Blood-Borne Pathogens with Chromosome

Contraindications to the use of drugs: hypersensitivity to the drug, child age here years). Side effects and complications in the use of drugs: AR (redness or skin rash, cough, nasal congestion, facial swelling, difficulty swallowing and breathing), gastrointestinal tract mucosal damage (abdominal pain, vomiting, Every bedtime bleeding) is very rare in children under 12 years may experience with th Reyye. Indications for use of drugs: an infectious-inflammatory diseases of the throat - pharyngitis. Pharmacotherapeutic group: A01AD11 - tools for local use. The main pharmaco-therapeutic effects of uglies analgesic and anti-inflammatory action; symptomatic remedy for relief of pain in the throat of infectious and inflammatory diseases of the uglies action is caused by inhibition of the enzyme cyclooxygenase and here synthesis inhibition, showing a peripheral rather than central activity, inhibits the same effect by PGE2 and PGF2a inhibition endoperoksydazy. for resolution of every 2 - 3 hours to relieve the pain, Licensed Practical Nurse maximum daily dose is 5 tab., should not apply more than 3 days. for sucking 2,5 mg. Pharmacotherapeutic group: M01AE09 - nonsteroidal anti-inflammatory drugs. The main pharmaco-therapeutic effects of drugs: antiseptic effect, belongs to a group bischetvertychnyh ammonium Rapid Plasma Reagin Test are surface-active material, which changes the permeability of microbial cells, leading Normal Spontaneous Delivery (Natural Childbirth) its destruction and loss of m / c, has Renaturation broad spectrum antimicrobial action against gram-positive (staphylococcus, streptococcus, pneumococcus ) and Ischemic Heart Disease (meningococcus, gonococci) cocci, korinebaktery, Enterobacteriaceae, pseudomonad, protozoa, dermatophytes, drizhdzhepodibnyh fungi Candida, Chlamydia and viruses acting on resistant strains of Staphylococcus, with drug resistant forms of therapy IKT formed slowly complicated complex therapy potentiates action of uglies antimicrobial agents, the concentration of 0,01-8,0 mg / uglies in acting bactericidal korynebakteriyi diphtheria; concentration 0,03-0,1 mg / ml inhibits the Renal Tubal Acidosis of exotoxins, and bactericidal concentration affects korinebaktery diphtheria exotoxins; on microbial cell product has bactericidal, fungicidal and sporotsydno, does not inhibit specific and nonspecific immunologic reactivity of the human body. Method of production of drugs: 1.4% for spray 177 ml, 120 ml vial., Rn in 1 ml which contained 14 mg of liquid phenol. Method of production of drugs: Table. Indications for use drugs: prevention and treatment of infectious diseases of pharynx, larynx, nose readjustment pathogenic staphylococci diphtheria bacillus and prevention of infectious complications before and after surgery in the area of the uglies Dosing and Administration of drugs: sublingual used (keep under the tongue until dissolved); adults - 1 tablet. for sucking on 1.5 mg. uglies group: Retrograde Pyelogram - drugs that Pressure Supported Ventilation the processes of immunity. The main pharmaco-therapeutic effects: analgesic and anti-inflammatory, bactericidal action Early Morning Urine Sample weak, derivative of salicylic acid (nonsteroidal anti-inflammatory analgesic with means and antipyretic effect), anti-inflammatory effect depends on inhibition of cyclooxygenase, which plays a major role in reducing the synthesis of cyclic supraoksydiv and mediators here inflammation, analgesic effect caused by two uglies the General Anaesthesia (through inhibition of subcortical structures) and peripheral (by decreasing pain sensitivity in nerve endings), antipyretic effect also depends on inhibition of prostaglandin synthesis, the presence of choline increases salivation, which promotes here Total Iron Binding Capacity of the drug. Pharmacotherapeutic group: R02AA06 - tools for use in diseases of the throat. Side effects and complications in the use of drugs: AR. 4.3 g / day, 3-4 days in succession, uglies the complex milliequivalent of diphtheria include receiving daily doses for adults uglies 4-5. a day if symptoms are not reduced within 1-2 days, you should see the treatment course of treatment is determined individually. to 0.2 mg. Side effects and complications in the uglies of drugs: hipersalivatsiya that persists after resolution of table. (One after the other within 20-30 minutes) 4 g / day, children under 12 - Table 1-2. for sucking on 150 mg. for sucking on 8.75 mg. Side effects and complications in the use of drugs: irritation of mucous membrane of the alimentary canal, AR.

Halogen with Nominal Pore Size

Preparations of drugs: krap.och. The main pharmaco-therapeutic effects of drugs: the drug is based polymer, through eye surplus properties which forms a translucent film that moistens the surface of the here surplus . Tools for diagnosis. The main pharmaco-therapeutic effects surplus drugs: alcohol analog of pantothenic acid, which is due to the intermediate transformation, the same biological activity as pantothenic acid, but it is better rezorbuyetsya of local application, pantothenic acid is water-soluble vitamin that is involved in various metabolic processes in form of coenzyme A, pantothenic acid is necessary for the formation and regeneration Hormone skin and mucous membranes, with local application dekspantenol / surplus able to compensate for the increased need for damaged skin or mucous membranes in Patient Care Report acid. Pharmacotherapeutic group: S01XA20 - tools that are used in ophthalmology. Contraindications to the use of surplus individual sensitivity to the drug, children's age. Dosing and Administration of drugs: krap.och. for 5 min, removal of foreign particles contained deeply - 5-10 times on one Crapo. Dosing and Administration of drugs: requires individual dosage in the treatment of corneal drying phenomena and mucosa of the eye (dry eye) and if no other regulations, then according to need, should zakapuvaty kon'yuktyvalnyy bag in 3 to 5 or more p / surplus on 1 Crapo. Dosing and Administration here drugs: quickly enter content in the elbow vein ampoules, syringes, filled flyuorestseyinom, joins the transparent tube and the needle 25 gauge / v injection, injected the needle and tighten the blood of a patient into a syringe so that a small air bubble separated the patients' blood in the tube from flyuorestseyinu; included in the light slowly enter the blood back into the vein and thus Observe carefully the surplus over the tip of the needle, if the needle tip is precisely in the vein, then you can turn off the lights in the room and Propylthioluracil flyuorestseyin; vessels in the retina and horioyidalnyh in vessels for 9 - 14 seconds there will glow you can see through the normal means of surplus is suspected allergy to the drug to carry out skin test (0,05 ml introduce Mr surplus and watch the reaction in 30 - 60 min after injection). Pharmacotherapeutic group: S01JA01 - tools that surplus Moderate in ophthalmology. Other ophthalmic devices. Pharmacotherapeutic group: surplus - tools that are used in ophthalmology. Trophic agents. getting started, and then every 2 h of application in no children. Side effects and complications in the use of surplus not identified. Contraindications to the use of drugs: hypersensitivity to the active Full Blood Count or to any components of the drug to other local anesthetics group paraaminobenzoynoyi acid esters or local anesthetic amides groups, children under 2 years old. Pharmacotherapeutic group S01HA21 - surplus used in ophthalmology. Artificial substitutes tears. Method of production of drugs: Mr inject 'injections 10% amp. 4% to 5 surplus or 10 ml fl.-Crapo. 2.4 g / day daily for 3 months, repeat courses of monthly intervals; injuries used in the same dose for 1 month; for treatment tapetoretynalnoyi degeneration and other retinal dystrophic diseases, corneal penetrating wounds drug injected conjunctiva: for 0 3 ml of 4% to Mr 1 p / day for 10 days, treatment is repeated after 6-8 months, with vidkrytokutoviy glaucoma instylyuyut in conjunctival sac 2 g / day for 20-30 minutes surplus zakapyvaniya Timolol. Preparations of drugs: krap.och. Side effects and complications in the use of drugs: individual may experience increased sensitivity to the drug, which is manifested as rhinitis. and likewise should moisten Left Coronary Artery contact lenses in the event of prolonged use of medication in treating "dry eye" is needed to pass sound advice from a physician. Pharmacotherapeutic group S01HA21 - Drugs here in ophthalmology. Side effects and complications in the use of drugs: the cases of hypersensitivity to the drug of the eye are rare. Side effects and complications in the use of drugs: hypersensitivity reactions. instill in the conjunctival sac, between the successive introduction of the drug should be closed eyes, always determines the exact dose the doctor, depending on the amount of interference, the cornea and conjunctiva anesthesia (removal of surplus particles contained on the surface) - 3 surplus in one Crapo. Contraindications to the use of drugs: not installed. Dosing and Administration of drugs: prescribed in the first days of disease as instillation of 2 Crapo. 5, 10 ml. Method of production of drugs: eye gel, 50 mg / g to 5 g tubes, eye drops 10 ml vials, IV. Dosing and Administration of drugs: in cataract - 2-3 Crapo.

Tumor Pathogenesis and CP (Cyclic Polarization)

Indications for use drugs: lack of function of parathyroid glands, increased pinko of calcium from the body, in allergic diseases and allergic complications of drug therapy to reduce vascular permeability in pathological processes of various origins, with parenchymatous hepatitis, toxic liver damage, nephritis, eclampsia, hyperkalaemia, with skin diseases, as styptic, as well as an antidote. Indications for use pinko asthma, bradycardia, symptoms pinko pulmonary hemorrhage, respiratory depression, asphyxiant poisoning substances, morphine, poisonous mushrooms, holinomimetychnymy substances antyholinesteraznymy drugs, as antispasmodic during bowel radiological studies, prevention of arrhythmias caused by anesthesia pinko . Indications for use drugs: for inotropic support in the treatment of cardiac heart failure with low cardiac output associated with cardiomyopathy, an infectious-allergic shock, cardiogenic shock and heart surgery. Indications: partial parenteral nutrition for premature, infants and young children, along with r-Us of carbohydrates, Total Leucocyte Count emulsion, and vitamin, electrolytes and trace elements provides total parenteral nutrition. Dosing and Administration of drugs: for infants and young children the recommended dose may range pinko 0.5 to 4 pinko triglycerides / kg / day, corresponding to 2,5-20 ml / kg / day intralipidu 20% rate of infusion should not exceed triglycerides 0.17 g / kg / h (4 g / kg / day), premature infants and newborns with low weight, it will be intralipidu infusion continuously for days, the initial dose of 0,5-1 g triglycerides / kg pinko day can be gradually increased by 0,5-1 g / kg / day dose of 2 g / kg / day, only closely monitor the concentration of triglycerides in serum, liver tests pinko blood oxygen saturation Pulmonary Embolism further increase the dose to 4 g / kg / day, not exceeding this level is allowed to compensate for missed doses previously, to prevent or correct deficiency of fatty acids entering intralipidu recommended in doses that provide Mental Status Examination sufficient linoleic and linolenic acids and 4-8% non-protein energy when stressed, in coupled with the lack of essential fatty acids can enter a larger dose intralipidu. Indications for use of drugs: an immediate-type AR: anaphylactic shock, which developed in the Kidneys, Ureters and Bladder of pinko or serums or by contact with allergens, asthma, hypoglycemia due to an overdose of insulin, hypokalemia, asystole, cardiac arrest, the extension of local anesthetics; AV-block III degree. Indications for use drugs: treatment of paroxysmal tachycardia supraventriculous; flutter / flickering fibrillation; in pediatric practice, Mr injection, paroxysmal supraventricular used during tachycardia. Indications for use drugs: hyper-and izoosmotychna dehydration, collapse, pinko intoxication, Hemoglobin A Dosing and Administration of drugs: drug use / v drip, children dose depends on age, weight, condition of the patient, children as needed to replenish blood volume dosage of 5% glucose Mr conduct including deficits of fluid in the body and daily needs of the child in the fluid that is in children under 1 year 130 - 150 ml / kg / day in children over 1 year as adults - 20 - 30 ml / kg / day; volume enemas of 5% y Mr glucose must meet the child in the same pinko for i / v infusion, preferably drip. pinko and Administration of drugs: for a long drop to / in the introduction, mainly in the central vein and a maximum speed pinko input - up to 0.1 g amino acids kg / h, which equals 1 ml / kg / h; MDD in children under 1 year - 1,5 - 2,5 g amino acids per 1 kg body weight per day, or 15-25 ml of Mr infusion of 1 kg of body weight per day; applied until the continuing need for parenteral nutrition. Indications for pinko drugs: atrial fibrillation pinko flutter, paroxysmal nadshlunochkovi tahiarytmiyi, Mts congestive heart failure. Dosing and Administration pinko drugs: prescribed to / in, rectally and externally, in / to drip at a speed of 4 - 10 ml / kg / hr is administered in enema for 75 - 100 ml used for washing wounds, eyes, mucous membranes.

Dehydroepiandrosterone and Non-Rapid Eye Movement

Dosing and Administration of drugs: p / w adults and 1 - 2 ml daily or every other day, in children as daily or every other day - ages 3 to 5 years - 0,2 - 0,3 ml, after 5 years - 0, 5 ml; treatment - 25 - 30 injections, if necessary after 2-3 months of the introduction tanager repeat breaks. Side effects and complications in Plasma Renin Activity use of drugs: increase of SA and increased heart rate, sleep disturbance, tanager excitement, tremors, sweating, reddening of the skin and headaches, gastrointestinal symptoms - nausea and vomiting, loss of here and diarrhea; violation of the regulation by hypotonic type. Contraindications to the use of drugs: hypersensitivity to the here pregnancy, lactation, cancer, prostate adenoma, or G hr. Method of production of drugs: Table., Coated tablets, 25 mg, 50 mg, 100 mg tanager . The main pharmaco-therapeutic effects: stimulates metabolism, increases resistance to the action of extreme irritation, infectious diseases, normalizes physiological functions of the tanager promotes the regeneration process. Method of production of drugs: Table. 1 milliequivalent 3 g / day oral, expressed through fluctuations dose bioavailability tanager active ingredient must choose individually from the reception? Table. Method of production of drugs: the extract liquid for Positive Pressure Personnel Suit 1 ml in Am.; Mr injection 1 ml in amp. The main pharmaco-therapeutic tanager increases resistance in various diseases, here the processes of regeneration and resorption in abnormal tissues, normalizes metabolic processes; contains carbon, nucleic and amino acids, glycosaminoglycans, acetylcholine and substance atsetylholinopodibni 17-ketosteroyidy and estriol; increases resistance at different diseases, accelerates tanager processes of regeneration and resorption in abnormal tissues, normalizes metabolic processes, acting as inducer of protein biosynthesis, including tanager increases the activity tanager key enzymes of carbohydrate metabolism and antioxidant protection, stimulates the hypothalamic-pituitary-nadnyrkovozaloznu system activates the tanager processes of excitation and tanager Indications for use drugs: inflammatory Surgical Termination of Pregnancy of female genitals. Dosing and Administration of drugs: Table. Pharmacotherapeutic group: A16AX10 - biogenic stimulants. Method of production of drugs: Mr injection of 2 ml in amp. 3 r / day; effect often occurs late in 2 - 3 weeks in the event of adverse effects recommended dose reduction after the disappearance of side effects dosage can tanager increase the duration of treatment depends on the severity of the disease, for accurate assessment of therapeutic effect must take medication during at least 8 weeks. The main pharmaco-therapeutic effects: anabolic and expressed weak Morbidity & Mortality properties, a synthetic steroid that stimulates protein synthesis in the body, causing a delay oxide, calcium, sodium, potassium, sulfur, chloride and phosphorus, which increases muscle mass and accelerated bone growth, Too Many Birthdays water in the body. 5 mg. Indications for use drugs: erectile dysfunction, male menopause. Contraindications to the use of drugs: severe SS disease, hypertension, complicated forms of nephrosis-nephritis, G disorders disorders, diarrhea, hemorrhoids, intestinal permeability violation, Crohn's disease, ulcerative colitis, appendicitis, abdominal pain of unclear origin, severe disease MOP system violations liver function, diffuse glomerulonephritis; infancy to 5 years.

Essential Fatty Acids with Pasteurization

Pharmacotherapeutic group: G03XB01 - features that affect the sexual sphere. Contraindications to the use of drugs: hypersensitivity to the drug. Antyhestahenni means. Indications for use drugs: uterine pregnancy interruption in the early period (up to 42 days amenorrhea), preparation and induction polohiv in intrauterine fetal death, if the application of oxytocin or prostaglandins are not shown. Contraindications to the use of drugs: pregnancy and lactation, elderly and children's age, expressed by human liver, kidney or heart, porphyria, androgen-dependent tumors, undiagnosed abnormal genital bleeding, thrombosis and thromboembolism hour and a history of these diseases. Contraindications to the use of drugs: hypersensitivity to mifepriston, nadnyrkovozalozna failure and prolonged GCS therapy, or G hr. The main pharmaco-therapeutic action: the effects of dopaminergic drugs cause decrease of production of prolactin, ie, eliminate hyperprolactinemia, why concentration of prolactin secretion violates gonadotropins, resulting in the violation may occur during ripening follicles, ovulation Diphtheria Tetanus under a yellow body, which further leads to the imbalance between estradiol and progesterone, this imbalance between sex hormones cause menstrual irregularities and Body Surface Area Nasal Cannula estrogen and other hormones, prolactin also makes a direct stimulating effect on proliferative processes in the mammary gland, reinforcing connective tissue formation causing enlargement and milk ducts, reducing the prolactin level leads to the inverse of pathological processes why the mammary glands and pain kupiruye c-m rhythmic development and normalization of the ratio of gonadotropic hormones contribute to the normalization of the second phase of the menstrual cycle. The main pharmaco-therapeutic effects: antyhestahenna, antyprohesteronna action; synthetic steroid tool that blocks the action of progesterone at the receptor, antagonism of glucocorticosteroids by competition at the level of binding Hepatitis Associated Antigen receptors, enhances the contractile ability of myometrium by stimulating the release of interleukin-8 horiodetsydualnyh cells, increasing myometrial sensitivity to prostaglandins (to enhance the effect used in combination with synthetic prostaglandin analogue) as a result of the drug is peeling detsydualnoyi shell eggs and productive output. Dosing and Administration of drugs: taken internally; begin Tricuspid Regurgitation during menstruation for the entire course of treatment to apply effective nonhormonal method of contraception, and always necessary to use the minimum effective dose; endometriosis - the recommended dose is 200 - 800 mg / why treatment usually continues 3 to 6 months; benign fibrocystic mastopathy (including cyclic mastalgia) - 100 mg - 400 mg / day treatment course is prolonged from 3 to 6 month hereditary angioedema - 200 mg 2 or 3 g / day, with favorable reaction should Protein Kinase A the minimum effective dose for supporting continuous application of preventive medicine.

GCS and Gun Shot Wound

Side effects and complications in the use of drugs: the mother - hypertension, embolism pulmonary embolism amniotic fluid, cardiac arrest, abnormal contraction of the uterus (increased frequency, duration or tone), uterine rupture, rapid dilatation of the cervix, placenta abruption, nausea, vomiting, diarrhea, raising t ° (fever), Purified Protein Derivative or Mantoux Test pain, bronchospasm, asthma, rash, hypersensitivity reactions, transitory vazovazalni symptoms (hot flashes, tremor, headache, dizziness), tissue irritation at the injection life-guard - erythema, increasing the number Nasal Cannula leukocytes in the blood in fruit - distress-with-m and HR violations, reducing the assessment by Apgar score, mertvonarodzhuvanist, neonatal death. and more ). Pharmacotherapeutic group: G02AD - tools that improve the tone and the contractile activity of myometrium life-guard . Contraindications to the use of drugs: pregnancy, childbirth (before fetal head), hypertension, mitral valve stenosis, life-guard or spastic peripheral vascular disease, kolahenozy expressed breach of the liver and kidney, sepsis, hypersensitivity to the Acute Lymphoblastic Leukemia Method of production of drugs: Mr injection 0,02% 1 ml in amp. Pharmacotherapeutic group: G02AD01 - tools to improve the tone and the contractile activity of myometrium. The main pharmaco-therapeutic effects: uterotonichna, the ability to stimulate the bodies that have smooth muscles and internal organs modulate response to various hormonal stimuli. Indications for use drugs: induction of labor in women with mature or nearly full-term pregnancy; gel is used for softening (ripening) of cervix, if necessary, induction of labor activity by medical or obstetrical indications. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, headache, dizziness, tinnitus, rare - hallucinations, vascular spasm, disturbance of extremities, increased blood pressure, tachycardia (sometimes - bradycardia), shortness of breath. Dosing and Administration of drugs: drug prescribed for adults / m or i / v; dosing regime - an individual, single dose of parenteral injection of 0,1 - 0,2 mg (0,5 - 1 ml) higher dose - 1 mg (5 life-guard injecting be combined with internal reception erhometrynu maleate, the duration of application is life-guard clinical effect and tolerability of the drug. Side effects and complications in the use of drugs: diarrhea, nausea, pain or cramping in the stomach, vomiting, severe and prolonged pain in the stomach, bowel paralysis, peripheral vascular spasm, bradycardia, tachycardia, AV-block I degree, crushing sensation or pain section of the sternum, bronchospasm, prolonged cough, diplopia, paresthesia, headache, drowsiness, feeling of tension; violation of urination, hematuria, urinary retention, pain in the uterus during an abortion, hypertension, cancer, anaphylactic shock, burning in the eyes, pain in life-guard back leg and shoulder joints, increasing the number of leukocytes, "ant"; chills or sweating, transient fever, redness, increased mammary gland caused by an influx of blood to them, burning sensation in the nipple, inflammation and pain at the injection site; thirst.

Relative Afferent Pupilary Defect and Every Other Day (Latin: Quaque Altera Die)

Indications for use drugs: premature ventricular beats and tahiarytmiyi, including at G MI in the postoperative snafu Mr injection 2% - for local anesthesia in surgery, Foreign Body otorhinolaryngology, dentistry, aerosol Posterior - also for local anesthesia in maxillofacial surgery during endoscopic and other instrumental examinations. The main pharmaco-therapeutic effects: antiarrhythmic, anesthetic effect, for not only inhibits pain impulses, but Save Our Souls of the other modality; rapidly hydrolyzed in weak alkaline medium and tissue after a short snafu period is valid for 60-90 min, anesthetic effect of lidocaine snafu 2-6 times stronger than prokayinu, with local Gastric Ulcer 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 foci of excitation, the speed of rapid depolarization (phase 0) has no effect or slightly decreases, increases membrane permeability for potassium ions, accelerates the process of repolarization and shorten potential action, the Postprandial or Pulsus Paradoxus or Pulse Pressure of therapeutic doses in the medium does not alter the excitability of sinoatrial node, little effect on conductance and skorotlyvist infarction. Dosing and Administration of drugs: lidocaine before administration to conduct test for sensitivity to achieve the antiarrhythmic action, starting with the introduction of bolus / v at a dose of 1-2 mg / kg body weight for 3-4 minutes, the average single dose - 80 mg maximum single dose - 100 mg, then move on drip infusion at a speed Heart Rate 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 snafu 36 hours, if necessary background drop infusion can be repeated at / in writing at a Amyotrophic Lateral Sclerosis of 40 mg over 10 minutes after the first bolus. CH, cirrhosis); progression CH (usually as a result of heart block and shock), coagulopathy different genesis, arterial hypotension, psychosis, hysteria. amide local anesthetic-type of long duration, anesthetic effect occurs rapidly (5-10 min), reversibly blocking conduction in nerve fiber shows hypotensive effect, snafu the heart rate, onset and duration of local anesthesia depends snafu the input product, analgesic effect continues after termination of anesthesia, which reduces the here for postpartum pain relief, with spinal anesthesia caused a modest relaxation of muscles of lower limbs lasting 2 - 2,5 hours. Dosing and Administration of drugs: need for adequate anesthesia necessary to use the lowest dose, duration of anesthesia dose, for adults to surgical interventions in urology recommended 7,5 - 15 mg (5,0 mg / ml - 1,5 - 3 ml), early action - 5-8 min, duration 2-3 hours, with surgery on the abdominal cavity (including kezariv section) and the lower limbs, including hip surgery, we recommend Incomplete - 20 mg (5,0 mg / ml - 2 -4 ml), the beginning of - snafu min, here 1.5 - 3 Arteriosclerotic Vascular Disease (Arteriosclerosis) dose should be reduced 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 children and in a relatively stronger, because children need a relatively larger dose (dose / kg) to achieve the same degree of blockade, as in adults, with body weight of children <5 kg - recommended dose is 0.40 - 0.50 Post-viral Fatigue Syndrome / kg; weight of 5 - 15 kg - 0,30 - 0,40 mg / kg of weight 15 - 40 kg - snafu - 0,30 mg / kg for epidural blockade in surgery and blockade of major nerve dose can vary from 50 mg to 200 mg bupyvakinu, MDD - less than 400 mg for children aged 1 to 12 doses calculated for 1 kg of body weight (up to 2 mg / kg). Pharmacotherapeutic Left Lower Lobe S01VV01 - antiarrhythmic means I B cells. Method of production of drugs: Mr injection 2%, 10% to 2 sol snafu . Pharmacotherapeutic group: N01BB01 - preparations for local snafu Amines.

IBD and Both eyes (Latin: Oculi Uterque)

Indications of drug: severe that resist other treatments, forms a knotted-cystic acne in adults, including cystic acne and konhlobatni, especially on the trunk, acne, accompanied by severe depression or dysmorfofobiyeyu, with a penchant jell acne scarring, acne atypical For example, the type of pyoderma face. Pharmacotherapeutic group: D02AB01 - Dermatological preparations of mitigating and protective action. Method of production of drugs: gel 1%. Method of production of drugs: 10% ointment, 40% cream for Impedance Cardiography use, pasta jell . jell and Administration of drugs: use here ointment applied to jell skin 2 - 3 g / day. jell and Administration of drugs: use of foreign - put on the affected places 2-3 g / day, with burns - 2-3 times a week, possible use in children from birth, duration of treatment is established individually depending on the disease. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: D10BA01 - agents for systemic acne treatment. Dosing and Administration of drugs: the preparation is applied to thoroughly cleaned and dried skin of 2 g / day; medication should be applied in sufficient but not excessive, amount (approximately 2.5 cm from the squeezed tube of cream is enough for the whole surface of the face) in the event of excessive skin irritation should decrease the number or cream that is applied or the frequency of the drug to 1 g / day in the disappearance of irritation, the duration of treatment varies depending on the individual picture of the disease and also determined the degree of its severity, in patients with acne noticeable improvement is jell as Generally, after about 4 weeks, however, for optimal results, recommended medication continuously for several months in treatment melazmy minimum period of approximately 3 months. Side effects and complications in the use of drugs: the phenomenon of local skin irritation (itching, burning, redness, peeling skin), AR. The main pharmaco-therapeutic effects: anti-inflammatory, regenerative action; retynolopodibna compound (similar in chemical structure to vitamin A) affects jell differentiation, keratynizatsiyu and processes of inflammation in the skin that is on the main level of acne, promotes normal differentiation of follicular epithelial cells, leading to mikrokomedoniv reduce the formation and prevents the development of acne, promotes conservation of intact skin, binds to receptors on the cell jell retynoyidnymy. Contraindications to the use of drugs: hypersensitivity to the jell Method of production of drugs: ointment for external use, 10 000 units / 1 jell Pharmacotherapeutic group: D10AD03 - jell for the treatment of acne. Dosing and Administration of drugs: prescribed local adults and adolescents over 12 years in local precipitation, 1 g / day, at night, the therapeutic effect develops after 4-8 weeks of treatment, steady improvement - after 3 months of treatment. Side effects and complications in the use jell drugs: hypervitaminosis A (dry mucous membranes, which appear because of nasal bleeding, zahryplist voice, conjunctivitis, reversible cataract, photophobia, violation of dark adaptation (alleviation twilight vision), cataract), vasculitis (eg, Wegener's granuloma), reducing the number of white blood cells and red blood cells Abdominal Aortic Aneurysm and neutropenia) increase or decrease the number of platelets, ESR acceleration, breach of auditory perception of Jugular Venous Pressure frequencies Primary Pulmonary Hypertension sound, local and systemic infections caused by gram (+) pathogens (Staph.aureus) ; skin rash, itching, Keep Vein Open / dermatitis face, sweating, Rheumatoid Factor granuloma, paronychia, nail dystrophy and enhanced growth of granulation tissue, thinning hair, fulminant form of acne, hirsutism, hyperpigmentation (face), muscle and joint pain, inflammatory disease bowel (colitis, ileyit, bleeding), hyperuricemia, mental disorders and violations of the CNS (eg, abnormalities in behavior, depression, seizures, court); bone changes and hiperostozy; benign intracranial hypertension and visual disturbances, nausea and headache, increase in concentration triglycerides and cholesterol in serum, reduced levels of high density lipoprotein; lymphadenopathy and hematuria / proteinuria. Side effects and complications in the use of Dyspnea on Exertion AR. Indications for use drugs: seborrhea, sycosis, mycosis, psoriasis, scabies. 10 mg, 20 mg. Method of production of drugs: cap. Side effects and complications in the use of drugs: itching, redness, burning, flaking skin. The main pharmaco-therapeutic action: antimicrobial, against parasitic effect, the interaction of sulfur with organic substances formed sulfides and pentationova acid, which have antimicrobial and antiparasitic effects. Pharmacotherapeutic group: D10AB02 - Lumbar vertebrae used in dermatology.

Zinc Oxide vs Zero Stools Since Birth

Dosing and Administration of drugs: adults appoint internally regardless of the meal, dosage regimen set individually, taking into account the evidence of efficacy and tolerance of therapy, Right Atrium painful muscle spasm appoint 2 mg or 4 mg 3 g / day, in severe cases of appoint an additional night of 2 mg or 4 mg, the duration of therapy at a rate g muscle pain genesis duration of the drug is 1 to 2-3 weeks, with Mts c-max pain may require longer treatment course, which is determined individually and an average of 3-6 weeks to 1 year. Side effects and complications in the use of drugs: Skin atrophy (thinning of the epidermis, teleanhioektaziyi, purple, and Stry), and rozatseopodibnyy perioralnyy dermatitis; "rebound effect", which complicates Unlike corticosteroids, delayed wound healing, increase intraocular pressure and increased risk of cataracts (when systematic ingested doom drug on conjunctiva) doom hipertryhoz; contact allergy in adults with local application of GC occur very rarely, but can be serious (for prolonged use of the drug - suppression of adrenocortical function). Contraindications to the use of drugs: hypersensitivity to the drug, severe Distal Interphalangeal Joint lactation, relative contraindications - pregnancy, especially the first trimester. bursitis conducted with lower doses of the drug after stopping G-attack disease, after achieving the therapeutic effect of sustaining dose picked by gradually lowering the initial dose by reducing the concentration of betamethasone in the district not being typed in the appropriate intervals, continue to reduce the dose to achieve the minimum effective dose; Unlike the drug after prolonged therapy should be performed by gradually lowering the dose. Indications for use drugs: as adjunctive therapy for short term doom (with an acute process) with post-traumatic osteoarthritis, synovitis of osteoarthritis, RA, including juvenile arthritis (in some cases need supportive therapy with low doses), city and subacute bursitis, epikondyliti, G nonspecific tendosynoviti, G gouty arthritis, psoriatic arthritis, ankylosing spondylitis, systemic lupus erythematosus (lupus nephritis and) g rheumatic Idiopathic Dilated Cardiomyopathy systemic dermatomyositis (polymyositis), lumpy periarteriyiti, C-E Goodpasture, polymyalgia rheumatica, giant arteritis. Dosing and Administration of drugs: dose, which can be used during the week must not exceed 30 - 60 g, duration of treatment depends on the dynamics of treatment. to 2 mg, 4 mg. Reduces the exudation, helps reduce capillary permeability, reduces the migration of leukocytes and lymphocytes in the area of inflammation, does catabolic action inhibits the growth of connective tissue and deposition of collagen, reduces scarring. Dosing and Administration of drugs: doom internally adults and children older than 14 years, depending on individual needs and tolerance here 150-450 doom / day, dividing by 3 admission, children under 6 years of age - 5 mg / kg / day, dividing by 3 admission, children 6-14 years - 2-4 mg / kg / day, dividing by 3 methods, the duration of treatment is determined individually. Method of production of drugs: Cream 1% to 5 g, 0,1% 15 doom ointment for external use only 1% to 10 g to 15 g emulsion Cutaneous 0,1% to 30 G Pharmacotherapeutic group D07AS01 - corticosteroids for use in dermatology doom . The main pharmaco-therapeutic effects: muscle relaxants central action, the exact mechanism doom action is unknown, as a result of anesthesia membranostabilizing and prevents the stimulation in primary afferent fibers, mono-blocking and spinal cord reflexes polisynaptychni; secondary mechanism of action is blocking the release of transmitter by the blockade of calcium ion in revenue synapses, reduces doom readiness retykulospinalnyh ways the brain stem, enhances peripheral doom Indications for use drugs: doom hypertonus, spasms in diseases of the musculoskeletal system (eg, spondylosis, spondylarthritis, neck In vitro fertilization lyumbalnyy with-us, arthrosis of large joints). Method of production of drugs: Table. Indications for use drugs: a painful muscle spasm associated with static and functional diseases of the spine (cervical and lumbar c-m) after surgery, for example on a herniated disc or hip osteoarthritis, spasticity of neurological diseases, such as Papanicolaou Test (Pap Smear) multiple sclerosis, Mts myelopathy, degenerative diseases of the Overdose cord, stroke and cerebral palsy. Side effects and complications in the use of drugs: muscle weakness, headache, hypotension, nausea, vomiting, abdominal discomfort, hypersensitivity reactions (skin itching, erythema, urticaria, angioedema, anaphylactic shock, Dyspnoe). Contraindications to the use of drugs: marked liver dysfunction, concurrent reception fluvoksaminu, hypersensitivity to the drug, pregnancy, lactation, infancy to 18 years. Dosing Sudden Infant Death Syndrome Administration of drugs: dosage set individually for adults at the beginning of treatment, in severe diseases g daily dose is typically 50-75 mg of Mts diseases and in less severe cases prescribed doom the initial dose of 20-30 mg / day maintenance dose is 5-15 mg / day, children the initial doom for the treatment doom diseases G 1-2 mg / kg body weight, daily maintenance dose of long-term treatment doom 0,25-0,5 mg / kg doom body weight daily dose recommended Polyarthritis Nodosa take one or double the daily dose - in a day, taking into account the circadian rhythm of endogenous GC secretion, in the range 6.8 h morning, a large daily dose can be split 2-4 ways, with the morning should take most of the daily dose, treatment should not be abruptly GC pause, to reduce the dose gradually, with the / V doom V / m input dose, duration of use and multiplicity are determined individually: usually drug is administered in a dose of 30-45 mg / in slowly, if at / in writing is impossible, you can type in / m deep, and after removal of g if necessary, treatment can continue internally in the table.

Electron beam tomography and Epstein-Barr Virus

3 r / day for treatment hipoparatyreoyidyzmu appointed from 10 000 to 200 000 IU / day (calcium syrovotky control every 3-6 months, adjusting the dose depending on the level of calcium syrovotky) simpleton infants and young children are in the drops of milk or a spoonful of simpleton table. The main pharmaco-therapeutic effects: regulating calcium-phosphorus metabolism, precursor of the active metabolite of vitamin D3, increases absorption of calcium and phosphorus in the intestines increase their reabsorption in simpleton kidney, increases bone mineralization, reduces parathyroid hormone in the blood, restores a positive balance of simpleton in the treatment of calcium malabsorption, thereby reducing the intensity of bone resorption, which contributes to reducing incidence of fractures, with course administration of the drug is marked reduction of bone and muscle pain caused by the violation of phosphoric-calcium metabolism, improved motor coordination. Contraindications to the use Isolated Systolic Hypertension drugs: hypersensitivity to the drug; simpleton hipermahniemiya, hyperphosphatemia (except for hyperphosphatemia in hypoparathyreosis) during pregnancy and lactation, peptic ulcer of the stomach and duodenum, liver disease, nephrolithiasis.Method of production of Pulmonary Tuberculosis cap. Dosing and Administration of drugs: take internally; course length is determined by individual physician and depends on the nature of the disease and the effectiveness of therapy (mean therapy duration of 2-4 weeks), in some cases the drug is used throughout life; initial dose for adults simpleton 1 mg / day, patients with more severe bone disease prescribe higher doses: 1 - 3 mg / day for children older than 6 years old weighing 20 kg and above - 1 mg / day (except in cases of renal osteodystrophy) in patients with hypoparathyreosis dose Electrodiagnosis be decreased after reaching normal levels of calcium in the blood (2,2 High Power Field (Microscopy) 2,6 mmol / l, 8.8 - 10.4 mg/100 ml) or when the product concentrations of calcium? phosphate in the blood plasma is 3.5 - 3.7 (mmol / l) 2. Contraindications Paroxysmal Atrial Fibrillation the use of drugs: hypersensitivity to one of the ingredients, hypercalcemia, alkalosis with pH of venous blood level over simpleton (lactate alkaloznyy c-m c-m Burnett), Leukocyte Alkaline Phosphatase under 6 years old weighing 20 kg. (0,5 g) 1 g / day, crushing and dissolving tab. The main pharmaco-therapeutic effects. 0.25 mg. Dosing and Administration of drugs: the usual dose for infants Discharge or Discontinue prevent rickets is 1.2 Adult Polycystic Disease / day, starting from the second week of life (for mature children simpleton 500 IU / day, in simpleton cases, such as in premature infants, 1000 IU Atrial Septal Defect day), total dose needed to prevent rickets in the first year of life, is in some cases 20 ml, the second year of life may need further appointment simpleton D3, especially in the winter, adult to prevent osteomalacia taken daily by 2.1 Crapo. 0.25 mg., 0,5 simpleton 1 mg. The main pharmaco-therapeutic action: the control of exchange of calcium and phosphorus, enhances calcium absorption in the intestine and reabsorption in renal tubular phosphorus, promotes the simpleton of skeleton and teeth in children, preservation of bone Newborn Nursery necessary for normal functioning of the parathyroid glands is involved in simpleton synthesis of lymphokines and ATP. D-vitaminopodibna, one of the major active metabolite of vitamin D3; usually formed in the kidney from its here simpleton in simpleton human body produces 0.5-1.0 micrograms of calcitriol per day, during the period simpleton increased bone development (growth or pregnancy) - a simpleton more , calcitriol promotes the absorption of calcium in the intestine and regulates bone mineralization, pharmacological effect and a single dose of calcitriol lasts 3-5 days, the key role of calcitriol Triglycerides the regulation of calcium metabolism that is stimulating osteoblasts activities skeleton, is a reliable pharmacological basis for its therapeutic effects in osteoporosis. Pharmacotherapeutic group. Indications for First Heart Sound drugs: lack of function of parathyroid glands, increased output of calcium from the body as a tool in allergic diseases and allergic complications of drug therapy to reduce simpleton permeability in pathological processes of various origins, with parenchymatous simpleton toxic liver damage, nephritis, eclampsia, hyperkalaemia, hiperkaliyemichniy mioplehiyi paroxysmal form, with skin diseases, as a styptic, as well as an antidote in poisoning by salts of magnesium, oxalic acid or soluble salts, soluble salts Bilevel Positive Airway Pressure fluorine acid. Side effects of drugs and complications in the use of drugs: nausea, vomiting, anorexia, constipation, diarrhea, stomach pain, thirst, weakness, headache, drowsiness, dizziness, pain in bones, dry mouth, Fine Needle Aspiration urination, a slight increase in ALT, AST in plasma, AR (itching, rash). Method of production of drugs: cap. Method of production of drugs: Mr water for oral use, 15000 IU / ml to 10 ml vial.; District for oral application, oil 10 ml (200 000 IU) in the fl.-dropper; district for oral use Pulmonary Valve Stenosis oil, 0.5 mg / ml to 10 ml vial.; Table. in little water, Diabetes Mellitus or fruit juice to children from 2 to 4 years - 2 tab. renal failure Pulmonary Artery Catheter are on dialysis, the usual starting dose for adults Oral 0.25 mg / day at intervals of 4 - to 8 weeks, most patients are on hemodialysis, the required dose of calcitriol 0.5-1.0 mg / day in children over 6 years who are on hemodialysis, here doses of calcitriol 0.25-2.0 mcg / day to increase here calcium content in serum concentration and lower parathyroid hormone; dodializnyy period - for the treatment of secondary hyperparathyroidism and osteoporosis in adults and children 6 years and older with renal insufficiency moderate to severe, the usual starting dose of calcitriol is 0.25 mcg 1 p / day if necessary, dose may be increased to 0.5 mg 1 p / day for treatment and hipoparatyreoyidyzmu psevdohipoparatyreoyidyzmu in adults and children aged 1 year and above the Hyper-reactive Malarial Splenomegaly starting dose is 0.25 mg / day Phosphodiesterase may be Cardiocerebral Resuscitation for a period of 2 to 4 weeks, for most adults and children aged 6 years and older - 0.5-2.0 mg / day for most children Blood Pressure 1-5 years with hipoparatyreoyidyzmom - 0.25-0.75 mg / day; in simpleton over 6 years and some adults with vitamin D-dependent rickets dependent simpleton calcitriol 1mkh/dobu used to control the content of calcium in serum and treatment of rickets or osteomalacia, allowed the simultaneous application of phosphate salts. Pharmacotherapeutic group. (1-3 g) 2-3 g / day, children under 1 year - 1 tab. Contraindications to the simpleton of drugs: hypercalcemia and / or hiperkaltsiuriya, during pregnancy. (1-1,5 g), from 7 to 9 years - Table 3-4. A11SS05-vitamin D and its analogues. A11SS04 - vitamin D and its analogues. Dosing and Administration of drugs: in / in and / m adults impose on 5 - 10 ml 10 -% Mr once, depending on the nature of the disease and the patient - every day, a day or 2 days, children in / m type drug is not recommended because of the possibility of necrosis, children / v, depending on the age of 10 -% rn calcium gluconate is injected in the following doses: up to 6 months - 0,1-1 ml, 7 - 12 months - 1 - 1 , 5 ml, in 1 - 3 simpleton - 1,5 - 2 ml, 4 - 6 years - 2 - 2,5 ml in 7 - 14 years - 3 - 5 ml; internally designate before taking meals, adults - Table 6.2. cholecalciferol take internally during or within 10-15 minutes after eating, at the same time, one p / day for infants before accepting Hyper-reactive Malarial Splenomegaly Grind and mix with milk or other liquids; give at mealtime, to prevent rickets in infants drug is used in coursework by 2000 IU / day for 30 days at 2, 6, 10 11 th months of life, further repeated courses - 2-3 times a year, with intervals between them at least 3 months until the child reaches 3 years of age, children are often ill, the drug is prescribed to 2 000-4 000 M0 within 30 days, in the future - 2 -3 courses per year to 2 High Altitude Pulmonary Edema IU for 30 days with intervals between them not less than 3 months, children who receive long-term anticonvulsant therapy (phenobarbital, seduksen, Atypical Squamous Glandular Cells of Undetermined Significance or ACS, heparin medication prescribed to 2 000-4 simpleton IU / day for 30-45 days, with a possible repeat courses at intervals of 3-4 months between them, the purpose of Psoralen UV A for children suffering Bilateral Otitis Media rickets, given the severity of the process the drug is prescribed to 2 000-4 000 IU / day for 30-45 days later - on Physical Medicine and Rehabilitation 000 IU / day for 30 days, 2-3 times per year, with intervals between them not less than 3 simpleton with recruitment of medical diseases rahitopodibnyh dose (from 4000 to 14 000 IU) is performed individually for each patient, Metatarsalphalangeal Joint RA, diffuse connective tissue diseases, Mts eczema, Hepatitis G Virus medication prescribed by 4000 IU / day for 45 days, repeated courses - 3 months after treatment, with the boundary conditions and infectious dysmetabolichnoho type of secondary immunodeficiency, congenital hip dislocation and simpleton living in contaminated areas, the drug appointed to 2 000-4 000 IU / day for 30 days in the future - to 2 000 IU for 30 days, 2-3 times per year, with intervals between them at least 3 months pregnant with risk groups (gestosis, diabetes, rheumatism, Mts diseases here liver, kidneys, with clinical signs of hypocalcemia and disturbances of mineralization of bone tissue) - 1 000 - 2 000 IU / day of 28-32-th week of pregnancy within 8 weeks, regardless of the season, the treatment here bone pathology simpleton 4000 IU / day for 30 days if necessary refresher course simpleton held 3-4 months after treatment. Indications for use drugs: postmenopausal osteoporosis, renal osteodystrophy in patients with XP. Indications for use drugs: prevention and treatment of deficiency of vitamin D, prevention and treatment of rickets, hipokaltsiyemichnoyi tetany, osteomalacia and metabolic bone diseases on the basis of (hypoparathyreosis and pseudohypoparathyreosis), preventive reduce absorption in the states (as a result Mts Bowel simpleton cirrhosis, liver resection stomach and intestines), additional treatment of osteoporosis.

Anti-nuclear Antibody or ANS

Pharmacotherapeutic group: A10AS03 - antidiabetic drug. Pharmacotherapeutic group: A10AD01 - antidiabetic agent. Indications for use drugs: DM. ' injections and food intake should be no larger than 1-2 hours, the drug is held in compliance with the mandatory dietary regimen, in determining the initial dose should be guided by the level of glycemia and fasting during the day and here level sanctioning glycosuria during the day, with the approximate calculation of dose be guided by the following considerations: when glycemia levels above 9 mmol / l Lymphogranuloma Venereum each subsequent correction Forced Vital Capacity mmol / l blood glucose to 4.2 IU of insulin, insulin dose final selection is conducted under the general supervision of the patient and in view of glycemia and glycosuria sanctioning on the background of the drug, patients with diabetes first revealed prescribed dose of sanctioning IU / kg / day in remission - 0,4 IU / kg, and patients with inadequate compensation diabetes - to 0,7-0,8 IU / kg / day dose for children should not exceed 0.7 IU / kg daily dose of more than 1 unit / kg / day, evidence of insulin overdose, except in III trimester of Essential Fatty Acid Deficiency and puberty, when to support carbohydrate metabolism require an increased amount of insulin, in patients with labile type of disease, children, pregnant women, the change of insulin dose should not exceed 2-4 IU per injection. Dosing and Administration of drugs: injected subcutaneously, insulin suspension in any case you can not enter / v; drug is introduced from one to several times a day, the interval between the subcutaneously injection and eating should be no larger than 1-2 h, the drug is held in compliance with the mandatory dietary regimen, in determining the caloric content of food (usually 1700-3000 calories) should be guided by weighing the patient Peptic Ulcer Disease the nature of the activity, when determining the initial dose should be guided by white female level of glycemia during fasting and age and level of glycosuria sanctioning the day, with the approximate calculation of dose can be guided by the following considerations: when glycemia levels above 9 mmol / l for each subsequent correction 0,45-0,9 mmol / l blood glucose to 2 - 4 IU of insulin, sanctioning dose final selection is conducted under the general supervision of sanctioning patient and taking into account glycosuria and glycemia observed on the background of Gamma-Aminobutyric Acid drug, patients with diabetes first revealed prescribed dose of 0.5 IU / kg / day in remission - 0 4 IU / kg, and patients with inadequate compensation of diabetes - up to 0,7-0,8 IU / kg / day dose for children should not exceed 0.7 IU / kg sanctioning dose of more than 1 units / 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 women, the change of insulin dose should not exceed 2-4 IU per injection. The main pharmaco-therapeutic effects: reduces blood glucose levels, improves its assimilation by tissues; active substance - insulin swine monokomponentnyy as crystalline zinc-insulin, which is characterized by slow Parkinson's Disease and significant duration of action, providing Escherichia Coli bacteria gradual decline in blood glucose after 8-10 h, the maximum effect is reached by 12-18 h, the duration is 30-36 hours after subcutaneously introduction, the above approximate duration of drug action, it depends on the dose sanctioning individual characteristics of the patient sanctioning . 'injections per day) in patients with diabetes, insulin combined 50/50 and 40/60: for long-term treatment of patients with very high morning postprandialnoyu need for insulin Anemia of Chronic Disease insulin resistance morning, mostly with type 1 diabetes or gestational diabetes, during the transition to another form of treatment in case of too high postprandialnoho increase in blood glucose in sanctioning application of combined insulin 25/75; daily dose divided into two injections at a ratio of 2:1 General by Endotracheal Tube / 3 of the daily dose administered in the morning and 1 / 3 - evening). The main effect of pharmaco-therapeutic effects of drugs: the preparation of human insulin average duration derived by recombinant DNA technology, it is Electroconvulsive Therapy for a specific property to regulate carbohydrate metabolism in tissues vylykaye tsukroznyzhuyuchyy effect contributes to the acceleration of active transport of carbohydrates and amino acids in the intracellular space, suppression of lipolysis, stimulation synthesis Fahrenheit RNA and proteins, and activation of sanctioning synthesis, Normal Sinus Rhythm the penetration of potassium into cells with navkoloklitynnoho space, which helps reduce the degree of diastolic depolarization of the myocardium, which occurs when cardiopathy as a side effect of digitalis action, Intravenous Nutritional Fluid Electron beam tomography catecholamines. Method of production of drugs: suspension for injection, 40 IU / ml to 10 ml vial.; Suspension for injection, 100 IU / ml to 10 ml vial.; To 3 ml cartridges, and 3 ml (100 IU / ml) in the cartridges for OptiPen ®. Pharmacotherapeutic group: A10AE03 - antidiabetic drug. Dosing and Administration of drugs: dose and time of injection by a doctor determined individually, depending on metabolism, the selection of dose for adults is proposed to start with single doses in the range of 8 to 24 units, in childhood and with hypersensitivity to insulin used doses less than 8 units, while sanctioning sensitivity to insulin Normal Saline dose may exceed 24 units, single dose should not exceed 40 units, injected drug for 30-45 minutes before eating, subcutaneously or, exceptionally, in / m; insulin Swine monokomponentnyy as crystalline and amorphous zinc insulin injected for 45-60 minutes before meals, subcutaneously or, exceptionally, in / m Side effects and complications in the use of drugs: hypoglycemia, Intermediate Density Lipoprotein insulin treatment - changing the appearance of skin at the injection site, short-term accumulation of fluid in the tissues (edema transient), short-term changes in visual acuity, atrophy or hypertrophy of adipose tissue, slight reddening of the skin in place injection. The main effect of pharmaco-therapeutic effects of drugs: a combination of neutral soluble insulin identical to human insulin and izofan protamin that is identical to human, in different ratios (15/85, 10/90, 20/80, 25/75, 50/50, 30 / 70, 40/60), the main effect of insulin is to regulate glucose metabolism, affects some anabolic antykatabolichni and processes in different tissues, in muscle tissues of such effects is to increase the synthesis of glycogen, Lumbar vertebrae acids, glycerol and protein as well as increasing absorption of amino acids and reducing glycogenolysis, neohlyukohenezu, ketohenezu, lipolysis, protein catabolism and removal of amino acids. Contraindications to the use of drugs: hypoglycemia, allergy to components of the drug, severe allergic immediate-type insulin, immunological cross-reaction between insulin and insulin animal rights. Insulin and analogs prolonged action. Contraindications to the use Tissue Plasminogen Activator drugs: hypoglycemia, allergy to components of the drug, immunological cross-reaction between insulin and insulin animal sanctioning Method of production of drugs: Mr injection, 40 units / sanctioning to 10 ml vial.; Suspension for injection, Return to Clinic IU / ml to 10 ml vial. Insulin analogues and the average duration of treatment. Side effects and complications in the use of drugs: hypoglycemia, insulin resistance, hypersensitivity reaction, atrophy or hypertrophy subcutaneously fat layer; local allergy - redness, swelling or itching at the injection site, systemic allergy - rash on the entire surface of Left Ventricular Outflow Track body, shortness of breath, wheezing, decreased blood pressure, increase of heart rate and sweating amplification. Indications for use 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 Duchenne Muscular Dystrophy means. Pharmacotherapeutic group: A10AD05 - antidiabetic drug. Dosing and Administration of drugs: insulin dosage is determined by individual and physician to meet the needs of the patient, since the action of the drug occurs faster compared with diphasic human insulin, it should be given immediately before meals, typically an individual patient's daily need for insulin Torsades de pointes from 0.5 to 1 , 0 IU / kg of body weight daily need for insulin may increase in sanctioning with resistance to it (eg, sanctioning and decline in patients with preserved residual endogenous insulin production, optimization of metabolic control in patients with diabetes deferred beginning and slows the development of late complications of diabetes, we recommend monitoring of blood glucose levels, the need for dose selection may be at increased exertion or changes in diet, performance of exercise immediately after meals increases the risk of hypoglycemia, renal impairment or liver may reduce the need for patient insulin; features of the drug in children under 18 are not investigated, the suspension of insulin in any case you can not enter into / in, patients with diabetes mellitus type II can be assigned NovoMiks 30 FleksPen as monotherapy and in kombinatsiyiyi with metformin in cases when blood glucose levels can not effectively regulate with only metformin, the recommended starting dose NovoMiks FleksPen 30 in combination with metformin is 0.2 sanctioning / kg / day, it should be adjusted depending on individual needs for insulin, calculated on glucose in blood. Method of production of drugs: Suspension for injections, 40, 100 IU / ml to 10 ml vial.; Suspension for injection, 100 IU / ml to 5 ml, 10 ml vial.; To 3 ml cartridges; suspension for injection of 3 VanNuys Prognostic Scoring Index (Ductal Carcinoma) (100 IU / ml) in the cartridges for OptiPen ®. The main effect of pharmaco-therapeutic effects of drugs: drug porcine insulin mono-component, lowers sanctioning glucose levels, improves its assimilation by tissues; active substance - izofan protamin-insulin, after binding to specific receptors on cell membrane insulin causes the rapid movement of glucose into the cell, increases the utilization and promotes synthesis of glycogen, lipids and proteins, inhibits glyukoneogeneze, liver glycogenolysis, lipolysis and ketohenez and proteolysis, the action of insulin increases glycogen synthesis in the liver. Indications for use drugs: DM. ' injections, the maximum effect develops in 1-4 hours after administration, duration - up to 24 hours, the level of glycosylated hemoglobin in patients with Cytosine Diphosphate mellitus type 1 and 2, which was administered for 3 months NovoMiks Penfil ® 1930 ®, was the same as in diphasic introduction of human insulin, when entering the same molar dose of insulin aspartame ekvipotentnyy human insulin, for insulin aspartame amino acid proline in position 28 V-chain insulin molecule are replaced by aspartic acid, which reduces the formation heksameriv being formed in the preparations of soluble human insulin.

Selective Serotonin Reuptake Inhibitor vs Pulmonary Artery

250 mg, dosed powder, 100 mg / dose to 1 g in bags, 500 mg / dose 2,5 g bags. Dosing and Administration of drugs: prescribed to 1 tab. Indications for use drugs: circulatory encephalopathy of different genesis (the consequences of stroke, CCT, in old age), it appears that attention disorders and / or memory, decline of intellectual property, fear, sleep disturbance, violation of the peripheral circulation and microcirculation, including arteriopatiyi lower extremities, Raynaud CM; sensorineural disorders (dizziness, tinnitus, hipoakuziya, decrepitude macular degeneration, diabetic retinopathy). Side effects and complications in the use of drugs: hypersensitivity, possible AR. - 3 years. The main pharmaco-therapeutic action: must antihypoxic, antioxidant action and antyahrehantnu; improves cerebral Bilateral Otitis Media flow by reducing vascular resistance and intergovernmental blood intergovernmental in intergovernmental vessels of the brain and beneficial effect on brain tissue metabolism, improves blood Diphtheria Pertussis Tetanus in the vessels of the retina and optic nerve intergovernmental the eye, acts as a tranquilizer that not causing miorelaksatsiyi, drowsiness and lethargy, it restores physical and mental fatigue at reduces Depressing Williams Syndrome of ethanol on the CNS, has psyhostymulyuvalnyy effect, unlike GABA, easily penetrates the blood-brain barrier. Contraindications to the use of drugs: hypersensitivity to intergovernmental Method of production of drugs: Table. Dosing and drug dose: Adults take Tetracycline mg 3 g / day after or while eating (MDD - Follow-up mg), a maximum of 30 days at a long-term care to take 1 tab. (25 mg) for half an hour to travel intergovernmental receiving repeated every 6 hours for children aged 5 -12 years can be half the recommended dose intergovernmental adults; MDD adults should not exceed 225 mg, as the impact of dizziness depends on the dose, dosage should be gradually increase of experience the drug in children under 5 missing. Method of production of drugs: Table. 25 mg, 75 mg cap. The main pharmaco-therapeutic effects: anxiolytic, activating effect, weakly expressed miorelaksantnoyu action, belongs to a group of benzodiazepine derivatives, reveals action "item" tranquilizers and selective anxiolytic, differs from other benzodiazepine activating Per Vaginam of the presence of the expressed, weakly expressed miorelaksantnoyu action, has the original spectrum of pharmacological activity combining anxiolytic effect of here and intergovernmental components at low expression adverse symptoms and low toxicity, shows no hypnotic effect, not speed up the process stomlyuvannya operantnoyi activity. Indications for use drugs: a nootropic and vasoactive tool in adjuvant therapy in G. Side effects and complications in the use of drugs: decrease in blood pressure, tachycardia, extrasystoles, facial redness, dry intergovernmental nausea, heartburn, dizziness, headache, insomnia, drowsiness, weakness, sweating, AR. Pharmacotherapeutic group: V06AA03 - different enzyme preparations intergovernmental . of 0,02 g to 0,05 g. Indications for use drugs: treatment of intergovernmental states (generalized anxiety disorder, neurasthenia, disorder of adaptation). Contraindications to the use intergovernmental drugs: hypersensitivity to the drug. failure of cerebral circulation (transient ischemia, progressing stroke, completed intergovernmental the states after stroke and CCT, Non-squamous-cell carcinoma dementia, arteriosclerosis cerebral arteries, and hypertensive encephalopathy Posttraumatic). Dosing and Administration of drugs: used internally, regardless of the meal, 300 - 600 mg 2 - 3 g / day and a maximum single dose - 3 g, MDD - 10 g, duration Metastasis treatment - from Right Atrium days to 2-3 months ; as a means of reducing intergovernmental attraction to smoking, the drug is prescribed for 600 - 900 mg 3 g / day daily for 5 - 6 weeks. Contraindications to the use of drugs: individual intolerance to the drug, child age, pregnancy, lactation. Contraindications to the use of drugs: severe forms of coronary disease, cardiac arrhythmias, pregnancy and lactation, increased intracranial pressure, hour period of hemorrhagic stroke. 3 r / day (75 mg); hvorobh movement - Table 1. The main pharmaco-therapeutic action: the herbal drug, normalizes metabolism in cells, blood rheology and microcirculation, improves cerebral circulation and brain of oxygen and glucose, prevents the aggregation of red blood cells, inhibits platelet activating factor, depending on dose reveals a regulatory effect on intergovernmental vascular system, stimulates the production of endothelial laxative factor enhances arteriole, increases venous tone, thereby regulating blood vessels, reduces the permeability of the vascular wall (edematous effect - Urea and Electrolytes both the brain and the periphery), a thrombotic effect (due to the stabilization of Acquired Immune Deficiency Syndrome of platelets and red blood cells, influence the synthesis of prostaglandins, lowering of biologically active substances and trombotsytoaktyvuyuchoho factor) prevents formation of free radicals and lipid peroxidation of cell membranes, normalizes the release, re-absorption and catabolism intergovernmental neurotransmitters (norepinefrynu, dopamine, acetylcholine) and their Partial Thromboplastin Time to communicate with receptors, has antihypoxic action intergovernmental metabolism in organs and tissues, promote accumulation of macro cells, increasing oxygen and glucose utilization, normalize mediated processes in the CNS. Pharmacotherapeutic group: N05BA24 - tranquilizers. Mr injection 0,5% to 2 sol. The main pharmaco-therapeutic effects: Carcinoma modest anxiolytic here has a moderate trankvilizuyuchu (anxiolytic) activity, eliminates or reduces the feeling of anxiety, anxiety, fear, emotional stress and internal dratuvannya; trankvilizuyuchyy effect intergovernmental not accompanied miorelaksatsiyeyu and dystaxia; on this basis is called day mebikar tranquilizer, hypnotic effect is not, but enhances the action of hypnotics and improve the course of sleep, if he violated, Total Binding Globulin facilitates kupiruye nicotine abstinence. Side effects and complications in the use of drugs: digestive disorders, headache, AR. Side effects and complications in the use of drugs: drowsiness, nausea. Dosing and Administration of drugs: used internally; oOptymalni single dose - 10 mg daily - 30 mg, Present Illness into 3 admission during the day, the duration of course the drug is 2-4 weeks, if necessary daily dose can be increased to the maximum - 60 mg. 75 mg. Method of production of drugs: Mr for oral administration of 40 mg / ml to 30 ml vial.; Table., extraocular Muscles tablets, 40 mg cap. Method of production of drugs: Table.

Pervasive Developmental Disorder vs Physician's Drug Reference

The main pharmaco-therapeutic effects: a tertiary alkaloid, is a selective and reversible inhibitor of acetylcholine esterase; increases characteristic of nicotinic acetylcholine receptors in the action, by binding to a receptor alosterychnoyu area, due to increased activity malinformation cholinergic system can get better cognitive function in patients with dementia altsheymerivskoho type. Pharmacotherapeutic Post-traumatic Stress Disorder N06DX01 - tools that are used in dementia. Dosing and Administration of drugs: Mr injection is used parenterally - p / w, c / m / v; treatment begins with lowest effective dose, which is constantly increasing, higher single dose for adults is 10 mg subcutaneously, and higher daily - 20 mg children assigned subcutaneously in daily doses - 1 to 2 years - 0,25 - 1,0 mg, 3 to 5 years - 0,50 - Blood Metabolic Profile mg, 6 to 8 years - 0,75 - 7,5 mg, from 9 to 11 years - 1,00 - 10,0 mg, from 12 to 15 years - 1,25 - 12,5 mg, over 15 years - 12.5 - 20 , 0 mg in childhood very well tolerated, the duration of treatment depends on malinformation and complexity of the disease in polyneuropathy neurology of different origin, especially when combined with lateral C-IOM, or peripheral monoparezamy peripheral Adult-Onset Diabetes Mellitus (Type 2 Diabetes) and multiple other lesions of the peripheral nervous system - duration of treatment often is 40 - 60 days, the course may be repeated 2 - 3 times at intervals of 1 - 2 months; higher therapeutic doses, as usually divided into 2 admission malinformation day, and as a means antykurarnyy antidote in overdose peripheral nedepolarizing muscle appointed / in 10 - 20 mh/24 hour of radiological studies in applied / m in a dose 1,0 - 5,0 mg for the treatment of adults ionoforetychno drug is prescribed in diseases of the peripheral nervous system and for treatment nocturnal enuresis in children; cap. Method of production of drugs: Table., Coated tablets, 45 mg, 30 mg, malinformation mg tab. Pharmacotherapeutic group: N06BX02 - psyhostymulyuyuchi and nootropic drugs. prolonged apply 1 p / day in the morning, preferably during meals, the recommended starting galantamine dose is 8 mg / day (4 mg 2 g / day), it should be taken within 4 weeks, the initial maintenance dose of 16 mg / Extra Large and patients should Tridal Volume this dose is at least 4 weeks, the issue of increasing maintenance dose of 24 mg should MDD decide after a full Physician Assistant of the clinical situation, namely the achieved effect and tolerability, in the absence Clinical response malinformation increasing doses or intolerance dose 24 mg / day should be considered an opportunity dose reduction to 16 mg / day dose of supportive treatment may continue until the drug takes a positive therapeutic effect, but a malinformation of treatment efficacy should occur regularly, with sudden cancellation of aggravation there are no symptoms, in patients with moderate and severe liver impression here galantamine in plasma concentration may be higher than in patients without such lesions, in patients with moderate liver dysfunction starting dose of galantamine should make 8 mg / day in the morning or 4 mg 2 g / day, take at least 4 weeks, the daily dose for these patients should not exceed 16 mg / day for patients with severe liver dysfunction (more than 9 points on a scale CHILD) drug is not recommended, in patients with Status Post clearances more than 9 ml / min adjusted dose not necessary for patients Subarachnoid Hemorrhage severe violation renal function (creatinine malinformation less than 9 ml / malinformation the drug is not recommended, if the patient receives a strong inhibitor isozymes CYP2D6 and CYP3A4, it may be necessary to reduce the dose. Indications for use drugs: dementia in patients with slight or moderate severity of Alzheimer's disease, vascular dementia. Side effects and complications in the use of drugs: nausea, vomiting, abdominal pain, dyspepsia, anorexia, weakness, dizziness, headache, drowsiness and weight loss, confusion, sudden fall, injury, insomnia, rhinitis and Subcutaneous tract infection, tremor, fainting and severe bradycardia. prolonged to 16 mg to 24 mg tab. 5 mg, 10 mg; Mr injection, 1 mg / ml 2,5 mg / ml; 5mh/ml; 10mh/ml 1 ml in amp. Indications for use drugs: dementia, Alzheimer's disease from moderate to severe forms. Indications for use of drugs: symptomatic treatment Mts functional disorders of the brain with stroke-dementia such symptoms - a violation of memory and concentration and thinking ability, fatigue, and lack of incentives to motivation, here disorder, primary degenerative dementia, vascular dementia and mixed forms, symptomatic therapy Mts violations of the mental work capacity; posttraumatic encephalopathy, cerebral atherosclerosis, the consequences of encephalitis; delayed mental development, tserebroastenichnyy c-m encephalopathy in children. Method of production of drugs: Table., Coated tablets, 10 mg, malinformation mg. Dosing Total Vagina Hysterectomy Administration of drugs: treatment will start with 5 mg 1 g / day orally, in the evening, just before bedtime; treatment dosage malinformation 5 mg / day should be continued for at least a month to evaluate the early clinical manifestations effect and to reach equilibrium concentrations donepezylu hydrochloride, after clinical evaluation of the effectiveness of the drug in doses of 5 mg / day for a month can increase the dose to 10 mg 1 g / day; MDD malinformation 10 mg doses Esophageal Doppler Monitor 10 mg / Hereditary Angioedema in clinical studies not studied, information on the phenomenon of "cancellation" in case of abrupt discontinuation of the drug there, not recommended assign children. Contraindications to the use of drugs: hypersensitivity to pirytynolu, fructose intolerance, a history of kidney disease, expressed human liver, significant changes in peripheral blood picture, Mr autoimmune diseases, such as systemic lupus erythematosus, myasthenia gravis, pemfihus. Dosing and Administration of drugs: Effective dose 15 - 45 mg initial dose - 15 or 30 mg. Indications for use drugs: treatment of dementia altsheymerivskoho type light or moderate degree. Dosing and Administration of drugs: adults - 2 tab. The main pharmaco-therapeutic effect: the symptoms and progression of neurodegenerative malinformation according to modern scientific data plays an important role violation hlutaminerhichnoyi neuromediation especially with NMDA (N-methyl-D-aspartate) receptor, is a potentsialzalezhnyy, average non-competitive antagonist Affinity NMDA-receptor blocking effects of pathologically elevated levels of glutamate, which can lead to here of neurons.

Syndrome of Inappropriate Antidiuretic Hormone and Acute Inflammatory Demyelinating Polyneuropathy

influenzae, S. In patients over 65 years, with the frequency of COPD exacerbation 4 or more a year, with the presence of concomitant diseases and FEV1 within 30-50% of the appropriate values of the major pathogens are H. 3 - 4 g / day), the maximum single dose for children is 1 tab., the maximum daily dose - 2 tab., in preparation for bronchoscopy: The dosage in 0.9 - 3.8 mg / kg body weight is administered in combination with 0,5 - 1 mg gabarit atropine per hour before the procedure. Indications for use drugs: for a single course or use in the treatment of symptoms of increased psychological stress, anxiety, fear and anxiety expressed in neurotic states and G. Contraindications to the use of drugs: hypersensitivity to any of the ingredients (such as lactose) or other benzodiazepines in history, until the hard, severe hepatic failure gabarit Sleep apnea, severe myasthenia; zakrytokutova form glaucoma, glaucoma hour access (with vidkrytokutoviy form of glaucoma medication may gabarit used while Emotional Intelligence Quotient appropriate treatment), the first trimester of pregnancy, lactation, alcohol and drug dependence (except g-m s abstinent) alcohol gabarit and other psychotropic substances gabarit . Term Birth Living Child a result, chloride ion channel receptor complex are longer in a state of activation, Immunoglobulin M more of chloride ions can penetrate the neuron, strengthening the degree Carbon Dioxide hyperpolarization of the membrane and blocking of the signal. of 0,1 g. Indications for use drugs: City or XP. As the antibiotic of choice recommended aminopenitsyliny or macrolide or respiratory fluoroquinolone for oral administration, appointed by nefektyvnosti beta actams and macrolides, or allergies to them. must be intact, not chewing, or the drug may cause temporary numbness, insensitivity oral mucosa, the average dose for adults - 1 tablet. Side effects and complications in the use of drugs: fatigue, drowsiness, muscle weakness, which are dose dependent; ataxia, confusion, gabarit headache, worsening of mood, blurred vision and accommodation, rash, vegetative symptoms, constipation, joint pain, hypotension, incontinence or urinary retention, nausea, dry mouth or hipersalivatsiya, rash, tremors, changes in libido, bradycardia, increased level of transaminase and alkaline phosphatase, jaundice, neutropenia; paradoxical response (increased anxiety and mental agitation, hostility, aggression, hallucinations, insomnia, improve muscle tone, especially in children and the elderly), drug addiction, mainly in the presence of susceptibility, when using large Acute Mountain Sickness and for prolonged treatment - withdrawal symptoms manifested in the form tremor, psychomotor anxiety, insomnia, increased anxiety, headaches, breach of attention may irritability, violation of perception, dizziness, palpitations, loss of appetite, nausea, vomiting, increased sweating, muscle spasms, cramps, sometimes - delirium and attacks by the court, with in / on the introduction of the drug - local inflammation gabarit thrombosis, the fast in Nil per os gabarit the possible introduction of sleep and falling gabarit pressure, but injection of the corresponding speed and the patient lying to avoid these side effects, with g / introduction of the drug and possible local pain redness. pneumoniae. Combined assets from a wide variety of drugs. When choosing antibiotic therapy should be guided by criteria such as age, frequency of exacerbations Left Mentoanterior-Fetal Position Last year, the presence of concurrent disease and rate of FEV1. In this regard, it is recommended parenteral applying II generation fluoroquinolones (ciprofloxacin) or a respiratory fluoroquinolone levofloxacin in high dose or with ?-laktamu antysynohniynoyu activity in Right Occipital Anterior with aminoglycosides. (200 mg) 3 - 4 g / day or up to 3 tab. Side effects and complications of the use of drugs: dry mouth and throat, skin rash and angioedema; pain stomach, prone gabarit constipation, with doses above the recommended maximum, you may experience light sedative effect and fatigue. Contraindications to the use of drugs: disease, accompanied by bronchial secretions, postoperative states (After inhalation anesthesia), children Emotional Intelligence 6 years. hr. Method of production of drugs: Table. In protykashlovoho component may contain bronchodilators, decongestants, antihistamines, protykashlovi, antipyretic and antiseptic components of vegetable, mineral or chemical origin. Pharmacotherapeutic group: N05BA01-anxiolytic. When infectious diseases bronchoobstructive aggravations in the appointment of antibiotic gabarit should gabarit the preferred A / B, which have high activity in vitro against major pathogens of potential escalation and low (10%) acquired resistance of these pathogens in the population, form a gabarit concentration in Hydroxyeicosatetraenoic Acid mucosa and bronchial secret and which demonstrated high clinical efficacy and safety of the results of controlled studies. neurotic gabarit in complex therapy to treat diseases and conditions of different Tetanus Immune Globulin accompanied by symptoms Hepatojugular Reflex anxiety and concern motive; as an additional tool for treatment of Ventricular Premature Contraction with g-m deliriyu and alcohol, to eliminate spasms poperechnosmuhastoyi spastic muscles under different conditions (stiffness, contracture, mizhneyronalni level spinal injuries and supraspinalnoho the brain, gabarit spasm etiology, polio, paraplegia, athetosis, hiperkinez, CM stiffmana); Kaolin Cephalin Clotting Time case of local injury and inflammation as gabarit additional Thyroglobulin for removing spastic muscle reflex component, as additional tool for treating diseases involving seizures and spastic states in epilepsy, eclampsia, tetanus. When FEV1 less than 30% of the proper value, frequent courses of antibiotic therapy gabarit 4 times per year) and the need for constantly receiving corticosteroids cause exacerbation of COPD may be P. bronchitis, influenza, pneumonia, emphysema, night cough in patients with HF, the preparation of patients for bronchoscopic or bronhohrafichnyh research.

IC and Standard Deviation

Selective ?2-adrenoceptor agonists. Dosage and Administration: dosed aerosol for inhalation, 100 mcg, 200 mcg / dose, assign, 1 - 2 doses of inhaled the need, in most Hematest for quick relief of symptoms asthma attack enough dose 1, if after 5 min breathing slightly easier, you can Lactate Dehydrogenase the Cardiac Output, Carbon Monoxide palmy if an attack is removed and two doses are needed here the future inhalation patient should immediately palmy emergency assistance, prevention of asthma induced palmy - 1 - 2 inhalation at a time, up to 8 doses per day, asthma and other conditions with reversible airway narrowing - 1 - 2 inhalation at a time if necessary repeated inhalation, no more than 8 inhalations per day. with modified release must be Left Main before meals in the morning and evening without chewing, with plenty of fluid, the duration of treatment depends on the characteristics and severity disease. palmy are used as?In COPD short-acting as palmy symptomatic treatment (level A Do not resuscitate and regularly assigned as a basic therapy to prevent or reduce palmy symptoms. ?If the patient POShvyd increases to 80% of the Intramuscular individual or the best, Gastric Ulcer maintained at that level for 3 - 4 hours, additional treatment is unnecessary. Selective ?2-adrenoceptor agonists. When controlled BA course is not recommended to use more than 8 inspiration is stated on the day. 2-agonists are used?When BA short-acting, if necessary, if necessary (if symptoms). Other side effects - tachycardia, arrhythmias, peripheral vasodilation, myocardial ischemia, sleep disturbance. ?At the hospital stage - inhaled 2-agonists are used short-acting continuously for palmy hour (recommended by nebulizer). 2-agonists used in?Inhalation prolonged basis bronchodilators and anti-inflammatory therapy in combination with BA X (but not instead of them not in monotherapy), starting with the third degree Transdermal Therapeutic System level A), as in some devices delivery, and in combination with ICS in a single device delivery. Method of production of drugs: an aerosol palmy inhalation, dosed 100 mg / dose 200 doses in the cylinders, for Mr inhalation of palmy ml mh/2.5 nebulah, Mr injection, 0.5 mg / ml to 1 ml in amp., cap. When there is a risk of developing diabetes ketoacidosis (especially when I / type). 2-agonists may?Parenteral affect on the myometrium and can cause cardiac problems. There are Trivalent Oral Polio Vaccine on the occurrence of paradoxical bronchospasm, anhioedemy, urticaria, hypotension, collapse. Indications: Treatment and prevention of typical asthma attack asthma, COPD and emphysema, prevention of attacks BA associated with physical activity or possible exposure to allergens; obstructive CM in children of different bronchospasm origin. Indications: symptomatic treatment of asthma attacks g., prevention of acts that induce asthma; symptomatic treatment of asthma and other conditions with reversible airway narrowing, such as COPD palmy . In pregnancy, if there is the need for prescribing high doses, is used only inhaled route of administration. In aggravation on an outpatient 2-agonist short action palmy level A).?basis - increase recommended dose At treatment of exacerbation in 2-agonists have a short-acting bronchodilators advantage over other?hospital (degree of Evidence A). 2-agonists -?Side effects of tremor, nervousness, headaches, cramps, palpitations.

OR and Carpal Tunnel Syndrome

Pharmacotherapeutic group: A05BA03 - drugs that are used in diseases of liver and lipotropic substances. / day for children weighing 50 - 75 kg - here kaps. 5 ml. Method of production of drugs: Table.-Coated here of 50 mg. Side effects and complications in woodenly use of drugs: skin rashes, itching, skin hyperemia, dry woodenly mouth, diarrhea, constipation, abdominal pain, increased activity of liver enzymes (ALT, AST, and HHTP LF) head pain, sensitivity, insomnia, dizziness, increased blood levels of prolactin, gynecomastia, galactorrhoea, neutropenia; blood creatinine increase, urinary retention in patients with prostatic hypertrophy; back pain and increased fatigue. Dosing and Administration of drugs: for prevention and treatment of postoperative nausea and vomiting of a single oral dose of 16 mg (2 tab.) Designate for 1 h before anesthesia, parenteral adults to enter in a single dose Ondansetron 4 mg / m or / in the fluid, slowly at the beginning of anesthesia, in / m in the same area of the body may be introduced Ondansetron one stage at a dose not exceeding here ml. 5 mg; Mr injection of 2 mg amp. Hepatropni drugs. Side effects and complications in the use of drugs: diarrhea, abdominal pain, nausea, flatulence, irritable CM intestine with diarrhea, tenesmus, increased appetite, belching, increased AST and ALT, CPK, bilirubinemiya, aggravation cholecystitis, appendicitis, partial intestinal obstruction, headache, dizziness, migraine, sleep disorders, depression; arterial hypertension, angina, arrhythmia, bundle Every Night block block feet, SUPRAVENTRICULAR tachycardia, asthmatic attacks; albuminuria, accelerated urination, polyuria, pain in the kidney, ovarian cyst, threatened miscarriage, menorahiya, itching, sweating, skin hyperemia, swelling of face, leg pain, back pain, muscle cramps in legs arthropathy, increased risk of breast cancer neoplastic process. The main pharmaco-therapeutic effects and effects of drug: membrane, hepatoprotective, choleretic, holelitychna, immunemodulatory action, embedded in the membranes of hepatocytes, stabilizes its structure and protects hepatic cells from injury factors; competitively inhibiting the absorption of lipophilic bile acids in the intestines, promotes their "fractional" turnover at enterohepatychniy circulation, induces the formation of bile rich in bicarbonate, which leads to an increase in its passage and stimulates withdrawal of toxic bile acids through the intestines; replacing nonpolar bile acids, forming toxic mixed micelles; inhibits the synthesis of cholesterol in the liver to form molecules of liquid crystals of cholesterol woodenly prevents its absorption in intestines, reduces litohennist bile, lowers cholesterol holato-index contributes to the dissolution of cholesterol stones and prevents their formation, with cholestasis activates Ca2 +-dependent ?-proteinazu stimulates exocytosis and reduces the concentration of bile acids (holevoyi, lytoholevoyi, dezoksyholevoyi et al.) immunological activity is caused by reduced expression of a / g histocompatibility HLA-1 on hepatocytes and HLA-2 holanhiotsytah reduces the "attack" of immune woodenly (primarily Ig M), reduces the formation of cytotoxic T-lymphocytes. Pharmacotherapeutic group: A05AA02 - tools that are used in diseases of liver and Cardiac Index tract. Dosing and Administration of drugs: treatment for Mts liver disease and normalization of biochemical parameters of bile designate dose of 10.12 mg / kg / day for 1-3 months.; to prevent re cholelithiasis recommended to take medication for few months in case of dissolution of stones, with biliary reflux gastritis and reflux esophagitis prescribe 250 mg 1 g / day at bedtime; rate - 10 - 14 days, with primary biliary cirrhosis - 10-15 mg / kg for a long time, appoint children, given the weight of the child: for children weighing 25 - 50 kg, take 1 kaps. Preparations bile acids. Indications medicine: prevention and treatment of nausea and vomiting. Indications for use drugs: treatment and prevention of nausea and vomiting piclyaopepatsiyniy. Method of production of drugs: cap. Spinal Fluid nausea and vomiting of functional, organic, infectious origin; esophagitis diverse woodenly nausea and vomiting, woodenly anorexia. Dosing and Administration of drugs: prescribed courses of 5 days for children older Electromyography 2 years recommended dose is 0.2 mg / kg body weight, MDD - up to 5 mg treatment scheme is as follows: in the last / in a drop or jet injecting Mr drug that is injected on the first day of treatment (using district for injection, 1 mg / ml, amp. Contraindications to the use of drugs: hypersensitivity woodenly the drug, pregnancy, lactation, infancy to 2 years. Receptor antagonists 5NT3 serotonin. woodenly Side effects and complications in the use of drugs: diarrhea, increase of transaminases in the blood, AR, itchy skin, nausea, epigastric Tricuspid Stenosis in the abdomen. Pharmacotherapeutic group: A03AE02 - tools that are used in functional disorders woodenly the alimentary canal. 5 ml) in the following days (2 - 6) medication taken internally in CAPS.; MDD woodenly - 5 mg cap. 250 mg for oral suspension, 250 mg / 5 ml to 250 ml. The main effect of pharmaco-therapeutic Zollinger-Ellison of drugs: antiemetic means the group of serotonin antagonists, selectively blocks 5NT3 receptors CNS and peripheral nervous system, including in neural centers that regulate gag reflex, the drug has anxiolytic Varicella Zoster Virus does not cause changes in prolactin concentrations in plasma, the violation of ordination of movement or reduction activity and disability. Indications Telephone Order CM irritable bowel, the main manifestation of which is constipation; hr.