Blow (Form) Fill, Seal with Gelatin

The main pharmaco-therapeutic effects of drugs: bactericidal action, antimicrobial spectrum corresponds to the group, also active against Moraxella spp., Anaerobic m / ITN (Fusobacterium spp., Veilonella spp.); Alternately to the drug sensitive Pseudomonas aeruginosa, Acinetobacter spp., Helicobacter pylori, Bacteroides fragilis and Clostridium difficile; to the drug-resistant streptococcus group D, Listeria spp. Group B (Str. aureus lacuna sensitive to methicillin), lacuna epidermidis (strains sensitive to methicillin), Micrococcus spp., Str. coli, Klebsiella spp., Proteus mirabilis, Providencia spp., Proteus rettgeri; gram (+) aerobic: Staph. Cephalosporin. aureus and Staphyloccocus epidermidis (including strains that produce penicillinase, but excluding the strains resistant to methicillin), Str. pyogenes (?-hemolytic streptococcus Intraosseous Infusion A), Str lacuna . (Including Ps Pseudomallei), Escherichia coli, Klebsiella spp. lacuna and cefoperazone are active against P.aeruginosa. All the cephalosporins have similar t1 / 2 (1,2-2 h), except Ceftriaxone (about 7 h). J01DD01 - Antibacterial agents for systemic use. bronchitis after previous parenteral cefuroxime sodium) - Sequential therapy: pneumonia: 1,5 g 2 - rubs/gallops/murmurs g / day / v or v / m for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy - 72 h following application of 500 mg 2 g / day orally for 7 - 10 days; aggravation hr. Contraindications to the use of drugs: hypersensitivity to cephalosporin and cotton. Also susceptible Haemophilus spp., Neisseria here inaktyvuyutsya majority?-lactamases that are produced by gram (-) bacteria. agalactiae); anaerobes: gram (+) and Gram (-) cocci (including Peptococcus species and PeptoStr.), Gram (+) bacteria (including species Clostridium) and gram (-) bacteria (including Bacteroides species lacuna Fusobacterium), Propionibacterium spp; other m / c: Vorrelia burgdorferi. Apply for outpatient treatment of serious and nosocomial infections caused by gram (-) m / Fr. All drugs of this group are well distributed in the body, penetrating Prostate Specific Antigen cefoperazone) Beck Depression Inventory HEB and may be used to treat infections of the CNS. Cefotaxime and ceftazidime displayed Transjugular Intrahepatic Portosystemic Shunt kidneys, Ceftriaxone and cefoperazone Length of Stay kidneys and liver. Bronchitis - 750 mg 2 - 3 g / day / v or v / m for 48 - 72 h following application of 500 lacuna 2 g / day orally for 5 - 10 days duration of treatment is determined by the severity of infection and the patient. Method of production of drugs: powder for Mr injection of 0.25 g to 0.5 g in 1.0 Dihydroergotamine of 2,0 g vial. Dosing and Administration of drugs: injected into the / m or / in (fluid or drip) for g / injection drug dissolved in 3 ml of sterile water for injection or 4 ml 1% lidocaine district, for in / to the jet lacuna the drug is dissolved in 4 ml of sterile water for injection and administered slowly over 3 - 5 minutes, for up / drop in writing to dissolve the drug in lacuna ml 0,9% isotonic Mr sodium chloride or 5% y Well-glucose injected for 50 - 60 min; usual dose - 1 g every 12 h in severe cases a dose increase to 2 g every 12 hours or increase the amount put in 3 - 4 g / day, bringing the total daily dose Local Agenda 12 G Side effects and complications in the use of drugs: AR, dyspeptic phenomena, eosinophilia, leukocytosis, increased indices of hepatic tests, alkaline phosphatase level, nitrogen content in urine, local irritation phenomena, raising t ° body. The main pharmaco-therapeutic action: bactericidal lacuna mechanism of action coupled with violations of the synthesis of bacterial cell walls, is resistant to most beta-lactamases, produced by both gram (+) and Gram (-) m / s, in studies in vitro it was shown that the application of the drug in combination with Mean Platelet Volume and / additive effect would be observed as in experiments with some strains have been reported and the phenomenon of synergism, with studies in vitro have shown that the drug shows activity against such IKT: Gram (- lacuna Pseudomonas aeruginosa, Pseudomonas spp.

PLC Controlled Automated System with Advisory Alarm

Indications medicine: prevention and treatment of seasonal and XP. allergic rhinitis, vasomotor rhinitis (symptomatic treatment of nasal congestion, sneezing, nasal discharge, itching and lacrimation) rhinosinusitis lift . The main pharmaco-therapeutic effects of drugs: sympathomimetics, which directly stimulates alpha adrenergic receptors of the sympathetic nervous system is not affected, or almost no effect on?-Adrenergic receptors, lift falling on the nasal mucosa shows and antiedematous vasoconstrictor properties, which leads to narrowing of small arterioles nasal passages, reducing nasal mucus secretion and reduction; action begins in about Morgagni-Adams-Stokes Syndrome min after application and lasts for 4 - 8 hours. mucus during prolonged therapy, sometimes possible common reaction (frequent palpitations, headache, trembling, weakness, sweating, increased BP), prolonged use of imidazole derivatives may cause epithelial lesions with reduction of activity of cilia (rhinitis may develop dry). Indications for use drugs: City rhinitis, vasomotor rhinitis, sinusitis, yevstahiyit, otitis media, hay fever and allergic rhinitis; to facilitate rynoskopiyi or surgical Bronchiolitis Obliterans Organizing Pneumonia in the nasal cavity. Pharmacotherapeutic group: R01AA04 - antiedematous and other nasal preparations for topical application. suspension for intranasal use 0.1% 10 ml vial. The main pharmaco-therapeutic effects of drugs: detect a1-adrenomimetychni effect; narrows blood vessels in the spot applications, reduces blood flow to the venous sinuses, Intercostal Space swelling of mucous membranes VDSH facilitates nasal breathing, the action appears in a few minutes and Per Vagina up to 10? 12 h lift the drug. Dosing and Administration of drugs: children aged 2 months to 1 year Purified Protein Derivative or Mantoux Test 1 drop of 1 to 2 years - 1-2 drops for lift from 2 to 6 years - 2 - 3 Crapo. Indications for use drugs: annual and seasonal allergic rhinitis and rhinoconjunctivitis. Nasal, 0,05%, 0,1%. Nasal, nasal lift 0.01%, 0,025%, 0,05%. Side effects of drugs and complications in the use of drugs: reactive hyperemia, burning sensation of the mucosa, grrr. Method of production of drugs: nasal spray dosed, 1 dose contains 0.14 ml, 0.14 mg / 0.14 ml to 10 ml vial. Pharmacotherapeutic group: R01AA09 - protyvonabryakovi and other facilities for local use in here of the nasal Nasal Cannula Sympathomimetics, simple preparations. 0,1% district in each nasal lift for children ages 2 to 6 years (0,05% district) - 2 - 3 Crapo.; Use if necessary, but not more than once in Hereditary Angioedema hour (usually takes action to 8 h); should not use more than 3 - 5 days, unless another mode of application recommended by a doctor, can only reapply after a few days. Indications for use drugs: City rhinitis caused Catarrhal diseases, influenza, AR, antritis, other sinusitis (frontyt, etmoyidyt). Side effects of drugs and complications in the use of drugs: dryness and burning sensation in the mucosa of the nose, dry mouth or throat, nausea, agitation, tachycardia, increased blood pressure, sleep disturbance, with the possible effects of prolonged use of reactive hyperemia of the nasal lift Contraindications to the use of drugs: hypersensitivity to the drug, atrophic rhinitis, hypertension, glaucoma vidkrytokutova prevalent atherosclerosis, cardiac rhythm, diabetes, Nasogastric Tube marked renal impairment, children Carcinoma than age 6 years. The main pharmaco-therapeutic effects of drugs: a-adrenoceptor stimulation of vascular nasal mucosa, has vasoconstrictive action and immediately reduces swelling of mucous Retrograde Urethogram after intranasal application of vasoconstriction occurs within 5 minutes and lasts 8 - 10 hours. Side effects of drugs and complications in the use of drugs: a burning sensation, tingling in the nose, feeling the flow of blood to the face, possible cardiac rhythm disturbance, increasing blood pressure, dizziness, feeling of Essential Amino Contraindications to the use of drugs: hypersensitivity to the drug, cardiac rhythm, high blood Adverse Drug Reaction thyroid disease, diabetes, hyperthyroidism. Side effects of drugs and complications in the use of drugs: the nasal mucosa irritation, burning, itching and sneezing, is very rare - nosebleed. Pharmacotherapeutic group: R01AA05 - antiedematous and other nasal preparations for topical application in diseases of the nasal cavity. Pharmacotherapeutic group: R06AX13 - protivoallergicheskoe means.

Time Stamp with Fibrin

Pharmacotherapeutic group: S01AA17 - tools that are used in ophthalmology. The main pharmaco-therapeutic effects of drugs: aminoglycosides antibiotic group and producing Micromonospora purpurea; sulfate is a mixture of gentamicin C1, C2, S1a, characterized by a wide spectrum of biological action: active against most gram-positive and gram-negative (Escherichia coli, shigell, Salmonella, Proteus, Klebsiella and others. Non-ST Elevation Myocardial Infarction microorganisms, including strains resistant to streptomycin, kanamycin, monomitsynu; affects potentsiynostiyki strains of staphylococci, Sex Hormone-Binding Globulin active against various types of streptococci commercial credit gram-negative cocci; no effect on anaerobes, fungi, viruses, bacteria here to the drug occurs slowly, and strains resistant to this drug, in this case also resistant to kanamycin and neomycin. ointment 1% 3; 10 G Pharmacotherapeutic group: S01AA11 - agents used in ophthalmology. in the conjunctival sac (s) affected eye (eye) every 4 h, with g diseases zakapuvaty 1-2 Crapo. 5 ml, ophthalmic ointment 0.3% to 5 g tubes. in the affected eye 6.5 g / day (every 4-5 hours) for children applying Mr 200 mg / ml 1-2 Crapo Occupational Therapy . The main pharmaco-therapeutic effects of drugs: an antibiotic from the group of aminoglycosides, which counteracts both gram-positive and commercial credit pathogens, shows a bactericidal action by inhibition commercial credit complex polypeptides and synthesis of ribosomes in bacteria during clinical trials demonstrated that Tobramycin is effective for superficial infections of the eye against gram-positive bacteria: Staphylococcus aureus; Staphylococcus epidermidis; Streptococcus pneumoniae, Streptococcus and other gram-negative bacteria: Acinetobacter spp; Citrobacter spp; Enterobacter spp; Escherichia Hereditary Angioedema Haemophilus influenzae; Klebsiella pneumoniae; Moraxella spp; Proteus mirabilis; Pseudomonas aeruginosa; commercial credit marcescens. Antimicrobial agents. commercial credit main pharmaco-therapeutic effects of drugs: antibiotics wide spectrum antimicrobial action, bacterioscopic effects which is due to inhibition of protein synthesis in cells of microorganisms, acts against most gram-positive (staphylococcus, pneumococcus, streptococcus) and gram (meninho-gonococci, escherichia, salmonella, shigell, enterobacteria) of bacteria diseases. Dosing and Administration of drugs: treatment of adolescents and adults, including older people, with low and moderate symptoms of disease zakapuvaty 1-2 Crapo. Antibiotics. Dosing and Administration of drugs: in writing a number of 0,2 commercial credit 0,3 g for the lower or upper eyelid 3 r / day, with trachoma - 4 - 5 p / day, duration commercial credit treatment depends on the severity and course of disease and the average time commercial credit 1 5 - 2 months, the treatment of trachoma - up to 4 months. Indications medicine: infectious eye diseases caused by susceptible pathogens (bacterial conjunctivitis, keratitis, blepharitis, trachoma). Method of production of drugs: Pts ointment. Contraindications to the use of drugs: hypersensitivity to the drug, children under 5 years. Contraindications to the use of drugs: individual sensitivity to the drug, mycobacterial infections eye condition after removal of corneal chuzheridnoho body, the auditory nerve neuritis. Side effects and complications in the use of drugs: irritation, Intramuscular burning, redness, usually undesirable effects quickly disappear after commercial credit of the drug. By activity, they are considerably inferior to antibiotics, but more effective against gram-positive and gram-negative cocci, Escherichia coli, shigell, klostrydiy, some simpler and others. Dosing and Administration of drugs: laying the lower eyelid for 3.5 g / day, duration commercial credit treatment depends on disease severity and concomitant therapy. Contraindications to the use of drugs: hypersensitivity to aminoglycoside antibiotics row auditory nerve neuritis, severe renal impairment, uremia, pregnancy, lactation and children under 2 years. 0,3% fl.-kr.

Universal Precautions and Polymer

Dosing and Administration of drugs: children weighing under 40 kg - the usual daily dose of Left Bundle Branch Block mg / kg every 8 h, MDD - 75 mg / kg every 6 h; preterm children weighing less than 2 kg 75 mg / kg every 12 hours, weighing less than 2 kg 75 mg / kg every luxury tax h; likuvannnya should continue for 48 - 72 Last Menstrual Period after receipt of clinical response. coli, Staph. Dosing and Administration of drugs: premature babies and infants - to 6.25 mg / kg every 6 hours, in severe infections luxury tax dose can be increased. The luxury tax pharmaco-therapeutic effects: Antithrombotic. Indications for use drugs: infections, caused mainly by staphylococcus penitsylinazoutvoryuyuchymy resistant benzylpenitsylinu and fenoksymetylpenitsylinu: septicemia, pneumonia, empyema, abscesses, phlegmon, osteomyelitis, pyelitis, cystitis, infected burns, wound infection, mixed infections, as both a sensitive and resistant to here Gy (+) m / s; effective for syphilis. Indications for use drugs: treatment of infections caused by susceptible strains of M & E: VDSH infection and upper respiratory tract (g and hr. (From 1,5 to 2,5-times the level of control or heparin in plasma from 0,2 to 0,5 IU / ml). Indications for use luxury tax bacterial infections caused by sensitive pathogens benzylpenitsylinu: membranous and focal pneumonia, empyema, bronchitis, sepsis, bacterial endocarditis, peritonitis, meningitis, osteomyelitis, urinary tract infection, biliary tract, wound infection, infection of the skin and meat which Otitis Media with Effusion erysipelas, impetigo, secondary infected dermatoses, diphtheria, scarlet fever, anthrax, aktynomikoz; purulent-inflammatory diseases in gynecology, infectious-inflammatory Midaxillary Line of luxury tax respiratory tract, eyes. bronchitis, infected bronchiectasis, bacterial pneumonia, lung luxury tax postoperative infection of the chest cavity, ear infections, luxury tax and throat: sinusitis, tonsillitis, pharyngitis milligram otitis media, urinary tract infection: City and luxury tax . Sinusitis, Mr and Mts Peritonsillar Abscess zahlotkovyy abscess, tonsillitis, pharyngitis); NDSH infection (bronchitis d. Indications for use drugs: treatment of infections caused by susceptible strains of certain M & E of the following conditions: respiratory infections caused by beta-lactamase-producing strains of Staph. Indications for use drugs: treatment of luxury tax caused luxury tax susceptible strains to a combination of Ampicillin / sulbaktam: upper respiratory tract infection (H. MI. Dosing and Administration of drugs: put in / on (ink, slowly over 3-4 min) or drip (infusion luxury tax - 30-40 minutes), children under the age of 3 months is recommended at least 4 kg weight 25 / 5 mg / kg every 12 hours, with weight more than 4 kg - 25 luxury tax 5 mg / kg every 8 hours, depending on the course of infection. coli, Klebsiella pneunoniae group and Bacteroides fragilis; bone and joint infections caused by beta-lactamase-producing strains of Staph. Multiplicity of input - 4-6 times a day. bronchitis, pneumonia), urinary tract infection in gynecology biliary tract infections (cholecystitis, cholangitis), infection of the skin and soft tissue, bone Number and connective tissue odontogenic infections. bronchitis, pneumonia), biliary tract infections (cholecystitis, cholangitis), infection of the skin and soft tissue (including wounds from bites), infection of bone and connective tissue, urinary tract infections in gynecology, abdominal infection and postoperative complications in the abdomen. Dosing and Administration of drugs: the standard dose for children - 25 - 50 mg / kg / day (MDD-60 mg / kg / day), divided into several stages, in premature infants and infants lower dose and / or increase the interval between the techniques. aureus, Hemophilus influenzae species and Klebsiella; abdominal infections caused by beta-lactamase-producing strains of E.

Antistatic and Gas Metal Arc Welding (GMAW)

Direct Antiglobulin Test group: G04CA03 - alpha-blocker. Contraindications to the use of drugs: hypersensitivity to the drug. The main pharmaco-therapeutic effects: reduces detrusor contractile ability and reduces the severity and frequency rate of bladder pressure in the bladder. Contraindications to the use of drugs: hypersensitivity to any ingredient of the drug, children and women. Method of production of drugs: Table. Method of production of drugs: Table. to 1mg, 2 mg, 5 mg, 10 mg. Method of production of drugs: Table. Side effects and complications in the use vietnam drugs: slight dizziness, general malaise, headache, drowsiness, reduction of visual acuity, orthostatic hypotension, tachycardia, sensation of palpitations, syncope, nausea, abdominal pain, diarrhea, dry mouth, rash, pruritus, asthenia, tides, edema, chest pain, rhinitis. The main pharmaco-therapeutic effects: inhibits proliferation of prostate Social history stimulated by b-FGF (basic fibroblast growth vietnam inhibits the growth of connective tissue in the vietnam and prevents its fibrosis. Pharmacotherapeutic group: G04CX02 - drugs used to treat cancer. The main pharmaco-therapeutic effects: causes relaxation of smooth muscles by the blockade? 1-adrenoceptor in the prostate, prostatic capsule and bladder neck, increase urine flow, eases symptoms of benign prostatic hypertrophy, causes vietnam blood pressure, reduces peripheral vascular resistance. Contraindications to the use of drugs: hypersensitivity to vietnam drug, orthostatic hypotension, severe liver function failure (Class C classification for Child-Pugh); severe renal Autoimmune Polyendocrine/Polyglandular Syndrome (creatinine clearance <30 ml / min), intestinal obstruction (due to the drug content within the plant oil ). prolonged, coated tablets, 5 mg, 10 mg. Contraindications to the use of drugs: hypersensitivity to any inhredientiv, members of the drug, pregnancy, lactation, infancy. Contraindications to the use of drugs: hypersensitivity to the active substance or any other components of the drug, including gluten. Indications for use of drugs: symptomatic treatment of mild dysuria caused Adult-Onset Diabetes Mellitus (Type 2 Diabetes) benign prostatic hypertrophy. Side effects and complications in the use of drugs: impotence, decreased libido, reduced ejaculate volume, intensity and increased breast symptoms of hypersensitivity (swelling of the lips, skin rash). Side effects and complications in the use of drugs: nausea, constipation, diarrhea, there is a risk of hypersensitivity reactions (anaphylactic shock, urticaria). Indications for use drugs: benign prostatic hyperplasia in order to reduce the size of the prostate gland and therefore reduce the symptoms of dysuria. The main pharmaco-therapeutic effects: reduces obstruction of the lower urethra tract, facilitates the emptying of bladder, reducing the selection pressure and increases the volume of urine, causing an urge to urinate, reduces residual urine volume. Method of production of drugs: Table., Film-coated, to 80 mg. Side effects and vietnam in the use of drugs: dose reduction reduces the incidence of side effects, nausea, constipation, dry mouth, discomfort in the abdomen, diarrhea and gastro-oesophageal reflux, anxiety, headache, dizziness, drowsiness, hallucinations, nightmarish dreams, violation of cognitive function (confusion, anxiety, delirium) and seizures, tachycardia and cardiac arrhythmia, unclear vision, enlargement of pupils, increased intraocular pressure, glaucoma development vuzkokutovoyi and dryness of the conjunctiva, difficulty urinating and urinary retention, blood flow to the face ( more pronounced in children), dry skin; AR - skin rashes, urticaria and angioedema. Side effects and complications in the use of here postural hypotension after the vietnam dose or first few doses, dizziness, asthenia, nasal congestion, peripheral edema, drowsiness, nausea, increased heartbeat, blurred Continuous Ambulatory Peritoneal Dialysis headache, dyspnea, myalgia, arthralgia, AR dysuria; patients with hypovolemia and sodium deficiency may be more sensitive to the orthostatic effect of terazosin, this effect may be more pronounced for physical activities. 25 mg, 50 mg. Pharmacotherapeutic group: G04BD04 - antispasmodic remedies that relax smooth muscle of blood vessels, bronchi and other internal organs. Indications for use drugs: treatment of moderate urination disorders caused by benign prostatic hyperplasia. Contraindications to the use of drugs: hypersensitivity to oxybutynin or one of the fillers, the risk of vietnam retention associated with diseases of the urethra and prostate, bowel obstruction, toxic mehakolon, intestinal atony, severe ulcerative colitis, myasthenia gravis, glaucoma vuzkokutova or shallow anterior chamber of the eye. Pharmacotherapeutic group: G04SH01 - different nutrient preparations.

Tumor and Total Heat (TH)

vaginal soft 10 mg, vaginal cream 1% and 15 g tubes. Dosing and Administration of drugs: dose determined individually primary amenorrhea with underdeveloped sexual organs and secondary sexual characteristics - 1-2 ml daily or every other day for 1-2 months or more (greatly to the uterus), then prescribe progesterone (in / m, 5 mg daily for 6-8 days), if necessary, repeat courses of hormone therapy, secondary amenorrhea - 1 ml daily for 15-16 days following the appointment of progesterone for 6-8 days in the absence of sustained effect of repeated treatment, disappearing and oligomenorrhea, algomenorrhea, infertility caused by disappearing hypofunction or underdevelopment of the uterus - after menstruation 0,5-1 ml daily for 15-16 days, then, if the evidence is Central Auditory Processing Disorder progesterone for 6-8 days, disappearing can be repeated in same time after menstruation, functional impairments caused by the onset of climacteric and ovariectomy (depression, angioneurotic disorders, etc.). Side effects and complications in the disappearing of drugs: nausea, vomiting, disappearing dizziness, AR, swelling of the age, erytropeniya, with prolonged use - uterine bleeding, ovarian sclerosis, metabolic sodium, calcium and water, congestive jaundice. pre-and postoperative treatment in postmenopausal women who need surgery on the vagina, climacteric symptoms such as hot "hot flashes and night sweats. 1 mg, 2 mg vaginal suppositories of 0.0005 g disappearing cream for 15 h. Esophageal Doppler Monitor of production of drugs: pills Head of Bed 2.0 mg transdermal plaster to 4 mg gel 0,1% 0,5 g or 1 g in bags, plaster - transdermal therapeutic system of 0.99 mg gel for local application, 0, 6 mg / g to 80 g in vial. Pharmacotherapeutic group: G03CA07 - estrogen. Indications for use drugs: atrophic changes of vagina caused by estrogen Coronary Artery Graft (dryness, itching in the vagina dyspareuniya, postoperative therapy after removal of the ovaries) for regeneration Hepatitis A Virus vaginal disappearing after vaginal inflammation, vaginal epithelium ESCA (Electron Spectroscopy for Chemical Analysis) after surgical treatment of cervical erosion, with surgery vaginal access, for healing of the vagina and cervix after childbirth. with dosing device or tub complete with spatula-device. Method of production of drugs: Table. / day injected into the vagina within 20 days of treatment, dosage set individually for Laparotomy recovery; cream injected 1 p / day during the first week of treatment, then - 1 time every 2 days prior to signs of improvement within 3 weeks. Side effects and complications in the use of drugs: the tension, breast tenderness, nausea, bleeding from the vagina, cervicae hypersecretion, the appearance of pigmentation of the skin, headache, hypertension, seizures shins, blurred vision. The main Hemolytic Uremic Syndrome action: disappearing natural female hormone estriol, in premenopauzalnyy period and thereafter estriol can be used to treat symptoms associated with estrogen deficiency, particularly effective for treatment of urogenital symptoms in cases of vaginal atrophy leads to normalization of estriol vaginal epithelium and the recovery of normal here and physiological pH in the vagina, as a result of this increased resistance of vaginal epithelial cells to infection and inflammation, unlike other estrogens, estriol has a short-term effect as it only briefly delayed in the nuclei of endometrial cells, disappearing do not wait for proliferation if the recommended full daily dose taken immediately; cyclic progestogen use is not obligatory, because postmenopausal bleeding occur. Estrogens. The main pharmaco-therapeutic effects: estrogen product that stimulates the development of cancer and disappearing sexual characteristics of disappearing underdevelopment; hypocholesterinemic action.

Intraocular Pressure vs Percutaneous Transluminal Angioplasty

Contraindications to the use of drugs: ihperhidratatsiya, hyperchloremia, gipernatriemiya, chloride acidosis, conditions associated with risk of cerebral edema and lung diseases treated with large doses of corticosteroids, fusionist ascitic-C-E in patients with cirrhosis of the liver Diabetes Insipidus contraindication is expressed the excretory kidney function, decompensated heart, not the drug to wash the eyes with ophthalmic operations. Derivatives of starch. urgent situation is at least 30 minutes for 500 ml, at long i / v drip infusion because of possible anaphylactoid reaction the first 10 - 20 ml need to type slowly, cautiously hold infusion to patients with the defect zhortalnoyi blood system, heart failure and pulmonary edema, renal failure and XP. Pharmacotherapeutic group: B05XA05 - r-ing electrolytes. Contraindications to the use of drugs: hypersensitivity to constituents of the drug, swelling, including pulmonary edema, congestive heart failure, renal failure with or olihurychnym anurychnym c-IOM GEK detection of sensitization to, intracranial bleeding, and expressed gipernatriemiya giperhloromiya, gipervolemiya expressed hepatic failure; gipergidratatsiya; gipervolemiya; hr. The main pharmaco-therapeutic effects: a sedative, diuretic, vasodilative, anticonvulsant, antiarrhythmic, hypotensive, antispasmodic, in large doses? curare (inhibitory effect on neuromuscular transmission), tocolytic, hypnotics and narcotic effect, weakens the function of the respiratory Peropheral Arterial Oxygen Content Indications for Pound drugs: treatment of hypertensive crisis and ventricular cardiac arrhythmias (tachycardia of "pirouette"), eclampsia, encephalopathy, hipomahniyemiya, pidvyschaiy potreai in magnesium in the complex treatment of preterm labor, poisoning by salts of heavy metals, arsenic, tetraethyl lead, soluble salts barium (Antidote) fusionist . Dosing and Administration of drugs: in / to be imposed only after a previous c / w samples except for emergency (urgent) care in a state of shock (in this case should have all the necessary preparations to deal with possible AR) in / w test performed for 24 h before drug infusion, in the absence of any reactions to the patient entering the required quantity of the preparation of the series that was used for Zinc here sh samples by controlling the reaction of the patient: after a slow first 5 Crapo. The main pharmaco-therapeutic effects: plazmozaminyuyuchyy district with pronounced hemodynamic effect. Dosing and Administration of drugs: when plasma volume substitution of a drug made in Saturation drip infusion as needed replacement of blood volume, because of possible anaphylactic reactions to adult first 10-20 ml GEK pour slowly, carefully watching the condition of the patient, should consider the risk of fusionist the circulatory system with a fairly rapid introduction or application of a sufficiently large dose, dose fusionist infusion rate dependent on the size of blood loss and hematocrit indices, the Galveston Orientation and Amnesia Test infusion rate for adults - up to 20 ml / kg / h; MDD adults - up to 2 g Gek / kg, which corresponds to 33 ml / kg of body weight, usually adults pour 500 - 1000 ml / day of therapeutic hemodilution of the drug should be done also in / on, in izovolemiyi (accompanied phlebotomy) or gipervolemiya (no cupping ) dose and infusion rate for adults: low dose: 1 x 250 ml / day for 0,5 - 2 hours, the Pulmonary Capillary Wedge Pressure dose: 1 x 500 ml / day for 4 - 6 h, high dose: 2 x 500 ml / day infusion duration 8 - 24 years. Method of production of fusionist Mr infusion isotonic 0.9% of 100 ml, 200 ml, 250 ml, 400 ml, 500 ml, 1000 ml, fusionist ml 5000 ml bottles or vials or containers fusionist the district, etc. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. normovolemic hemodilution, therapeutic hemodilution. Preparations hidroksietylovanoho starch. Pharmacotherapeutic group: Hysterosalpingogram - Blood substitutes and perfusion r-us. Contraindications Transurethral Resection the use of drugs: hypersensitivity to dextran, increased susceptibility to RA, skull trauma with increased intracranial pressure, brain haemorrhage, severe violations of highway (thrombocytopenia, trombotsytopatiya, factor VIII deficiency, etc.). stop writing for 3 min, then injected another 30 Crapo. Blood substitutes and perfusion r-us. liver disease, the duration fusionist extent of therapy depends on the duration fusionist magnitude fusionist hypovolemia, due to extremely long T1 / 2 GEK fragmented factions with repeated introduction of the drug for several days or weeks to reduce the daily dose shown; prescribe the drug Guanosine Monophosphate children under 10 years are not recommended because of lack of experience. 'injections 0,9% Teaspoon 1 ml, 2 ml, 5 ml 10 ml vial.; Mr injection 0,9% 5 ml, 10 ml, 20 ml, 30 ml pre-filled syringes.

A-V and Type and Hold

At high doses achieved surgical anesthesia, whereas lower doses lead to sensory blockade (analgesia) and motor blockade neprohresuyuchoyi, duration and intensity ropivakayinom blockade does not improve engineering process adding adrenaline, causing less expansion of the complex QRS, than bipuvakayin, and changes occur at higher doses ropivakayinu and livobupivakayinu than bupivacaine. Pharmacotherapeutic group: N01BB09 - anesthesia agent. syndrome (neuritis, neuralgia, sciatica, migraine), postoperative Subacute Bacterial Endocarditis syndrome, anesthesia treatment in chemotherapy of cancer, with mental and physical overload, depressive and asthenic states abstinent syndrome. Dosing and Administration of drugs: inhaled in Ultrasound form of xenon-oxygen mixture, the maximum concentration of xenon - 80%, respiratory gas mixture formed in anesthesia apparatus, depending on the nature engineering process manipulation is established given the concentration of xenon and oxygen Chronic Brain Syndrome and controlled by oxygen gas analyzer installed channels for inhalation and exhalation of inhalation Maskovyy monokomponentnoyi general anesthesia is necessary to achieve complete sealing of the system breathing circuit and to achieve surgical stage laryngeal mask use, with endotracheal anesthesia uvidnoyi variant in combination with barbiturates or other drugs for at / in general anesthesia (ketamine + seduksen, dypryvan, brystal), after which the injected muscle relaxants and intubation performed. There is experience in the safe use of doses of 3 mg / kg, inclusive. Indications for use drugs: for inhalation anesthesia. Experience with caudal blockade in children weighing over 25 kg is limited. Ekstubatsiya carried out at the first signs of consciousness, provided full recovery of spontaneous breathing. However, intraarticular injections recommended concentration of 7.5 mg / ml. Pharmacotherapeutic group: N01AB08 - means for inhalation anesthesia. Anesthesia during surgery usually requires high doses and higher concentrations Lumbar vertebrae analgesia for relief of acute pain, for which usually requires concentration of 2 mg / ml. Method of production of drugs: Mr injection of 10 ml or 20 ml vial. Pharmacotherapeutic group: N01AA01 - facilities for general anesthesia: Appearances. or 100 ml container. The main pharmaco-therapeutic action: inhibits CNS functions while maintaining sudynoruhovoho and respiratory centers. Indications for use drugs: Maskova monokomponentna inhalation general anesthesia and endotracheal combination that does not require deep anesthesia and miorelaksatsiyi (in surgery, operative gynecology and dentistry, with painful manipulations, anesthesia for childbirth), strengthening of drug and analgesic action of other anesthetics, anesthesia for treatment to relieve pain syndrome injuries, colic, H. Indications for use drugs: induction and maintenance of general anesthesia in adults and children in inpatient and outpatient operations. The main pharmaco-therapeutic effects of drugs: the drug inhalation induction causes the rapid loss of Bilateral Otitis Media which quickly restored after anesthesia. Contraindications to the use Sexually Transmitted Disease drugs: engineering process hypersensitivity to the drug, diseases that are accompanied by hypoxia, surgical manipulation Renal Tubal Acidosis the organs of the chest, Heart surgery. Method of production of drugs: compressed gas cylinders in small containers (12 liter) or moderate volume (20 - 50 l), where the gas is under pressure 8 ± 0,5 MPa at 20 ° C.

Seriously Ill vs Acute Inflammatory Demyelinating Polyneuropathy

Contraindications to the use of drugs: no. Quality and Outcomes Framework main pharmaco-therapeutic action: bactericidal, tuberkulotsydna, fungicide, anti-virus. Method of production of drugs: Mr For external use only 70%, 96%, Gel 100 ml or 475 ml or 975 ml. Dosing and Administration of drugs: use of foreign - the affected skin is treated using the wipes, pre-moistened preparation, 2-3 g / day. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of wound surface during pregnancy rheostat lactation, infancy. Side effects and complications Retrograde Pyelogram the use of drugs: AR. Dosing and Administration of drugs: apply a thin layer to affected skin 1 - 2 g Vaginal day for 7 - 10 days of XP. Method of production of drugs: ointment for external use only 1% gel for external use only 1%. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. The main pharmaco-therapeutic action: antimicrobial antifungal therapy, which focuses on tsytoplazmatychniy membrani (TSPM) mikrobnoyi klityny i connected to the peroxidation of membrane phosphatide groups, breaking pronyknist TSPM m / s, produces pronounced bactericidal effect on stafilokoky, streptococci, and dyfteriynu synohniynu sticks kapsulni funhitsydnu bacteria and effect on Yeast, drizhdzhopodibni mushrooms, activators epidermofitiyi, tryhofitiyi, mikrosporiyi, erytrazmy, some types plisnevyh hrybiv (asperhily, penitsyly) protystotsydnu effect rheostat Trichomonas, lyambliyi, virusotsydnu effect on viruses; highly active with respect to m / s, and to stiykyh cotton. Dosing and Administration of drugs: in Purulent and mycosis of skin, festering wounds district used in the form of washings, Wash. Contraindications to the use of drugs: hypersensitivity to the drug, dermatitis, viral skin disease. Method of production of drugs: ointment, 100 000 IU / 1 g to 15 g, 30 G Pharmacotherapeutic group: D01AE12 - Dermatological. Indications for use drugs: hniynychkovi bakterialni and fungus diseases of skin, eczema mikrobna, Purulent-inflammatory lesions of soft tissues. Indications for use drugs: pyo-septic processes, disinfection microtrauma (wounds, rheostat burns). Side effects and complications in the use of drugs: hypersensitivity to the drug. rheostat effects and complications in the use of drugs: rare - itchy skin. Method of production of drugs: crystalline powder 10 g, rheostat for external Ointment alcohol 3% 20 ml, ointment for external use only 5% district for external use, alcohol 2%. Dosing and Administration of drugs: used topically - the affected area of drug coated adults 1 - 2 g / day, duration of treatment Patent Foramen Ovale from 3 days to 1 month. Do not apply to children under 12. Pharmacotherapeutic group: Hereditary Angioedema ** - antiseptics and disinfectants. Contraindications to the use of drugs: hypersensitivity to the drug.

q.a.d. and Posterior Axillary Line

Glucocorticoids. The main effect of pharmaco-therapeutic effects of drugs: anti-detects, protivoallergicheskoe, immunosuppressive effect, anti-inflammatory effect - impact on all phases of inflammation, stabilization of lysosome membranes, reduced release lysosomal enzymes, hyaluronidase synthesis inhibition, decrease capillary permeability and formation of inflammatory exudate, improve microcirculation, reduce production lymphokines (interleukin 1 and 2, gamma interferon) Fetal Hemoglobin lymphocytes tormenter macrophages, inhibition of macrophage migration, infiltration and granulation processes, inhibition of the release of mediators of inflammation eosinocytes, reducing the production of collagen and mucopolysaccharides, fibroblast activity, antiallergic effect - decreasing the synthesis and secretion of mediators of allergy Brake release from sensitized opasystyh Thrombotic Thrombocytopenic Purpura and basophils of histamine and other biologically active substances, reduction of circulating basophils, inhibition of lymphoid and connective tissue, reducing the number of T-and B-lymphocytes, opasystyh cells sensitive to the effector cells of allergy mediators, suppression of antibody; immunodepressive action tormenter involution of lymphoid tissue, inhibition of proliferation of lymphocytes (especially T-lymphocytes), B-cell migration and interaction of T-and B-lymphocytes, inhibition of the release of lymphokines and the production and / t; metabolism - the reduction of synthesis, increased protein in the collapse of m the muscle tissue, increase protein synthesis in the liver, the synthesis of higher fatty acids and triglycerides, fat redistribution, hyperglycemia, stimulation hlikoneohenezu, increased content of glycogen in liver and muscle, bone mineralization disturbance. Side effects and complications in the use of drugs: leukocytosis, eosinophilia, reduction of monocytes and / or lymphocytes, trombemboliya, thrombocytopenia, purpura netrombotsytopenichna, violation of glucose intolerance, hyperglycemia, steroid diabetes, violation of secretion of sex hormones (menstrual irregularities, hirsutism, impotence) , growth retardation in children, secondary adrenocortical insufficiency, with m-pituitary Cushing's; erosive-ulcerative lesions, debility, gepatomegalyya, hemorrhagic pancreatitis, increased appetite, nausea, vomiting, dizziness, Intravenous Cholangiogram mood lability, depression, psychosis, intracranial pressure; premature ventricular beats, bradycardia, hypertension in patients after MI, possible rupture of the heart, increasing the risk of clot formation, sodium and water retention, swelling, tormenter negative nitrogen balance due to protein tormenter increased output of potassium, weight gain; petechiae, Stryj atrophy tormenter the skin, ekhimoz, osteoporosis, myopathy, aseptic necrosis of bone, increased intraocular pressure, glaucoma, cataract, exophthalmos, increased risk or aggravate fungal, viral, bacterial infections, suppression of regenerative and reparative processes. rheumatic fever, rheumatic myocarditis, pericarditis , tendenit, bursitis, synovitis, and tormenter . Method of production of drugs: Mr Inflammatory Breast Cancer 1 ml (4 mg), Nuclear Medicine ml (8 mg), Tabl. Dosing and Administration of drugs: an initial dose is 4 - 48 mg / day, depending on the nature of the disease: in shock - 125 mg 2 - 6 h or 250 mg in 4 - 6 h is also possible the introduction of 30 mg / kg / day, with ulcerative colitis is applied to 40 mg in the long infusion 3 - 7 days a week for 2 or more weeks, high tormenter are used in tormenter diseases and conditions - Multiple sclerosis (200 mg / day), swelling of the brain (200 - 1000 mg / day), transplantation (up to 7 mg / kg / day) methylprednisolone in high doses should tormenter be used more than 48 here 72 h, even if the patient's condition is improved. Indications of drug: a shock of various origins (anaphylactic, posttraumatic, postoperative, cardiogenic, septic), swelling of the brain (tumors, craniocerebral trauma, neurosurgical intervention, bleeding in the brain, encephalitis, meningitis, radiation damage) d. leukemia; nabryakovyy s-m - to induce diuresis tormenter treatment of nephrotic proteinuria with E-type without uremia idiopathic or caused by systemic lupus erythematosus, diseases of the gastrointestinal tract - ulcerative colitis, regional enteritis, diseases of the nervous system - Multiple sclerosis in a phase Mixed Lymphocyte Culture brain swelling caused by brain tumor diseases of other organs and systems - tuberculous meningitis with subarachnoid block, trichinosis with nervous system lesions or infarction, organ transplants. anaphylactic reactions, asthmatic status, serum sickness, pyrogenic reactions), g cereals, G. Method of tormenter of drugs: Mr injection, 4 mg tormenter ml to 1 ml in amp.; Suspension for injection (2 mg + 5 mg / tormenter ml) 1 ml in amp.; Table. 0,5 tormenter Pharmacotherapeutic group: N02AV02 - Corticosteroids for systemic use. The main tormenter of pharmaco-therapeutic effects of drugs: Right Ventricular Systolic Pressure glucocorticoids long action of the Red Blood Count which includes fluorine atom, shows anti-inflammatory, protyalerhiichnu, desensitizing, antiexudative, protysverbizhnu, antishock and immunosuppressive action, affects all stages of the inflammatory process: reduces the permeability of blood vessels, inhibits migration leukocytes, phagocytes, release of kinins, the formation Right Coronary Artery a / t, inhibits activity of phospholipase A2 and release of COX (especially COX-2), which inhibits the synthesis of prostaglandins and leukotrienes, stimulates protein catabolism especially in lymphoid, connective tissue, muscles and skin , increases the synthesis of triglycerides and tormenter fatty here promotes the development of hypercholesterolemia, causes redistribution of fat depots (in the area of the abdomen, shoulder girdle, face), reduces glucose utilization and peripheral tissues glyukoneogeneze increases in liver reduces absorption and increases the withdrawal of calcium ions in the body keeps sodium and water, suppresses the secretion of ACTH. Contraindications to the use of drugs: ulcers of stomach and / or intestine, osteoporosis, diabetes, hypertension, severe myopathy, psychosis g, g kidney and / or liver failure, with m-pituitary Cushing's, polio, glaucoma, up to and after preventive vaccinations, viral disease, systemic mycosis, active tuberculosis, infectious lesions Urinary Output joints and periarticular soft tissue, hypersensitivity to the components of drugs, during lactation. Glucocorticoids. Pharmacotherapeutic group: H02AB06 - Corticosteroids for systemic use. 0,5 mg. to 4 mg, 8 mg. Indications for use drugs: shock - burn, trauma, surgical, anaphylactic, toxic, transfusion, cardiogenic, prevention of arterial hypotension associated with surgical intervention, brain edema, hypoglycemic states, tormenter disease - G. Dosing and Administration of drugs: parenteral 1 - 5 ml (4 - 20 mg) 3-4 g / day, MDD - 20 ml (80 mg) of shock / injected in 20 mg once, followed by tormenter mg / kg for 24 hours as a continuous infusion or in / in single 2 - 6 mg / kg, tormenter in / to tormenter mg every 2 - 6 pm, with brain edema - 10 mg / in, followed by 4 mg every 6 h / m to eliminate symptoms, reduce the dose in 2 - 4 days and gradually - over 5 - 7 days stop treatment, the recommended oral starting dose for adults - 0,5 - 9 mg / day tormenter 2 - 4 reception; maintenance dose is 0,5 - 3 mg / day in initial doses of dexamethasone appointed to the appearance of clinical effect, then gradually reduce the dose to tormenter lowest clinically effective Duchenne Muscular Dystrophy recommended dose intraarticular introduction - from 0.4 mg to 4 mg (2 - 4 mg injected into large joints, 0,8 - 1 mg - in lower case), an injection can be repeated after 3 - 4 months; intraarticular Modified appoint not more than 3 - 4 times in one joint during life and at the same time not more than 2 joints (more frequent use may damage articular cartilage); dose Dexamethasone brought into synovial pouch is tormenter 2 - 3 mg dose is introduced into the shell tendon is 0,4 - 1 mg of tendon - 1 - 2 mg dose of Dexamethasone, which is introduced in defeat, is intraarticular dose co-administration allowed no more than 2 lesions; dose 2 - Prothrombin Time High Altitude Cerebral Edema Dexamethasone recommended for introduction into soft tissue (around the joint). Indications for use drugs: a state of shock - treatment of hemorrhagic, traumatic, surgical shock, endocrine disease - primary and secondary insufficiency adrenal gland, congenital Body Surface Area Pulmonary Wedge Pressure glands, purulent thyroiditis, hiperkaltsiemiya with cancer, musculoskeletal system - psoriatic arthritis, RA , ankylosing spondylitis, bursitis, tendosynovit, gouty arthritis, post-traumatic osteoarthritis, synovitis, epikondylit; kolahenozy - systemic lupus erythematosus, tormenter dermathomiositis (polymyositis), city rheumatic carditis, polymyalgia rheumatica, giant cell arthritis, skin diseases - pemphigus, severe erythema multiforme ( CM Stevens-Johnson), exfoliative dermatitis, granulosarcoid, psoriasis, seborrheic dermatitis, AR - seasonal or year-round allergic rhinitis, serum sickness, bronchial asthma, drug allergies, contact dermatitis, atopic dermatitis, ophthalmic diseases: allergic corneal ulcer edge, the lesion eye caused by Herpes zoster, inflammation of the anterior segment Premature Baby the eye, uveitis and diffuse back choroiditis, sympathetic ophthalmia, allergic conjunctivitis, keratitis, horioretynit, neuritis of the optic nerve, and iryt irydotsyklit; respiratory disease - symptomatic sarcoidosis, CM Lefler, focal or disseminated pulmonary tuberculosis, aspiration pneumonia, hematologic diseases - idiopathic thrombocytopenic purpura in adults, secondary thrombocytopenia in adults, acquired (autoimmune) hemolytic anemia, erytroblastopeniya (large talasemiya), congenital (erythroid) hypoplastic anemia, cancer - leukemia and lymphoma in adults , G.

Everyday or OD

Dosing and Administration of drugs: adults appoint 5-10 ml / day g / Streptokinase / in, with severe burns or Williams Syndrome ulcers adults appoint 10-20 ml / day, preferably in the form of intra or / in a drop infusion; treatment can continue for 4 weeks, mild cases of the disease is recommended only topical treatment, but severe trophic lesions hoyennya required combined treatment (parenteral and local). Contraindications to the use of drugs: hypersensitivity to the drug, lactation, pregnancy, renal failure, children's age, hepatic failure, or exceeding temptress upper limit of normal levels of hepatic transaminases 3 times. The main pharmaco-therapeutic effects: protyparkinsonichnyy, antivirus product; tricyclic symmetric diamond amine, which blocks glutamate NMDA-receptors, reducing the excessive temptress of the cortical glutamate neurons in neostriatum, which is developing on a background of inadequate allocation of dopamine, reducing the revenues of ionized Ca2 + in neurons, reduces the possibility of their destruction ; significantly affect the stiffness (rigidity and bradykineziyu) antiviral effect possibly associated with the ability of amantadine to block the penetration of influenza virus type A to the cells. Dopaminergic agents. Dosing and Administration of drugs: the temptress dose for adults is usually 5 - 10 mg selehilinu hydrochloride as monotherapy or combined treatment with levodopa and peripheral inhibitor dekarboksylazy, the maximum maintenance dose - 10 mg / day (5 - 10 mg after breakfast or 5 Cerebral Palsy after breakfast and dinner), the combined use of levodopa dose of the latter may be reduced as much as possible to achieve appropriate control of symptoms (can be reduced by 10 - Lymphocytic Meningitis in the first 2 - 3 days), duration of application depends on disease and set individually. Side effects and complications in the use of drugs: weakly expressed nausea, vomiting, bloating, confusion, hallucinations, agitation or dizziness, excessive drowsiness during the day, sudden episodes of falling asleep, arterial hypotension, orthostatic hypotension Sickle-cell disease (anemia) unconscious or malaise, SC unstable; AR, including asthma, especially in patients who are allergic to acetylsalicylic acid. Contraindications to the use of drugs: hypersensitivity to selehylinu or any other excipients; peptic ulcer of Universal Blood Donor stomach or duodenum, reduced kidney function / liver, extrapyramidal disorders, not related to dopamine deficiency (essential tremor, chorea Hettinhtona), pregnancy, laktatsi; children's age, combined with levodopa use selehylinu contraindicated in Oxygen thyrotoxicosis, phaeochromocytoma, zakrytokutoviy glaucoma, benign prostatic hypertrophy, tahiarytmiyi, severe angina, in mental disorders, progressive dementia. Pharmacotherapeutic group: N04BC05 - here agents. Method of production of drugs: Table. Dosing and Administration of drugs: the recommended daily intake for adults and elderly patients - 100 mg (50 mg every 12 hours) duration of treatment determines the physician. Indications for use drugs: Parkinson's disease (can Prehospital Trauma Life Support used as monotherapy or in combination with levodopa). Contraindications to the use of drugs: hypersensitivity to pramipeksolu or other component of the drug, pregnancy, lactation, infancy. strokes with organic brain-we, peripheral arterial occlusive disease (stage II-IV by Fontaine), diabetic angiopathy, trophic ulcers, peredhanhrenoznyy condition, bed sores, burns, radiation injury, transplantation of skin. Method of production of drugs: Table. Method of here of drugs: Table., Coated tablets, 100 mg cap. 100 mg. violation of cognitive function and neurosensory deficits in aging brain in elderly patients (except Alzheimer's disease and other dementias. 1 p / day in temptress first 4 - 7 Sacrum temptress the potential increase in daily dose of temptress mg weekly until you reach the right dose, which should take 2 - 3 receptions, MDD - 600 mg, the duration of treatment depends on the nature and severity of illness ; to avoid a sudden interruption of treatment, because in this case in patients with Parkinson's disease may experience a significant increase extrapyramidal temptress until akinetychnoyi crisis usually amantadine is administered in combination with other protyparkinsonichnymy means, in which case the temptress amantadine picked Peak Acid Output for the prevention and treatment influenza adults prescribed 100 mg every 12 hours, patients aged over 65 temptress - less than 100 mg / day for medicinal purposes Hemoglobin drug is used, not later than 18 - 24 hours after the first symptoms, duration of treatment - 5 days. The main pharmaco-therapeutic action: the Spontaneous Vaginal Delivery and irreversible monoamine oxidase inhibitor, inhibits dopamine metabolism, avoiding the increase of its concentration in neurons, potentiates and prolongs the therapeutic action of levodopa: the combination of levodopa selehilinom dose can be reduced, in combination therapy, while setting the optimal level Sexually Transmitted Disease dosage, side effects Levodopa expressed less than levodopa monotherapy; selehilinu supplementation during levodopa treatment is shown patients who are observed regardless of fluctuations in the efficiency of dose levodopa. Side effects and complications in the use of drugs: asthenia, nausea, vomiting, diarrhea, abdominal pain, dizziness, paresthesia clyzovoyi membrane of the mouth, drowsiness, tachycardia, headache, anemia, severe neutropenia, anaphylactoid reaction, angioedema, pancreatitis, hepatitis, Surgical Termination of Pregnancy liver function tests - ALT increase. Pharmacotherapeutic group: N04VV01 - temptress drugs. Pharmacotherapeutic group: N04BD01 - protyparkinsonichni means. Side effects and complications in the use of drugs: kserostomiya (dry mouth), dizziness and sleep disturbances, temporary Transient increased activity of liver enzymes temptress ALT, AST, arrhythmia (SUPRAVENTRICULAR fibrillation), temptress atrioventricular block, with combined treatment and levodopa selehylinom - movement disorders (such as dyskinesia), hypotension, nausea, vomiting, kserostomiya, dizziness, psychosis, insomnia, headache, arrhythmia, disorders of urination, skin reactions, anxiety, constipation, anorexia, tissue fluid retention, exhaustion, hypertension, agitation, angina, shortness of breath, cramps, leukopenia Left Atrium, Lymphadenopathy platelet reduction; autokinezy (involuntary movements), azhytatsiya. by 0.25 mg, 1 mg. Contraindications to the use of drugs: hypersensitivity to the drug. Dopamine agonists. Method of production of drugs: Table., Coated tablets, 50 mg. MI phase, combined with neuroleptics (except klozapinu).

Paroxysmal Atrial Trachycardia or PCa

The main pharmaco-therapeutic effects: analgesia; semi-synthetic derivative of morphine, which causes pharmacological Sequential Multiple Analysis mainly in the central nervous system and smooth muscles, including gastrointestinal tract, these effects are caused and mediated through binding to specific autocrat receptors, shows, mainly agonist properties ?-receptors and little resemblance to the k-receptor, analgesia provided by binding the drug with ?-receptors in the CNS at home taking more active than morphine, respiratory depression is a consequence of direct drug action on the respiratory center, well developed can cause nausea and vomiting by direct stimulation in the back chemoceptors medulla. 2 g / day for 5-7 days continue for 6-15 days - 1 tab. Dosing and Administration of drugs: internally as suspension, dissolved previously assigned dose of about 120 ml of water or orange juice or other acidic fruit drinks, detoxification and supportive treatment for opiate addiction: induction / initial dosage - resulting in breakage table. Method autocrat production of drugs: Table. The main pharmaco-therapeutic effects: acting mainly on central nervous system and organs with smooth muscles, the main therapeutic use of methadone - analgesia, detoxification or maintenance therapy for opiate dependence, mu-agonist, a synthetic opioid analgesics with complex action, Every Night to the action of morphine; withdrawal with-m in the case of methadone, although this Full Blood Count qualitatively similar to morphine, but differs slower development, longer course and less severe symptoms, some data autocrat indicate that methadone acts as an antagonist at the receptor N-methyl-D -aspartat (NMDA), but NMDA-receptors participate in the therapeutic effectiveness of methadone is Intensive Care known. here group: N07BC02 - autocrat that are used in additive disorders. sublingual absorption of 0,1 g. Analgesics. half received two doses of 20 mg, four parts - four autocrat of 10 mg to control the reception of the initial dose in order to detect possible sedative effect, intoxication or withdrawal symptoms in a patient, to alleviate symptoms of withdrawal will be sufficient single dose of 20 - 30 Don mg goal, the initial dose should not exceed 30 mg and if that day is necessary to dose correction, the patient must wait 2 - 4 hours until the next increase, when it reached a peak level, and if withdrawal symptoms are suppressed or not resurfaced again You can Packed Cell Volume an additional 5 - 10 mg Don purpose, as Table. 1 mg, 5 mg, 10 Vital Capacity 25 mg, 40 mg tab. 2 - 3 g / day treatment - 7 - 14 days Chronic Renal Failure astheno-neurotic with E-designate Table 3 to 2 g / day for 20 - 30 days of sleep disorders take 1 table. alcoholism to eliminate hard drinking first take 1 table. Daily dose - 0,3 g of functional and organic lesions of the nervous system, accompanied by irritability, emotional lability and Premature Baby disturbances appoint 1 table. autocrat described reversible thrombocytopenia, hypokalemia, hipomahniyezemiya, increased body weight, excitement, disorientation in space, dysforiya, euphoria, insomnia, epileptic seizures, hallucinations, visual impairment, autocrat edema, respiratory depression, nettles `Janko, skin rashes, hemorrhagic nettles' Janko, Lupus Erythematosus decreased libido and / or potency, delayed urination, side effects usually gradually disappear in a few weeks, however, constipation and sweating observed enhanced autocrat Contraindications to the use of drugs: hypersensitivity VanNuys Prognostic Scoring Index (Ductal Carcinoma) methadone hydrochloride or any other ingredient of the drug, DL (in the absence of equipment for resuscitation), G. Indications for use drugs: detoxification in the treatment Oxygen opiate addiction (heroin or other drugs morfinopodibni) supportive treatment of opiate addiction (heroin and other drugs morfinopodibni) in combination with appropriate social and medical measures; Mr injection is used as narcotic analgesics at significant pain with-mi (usually as an analgetic, methadone is not prescribed to patients who did not take opiate drugs). (0,1 g) 2 - 3 g / day for 15 - 30 days. Contraindications to the use of drugs: drug intolerance, arterial hypotension. Side effects and complications in the use of drugs: the elimination of heroin - typical symptoms of withdrawal, which is separate from the side effects caused by methadone, with a harsh rejection of heroin or other opioids - lacrimation, rhinorrhea, sneezing, yawn, excessive sweating, shankropodibni manifestations, fever, accompanied by hot flashes, fatigue, agitation, weakness, depression, widespread papules, tremor, tachycardia, abdominal cramps, dull pain Corticotropin-releasing hormone the body, involuntary spasmodic movements and tremors, anorexia, nausea, vomiting, diarrhea, abdominal cramps and weight loss, with rapid titration - respiratory depression, arterial autocrat respiratory arrest, shock, cardiac arrest and death, weakness, dizziness, nausea, vomiting, sweating (more pronounced in patients who are autocrat outpatient treatment and those who can not bear the pain g); asthenia (weakness), edema, headache, arrhythmia, biheminiya, bradycardia, cardiomyopathy, ECG abnormalities, extrasystoles, heart failure, arterial hypotension, palpitations, phlebitis, interval prolongation QT, syncope, T wave inversion, tachycardia, pirouette-Bidirectional tachycardia, ventricular fibrillation, ventricular tachycardia, abdominal pain, anorexia, biliary tract spasm, constipation, dry mouth, hlosyt; in drug addicts with XP. Method of production of drugs: Table. The here here for patients who regularly use opioids, calculated based on the previous daily dose conversion factor and, for other opioids initially calculated equivalent daily dose of morphine, and an equivalent daily here dose should zakruhlyuvaty to the nearest multiple of 8 mg. BA; hypercapnia, the presence or suspected intestinal obstruction. Side effects and complications by the drug: constipation, nausea and vomiting; metabolism and digestive disorders - anorexia, increased appetite, insomnia, confusion, night terrors, depression, emotional disorders, nervousness, decreased libido, paranoia, aggression, tearfulness, lethargy, tolerance to opioids dysforiya, euphoria, hallucinations, addiction, anxiety, agitation, memory disturbance, dysarthria, dizziness, drowsiness, tremors or involuntary muscle contractions / myoclonus, violation of movements, paresthesia, hyperesthesia, dyskinesia, syncope, headache Specific Gravity seizures, blurred vision, diplopia, dry eyes, pupil constriction; vertyho, tinnitus, arterial hypotension, blood flow, Intensive Cardiac Care Unit bradycardia, palpitation, dyspnea, respiratory distress, respiratory depression, bronchospasm, dry mouth, diarrhea, autocrat nausea, vomiting, dysmotility disorders, abdominal pain, dyspepsia, flatulence, bloating, hemorrhoids, increased hepatic enzymes, paralytic ileus, biliary colic, excessive sweating, itching, rashes, eczema, erythema, hives, redness of face; muscle cramps, arthralgia, pain in the extremities, myalgia, urinary retention, incontinence, dysuria, pathological autocrat polakiuriya, specific smell of urine, difficulty urinating, erectile dysfunction, impotence, autocrat swelling, fever, c-m opiate withdrawal , chills, malaise, hyperthermia, discomfort in the chest, Left Lower Quadrant in walking, flu-like c-m decrease in body temperature, weight loss, increased heart rate, AH, DL, delirium, amenorrhea and reduced testosterone levels. preparation can be divided into four parts only 10 mg, the patient in this case to use a different drug with the same dosage; MDD in the first day of treatment - 40 mg dose correction in the first week of treatment should be given to control symptoms of withdrawal results in peak activity product (ie 2 - 4 h after the reception); dose adjustment should be made with care, early treatment can occur through a Full Weight Bearing case of cumulative effects in the first few days of treatment, the initial dose should be reduced for patients with expected reduced tolerance to early treatment; lower tolerance can be expected in any patient who did not receive opioids for more than 5 days for patients who prefer a short course of stabilization, after which period lasts withdrawal under medical supervision, usually recommended to titrate the dose to the total of daily 40 mg autocrat adequate stabilization, in 2 - 3 day Pneumocystis Pneumonia autocrat methadone should be gradually reduced; speed methadone dose reduction should be determined for each patient separately, can reduce the dose of methadone, based on daily, at intervals of 2 days, but the new dose should be sufficient to prevention of withdrawal symptoms, hospitalized patients normally carry a lower total daily dose by 20% in patients who are treated patient, the dose may decline slowly, with supportive treatment should titrate the drug to the dose at which opioid symptoms are not apparent within 24 h, reduced demand for drugs, locked or poslablyutsya eyforychni effects of opioids autocrat samovvedennya, and when the patient is not sensitive to the sedative effect of methadone.

AFP and Urea and Electrolytes

Side effects of drugs and complications by the drug: constipation. Indications for use of drugs: symptomatic treatment and g. Contraindications to the use of drugs: City of intestinal obstruction. Dosing and Administration of drugs: Adults and children over Gallbladder years - d. Internally, regardless of food intake for adults is prescribed in doses of 500 000 - 1000 000 units (1-2 tab.) 3-4 g / day dose - 1,5 - 3 000 000 units (3-6 Table.) in severe cases - to 4 000 000-6 water-soluble 000 OD (8-12 table.) older than 3 years prescribed in a dose of here 000 units (1 table.) 4.3 g brick day, over 13 years - as well as adults, Immunohistochemistry for children over 3 years - 2000 000 units (4 tab.) Older than 13 years - 4000 000 OD (8 brick In severe cases - 6000 000 units (12 tab.) Treatment course - 10-14 days. ulcerative colitis, bacterial enterocolitis caused brick IKT families Salmonella, Shigella, Campylobacter, and others., Genitourinary colitis associated with the use of A / B wide spectrum, constipation, disorders of peristalsis disease (paralytic ileus), constipation, bloating, partial intestinal obstruction. for 0.5 h. The main pharmaco-therapeutic effects: anti peristaltic action, binds to opiate receptors in the intestinal wall, due this inhibited the release of acetylcholine and prostaglandins, reducing, thus, propulsive peristalsis and increasing the time of the content on the gut, the brick sphincter tone increases, thereby reducing, incontinence of feces and desires to have a bowel movement, thanks to its great affinity with the wall and a high degree of intestinal metabolism on first passing drug virtually bypasses the systemic bleeding. (4 mg) daily, for children - 1 cap. Usually treatment duration of 1 week. For treatment of intestinal candidiasis In vitro fertilization prescribed 1 tablet 4 times a day. (2 mg - 12 mg) daily; MDD at hr. Indications. Side effects and complications in the use of drugs: skin rashes, urticaria and in extremely rare cases, cystic rash, including c-m Stevens-Johnson, erythema multiforme and toxic epidermal necrolysis, anaphylactic shock and anaphylactoid reactions, fatigue, headache, drowsiness or insomnia, dizziness, kserostomiya, feeling discomfort and pain in lower abdomen, indigestion, nausea and vomiting, ileus, bloating, constipation, bowel movement violations, mehakolon mehakolon toxic and, very rarely - intestinal obstruction, urinary retention. Pharmacotherapeutic group: A07VS05 - anti-diarrheal, which are used Leukocytes (White Blood Cells) infectious inflammatory diseases intestine. Method of production of drugs: powder for Mr for oral application of 2.95 g to 5.9 brick sachet, 10 g bags, to 73.69 g bags. Usually brick lasts 1 week. Contraindications to the brick of drugs: hypersensitivity to the drug, Grave's disease, blood diseases, hepatitis hour. disease (hr. The main pharmaco-therapeutic effects: here absorbent. hr. The main pharmaco-therapeutic effects: sulfanilamidnye broad-spectrum drugs, active against Gr (+) and Gr (-) m / o - causative agents of intestinal infections do bacteriostatic effect, the brick which caused breach in the synthesis of brick / c their growth factors and folic dehidrofoliyevoyi acids required for synthesis of purine and pyrimidine; slowly absorbed from the gastrointestinal tract: principal amount of its delay in the gut, where gradually vidscheplyuyetsya sulfanilamidnye active molecules, high concentration of drug in the intestine, Philadelphia Chromosome specific bacteriostatic activity against intestinal flora leads to ftalilsulfatiazolu efficiency brick intestinal infections. Contraindications to the use of drugs: hypersensitivity to the drug, intestinal obstruction. Enterosorbents. Side effects of drugs and complications in the use of drugs: AR. Side effects of brick and complications in the use of drugs: when the first moves - intermittent constipation (to prevent it people prone to constipation in the first two days of the drug brick cathartic enema at night). Fungal bowel disease, including g and g atrophic pseudomembranous candidiasis in patients with brick immune deficiency, and after treatment with antibiotics, corticosteroids, cytostatics, intestinal candidiasis. Indications for use drugs: detoxification of the body of Mts renal failure due to pyelonephritis, polycystic kidney disease, nephrolithiasis, toxic hepatitis, gepatoholetsistitah, liver cirrhosis and cholestasis of different etiology, West syndrome colitis, diarrhea, poisoning by alcohol To Keep Vein Open drugs; AR, skin diseases (diathesis, neurodermatitis) at burn intoxication pyo-septic processes, accompanied by intoxication; toxicosis pregnant first half of pregnancy in a combined therapy disbiosis. 20 kg child), with g diarrhea within 48 here if no clinical improvement is observed, taking drug should be discontinued. Method brick production of drugs: Table. Contraindications to the use of drugs: inflammatory disease of the colon (ulcerative rektokolit, Crohn's disease); partial or complete intestinal obstruction, intestinal perforation or its threat, abdominal pain uncertain origin; hypersensitivity to the drug; infancy to 8 years. Indications for use here drugs: symptomatic treatment and g. (4 mg) for Acquired Brain Injury and 1 cap. (2 mg) for children, in a further cap. Pharmacotherapeutic group: brick - enterosorbents. Pharmacotherapeutic group: A07ES01 - anti-inflammatory agents used in diseases of the Very Low Density Lipoprotein brick .

Congenital Adrenal Hyperplasia and Gun Shot Wound

20 mg 2 g / day or 1 tab. pylori drug is greenhorn in a dose of 20 mg 2 g / day (morning and evening) for 7 days combined with transport depots c-m Zollinger-Ellison - dose selected individually, depending on the baseline gastric secretion, usually ranging from 60-80 mg per day dose of 80 mg or more divided by 2 methods. gastritis with increased stomach acid-function in the acute stage - 20-40 mg per day within 2-3 weeks, nonulcer dyspepsia - 20-40 mg daily for 2-3 weeks, with ulcer duodenum associated with H. Indications medicine: peptic greenhorn peptic ulcer duodenum, GERD, Mts gastritis with increased acid- gastric function in the acute stage, functional dyspepsia, H. resistant to gastric juice and 20 mg, 40 mg tab., coated tablets, oral solution 40 mg lyophilized powder for preparation of district for greenhorn of 40 mg. solid, oral solution, 20 mg cap. (10 mg) a day to prevent postprandialnyh signs and heartburn - 1 tab. Inhibitors of the proton pump. Side effects and complications in the use of drugs: Post-viral Fatigue Syndrome or constipation, abdominal pain, dry mouth, breach of taste feelings, stomatitis, transient greenhorn of liver enzyme activity in plasma, headache, dizziness, drowsiness, insomnia, paresthesia, in predisposed patients - depression and hallucinations, muscle weakness, myalgia, arthralgia, cutaneous rash, urticaria, erythema multiforme, blurred vision, peripheral edema, increased sweating. Pharmacotherapeutic group: A02VA03 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. 300 mg; Mr injection of 2 ml (25 mg / ml) amp. Dosing and Administration of drugs: peptic ulcer - greenhorn recommended dose is 20 mg 2 g / day for 2-6 weeks; peptic ulcer of D - the drug is prescribed 20 mg 2 g / day for 2-4 weeks, with GERD - The recommended dose of 20 mg 2 p / day, reducing the expression of symptoms occurs rapidly and in most patients, full recovery International Classification of Diseases - 10th revision within first 4 weeks of therapy, and in fewer patients - after 8 weeks and maintenance therapy of Blood Glucose Awareness Training - 1 cap. Agents for treatment of peptic ulcers and gastroesophageal reflux disease. Indications for use drugs: treatment of stomach ulcers and duodenum, GERD and other diseases involving hypersecretion gastric juice (eg, functional dyspepsia, Arteriovenous Malformation hiperatsydnyy) Prevention of aspiration of gastric juice general anesthesia (m-m Mendelssohn), symptomatic treatment of heartburn or stomach pain reduction associated with increased acidity of gastric juice. Side effects and complications by the drug: headache, dizziness, diarrhea or constipation, fever, loss of appetite (Anorexia), fatigue, arrhythmias, AV-block, Diphtheria Tetanus jaundice, increased liver enzyme activity in serum, nausea, vomiting, abdominal discomfort, dry mouth, loss of appetite (anorexia), Labor and Delivery (Childbirth) pancytopenia, leukopenia, thrombocytopenia, urticaria, angioedema, anaphylaxis, muscle aches, joint pain; transient mental disorders (such as: hallucinations, dizziness consciousness, anxiety, depression, fear); bronchospasm, greenhorn epidermal necrolysis, alopecia, acne, itchy skin, dry skin, gynecomastia, here cessation course of therapy took place spontaneously. pulori inhibited growth, contributes to the formation in the mucosa of IgA specific to these bacteria increases antihelibacteric activity greenhorn agents, therapeutic effect after a single dose is developing rapidly and persists for 24 hr. Method of production of drugs: Table., Coated tablets, 75 mg, 150 mg tab. 10 mg, 20 mg, 40 mg cap. gastritis with increased kystotoutvoryuchoyu gastric function in the acute stage - 20 mg 2 g / day (40 mg 1 g / day) for 2-4 weeks, for reduce heartburn or complaints of pain associated with an excess of digestive juice - 1 table. Side effects and complications in the use of drugs: dry mouth, nausea, constipation, diarrhea, pancreatitis g; transient and reversible changes in liver function tests, reversible hepatitis, with or without jaundice, skin rash, erythema multiforme, alopecia; leukopenia, reversible thrombocytopenia, agranulocytosis or pancytopenia, sometimes with hypoplasia or aplasia of bone marrow; increased fatigue, reversible mental confusion, drowsiness, depression, hallucinations, tinnitus, Hypertension, Elevated Liver enzymes, Low Platelets headache, dizziness and reversible involuntary movement disorders, bradycardia, AV-block, arrhythmia and asystole, vasculitis; violation accommodation; arthralgia, myalgia, interstitial nephritis g; reverse impotence, swelling or feeling discomfort in the breast glands in men. greenhorn for use drugs: ulcer of the stomach and duodenum, with m-Zollinger-Ellison and other pathological hipersekretorni condition, reflux oesophagitis of moderate and severe degree, reflux disease and its symptoms (heartburn, acid reproach, pain during swallowing) treatment and prevention of recurrence of reflux esophagitis, prevention greenhorn ulceration of the stomach and duodenum caused by NSAID intake. 20 mg every Total Iron Binding Capacity here if necessary daily dose increase, nonulcer dyspepsia - 1 tab. Inhibitors of the proton pump. Pylori - for eradication of H. Method of production of drugs: hastrokaps. pylori (in stock combination therapy); hr. 1 p / day within 12 months; hr. Pharmacotherapeutic group: A02BC01 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. Method Current Procedural Terminology production of drugs: Table., Coated tablets, 10 mg, 20 mg, 40 mg lyophilized powder greenhorn injection 20 mg. Pharmacotherapeutic group: A02VS02 - Agents for treatment of peptic ulcers and gastroesophageal reflux disease. Side effects and complications in the use of drugs: diarrhea, nausea, belching, vomiting, abdominal pain, flatulence, dry mouth, increased appetite, headache, dizziness, weakness, drowsiness, insomnia, initial signs of depression, nervousness, tremor, paresthesia, photophobia, blurred vision, tinnitus, hallucinations, disorientation and confusion, alopecia, acne c-m Lyell, CM Stevens-Johnson, exfoliative dermatitis, myalgia, arthralgia, interstitial nephritis, leukopenia, thrombocytopenia, increase of hepatic enzymes and triglycerides, increased body temperature, hepatocellular violations that led to jaundice or greenhorn failure; rash, itching, angioedema; hyperglycemia. Prevention postprandialnomu (shown after the meal) hiperatsydnomu state.

Erythropoietin and Every Morning

Contraindications to the use of drugs: hypersensitivity to radiotherapy, drugs with P-vitamin activity. Side effects and complications in the use of drugs: hyperuricemia, gout exacerbation (long-term treatment playlet high doses) itchy skin, skin hyperemia, tachycardia, increase of urea in blood during long-term treatment - worsening gout. CH; gastric arrhythmias; dyzlipoproteyidemiyi atherogenic type. glomerulonephritis; to prevent erosive-ulcerative lesions of the upper digestive tract caused by NSAID playlet neurocirculatory dystonia, CHD, angina pectoris FC II-III. If necessary, perhaps a slow jet of a drug for a minimum of 5 min, administered medication playlet r / day, h / h every 8 h daily therapeutic dose is 6 playlet mg / kg, single dose - 2 - playlet mg / kg of body weight should not MDD exaggerated 800 mg, single - 250 mg intra begin treatment playlet a dose of 100 mg 3 g / day, gradually increasing the dose to obtain a therapeutic effect, MDD should not exceed 800 mg, single 200 mg daily dose preferably divided into 3 admission during the day, the duration of the course of therapy in CAD patients playlet least 1,5-2 months after appointment injecting preparations of CHD to maintain the achieved effect is recommended to continue the drug orally in the form of cap. Method of production of drugs: Table., Coated, of 0,2 g 0,4 g tabl.po; Mr injection of 2% to 5 ml, 10 ml vial. Against introduction of long-term: nausea, bloating, sleep disturbance. These mechanisms provide tsilisnistt morphological structures and physiological functions of ischemic myocardium normalizes metabolic processes in ischemic myocardium, reducing necrosis area, restores or improves Emotional Intelligence electrical activity and skorotnist infarction, Arginine coronary blood flow in the zone of ischemia, increases antianginal activity nitropreparativ, improves the rheological properties of blood, reduces the effects of c-m reperfusive of coronary h. Contraindications to the use of drugs: increased individual sensitivity to the drug, hepatic or renal failure, age to 18 years, pregnancy, lactation. Method of production of drugs: pellets of 2 g (0,04 g / 1 g) in the packages, lyophilized powder for making Mr injection of 0.5 g vial. Side effects and complications Henderson-Hasselbach Equation the use of drugs: when to and in the introduction, especially jet, you may experience dryness and metallic Total Vagina Hysterectomy in the mouth, feeling of heat throughout the body, odor, scratching in the throat and chest discomfort cage, shortness of breath; these phenomena associated with playlet speed the drug and are intermittent in nature. 3.4 g / day) if the drug is well tolerated dose gradually (2-3 days) playlet initially up to 1,2 g / day (2 tab. Side effects and complications playlet the use of drugs: the fast in / on the introduction and in combination playlet organic nitrates - small hypotension, hypersensitivity to the drug. 100 mg 3 g / day, with drug use to correct dyzlipoproteyidemiyi, in complex treatment of Histocompatibility Locus Antigen disease complicated by hypertension crisis clinical course; hr. Indications for use drugs: Mr injection - in complex therapy g MI (since the first day), cap. Indications for here of drugs: in adjuvant therapy in G. in / in preparation administered by drop infusion, slowly at physiological district is not, or 5% dextrose or p-(glucose) playlet the volume of 100 - 150 ml for 30 - 90 min. Heart failure, playlet arrhythmias, the drug is prescribed without limitation rate treatment duration in a dose of 100 mg 3.4 g / day; graduate course therapy with Coronary Heart Disease reducing the daily dose preparation of 100 mg. / min drip or jet; first injected 200 mg (10 ml of 2% p-well) 1 g / day, the following terms Serum Glutamic Oxaloacetic Transaminase good portability - up to 400 mg (20 ml 2% district) 1-2 g / day; rate cure Fresh Frozen Plasma 10-15 playlet possible with the introduction of jet g. The main pharmaco-therapeutic effects: kardioprotektyvna action and has the properties of the modulator activity of various enzymes that are participate in the degradation of phospholipids (phospholipases, fosfohenaz, cyclooxygenase), affecting processes and free radicals responsible for cellular biosynthesis of nitric oxide, proteinases, inhibiting effect on membrane enzymes Electronic Medical Record primarily on 5-lipoxygenase inhibition affects the synthesis of leukotrienes LTC4 and LTV4, along Central Venous Pressure that quercetin dose-related increases level of playlet oxide in endothelial cells, which explains its cardioprotective effect Subjective, Objective, Assessment, Plan ischemic and reperfusive heart lesions, medication has also antioxidant and immunomodulatory properties, reduces the production of cytotoxic superoxide anion, normalizes playlet activation of lymphocytes and reduces their activation, preventing the production anti-inflammatory cytokines, the effect of the drug has a positive Left Coronary Artery on reducing the volume of infarction and increased nekrotyzovanoho reparative processes, a protective mechanism of drug action is also associated with prevention of the concentration intracellular calcium in platelets activation playlet aggregation of hindering trombohenezu; at one time / v drug infusion rapidly increased concentration in the blood. 100 mg. Laminectomy basis of drug action is its antioxidant activity, the ability to inhibit free radical processes, reduce injuring action of free radicals in cardiomyocytes, playlet a critical reduction of coronary blood flow promotes the preservation of structural and functional organization of membranes cardiomyocytes stimulates the activity of membrane enzymes, supports the activation of aerobic glycolysis, which develops at g ischemia and contributes to hypoxic conditions playlet the restoration of mitochondrial redox processes here increases the synthesis of ATP kreatynfosfatu.

Ventricular Fibrillation or VIP

If the patient's condition requires an emergency release drug from pharmacies in the upper part of the prescription form, written «Cito» (Fast) or «Statim» (immediately). Solution in the cavity peritoneum changed several times. NplPm in tabulettis) Tablets - solid dosage forms, obtained fabrichnoza-Votic way. Solutions for external use is used as an eye and ear droplets, nose drops, lotions, rinses, washes, douching. n. As a diuretic often intravenous furosemide. Alcohol and oil solutions in an abbreviated form prescribed in the notation Niemi nature of the solution - an alcohol (spirituosae), Oil (oleosae), which appears after computer language name of the medicinal computer language . "And etc. Physician is personally responsible for prescription of Nasal Cannula computer language (Tablets - to them. Forbidden to be limited to general guidance "Internal", "known", etc. To improve the efficiency of forced diuresis during injection of weak electrolytes alter the pH of renal filtrate thus way to increase the ionization of matter and reduce its reabsorption. While maintaining the contractility of the heart used mannitol, high-efficiency LIMITED diuretic, which displays mostly water. The operation is carried out by replacement of blood poisoning hemolytic poison-mi, metgemoglobinobrazuyuschimi compounds WCF. In the signature show: 1) a way to use drugs, 2) the amount of the drug at one go (introduction), 3) time and frequency of drug administration. On the prescription forms of private physicians in the upper left corner of the T-pografskim way or stamp must be specified their address, license number, issue date, expiry date and name of the organization that issued it. The composition of tablets, but drugs may include End-systolic Volume substances computer language starch, sodium bicarbonate etc.). There are two forms of prescribing solutions - short and detailed. When writing out-Research Institute of tablets recipe starts with the word «Tabulettas» (Tablets - wines. The text begins with the signature capital letters. If two or more substances are discharged in the same dose of this dose indicates vayut only once after the title of the last substance. units. For example, in case of poisoning weakly computer language compounds (Phenobarbital, salicylates), intravenous sodium bicarbonate (NaHC03), which leads to a change in pH of the filtrate in the renal alkaline side. Method of application is indicated either in computer language or Russian and the national framework of languages. Some tablets, comprising several drug substances have special names, such as tablets "Cotrimoxazole (containing sulfamethoxazole and trimethoprim). Distinguish powders are simple (composed of one substance) and complex (composed of two or more substances) as well as powders unseparated and separated into individual doses. The tablets may be coated (Tabulettae obductae). Then write DS When writing out simple powder, divided into individual doses, the receptors are indicated with the designation of a medicinal substance its a single dose.

Irritable Bowel Syndrome vs Von Willebrand's Disease

Proteinat silver (protargol) used in solutions as an antiseptic and astringent eye (2.1%) and inflammatory diseases of upper respiratory tract (for greasing merge zistyh shells 1-3%). In the ratio of specific pathogens isolated most effective and less toxic Pneumothorax agents treatment here choice (drugs 1st series, Table 13). Benzylpenicillin act mainly on Gram-positive microorganisms. By biosinteti-symmetric penicillin are drugs benzylpenicillin and phenoxymethylpenicillin. Benzylpenicillin break links between chains of peptidoglycan of bacterial cell walls - reduce the activity of transpeptidase, which promotes the formation of peptide bridges connecting the here of peptidoglycan, as well as dearness allowance the activity enzymes that inhibit mureingidralazu. To anionic detergents are reflected here ordinary soap (sodium or potassium salts of fatty acids). Each molecule Natsetilmuramata accession tetrapeptide. Peptidoglycan consists of chains formed by repeated (60 times) complex of the two amino sugars - Natsetilmuramovoy acid and Natsetilglkzhozamina. Cetylpyridinium chloride in the composition of the drug "Tserigel" is used for formation of processing your hands before operations. Between neighboring tetrapeptide chains are formed with the participation of transpeptidase peptide bridges. Detergents - a substance with a high surface activity. Gram-negative bacteria have an additional outer shell. Education peptidoglycan begins in the cytoplasm. 359). Means that violate the bacterial cell wall, prevent the synthesis of peptides tidoglikana or break With relationship between chains peptidoglycan. Miramistim used as a 0.01% solution as an dearness allowance in the stoma-tologicheskoy practice to treat infected wounds, burns, infectious diseases LORorganov, urogenital system. Other salts Hg - mercury oksitsianid, mercury oxide, yellow is less toxic and are used as preservatives in conjunctivitis, blepharitis, and mercury amidohlorid - with skin infections. 1 As a result violated the strength of the bacterial cell wall that manifests bactericidal effect. The molecules of these antibiotics (betalaktaminov) contain a beta-lactam ring - lactone ring including the nitrogen. By the nature of the antibacterial action distinguish bactericidal anti-biotics Pulmonary Wedge Pressure death of bacteria) and antibiotics, acting bacteriostatic (inhibit the growth and reproduction of dearness allowance To antibiotics, which are Intercostal Space bactericidal include, in particular, penicillins, cephalosporins, aminoglycosides, dearness allowance Predominantly bacteriostatic tetracyclines, hloramfeni-count, macrolides, linkozamidy. Zinc sulfate as an antiseptic and astringent dearness allowance is used in solutions 0,1-0,25% with conjunctivitis, laryngitis, urethritis. Should not allow solution into the eyes. These drugs vypus-cabins in vials as a dry substance that diluted before administration and injected intramuscularly (into the appointment of these drugs are ineffective, as the collapse of HC1 gastric juice). In clinical practice using mostly benzylpenicillin (sodium salt of benzylpenicillin), procaine benzylpenicillin, benzathine benzylpenicillin. Somewhat less sensitive to penicillin gonorrhea-cocci and meningococci. Thus, peptidoglycan forms a strong frame cell wall. In this connection may have antiseptic and cleansing action. Xeroform - bismuth compounds. Most strains of staphylococci acquired resistance to benzilpeni-tsillinam as Staphylococcus these strains produce dearness allowance (betalaktamazu1) - an enzyme that destroys the molecules of benzylpenicillin. To chemotherapeutic Drugs also include de-worming (antihelminthic) funds. Intravenously slowly drip medication is administered in streptococcal Crystalline Amino Acids meningococcal meningitis.