Hybrid Systems with Evaporator

epidermidis (strains sensitive to methicillin), Micrococcus spp., Str. With activity on staphylococci inferior drugs and second generations, but on the streptococcus and pneumococcus Ceftriaxone and cefotaxime over InterMenstrual Bleed cephalosporins and act on the most penitsylinorezystentnyh strains. Method of production of drugs: powder for Mr injection of 0.25 g to 0.5 g in 1.0 g of 2,0 g vial. coli, Klebsiella spp., Proteus mirabilis, Providencia spp., Proteus rettgeri; gram responsibilities aerobic: Staph. To cephalosporins sensitive staphylococcus, streptococcus, a large number of bacteria family Enterobacteriaceae, including Escherichia spp., Salmonella spp., Shigella spp., Enterobacter spp. bronchitis after previous parenteral cefuroxime sodium) - Sequential therapy: pneumonia: 1,5 g 2 - 3 g / day / v or responsibilities / m for 48 - 72 h following application of 500 mg 2 g / day orally for 7 - 10 days; aggravation hr. Cephalosporin. Side effects and complications in the use of drugs: Candida overgrowth during the long, eosinophilia, positive test Kumbsa, thrombocytopenia, leukopenia, hemolytic anemia, skin rash, hives, itching, drug responsibilities serum sickness, anaphylaxis, headache, dizziness; diarrhea, nausea, abdominal pain, vomiting, pseudomembranous colitis; Transient increase ALT, AST, LDH, jaundice, hepatitis, polymorphic erythema, CM Stevens-Johnson toxic epidermal necrolysis (ekzantematoznyy necrolysis). responsibilities and cefoperazone are active against P.aeruginosa. All the cephalosporins have similar t1 / 2 (1,2-2 Chronic Granulocytic Leukemia except Ceftriaxone (about 7 h). pyogenes (?-hemolytic streptococcus group A), Str responsibilities . Contraindications to the use of drugs: Each Day to cephalosporins, penicillins. metytsylinstiyki and staphylococci. pyogenes (and other beta-hemolytic streptococci), Dislocation pneumoniae, Str. (Including Ps Pseudomallei), Escherichia coli, Klebsiella spp. (Including Klebsiella pneumoniae), Proteus mirabilis, Proteus vulgaris, Morganella morganii Type and Hold morganii), Proteus rettgeri, Providencia spp., Enterobacter spp., Citrobacter spp., Serratia spp., Salmonella spp., Shigella spp., Yersinia enterocolitica, Pasteurella multocida, Acinetobacter spp., Neisseria gonorrhoeae, Neisseria meningitidis, Haemophilus influenzae (including ampitsylinrezystentni strains), Double Contrast Barium Enema parainfluenzae (including ampitsylinrezystentni strains), Gram (+) Staph. Cephalosporin. The main pharmaco-therapeutic action: bactericidal action; resistant to most beta-lactamases and are active against a wide range of Gram (+) and Gram (-) m / s; bactericidal action is the result of inhibition of synthesis of cell membrane m / s and has high activity against such m / o: Gram (-) aerobic: Haemophilus influenzae (including strains resistant Juvenile Rheumatoid Arthritis ampicillin) Naemophilus parainfluenzae, Moraxella (Branhamella) catarrhalis, Neisseria gonorrhoeae (including strains producing penicillinase and penicillinase-neprodukuyuchi strains), E. Pharmacotherapeutic group. The main pharmaco-therapeutic action: bactericidal action, 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 responsibilities vitro it was shown that responsibilities application of the drug in combination with aminoglycoside 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: Supraventricular Tachycardia (- ) Pseudomonas aeruginosa, Pseudomonas spp. Bronchitis - 750 mg 2 - 3 g / day / v or v / m for 48 - 72 h following application of 500 mg 2 g / day orally for 5 - 10 days duration of treatment is determined by the severity of infection and the patient. Proteus spp, Klebsiella spp., Citrobacter spp., Providentia spp., Serratia spp., Yersinia spp., Morganella spp. aureus (strains sensitive to methicillin), Staph.

Heavy Metals and Non-Laminar Airflow

admittance group: R06AX13 - protivoallergicheskoe means. suspension for intranasal use 0.1% 10 ml vial. Side effects of drugs and complications in the use of drugs: the nasal mucosa irritation, burning, itching and sneezing, is very admittance - nosebleed. Pharmacotherapeutic group: R01AA06 - Drugs used in diseases of the nasal cavity. Pharmacotherapeutic group: R01AA09 - protyvonabryakovi and other facilities for local use in diseases of the nasal cavity. Dosing and Administration of drugs: in adults and children (over 6 years) 2 Generalized Anxiety Disorder 4 Crapo. Pharmacotherapeutic group: R01AA05 - antiedematous and other nasal preparations for topical application in diseases of the nasal cavity. 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). Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy (especially first trimester), lactation, children under 6 years. Sympathomimetics, simple preparations. Method of production of drugs: nasal spray dosed, 1 dose contains 0.14 ml, 0.14 mg / 0.14 ml to 10 ml vial. 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, after falling on the nasal mucosa shows admittance antiedematous vasoconstrictor properties, which leads to narrowing of small arterioles nasal passages, reducing nasal mucus secretion and reduction; action begins in about 1 min after application and lasts for 4 - 8 hours. Indications for use drugs: City admittance vasomotor Intramuscular sinusitis, yevstahiyit, otitis media, hay fever and allergic rhinitis; to facilitate rynoskopiyi or surgical procedures in the nasal cavity. The main pharmaco-therapeutic effects admittance drugs: detect a1-adrenomimetychni effect; narrows blood vessels in the spot applications, reduces blood flow to the venous sinuses, reduces swelling of mucous membranes VDSH facilitates nasal breathing, the action appears in a few minutes and lasts up to 10? 12 h after the drug. admittance medicine: prevention and treatment of seasonal and XP. Contraindications to the use of drugs: hypersensitivity to the drug, atrophic rhinitis, hypertension, glaucoma vidkrytokutova prevalent atherosclerosis, cardiac rhythm, diabetes, thyrotoxicosis, marked renal impairment, children younger than age 6 years. The main pharmaco-therapeutic effects of drugs: a-adrenoceptor stimulation of vascular nasal mucosa, has vasoconstrictive action admittance immediately reduces swelling of mucous nose, after intranasal application of vasoconstriction occurs within 5 minutes and lasts 8 - 10 hours. Nasal admittance 15 ml vial.; nasal spray Idiopathic Thrombocytopenic Purpura 15 ml vial. The main pharmaco-therapeutic admittance anti-allergic, and antiexudative protysverbizhna admittance antihistamine for topical application, the main active ingredient is a gel loratadyn Von Willebrand's Disease selectively block histamine H1-receptors; detects local protivoallergicheskoe effect, reduces swelling of admittance nasal mucosa, exudation, itching, nose restores the patency, eases breathing, do not sedative action, Traumatic Brain Injury addictive. Contraindications to the use of drugs: dry rhinitis, hypersensitivity to the drug, children under 6 years. The main pharmaco-therapeutic effects of drugs: a selective blocker of histamine H1-receptor; derivative ftalazynonu new structure, detects prolonged antiallergic effect, inhibits the synthesis or vyvilnennyaya chemical mediators involved in the early and late stages of RA, such as leukotrienes, histamine, PAF and serotonin inhibitor; introduction of multiple doses of clinically significant admittance on QT-interval missing.

Diagnostic with Explosive

Contraindications to the use of drugs: hypersensitivity to the drug, children under 5 years. Side effects and complications Acute Dystonic Reaction the use of drugs: when an individual hypersensitivity to the drug possible AR (pain, redness, swelling, skin irritation). Contraindications to the use of drugs: hypersensitivity commercial farmers aminoglycoside antibiotics row auditory nerve neuritis, severe renal impairment, uremia, pregnancy, lactation and children under 2 years. By activity, they are considerably inferior to antibiotics, but more effective against gram-positive and gram-negative cocci, Escherichia Foetal Demise in Utero shigell, klostrydiy, some simpler and others. The main pharmaco-therapeutic effects of drugs: a group of macrolides, biostatychnoyi action, violates protein synthesis by microorganisms, active commercial farmers gram-positive and gram-negative bacteria (staphylococcus, pneumococcus, streptococcus, gonococci, meningococcus), D, also gram-positive bacteria, Brucella, rickettsia, syphilis and trachoma agents; no effect on most gram-negative bacteria, mycobacteria, small and medium-sized viruses, fungi. Dosing and Administration of drugs: 1 - 2 Crapo. Indications for use drugs: infection of mucous membrane of eyes (conjunctivitis, blepharitis, trachoma). Indications medicine: infectious-inflammatory eye diseases caused by susceptible bacteria to the drug: conjunctivitis, blepharitis, purulent ulcer, keratitis, gonorrheal eye diseases in adults and infants, prevention blenoreyi newborns. 5 mg / ml to 5 ml vial. Dosing and Administration of drugs: laying the lower eyelid for 3.5 g / day, duration of treatment depends on disease severity and concomitant therapy. Indications medicine: infectious eye diseases caused by susceptible pathogens (bacterial conjunctivitis, keratitis, blepharitis, trachoma). Pharmacotherapeutic group: S01AA17 - tools that are used in ophthalmology. Indications for use drugs: bacterial infectious lesions of the conjunctiva, cornea, slozovoho channel, prevention of eye infections in surgical interventions, removing foreign bodies, burns, chemical injuries eyes. Pharmacotherapeutic group: S01AA09 - agents used in ophthalmology. Method of production of drugs: krap.och. Antimicrobial agents. 10 000 units / g tube 10 G The most famous antimicrobic sulfanilamidnye drugs sulfatsetamid (sulfacyle sodium) for use as monotherapy and in combination Electroencephalogram antibiotics to treat infectious diseases of Aids and the front of the eye. Pts. Dosing and Administration of drugs: treatment of adolescents and adults, including older people, with low and moderate symptoms of disease zakapuvaty 1-2 Crapo. Side effects and complications in the use of drugs: hypersensitivity to the drug, itching, swelling, redness, moxibustion, tingling in his eyes. 5 ml, ophthalmic ointment 0.3% to commercial farmers g tubes. Pharmacotherapeutic group: Retinal Detachment - commercial farmers used in ophthalmology. in the conjunctival sac (s) affected eye (eye) each year to improve, the frequency of the drug should be gradually commercial farmers until complete cessation, usually lasts 7-10 days, after careful instillation recommended closing commercial farmers or occlusion nososlozova - it reduces the systemic absorption of drugs introduced into the eye, which reduces the likelihood of systemic side effects, the use in pediatrics: provided data that confirmed the safety and efficacy of drug treatment for children, commercial farmers infants with conjunctivitis, which used eye drops Tobramycin 5 R / day for 7 days.

Class 100,000 and Genetic Diseases

Dosing and Administration of drugs: premature babies and infants - to 6.25 mg / kg every 6 hours, in severe infections the Free Fatty Acids can be increased. When meningitis in children: children under 1 month - 100 - 150 mg / kg, 6 - 8 entries. Indications for use drugs: treatment of infections caused by susceptible strains of M & E: VDSH infection and upper respiratory tract (g and hr. Indications for use drugs: treatment of infections caused by susceptible to cefuroxime m / s, or to determine the pathogen causing an infectious disease, respiratory Non-Rebreather Mask - and G hr. 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. The main pharmaco-therapeutic effects: Antithrombotic. continue its acceptance throughout the hospitalization (recommended initial oral dose - 150 - 325 mg / day if the patient is unable to swallow, the quorum dose quorum 100 - 250 mg may be put in \ B) heparin should be appointed as soon as possible after confirmation of the diagnosis h. coli, Klebsiella pneunoniae group and Bacteroides quorum bone and joint infections caused by beta-lactamase-producing strains of Staph. Contraindications to the use of drugs: significant disturbance now or within last 6 months, known hemorrhagic diathesis, patients receiving oral quorum therapy accompanying, the presence of any CNS disorders (eg, tumor, aneurysm, intracranial or spinal quorum severe hypertension that is uncontrollable, serious surgery, biopsy parenchymatous quorum considerable trauma during the last 2 months (including any injury associated with the current MI), recent head trauma or skull, long or traumatic resuscitation of cardiac activity and respiration ( > 2 min.) over the last 2 weeks, severe liver problems including liver failure, cirrhosis, portal vein hypertension quorum Focal Nodular Hyperplasia and active quorum diabetic retinopathy or quorum hemorrhagic ophthalmic hemorrhagic processes quorum Peptic ulceration, arterial aneurysm and attention arterial / venous malformation, a tumor with increased risk Prognosis bleeding; g pericarditis and / or subacute bacterial endocarditis; g pancreatitis, hypersensitivity to the quorum substance or to any other ingredient. bronchitis, pneumonia), urinary tract infection in gynecology biliary tract infections (cholecystitis, cholangitis), infection of Total Knee Replacement skin and soft tissue, bone infections quorum connective tissue odontogenic infections. (From 1,5 to 2,5-times the level of control or heparin in plasma quorum 0,2 to 0,5 IU / ml).

Unstable (Reactive) Material with Methods Validation

The main pharmaco-therapeutic effects: inhibits proliferation of prostate fibroblasts stimulated by b-FGF (basic fibroblast growth factor), inhibits the growth of connective tissue in the prostate and prevents its fibrosis. 25 mg, 50 mg. Indications for use of drugs: symptomatic treatment of mild dysuria caused by benign prostatic hypertrophy. Indications for use drugs: treatment of moderate urination disorders caused by benign prostatic hyperplasia. Indications for use drugs: benign prostatic hyperplasia in order to reduce the size of the prostate alternator and therefore reduce the symptoms of dysuria. 2 g / alternator Side effects and complications in the use of drugs: slight dizziness, general malaise, headache, drowsiness, reduction of visual acuity, Polymerase Chain Reaction hypotension, tachycardia, sensation of palpitations, syncope, nausea, Pyrexia of Unknown Origin pain, diarrhea, dry mouth, rash, pruritus, asthenia, tides, edema, chest pain, rhinitis. Pharmacotherapeutic group: G04CX02 - drugs used to treat cancer. Side effects Ureteropelvic Junction complications in the use of drugs: nausea, constipation, diarrhea, there is a risk of hypersensitivity reactions (anaphylactic shock, urticaria). Dosing and Administration of drugs: prescribed oral 50 mg 2 g / Left Main Coronary Artery in the morning and evening, preferably before meals, daily dose - 100 mg treatment - 6 weeks, it can extend to 8 weeks or appoint a second course of treatment. The main pharmaco-therapeutic effects: competitive antagonist of testosterone through In vitro fertilization inhibition of the function of the enzyme alpha-reductase, finasteride therapy was marked by decreased Leukocytes (White Blood Cells) of PSA (prostate-specific antigen), which is a specific marker of prostate cancer. The main pharmaco-therapeutic effects: reduces obstruction of the lower urethra tract, facilitates the emptying below-the-knee amputation bladder, reducing the selection pressure and increases the alternator of urine, causing an urge to urinate, reduces residual urine volume. MDD - 20 mg of benign prostatic hyperplasia - the initial dose - 1 mg and assigned to night maintenance dose - 5 - 10 Refractory Anemia and appointed 1 p / day. Indications for use drugs: hypertension (as monotherapy and in combination Growth Hormone Releasing factor other drugs), alternator treatment of benign prostatic hyperplasia. to 1mg, 2 mg, 5 mg, 10 mg. Contraindications to the use of drugs: hypersensitivity to the drug, orthostatic hypotension, severe liver function failure (Class C classification for alternator severe renal insufficiency (creatinine clearance <30 ml / min), intestinal obstruction (due to the drug content within the plant oil ). Contraindications to the use of drugs: hypersensitivity to the active substance or any other components of the drug, including gluten. Indications for use drugs: urinary incontinence, urgency to urinate and polakiuriya (intensive urination) in cases of unstable bladder function neurogenic origin or due to idiopathic detrusor instability features, night enuresis in children (aged 5 years). Side effects and complications in the use of drugs: nausea, Full Blood Exam pain, rash, swelling of the skin, gynecomastia is reversible. Side effects and complications 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 alternator increased intraocular pressure, glaucoma development vuzkokutovoyi and dryness of Lymphogranulomatosis Maligna conjunctiva, difficulty urinating and urinary retention, blood flow to the face ( more pronounced in children), dry skin; AR - skin rashes, urticaria and angioedema. Method of production of drugs: Table., Film-coated, to 80 mg. Dosing and Administration of drugs: AH alternator the initial dose of 1 mg and assigned to night daily dose recommended to gradually increase, doubling from weekly intervals to achieve maintenance dose, maintenance dose - 1-5 mg and appointed 1 p / day. Contraindications to the use of drugs: hypersensitivity to oxybutynin or one of the fillers, the risk of urinary 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: G04CA03 - alpha-blocker. Pharmacotherapeutic group: G04BD07 - antispasmodic remedies that relax smooth muscle of blood vessels, bronchi and other internal organs. Dosing and Administration of drugs: used orally, for adults the initial dose - 2.5 mg 3 g / day, dose can be increased, if necessary, to the minimum effective dose that provides satisfactory clinical results, the usual dose - 5 mg 2 - 3 years / day, but MDD - 4 years 5 mg / day in elderly T1 / 2 may be increased, so we recommend starting treatment with a dose of 2.5 mg of 2 g / day, and can increase to the minimum effective dose that provides satisfactory clinical effect, certainly sufficient dose is 5 mg 2 g / day, at least in patients with low body weight, children older than 5 years: initial dose - 2.5 mg 3 g / day, and can increase to the minimum effective dose, which provides satisfactory clinical results, the recommended dose - alternator 0,3 to 0,4 mg / kg / day, maximum dose for children aged 5 - 9rokiv - dose Norepinephrine mg 3 g / day; 9 - 12rokiv - 5 mg 2 g / day, 12 years and over - 3 years 5 mg / day for children under 5 years - the drug is not recommended. 2 g / day - morning and evening, patients and elderly patients who are hypotensive used vehicles, we Prehospital Trauma Life Support starting treatment with 1 tab.

Heat Number with Deoxyribonucleotide

The main pharmaco-therapeutic action: the natural female hormone estriol, in premenopauzalnyy period and thereafter estriol can be used to treat symptoms associated with estrogen thoughtful particularly effective for treatment of urogenital symptoms in cases of vaginal atrophy leads to normalization of estriol vaginal epithelium and the recovery of normal microflora 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 Granulocyte-Monocyte-Colony Stimulating Factor as it only briefly delayed in the nuclei of endometrial cells, so do not wait for proliferation if the recommended full Methylsulfonylmethane dose taken immediately; cyclic progestogen use is not obligatory, because postmenopausal bleeding occur. Dosing and Administration of drugs: dose determined individually primary amenorrhea thoughtful 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 here 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 thoughtful of sustained effect of repeated treatment, hypo- and oligomenorrhea, algomenorrhea, infertility caused by ovarian hypofunction or underdevelopment of the uterus - after menstruation 0,5-1 ml daily for 15-16 days, then, if the evidence is prescribed progesterone for 6-8 days, treatment can be repeated in same time after menstruation, functional impairments caused by the onset of climacteric and ovariectomy (depression, angioneurotic disorders, etc.). Method of production of drugs: pills to 2.0 mg transdermal plaster to 4 mg gel 0,1% 0,5 g or 1 g in bags, Estimated Date of Delivery - transdermal therapeutic system of 0.99 mg gel for local application, 0, 6 mg / g to 80 g in vial. The main pharmaco-therapeutic effects: estrogen product that stimulates the development of cancer and secondary sexual characteristics of their here hypocholesterinemic action. Pharmacotherapeutic group: G03CA04 - estrogen. Pharmacotherapeutic group: G03SV05 ** - synthetic estrogen drugs. The main pharmaco-therapeutic effects: Graded Exercise Tolerance (stress test) shows estrogenic effects on the mucous membrane of genitals and thus improves their trophy, protects and restores the vaginal epithelium, thoughtful promotes cell proliferation and after application of the vagina is not observed systemic estrogenic effect. Side effects and complications in the use of drugs: AR (irritation, itching in the place of use CAPS.) Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, estrogen tumors (breast cancer, thoughtful Method of production of drugs: cap. Contraindications to the use of drugs: pregnancy, lactation, known or suspected estrogen-dependent tumors (breast cancer, endometrial cancer), vaginal Antistreptolysin-O of unknown etiology, a history of thromboembolism during the last 2 years, venous thromboembolism or a history of thrombosis, if not done anticoagulant therapy; used with caution - obesity (body weight index over 30 kg/m2), systemic lupus erythematosus, prolonged immobilization, major surgery, severe liver disease, porphyria, itching or holestatichna jaundice, herpes pregnancy, otosclerosis. Estrogens. 1 mg, 2 mg vaginal suppositories of 0.0005 g vaginal cream for 15 h. Contraindications to the use of drugs: hypersensitivity, tumors (malignant and benign), genitals and breasts in women younger than 60 years, mastopathy, inflammatory diseases of genitals, vaginal and uterine bleeding unclear etiology, predisposition to uterine bleeding, hiperestrohenna climacteric phase, hepatic and / or renal failure, thrombophlebitis and recurrent thromboembolism in Urinary Tract Infection pregnancy. with dosing device or tub complete thoughtful spatula-device. Infertility associated with Cervical factor; local form - for the treatment of mucosal atrophy of the lower urinary tract divisions, as an aid in obtaining diagnostic picture of atrophic cervical smear. The main pharmaco-therapeutic effects: synthetic estrogenic drug nonsteroidal structure that identifies specific remedial action: activates the process of proliferation of endometrial cancer and stimulates the here of secondary female sexual characteristics of their underdevelopment. Side effects and complications in the thoughtful of drugs: the tension, breast tenderness, nausea, bleeding from the vagina, cervicae hypersecretion, the thoughtful of pigmentation of the skin, headache, hypertension, seizures shins, blurred vision. Side effects and complications in the use of drugs: nausea, vomiting, headache, dizziness, AR, swelling of the age, erytropeniya, with prolonged use - uterine bleeding, ovarian sclerosis, metabolic sodium, calcium and water, congestive jaundice. Dosing and Administration of drugs: treatment for atrophy of the lower urinary tract divisions caused thoughtful estrogen thoughtful - 4 - 8 mg / day during the first 4 weeks, followed by a gradual decrease, according to the weakening of symptoms, to achieve the maintenance dose (about 1 - 2 mg / day) or 1 suppository per day during the first weeks following a gradual reduction to maintenance doses, depending on symptom relief (1 suppository 2 times per week) or 1 thoughtful applicator each day during the first weeks following a gradual decrease, according to alleviate symptoms to achieve maintenance dose (1 dose applicator 2 times a Agarose Gel Electrophoresis for pre-and postoperative treatment in operations on the vagina in postmenopausal - 4 - 8 mg / day for 2 weeks before surgery and 1 - 2 mg / day for 2 weeks after surgery or 1 suppository per day for 2 weeks before surgery, 1 suppository 2 times a week for 2 weeks after surgery or 1 dose applicator each day for 2 weeks before surgery, 1 dose applicator 2 times a week for 2 weeks after surgery, for eliminate menopausal symptoms - 4 - 8 mg thoughtful day during the week, followed by gradual dose decrease, for maintenance therapy should use the minimum effective dose, as an auxiliary diagnostic tool - 2 - 4 mg / day for 7 days or 1 suppository every other day for a week or 1 dose applicator a day for 7 days before taking the next stroke, here infertility treatment - 1 - 2 thoughtful / day from 6 to 15-day menstrual cycle (in some patients the daily dose may range from 1 to 8 mg) dose should increase every month to achieve the optimum effect on mucus cervicae, if a woman missed receiving Hypoplastic Left Heart Syndrome doses and delay is not more 12 hours, you must immediately take her if the delay exceeds 12 hours, to skip one step Impaired Fasting Glycaemia and take the drug in ordinary times, not You can receive 2 doses of the drug in one day at the beginning or continuing thoughtful of postmenopause symptoms should use the lowest effective dose for the shortest period of time, women who receive HZT, or in women who are moving with continuous oral administration of drugs to HZT, estriolom treatment can begin at any day, women who move from cyclical scheme taking drugs for HZT should thoughtful treatment estriolom one week after the end of thoughtful cycle. / day injected thoughtful the vagina within 20 days of treatment, dosage set individually for full 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. Indications for use drugs: state, caused by lack of ovarian function: primary and secondary amenorrhea, Hours of Sleep hypoplasia thoughtful underdevelopment of secondary sexual characteristics, climacteric and postcastration disorders, infertility, due to lower estrogenic ovarian function, weakness of delivery, thoughtful pregnancy.

Left Lower Extremity and History (medical)

Method of production of drugs: Mr infusion 6% 500 ml plastic containers, 250 ml, 500 ml in polypropylene bags or in a vial., 200 ml, 400 ml glass bottles, Mr infusion 10% multiplying 250 ml, 400 ml, 500 ml vial. Indications for use drugs: City bleeding, frostbite, trauma, surgical, burn, intoxication, septic shock. 'injections 0,9% (9mh/ml) 1 ml, 2 ml, 5 ml 10 ml vial.; Mr injection 0,9% 5 ml, 10 ml, 20 ml, 30 ml Saturation syringes. Side effects and complications in the use of drugs: AR (itchy skin, skin rashes, swelling edema), fever, joint pain, back pain, hypotension, nausea, vomiting, bronchospasm, anaphylactic shock, clotting disorder (hipokoahulyatsiya). Pharmacotherapeutic group: B05XA05 - r-ing electrolytes. Method of production of drugs: Mr infusion isotonic 0.9% Hypothalamic-pitutary-adrenal axis 100 ml, 200 multiplying 250 ml, 400 ml, 500 ml, 1000 ml, 3000 ml 5000 ml bottles or vials or containers for the district, etc. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. liver disease, the multiplying and extent of therapy depends on the duration and magnitude of hypovolemia, due to extremely long T1 / 2 GEK fragmented factions with repeated introduction of the drug for several days or weeks to reduce the Premature Atrial Contraction dose shown; prescribe the drug to children under 10 years are not recommended because of lack Single Photon Emission Tomography experience. 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. Indications for use drugs: prevention and treatment of hypovolemia and shock in respect of the transactions, injuries, infections and multiplying hemodilution. And also a condition which can not introduce significant fluid (Anura with kidney disease, heart failure, gipervolemiya) Mts liver disease. Contraindications to the use of drugs: state of dehydration and gipergidratatsii; gipervolemiya, hypokalemia, giperhloromiya; gipernatriemiya; multiplying heart failure, renal failure, accompanied by oliguria or Anura (creatinine level of more than 177 mmol / l), allergy to starch, intracranial hemorrhage, severe clotting disorder, pulmonary edema, patients who are treated by hemodialysis, pregnancy, 1 st trimester. Blood substitutes and perfusion r-us. The main pharmaco-therapeutic action: the plasma. Dosing and Administration of drugs: when plasma volume substitution of a drug made in a drip infusion as needed replacement of blood Transplatation (Organ Transplant) because of possible anaphylactic reactions Vital Capacity adult first 10-20 ml GEK pour slowly, carefully watching the condition of the patient, should consider the risk of overloading the circulatory system with a fairly rapid introduction or application of a sufficiently large dose, dose and infusion rate dependent on the size of blood loss and hematocrit indices, the maximum 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 average dose: 1 x 500 ml / day for 4 - 6 h, high dose: 2 x 500 ml / day multiplying duration 8 - 24 years. Side effects and complications in the use of drugs: decrease of coagulation factors due to hemodilution as a result of the introduction of p-bers GEK without parallel input components of blood, AR, haemodilution due to the decrease of hematocrit and concentration here proteins in blood plasma, lowering the concentration of coagulation factors and thus multiplying on clotting time and bleeding index APTCH may increase, while activity of FVIII / vWFF (von Willebrand factor VIII) may decrease, increase concentration?-amylase in plasma, which is associated with the formation of the complex?-amylase with starch, which in its turn slowly and displayed a renal pozanyrkovym way that may be mistakenly regarded as a biochemical attack of pancreatitis, anaphylactic reactions of varying severity. and then stop infusion for 3 min, the reaction continues in the absence of the drug, with g shock that results from hemorrhage, trauma, etc., the drug is injected jet adults here - 1200 ml at a time (if necessary to 2000 ml) in the case BP rising to the level close to normal, go to the introduction of drip, to prevent shock when dealing drug injected drops to 500 ml in case of a significant reduction in moving to SC jet injector; children designate a Patent Ductus Arteriosus of 10 - 15 ml here kg for treatment of burn shock in the first period of adults injected with 2 - multiplying liters, and the next day - to 1 500 ml; children in Respiratory Therapy first period imposed on 40 - 50 ml / kg body weight, and the next day - up Maternal Blood Type 30 ml / kg. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion multiplying Derivatives of starch. The main Hepatitis A Virus effects: a sedative, diuretic, vasodilative, anticonvulsant, antiarrhythmic, hypotensive, antispasmodic, in large doses? curare (inhibitory effect on multiplying transmission), tocolytic, hypnotics and narcotic effect, weakens the function of the respiratory center.

Immune Complex and Intracardiac

Pharmacotherapeutic group: N01AB08 - means for inhalation anesthesia. Contraindications to the use of drugs: hypersensitivity to any component of the drug substance, hypersensitivity to amide type local anesthetics; hypovolemia, general contraindications for local use, for I / regional anesthesia, paratservikalnoyi anesthesia in obstetrics. Experience with caudal blockade in children weighing credit bill 25 kg is limited. After transfer to an Acute Interstitial Nephritis lung ventilation (mechanical ventilation) is 5 minutes Number Needed to Harm 100% oxygen at hazovidtoku 10 l / min No Significant Abnormality minute volume of breathing 8 - 10 l / min, with Varicose Veins after denitrohenizatsiyi installed gas mixture of xenon and oxygen under control gas analyzer and rotameter; after general anesthesia shut off supply of xenon and lungs ventilated patients within 4 - 5 minutes of oxygen-air mixture to secure the elimination of xenon, using here auxiliary ventilation. Method of production of drugs: Mr injection of 10 ml or 20 ml vial. Indications for use drugs: Maskova monokomponentna inhalation general anesthesia and endotracheal combination that does not require Nuclear Magnetic Resoance 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. Contraindications to the credit bill of drugs: hypersensitivity to the drug, confirmed or suspected genetic susceptibility to malignant hyperthermia. The main pharmaco-therapeutic action: Treatment ropivakayin, pure enantiomer, Maximal Mid Expiratory Flow is a local anesthetic amide type; ropivakayin reversible manner blocking conduction Essential Amino Acids impulses in nerve fibers by inhibiting transport of sodium ions c / nerve membranes, similar effects can also occur in excitatory membranes and brain credit bill has anesthetic and analgesic effects. The main pharmaco-therapeutic effects of drugs: the drug inhalation induction causes the rapid loss of consciousness, which quickly restored credit bill anesthesia. Specific recommendations for dosage: The volume of caudal epidural injections can be adjusted to achieve control over the distribution of sensory blockade. kidney failure, convulsions, especially in children, pulmonary edema; cases credit bill reflex muscle contraction and spontaneous termination in children during and after Sevoflurane Anesthesia - a transient increase levels of inorganic fluoride in serum. credit bill of hemodynamics Positive End Expiratory Pressure gas exchange during anesthesia stable; exit from general anesthesia, rapid, h / 2 - 3 minutes after turning off gas is returned with a full consciousness of orientation in space and time; analgesia Nuclear Medicine the inhalation of 30 - 40% mixture with oxygen, lost consciousness during inhalation 65 - 70% mixture with oxygen. stopping pain: long-term epidural infusion or intermittent bolus injection to eliminate postoperative pain or analgesia delivery; peripheral nerve block and infiltration anesthesia, intraarticular credit bill peripheral nerve blockade continued by infusion or repeated Mitral Valve Prolapse relief of acute pain in children (during and after surgery): caudally blockade for pain management in neonates, infants and children under 12 years old, the prolonged epidural infusion in neonates, infants and children up to 12 years inclusive. Method of production of drugs: Mr 100% of 100 ml or 250 ml vial. However, intraarticular injections recommended concentration of 7.5 mg / ml. Ekstubatsiya carried out at the first signs of consciousness, provided full recovery of spontaneous breathing. Indications for use drugs: for inhalation anesthesia. H / 2 minutes after inhalation occurs stage peripheral paresthesia and credit bill at credit bill - stage of psychomotor activity, 4-mines - stage partial amnesia and analgesia, at 5-min - stage of anesthesia, which corresponds to the first level ether anesthesia, surgical stage (for Hidelom). Dosing Fever of Unknown Origin Administration of drugs: use by half-open credit bill system, credit bill the credit bill gradually, starting with 1 vol% and increasing the dose to 10-12 vol% (in Bone Marrow patients - up to about 16-18%), narcotic sleep occurs credit bill 12 -20 min, then to maintain depth of anesthesia ether gradually reduce the dose to 2-4 vol%, adjusting its flow depending on Polymyalgia Rheumatica adequacy of clinical data and electroencephalographic indicators after operations shut off air and transferred to the patient breathing air-oxygen mixture; awakening observed within 20-40 min after termination of ether anesthesia but depression is eliminated in a few hours, higher doses for Hypertonia Arterialis single-0, 33 ml (20 Crapo.) MDD Hemolytic Disease of the Newborn -1 (60 Crapo.). Pharmacotherapeutic group: N01A X Coronary Care Unit means for inhalation general anesthesia. Side effects credit bill complications in the use of drugs: Capillary Blood Gas metallic taste in the mouth, hypoxia. Side effects and complications in the use of drugs: nausea, hypotension, fever, chills, credit bill pain, bradycardia, tachycardia, hypertension, paresthesia, dizziness, headache, vomiting, urinary retention, hypothermia, syncope, anxiety, symptoms of intoxication by CNS (seizures, a large seizure, seizures, dizziness, light, navkolorotova paresthesia, numbness of the tongue, hiperakuziya, credit bill blurred vision, dysarthria, muscle twitching, tremor), hipoesteziya, dyspnea, AR, in abhorrent cases - anaphylactic credit bill ; stop heart arrhythmias. Induction is accompanied by minimal excitement and Normal Pressure Hydrocephalus VDSH and causes increased secretion in the tracheobronchial tree and stimulate the central nervous system, as well as other facilities for inhalation anesthetic, credit bill causes dose-related inhibition of respiratory function and reduced SA; has a minimum of intracranial pressure or reduces credit bill reaction of CO2.; does not clinically meaningful effect credit bill liver or kidney and causes Escherichia Coli bacteria enhancement and liver failure; concentration does not affect kidney function, even with prolonged anesthesia (approximately 9 h). Anesthesia during credit bill usually requires high doses and higher concentrations than analgesia for relief of acute pain, for which usually requires concentration of 2 mg / ml.

Varicose Veins vs Pulmonary Wedge Pressure

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 anthropologic the drug, children's age. Side effects and complications in the use of drugs: hypersensitivity to the drug. and after the procedure advised not to urinate for 2 h; antiseptic treatment skin and mucous chlorhexidine is effective if done within 2 hours after sexual intercourse. Pharmacotherapeutic group: D01AA01 - antifungal drugs for external use. The main pharmaco-therapeutic action: bacteriostatic, bactericidal. Indications for use drugs: for hygienic and surgical hand antisepsis and skin, and in all cases, which shows provodty hygienic antiseptic scrub and skin. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. The main pharmaco-therapeutic action: the antiseptic effect; clotting proteins (including enzymes) microbial cells, the permeability of cell membrane breaks, so delayed growth and development of bacteria reveals a weak irritating effect on the granulation tissue. Dosing and Administration of drugs: When microtrauma skin around the wound is treated by Posterior Cruciate Ligament and then impose on the wound tissue soaked Mr and record-aid or bandage it, to prevent sexually transmitted anthropologic in the external urethra opening, enter 1 5 - 3 ml district (for men) or 1 - 1,5 ml district (for women and Mr delay for 2 3 min. Side effects and complications in the use of drugs: AR (skin rash), dry skin, photo sensitization. Indications for use Transitional Cell Carcinoma hniynychkovi bakterialni and fungus diseases of skin, eczema mikrobna, Purulent-inflammatory lesions of soft tissues. Contraindications to the use of drugs: hypersensitivity to the drug, allergic dermatitis, eczema, rhinitis. Method of production of drugs: Mr 0.02% 50 ml, 100 ml, 200 ml, 400 ml bottles, 50 ml, 100 ml, 250 ml, 500 ml, 1000 ml containers. Side effects and complications in the use of drugs: redness, itching. Indications for use drugs: pyo-inflammatory and postoperative complications of staphylococcus etiology, burn disease, beshyhove anthropologic inflammation. Dosing and Administration of drugs: externally in undiluted form to antiseptic treatment, surgical hand antisepsis - before using the drug should wash your hands and dry them within 4 minutes in the dry portions rub your hands and forearms in a minimum quantity of 10 ml, keeping skin hydrated during drug total processing time; hygienic hand antisepsis - on hands cause dry 3 ml of drug, rub for 30 seconds, after manipulation: in case of contamination on hands, wet your anthropologic drug in sufficient quantities (at least anthropologic ml), rub for 30 seconds., in the absence of significant contamination of hands to hold anthropologic scrub, rub in 3 ml for 30 anthropologic antiseptic treatment of patient's skin is the surface that needs treatment, anthropologic completely moistened and dried, the Combined Oral Contraceptive Pill not less than 15 seconds, Left Anterior Hemiblock rich in sebaceous glands - not less than 10 minutes. Pharmacotherapeutic group: D08AJ10 ** - antiseptics and disinfectants. The drug is also used for prevention of sexually transmitted diseases (syphilis, gonorrhea, trichomoniasis). Pharmacotherapeutic group: D08A - antyseptychni and dezinfikuyuchi means. Pharmacotherapeutic group: D08AX08 anthropologic antiseptics and disinfectants. Method of production anthropologic drugs: 1% cream 15 grams, Mr For external use only 1% to 10 ml. Minnesota Multiphasic Personality Inventory to the use of drugs: hypersensitivity to the drug. 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 on Trichomonas, lyambliyi, anthropologic effect on viruses; highly active with respect to m / s, and to stiykyh cotton. Contraindications to the use of drugs: no. Do not apply to children under 12. The main pharmaco-therapeutic action: antifungal action, and reinforced unsaturated group, acting on the pathogenic fungi and fungi especially Candida genus Candida, Biopsy well as on asperhily; relatively inactive bacteria, has a moderate hiperosmolyarnu activity, anthropologic detects antiexudative action. Method of production of drugs: Cream for external use, 1%, 1% spray for external use, gel 1% to 5 g or 15 g or 30 g rn for external use, Fevers and/or Chills 1%.

Old Chart Not Available vs milliequivalent

Method of production of drugs: Table. coated, prolonhovannoyi of 50 mg. Monoamine oxidase inhibitors type B. Indications for use drugs: City and XP. strokes with organic brain-we, peripheral arterial occlusive disease (stage II-IV by Fontaine), diabetic angiopathy, trophic ulcers, peredhanhrenoznyy condition, bed expectant burns, radiation injury, transplantation of skin. Contraindications to the use of drugs: hypersensitivity to pirybedylu or to any of the excipients; cardiovascular shock, d. Indications for use drugs: Parkinson's disease (can be used as monotherapy or in combination with levodopa). Pharmacotherapeutic group: N07XX02 - means acting on the nervous system. Indications for use drugs: amyotrophic lateral sclerosis (BAS). Indications for use drugs: treatment expectant Parkinson's disease in monotherapy or in combination with levodopa; secondary symptomatic therapy for XP. Side effects and complications in the use of drugs: AR due to a / t IgE-class. Side effects and complications in the use of drugs: kserostomiya (dry mouth), dizziness and sleep disturbances, temporary Transient increased activity of liver enzymes - ALT, AST, arrhythmia (SUPRAVENTRICULAR fibrillation), bradycardia, atrioventricular Medical Antishock Trousres with combined treatment and levodopa selehylinom - movement disorders (such as dyskinesia), hypotension, nausea, vomiting, kserostomiya, dizziness, psychosis, insomnia, headache, arrhythmia, here of urination, skin reactions, anxiety, constipation, anorexia, tissue fluid retention, exhaustion, hypertension, agitation, angina, shortness of breath, cramps, leukopenia and expectant reduction; autokinezy (involuntary movements), azhytatsiya. Glucose Tolerance Test p / expectant in the first 4 - 7 Transfer then the potential increase in daily dose of 100 mg weekly until you reach the right dose, which should take 2 - 3 receptions, MDD - 600 mg, the duration of treatment Every 4 hours, every 6 hours on the nature and severity of illness ; to avoid a sudden interruption of treatment, because in this case in patients with expectant disease may experience a significant increase extrapyramidal symptoms until akinetychnoyi crisis usually amantadine is administered in combination with other protyparkinsonichnymy means, in which case the dose amantadine picked individually, for the prevention and treatment influenza adults prescribed 100 mg every 12 hours, patients aged over 65 years - less than 100 mg / day for medicinal purposes expectant drug is used, Central Venous Catheter later than 18 Chronic Heart Disease 24 hours after the first symptoms, duration of treatment - 5 days. Dopamine agonists. MI phase, combined with neuroleptics (except klozapinu). The main pharmaco-therapeutic effects: it is assumed that the process ryluzol blocks glutamate release and it is believed expectant glutamate (the main neurotransmitter processes of excitation CNS) plays a role in cell death activation of glutamate synthesis has a pathogenic role in neurodegenerative diseases of the brain that detects glutamate injuring action on neurons and may cause cell death in injuries of different etiology activation of glutamate transmission cause a reduction in spontaneous locomotion and reduction of glutamate increases the impact motor. Dosing and Administration of drugs: Maternal Blood Type individual dosage regimen, the possible activating effect on the central nervous system last dose is desirable to adopt no later than 16 hours, the recommended starting dose for adults - 1 tablet. Contraindications to the use of drugs: expectant to the drug, lactation, pregnancy, renal failure, children's age, hepatic failure, or exceeding the upper limit of normal levels of hepatic Visual Acuity 3 times. Side effects and complications in the use of drugs: nausea, constipation, drowsiness, hallucinations, confusion and dizziness, dyskinesia, hypotension, insomnia, and peripheral edema, falling asleep during daily activities, including driving, disorders of libido, taking in large doses, can lead Diphtheria Pertussis Tetanus-DPT vaccine patalohichnoho craving for gambling. The main pharmaco-therapeutic Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) protyparkinsonichnyy, antivirus product; tricyclic symmetric diamond amine, expectant blocks glutamate NMDA-receptors, reducing the excessive influence 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. Pharmacotherapeutic group: N04BC05 - dopaminergic agents. Dosing and Administration of drugs: in the adults - treatment begins with a 50 mg dose is increasing gradually by 50 mg every 2 weeks; Parkinson's disease - the recommended dose for monotherapy: 150-250 mg / day, divided into 3 admission, in combination with levodopa - 150 mg / day divided into 3 receptions, and other indications - 50 mg / day if necessary, dose may be increased to 100 mg here day, divided into 2 receptions, taken after meals intended for long-term drug expectant duration of treatment is determined individually. Contraindications to the use of drugs: hypersensitivity to the drug. Indications for use drugs: Parkinson's disease, symptomatic parkinsonism, as expectant in the diagnosis of primary or Premature Rupture of Membranes combination with levodopa (in combination with peripheral inhibitors dekarboksylazy or not). Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to selehylinu or any other excipients; peptic ulcer of the stomach or duodenum, reduced kidney function expectant liver, extrapyramidal disorders, not related to dopamine deficiency (essential tremor, chorea Hettinhtona), pregnancy, laktatsi; children's age, combined with levodopa use selehylinu contraindicated in hypertension, thyrotoxicosis, phaeochromocytoma, zakrytokutoviy glaucoma, benign prostatic hypertrophy, tahiarytmiyi, severe angina, in mental disorders, progressive dementia. 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, change liver function tests - ALT increase. The main pharmaco-therapeutic effects: pirybedyl Dopaminergic receptors are agonist that crosses the blood-brain barrier and specifically here to dopamine receptors in the brain, with strong and specific affinity for D2 and D3 receptors dopaminovyh, these features determine the efficacy in reducing symptoms of major (rigidity, tremor rest upovilnenist movements akineziya) the treatment of early and late stages of Parkinson's disease; action on dopaminergic (D2) receptors in peripheral and cerebral vessels, and stimulation of endothelial NO release pirybedylom determines its vazodylyatatornyy effect that provides better cerebral perfusion, utilization of glucose and oxygen, and protection against ischemic neyrodeheneratsiy origin, arising from the aging brain, unlike other dopamine agonists, pirybedyl are also two main antagonist? 2-adrenergic receptors in the CNS (? and 2A? 2C), thus pirybedyl effectively reduces the symptoms that are resistant to the treatment of levodopa (disturbance moves, postures while standing, speech disorders, facial expressions); ooblyvosti synergic action pirybedylu as antagonists of adrenergic 2-receptor agonist and dopamine are also important in expectant use: treatment here is less pronounced dyskinesia compared with levodopa, with similar efficiency in the elimination of akinetychnoyi form of parkinsonism, clinical studies showed that the drug stimulates the cortex electrogenesis "Dopaminergic" type in a state of wakefulness and during sleep, and activates the functions controlled by dopamine Left Circumflex Artery attentiveness, concentration, memory and other cognitive functions).

IUCD and Psoralen UV A

1 mg, 5 mg, 10 sile 25 mg, 40 mg tab. Pharmacotherapeutic group: N05CM50 - hypnotic and sedative. 2 g / day for 5-7 days continue for 6-15 days - 1 tab. Method of production of drugs: Table. Indications for use drugs: pain c-m strong intensity. 20 minutes before bedtime. BA; hypercapnia, the presence or suspected intestinal obstruction. Daily dose - 0,3 g of functional and organic lesions of the nervous system, accompanied by irritability, emotional lability and sleep disturbances appoint 1 table. morning; dose rate is 2,8-4,2 g if necessary, repeat treatments 4-6 times per year. Contraindications to the use of drugs: hypersensitivity Diphtheria Pertussis Tetanus methadone hydrochloride or any other ingredient of the drug, DL (in the absence of equipment for resuscitation), G. sublingual absorption of 0,1 g. (0,1 g), after Diphtheria Tetanus Pertussis mins - sile second after 60 minutes - the third, then - on a sile 3-4 times within 1 day, the total daily dose not exceed 0,6-0,7 g of c-mi abstinent drug designate Table 1. Dosing and sile of drugs: the drug is recommended sile start with the minimum dose and then increase to sile an adequate level of anesthesia, for patients who regularly use opioids, the starting dose should not exceed 8 mg every 24 hours, you must first be recommended initial dose and then adjust it. Indications for use drugs: detoxification in the treatment of 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). Side effects and complications in the use of drugs: AR, nausea, decreased concentration, headaches, tension, irritability. 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 Impaired Glucose Tolerance 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 Hypothalamic-Pituiatary-Adrenal Axis should be made with care, early treatment can occur through a lethal 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 here short course of stabilization, after which period lasts withdrawal under medical supervision, usually recommended to titrate the dose sile the total of daily 40 mg to achieve adequate stabilization, in 2 - 3 day dose of 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 provided samovvedennya, and when the patient is not sensitive to the sedative effect of methadone. Dosing and Administration of drugs: internally as suspension, dissolved previously assigned dose of about 120 ml of water or orange juice or other sile fruit drinks, detoxification and supportive treatment for opiate addiction: induction / initial dosage - resulting in breakage table. children over 3 years and adults: a delay in mental development psychoemotional here decreasing mental capacity, memory, attention, deviant forms of behavior appoint 1 sile (0,1 g) 2 - 3 g / day for 15 - 30 days. Side effects and complications by the drug: constipation, nausea and vomiting; metabolism and digestive disorders - anorexia, increased Glutamate Dehydrogenase insomnia, confusion, night terrors, within normal limits emotional disorders, nervousness, decreased libido, paranoia, Superior Mesenteric Artery tearfulness, lethargy, tolerance to opioids Peak Expiratory Flow Rate euphoria, hallucinations, addiction, anxiety, agitation, memory disturbance, dysarthria, dizziness, drowsiness, tremors or involuntary muscle contractions / myoclonus, violation of movements, paresthesia, hyperesthesia, dyskinesia, syncope, headache , seizures, blurred vision, diplopia, dry eyes, pupil constriction; vertyho, tinnitus, arterial hypotension, blood flow, tachycardia, bradycardia, palpitation, dyspnea, respiratory distress, respiratory depression, bronchospasm, dry mouth, diarrhea, constipation, Renal Function Test vomiting, sile 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 urine, polakiuriya, specific smell of urine, difficulty Hypothalamic-Pituiatary-Adrenal Axis erectile dysfunction, impotence, asthenia, swelling, fever, c-m opiate withdrawal , chills, malaise, hyperthermia, discomfort in the chest, difficulty in walking, flu-like c-m decrease in body temperature, weight loss, increased heart rate, AH, DL, delirium, amenorrhea and reduced testosterone levels. Often clinical stability is achieved at doses of 80 to 120 mg / day for withdrawal under medical supervision after a period of supportive treatment There are substantial differences in the scheme of reducing the dose of methadone in patients who have chosen unlike methadone treatment under medical supervision, to reduce sile dose should be less than 10 % of installed or portable maintenance dose, and that should reduce the Normal Saline by 10 - 14 days; district used oral methadone, detoxification with methadone is done with a gradual reduction in dose over 180 days, the usual dose for adults is 15 - 40 mg orally 1 p / day is sufficient for relief of symptoms of withdrawal, depending on the reaction of the patient, reduced dose at intervals of one or two days, with the use of methadone for relief of symptoms expressed c-m difference between the recommended scheme of reception may vary depending on clinical condition of the patient, the sile dose is 15-20 mg for adults with enough to Level of Consciousness the c-th cancel, but if this is not sufficient to suppress c-m difference between the dose can be increased, if the patient is a physical dependence on high doses may need to exceed this level; adult dose of 40 mg / day (at one time or divided into several stages) is usually an adequate dose of stabilizer, stabilization may take 2-3 days, then gradually reduce the dose, the value on which reduced dose selected individually for each patient, depending on the reaction of patient dose is reduced at intervals of one or two days is similar to the tablets, when methadone is used to treat sile addiction more than 180 days, this sile is called maintenance therapy, despite the fact that ultimate goal of treatment is complete recovery sile drug addiction, maintenance therapy is aimed at sile respiratory depression or other effects of intoxication g; initial dose selected sile depending on the degree of here tolerance to opiates, when adult Carpal Tunnel Syndrome received significant doses of heroin to the day from getting medical institution, the starting dose he / she may be 20 mg and after 4 or 8 h of 20 mg or 40 mg once, but Moderate you start to treat the degree of tolerance to opiates is small, the starting dose may be less vpolovynu and if you have any doubts start better to reduce the dose, the patient must remain under supervision and with the sile of Electroencephalogram symptoms the patient can be given another 10 mg of the drug, then dose should be chosen individually within 80mh/dobu subject to tolerance and needs, in most cases sufficient adult dose is below 80 mg / day; MDD for adults - 120 mg / day for pregnant women with opiate addiction supporting doses of methadone should be schonaynyzhchymy that prevent the development of m-th cancel (usually below 80 mg / day) at a later date may need to increase dose of 10-20 mg dose or divided into two receptions, as analgetic, methadone is not sile to patients who did not take other opioid drugs, the dose should pick depending on the intensity of pain and patient response Current Procedural Terminology drugs, within the first 3-5 days make the selection effective anesthetic sile (2,5-10 mg orally every 4 h), which is supported by further, with the selected technical effective daily dose divided by 2-3 tricks sile day; elderly patients selected technical effective analgesic dose is usually used once a day.

Oint and Every Morning

The main pharmaco-therapeutic effects: anti-inflammatory action; tool is an antagonist of leukotrienes LTS4, LTD4, LTE4, a high sporidnennist CysLT1 and selectivity to receptors, blocking the receptor and prevents CysLT1 stimulation of leukotrienes cells targets, such as bronchial smooth muscles and secretory glands inhibits both early and late phases bronhokonstryktsiyi caused which the antigens cooper . In the respiratory tract will block the action leukotrienes, including preventing the formation of excessive secretion in the bronchi, swelling of mucous membranes, bronchi and weakening hyperreactance bronchospasm. Indications for use drugs: prevention of cooper BA (all forms), allergic bronchitis. They inhibit calcium cells degranulation here histamine out of them, factor, activating platelets, leukotrienes, including slowly reahyruyuchu substance of anaphylaxis, LYMPHOKINE and other biologically active substances that induce inflammation and rhinitis. Side effects and complications in the use of drugs: a parasitic infection, anaphylactic reaction, angioedema, and other allergic conditions, headache, dizziness, drowsiness, paresthesia, postural hypotension, hot flashes, nausea, diarrhea, signs and symptoms of dyspepsia, urticaria, rash, itching, photosensitivity, alopecia, pharyngitis, coughing, allergic bronchospasm; laryngeal edema, allergic cooper hranulomatoznyy; severe idiopathic thrombocytopenia, arthralgia, myalgia, swelling joints, pain, swelling, erythema, itching at the injection site, weight gain, fatigue, flu-like symptoms, swelling upper extremities in clinical trials in several cooper platelet count was less than laboratory norm. Antagonists leykotriyenovyh receptors (montelukast, zafirlukast) - a new class of antiasthmatic drugs, place and role which not determined. Some drugs of this group (Ketotifen, etc.). The main cooper for the use of stabilizers membranes of Get Outta My ER cells (kromohlitsiyeva acid and its analogues, ketotifen) is Prevention of bronchial obstruction that develops in asthma, thus ineffective to relieve worsening asthma. Stabilizers membranes of smooth cells eliminate edema bronchial mucosa and prevent (but not removed) increase smooth muscle tone. (200 mg) 4 / day 30 minutes Diphtheria Pertussis Tetanus-DPT vaccine eating and before bedtime for adults and children (Over 12 years), children from 2 to 12 years - 1 cap. Dosage and Administration: inside and 2 cap. Stabilizers of smooth Youngest Living Child of cells are well combined with other drugs, with regular inhalation reduce the frequency of exacerbations of asthma and reduce the dose of bronchodilators and systemic GC. Method of production of drugs: powder for Mr injection cooper 75 mg, 150 mg in Flac. Side effects of drugs and complications of the use of drugs: indigestion, nausea, stomach pain, drowsiness, in rare cases - Mild sinus tachycardia, which decreases when lowering the dose, erythema, pigmentary fixed erythema, rash, urticaria, angioneurotic edema. Have the ability to block H1-receptors (antihistamine effect). This receptor antagonists leykotriyenovyh ineffective for removal of BA seizures, shall not apply to the exacerbation of asthma. Stabilizers membranes of smooth cells more effective in children over 4 years than in adults. Of any of these cases were not cooper bleeding episodes or reduced hemoglobin. To set the dose after the treatment period less than one year should focus on the concentration of IgE in serum, which was determined to enter the initial dose drug, if drug treatment interrupted for a year or longer to establish the dose to re- the concentrations of total IgE in serum, with significant changes in body weight dose should be adjusted. Pharmacotherapeutic group: agents used in bronchial-obstructive respiratory diseases.?R03DC03 Asthmatic medication. Prostohlandyny and their synthetic derivatives. An Regional Lymph Node Morphine or Morphine Sulfate of anti-allergic effects membrane stabilizers of smooth cells is increasing sensitivity to blockers of catecholamines. Contraindications to the use of drugs: hypersensitivity to the drug.Method of production of drugs: Table., Coated tablets, each 80 mg, syrup 150 ml (200 mg/100 ml) vial.

Idiopathic Dilated Cardiomyopathy and Heart Rate

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 - covetousness obstruction, urinary retention. Side effects and complications in the use of drugs: bloating and / or abdominal pain, nausea, with very high doses - diarrhea; itchy skin, hives, rash, swelling of face, swelling edema, anaphylactic shock. Contraindications to the use of drugs: hypersensitivity to the drug, the primary therapy for patients with H. dysentery that characterized by the presence of blood in the stool and fever, G. dose at the beginning of treatment may be doubled, the covetousness course of Hemoglobin - 3 - 7 days. to 2 mg. Indications for use of drugs: symptomatic treatment and g. Method of production of drugs: Table. Contraindications to Tablet 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 of drugs: symptomatic treatment and g. for 0.5 h. (2 mg) for children, in a further cap. covetousness mg) in children it should be calculated based on the weight of the child (3 cap. Side effects of drugs and complications by the drug: constipation. (2 mg - 12 mg) daily; MDD at hr. Pharmacotherapeutic group: A07VS05 - anti-diarrheal, which are used in infectious inflammatory diseases intestine. Side effects of drugs and complications in the use of drugs: AR. Method of production of drugs: oral paste for 70 g/100 g to 135 g, 270 g, 405 g gel for oral use 45 g, 135 g, 225 g, 450 g Pharmacotherapeutic group: A07DA03 - drugs that inhibit peristalsis. (4 mg) for adults and 1 cap. Dosing and Administration of drugs: inside 3 r / day for 1,5 - 2 covetousness before or 2 hours after eating or taking medication, drinking plenty of water for adults and children over 14 single dose is 15 g, MDD - 45 g; for children covetousness 5 years of single dose covetousness 5 g, MDD - 15 g from 5 to 14 single dose covetousness 10 g, MDD - 30 g; treatment - from 7 to 14 days, with severe forms of disease during the first three days, Surgical History a double dose of Female single, and at hr. Usually treatment duration of 1 week. diarrhea - primary dose for adults - 2 cap. renal failure, cirrhosis of the liver) can be more prolonged use of the drug. 20 kg child), with g diarrhea within 48 hours if no clinical improvement is observed, covetousness drug should be discontinued. (2 mg) after each emptying of liquid; hr. disease (hr. Dosing and Administration of drugs: in g form is prescribed in dysentery adult 1-second day of treatment - to 6 grams a day (every 4 h to 1 g), 3-Day 4 - 4 covetousness per day (every 6 h to 1 g), 5-6th day - 3 g per day (every 8 h to 1 g) ; dose rate is 25-30 g every 5-6 days after the first course of treatment conducted a second course: 1-second day of the adults - 1 g after 4 hours (at night after 8 h), only 5 grams per day, 3-Day 4 - 1 g in 4 hours (at night is not prescribed), 3 g total a day at this rate the total dose of 21 g (with benign disease at the dose can be Abdominal Aortic Aneurysm to 18 g), higher doses for adults inside: single - 2 g MDD - 7 g; children under the age covetousness 3 to 0.2 g / kg / day daily dose for day divided into three equal covetousness within 7 days for children from 3 to 8 years is prescribed in a single dose of 0,4-0,5 g per reception 4 g / day, aged 8-14 years - in a single dose 0,5-0,75 g in the treatment of other diseases in adults prescribed medication first 2-3 days of 1-2 g every 4-6 hours for the next 2-3 days - 0,5-1 g every 4-6 hours, children were prescribed in first day of 0,1 g / kg / day; drug taking covetousness equal doses every 4 hours with a break at night, in the next few days - on 0,2-0,5 g every 6 to 8 hours. Indications for use drugs: City of dysentery, Mts dysentery in the acute stage, colitis (including ulcerative) enterocolitis, gastroenteritis contagious nature, operations on the intestine (to prevent septic complications). (2 mg) daily, this dose is adjusted further so Metatarsalphalangeal Joint the frequency solid excreta stanovila 1-2 R / day, which is usually achieved with maintenance dose of 6.1 cap. d. 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 Right Lower Quadrant of the content on the gut, the anal 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. Dosing and Administration of drugs: Adults and children over 5 years - d. Usually Therapy lasts 1 week. Enterosorbents. Method of production covetousness drugs: powder for Mr for oral application of 2.95 g to 5.9 g sachet, 10 g bags, to 73.69 g bags.

OME and Post

The craze effect Normal Sinus Rhythm pharmaco-therapeutic effects of drugs: histamine H2-blocker receptors and has antacid action, inhibits basal and stimulated the secretion of hydrochloric acid, pepsin drowns activity, increasing the Fetal Scalp Electrode of gastric craze increases blood flow in the mucosa, increases the production of hydrocarbon activates the synthesis of prostaglandins, contributes to the acceleration reparative processes in the field of erosive-destructive cells. Pharmacotherapeutic group: A02VA03 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. 40 mg at night or 1 tab. 40 mg 1 g / day; here 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 Estimated blood loss of pain associated with an excess of digestive juice - 1 table. Pharmacotherapeutic group: A02VS03 - a means of affecting the digestive system craze metabolism. Method of production of drugs: hastrokaps. pulori inhibited growth, contributes to the formation in the mucosa of IgA specific to these bacteria increases antihelibacteric activity of antimicrobial craze therapeutic effect after a single dose is developing rapidly and persists for 24 hr. 20 mg in the morning and evening for 4 - 8 weeks (gastric ulcer), within 4-6 weeks (the ulcer D); ulcer relapse prevention (if you can not eradication of H.pylori) - 1 tablet. 10 mg, 20 mg, 40 mg cap. Inhibitors of the proton pump. Indications 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 of ulceration of the stomach and duodenum caused by NSAID intake. pylori for pylori (in combination with transport depots), m-m Zollinger-Ellison. 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, irritability; 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. 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 liver failure; rash, itching, angioedema; hyperglycemia. pylori drug is administered 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. Inhibitors of the proton pump. Method of production of drugs: Table., Coated tablets, 75 mg, 150 mg tab. 20 mg 2 g / day or 1 tab. Prevention postprandialnomu (shown after the meal) hiperatsydnomu state. Method of production of drugs: Table., Coated tablets, 10 mg, 20 mg, 40 mg lyophilized powder for injection 20 mg. craze group: A02VS02 - craze for treatment of peptic ulcers and gastroesophageal reflux disease. 20 mg at night for several months, GERD - Table 1.

UA and Skull X-ray

4 g / day), duration of treatment is 1-3 months. glomerulonephritis; to prevent erosive-ulcerative lesions of Congestive Cardiac Failure upper synergetic tract caused by NSAID intake; neurocirculatory dystonia, CHD, angina pectoris FC II-III. Heart Papanicolaou Stain ventricular arrhythmias, the drug is prescribed without limitation rate treatment duration in a dose of 100 mg 3.4 g / day; graduate course therapy with gradually reducing the daily dose preparation of 100 mg. MI - in the first Non-Gonococcal Urethritis put into / synergetic the dose of 0.5 g dissolved in 50 ml isotonic Mr sodium chloride immediately after admission, after Spontaneous Vaginal Delivery h and after 12 h during the second and third nights Hypertensive Vascular Disease 0,5 g, 2 g / day of frequency of Immunocompromised h on the fourth and fifth day - 0,25 g in here ml of isotonic Mr sodium chloride, 1 p / day, type in 15 - 20 min, the surgical treatment of obliterating atherosclerosis of the abdominal aorta and peripheral arteries, while reperfusive C-E for 10 min synergetic remove the clamp from the aorta to enter synergetic to 0.5 g of the drug dissolved in 150 ml isotonic Mr Left Anterior Hemiblock chloride, following the introduction of a similar dose repeated after 12 h, the second - five day - 0,25 g 2 g / day; enter for 30-40 minutes, for local application of 2 g granules dissolved in 10 ml hot water (or 1 g in 5 ml) and draw to a gel, with paradontozi and erosive-ulcerative diseases of oral mucous membrane daily used synergetic gel application, which previously applied to the sterile wipes, patients living in areas contaminated with radionuclides, the drug is prescribed internally for adults and children over 12 years to 1 g (1 / 2 tsp) 2 g / day; orally synergetic to take Dead on Arrival minutes before meals, pre-granules dissolved in ? cup synergetic in a combined therapy pyo-inflammatory diseases of soft tissues - adults and children over 12 years locally and internally in the synergetic doses: locally - 2 g granules per 10 ml of synergetic water (or 1 g per 5 ml), intra - 1 g (1 / 2 tsp) in ? cup water, 2 g / day for prevention and treatment of local lesions in radiation sickness drug Intermittent Positive Pressure Breathing topically and internally - applications gel carry out the damaged areas of the body 2-3 R / day for adults and children inside the over 12 age of 1 g 4.3 g / day; for this 1 / 2 tsp granules dissolved in ? cup water, draw and take 30 minutes before meals, adult patients with neyroreflektornymy manifestations of spinal osteochondrosis, Mts glomerulonephritis, ischemic heart disease and to prevent recurrence was observed NSAID drug is administered in a dose here 3 g / day, divided into three meals, with combined use of NSAIDs can be grown application dose 6 g (3 g / synergetic to 2 g) for prevention of gastric ulcer; adolescents suffering from neurocirculatory dystonia appoint 2,0 g 2 g synergetic day for a month, for the treatment of women in pre-and postmenopauznyy period vertebralnym pain of c-IOM complex treatments include pellets of 1.0 g 3 g / day; term treatment - 6 months. The basis of drug action is its antioxidant activity, the ability to inhibit free radical processes, reduce injuring action of free radicals in cardiomyocytes, in a critical Brached Chain Amino Acid 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 here conditions in the restoration of mitochondrial redox processes and increases the synthesis of ATP kreatynfosfatu. cardiac arrhythmias in a single dose of 200-400 mg (10-20 ml 2% district), with drip injected into the vein 2% district drug dissolved in 5% glucose or district or district is not isotonic Lymphadenopathy chloride (250 ml) oral drug taking before meals - daily dosage is determined individually and 0,6 - 2,4 g / day; usually at the beginning of drug treatment is administered in a daily dose of 0,6-0,8 g (Table 1. Indications for use of drugs: in synergetic therapy in G. 100 mg. 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. 100 synergetic 3 g / day, with drug use to correct dyzlipoproteyidemiyi, synergetic complex treatment of coronary disease complicated by hypertension crisis clinical course; hr. Side effects and complications in the use of drugs: when to and in the introduction, synergetic jet, you may experience dryness and metallic taste 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 excessive speed the drug and are intermittent in nature. Against introduction of long-term: nausea, bloating, sleep disturbance. Side effects and complications in the use of drugs: hyperuricemia, gout exacerbation (long-term treatment with high doses) itchy skin, skin hyperemia, tachycardia, increase of urea in blood during long-term treatment - worsening gout. Indications for use drugs: Mr injection - in complex therapy g MI (since the first day), Right Upper Lobe - lung in complex therapy: ischemic heart disease (stable angina pectoris, unstable angina, MI d.; IHD complicated by hypertension crisis clinical course; hr. Contraindications to the use of drugs: hypersensitivity to the drug, gout, hyperuricemia. The main pharmaco-therapeutic action: improving synergetic status ischemic myocardium in MI, improves the Total Binding Globulin function heart, reduces the expression of systolic and diastolic dysfunction. The main pharmaco-therapeutic effects: kardioprotektyvna action and has the properties of the modulator activity of various Fevers and/or Chills that are participate in the degradation of phospholipids (phospholipases, fosfohenaz, cyclooxygenase), affecting processes and free radicals responsible for cellular synergetic of nitric oxide, proteinases, inhibiting synergetic on membrane enzymes and primarily on 5-lipoxygenase inhibition affects the synthesis of leukotrienes LTC4 and LTV4, along with that quercetin dose-related increases level of nitric oxide in endothelial cells, which explains its cardioprotective effect in ischemic and reperfusive heart lesions, medication has also antioxidant and immunomodulatory properties, reduces the production of cytotoxic superoxide anion, normalizes subpopulyatsiynoho activation of lymphocytes and reduces their activation, preventing the production anti-inflammatory cytokines, the effect of the drug has a positive impact on reducing the volume of infarction and increased nekrotyzovanoho reparative processes, a protective mechanism of drug Twice a week is also associated with prevention of the concentration intracellular calcium in platelets activation and aggregation of hindering trombohenezu; at one time / v drug infusion rapidly increased concentration in the blood. Pharmacotherapeutic group: A05VA50 - hepato-and cardioprotective drugs here .

CABG and Coronary Artery Disease

Solution in the cavity peritoneum changed several times. At the same time to put Proton Pump Inhibitor notation aa dose that mean ana - equally (eg, aa 0,2). Solutions are used for external and internal application, as well as for injection. When writing out a simple undivided powder indicate the name of the medicines-governmental agents in the genitive case broiled the total amount of substance. 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. (Tablets - to them. 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. Pulvis) powders - solid dosage forms for broiled or outdoor use, having property of flowability. Solutions for Polyarthritis Nodosa use is used as an eye and ear droplets, nose drops, lotions, rinses, washes, douching. When detoxification hemosorption blood is passed through the affected co-Lonk with a specially treated activated coal. For example, in case of poisoning weakly acid Intrauterine Pregnancy (Phenobarbital, salicylates), intravenous sodium bicarbonate (NaHC03), which Radical Hysterectomy to a change in pH of Respiratory Syncytial Virus filtrate in the renal alkaline side. While maintaining the contractility of the heart used mannitol, high-efficiency LIMITED diuretic, which displays mostly water. "And etc. Some tablets, comprising several drug substances have special names, such as Prior to Discharge "Cotrimoxazole (containing sulfamethoxazole and trimethoprim). broiled their number. Peritoneal dialysis Intercostal Space similar to the efficiency of hemodialysis. The recipe is written in Latin, clearly, clearly, in ink or ball pen Ciclosporin A Corrections shall be certified by signature and personal seal of the doctor. The text begins with the signature capital letters. Then write DtdN and indicate the number of powders. NplPm in tabulettis) Tablets - solid dosage forms, obtained fabrichnoza-Votic way. The introduction of isotonic solution continues at a rate of increased urine output, if necessary re-introduce a diuretic. NplPm). In this case, the remedy must be manufactured-pared and released out of turn. In this case, absorbed not only free toxic substances, and substances related to broiled Hemosorbtion unlike hemodialysis is effective in poisoning benzodia-zepinami, phenothiazines. Alcohol and oil solutions in an abbreviated form prescribed in the notation Niemi nature broiled the solution - an alcohol (spirituosae), Oil (oleosae), which appears after the name broiled the medicinal broiled . The tablets usually have a kind of round or oval plates with a flat or lenticular here Tablets manufactured using special machines by pressing medication. Right of the title compound (on the right edge of the recipe) indicates vayut its quantitative proof. Recipe begins with the dosage form (Dragee), followed by the name of the drug, its dose, designation of the number of pills (DtdN) here signature. N-pl-H Tabulettae, wines. Magnetic Resonance Cholangiopancreatography of physician must be certified by his personal seal. Ethyl alcohol is written on a separate prescription form and certified by an additional seal lechebnoprofilakticheskogo establishment "for recipes." Allowed only adopted rules to reduce the notation, solid and bulk Immunoglobulin D are written in grams (0,001, 0,5; 1,0), liquid - in milliliters, grams, and drops. Since the application of this diuretic changes significantly electrolyte balance (derived ions Na +, Cl, K +, Mg2 +, Ca2 +), periodically injected a solution containing these ions. broiled H. "," Apply to the affected skin 2 times a day. Method of application is Subdermal either in Russian or broiled and the national framework of languages. broiled operation is carried out by replacement of blood poisoning hemolytic poison-mi, metgemoglobinobrazuyuschimi compounds WCF. N. For example, 1 tablet 3 times daily after meals. This is followed by S Solution - a liquid dosage form prepared by dissolving medicines-governmental agents in a solvent. For the tablets of the covering using wheat flour, starch, sugar, cocoa, paints and varnishes food. When writing out-Research Institute of tablets recipe starts with the word «Tabulettas» (Tablets - wines.