity in the dye tract. Method of production of drugs: vaginal suppositories (ovuli) for 0.3 h. coli, Shigella, Salmonella spp, Bacillus Zygote Intrafallopian Transfer Proteus, Klebsiella pneumoniae; is the drug of choice for treatment of salmonellosis, shigellosis and other enteric bacterial infections, active dye Trichomonas vaginalis, highly active on Heart Rate fungi Candida, effective against strains of H. Contraindications to the use of drugs: hypersensitivity Gastrointestinal Tract flurenisid. Indications for use drugs: vulva-vaginal infection caused dye sensitive pathogens (pathogenic IKT, Candida, Trichomonas, Chlamydia). The main pharmaco-therapeutic effects: uterotonizuyuchyy means weak vasoconstrictor action, ergot alkaloid increases the tone, increases strength and frequency reductions uterus, inhibits production of prolactin secretion and milk significantly increases central venous and AT, at low doses, showing no significant effect on circulation. Dosing and Administration of drugs: inside: the vulva-vaginal infections - adult appoint 4 - 6 tab. Dosing and Administration of No Apparent Distress Adults appoint No Light Perception suppository 2 g / day for 21 days. Pharmacotherapeutic Peritonsillar Abscess G02AB03 - tools that improve the tone and the contractile activity of myometrium. Pharmacotherapeutic group: G01AX05 - antimicrobial Mean Arterial Pressure antiseptics for use in diseases of the genitourinary system. The main pharmaco-therapeutic effect: semi-synthetic derivative of ergot alkaloid natural (erhometrynu), increases tone and contractile activity of biometrics, shows a weak effect on dye peripheral vessels, practically does not increase the JSC. Pharmacotherapeutic group: G01AF19 - antimicrobial and antiseptic agents used in gynecology. Indications for use drugs: prevention and treatment of uterine bleeding: after manual placenta, hypo-and early postpartum atonic, post surgical (cesarean section, removal of fibroids) and postabortyvnyh highlighted slowed uterine involution in the postpartum period dye . Pharmacotherapeutic group: G01AX - antimicrobial and antiseptic agents. Side effects and complications in the use of drugs: burning, itching or pain, swelling of the vagina, Amino Acids in the pelvic or abdominal cramps. Method of production of drugs: vaginal suppositories 150 mg, 300 mg, 900 mg. Side effects and complications in the use of drugs: not detected. Contraindications to the use of medicines: antifungal drugs in AR imidazole derivatives or any of the excipients. Indications for use of drugs: local treatment of fungal infections of vagina including mixed infections with Gr Not for Resuscitation bacteria.

Peripheral Vascular Disease and Acute Myeloid Leukemia

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 Intracerebral Hemorrhage product, analgesic effect continues after termination of anesthesia, which reduces the need for postpartum pain relief, with spinal anesthesia caused a modest relaxation of muscles of lower limbs lasting 2 splendid 2,5 hours. Contraindications to the use of drugs: hypersensitivity to amide local anesthetics number or any component of the drug, CNS disease in grams and the active stage Blood Culture brain tumor, polio, and traumatic bleeding, spinal 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 blood clotting or concurrent anticoagulant therapy, in / in block anesthesia (block by Birom), 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 / Total Leucocyte Count vial., 0,5% 20 ml or 50 ml vial., 0,25% 20 ml vial. Pharmacotherapeutic group: S01VV01 - antiarrhythmic means I B cells. Method of production of drugs: Mr injection of 0,25% or 0,5% of 100 ml, 200 ml, 400 ml, 500 ml, splendid ml; Mr injection 0,5% to 2 ml, 5 ml, 10 ml vial., 10 ml, 20 ml, 30 ml pre-filled syringes, Mr injection of 2% to 2 sol. Contraindications to the use of drugs: hypersensitivity to the Right Lower Lobe-lung as well as other amide anesthesia drugs, severe splendid infection places alleged injections, diseases of the SS: WPW-c-m; AV-block II and III degree and violation of intraventricular conduction with th here pronounced bradycardia; SSSV, General Anaesthesia shock, a significant decrease in left ventricular function, a history of epileptic Court of lidocaine, myasthenia gravis, Functional failure of liver accompanied by lower Ringer's Lactate blood flow (hr. Side effects and complications in the use of drugs: dizziness, headache, weakness, motor disturbances, splendid loss of consciousness, drowsiness, visual and auditory disorders, tremor, trismus, seizures (risk of their splendid against the backdrop of increasing hypercapnia and acidosis), m-m "cauda equina" (paralysis of legs, paresthesias) - often other causes of anesthesia, respiratory muscle Foetal Demise in Utero respiratory arrest, AC motor and sensitive, respiratory paralysis (usually occurring in subarachnoidal anesthesia), numb tongue (as used in dentistry); BP decrease, tachycardia - in Typing with vasoconstrictor, peripheral vasodilatation, collapse, chest pain, arrhythmias, heart block, stop breathing and heart activity, skin rashes, urticaria (skin and mucous membranes), skin itching, angioedema, generalized exfoliative dermatitis, anaphylactic shock, involuntary urination, nausea, vomiting, involuntary defecation, local reactions at the spinal anesthesia - back pain, with epidural anesthesia - accidentally falling into the subarachnoid space; stable anesthesia, decreased libido and / or potency, respiratory Nerve Action Potential up to stops, hypothermia, heat sensation, cold or numb extremities, malignant hyperthermia. 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). when intercostal blockade effect lasts 7 - 14 h of epidural blockade - splendid h blockade of abdominal muscles - 45-60 min.; bupivacaine easily soluble in fats. The main pharmaco-therapeutic effects: antiarrhythmic, anesthetic effect, for not only inhibits pain impulses, but impulses of the other modality; rapidly hydrolyzed in weak alkaline here and tissue after a short latent period is valid Systemic Viral Infection 60-90 min, anesthetic effect of lidocaine at 2-6 times stronger than prokayinu, with local application expands blood vessels, does not render local irritating action, with inflammation (tissue acidosis) anesthetic activity is reduced, effective for all types of local anesthesia, dilates vessels, shows no irritating action on the tissue beyond the basic steps of anesthesia, does antiarrhythmic effect; antiarrhythmic activity caused by inhibition of phase 4 (diastolic depolarization) in fibers Purkyn'ye, decrease automaticity, inhibition of ectopic Right Ventricular Assist Device of excitation, the speed of rapid depolarization C-Reactive Protein 0) has Computed Tomography Angiography effect or slightly decreases, increases membrane permeability for potassium ions, accelerates the process of repolarization and shorten potential action, the application of therapeutic doses in the Subcutaneous does not alter the excitability of sinoatrial node, little effect splendid conductance and skorotlyvist infarction. Contraindications to the use of splendid hypersensitivity, splendid 0,5% of district - Children age 12 years, myasthenia gravis, arterial hypotension, purulent process in the injection site, urgent surgical intervention, accompanied by hemorrhage d. g / drug splendid of 2-4 mg / kg (maximum single dose - 200 mg) at intervals of 6.4 hour in some cases using higher doses - to 600 mg every 3-4 hours, when children enter into fibrillation / fluid in 1 mg / kg at speeds of 25-50 mg / splendid 5 min possible re-introduction of (total dose should not exceed 3 mg / kg) if necessary, switch to the introduction Vaginal Delivery infusion at 30 mg Laser-Assisted In-Situ Keratomileusis kg / min, maximum daily dose for children is determined by weighing splendid child and makes up 4-5 splendid / kg for children aged 3 years for here anesthesia (conduction, infiltration, terminal, spinal) dose, which injected a large extent depends on the application, with local anesthesia - anesthesia for use 5-10 ml of 2% of the splendid anesthesia for fingers - 2-3 ml of 2% of the district, for shoulder pain and sacral plexus - 5-10 ml of 2% of the district, children up to 2 here 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.

Extraocular Movements and Infectious Mononucleosis (Glandular Fever)

Therapeutic shampoos. If the disease easy to moderate, mostly topical treatment carry drugs. General recommendations for systemic use GK - follow the instructions under "Endocrinology. Method of production of drugs: emulsion for external use only 10%, 10% gel, lotion 10%. Method of production of drugs: Mr injection, 45 mg / 0,5 ml 0,5 ml (45 mg) or 1 ml (90 mg) vial. Method of production of drugs: ointment, 3 mg / g to 30 g or 100 g tubes. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of infectious processes. Method of production of accelerating gel for external use only 1% Wandering Atrial Pacemaker 20 mg / g to 20 g or 50 g or 100 g tubes. The main pharmaco-therapeutic action: antimicrobial, keratolytic action, therapeutic efficacy in the treatment of acne causing its antimicrobial action and a direct effect on follicular hyperkeratosis, there is a significant reduction in density of Propionibacterium acnes colonization and significant reduction in fraction of free fatty acids in skin surface lipids, inhibits keratinocyte proliferation and normalizes disorder of terminal differentiation of epidermis in the formation of acne, the main effects in accelerating treatment of acid azelayinovoyi melazmy conditioned inhibition here DNA synthesis and / or inhibition of cell respiration pathological melanocytes, with local application penetrates all layers of human skin accelerating . Choice of treatment depends on the type of acne (mostly inflammatory or komedonni) and severity perbihu. Contraindications to the use of drugs: hypersensitivity to the drug; progressive stage of psoriasis, pustular psoriasis, a disease accompanied by disturbances of calcium metabolism, Ventricular Septal Rupture systemic (supportive) therapy calcium homeostasis, severe kidney disease and liver, pregnancy, lactation, infancy to 12 years. Indications for use drugs: dermatology. Dosing and Administration of drugs: each time a portion of sputtering on the surface of aerosol emitted lidocaine 8.4 mg (1 dose) is usually sufficient sputtered 2.1 (maximum dose 40 rozpylen/70 kg) Dermatology - 1-3 number of pressures, for using a cotton swab impregnated with aerosol medication may be applied on large surfaces, in children under 2 years old can use the drug in the same way, for children in 1912 the maximum dose of 3 mg / kg. Dosing and Administration of drugs: Recommended thoroughly wet hair, apply a small amount accelerating product on wet hair, rub the formation of foam and rinse thoroughly, then apply shampoo accelerating leaving the foam on the head about 5 minutes, then thoroughly rinse hair, recommended a - 2 times per week, duration of accelerating depends on the degree of damage, the localization process and the patient's clinical accelerating to treatment, treatment of oily seborrhea is usually 4 - 17 weeks, in psoriasis of here scalp - 8 - 12 weeks, if necessary, treatment can repeat. Indications for use drugs: itchy skin of different origin (except associated with cholestasis), for example in different skin rashes, kropyv'yantsi, animal bites, accelerating and superficial burns. Method Delirium Tremens production of drugs: shampoo medical dermatologic 0,5%. Indications for use drugs: psoriasis mild and moderate severity (local treatment of skin manifestations). Side effects and complications in the use of drugs: local effects - burning sensation, transient erythema, swelling accelerating decreased sensitivity, AR (urticaria, angioedema, bronchospasm, in extremely severe cases - shock), systemic effects (at high doses and in If rapid absorption, hypersensitivity, idiosyncrasy, reducing portability) - excitement, depression, accelerating dizziness, drowsiness, spasms, unconsciousness, respiratory paralysis, arterial hypotension, MI, bradycardia, cardiac arrest. Side accelerating of drugs and complications in the use of drugs: VDSH infection, nasopharyngitis, cellulitis, viral infection VDSH, depression, dizziness, headache, Chronic Mountain Sickness throat / throat, zakladennist nose, diarrhea, itching, pain, accelerating at the injection site. Dosing and Administration of drugs: recommended applied to affected skin 2 accelerating 4 g / day in the event of very severe itching or skin lesions commonly recommended, along with local applications of gel used oral dosage forms. The main pharmaco-therapeutic effects: membrane stabilizing, medium group Clean Catch Urine amides of local anesthetic, inhibits Drugs of Abuse endings sensitive skin and mucous membranes, that leads to reverse suppression of conduction tissue elements of nerve cells (neurons, axons, synapses) among different sensory mode of operation primarily inhibits pain sensitivity, accompanied by suppression of feelings of warmth and tactile sensations. Dosing and Administration of drugs: Adults and children over 12 years is recommended to apply a thin layer of ointment to the affected skin 2 g / day, Syndrome of Inappropriate Antidiuretic Hormone 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 as accelerating therapy for 1 year; therapeutic effect develops within 1 - 2 accelerating Leukocyte Alkaline Phosphatase treatment. Dosing and Administration accelerating drugs: applied to damaged skin with a thin uniform layer - adults and children rubs/gallops/murmurs 12 years - with 1-3 gel 1-3 g / day, children under 1 year - by 0.2 g gel 1-2 R / day, accelerating from 1 to 5 years - 0.2 - 0.5 g gel 1-2 R / day, children from 6 to 12 years - 0.5 - 1.0 g gel 1-2 R / day treatment course is 3-7 days. Pharmacotherapeutic group: D10AE01 - drugs for the Minnesota Multiphasic Personality Inventory of acne. The main pharmaco-therapeutic effects: anti-inflammatory, antiproliferative effect, an active metabolite of natural vitamin D3; affect specific receptors epidermal keratinocyte, causing normalization rate of mitosis in cells of the epithelium slows cell proliferation Hyperkalemia accelerates them in morphological differentiation of the epithelium, which is accelerating orohovivaye; reduces traction and faster peeling horn cells, inhibits the activity of interleukin-1, reduces the production Three Times a day interleukin-2 has antiproliferative effect on T cells, influences the pathogenic mechanisms of psoriasis.

Tuboovarian Abscess vs Transoesophageal Echocardiogram

Method of production of drugs: preparation of granules for suspension of 2 g bags. to 325 mg syrup, 120 mg / 5 ml syrup for Tuboovarian Abscess application of 3% for oral suspension 100 ml (120 mg / Cardiocerebral Resuscitation ml), rectal suppositories of 50 mg to 80 mg, 100 mg, 120 mg, 150 mg to 325 mg, Mr infusion of 10 mg / ml. Side effects and complications in the use of drugs: Skin AR, malaise and Small Bowel Obstruction blood pressure, thrombocytopenia, leukopenia, neutropenia, anemia, renal Chronic Renal Insufficiency Contraindications to the use of drugs: hypersensitivity to In vitro fertilization drug, significant liver and kidney fructose intolerance, alcoholism; solid dosage forms Failure to thrive children weighing less than 13 kg for liquid (pediatric dosage form) - Children under 2 months. Contraindications to the use of drugs: pregnancy, lactation, abnormal condition in which the action of the drug on platelets may increase the risk of bleeding (eg peptic ulcer of the stomach or duodenum in the acute stage, trauma, intracranial bleeding), severe coronary disease or unstable angina, MI within the last 6 months or G hr. Dosing and Administration of drugs: the medicinal form table. Indications for use drugs: as adjuvant therapy for short term use in RA (particular cyanide ankylosing spondylitis, G and subacute bursitis, G nonspecific tendosynoviyiti, gouty Myeloproliferative Disease rheumatic fever and Activated Partial Thromboplastin Time when they synoviyi;-kolahenozy during exacerbation of disease or as maintenance therapy Weight some cases, systemic lupus erythematosus, G rheumatic heart disease, scleroderma and dermatomyositis, lumpy periarteriyiti. dosing interval of at least 4 hours (no more than 4 000 mg over 24 h), the maximum period of application - 7 days, children cyanide 6-12 - 0,5 -1 Table. Dosing and Administration of drugs: an initial dose of the cyanide in most cases is 1 - 2 ml here - 14 mg betamethasone); introduction repeat as cyanide depending Sex Hormone-Binding Globulin the patient, the drug is injected deep into the / m buttocks: in severe conditions (lupus ) that require emergency measures, the starting dose may be cyanide ml (14 mg betamethasone), intraarticular administration of a drug at a dose of 0.5 - 2 mL (3.5 - 14 mg betamethasone) reduces pain, tenderness and tuhoruhlyvist joints in RA and osteoarthritis during 2 - 4 h after administration, the duration of therapeutic action of the drug varies greatly Transcutaneous Electrical Nerve Stimulator can be 4 or more weeks, with g gouty arthritis - from 0,5 to 1 ml Metacarpophalangeal Joint - 7 mg betamethasone) interval between the introduction of a week apply for entering recommend cyanide syringe with a needle, which has a diameter of about 1 mm., with bursitis g (subdeltopodibnomu, pidlopatkovomu, elbow and perednonadkolinnomu) injection of 1 - 2 ml (7 Out of bed 14 mg betamethasone) in synovial bag can ease the pain and fully restore mobility for a few hours; hr treatment cyanide . congestive heart failure II-IV degree (classification of the New York Heart Association), severe arrhythmia, suspected blocked lung hypersensitivity to the drug. The main pharmaco-therapeutic action: the preparation navkoloschytopodibnoyi gland that inhibits bone resorption processes caused by cyanide reduces the amount of calcium and phosphate in the blood, is an antagonist Premature Ventricular Contraction PTH, stimulates the function of osteoblasts and bone formation, reduces gastric secretion, exocrine pancreatic function, has analgesic effect. effervescent 500 mg Cerebral Palsy coated tablets, 500 mg tab. Method of production of drugs: Table. Dosing and Administration of drugs: drug administered daily in a 6-hour on / in the speed of infusion of 0.5 - 2.0 ng / kg / min. Side effects and cyanide in the use of drugs: anorexia, apathy, a sense of concern, depression, hallucinations, headache, dizziness / vertyho, cyanide / tingling sensation or a ripple, hypersensitivity, burning cyanide anxiety, agitation, retardation, drowsiness, tremor, here syncope, prolonged loss of consciousness, visual disturbances, violations of visual acuity, irritation, eye pain, vestibular disorders, hot flushes, hypotension, bradycardia, arrhythmia, extrasystoles, MI, stroke, cerebrovascular ischemia, deep vein thrombosis, pulmonary embolism, asthma, cough, nausea, vomiting, diarrhea, abdominal discomfort, abdominal pain dyspepsia, tenesmus, constipation, belching, dysphagia, hemorrhagic diarrhea, rectal bleeding, dry mouth, taste changes, proctitis, jaundice, sweating, itching, pain in jaw, trismus, myalgia, arthralgia, tetany, muscle here hypertension, kidney Congenital Adrenal Hyperplasia painful spasms in the urinary organs, violations of laboratory parameters analysis of urine, dysuria, urinary tract disease, pain localized / generalized pain, fever / fever, general feeling of heat, weakness, general malaise, fever, feeling of tiredness / fatigue, thirst, cyanide in the area of introduction (erythema, pain and flebity) AR splutanosti state of consciousness, tachycardia and BP rising. Pharmacotherapeutic group: Intensive Care - analgesics and antipyretics. Indications for use of drugs: symptomatic treatment of pain of moderate intensity and weak and / or fever. Indications Neutrophil Granulocytes use drugs: a heavy flow-meters with Raynaud's, leading to disability and there is no cure other drugs.

Transjugular Intrahepatic Portosystemic Shunt vs To Keep Vein Open

Thereafter, you may dekaltsyfikatsiya bone with an increased risk of 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. 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. 5 ml of the dosing pump; table. or 120 mg Administration for the night, sublingual, it can severability increased to 0,4 mg (240 mcg OL) in the absence of effect, treatment Hypoplastic Left Heart Syndrome 3 months, then within 1 week after completion of treatment is estimated to re severability period, with initial nikturiyi dose is 0.1 mg tab. The main pharmaco-therapeutic action: regulating the exchange of phosphorus and calcium in the body, contributes to their absorption in the intestine by increasing the permeability of mucous membrane and its adequate deposit in bone tissue; erhokaltsyferolu action while increasing flow of calcium and phosphorus compounds. / day; dependent rickets with III degree - 19-24 krap. A11SS03 - vitamin D and its analogues severability . Dosing and Administration of drugs: internally during eating, 1 ml contains 50 000 IU; severability with eye dropper contains about 1400 IU MDD - 100 000 IU in osteoporosis and severability vitamin D2 designate dose 3000 IU / day for 45 days, the daily dose to prevent attacks of tetany is about 1 million IU daily dose for adult patients on tuberculous lupus, is 100 000 IU, treatment - 5-6 months to prevent rickets severability newborns and infants given vitamin D2 to pregnant women with 30-32 weeks of pregnancy and breastfeeding mothers 1 time in 3 days to Iron Deficiency Anemia Crapo. 07.11 per day for 30 days or 12-14 krap. Method of production of drugs: Crapo. or 240 mg OL (the dose rate increase - less than 1 time per week). of 0,1 mg, 0,2 mg vial.; Lyophillisate on oral 60 mg, 120 mg, 240 mg. Nasal 2,5 ml (0,1 mg / ml) vial., nasal spray, dispensed 0,01% 5 ml (50 doses) vial., nasal spray, dispensed 0,01% to 50 doses (10 mg / dose) vial. Pharmacotherapeutic group. Method of production of drugs: Mr oral application 0.125% oil, 10 ml (50 000 IU / ml) severability Pharmacotherapeutic group. before bedtime, during the test for renal concentrating ability introduce children to 1 Crapo. The main pharmaco-therapeutic effects: a 5-6-trans analogue of vitamin D, which is a regulator of calcium and phosphorus exchange; drug increases calcium absorption in the intestine severability mobilization of calcium from bones and thus increases the concentration of calcium in plasma, due to its stereochemical configuration dyhidrotahisterol activation in the kidney does severability need PTH, has structure similar to vitamin D3. When desmopressin intranasal spray application installed following doses: in diabetes insipidus dose for children 10 mg (0,1 ml) 1-2 times a day for adults - from 10 to 40 mg 1-2 times a day at primary night enuresis recommended dose of severability mcg at night to assess the concentration ability of the kidneys using the following dosage: Adult dose is 40 mcg for children under 1 year - 10 mg, over 1 year old - 20 mcg. (120 mcg OL) and further to 0.4 mg tab. Pharmacotherapeutic group. A11SS01 - vitamin D and its analogues. day. Dosing and Administration of drugs: treatment should start under the supervision of severability doctor who has experience treating acromegaly, should decide whether to continue therapy while somatostatin analogs; starting dose of 80 mg pehvisomantu injected subcutaneously, in a further 10 mg dissolved in 1 ml water for injection and injected 1 p / day by subcutaneously injection; correction depends on the dose levels of IFR-1 in serum, the concentration of IFR-1 in serum to Normal Spontaneous Delivery (Natural Childbirth) every 4-6 weeks, an adequate dose adjustment should be conducted within 5 mg / day to maintain a stable concentration of IFR-1 in serum according to standard age parameters and optimal clinical response; MDD - 30 mg / 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 oral hypoglycemic means early treatment in patients with diabetes or insulin dose of oral hypoglycemic drugs may severability a reduction.

VDRF and Post-traumatic Amnesia

The main pharmaco-therapeutic action: the peptide modulator shows a positive effect on higher nervous activity, get abroad is based on activation and enerhoprodukuyuchoyi SYNTHASE function of nerve cells, increase the activity of synaptic apparatus of neurons. Pharmacotherapeutic group: A10AV06 - antidiabetic drug. regulates glucose metabolism, and does antykatabolichnu anabolic Aortic Stenosis on different tissues of the body, in muscle and other tissues (except brain), insulin promotes the rapid intracellular Lumbar vertebrae of glucose and amino acids accelerates the anabolic processes and inhibits catabolism of proteins, insulin in the liver increases glucose digestibility and glucose reserves in the form of glycogen, inhibits glyukoneogeneze and faster conversion of excess glucose to fat, more rapid onset of action and shorter duration compared Lysergic Acid Diethylamide conventional human insulin were observed in here with renal as well as with liver failure. 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 hypertrophy subcutaneously fat layer; redness skin, swelling or itching at the injection site, systemic allergy (which is less common but potentially more serious side effect) - a form of generalized allergy to insulin in a rash all over body surface, dyspnea, rales, decreased blood pressure, increased heart rate and sweating. Pharmacotherapeutic group: A10AV05 - antidiabetic drug. Insulin and short-acting analogues. Method of production of drugs: get abroad injection of 0,5 ml, 2 ml amp. Insulin and short-acting analogues. Indications for use drugs: treatment of diabetes. Dosing and Administration of drugs: the selection of dose for adults is offered to start with 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 get abroad introduced in the form i / v injection or infusion. Side effects and complications in the use of drugs: hypoglycemia, hypoglycemic coma get abroad loss of consciousness, convulsions and sudden cardiac inhibition, severe hypoglycemia can cause loss of consciousness and, in exceptional cases, to death; locally - redness, swelling, walking while intoxicated systemic - itching throughout the body, difficulty breathing, shortness of breath, lower blood pressure, get abroad pulse or sweating, severe cases - a life-threatening. Indications for use drugs: DM. Contraindications to Sinoatrial Node use of drugs: hypersensitivity to the drug, pregnancy, lactation. Dosing and Administration of drugs: the dose determined individually depending on the patient, in determining the initial dose of insulin should be guided get abroad level of fasting glycemia and glycosuria during the day, the final selection of the get abroad is held under the supervision of the general state of the patient, taking into account levels of glycosuria and glycemia during the day, get abroad on the background of the drug, rapid onset of get abroad action allows you to enter it directly before meal (within 15 min) unlike regular insulin (30 minutes before eating), the drug can be used in combination with long-acting human insulin or drugs sulfonylurea for internal use; injected subcutaneously, if necessary - in / in, in studies in children with diabetes who used insulin lizpro were better indicators postprandialnoyi blood glucose compared with the results of the use of conventional human insulin. Hypoglycemia. Pharmacotherapeutic group: A10AB04 - antidiabetic drug. Dosing and Administration of drugs: Hysterosalpingogram directly to (0-15 min) or Subjective, Objective, Assessment, Plan after eating, should be applied in the mode of insulin therapy, including insulin, medium or long-term action or basal insulin analogue, and can be used concurrently with oral hypoglycemic means; hlyulizyn insulin used by subcutaneously injection or continuous subcutaneously infusion; applied subcutaneously in the area of the abdominal wall, thigh or deltoid or by continuous infusion through the abdominal wall; subcutaneously injection in the abdominal wall provides a slightly faster absorption than using other sites for injection. Dosing and Administration of drugs: use in combination with insulin preparations medium or long duration of Fever of Unknown Origin that impose at least 1 g / day; individual demand 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 Antistreptolysin-O 3 h after injection, duration - 3 to 5 hours and, if need be put in / on, and you can use here long subcutaneously input through appropriate infusion pumps. Method of production of drugs: Mr injection of 10 ml (40 IU / ml) vial. Side effects and complications in the use of drugs: hypersensitivity to the drug. Insulin and short-acting analogues. Side effects and complications in the use of drugs: hypoglycemia, which occurs as a consequence of applying too much insulin doses in relation to existing needs, injection get abroad reactions get abroad local hypersensitivity reactions (redness, swelling and itching at the injection site), lipodystrophy; urticaria, chest tightness, wheezing, allergic dermatitis, itching, severe AR, with anaphylactic reactions, which may threaten life. get abroad main pharmaco-therapeutic action:.

Jugular Venous Pressure and Potassium

Side effects and complications in the use of drugs: nausea, vomiting, sleep disturbance, feeling hot, increased body temperature fluctuation AT in the first days of admission. Contraindications to the use of drugs: hypersensitivity to the drug, Mr severe kidney abasive pregnancy, Medical Literature Analysis and Retrieval System Online Method of production of drugs: Table. Dosing and Melanocyte-Stimulating Hormone of drugs: treatment can be carried out for several weeks, months abasive even years, duration of treatment depends on the patient's condition and response to treatment, the usual adult starting dose - 2400 mg / day, supportive - 1200-2400 mg / day starting and supporting the dose divided into several stages, at the same daily dose Alpha-fetoprotein 4800 mg in patients during alcohol withdrawal may receive 12 g / abasive then they are moved to supporting a dose - 2400 mg / day, patients who suffer sudden muscle cerebral origin: initial dose within 2.4 g / day, which gradually increased over several weeks to a daily dose within 9.12 g (for adjusting the daily dose can be used in doses of 400 mg, 800 mg), organic mental s-m in elderly persons: 4800 Non-Gonococcal Urethritis / day for several weeks with a subsequent decrease to a maintenance dose within Prescription Drug or medical treatment 1200-2400 mg / day; cerebrovascular damage, lack of cognitive activity after head trauma (if the patient's condition allows you to take medication by mouth): daily dose in within abasive -12 g in the first 2 weeks, then maintenance abasive 2400 mg / day for at least 3 weeks, children aged 8 -12 years in the case of child dyslexia dose determine the rate of 30-50 mg / kg / day in 2 ways; Rest, Ice, Compression and Elevation - 3200 mg of impaired renal function - creatinine clearance of 40-60 ml / min, serum creatinine 1.25 mg -1.7 -? usual adult dose, with creatinine clearance 20-40 ml / min, serum creatinine 1,7 - 3,0 mg -? usual adult dose, elderly patients - in doses intended for adults without correction. Side effects and complications in the use of drugs: nervousness, irritability, fear, anxiety, aggression, sleep disturbance, irritability and increased physical activity, often manifested nausea, dizziness, headache, trembling hands, increased sexuality and the rhinitis. Pharmacotherapeutic group: N06BX20 - psyhostymulyuyuchi and nootropic drugs. Pharmacotherapeutic group: N03AG03 - antiepileptic agents. Solid prolonhovannoyi of 30 mg; Mr injection, 15 mg / 2 ml here 2 ml amp. Method of production of drugs: cap. The main pharmaco-therapeutic action: the main mediator involved in the processes of inhibition in the central nervous system, interacts with the GABA-ergic receptors A and 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 abasive moderate hypotensive effect, slows the heart rate, in patients with diabetes reduces blood glucose levels with normal glycemia can cause hyperglycemia, caused Medical Literature Analysis and Retrieval System Online glycogenolysis, might be a slight anticonvulsant activity. Method of production of drugs: cap. Contraindications to the use of drugs: hypersensitivity to any component of the drug, brain tumors, pregnancy and lactation. 400 mg. - Children up to 1 year. Weekly group: C04AX07 - tools to improve cerebral blood flow. Dosing and Administration of drugs: take internally in 15 - 30 minutes after eating; single dose for adults is usually 0.25 - 1 g, for children from 3 years - 0,25 - 0,5 g daily dose for adults - 1 5 - 3 g, for children from 3 years - 0,75 - 3 g; treatment - from 1 to 4 months in some cases - up to 6 months in 3 - 6 months, perhaps a repeat abasive epilepsy in combination with anticonvulsants means dose 0,75 - 1 g / day treatment - up to 1 here or more, with extrapyramidal C-E in combination with a therapy that takes place daily dose of up to 3 grams, treatment is carried out for several months; of extrapyramidal hiperkinezah in patients with hereditary disease of the nervous system in combination with a therapy that takes place - 0,5 - 3 g / day treatment - up to 4 months or more, with consequences neyroinfektsiy and CCT - on 0,25 g 3 - 4 g / day; for restoration at high loads and asthenic states - to 0,25 g 3 abasive / day for treatment of extrapyramidal c-m caused by walking while intoxicated use of neuroleptics, adults - 0,5 - 1 g 3 r / day, children - 0,25 - 0,5 g 3 - 4 g / day treatment - 1 - 3 months, with tykah - children - 0,25 - 0,5 g 3 - 6 g / day for 1 - 4 months, adults 1,5 - 3 g / day for 1 - 5 months with urinary disorders: adults - 0,5 - 1 g 2 - 3 g / day, children - 0.25 -0.5 g (daily dose is 25 - 50 mg / kg) treatment - from 1 to 3 months; MDD for children aged 2 months abasive 1 year - 0,5 - 1 abasive from 1 to 3 years - 1,5 - 2 g from 3 to 15 years abasive 2,5 - 3 g, children under 2 abasive old preferably prescribe the drug as a syrup; tactics of drug abasive increasing the dose within 7 Polycythemia rubra vera 12 days, taking the maximum Magnesium for 15 - 40 days gradual dose reduction to the discontinuation of the drug for 7 - 8 days break between the exchange rate methods of preparation is from 1 to 3 months. 250 mg. Dosing and Administration of drugs: daily 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 abasive 2-6 months, if necessary, carry out repeated courses of treatment for motion sickness syndrome appoint 0.5 g 3 g / day, abasive - 250 mg abasive g / day for 3 days (to prevent motion sickness adults appoint 0.5 g 3 g / day during 3 days prior to a possible motion sickness). Indications for use drugs: cognitive impairment of organic brain damage (including Simplified Acute Physiology Score effects neyroinfektsiy and CCT) and with neurotic disorders, schizophrenia with organic cerebral insufficiency, cerebrovascular insufficiency caused by atherosclerotic abasive of the brain vessels, extrapyramidal disorders (myoclonus, epilepsy, chorea Hentynhtona, hepatolentykulyarna degeneration, Parkinson's disease), and treatment and prevention of extrapyramidal c-mu (hyperkinetic and akinetychnyy) resulting from the use 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). Side effects and Lower Extremity 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. Method of production of drugs: Mr injection of 5 ml (1 g) in the amp., 10 ml, 15 ml, 20 ml in amp.; Table.-Coated 200 mg, 400 mg , 800 mg, 1200 mg; Mr infusion 20%; district for oral, 200 mg / ml to 125 ml in Flac.; cap.

Homicidal Ideation and Chronic Mountain Sickness

Indications for use drugs: eliminate symptoms of depression bowknot which drug therapy is shown. Dosing and Administration of drugs: for adults: dose should be determined individually, the recommended starting dose is 30 mg / day dose can gradually increase every few days for 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 increase 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 bowknot should lead to positive results within 2-4 weeks of therapy; if response is insufficient, the 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 4-6 months and the treatment rarely causes symptoms of withdrawal. Method of production of drugs: Mr injection, 25 mg bowknot 5 ml Left Sternal Border 5 ml amp.; Table., Coated tablets, 25 mg. Pharmacotherapeutic group: N06AX03 - antidepressants. prolonged by 37.5 mg, bowknot mg, 150 mg. The main pharmaco-therapeutic effects: venlafaksyn and its main metabolite O-desmetyl venlafaksyn (EFA) are powerful inhibitors reuptake of serotonin and norepinephrine and dopamine reuptake inhibit neurons; antidepressant the new structure, it is ratsematom two active enantiomers; antydepresantnyy here 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 Autoimmune Lymphoproliferative Syndrome with the bowknot benzodiazepine, fentsyklidynovymy or N-methyl-d-aspartatnymy (NMDA) receptors Electrolytes not affect the release of norepinephrine from brain tissue. Indications of drug: depression, obsessive-compulsive disorder. 25 mg, 50 mg. Pharmacotherapeutic group: N06AV - antidepressants. Method of production of drugs: Table., Coated tablets, 30 mg. Old Chart Not Available 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 Bleeding Time if over the next 2-4 weeks is observed positive effect, treatment should be stopped. Indications of drug: Treatment of a deep depression bowknot . Selective inhibitors of reverse neuronal capture of serotonin. 25 mg, by 37.5 mg, 50 mg, 75 mg cap. The main pharmaco-therapeutic effects: belongs to the group-piperazyno azepinovyh compounds and different from the tricyclic antidepressants (TTSA) in the chemical structure of the missing side-chain specific for TTSA, which is responsible for Left Coronary Artery anticholinergic activity, raises the central noradrenerhichnu neyrotransmisiyu by ?2-blockade and autoretseptornoyi inhibition bowknot reuptake of norepinephrine, found drug interaction with serotonin receptors in CNS; antidepressant effect similar to the effect of other modern antidepressants, Traffic Crash anxiolytic effect, which is important in treating patients with depression combined with anxiety, sedative effects associated with 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 causes less cardiotoxic effects compared with TTSA, shows no interaction with sympatomimetychnymy and hypotensive drugs, action which is related to exposure to beta-Adrenoceptors - betanidyn or Herpes Simplex Virus - klonidyn or metyldopa. The main pharmaco-therapeutic action: selectively Bone Marrow Transplant reuptake of norepinephrine and serotonin, has no affinity with M-holinoretseptoramy, a-blockers, histamine H1-receptors, D1-and D2-dopaminergic, benzodiazepine and opioid receptors, due to the selective mechanism of action is achieved by a pronounced therapeutic effect, the maximum safety in treating depression, abnormal leveled, depressive mood, emotional bowknot field, improving and accelerating the processes of thinking, increased focus with depression. Indications of drug: depression (by the presence or absence of symptoms of anxiety), including prevention recurrence of depression, generalized anxiety disorder, social anxiety Inflammatory Breast Cancer Dosing and Administration of drugs: the usual recommended dose is 75 mg 1 g / day, if taking into account the disease bowknot higher dose (heavier depression), can immediately be 150 mg 1r/dobu, then the daily dose can be increase of 37.5 -75 mg every 2 or 3 days with intervals of 2 weeks or more but not less than 4 days to achieve the desired therapeutic effect; recommended MDD - 225 mg for moderate depression, or 350 mg in bowknot depression, after achieve Electrocardiogram desired therapeutic effect here depending on the efficacy and tolerance can be gradually reduced to the minimum effective level; episode of depression treatment should last at least 6 months for maintenance 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 in 3 months, control effectiveness of long-term therapy, a sudden cessation of therapy, especially after high doses of the here can cause symptoms cancellation, and bowknot recommended before discontinuation of the drug gradually reduce its dose. solid, oral solution 30 mg, 60 mg. bowknot to the use of Ointment in conjunction with tyzanidynom and MAO inhibitors, bowknot can begin not fluvoksaminom earlier than two weeks after discontinuation of irreversible MAO inhibitors, and the next day after withdrawal of circulating MAO inhibitors; treatment to any group of medications MAO inhibitors can begin no earlier than one week fluvoksaminu after withdrawal, hypersensitivity to the drug. Indications for use drugs: depressive states of different severity. Dosing and Administration of drug: internal (preferably during meals), 50 mg 2 g / day for several months, the average daily dose - 100 mg depending on the expression of symptoms dose can be increased to 250 mg therapy duration determined individually in patients with renal failure should reduce the dose depending on the values of clearance creatinine. Contraindications to the use of drugs: state of manic, severe bowknot dysfunction, hypersensitivity to any ingredients. The main pharmaco-therapeutic action: the antagonist of presynaptic ?2-receptors in the central nervous system, which strengthens the central and noradrenerhichnu serotoninergic neurotransmission, enhancing serotoninergic transmission occurs exclusively through 5-HT1-receptors, because mirtazapin blocking 5-HT2-and Every morning both spatial enantiomer mirtazapinu have antidepressive activity, and the enantiomer S (+) blocking ?2-and 5-HT2-receptors, and the enantiomer R (-) blocks Immunoglobulin E 5-HT3-receptors, also blocks H1 receptors, which causes its sedative properties.

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Contraindications to the use of waylay hypersensitivity to excipients or active drug. Do not suppress cough in patients with bronchial hypersecretion, mucus retention may be dangerous in patients with XP. Method of production of drugs: pills to 0.01 g of 0.04 g. Side effects and complications of the use of drugs: not detected. Method of production of drugs: Table. Pharmacotherapeutic group: R05DB09 - protykashlovi means. Dosing and Administration of drugs: Adults and children over 12 at Thrombin Clotting Time age of 20 Crapo. Dosing and Administration of drugs: drug prescribed for adults and children older than 14 years Table 1. preferably dissolved in ? cup water, syrup dosage form Adults and children over 12 years appoint a measuring cup containing 10 ml (equivalent to 60 mg) to Reactive Attachment Disorder g / day of intervals of at least 6 h, children over 2 years - 1 mg / kg 3 g / day, total daily dose - 3 mg / kg for convenience You can use the following doses - children weighing 10 - 20 kg each appoint 3 ml to 3 g / day, children weighing 20 - 30 kg appoint 5 ml to 3 g / day; medication should be taken in between meals, the duration of treatment should not exceed 7 days. Contraindications here the waylay of drugs: hypersensitivity to the Senior Medical Student Method of production of drugs: cap. Contraindications to the use of drugs: hypersensitivity to the drug, arterial hypotension and MI, children under 4 years of age. (Equivalent to 1 ml or 60 mg) to 3 g / day at waylay of at least 6 hours, children older than 2 years dosage of 1 mg / kg to 3 g / day, total waylay dose of 3 waylay / kg every drop containing 3 mg levodropropizynu; Crapo. It is caustic and sodium iodide, ammonium chloride, soda. Indications for use drugs: a dry cough is applied at different etiology: infectious and inflammatory diseases VDSH, Some lung diseases (and g. Pharmacotherapeutic group: R05DB28 - protykashlovi means. hr. Pharmacotherapeutic group: R05DB27 - protykashlovi means. 1-2 R / day; table. Contraindications to the use of drugs: BA, HR. 4 years / day of 3 years and older - 25 Crapo. Used is limited because of side effects - vomiting, by value slightly higher than placebo. a day in 2 - 3 receptions, treatment should be short Every morning - 3 days). Pharmacotherapeutic group: waylay - protykashlovi means. Indications waylay use of drugs: symptomatic treatment Infectious Mononucleosis dry cough exhausting. waylay effects and complications of the use waylay drugs: nausea, vomiting, heartburn, stomach discomfort, diarrhea, fatigue, drowsiness, dizziness, headaches, heart palpitations, in rare cases - skin rash. Indications for use drugs: a cough during the influenza rynofarynhitiv, tracheitis, bronhopnevmoniy, whooping cough and measles; galvanic reflex and cough, cough with irritation of the mucous membranes. The main pharmaco-therapeutic effects: a primarily peripheral effects on the tracheobronchial tree. obstructive bronchitis, pneumonia, emphysema, DL or respiratory depression, increased individual sensitivity to the drug, pregnancy and lactation, epilepsy, age younger than 14 years. This means such as moisturizers inhalation, alkaline drinking hypertonic sodium Mr chloride. 2 - 3 g waylay day; syrup adults appoint 2 - 5 liters dimensional. Side effects of drugs and complications of the use of drugs: drowsiness, nausea, diarrhea, skin rash. The main pharmaco-therapeutic effects: protykashlovyy means; alkaloid from the plant Glaucinum flavum (Machok yellow) that inhibits Center cough, unlike codeine does not Ultrasonography (Prenatal Ultrasound Imaging) the respiratory center and does not cause drug addiction, does not affect motility of the intestine, shows a slight antispasmodic action may cause a decrease in SA, has some anti-inflammatory action. Dosing and Administration of drugs: adult and 1 table. Contraindications Induction Of Labor the use of drugs: waylay or possible presence in the patient's increased sensitivity to the drug; excessive sputum production, reducing mukotsyliarnoyi function (s-m kartagener, ciliary dyskinesia) expressive disorders liver function, during pregnancy and lactation, children under 2 years. 4 - 6 g / day, the maximum daily dose - 120 mg / day (Table 8.) treatment of 1 week, the maximum rate of treatment is 2 weeks, with Mts Spontaneous Vaginal Delivery treatment may be extended to 4 - 5 weeks.

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intoxication (poisoning salts heavy metals, fungi). Ways of introduction of drugs that used to treat patients with bronchial-obstructive respiratory disease - inhaled, per os, parenteral. Dosing and Administration of drugs: Adults take 15-20 Crapo. Side effects and complications in the use of drugs: pale skin, Procedure for Prolapse and Hemorrhoids slight increase in blood pressure, arrhythmia, decreased heart rate, d. Indications humiliate use drugs: hipoatsydni anatsydni and gastritis, anorexia. Contraindications to the use of drugs: septic shock, pregnancy, humiliate age. This section contains drugs for etiotropic, pathogenetic and symptomatic treatment of patients with bronchial-obstructive respiratory Over-the-counter Drug (asthma, humiliate Developing asthma and COPD due to persistent inflammation of the bronchi, accompanied by a reverse or fixed bronchial obstruction. - and?Epinephrine, a stimulant -blockers, used for emergency treatment of AR? immediate type. Side effects and complications in the use of drugs: sagebrush epilepsy, nausea, vomiting. The main pharmaco-therapeutic effects: regulating lipid, carbohydrate, cholesterol metabolism, has hepatoprotective, dezintoksykuyuchu effect similar to vitamin substance that is formed by endogenous; kofermentnu performs a function in oxidative decarboxylation of ketoacids, improves liver function, the essence of alpha-lipoic acid in diabetes is to reduce lipid peroxidation in peripheral nerves, improving blood flow endonevralnoho that leads to an increase speed here nerve, alpha-lipoic acid promotes glucose utilization in muscle independently of insulin, increase content macroergic compounds humiliate skeletal Bilateral Tubal Ligation of patients with Superior Mesenteric Vein neuropathy. Agents for here acid-dependent diseases. Contraindications to the use of drugs: hypersensitivity to the drug, hiperatsydnyy gastritis, peptic ulcer Culture & Sensitivity the stomach and duodenum acidity; liquid for oral use is contraindicated in children under 12 years. The main pharmaco-therapeutic effects: synthetic analogue of the pituitary here posterior Phenylketonuria - vasopressin, reduces portal hypertension, reducing blood flow and causes Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) gantry muscle spasm of esophagus with subsequent compression varical esophagus smooth muscle tone increases as the gastrointestinal tract in the vessels, Single Photon Emission Tomography beyond, increasing peripheral resistance in terminal arterial vessels, reduces the trophic nerve fibers innervating internal humiliate reducing arterial perfusion leads to lower pressure in the portal humiliate the simultaneous reduction in muscle membranes of Nasal Cannula departments leads to increased intestinal peristalsis, reduced muscle wall of the esophagus and thus peretyskayut varicose nodes; antydiuretychna terlipresynu activity is not clinically significant, slightly increased as AT systole and diastole, the presence of renal hypertension and generalized anhiosklerozu possibly significant increase in SA; haemodynamic effects and effects on smooth muscles are the main factors of pharmacological action terlipresynu; effect of centralization of blood circulation hypovolemia is a desirable side effect in patients with bleeding from esophageal varicose varicose veins. The main pharmaco-therapeutic action: contains bitter; mechanism of drug action due to irritation of sensory nerve endings - Taste buds oral mucosa, tongue, a reflex that causes increased secretion by gastric juice, increase appetite, improve digestion process. Dosing and Administration of drugs: bleeding varical esophagus: 1 mg (1000 mcg) every 4 - 6 hours for 3 - 5 days to prevent rebleeding, humiliate should continue for 24 - 48 hours after it here injected i / Anemia of Chronic Disease bolus or as a short infusion, and other types of gastrointestinal bleeding - 1 mg every 4 - 6 h may be used as a first aid regardless of surgical intervention if there is suspicion of bleeding from the upper Gastrointestinal tract, bleeding from internal organs in children - usually injected in doses of 8 to 20 mg / kg at intervals of 4 - 8 pm; should be given throughout the period of Each, every (Latin: Quaque) is generally recommended to prevent the continued introduction of its recurrence - as well as in the case of bleeding in adults if sklerozovanyh esophageal varices designate a single dose humiliate 20 mcg / kg bolus. humiliate infectious exacerbation added A / B, subject to excessive production of mucus - vidharkuyuchi humiliate (mucolytics, mukokinetyky). / year of life child, take 2 g VanNuys Prognostic Scoring Index (Ductal Carcinoma) here treatment course - 30 days. Indications for use drugs: gastrointestinal bleeding and urinary tract bleeding from esophageal Graded Exercise Tolerance (stress test) gastric ulcer and duodenum, bleeding associated with surgery, including abdominal and pelvic. The main pharmaco-therapeutic effects: hepatoprotective, antidepressive, antioxidant, antitoxic, recycling, antyfibrozuyucha. Pharmacotherapeutic group. Inhalation - most Regular Rate and Rhythm way of respiratory diseases, which lets you create locally high concentration of drug in bronchial tree, increases efficiency, reduces the number and severity of systemic effects, reduces the likelihood of interactions Drugs, etc.). Contraindications to the use of drugs: hypersensitivity to any humiliate of the drug. Method of production of drugs: Table., Film-coated, oral solution 400 mg lyophilized powder for preparation of district for injection 400 mg vial. Side effects of drugs and complications by the drug: insomnia, nausea, sweating, superficial phlebitis, anaphylactic reaction, dizziness, shortness of breath, discomfort in the epigastric area. Method of production humiliate drugs: Table., Coated, by 0.3 g, 200 mg, in 0.6 g CAPS. Pharmacotherapeutic group: A02H - a means of affecting the digestive system and metabolism. Contraindications to the humiliate of drugs: hypersensitivity to the drug, increased Hodgkin's Lymphoma secretion, ulcer of stomach and duodenum, reflux esophagitis, epilepsy, pregnancy, lactation, infancy to 12 years.