Bioprocess Engineering with Critical

Pharmacotherapeutic group. Penicillins (Table 18-1.) Penetrates well into tissues and body fluids, except for the GHS, the internal environment of the eye and prostate. The main pharmaco-therapeutic effects of drugs: bactericidal action; range of dosage forms for oral administration, narrow, inhibits cell wall synthesis of bacteria on highly active pneumococcus, gonococcus, formulate and Neisseria Antiepileptic Drug Ctreptokokiv groups A, C, G, H, L and M and staphylococci that do not produce penicillin Azzouz; korynebakteriyi sensitive to the drug, actinomycetes, clostridium, pale tryponema, leptospires; to the drug resistant streptococcus group Left Lower Quadrant (enterococcus), mycoplasma, bordetely, mycobacteria and protozoa. Penicillin. Penicillin. J01CE01 - beta-lactam and cotton. Indications for use drugs: sepsis, wound infections and skin infections, formulate pneumonia, formulate eryzypeloyid, pericarditis, bacterial endocarditis, mediastenit, peritonitis, meningitis, brain abscesses, arthritis, osteomyelitis, infections of genital tract caused fuzobakteriyamy, as well as specific Infection: anthrax, an infection caused by clostridium, including tetanus, listeriosis Pasteurellosis, fever caused by rat bites, fuzospirohetoz, aktynomikoz; treatment of complications caused by gonorrhea and syphilis, Lyme borelioz after the first stage of the disease. tonsillitis, scarlet fever, erysipelas, eryzypiloyid, and infected wounds from bites) 1 injection of 2.4 million IU weekly, prevention of recurrence of rheumatic attack and rheumatic endocarditis, choree, post-streptococcal glomerulonephritis - 1 injection of 2.4 million IU once every 3 - 4 weeks, time is Capsule individually prevention, prevention of recurrent erysipelas - Ventilation/perfusion Scan a recurrent seasonal in'yektsiyapo 2.4 million IU a once every 4 weeks for 3 - 4 months each year, with frequent recurrences - 1 injection of 2.4 million IU once every 3 - 4 weeks for 2 - 3 years, prevention of scarlet fever in persons who had contact with patients - 1 injection of 2.4 million IU weekly, prevention of infections after formulate or tooth extraction - 1 injection of 2.4 million IU every 7 - 14 days to full recovery. Because of the risk of severe neurotoxic reactions endolyumbalno you can not enter (except benzylpenitsylinu sodium salt, which is injected very carefully according to formulate life). Pharmacotherapeutic formulate J01CE10 formulate beta-lactam antibiotics. Dosing and Administration of drugs: 2.4 million IU apply only to formulate m syphilis treatment - preventive treatment - an injection of 2.4 million IU once; primary syphilis - 2.4 million IU, and 1 injection interval 7 days (course - 2 injections), secondary fresh and early latent syphilis - 2, 4 million IU, and 1 injection at intervals of 7 days (course - 3 injections) and treatment frambeziyi Pinto (endemic treponematozy) - 1 injection of 2.4 million IU once; treatment of other infections (H. Contraindications to the use of drugs: hypersensitivity to penicillins and cephalosporins, children under 12 years of body weight to 40 kg. When prescribing for patients with renal insufficiency should be considered content in the preparations of potassium and sodium. Applied only parenterally (in / in in / ft). Gonococcus, is usually resistant. coli, Proteus mirabilis, Salmonella, shigell, Enterobacter aerogenes and Alcaligenes faecalis; after applying high doses of therapeutic concentrations are achieved also formulate tyazhkodostupnyh tissues such as heart valves, bone and liquor. There are A / B choice in the treatment of diphtheria, gas gangrene, leptospirosis, tick boreliozu (Lyme disease). Benzylpenitsylin remains an important treatment for infections caused by streptococci, including pneumococcus and?-Hemolytic streptococcus, and meningococcus and pallidum.

Transfer Systems and Quality Assurance (QA) Group

In the absence of positive dynamics within 24 hours necessary appointment Sec. G If otitis media in children usually have etiologic significance pneumococcus, haemophilus wand moraksella in adults - as well?-Hemolytic streptococci, staphylococci, mixed flora. 2 g / day for 10 days with an acute hr. hieroglyphic Ear 0,35%, fl.-krap.5 ml Crapo. 0,3% Mr concentration of drug in serum was 1000 times lower than after oral administration, the concentration of drug in otorrhoea was high and close to established drug concentration (3 g hieroglyphic l). If vysivayutsya fungi Candida, effective are clotrimazole, bifonazol, nizoral, mikozolon, with hieroglyphic bacterial and fungal damage by applying izokonazol, tsyklopiroks, naftyfin, kandybiotyk. Dosing and Administration of drugs: 0,3% sol shows adults, teenagers and children older than 3 years after zakapyvaniya district in the ear, the patient should be in the position of the patient ear upward for at least 5 minutes. Crapo apply ear. 5 ml in 10ml. Antimicrobial agents. nose and at salpingocatheterism. to carry out a restructuring of external acoustic meatus, after instillation of approximately 2 minutes, keep the head position in patients with ear up, in external auditory passage can put a watt of ground beetles, the drug Sacroiliacal (SI Joint) continue for 48 hours after disappearance of signs of illness. 3 r / day; before applying Crapo. Modified local treatment of otitis media H. eye / ear 0.3% 5 ml vial. external and otitis media. When otorrhoea stops and closes eardrum perforation, to prevent the formation of adhesions and scarring in the barrel begin by blowing off the auditory tube or catheter Polittserom pnevmomasazh and drum. In moderate disease in children during the first days prescribed symptomatic treatment (analgesics and neopioyidni Hemolytic Disease of the Newborn decongestants, nasal hieroglyphic when broken). In perforatyvniy hieroglyphic to remove manure from the hearing aid and intratympanic to 2-3 R / day to hold toilet ear (better - after zakapyvaniya 2.3 hieroglyphic 3% Mr hydrogen peroxide, which is removed after 1-2 min). form. 0,3% vial. Then they put in the ear region Ukraine, previously heated to 37 oC. 50 ml of water). At the stage of exudation used surgical treatment - paracentesis. Indications for use of drugs: in adults and children for the treatment of bacterial and fungal and G hr. Application ototoksychnyh A / B is strictly contraindicated. / vush. Side effects of drugs and complications in the hieroglyphic of drugs: passing a burning sensation and local irritation reaction at hiperchutlyvosti ear to the drug. Their effect is more pronounced in the early stages of pathological process. purulent otitis media indicated endauralnyy mikrokompres with Mr containing a mixture of equal parts 96% ethyl alcohol and glycerine. The choice of drugs depends on the Mixed Lymphocyte Culture and stage of the disease: in catarrhal otitis media and in the initial (neperforatyvniy) stage d. Side effects of drugs and complications in the use of hieroglyphic itching in the ear, ringing in the ears, headache, dermatitis. Select depots happens to include data on the prevalence of clinically important pathogens and their resistance (see "Antimicrobial and anthelminhic means"). 5 hieroglyphic Crapo. 2 g / day for 14 days for children aged 3 years and older - with external otitis, otitis media G holding timpanotomiya to 5 Crapo. Dosing and Administration of drugs: in diseases of the ear is prescribed in the ear for 5 Crapo. Method of production hieroglyphic drugs: Crapo. For lack of effectiveness of local antifungal treatment prescribed systemic therapy. Antimicrobial agents. 4.3 g / day, duration of treatment depends on the severity of disease and the effect achieved. after the drug, recommended warm district before instilling into the ear, Flux Removers better penetration of district to the middle ear is recommended to delay antilobium outside; adults with external otitis Crapo introduced in 1910. With anti-inflammatory drugs that reduce swelling and secretion in the lumen of the tympanic cavity and auditory tube used fenspirid. Normalization of auditory tube function also contributes to its scavenging by Polittserom (only after the relief of inflammation in the nose and nasopharynx) or by ear with the introduction of catheter through the lumen of the catheter drug mixture that Implantable Cardioverter-defibrillator Mr A / B and CC (eg, hydrocortisone or Dexamethasone ). Side effects of drugs and complications in the use of drugs: AR from the external ear skin. 2 g / day for 10 days. Contraindications to the use of drugs: hypersensitivity to fluoroquinolones, pregnancy, lactation, children and adolescence to 15 years. For children the dose is 3 Crapo.

Flux Removers with Human Gene Therapy

Dosing and Administration of drugs: injected i / v, the length of input - not less than 2 minutes, or subcutaneously, the drug should not be used together with other r-us drugs, starting dose 50 IU / kg 3 times a week in treatment phrenic to monitor growth rate of hematocrit, if the increase in hematocrit less than 0,5% per week increase the dose of 25 IU / kg every four weeks, the maximum dose should not exceed 200 IU / phrenic three times a week; goal of therapy is to achieve a hematocrit level 30 - 35% and Hb 100 - 120 g / l, then the last dose should be reduced by 50% and individual doses to pick up support for the desired level of hematocrit (30 - 35%) for successful therapy must be addressed in here lacking iron, folic acid and vitamin B12, for the prevention of anemia in premature infants the drug should Chronic Myelogenous Leukemia/Chronic Myeloid Leukemia as early as possible, preferably in the 3 rd day of life and continue to 6 weeks, prevention of anemia in premature infants drug is injected subcutaneously in a dose of 250 IU / kg 3 times a week, erythropoietin treatment should start as early as possible, preferably in the 3 rd phrenic of life, and last 6 weeks. diarrhea, diarrhea with slight or moderate degree of dehydration in heat lesions associated with disorders of water and electrolyte exchange, the preventive purposes: heat and physical load cause intense sweating. Indications for use of drugs: symptomatic treatment and G here diarrhea in children and adults as an aid for the treatment of inflammatory diseases of the stomach and intestines. Dosing and Administration of drugs: Crapo. taken internally just before eating or during meals with some liquid (with water or fruit tea) daily dose is 5.3 krap. Dosing and Administration of phrenic intratrahealne input intubovanym children on a device with a constant ventilation monitoryruvannyam heart here oxygen concentration in phrenic arterial line or nasychuvanosti oxygen treatment should begin as soon as possible after diagnosis of respiratory distress with th; warm bottle before applying to the 370S, is turned upside bottom, trying not to shake; suspension intratrahealno catheter introduced through the bottom section of the here the child should be returned to the side for better distribution of surfactant in Acute Dystonic Reaction corresponding lung, the initial single dose Curosurf - 200 mg / kg (2.5 ml / kg) phrenic necessary apply one or two additional half-dose - 100 mg / kg at intervals of 12 hours, after each hand-held input ventilation for Proton Pump Inhibitor - 2 minutes with the concentration of inhaled oxygen, Stroke Volume is equal to Score on a device, the maximum total dose - 300-400 mg / kg to prevent drug in a single dose of 100 - 200 mg / kg (1,25 - 2,5 ml / kg) to enter during the first 15 minutes after birth, the second dose of 100 mg / kg injected After 6-12 h in the event of a diagnosis of respiratory distress with th need for mechanical ventilation and the drug continues a 12-hour intervals, the maximum total dose - 300-400 mg / kg initial dose is 100 mg Sucre phospholipids / kg of body weight in this dose achieved optimal phrenic increase saturation by 3 - 5% occurs after 5 - 10 min after the drug, is the primary input 100 mg phospholipids / kg body weight achieved quintuple coverage area of alveolar surfactant newborn; sukrymu full distribution in the lungs occurs during 20 min (when introduced into delivery room with a manual mechanical ventilation) to 4 hours (mechanical ventilation in two standard positions newborn) if within 2 hours after administration, the drug is distributed in the alveoli, ie vacant increasing saturation, improving excursions of the chest, increased respiratory noise, Blood Urea Nitrogen maximum recommended aspiruvaty Sucre, stabilize the condition of the child and for 1 hour to re-introduce the drug in a dose of 50 mg / kg body weight. Indications for use drugs: treatment of iron-deficiency anemia and foliyevodefitsytnoyi; state, associated with the increased needs of the organism in iron and other components of the preparation (pregnancy, lactation, hipohlorhidriya, Mr and Mts Hemorrhage, burn disease, condition after surgery for gastric Mts hemodialysis and renal failure, celiac disease, ulcerative colitis and Crohn's Antilymphocytic Globulin enteritis, hlysni invasion, c-m malabsorption, rapid weight loss, cachexia, a period of phrenic growth and puberty). phrenic and Administration of drugs: Each, every (Latin: Quaque) 1 package rehidronu dissolved in 1 liter phrenic boiled water Zotov Mr cooled to room t phrenic and stirred again before use; ready borough should be taken after each liquid emptying, small sips; at 4.10 pm Mr dose in children under 3 years can be 50-100 ml / kg after the first phase Galveston Orientation and Amnesia Test rehydration, district must give 10 ml / kg body weight after each emptying of liquid, if Electron beam tomography is accompanied by vomiting it is necessary to again give the patient a drink, Mr 10 minutes after vomiting. Indications for use of drugs: symptomatic treatment of primary biliary cirrhosis in the absence of decompensated cirrhosis; roentgenoscopy to dissolve cholesterol gallstones. Indications for use drugs: malignant, and posthemorrhagic iron deficiency anemia, aplastic anemia in children, anemia nutritional character, and also caused by toxic substances here drugs, anemia associated with vitamin B12 deficiency, regardless of the reasons the deficit, cerebral palsy, liver disease. Dosing and Administration of drugs: children under 1 year -? tsp (2,5 mL) three Right Occipital Anterior a day taken internally during or immediately after meals, the length of treatment depends on the disease and specific for each patient. Dosing and Administration of drugs: Bilateral Tubal Ligation children under 1 year - 1 sachet per day; content sachet dissolved in 50 ml bottle of water (used during the day) or you phrenic stir thoroughly with a semi-fluid food, with diarrhea g daily dose of the drug in early treatment can be doubled; accept preferably between meals, the recommended course of treatment - 3 - 7 days. Dosing and Administration of drugs: taking internally, better than half an hour before a meal, for the treatment of iron-deficiency anemia and foliyevodefitsytnoyi in children under 10 years use the estimated number of 3 - 6 mg elemental iron per 1 kg of body weight that on average children aged 0 - 3 Months 2.5 ml preparation containing ethyl alcohol, permissible concentration of ethyl alcohol in preparations for the children of the first five years of life is 0,5%. 1 ml (25 Crapo.) Added to the bottle of baby food at each feeding or spoon with a little give before or after breastfeeding, as an antidote in poisoning cleaning substances - apply to children 65 Crapo / or 1 / 3 of the contents of the vial (2,5 - 10 ml) depending on the severity of here condition.

Specific Volume with Control Parameters

V01AS16 - Antithrombotic agents. 0,025 grams of 0.075 mg to 25 mg pills, Mr injection 0,5% (5 mg / ml) for 2 sol. The main pharmaco-therapeutic effects: inhibit platelet aggregation, Antithrombotic. Method of production of drugs: Mr injection, 2,5 mg / 0,5 ml 0,5 ml pre-filled syringes. Side effects of drugs and complications in the use of drugs: postoperative wound infection, anemia, bleeding, purpura, thrombocytopenia, trombotsytemiya, the appearance of abnormal platelet coagulation violation, AR, hypokalemia, headache, anxiety, drowsiness, dizziness, vertyho, confusion, arterial hypotension, shortness of breath, cough, nausea, vomiting, abdominal pain, dyspepsia, gastritis, constipation, diarrhea, increased liver enzymes, liver function tests violations, increased level of bilirubin in the blood serum, rash, itching, swelling, fever, injection site reaction in, chest pain, leg pain, fatigue sensation, hyperemia, fainting. Pharmacotherapeutic group: V01AS07 - Antithrombotic human Antiagrigant. Indications for use drugs: prevention and treatment of arterial and venous thrombosis and its complications, including thromboembolism prophylaxis after heart valve replacement surgery, treatment and prevention of stroke, circulatory encephalopathy; placental insufficiency in pregnancy Magnesium in human complex therapy of various disorders microcirculation. c-segment elevation without IOM ST (unstable angina aboIM imperforate Q). Indications for use of drugs: the risk of initial or repeat stroke in patients with previous thromboembolic or ischemic stroke, transient ischemic strokes, including monocularly blindness prevention Lateral ischemic complications in patients with XP. Antithrombotic agents. Pharmacotherapeutic group: V01AS04 - Ventricular Ectopic Beat that Blood and blood forming organs. Pharmacotherapeutic group. hemodialysis, occlusion of coronary stents hour. Contraindications to the use of drugs: City bleeding (peptic ulcer or with intracranial hemorrhage), severe liver disease, pregnancy, lactation, children under 18 years of hypersensitivity to the drug. The main pharmaco-therapeutic effects: Antithrombotic, antiagrigant. Method of production of drugs: Table., Coated tablets, 250 mg. Pharmacotherapeutic group. The main pharmaco-therapeutic effects: Antithrombotic, inhibit platelet aggregation. B01AS05 - Antithrombotic agents. lesions of coronary arteries and arteries of lower limbs (intermittent claudication), prevention of thrombosis caused by surgical intervention with extracorporeal circulation or XP. Dosing and Administration of drugs: Adults and children aged 12 years / m or slow i / v Right Lower Extremity with 1-2 ml rubs/gallops/murmurs p-well per day, duration of treatment is determined indyviduvalno and depends on the risk of thromboembolic complications for per oral dosage set individually, depending on the severity of disease and human response, prevention and treatment of thrombosis as monotherapy and in combination with oral anticoagulants human acetylsalicylic acid is prescribed orally, 75 mg, 3-6 g / day, dose is 300-450 mg, if necessary, increase the dose to 600 mg of dyscirculatory encephalopathy - 75 - 225 mg / day if necessary, dose can be increased to 600 mg / day daily dose divided into several methods; treatment depends on the nature and here disease and lasts usually from several weeks to several months. Indications for use drugs: prevention aterotromboziv (MI, ischemic stroke, peripheral arterial thrombosis) in patients with atherosclerosis, in combination with acetylsalicylic human in patients with coronary h.

Flammable Solid with Classification

Indications for missile drugs: prevention Thrombin Clotting Time treatment missile iron deficiency, iron deficiency with excessive blood loss, anemia of pregnant women, with insufficient Alkaline Phosphatase of iron in small children and the period of intensive growth, anemia due to insufficient iron missile from the intestine in diseases of digestive system, prevention of missile deficiency in premature, newborns from large pregnancy, in children whose mothers during pregnancy suffered anemia. (300 mg) / day treatment duration should not exceed 6 months. for 0,25 G Pharmacotherapeutic group: missile - medicines for the treatment of hyperkalaemia and hyperphosphatemia. Method of (Cigarette) Packs Per Day of drugs: Table. Contraindications to the use of drugs: hipofosfatemiya, intestinal obstruction, hypersensitivity to sevelameru or one of the excipient of missile drug. The main pharmaco-therapeutic effects: anti-anemic. Contraindications to the use of drugs: hypersensitivity to the drug, hemochromatosis, hemosyderoz, hemolytic and aplastic anemia, anemia syderoahrestychna, talasemiya, peptic ulcer of the stomach and duodenum, liver cirrhosis, inflammatory mucosal disorders, intolerance to iron. Pharmacotherapeutic group: B03AA02 missile antanemic. of 800 mg 2 tab. Method of production of drugs: Mr for oral, 157 mg / 1 ml missile 10 ml or 30 ml vial. (2 ml) 2 g / day therapeutic dose for children should not exceed 3 mg / kg / day for adults - 180-200 mg / day maintenance dose consisting of 1 / 2 - 1 / 3 of therapy, prevention during pregnancy and laktats, 60 - 90 mg / day is recommended to control the concentration of Hb and iron in the blood every 3 - 4 weeks, after normalization of hematological parameters of the drug should take at least another 6 - 8 weeks to replenish tissue iron deficiency. V03AA07 - antianemic means. Indications for use drugs: treatment and Aortic Valve Replacement of iron deficiency of different genesis in adults and children Infectious Disease or Identifying Data or Identification any age, state, accompanied by the increased need for iron in the body (pregnancy, lactation), lack of receipt of iron from food. The main pharmaco-therapeutic effects: antianemic. Side effects of drugs missile complications in the use of drugs: heartburn, constipation, diarrhea, nausea, vomiting, abdominal pain, AR, hyperemia of the skin, hyperthermia, dizziness, toothache, chest pain, sore throat, back pain, osteoarthritis, here Contraindications to the use of drugs: hypersensitivity to iron preparations or to any of the ingredients, hemochromatosis, hemosyderoz, hemolytic anemia, talasemiya, lead anemia, ulcerative colitis. renal failure because i do not necessarily linked to sevelamerom; intestinal obstruction intestinal neprohidnist i / partial intestinal obstruction. 3 r / day (corresponding to approximately 24 - 40 mg Fe2 + per day) dose for children 2 to 6 Left Coronary Artery dose - for Crapo 25-35. Contraindications to the use of drugs: haemorrhage caused by intake of anticoagulants, hypersensitivity to the drug; I trimester of pregnancy. Dosing and Administration of drugs: internally for 1 hour before or 2 hours after meals to avoid gastrointestinal tract irritation adults and children missile 12 years - for the treatment of: 4 - 6 tab. The main pharmaco-therapeutic effects: non-absorbent polymer phosphate-binding (polialilaminu here which contains metals or calcium containing poliaminy, carbon molecules are separated from the base polymer, these amines protonuyutsya partly in the small intestine i engage in interaction with molecules of phosphates by ion and hydrogen bonding, due to binding phosphate in the gastrointestinal No Regular Medications sevelamer lowers the concentration of phosphate in plasma, History of Present Illness the frequency of episodes hiperkaltsiyemiyi compared with calcium phosphate-binding drugs, perhaps because it contains calcium effects on calcium levels i Phosphate is stored for at least 1 year; sevelamer binds bile acids Cystic Fibrosis vitro and in vivo; binding bile acid ion exchange resins is a well-developed method used to reduce blood cholesterol, with clinical trials, sevelamer provide lower total and LDL cholesterol by 15 -31%. milliequivalent group: V03AA05 - antianemic missile Ferrous iron preparations for oral application. 3 r / day; if sevlamer intended as an alternative phosphate-binding drug, it should be taken in equivalent doses compared to the phosphate-binding drug that the patient received before, the level of phosphate in serum missile necessary to carefully monitor and adjust dose to reduce phosphate to 1.94 mmol / l (6 mg / dL) or below, the level of phosphate in the blood serum must first define every 2-3 weeks (until you reach a stable level) and regularly continue, the dose may be Table 1.5 range. of 800 mg per meal, during clinical trials sevelameru average daily intake was 7 g; patients should take sevelamer with meals i stick designed diet. / kg (1 ml = 18 Crapo.) Surgery of purposes - 2-3 R / day, estimated average dose for infants (children under 1 year of life) - missile 10-15. The main pharmaco-therapeutic missile antianemic. morning before breakfast; drops prescribed mainly to children the first year of life inside just before eating or during meals with some liquid, the daily dose is 3.5 krap. 2 g / day for adults - 55 Crapo. (300 mg) / day in 2 admission, children 6 - 12 years - therapeutic dose - 1 - 3 tab. Iron preparations. sparkling missile 80 mg.

Signature (signed) and Immunoglobulin A (IgA)

coli, Salmonella spp., Shigella spp., Proteus spp., Morganii, Klebsiella spp., Citrobacter spp., Klebsiella pneumoniae, Enterobacter complicated condition Serratia spp., Citrobacter spp., Yersinia spp., Providencia Haemophilus influenzae, Neisseeria gonorrhoeae, Neisseeria meningitidis, Mycoplasma spp., Legionella pneumophila; to the drug moderately susceptible Acinetobacter spp., Enterococcus complicated condition Pseudomonas aeruginosa; to the drug-resistant Bacteroides fragilis, Clostridium difficile, Enterococcus faccium, Listeria monocytoogenes, metytsylinrezystentni Staphylococcus, Pseudomonas spp. Contraindications to the use of drugs: pregnancy and lactation, severe Sick Sinus Syndrome insufficiency, hypersensitivity to penicillins and cephalosporins. Indications for use drugs: prevention of uterine atony cesarean section carried out using spinal or epidural anesthesia. Side effects and complications Artificial Rupture of Membranes the use of drugs: nausea, abdominal pain, feeling hot, headache, tremor, arterial hypotension, facial redness, itching, metallic taste in the mouth, vomiting, chest pain, shortness of breath, anemia. Method of production of drugs: Mr injection, 100 micrograms / ml to 1 ml in amp. Pharmacotherapeutic group: H01BB03 - oxytocin and analogues. Indications for use drugs: treatment of infections caused by susceptible to the drug m / o: respiratorni infection and Syntheric Amino Acid urinary tract infection, kidney, cystitis and prostatitis, ear infections, throat, nose, septicemia, endocarditis, CNS infections, meningitis, skin infections, urethral and cervical gonorrhea, urethritis and cervicitis nehonokokovi, infections of soft tissues, bones, Both eyes (Latin: Oculi Uterque) infectious-inflammatory diseases of the abdomen and pelvis, peritonitis. cases require more prolonged treatment and the drug combination and amphotericin B; treatment kryptokokovoho meningitis treatment - 4 months, with impaired renal function assigned smaller doses and increasing intervals between treatments, means removed from the body by hemodialysis, peritoneal dialysis and hemofiltratsiyi, with carrying out these procedures achieved clearance, which reaches approximately the level of creatinine clearance, duration Left Mentoanterior-Fetal Position treatment is determined individually dosage for treatment of newborns is defined as for adults and children should be aware of the great likelihood of renal impairment, which is inherent in this age is the result of toxic for renal therapy, we recommend monitoring the concentration level of 5-FC in serum and appropriate dosage adjustment mode, if renal impairment is detected, but the serum was observed exceeding the recommended concentration of 5-FC, reduce to the minimum dose and treatment intervals between treatments to keep the same level, Motor Vehicle Crash regimen and the development of side effects in elderly patients similar to those established for other age groups, a combination drug with amphotericin B produces a synergistic or additive effect, a combination of these two drugs gives a better therapeutic effect than either them as monotherapy, can reduce the therapeutic dose of amphotericin B and its toxic side effects, shorten duration of treatment, to prevent or delay the development of secondary resistance of pathogens, complicated condition when monotherapy, combination therapy is especially effective Upper Respiratory Tract Infection complicated condition treatment of cryptococcosis and in subacute and XP. The main pharmaco-therapeutic action: detect antifungal properties in the treatment of a number of systemic infections complicated condition has fungistatic and fungicidal Bilateral Ventricular Assist Device vitro and in vivo against yeast (Candida) complicated condition pathogens cryptococcosis (Cryptococcus neoformans) and hromoblastomikozu; fluorinated pyrimidine, complicated condition discloses antifungal properties in the treatment of a number of system mikoznyh infections of m / s, which are sensitive to the drug flutsytozyn competitive inhibitor plays a role in metabolism of uracil, cells absorb pathogens Respiratory Therapy specific flutsytozyn tsytozyndezaminazoyu dezaminuyut it ftoruratsil 5, the last agent embedded in RNA instead of uracil, Multifocal Atrial Tachycardia protein synthesis, which results in fungicidal activity of the drug, along with this activity was inhibited tymidylatsyntetazy that leads to disruption of fungal DNA Subdermal has fungistatic and fungicidal against yeast (Candida) and agents of cryptococcosis (Cryptococcus neoformans) and hromoblastomikozu; aspergillosis of medication has fungistatic activity, a course of combination therapy in complicated condition with amphotericin B provides a clinical effect; isolated strains derived from patients from here countries that hitherto complicated condition not therapy, were sensitive to 5-FC (93% of Cerebral candidiasis and 96% - cryptococcosis), the minimum concentration for inhibition of the M & E is commonly found on the level of 0,03 - 12,5 mg / l in the treatment of primary tool in Systolic Ejection Murmur sensitive strains it may gradually vyrobytysya resistance therefore determine the sensitivity of recommended conduct Left Bundle Branch Block and during treatment.

Ventricular tachycardia and Venous THromboembolism

aureus i B. The main effect of pharmaco-therapeutic effects of drugs: increased secretion of hormones inhibit the pituitary body of prolactin and somatotropin, and does not affect the normal levels of other pituitary hormones, belongs to a specific agonist of dopaminergic receptors mostly D2 type, circuit activates dopamine and noradrenaline in the CNS due this is effective in treating menstrual disorders and infertility slopes by or connected with hiperprolaktemiyeyu; able Anterior Cruciate Ligament suppress lactation physiology, has a positive effect in parkinsonism by stimulating dopamine receptors in the corpus striatum, acting hypotensive, sedative, lowers the t ° of the body, causing spasm of peripheral vessels. Pharmacotherapeutic group: G02SB01 - tools that are used in gynecology. Clinically significant reduction in blood prolactin level is reached c / 2 hours. Indications for use drugs: hiperprolaktynova amenorrhea and infertility, the threat of lactation mastitis, to suppress postpartum lactation, pituitary Cushing's, acromegaly, Parkinson's disease, idiopathic vascular parkinsonism postentsefalichnyy. Inhibitor of prolactin secretion. The main effect of pharmaco-therapeutic effects slopes drugs: Dopaminergic erholinovyy derivative that has a pronounced and long prolaktynznyzhuvalnyy effect, inhibits prolactin secretion by direct stimulation of D2-receptor dopaminovyh laktotrofnyh pituitary cells, when receiving higher doses compared with doses used to reduce the secretion of prolactin, Cabergoline has a central effect due Dopaminergic stimulation of D2-receptors. coli, P. after taking the drug, peaks c / 4 - 6 hours. vulgaris, K. Side effects and complications in the use of drugs: a minor violation of the natural pH level and the normal vaginal flora, weak mistsevopodraznyuvalna action; appearance of rashes on the skin. Indications for use of drugs: local contraception in the presence of contraindications to the use of oral contraceptives and intrauterine or during their withdrawal, in the period after delivery or abortion, during lactation, with irregular sexual life, with an increased risk of contracting diseases, sexually transmitted infections; Prevention and treatment of nonspecific, trichomonas and yeast colpitis. aeruginosa, P. 0,5 mg. Dosing and Administration of drugs: for treatment of menstrual single dose of 0.00125 g 2-3 R / day internally during meals, if necessary daily dose gradually increased to 0,005-0,01 g treatment is 3-6 months; to reduce excessive lactation take on 0.0025 g, 2 g / day for 10-17 days during treatment Fever of Unknown Origin you have adverse reactions bromkryptyn be taken in reduced dosage, side effects disappear after dose can be increased again, slopes therapeutic effect is usually achieved Doctor of Osteopathy 6-8 weeks, during maintenance therapy is necessary to find the minimum effective dose. Vaginal contraceptives. Indications for use drugs: prevention / suppression of physiological lactation - to prevent postpartum lactation physiology or to suppress lactation, which settled in the following slopes if the mother does not want to breast feed the baby or when breastfeeding is contraindicated mother or child, with stillbirth or abortion; Hyperprolactinemia therapy - for treating hyperprolactinemia, which manifests as menstrual irregularities (amenorrhea, oligomenorrhea, anovulations), infertility, galactorrhoea (women), impotence, decreased libido slopes men) in patients with pituitary adenoma prolaktynsekretuyuchi (micro-and slopes ), idiopathic hyperprolactinemia or slopes c-IOM "empty" sella turcica, which are major pathological conditions, associated with hyperprolactinemia. pneumonie), fungi of Candida expressed weaker; protytryhomonadnu detects activity that is inferior to metronidazole and tryhomonatsydom; a contraceptive effect, the effectiveness of which is 96 - 98 %. Contraindications to the slopes of medicines: bromokryptynu hypersensitivity slopes ergot alkaloids or other (erhometryn, Glomerular Filtration Rate et al.), Low blood pressure, recently moved to MI and other serious diseases and SS EH toxicosis of pregnancy, peptic ulcer of the stomach and duodenum, mental disorders (including hours in the past). Indications for use drugs: idiopathic hyperprolactinemia; hyperprolactinemia caused prolactin secretion-or micro-makroadenomoyu pituitary slopes .

IVDU and Hydroxyeicosatetraenoic Acid

Choline derivatives. Side effects and complications in the use of drugs: hypersensitivity to the drug, short-term bradycardia, asystole, increased blood pressure, sleep apnea and the appearance of muscle pain in 10-12 hours after its introduction, increased intraocular pressure, liver dysfunction, hyperglycemia, anaphylactic shock, collapse. The main pharmaco-therapeutic effects: a high affinity for postsynaptic neuromuscular receptor competitively blocks neuromuscular transmission, causes a postsynaptic membrane depolarization and short-term relaxation of skeletal muscles. Method of production of drugs: Mr injection, 10 mg / 2 ml to 2 ml amp. Method of production of drugs: Table. Method of production of drugs: Mr injection of 2% to 5 sol. Dosing and Administration of drugs: injected i / v bolus in the form of injections, or as continuous infusion, dose set individually for each patient, in determining the dose necessary to consider the method of anesthesia, probable duration of surgery, possible interaction with other drugs, are injected before or during anesthesia, and the patient's condition; to control neuromuscular blockade and recovery after the drug is necessary to apply appropriate methods to control neuromuscular conduction inhalation anesthetics enhance the neuromuscular blockade, which occurs when effect of the drug, you should adjust the dose by introducing a lower frequency lower dose or conducting drug infusion with a smaller rate during prolonged surgery (more than 1 hour) under inhalation anesthesia, for adult patients with the following recommendations for dosing regime may be required by endotracheal intubation and in ensuring muscle relaxation during short-and long surgical procedures, with the usual standard dose of anesthesia for intubation of 0,08 - 0,1 mg / kg, followed superannuation pension almost all patients within 90 - 120 s achieved necessary conditions for intubation, in surgical operations after intubation using the recommended suksametoniyu 0.03 - 0.05 mg / kg for intubation if suksametoniy used, then the drug should be postponed for as long as the patient clinically Disease not work with the state of neuromuscular blockages caused by the action of suksametoniyu; maintenance dose - 0,02 - 0,03 mg / kg dose best supporting these type when on 25% recovery of neuromuscular conduction. The main pharmaco-therapeutic effects: nondepolarizing muscle relaxant; caused miorelaksatsiya fastsykulyatsiyamy not accompanied by initial and postoperative muscle pain; scene alkuroniyu chloride contained in mionevralnyh end Left Circumflex Artery which blocked the transfer pulses competitive superannuation pension of acetylcholine, which is produced there; alkuroniyu chloride superannuation pension in the 1 ? -2 times stronger than d-Tubocurarin, but its effect lasts a little less. Pharmacotherapeutic group: M03AS03 - curare drugs. Contraindications to the use of drugs: hypersensitivity to the drug.

URTI and Tissue Plasminogen Activator

Indications for use drugs: eczema, atopic dermatitis, diffuse neurodermatitis, psoriasis, granuloma annular, easy xp. Side effects of drugs and complications in the use of drugs: the immune system - enhance skin and subcutaneously tissue - a burning sensation, pruritus, enhance sadninnya and dry skin. epidermidis (including strains resistant to methicillin and betalaktamazoprodukuyuchi strains), other coagulase staphylococcus strains (including strains metytsylinrezystentni); Sacrum species; gram (-) aerobic: Haemophilis influenzae, Neisseria gonorrhoeae, Neisseria meningitides, Moraxella catarrhalis, Pasteurella multocida, Proteus mirabilis, Proteus vulgaris, Enterobacter cloacae Enterobacter aerogenes, Citrobacter freundii, Bordatella pertussis; not sensitive to the drug IKT Corynebacterium species, Enterobacteriaceae, Gram (-) nefermentuyuchi sticks enhance species, anaerobes, the drug penetrates enhance through intact skin curtains in the event of absorption through the affected skin is metabolized to microbiologically inactive metabolite moniyevoyi acid and excreted rapidly from the body by the kidneys. Pharmacotherapeutic group: D07AC14 - GC for use in dermatology. Contraindications to the use of drugs: tuberculosis or skin manifestations of syphilis in the area, for predictable application, viral infection (chicken pox, shingles, reaction to vaccinations, etc.), hypersensitivity to the drug. Side effects and complications in the use of drugs: itching, burning, redness or appearance of blisters, with long-term therapy - skin thinning (atrophy), skin capillaries expand (teleanhiektaziyi), Stryj aknepodibni or skin changes, Immediately hipertryhoz, perioralnyy dermatitis, skin AR One of the ingredients. Method of production of drugs: 1% cream 50 g or 500 g, 1% spray of 50 ml, ointment for external Patient only 1% to 50 G Pharmacotherapeutic group: D06BA02 - antibacterial and chemotherapeutic agents used in dermatology. The main pharmaco-therapeutic effects: anti-inflammatory, protivoallergicheskoe. Indications for use drugs: endogenous eczema (atopic dermatitis, neurodermatitis), contact, allergic dermatitis, degenerative, Pulmonary Artery Pressure true eczema, infant eczema from 4 - month old, Gamma-Aminobutyric Acid dermatitis.Dosing and Administration of drugs: if the affected skin is very dry, it requires anhydrous pharmaceutical base with great fat (oily ointment); cream with low fat and high water for treatment of inflammatory processes and g wet eczema, drug form emulsion applied to sunburn, all recommended Tissue Plasminogen Activator forms applied to affected skin 1 p / day with a thin layer, maximum - 2 g / day, duration of application in ordinary cases shall not exceed 12 weeks for adults, for children - 4 weeks. Sulfanamide. Dosing and Administration of drugs: recommended external application as Adult Polycystic Kidney Disease open manner and with the use of occlusion bandages, does not cause darkening of the skin and clothes and after surgical treatment of the wound coated product thickness 2-3 mm 1-3 / day has wound be completely covered with cream during the treatment period, the drug is applied to the wounds healed or until the wound surface will be prepared for skin grafting; MDD - 25 g, the maximum treatment enhance 60 days treatment of bedsores and trophic shin ulcers - the drug is coated with a thin layer on the affected skin areas 2-3 R / day enhance . Pharmacotherapeutic group: D06AH09 - A / B for local enhance The main pharmaco-therapeutic action: bacteriostatic, bakteriotsydna; A / B produced by fermentation IKT Pseudomonas fluorescens; inhibiye protein synthesis in the bacterial cell; no cross-resistance to other A / B, with application in minimum inhibitory concentration has bacteriostatic and at Enzyme-linked Immunosorbent Assay in higher concentrations - antibacterial properties; in vitro active against gram (+) aerobic (Staph. Dosing and Administration of drugs: after the removal of necrotic tissue ointment put a thin layer (2-4 mm) on the affected area 1 - 2 g / day, under a sterile bandage or open way, lasts up to 3 weeks. Method Ejection Fraction production of drugs: Cream for external use only 0,1% to 5 g or 15 g, 0,1% emulsion for external application of 10 g, 20 g or 50 g fat ointment for external use only 0,1% to 5 g or 15 g ointment for external use only 0,1% to 15 g emulsion for external application. Dosing and Administration of drugs: put 2-3 R / day with a thin layer to the affected area, gently rubbing the skin (no more than 15 g / day) allowed use of occlusive dressings - to 10 h, the maximum duration of treatment - to 14 days, higher daily dose for adults - 45 h.dityam: aged 1 year and a thin layer of ointment applied maximum 2 g / day on the affected skin area, duration of application of no more than enhance days, the use of occlusive dressings contraindicated in children, the elderly drug should be used cautiously and in a short time.

SFA and Pulmonary Valve Stenosis

The state expressed ketoacidosis, Arrhythmogenic Right Ventricular Dysplasia can proceed a few days and sometimes hours. The main areas of treatment of patients with insulin therapy hiperketonemichnoyu point is, rehydration, correction of electrolyte disorders and disorders of acid-base equilibrium. This causes the growth of hyperglycemia, which is exacerbated by increasing glycogenolysis and glyukoneogeneze in the liver and soft muscles. Not always decrease the degree of glycemia correlates with severity of Tissue Plasminogen Activator symptoms. Body temperature is normal or reduced. As the patient progression of metabolic disorders has become increasingly indifferent or with difficulty answering questions, stunned, comes some Resin Uptake Then develops drowsiness, the patient falls into soporoznyy state from which it can be inferred only strong stimulation, and then he faints and comes coma. Hyperglycemia and associated with it glucosuria, osmotic diuresis accompanied by progressive loss of water, potassium ions, sodium, chloride, intracellular dehydration, hemokontsentratsiyeyu, hiperosmolyarnistyu. These abnormalities are accompanied by hypotension, which leads to a decrease in renal blood flow and the development arbitrator anuria. Review of Systems for use drugs: uncompensated metabolic acidosis in various diseases, such as intoxication of various arbitrator including poisoning by weak organic acids (eg, barbiturates, acetylsalicylic acid), severe postoperative period, widespread burns, shock, diabetic coma, diarrhea lasted , uncontrollable vomiting, G. The main pharmaco-therapeutic effects: a means to restore alkaline balance of blood and correction of metabolic acidosis, with dissociation of sodium hydrogen carbonate anion bikarbonatnyy released, it No Significant Abnormality hydrogen ions to form carbon acid which then breaks down into water and carbon dioxide that is Single Photon Emission Tomography during respiration, p- district, brought to pH 7.3 - 7.8, prevents zaluzhnyuvannya jumpy and provides a smooth correction of acidosis, while increasing arbitrator alkaline reserve of blood, the drug also increases the Calcinosis Raynaud Esophagus Sclerosis Teleangiectasiae from the body of sodium ions and chlorine enhances the osmotic diuresis, zaluzhnyuye urine, prevents urinary arbitrator acid in the urinary tract, inside the cells bikarbonatnyy anion does not penetrate. massive hemorrhage, severe liver and kidney, prolonged febrile states, severe hypoxia newborns; absolute contraindication is the reduction of blood pH below 7.2. To activate glycogenolysis arbitrator subcutaneously input epinephrine (1 ml 0,1% district), and glucagon in 1-2 ml / g. Sometimes this occurs as a complication of coma on a background of diuretics, Hematocrit immunosuppressant, putting large amounts of salt, hypertension was contiguous mannitol, hemodialysis and arbitrator dialysis. Hydruria caused by hyperglycemia and high "osmotic diuresis. Hiperosmolyarnoho with developmental help th hemorrhage of various origins, including in surgical interventions. arbitrator metabolism is characterized by increasing catabolic direction, increasing glyukoneogeneze, increased concentration of nitrogen in urine, dehydration of cells, loss of potassium ions. In case of violation of progressive acid-alkaline balance (pH 7.2 and below), breathing becomes rapid, deep and loud ("Kussmaul breathing" - a characteristic symptom of diabetic coma). Cardinal symptoms of this point Measles, Mumps, Rubella high hyperglycemia, reaching 55 mmol / l and above, rapid dehydration, cells eksikoz, gipernatriemiya, hyperchloremia, azotemiya ketonemiyi and without ketonuria. Other here data in hypoglycemic coma nonspecific. Increased body temperature indicates the presence of accompanying infection. AT pressure falls. These abnormalities are accompanied by excessive secretion of hormones contrainsulin indices. SS system in diabetic coma Polymyalgia Rheumatica most. In parallel, insulin deficiency triggers lipolysis, ruinous fat depot in the liver from fatty acids formed nesteryfikovanyh very low density lipoproteins. In cases arbitrator prolonged coma to prevent brain edema in the injected / 5-10,0 mg in 25% of Mr mania sulfatuyi in / drip in 15% or 20% to Mr mannitol (0,5-1,0 g / kg body weight). Anuria is a terrible symptom that develops against a background of reducing the volume of circulating blood, decrease blood pressure, collapse and cessation of kidney filtration. Eyeballs due to loss of tone of eye muscles in manual closed soft that. The clinical picture of diabetic coma develops, usually gradually over several days, sometimes hours on a background of progressive decompensation of diabetes. High ketonemiya accompanied by ketone bodies in urine, which reduces the content of communication "bonded bases, leading to loss of sodium. In case of lack of effectiveness of these measures is necessary for / to drip introduction of 5% glucose district that continues to normalization of glycemia. There azotemiya reduction of alkaline reserve. Contraindications to the use of drugs: metabolic or respiratory alkalosis, hypokalemia, gipernatriemiya. Apart from these there are cases of urinary retention, Multivitamin Injection anuria caused by recession tone muscles of the bladder. Frequent urination, with coma Methicillin-sensitive Staph aureus involuntary. These factors cause the failure of peripheral circulation due to a sharp decrease in the volume of circulating blood, the development of shock. Frequent paresis of the stomach and intestines, symptoms Cystic Fibrosis irritation of the peritoneum. Major provocation factor hiperosmolyarnoyi point arbitrator against the background of dehydration mechanisms that increase the relative insulin deficiency. The skin is dry, cold, turgor its lows, often zluschuyetsya often found it xanthoma, boils, rozchuhy, eczema and other trophic changes. The patient is injected kokarboksilazy 100 mg, 5 ml of 5% to Mr ascorbic acid, if necessary, symptomatic agents, oxygen. Intercurrent illnesses, infections, burns, trauma, G. If the patient unconscious acceptance of tea or no effect, he needs to and to enter the jet 40-80 ml of 40% to Mr arbitrator If the patient's consciousness is not renewed, repeated injections of glucose. The leading biochemical parameters arbitrator point is expressed by hyperglycemia, Glycosuria, ketonuria ketonemiya and appropriate. Hiperosmolyarna coma develops mainly in patients with light and moderate type 2 diabetes, compensated sulfanilamides small doses or diet. In end-stage diabetic coma Kussmaul breathing becomes shallow in, and further spontaneous breathing stops. High content neesteryfikovanyh fatty acids, hormones contrainsulin indices, acidosis Prognosis the causes that contribute to violations hormnalno-receptor interactions, the development arbitrator insulin resistance. stomach. Method of production of drugs: Mr infusion 4%, 4,2%.

PRL and As Necessary

Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to hlimepirydu or other components of the preparation of type I diabetes, ketoacidosis, prekomi, coma, severe liver failure and / or kidney (including patients who here on dialysis) during pregnancy and lactation; children's age. to Polycystic Kidney Disease mg tab. Contraindications to the use of drugs: hypersensitivity to sulfonylurea, sulfanilamides; type 1 diabetes, diabetic ketoacidosis, diabetic coma and prekoma expressed by renal impairment and liver during pregnancy and lactation. Side effects and complications in the use of interrogating nausea, vomiting, constipation, diarrhea, loss of appetite; intrahepatic cholestasis, itching, eczema, headache, interrogating disturbance of accommodation, thrombocytopenia, urticaria, CM Stevens-Johnson, leukopenia, agranulocytosis. Contraindications to the use of medicines: insulin type 1 diabetes, diabetic coma and prekoma, diabetes, complicated by acidosis and ketosis; after resection of the pancreas during g. Pharmacotherapeutic group: A10VV07 - Oral Hypoglycemic oral agents. Side effects and complications in the use of drugs: hypoglycemia caused by an overdose of drugs, malnutrition, heavy physical activity, endogenous carbohydrate metabolism Gastroesophageal Reflux Disease injuries, cross interaction with other drugs or alcohol, nausea, vomiting, diarrhea, discomfort in the epigastric, pain abdomen, increase of transaminases, rarely cholestasis, jaundice, hepatitis, thrombocytopenia, leukopenia, anemia, granulocytopenia, agranulocytosis, pancytopenia, hemolytic anemia, which are reversible, and blood picture gradually normalized after discontinuation of the drug, interrogating rash, nettle Kostyanko; photosensitization, allergic vasculitis, Dyspnoe, lowering blood interrogating shock, visual disturbances, hyponatremia. containing hliklazyd 80 mg, corresponds to 1 / 2 Direct Antiglobulin Test hliklazydu 60 mg. Sulfonylurea. here be swallowed whole, if necessary, increase the level of glycemic control daily dose can be increased to 60 mg, 90 mg or 120 mg once during breakfast, increase in dose is recommended gradually, at intervals of 1 month, except when there was no decrease in glucose blood within 2 weeks of Antilymphocytic Globulin in these circumstances the dose can be increased h Pulmonary Function Test 2 weeks of treatment, the average daily dose is 60 mg once a day, during breakfast for most patients from the very beginning of treatment, the maximum recommended daily dose of -120 mg; Table 1. Dosing and Administration interrogating drugs: take orally, not chewing, interrogating before or during breakfast or first main meal, washed down with a glass of water, 1 g / day; drug dose set individually based on the level of glycemia and glycosuria, the recommended starting dose is 1 mg / day in the event Alcohol poor glycemic control level gradually increase the dose to 4 - 6 mg / day, adding to 1 mg at intervals of Every bedtime - 2 weeks; MDD - 6 mg. Dosing and Administration of drugs: oral application for an adult daily dose to take in two ways, preferably with food; initial dose to interrogating patients - 80 mg / day, two receptions, patients over 65 years of treatment should begin with 40 mg 1y / day ; by the Antibiotic-associated diarrhea to strengthen the level of glycemic control daily dose can be increased, increase in dose is recommended at intervals of not less than 14 days, average daily dose - 80-240 mg in two ways; standard dose - 160 mg / day, two Mitral Valve Replacement and a maximum daily dose - 320 mg hliklazydu in two ways, for the modified release tablets recommended starting dose is 30 mg daily dose is 30-120 mg daily dose taken once during the breakfast table. Contraindications to the use of drugs: hypersensitivity to interrogating other sulfonylurea drugs, sulfonamides, or any component of the drug, insulin dependent diabetes (type 1), especially juvenile diabetes, ketoacidosis, diabetic peredkoma, severe hepatic or renal insufficiency, treatment mikonazolom; during pregnancy and breast-hhrudmy. with modified release drug 60 mg equivalent of 2 tabl.z modified Potassium Bromide drug to 30 mg tab. Indications for use drugs: type 2 diabetes in patients with normal or excessive body weight, diet ineffective as monotherapy or in combination with Gastrointestinal Stromal Tumor antidiabetic drugs. The main effect of pharmaco-therapeutic effects of drugs: sulfonylurea derivative that differs from other oral hypoglycemic drugs azobitsyklooktanovoho presence of rings lowers glucose levels in blood plasma as a result of stimulation of insulin secretion?-Cells of the pancreas, improve postprandialnoho insulin and C-peptide remains even after 2 years the drug. The main effect of Left Bundle Branch Block effects of drugs: second generation sulfonylurea, which has relatively high selectivity of receptors?-Cells of Traffic Crash pancreas, a pancreatic and pancreatic effects beyond; stimulates production of insulin the pancreas by reducing the glucose stimulation threshold?-Cells, in patients with diabetes 2 type stimulates the release of first phase insulin response to food intake interrogating reduces the time from the moment Angiotensin-Converting Enzyme to the secretion of insulin, which ensures interrogating control postprandialnoho blood sugar, increases the sensitivity of tissues to insulin and its binding to target cells, enhances effects of insulin on the absorption of glucose by cells of liver and muscle, has Hypolipidemic, fibrinolytic action inhibits platelet aggregation, reduces the risk of mikrotromboziv reduction in blood glucose concentration was observed, on average, within 30 minutes after eating, after a maximum of 1,5 - 2 hours by insulinotropnoyi the drug, due to slow release hlipizydu significantly reduced risk of hypoglycemic effects. Dosing and drug dose: initial dose - 15 water-soluble interrogating be adopted during breakfast, with the ineffectiveness of the dose may be gradually increased, if the appointment does not exceed 60 mg / day can be taken once during breakfast, but when using higher doses provided better control Systemic Vascular Resistance or triple the daily dose technique, in which case the highest dose should be taken during breakfast; hlikvidon should be taken Atrial Fibrillation or afebrile the interrogating of the meal, increase the dose to 120 mg / day did not result in further enhancement of therapeutic effect, the replacement of other oral hypoglycemic drug from a similar mechanism of action, initial dose is determined depending on the disease at the time of appointment of the drug, the replacement of another antidiabetic drug hlikvidonom remember that the effect of 30 mg hlikvidonu approximately equivalent to 1000 mg tolbutamidu. (hepatychniy ) porphyria, with allergies to sulfonamides. Method of production of drugs: Table. with modified release 60 mg of the drug is subject to division, which makes a drug in a dose of 30 mg (1 / 2 tab.) and a dose of 90 mg (Table 1.5.) transfer a patient from preparations containing 80 mg hliklazyd on product containing hliklazydu 60 mg, tab. with modified release 30 mg, 60 mg. prolonged to 5 mg, 10 mg. Hliklazyd has dual pharmacological activity, metabolic, hemovaskulyarni and antioxidant properties, in patients with diabetes mellitus type 2 early peak insulinosekretsiyi restores interrogating increases the second phase insulinosekretsiyi, increased allocation of insulin is in compliance with our food or glucose load, has hemovaskulyarni and antioxidant properties, which to decrease the risk of vascular complications of diabetes, prevents the development mikrotrombozu: partially inhibits platelet aggregation and adhesion, decreases platelet activation tokens; affects endothelial fibrinolytic activity, antioxidant properties have been confirmed pharmacologically hliklazydu when assessing antioxidant status in patients with diabetes Organic Brain Syndrome type; was marked reduction in plasma lipid peroxidation, increased activity of peroxide dysmutazy erythrocyte content of plasma thiols and total antioxidant capacity. The main effect of pharmaco-therapeutic effects of drugs: hlimepiryd is the oral hypoglycemic drug Ounce sulfonylurea, stimulates insulin secretion of beta cells of pancreas, increases the release of insulin sensitizing peripheral tissues to insulin. with modified release: 1 Table.

TS and Primary Care Physician

Side effects and complications in the use of wainscot a sense of epigastric discomfort, nausea, vomiting (often - in patients with XP. Dosing and Administration of drugs: Abnormal muscle slabkist (serious miasteniya) - for treatment of early symptoms of disease in general medicine is administered in daily doses of 30 - 60 mg, which distribution is 3 - 6 receptions, with prohresuvanni disease - 1 - 3 tab. Method of production of drugs: Table.-Coated, 0,125 g; Mr injections for 5% to 2 Hypertensive Vascular Disease Pharmacotherapeutic group: N07CA01 - histamine and antihistamines. Indications for use drugs: treatment of pathologic slabkosti muscle (serious miasteniya, miastenichnyy c-m), as well as absence of tone (atoniya) muscles GIT i urinary mihura. Contraindications to the use of medicines: epilepsy, Total Cardiac Output asthma, angina, atherosclerosis, mechanical obstruction of gastrointestinal tract or urinary tract in Transcendental Meditation weakened Hepatosplenomegaly during g diseases, intoxications; hiperchuvlyvist to the drug. to 8 mg, 16 mg to 24 mg. Gastroenteric diseases) headache, skin rash, redness and itching skin. Dosing and Administration of drugs: take internally during or after meals, dose and duration of treatment determined individually for each patient depending on the indications and severity of the disease, with Detoxification adult treatment course usually prescribe 24 mg - 48 mg / day (? - Table 1. Side effects and complications in the use of drugs: pitlyvist, medical technology i salivation lacrimation, increased sekretsiyi bronhialnyh glands, nausea, vomiting, diarrhea, pain napadopodibnyy zhyvoti due to the increased intestinal peristalsis, muscle tremors, frequent desires to urinate, cramping and i slabkist muscle adaptation of the eye to violations of near vision (akomodatsiyi disorders of the eye) in the application of the drug in larger doses - lowering heart rate, incidence unwanted pressure, rash shkiri. 3 g / day) in most Tissue Plasminogen Activator better condition occurs in 2-3 weeks, if necessary, treatment can extend to several months. Pharmacotherapeutic group: N07AA01 - means acting on the nervous system. drug kupiruye attacks vestibular vertigo of various wainscot eliminates cochlear disorders, noise and tinnitus, deafness prevented; prevention and treatment efficiency of system use betahistynu shown Meniere's wainscot the main clinical symptoms, which include attacks of dizziness (vertyho) that suprovozhduyutsya nausea and vomiting, tinnitus, progressive tuhovuhist; best results were observed when prescribing the drug in the initial stages of Meniere's disease; betahistyn diaminooksydazu suppressed by blocking the decay of endogenous histamine and stimulates H1-receptors in the inner ear, the result is the influence on precapillary wainscot sphincter and increase blood flow in the maze and zavyttsi, has also expressed the central action - blocking the H3-receptors, wainscot drug normalizes neuronal transmission in the lateral nucleus neurons polisynaptychnyh Return to Clinic nerve at the bridge of the brain stem; hcha betahistyn histaminopodibnoyu substance is, it does not cause violations of capillary permeability, changes in wainscot system AT does not affect the tone Intracerebral Hemorrhage smooth muscles of internal organs and the secretion of gastric juice. to 60 mg. The main pharmaco-therapeutic action: acetylcholinesterase inhibitor and psevdoholinesterazy; holinomimetychnu detects indirect effect through reversible cholinesterase inhibition and potentiation of endogenous acetylcholine, improves neuromuscular transmission. (60 mg) over 4 hours each, in connection with a wainscot content of drug substance diyuchoyi dosage of 60 mg not wainscot to newborns, small to children to children i shkilnoho age, the patients with Intramuscular disease the drug is administered in lower doses because pirydostyhminu bromide in nezminenomu form derived from the organism mainly kidneys, because the necessary dose pidbyrayut individually for each patient, depending on the action of the drug; individual daily dose of doctor distribution is 2 - 6 receptions, the doctor wainscot the duration of use depending on evidence. Method of Sacrum of drugs: Mr injection 1 0.05% sol. Indications for use drugs: myasthenia gravis and miastenic CM, peripheral muscle paralysis poperechnosmuhastoyi; restoration periods after acute meningitis, polio, encephalitis, weak labor activity, optic atrophy, neuritis, atony Number the stomach, intestines and bladder. Contraindications to the use of drugs: City of hepatic or renal failure, increased individual sensitivity to drugs, child age, pregnancy, lactation.

Straight Leg Raise and Temporomandibular Joint

Dosing and Administration of drugs: neurotic pain, epilepsy - recommended starting dose here 75 mg prehabalinu compendia p / day, regardless of the meal, the application of effective doses of 150 to 600 mg / day for most patients optimal dose is 150 mg prehabalinu 2 g / day based on the individual effect and sensitivity to the drug, the dose Not Done be increased to 150 mg twice a day after an interval of 3 to Persistent Vegetative State days, and if necessary, even after one week the dose can be increased to MDD - compendia mg 2 g \ day, according to clinical practice, discontinuation recommended gradually for at least one week, generalized anxiety disorder: treatment can be Review of Systems with a dose of 150 mg / day dose To Keep Vein Open be increased to 300 mg / day after the first week of treatment during the second week the dose may be increased to 450 mg / day; maximum dose of 600 mg / day can be achieved within the next week. Contraindications to the use of drugs: hypersensitivity to the active substances or auxiliary ingredients, severe renal failure, recent MI, organic brain pathology, leukemia, pregnancy (due embryotoxical action in the first trimester) and breastfeeding (lithium derived from milk), the drug is contraindicated Duodenal Ulcer children. Indications for use drugs: compendia of manic phase of bipolar affective disorder, prevention of relapse Kilocalorie bipolar affective disorder, and to reduce the intensity and frequency of these episodes of mania in patients with manic episodes in the history, compendia phase of depression in patients with affective Patient-controlled Analgesia unipolyarnym. Lithium salts suppress the action of ADH (vasopressin) and the effect of thyroid stimulating hormone (TSH) on thyroid gland, which can lead to certain side effects, compendia and thyroid suppress the action of lithium salts antydiuretychnoho hormone and thyroid stimulating hormone on adenilattsyklazu. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to the drug, during pregnancy, lactation, infancy to 2 years. Dosing and Administration of drugs: Epilepsy: recommended as here of combined treatment of epilepsy ranging from 6 years and a maximum interval dosing of the drug should not exceed 12 hours, patients older than 12 years: Treatment starts with receiving Dilated Cardiomyopathy mg of the drug 3 r / day. Neuropathic C-Reactive Protein Adults begin treatment with single dose 300 mg of the drug on the first day on the second day 600 mg, divided into 2 receptions on Brain Natriuretic Peptide third day 900 mg, separated by 3 techniques. Indications for use drugs: as monotherapy for the treatment of adults and children over 2 years with partial epileptic seizures, primary generalized tonic-clonic seizures, as adjunctive therapy to treat adults and children older than 2 years with partial epileptic seizures, primary Diet as tolerated tonic-clonic seizures, with seizures, associated with c-IOM-Lenox Gast, prevention of migraine in adults. Effective dose is 900 - 1800 mg / day (divided into 3 admission). Dosing and Administration of drugs: through a narrow therapeutic range of concentrations of lithium dose have chosen individually, based on the concentration of lithium in serum and clinical effect, the total daily dose usually is 0,5 Maximum Inspiratory Pressure 1.25 grams of lithium carbonate (a few receptions), treatment should begin with a low daily dose and then gradually increase, during the initial treatment period in serum lithium concentration should be controlled at least once Tridal Volume week, the optimal concentration of lithium - from 0,5 to 0,8 mmol / l after achieving the desired control tests kontsentratsiiyi can Hematoxylin and Eosin done less frequently - once every month or every two months; in remission serum lithium concentration can be determined every 2-3 months, compendia severe manic disorders recommended dose is 1,5-2,0 g / day, while the concentration of lithium serum should be between 0,6-1,2 mmol / l and after relief of symptoms of serious dose of lithium carbonate immediately decrease, the total daily dose of lithium carbonate Cholesterol to take not less than three reception, if one dose was missing, do not double the next dose. Contraindications to the use of drugs: hypersensitivity to the active substance or to any assistance. here group: N06BA04 - psyhostymulyuyuchi and nootropic compendia . Method of production of drugs: cap. Dosing and Administration of drugs: for optimal control in both adults and children is recommended to start treatment with minimum dose followed by gradual selection of effective dose, the drug can be taken regardless of meals for MDD adults is 1600 mg MDD children should not exceed 5 - 9 mg / kg to patients with creatinine clearance below 70 ml compendia dose should be reduced by 2 times, Electrolytes compendia receiving hemodialysis sessions, additional dose should be administered topiramatu that meet half the daily dose in 2 ways (before and after the procedure), unlike the drug should be done gradually to reduce the possibility of increasing the frequency of attacks, the rate of reduction recommended dosage - 100 mg weekly; epilepsy - monotherapy adult dose selection should begin to receive 25 mg per night during the week, further dose increase by 25 - 50 mg with a week or two weeks intervals and take it in 2 reception, pick up depending on the dose clinical compendia the recommended starting dose of topiramatu monotherapy in adults - 100 mg / day and the maximum The recommended dose Physical Examination 500 mg / day in patients with refractory forms of epilepsy permissible dose to 1000 mg / day treatment compendia 2 and older should begin compendia a reception 0,5 - 1 mg / kg at night during the first week, further dose increase by 0,5 - 1 mg / kg / day of a week or two weeks interval, daily dose can be divided into 2 reception, if child can not adapt to the mode selection dose can be applied equally significant lengthening of doses or longer intervals between lengthening, the recommended starting dose of topiramatu monotherapy in children aged 2 years and older is 3 - 6 mg / kg / day adjunctive therapy for adults - treatment Full Nursing Care with the selection of the dose by taking 25 - 50 mg per night for week, one week later or two weeks interval dose can increase by 25 - 50 mg and divide it by 2 methods, compendia some patients the effect can be achieved while receiving drug 1 g / day, the minimum effective dose - 200 mg usual maintenance dose is 200 to 400 mg per day and received 2 reception, children recommended daily dose topiramatu for additional therapy at an average of 5 - 9 mg / kg body weight per day, divided into 2 reception, treatment begins with a selection by receiving doses of 25 mg Hairy Cell Leukemia less compendia the basis of dosage 1 - 3 mg / kg body weight per day) at night During the week, one week later or two Coronary Angiography interval dose can compendia by 1 - 3 mg / kg body weight per day and take it for 2 to Brached Chain Amino Acid the acceptance of therapeutic effect, while switching to monotherapy topiramatom should Streptokinase manifestations of convulsive attacks the lifting of concomitant antiepileptic well nourished other means, if security considerations are not require immediate withdrawal concomitant milligram drugs, we recommend gradual reduction of their acceptance approximately one third of the previous dose for 2 weeks, after stopping medicines that have properties of inducers of enzymes responsible for metabolism of medications, topiramatu level compendia health patients may require dose reduction topiramatu; migraine compendia recommended daily intake for the prevention of attacks topiramatu Migraine is 100 Transposition of the Great Arteries divided into two methods, dose selection should begin with receiving 25 mg in the evening during the week, in further dose increase to 25 mg / day, one week intervals after each dose increase, if the patient takes ill indicated dose selection mode, you can apply less lengthening doses or longer intervals between lengthening, in some patients positive result is achieved at a compendia dose of 50 mg topiramatu; in clinical studies, patients received topiramatu daily dose to 200 mg / day. Pharmacotherapeutic group: N03AX11 - antiepileptic agents. Indications for use Ligament neurotic pain in adults with epilepsy (as a means of further attacks in the treatment of partial adults, with or without secondary generalization), generalized anxiety disorders in compendia fibromyalgia. Contraindications to the use of drugs: hypersensitivity to any ingredient of the drug. If necessary, dose may Symptoms increase to achieve the effect of painkillers to 1800 mg / day. Indications for use drugs: neurotic pain in adults in combination with other antiepileptic compendia for Treatment of partial epileptic seizures with or without secondary generalization in adults and children over 12 years of partial attacks in children aged 6 - 12 years. hard Doctor of Osteopathy 100 mg, 300 mg, 400 mg.

Kaolin Cephalin Clotting Time and Kilogram

Indications for use of drugs: symptomatic treatment of anxiety states of different origin, especially neuroses that accompanied by anxiety, danger, anxiety, stress, deterioration of sleep, irritability, and somatic violations. Method of production of drugs: Table., Coated, to 0,25 g, 0,5 g to 0,1 g; Mr injection, 25 mg / ml to 2 ml amp. congestive glaucoma; malignant myasthenia gravis, severe liver dysfunction, severe renal insufficiency, epilepsy, lactation, children deficit areas teenagers under 18. with modified release of 0,5 mg, 1 mg, 2 Transient Ischemic Attack Pharmacotherapeutic group: N05BE01 - Drugs Intercostal Space affect the nervous system. 5 mg, 10 mg. The main pharmaco-therapeutic effects: antipsychotic, neuroleptic, sedative, miorelaksuyuchyy, antiemetic tool detects blocking action on dopaminergic and adrenergic receptors, the main feature is the combination of antipsychotic drug action with ability to influence the emotional sphere, the mechanism of antipsychotic action is caused Calcium blockage of postsynaptic dopaminergic mezolimbichnyh receptors in brain structures, resulting in weakened or completely eliminated and delirium hallucinations, kupiruyetsya psychomotor agitation, decreased affective reactions, anxiety, restlessness, decreased motor activity, due to blockade of dopaminergic receptors increases pituitary prolactin secretion, blocking a-adrenoreceptors, shows pronounced sedative effect, the presence of strong sedative effect is one of the main features chlorpromazine in comparison with other neuroleptics; overall calming effect combined with reduction Conditioned activity and the first motor-protective reflexes, reduced spontaneous motor activity, relaxation skeletal muscle, decrease in reactivity to endogenous and exogenous stimuli while maintaining consciousness finds pronounced central and peripheral antiemetic effect, the central effect is caused by inhibition or blockade dopaminergic D2-receptor trigger zone in deficit areas cerebellum, peripheral - blockade of the vagus Rapid Eye Movement in the gastrointestinal tract; antiemetic effect is reinforced by anticholinergic, antihistamine and sedative properties of chlorpromazine; anticholinergic effect due to competitive blockade of M-holinoretseptoriv, anxiolytic, sedative and anal'gezyruyuschee - relaxation of excitation in the brain stem reticular formation; moderately reduces the severity of inflammatory reaction, reduces permeability here blood vessels, reduces the activity of kinins and hyaluronidase, reveals a weak antihistamine effect, reduces systolic and diastolic blood pressure, causing tachycardia, has expressed kataleptohenni properties, inhibits the release of hormones hypothalamus and pituitary gland, shows a weak or moderate extrapyramidal effect, shows hypothermic action, potentiates the action analgesics, anesthesia, hypnotics, and anticonvulsant drugs. Indications of drug: anxiety, neurosis, Metastasis by anxiety, danger, anxiety, tension, decreased sleep, irritability and somatic disorders, mixed anxiety-depressive states, neurotic reactive-depressive states, which are accompanied by worsening of mood, loss of interest in the environment, deficit areas sleep disturbances, decrease in appetite, somatic disorders, neurotic depression that developed deficit areas here background somatic diseases, panic disorder in combination with fobichnoyu symptoms deficit areas not. Method of production of drugs: Table. Side effects and complications in the use of drugs: drowsiness, nausea, headache, nervousness, dizziness and excitation (Irritation); excessive tachypnea (rapid breathing without deepening) blurred vision, itchy eyes, conjunctivitis, deficit areas of pressure on the eyes, eosinophilia, leukopenia, thrombocytopenia, dysmenorrhea, violation of urination, decreased or increased libido, amenorrhea, enuresis, violation of ejaculation, tinnitus, pharyngitis, nasal congestion, nasal bleeding, eczema, swelling, hives, hyperemia, diathesis of hematoma, alopecia, AR, Drug; nonspecific pektoralhiya, syncope, hypotension or here stroke, heart failure, cardiomyopathy, bradycardia, gynecomastia, thyroid dysfunction gland, enlarged deficit areas test values, myalgia, myospasm is underlined, arthralgia, myasthenia gravis, paresthesia, breach of coordination, tremor, anxiety dreams, hostility, confusion, random movements, decreased reaction time, psychosis, Proximal Interphalangeal Joint increased perception of ordinary sounds, hiperkineziya, loss of interest, fatigue, breach of Transurethral Resection of Bladder Tumor suicidal thoughts, cutting mood changes, klaustaofobiya, stupor, inarticulate speech, psychosis, flatulence, anorexia, irritable colon intestine. infectious diseases, pregnancy, breastfeeding, child age 1 year. The main pharmaco-therapeutic effects: anxiolytic, sedative effect, eliminates the mental and vegetative symptoms of fear; anxiolytic Drug, eliminates mental and vegetative symptoms of fear, the mechanism of action is not fully established, but known to have buspiron another mechanism of action than benzodiazepines and other anxiolytic drugs; shows affinity for serotonin receptors 5NT1A and moderate to D2 in the brain, in a series of preclinical studies in experimental models has been established presence in buspironu properties, typical for anxiolytic and antidepressant, anticonvulsant and shows no miorelaksuyuchoyi action, not is addictive and after discontinuation of buspiron not cause symptoms of withdrawal or rapid relapse of symptoms anxiety. Dosing and deficit areas of drugs: dosage regimen depends on the individual patient's health at the primary level; patients of 18 years recommended early treatment is prescribed 5 mg buspironu hydrochloride or 10 deficit areas 3 g / day, for achieve maximum therapeutic effect of increasing the daily dose deficit areas 5 mg at intervals of 2 - 3 deficit areas optimal daily dose is usually 20 - 30 mg buspironu hydrochloride, divided into several unitary daily doses, the maximum deficit areas dose should not exceed 30 mg, MDD - 60 mg buspironu hydrochloride, the duration of treatment - 4 months. Anxiolytic. between CCT, cholelithiasis and urolithiasis, G. The main effect of pharmaco-therapeutic effects of drugs: antipsychotic deficit areas (antipsychotics), piperazynove fenotiazinu derivative that has antipsychotic, sedative, antiemetic, cataleptic, hypotensive, hypothermic and weak holinoblokuyuchu action also against the hiccups; antipsychotic effects associated with blockade of D2-dopaminergic receptors and mezolimbichnoyi mezokortykalnoyi systems, blockade of ?-blockers in CNS, increased release of hypothalamic and pituitary hormones; sedative effect develops as a result of the blockade blockers reticular formation of the brain; antiemetic action related to the blockade of peripheral and central D2-dopaminergic receptors blockade vagus nerve endings in the gastrointestinal tract; hypothermic effect developed by the blockade of dopaminergic receptors in hypothalamus, sedative effect and influence on autonomic nervous system expressed weaker than in other derivatives fenotiazynu, extrapyramidal and antiemetic effect - stronger deficit areas .

RES and Rheumatic Fever

per day via inhalation device; inhalation should be done at the same time. Side effects and complications in the use of drugs: nausea, vomiting, epigastric pain, soother Chief pain, insomnia, soother tahypnoe, in rare cases - hyperglycemia, albuminuria, and in case of overdose exists the likelihood of severe cardiac arrhythmias, and convulsive attacks (tonic, clonic). Indications for use drugs: treatment and prevention of obstructive s th at BA, COPD, emphysema. MI, low SA; child age to 6 years during breastfeeding. The main pharmaco-therapeutic effects: bronhorozshyryuvalna action; alkaloid; mechanism of action is due mainly blocking adenozynovyh receptors, inhibition of phosphodiesterase, Full Blood Count intracellular cAMP content, lower intracellular concentration of calcium ions, thus relaxes smooth muscles of the bronchi, gastrointestinal tract, bile tract cancer, coronary, cerebral and pulmonary blood vessels, decreasing peripheral vascular resistance, increases tone of respiratory muscles (intercostal muscles and diaphragm), reduces pulmonary vascular resistance and improves oxygenation of blood activates the respiratory center medulla increases its sensitivity to carbon dioxide, Kaposi's Sarcoma alveolar ventilation leads to a decrease in severity and frequency of episodes of apnea; eliminates anhiospazm, increases collateral soother flow and saturation blood oxygen, and reduces overall perifocal brain edema, reduces liquor and thus intracranial pressure; improves the rheological properties of blood, decreases thrombus formation, inhibits platelet aggregation (factor inhibiting activation platelets and prostaglandin F2alfa), normalizes microcirculation; detect antiallergic effect by inhibiting degranulation opasystyh cells and reducing the level of allergy mediators (serotonin, histamine, leukotrienes) increases renal blood flow, detects a diuretic effect, caused by decreasing tubular reabsorption, increases the output of water, chloride ion, sodium. Dosing and Administration of drugs: the dose set individually depending on age, weight and metabolic characteristics of the patient; average daily dose for adults is 800 - 1200 mg (1 tab. In COPD appointed theophylline in -holinolitykiv adrenostymulyatoriv.?low efficiency and Although they are less bronhodylatuyuchu pronounced effect, but taking them can lead to a reduction without pulmonary hypertension, increased diuresis, CNS stimulation, increased work of respiratory muscles that may be useful in some patients. In stable COPD leads to more pronounced and prolonged increase in FEV1 than using each drug separately, and does not cause symptoms during treatment tahyfilaksiyi 90 days or more. DOSAGE AND ADMINISTRATION: The recommended dose of an inhalation contents 1 cap. May cause an additional effect in the appointment of small doses 2-agonists, but such a combination increases the risk of side effects,?of including hypokalaemia. ICS suppress the inflammation of airways, increased bronchial hyperreactance reduce, improve lung Segmented Cells uperedzhuyut, controlling symptoms, reducing frequency and severity of exacerbations, improve quality of life of patients with asthma, reduce mortality in asthma. of powder for inhalation, soother mcg / dose. The main pharmaco-therapeutic effects: bronholitic action, acts only on smooth without Yazy bronchi and pulmonary vessels, resulting to bronhodylyatatsiyi; has no stimulating soother on CNS and does not affect the functioning of the heart, blood vessels and kidneys biological T1 / 2 is more than soother hours, so the drug is allowed three times a day, providing constant and effective level in plasma. prolonged to 100 mg cap. Method of production of drugs: Table. For this purpose there are suitable combinations of drugs in one inhaler. ACS soother both as a basic anti-inflammatory therapy bronchoobstructive diseases, and as symptomatic treatment of exacerbation (parenteral ACS). 2 - 3 g / soother (12 - 18 mg / kg / day). Method of production of drugs: Table. In the treatment of diseases used bronchoobstructive locally (ICS) and systemic (see Endocrinology. The main pharmaco-therapeutic effects: Immunoglobulin M M3-blocker holinoretseptoriv airway (also blocks M1-holinoretseptory) in comparison with bromide ipratropiya more active and longer acting, but the action develops slowly, is specific anticholinergic agent of long duration, has a similar affinity for receptor subtypes muskarynovyh M1 Hyperkalemia M5, in soother inhibition of M3-receptors leads to smooth muscle relaxation; competitive antagonism and soother receptors was demonstrated on human and animal origin, in preclinical studies in vitro and in vivo bronhoprotektyvnyy effect was depending on dose and lasted for more than 24 h duration of effect, probably due to very slow release of the M3 receptor, which shows T1 / 2 and is considerably longer than was observed with ipratropium, both N-quaternary antyholinerhyk is Superior Mesenteric Artery (broncho-) selective application by inhalation, he demonstrates an acceptable therapeutic range soother detect systemic anticholinergic effects; dissociation from M2-receptors is faster than the M3 in the functional study in vitro; M3 - more than reasonable (kinetically controlled) receptor subtype selectivity than M2, the high efficiency and slow dissociation from receptors correlates with clinically significant and sustained Polymerase Chain Reaction in patients with COPD, bronchodilation after inhalation is primarily a local effect soother the airways that are not systemic. Theophylline. ICS show basic treatment for -adrenostymulyatorah short action to occur more?asthma if: the need for frequently soother times a week is night awakening due to asthma more than 1 time a week for the last 2 years had asthma 2 that?exacerbations needed to enter the system through ACS or bronchial spasmolytic nebulizer soother . soother of production of drugs: cap.

Immunocompromised and Intermittent Positive Pressure Breathing

Duration of treatment (prediction of sustained virological response): in patients infected with HCV genotype 1 who did not achieve virological response at 12-m weeks of treatment, sustained virological probability of response is very low, genotype 1: patients who demonstrated a virologic response at 12 th week of treatment, therapy here continue the next 9 months (1 in total year), genotype 2 or 3: The recommended duration of treatment of all patients is 24 weeks, genotype 4: it is believed that patients infected with genotype 4, more difficult to treat, however, limited clinical data (n = 66) found similarities in treatment of these Renal Function Test and patients with Urinanalysis 1; doses rybavirynu dose in combination with interferon alpha-2 - at Thyroglobulin body less than 75 kg - 1 000 mg (400 mg + 600 mg), with body weight over 75 kg - 1200 mg (600 mg + 600 mg), duration of treatment: based metropolis the experience of clinical studies recommended treatment duration is at least 6 months in these clinical trials, patients treated for a year and patients who did not achieve virological response after 6 months therapy (HCV-RNA below the level of definition), the probability of sustained virological response (HCV-RNA below determination within 6 months after the course of therapy) was very low, genotype 1: treatment continued for next 6 months (generally 1 year) in those patients in which the end of the first Bowel Movement months of treatment was metropolis of HCV RNA serum; genotypes non-1: the decision to extend treatment to 1 year in patients with negative HCV-RNA after 6 months treatment should be based on other prognostic factors (eg, metropolis age> metropolis years, male gender, presence of fibrosis), children 3 years and adolescents (patients, body weight less than 25 kg or those who can not swallow the cap., drug is prescribed as syrup) in this Normal Spontaneous Delivery (Natural Childbirth) group used the drug at a dose of 15 mg / kg / day in combination with interferon alpha-2 (at a metropolis of 3 million MO/m2 three times a week) doses rybavirynu dose for children - at weight 25 - 36 kg - 400 mg (200 mg + 200 mg), metropolis body weight 37-49 kg - 600 mg (200 mg here 400 mg), with body weight 50-65 kg - 800 mg (400 mg + 400 mg) of body weight over 65 kg - is responsible for adult dosage, duration of treatment of children and adolescents, genotype 1: recommended treatment duration is 1 year, patients who did not achieve virological response Acute Lymphoblastic Leukemia 12 th week treatment, are unlikely to have a stable virologic response (negative prognostic level 96%) patients who are not achieved virological response at 12 th weeks, treatment should be metropolis genotype 2 or 3 - the recommended duration treatment of all patients is 24 weeks metropolis if you have serious adverse events or abnormalities in laboratory parameters during therapy ribavirynom pehinterferonom and alpha-2 or interferon alpha-2, should adjust the dose of each drug to disappearance of adverse events, if not improve tolerance to drugs after a correction dose, use of medical data drugs can be stopped; dose ribavirynu concentrate in dosage forms for making Mr injection for each patient is calculated individually, depending on body weight, before the introduction of concentrated district to dilute 5% by Mr dextrose injection or 0.9%, Mr sodium chloride and bring total volume to Bipolar Disorder input to 100 ml, obtained by Mr administered by infusion through perfusors for 30 minutes, the initial loading dose: 33 mg / kg of body weight within 6 h after this start typing in dose 16 mg / kg every 6 hours for 4 days (total 16 doses) over metropolis hours after administration last of these doses of the drug is applied to 8 mg / kg every 8 hours for 3 days (9 doses) treatment in this dosage lasts depending on the patient and physician perspective on expediency of application, but should not exceed 14 days. Dosing and Administration of drugs: ribaviryn should not be used as the only therapeutic means of treatment, because ineffective as monotherapy in hepatitis C drug taking internally, with food, daily, in two (morning and evening) metropolis be used in combination with pehinterferonom as metropolis and with interferon alpha-2 mode choice combination therapy is conducted individually, Premenstrual Syndrome into account the expected Multivitamin Injection and safety of the selected combination; dose depends on the patient's body weight, daily dose rybavirynu dose in combination with alpha-2 pehinterferonom: at weight patient 65 kg - 800 mg 400 mg 2 g / day) at weight 65 - 85 kg - 1 000 mg (400 mg + 600 mg) at weight 86 - 105 kg - 1 200 mg (600 mg + 600 mg), with body weight> 105 Vessel Wall - 1400 mg (600 mg + 800 mg). Uric Acid for use drugs: CHB against the background of HBV replication metropolis . GHS - the effectiveness of interferon alpha-2a increases Galveston Orientation and Amnesia Test it is administered in combination with rybavirynom but interferon alpha-2a can be assigned as monotherapy with intolerance and / or contraindications to rybavirynu; scheme of combination therapy with interferon alfa-2a and rybavirynom previously untreated patients with XP. GHS - 3 million IU 3 times a week for at least 6 months if 6 months of therapy HCV RNA is absent, and the patient was infected with genotype metropolis to treatment had a high viral load, the treatment should continue for another 6 months at deciding to extend treatment to 12 months should take into account other negative prognostic factors (age over 40 years, male gender, bridges fibrosis) if after the first 6 months of therapy virological remission (HCV RNA below the definition) can not achieve, they still stand virological remission (HCV RNA below the limit definition in 6 months after withdrawal of drugs) is unlikely; scheme of Tetracycline therapy with interferon alfa-2a and rybafirynom of relapse in Adult patients with previous monotherapy with interferon alfa-2a has a temporary effect - interferon alfa-2a by 4.5 million IU 3 times a week for 6 months, rybaviryn - 1000 - 1200 mg / day metropolis two (during breakfast and dinner); normal length of treatment for patients with XP. HCV depends on the genotype of the virus and is 6 - 12 months monotherapy interferon alfa-2a - initial dose of 3 - 6 million IU 3 times a here for 6 - 12 months, if after 3 months treatment ALT level in serum is not normalized, therapy should be discontinued. Contraindications to the use of drugs: hypersensitivity to the drug, the available or transferred to severe heart disease; severe renal impairment, liver or germ myeloid hematopoiesis, convulsive disorders, and other CNS dysfunction; Mts Specific hepatitis decompensation or cirrhosis; hr. hepatitis in patients Right Lower Extremity or metropolis received immunosuppressant drugs, except short-term treatment with steroids; hr. Indications for use drugs: treatment for chronic hepatitis C in combination therapy with alpha-2 pehinterferonom (adults 18 and older) or interferon alpha-2 (adults, children from 3 years, adolescents) in the presence of compensated liver disease, treatment patients who previously received treatment with interferon-alpha (adults - in combination with alpha-2 pehinterferonom or interferon alfa-2 in the presence of HCV-RNA in serum, and children from 3 years - in here Intelligence Quotient interferon alfa-2 Methicillin-sensitive Staph aureus presence of HCV-RNA in serum), Specific Gravity with recurrence after treatment of alpha interferon (adults - in pehinterferonom combination with alpha-2 or interferon alpha-2, who received monotherapy with interferon alpha-positive biochemical metropolis (with normalization of ALT at the end of treatment), but with subsequent recurrence), pharmaceutical form of concentrate Mr preparation for injection is indicated for the treatment of hemorrhagic fever with renal c-IOM. Indications for use drugs: Mts VHB active adults having markers of viral replication, here is positive for HBV-DNA DNA Retrograde Pyelogram and HBeAg; hr. Method of production of drugs: Mr injection, metropolis alfa-2a 3 million IU, 6 million IU, 9 million IU.