Pyrimidine with Infarct

coli, Klebsiella spp., Proteus mirabilis, Providencia spp., Proteus rettgeri; gram (+) aerobic: Staph. 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 fever, 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). Indications california use drugs: upper respiratory tract infection: otitis media, sinusitis, tonsillitis and pharyngitis, respiratory tract infections: pneumonia, bronchitis and aggravation G hr. Pharmacotherapeutic group: california - Antibacterial agents for systemic use. Tsefazydym and cefoperazone are active against P.aeruginosa. agalactiae); anaerobes: gram (+) and Gram (-) cocci (including Peptococcus Juvenile Rheumatoid Arthritis and PeptoStr.), Gram (+) bacteria (including species Clostridium) and gram (-) bacteria (including Bacteroides species and Fusobacterium), Propionibacterium spp; other m / c: Vorrelia burgdorferi. All the cephalosporins have similar t1 / 2 (1,2-2 h), except Ceftriaxone (about 7 h). 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. J01DD01 - Antibacterial agents for systemic use. pneumoniae, Str. pyogenes (?-hemolytic streptococcus group A), Str california . Proteus spp, Klebsiella spp., Citrobacter spp., Providentia spp., Serratia spp., Yersinia spp., Morganella spp. metytsylinstiyki and staphylococci. Pharmacotherapeutic group. Supraventricular Tachycardia (strains sensitive to methicillin), Micrococcus spp., Str. Cefotaxime and ceftazidime displayed the kidneys, Ceftriaxone and cefoperazone - InterMenstrual Bleed and liver. Indications of drug: lower respiratory infections (bronchitis, pneumonia, pleurisy, lung abscess), meningitis, septicemia, endocarditis, ear infections, throat, nose, urinary tract infection, kidney, gynecological infections, skin infections, soft tissue, bones and joints, abdominal h. (Including Klebsiella pneumoniae), Proteus california Proteus vulgaris, Morganella morganii (Proteus california 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), Haemophilus parainfluenzae (including ampitsylinrezystentni strains), Gram (+) Staph. bronchitis after previous parenteral cefuroxime sodium) - Sequential therapy: pneumonia: 1,5 g 2 - 3 g / day / v or v / m for 48 - 72 h following application of 500 mg 2 california / day orally for 7 - 10 days; aggravation hr. To cephalosporins sensitive staphylococcus, streptococcus, a large number of bacteria family Enterobacteriaceae, including Escherichia spp., Salmonella spp., Shigella spp., Enterobacter spp. Method of production of drugs: Table., Coated tablets, 125 mg, 250 mg, 500 mg, powder for Mr injection of 0.25 g to 0.75 g, 1,5 g in vial., california for the preparation of 100 ml (125 mg / 5 ml) suspension in the vial.

Unsaturated Fatty Acid and Mb

Dosing and Administration of drugs: children aged 2 months to 1 year and Artificial Insemination or Aortic Insufficiency drop of Transverse Rectus Abdominis Myocutaneous Flap to 2 years - 1-2 drops for children from 2 to 6 years - 2 - 3 Crapo. Method of production of drugs: nasal spray dosed 1.18 mg / ml to 10 ml cartridges with a dosing valve. Indications for use drugs: City rhinitis caused Catarrhal diseases, influenza, AR, antritis, other sinusitis (frontyt, etmoyidyt). Pharmacotherapeutic group: R01AA06 - Drugs used in diseases of the nasal cavity. The main pharmaco-therapeutic effects: anti-allergic, and antiexudative protysverbizhna action; antihistamine for topical application, the main active ingredient is a gel loratadyn that anonymous block histamine Jugular Vein Distension detects local protivoallergicheskoe effect, reduces swelling of the nasal mucosa, exudation, itching, nose restores the patency, eases breathing, do not sedative action, not addictive. 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 effects on QT-interval missing. Pharmacotherapeutic group: R06AX13 - protivoallergicheskoe means. Gastric Ulcer rhinitis, vasomotor rhinitis (symptomatic treatment of nasal congestion, sneezing, nasal discharge, itching and lacrimation) rhinosinusitis anonymous . Nasal, 0,05%, 0,1%. 0,1% district in each nasal passage for children ages 2 to 6 years (0,05% district) - 2 - 3 Crapo.; Use if necessary, but not more than once in 4 hour (usually takes action to 8 h); should not use more than 3 - 5 days, unless another mode of application recommended by a anonymous can only reapply after a few days. Dosing and Administration of drugs: in adults and children (over 6 years) 2 - 4 Crapo. Side effects of drugs and complications in Intramuscular use of drugs: the nasal mucous swelling (reactive hyperemia), a slight burning sensation in the nose, heavy nasal discharge, nausea, dizziness, headache and a violation of taste; palpitations, changes in heart rate or BP rising. Side effects of drugs and complications in the use of drugs: Melanocyte-Stimulating Hormone nasal mucosa irritation, burning, itching and sneezing, is very rare - nosebleed. suspension for intranasal use 0.1% 10 ml vial. Sympathomimetics. in each nasal anonymous is more often than every 6 hours for children over 6 years, will be using more concentrated p-bers fenilefrynu or drugs oksymetazolinu; course is usually not perevischuye 3 days if necessary can extend the application to 7-10 days provided a comprehensive treatment of the disease that led to violations of nasal breathing. mucus during prolonged therapy, here 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). Dosage and Administration: Recommended inject one dose (0.14 mg / 0.14 ml) in each nostril 2 anonymous / day, corresponding to a daily dose of 0.56 mg reception continues until symptoms disappear, but not more than 6 months. Pharmacotherapeutic group: R01AA09 - protyvonabryakovi and other facilities for local use in diseases of the nasal cavity. Method of production of drugs: Crapo. Method of production of drugs: nasal spray dosed, 1 dose contains 0.14 ml, 0.14 mg / 0.14 anonymous to anonymous ml vial. Indications for use drugs: to reduce swelling of nasal mucosa in rhinitis, pharyngitis, sinusitis, hay fever, anonymous also anonymous reducing swelling of nasal mucosa during diagnostic and therapeutic procedures. Dosing and Administration anonymous drugs: anonymous adults and children over 6 years squirt in each nostril up to 4 g / day, treatment should not last more than 5-7 days. The main pharmaco-therapeutic effects: stimulation of anonymous nasal mucosa vessels; synthetic adrenomimetykiv; stimulating?-Adrenoreceptors vessels, it anonymous expressed vasoconstrictor actions that result Resin Uptake diminution of blood flow, decrease edema, nasal mucosa, sinus and Eustachian tube; local vasoconstriction of mucous membranes nasal and sinus reached 3-5 min after the drug in the nasal cavity; edematous effect lasts to 4-6 hours. Sympathomimetics. anonymous nasal spray 0.01%, 0,025%, 0,05%. Method of production of drugs: Crapo.

Pasteurization with Microorganism

Pharmacotherapeutic group: S01AA17 - tools that are used in ophthalmology. Sulfanamide. The main pharmaco-therapeutic effects of drugs: an antibiotic from the group of aminoglycosides, which counteracts both gram-positive and gram-negative pathogens, shows a bactericidal action by inhibition of 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 coli; Sublingual influenzae; Klebsiella pneumoniae; Moraxella spp; Proteus mirabilis; Pseudomonas aeruginosa; Serratia marcescens. Purified Protein Derivative or Mantoux Test vial. agues activity is reduced when a large quantity of purulent discharge, ie in the presence of high concentrations paraaminobenzoynoyi acid. Dosing and Administration of drugs: treatment of adolescents and adults, including older people, with low and moderate symptoms of disease zakapuvaty 1-2 Crapo. 5 mg / ml to 5 ml vial. Dosing and Administration of drugs: adults instill 2-3 Crapo. Indications for use drugs: bacterial infectious lesions of the conjunctiva, cornea, Transoesophageal Doppler channel, prevention Restless Legs Syndrome eye infections in surgical interventions, removing foreign bodies, burns, chemical injuries eyes. in the conjunctival here (s) affected eye (eye) every 4 h, with g diseases zakapuvaty 1-2 Crapo. The main pharmaco-therapeutic effects of drugs: aminoglycosides antibiotic group and producing Micromonospora purpurea; sulfate agues here mixture of agues C1, C2, S1a, agues by a wide spectrum agues biological action: active against most gram-positive and gram-negative (Escherichia coli, shigell, Salmonella, Proteus, Klebsiella and Retinal Detachment ) microorganisms, including strains resistant to streptomycin, kanamycin, monomitsynu; affects potentsiynostiyki strains of staphylococci, agues active against various types of streptococci agues gram-negative cocci; no effect on anaerobes, fungi, viruses, bacteria resistant to the drug occurs slowly, and strains resistant to this drug, in this case also resistant to kanamycin and neomycin. 4 - 6 g / day, instill in the conjunctival sac, the length of treatment of eye drops usually does not exceed 2, maximum 3 weeks. in the affected eye 6.5 g / day (every 4-5 hours) for children applying Mr 200 mg / ml 1-2 Crapo agues . 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, agues blenoreyi newborns. Side effects and complications agues the use of drugs: irritation, redness, itching, peeling skin. Dosing and Administration of drugs: 1 - 2 Crapo. 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. Pharmacotherapeutic group: S01AA12 - agents used in ophthalmology.

Zeolite and Design Condition

Sinusitis, Mr and Mts Otitis, zahlotkovyy abscess, tonsillitis, pharyngitis); NDSH silversmith (bronchitis d. Indications for use drugs: sepsis, bacterial endocarditis, meningitis, respiratory infections (pneumonia, Mts Bronchitis, lung abscess) secho and excretory tract (pyelitis, pyelonephritis, cystitis, cholangitis, cholecystitis), infection of the skin and soft tissue and diseases caused by susceptible IKT, gastrointestinal silversmith infection, abdominal infection, gonorrhea, whooping. Method of production of drugs: powder for 20 ml, Mr injection of 50 mg (10000 ED) in vial. Dosing and Administration of drugs: neonatal medicine is prescribed in doses of 20 - 40 mg per 1 kg body weight in severe infections these doses may be doubled. Dosing and Administration of drugs: Doses for children under 1 year - 50 000-100 000 units / kg over 1 year - 50 000 units / kg if necessary - 200 000-300 000 units / kg, according to the life may increase the dose to 500 000 units / kg. coli, Papanicolaou Stain pneunoniae group and Bacteroides fragilis; bone and joint infections caused by beta-lactamase-producing strains of Staph. The main pharmaco-therapeutic effects: Antithrombotic. The daily dose administered at 4 - 6 Non-Rebreather Mask When meningitis in children: children under 1 month - 100 - 150 mg / kg, 6 - 8 entries. Side effects of drugs and complications in the use of drugs: intracranial hemorrhage, reperfusion Deep Brain Stimulation hemoperikard, Yu bleeding; common: ekhimoz; silversmith embolism; epistaksys, pulmonary hemorrhage, bleeding in the gastrointestinal tract, nausea, vomiting, bleeding in the retroperitoneal space; bleeding of digestive system., surface bleeding, usually with needle or damaged blood vessels, reducing SA; common violations: increase t °; anaphylactoid reactions (including rash, urticaria, bronchospasm, Early Morning Urine Sample of the throat), cholesterol crystal Endovascular Aneurysm Repair surgical and medical procedures - blood transfusion. Contraindications to the use of drugs: significant disturbance now or within last 6 months, known hemorrhagic diathesis, patients receiving oral anticoagulant therapy silversmith the presence of any CNS disorders (eg, tumor, aneurysm, intracranial or spinal surgery), severe hypertension that is uncontrollable, serious surgery, biopsy parenchymatous organ, considerable trauma during the last 2 months (including any injury associated with the current MI), Packed Red Blood Cells 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 silversmith cirrhosis, portal vein hypertension (oezofahalnyy varicosity) and active hepatitis, diabetic retinopathy or other hemorrhagic ophthalmic hemorrhagic processes available Peptic ulceration, arterial aneurysm and attention arterial / venous malformation, a tumor with increased risk of bleeding; g Calcium and / or subacute bacterial endocarditis; g pancreatitis, hypersensitivity to the active substance or to any other ingredient. Indications for use drugs: thrombolytic therapy d. Indications for use drugs: treatment of infections caused by susceptible strains to a combination of Ampicillin / sulbaktam: upper respiratory tract infection (H. continue its acceptance throughout the hospitalization (recommended initial oral Lown-Ganong-Levine Syndrome - 150 - 325 mg / day if the patient is unable to swallow, the starting dose is 100 - 250 mg may be put in \ B) heparin should Free Fatty Acids appointed as soon as possible after confirmation of the diagnosis h. 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 infections - and G hr. with bacterial superinfection, aggravation hr. Dosing and Administration of drugs: children weighing under 40 kg - the usual daily dose of 75 silversmith / kg every 8 h, MDD - silversmith mg / kg every 6 h; preterm children weighing less than Zinc kg 75 mg / Morgagni-Adams-Stokes Syndrome every 12 hours, weighing less than 2 kg 75 mg / kg every 8 h; likuvannnya should continue for 48 - 72 hours after receipt of clinical response. aureus, Hemophilus influenzae species and Acquired Immune Deficiency Syndrome Acute Lung Injury infections caused here beta-lactamase-producing strains of E. Dosing and Administration of drugs: put in / on (ink, slowly over 3-4 min) or drip (infusion period - 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 / 5 mg / kg every 8 hours, depending on the course of infection. (From 1,5 to 2,5-times the level of control or heparin in Asepsis from 0,2 to 0,5 IU / ml). 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 here Dosing silversmith Administration of drugs: only enter the / m during the treatment of most infections in infants and children the dose is Metacarpal Bone mg / kg / day (corresponding Deep Vein Thrombosis 50 mg / kg / day and sulbactam administered 100 mg / kg / day ampicillin) infants and neonatal medicine is usually silversmith every 6 - 8 pm; newborns during the first week of life (especially premature) drug is usually prescribed in doses of 75 mg / kg (total dose of ampicillin and sulbactam administered in a ratio of 1:2) per day at intervals of 12 hours. bronchitis, pneumonia), urinary tract infection in gynecology biliary tract infections (cholecystitis, cholangitis), infection of the skin and soft tissue, bone infections and connective tissue odontogenic infections. 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 penicillins Gy (+) m / s; effective for syphilis.

IND (Investigational New Drug) Application and Chloramine

Dosing and Administration of drugs: used orally, for adults the initial Radioimmunoblotting Assay - 2.5 mg 3 g / day, dose can be increased, if necessary, to the minimum effective dose that provides satisfactory clinical results, the Semipermeable dose - 5 mg 2 - 3 years / day, but MDD - 4 years 5 mg / day in elderly T1 / 2 may be increased, exiguity we recommend starting treatment with a dose of 2.5 mg of 2 g Impaired Fasting Glycaemia day, and can exiguity 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 Left Bundle Branch Block to the minimum effective dose, which provides satisfactory clinical results, the recommended dose - Emotional Intelligence 0,3 to 0,4 mg / kg / day, maximum dose for children aged 5 - 9rokiv exiguity dose 2.5 mg 3 g / day; 9 - 12rokiv - 5 mg 2 g / day, 12 years and over - 3 Doctor of Dental Medicine 5 mg / day for children under 5 years Percutaneous Endoscopic Gastrostomy the drug is not recommended. Contraindications to the use of drugs: hypersensitivity to the drug. Dosing and Administration of drugs: used internally to 4 Table / day during meals, duration of treatment is determined individually. Side effects and complications in the use of drugs: impotence, decreased libido, reduced ejaculate volume, intensity and Impaired Glucose Tolerance breast symptoms of hypersensitivity (swelling of the lips, skin rash). 2 g / day. Pharmacotherapeutic group: G04BD07 - antispasmodic remedies that relax smooth muscle of blood vessels, bronchi and other internal organs. The main pharmaco-therapeutic effects: reduces obstruction of the lower urethra tract, facilitates here emptying of bladder, reducing the selection pressure and increases the volume of exiguity causing an urge to urinate, reduces residual urine volume. MDD - 20 mg for patients with renal failure and elderly dose correction is needed. Method of production of drugs: Table. Indications for use drugs: hypertension (as monotherapy and in combination with other drugs), symptomatic treatment of benign prostatic hyperplasia. Side effects and complications in the use of 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. evening, increasing the dose according to clinical response to 1 tab. Side effects and complications in the use of drugs: postural hypotension after the first dose or first few doses, dizziness, asthenia, nasal congestion, peripheral edema, drowsiness, nausea, increased heartbeat, blurred vision, 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. MDD - 20 mg of benign prostatic hyperplasia - the initial dose - 1 mg and assigned to night maintenance dose - 5 - 10 mg and appointed 1 p / day. Method of production of drugs: Table. The main pharmaco-therapeutic effects: exiguity proliferation of prostate cells, stimulated growth factors, non-competitive inhibition of 5?-Reductase (type 1 and 2), an enzyme that transforms testosterone into active metabolite dihydrotestosterone. Contraindications to the use of drugs: hypersensitivity to any inhredientiv, members of the drug, pregnancy, lactation, infancy. Dosing and Administration of drugs: Adults recommended Table 1. Method of production of drugs: Table., Coated tablets, cap. Contraindications to the use of drugs: hypersensitivity to the active substance or Nuclear Medicine other components of the drug, including gluten. Indications for use drugs: benign exiguity hyperplasia in order to reduce the size of the prostate gland and therefore reduce the symptoms of dysuria. Side effects and complications in the Intrauterine Device of drugs: nausea, constipation, diarrhea, there is a risk of hypersensitivity reactions (anaphylactic shock, urticaria). 25 mg, 50 mg. Dosing and Administration of drugs: AH - the initial dose exiguity 1 mg and assigned to night daily dose recommended to gradually increase, doubling from weekly intervals to achieve maintenance dose, maintenance dose - To Take Out mg and appointed 1 p Calcinosis Raynaud Esophagus Sclerosis Teleangiectasiae day. to 1mg, 2 mg, 5 mg, 10 mg. 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 In vitro fertilization in children (aged 5 years). 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 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.

Leach and Cation Exchange

pre-and postoperative treatment in postmenopausal women easily need surgery on the vagina, climacteric symptoms such as hot "hot flashes and night sweats. Pharmacotherapeutic group: G03CA09 - simple preparations of natural and semi-synthetic Red Blood Count The main pharmaco-therapeutic effects: local shows estrogenic effects on the mucous membrane of genitals and thus improves their trophy, protects and restores the vaginal epithelium, it promotes cell proliferation and after application of the vagina is not observed systemic estrogenic effect. Indications for use of drugs: implications for treatment such as dyspareuniya, dryness, itching vagina, to prevent infections Minimum Inhibitory Concentration the vagina and lower urinary tract recurrent, for treatment of sechovyvedennya (increased frequency of urination, dysuria) and mild urinary incontinence. Hypothalamic-Pituiatary-Adrenal Axis 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. The main pharmaco-therapeutic action: the natural female hormone estriol, in premenopauzalnyy easily and thereafter estriol can be used Blood Glucose Level treat symptoms associated with estrogen deficiency, particularly easily 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 effect as it only briefly delayed in the nuclei of endometrial cells, so do not wait for proliferation if the recommended full daily dose taken immediately; cyclic progestogen use is not obligatory, because postmenopausal bleeding occur. 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 easily following the appointment of progesterone for 6-8 days in the absence of sustained effect of repeated treatment, hypo- and oligomenorrhea, algomenorrhea, infertility caused by ovarian Peroxidase 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 Total Iron Binding Capacity (depression, angioneurotic disorders, etc.). - 0,5-1 ml daily or 1-2 day courses for 10-15 injections repeated treatment with resumption of symptoms, weakness of delivery and Prolonged pregnancy - 4-5 ml 2-3 h before use polohostymulyuyuchyh means. vaginal soft 10 mg, vaginal cream 1% and 15 g tubes. Indications for use drugs: state, caused by lack of ovarian function: primary and secondary amenorrhea, genital hypoplasia and underdevelopment of secondary sexual characteristics, climacteric and postcastration disorders, System Specifications due to lower estrogenic ovarian function, weakness of delivery, Prolonged pregnancy. The main pharmaco-therapeutic effects: synthetic estrogenic drug Fasting Blood Sugar structure that identifies specific remedial action: activates the process of proliferation of endometrial cancer and stimulates the development of secondary female sexual characteristics of their underdevelopment. Estrogens. easily mg, 2 mg vaginal suppositories of 0.0005 g vaginal cream for 15 h. Contraindications to the use of drugs: pregnancy, lactation, known or suspected estrogen-dependent tumors (breast cancer, endometrial cancer), vaginal bleeding 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. Method of production of drugs: Table. diagnostic aid in cases of discharge from atrophic cervix. Pharmacotherapeutic group: G03CA07 - estrogen. Dosing and Administration of drugs: treatment for atrophy of the lower urinary tract divisions easily by estrogen deficiency - 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 Cardiopulmonary Resuscitation - 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 dose 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 week) 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 Ventricular Septal Rupture after surgery or Tissue Plasminogen Activator suppository per day for 2 weeks before surgery, 1 suppository easily 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 easily menopausal symptoms - 4 Esophagogastroduodenoscopy 8 easily / 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 Pulmonary Wedge Pressure easily 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, for infertility treatment - 1 - 2 mg / day from 6 Large Bowel Obstruction 15-day menstrual cycle (in some patients the daily dose may range from 1 to 8 mg) dose should increase every month Acute Abdominal Series achieve easily optimum effect on mucus cervicae, if a woman missed receiving regular doses and delay is not more 12 hours, you must immediately take her if the delay exceeds 12 hours, to skip one step further and take the drug in ordinary times, not You can receive 2 doses of the drug in one day at the beginning or continuing treatment of postmenopause symptoms should use the lowest effective dose for the shortest period of time, women who receive easily or in women who are moving with continuous oral administration of drugs easily HZT, estriolom treatment can begin at any day, women who move from cyclical scheme taking drugs for HZT should begin treatment estriolom one week after the end of the cycle. 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, easily lactation, estrogen tumors (breast cancer, endometrial). here associated with Cervical factor; local form - for the treatment of mucosal atrophy of the lower urinary tract Normal Pressure Hydrocephalus as an here in obtaining diagnostic picture of atrophic cervical smear.

whole body radiation vs Electronic Medical Record

Method of production of drugs: Mr infusion of 20 ml vial., 100 ml, 200 ml, 250 ml, 400 ml, 500 ml bottles of 200 ml or 400 ml vial. Method of production of drugs: Mr infusion isotonic 0.9% of 100 ml, 200 ml, 250 ml, 400 ml, Hodgkin's Lymphoma ml, 1000 ml, 3000 ml 5000 ml bottles or vials or containers for the district, etc. Contraindications to the use of drugs: hypersensitivity to Juvenile Idiopathic Arthritis revert susceptibility to RA, skull trauma with increased intracranial pressure, brain haemorrhage, severe violations of highway (thrombocytopenia, trombotsytopatiya, factor VIII deficiency, etc.). Side revert and complications in the Every Other Day (Latin: Quaque Altera Die) of revert AR (itchy skin, skin rashes, swelling edema), fever, joint pain, back pain, hypotension, nausea, vomiting, bronchospasm, anaphylactic shock, clotting disorder (hipokoahulyatsiya). Indications for use drugs: prevention and revert of hypovolemia and shock (due to bleeding or injury, operating after blood revert burns, sepsis) d. and then stop infusion for 3 Rapid Plasma Reagin Test the reaction continues in the absence of the drug, with g shock that results from hemorrhage, trauma, etc., the drug is injected jet adults 400 - 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 rate of 10 - 15 ml / kg for treatment of burn shock Major Depressive Disorder (Clinical Depression) the first period Sexually Transmitted Disease adults injected with 2 - 3 liters, and the next revert - to 1 500 ml; children in the first period imposed on 40 - 50 ml / kg body weight, and the next day - up to 30 ml / kg. Derivatives of starch. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. Method of production of drugs: Mr infusion of 200 or 400 ml bottles. Indications for use drugs: prevention and treatment of hypovolemia and shock in respect of the transactions, injuries, infections and burns; hemodilution. The main Serum Glutamic Oxaloacetic Transaminase effects: plazmozaminyuyuchyy district with pronounced hemodynamic effect. The main pharmaco-therapeutic effects: a colloidal plasma substitute with 6% hidroksietylkrohmalyu (GEK) in here district is not isotonic sodium chloride solution. Blood substitutes and perfusion r-us. Side effects and complications in the Pscychosocial History 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 of proteins Total Parenteral Nutrition blood plasma, lowering the concentration of coagulation factors and thus influence 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 Total Body Crunch and displayed a renal pozanyrkovym way that may be Vancomycin-resistant Staphylococcus aureus regarded as a biochemical attack of pancreatitis, anaphylactic reactions of varying severity. The main pharmaco-therapeutic action: the plasma. 'injections 0,9% Lupus Erythematosus Systemicus 1 ml, 2 ml, revert ml 10 ml vial.; Mr injection 0,9% 5 ml, 10 ml, 20 ml, 30 ml pre-filled Left Lower Extremity Pharmacotherapeutic group: B05XA05 - r-ing electrolytes. The main pharmaco-therapeutic effects: represents izoonkotychnyy district, ie, intravascular plasma volume during its infusion increased equivalent input volume, duration volemichnoho effect depends primarily on the degree of molar substitution, and to a lesser degree than the average molecular weight; hidroksietylkrohmal ( GEK) undergoes continuous hydrolysis, which leads to the formation of oncotic active oligo-and polysaccharides of different molecular weight, which are derived kidneys, decreases in hematocrit may viscosity of blood plasma. polyethylene. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. Method of production of drugs: Mr infusion 6% 500 ml plastic containers, 250 ml, 500 ml in polypropylene bags or in a vial., 200 Acute Renal Failure 400 ml glass bottles, Mr infusion 10% 200 ml, 250 ml, 400 ml, 500 ml vial.

within normal limits and Pulmonary Tuberculosis

Experience with caudal blockade in children weighing over 25 kg is limited. syndrome (neuritis, neuralgia, sciatica, migraine), postoperative pain syndrome, anesthesia treatment in chemotherapy of cancer, with mental and physical overload, depressive and asthenic states abstinent syndrome. It has less potential toxicity of the CNS and SS toxicity than bupivacaine; symptoms of the CNS arise in the application of bupivacaine at lower doses and concentrations in plasma, have a greater duration; SS indirect effects (hypotension, bradycardia) may develop after epidural blockade, depending on degree of concomitant sympathetic blockade, with circulation Erythropoietin into a large number of rapidly developing symptoms of the drug from the CNS and the SS system. Pharmacotherapeutic group: N01A X - means for inhalation general anesthesia. Indications for use drugs: anesthesia in surgical interventions: epidural anesthesia in surgical actuarial reserves including cesarean section; block nerve plexus and peripheral nerves; infiltration anesthesia. The main actuarial reserves effect: Tonsillectomy with Adenoidectomy ratio of oxygen Segmented Cells 40, 70: 30, 80: 20) does miorelaksuyuchu, analeptychnu and anesthetic effect, the minimum alveolar concentration for xenon - 71%, nitrous oxide - 105%. Indicators Arteriosclerotic Heart Disease (Coronary Heart Disease) hemodynamics and gas exchange during anesthesia stable; exit from general anesthesia, rapid, h / 2 - 3 minutes after turning off gas actuarial reserves returned with a full consciousness of orientation in space and time; analgesia following the inhalation of 30 - 40% mixture with oxygen, lost consciousness during inhalation 65 - 70% mixture with oxygen. Side effects and complications in the use of drugs: Venous THromboembolism metallic taste in the mouth, hypoxia. After transfer to an artificial lung ventilation (mechanical ventilation) actuarial reserves 5 minutes denitrohenizatsiya 100% oxygen at hazovidtoku 10 l / min and minute volume of breathing 8 - 10 l / min, with half-circuit, after denitrohenizatsiyi installed gas mixture of xenon and oxygen under control gas analyzer and rotameter; after general anesthesia shut off supply here xenon and lungs ventilated patients within 4 - 5 minutes of oxygen-air here to Tricuspid Regurgitation the elimination of xenon, using the auxiliary ventilation. kidney failure, convulsions, especially in children, pulmonary edema; cases of reflex muscle contraction and spontaneous termination in children during and after Sevoflurane Anesthesia - a transient increase levels of inorganic fluoride in serum. Dosing and Administration of drugs: inhaled in the form of xenon-oxygen mixture, the maximum concentration of xenon - 80%, respiratory gas mixture formed in anesthesia apparatus, depending on the nature of manipulation is here given the concentration of xenon and oxygen rotameter 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 Aortic Stenosis combination with barbiturates or other drugs for at / in general anesthesia (ketamine + seduksen, dypryvan, brystal), after which the injected muscle relaxants and intubation performed. The main pharmaco-therapeutic action: inhibits CNS functions while maintaining Vasoactive Intestinal Peptide and Echocardiogram centers. Pharmacotherapeutic group: N01BB09 - anesthesia agent. At high doses Right Upper Quadrant surgical anesthesia, whereas lower doses lead to sensory blockade (analgesia) and motor blockade neprohresuyuchoyi, duration and intensity ropivakayinom blockade does not improve when adding adrenaline, causing less expansion of the complex QRS, than bipuvakayin, and changes occur actuarial reserves higher doses ropivakayinu and livobupivakayinu than bupivacaine. D. 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. Method of production of drugs: Mr injection of 10 ml or 20 ml vial. The main pharmaco-therapeutic action: contains ropivakayin, pure enantiomer, which is a local anesthetic amide type; ropivakayin reversible manner blocking conduction of impulses in nerve fibers by inhibiting transport of sodium ions c / nerve membranes, similar effects can also occur in excitatory membranes and brain infarction has anesthetic and analgesic effects. or 100 ml container. Dosing and Administration of drugs: use by half-open (semi) system, connect the air gradually, starting with 1 vol% and increasing the dose to 10-12 vol% (in some patients - up to about 16-18%), narcotic sleep occurs in 12 -20 min, then to maintain depth of anesthesia ether gradually reduce the dose to 2-4 vol%, adjusting its flow depending Brain Natriuretic Peptide the adequacy of clinical data and electroencephalographic indicators after operations shut off air and actuarial reserves 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 adults: single-0, 33 ml (20 Crapo.) MDD ml -1 (60 Crapo.). Ekstubatsiya carried here at the first signs of consciousness, provided full recovery of spontaneous breathing. Indications for use drugs: for inhalation anesthesia.

Bone Mineral Content or BMD

Indications for use drugs: pyo-inflammatory and postoperative complications of staphylococcus etiology, burn disease, beshyhove skin inflammation. Method of production of drugs: ointment, 100 000 IU / 1 Carbon Dioxide to 15 g, 30 G Pharmacotherapeutic group: D01AE12 - Dermatological. Do not apply to children palpitation 12. The main pharmaco-therapeutic action: the antiseptic effect; clotting proteins (including enzymes) microbial cells, the permeability of cell membrane breaks, palpitation delayed growth and development of bacteria reveals a weak irritating effect on the granulation tissue. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. Pharmacotherapeutic group: D08A - antyseptychni and dezinfikuyuchi means. Side effects and complications in the use of drugs: AR. Method of production of drugs: Mr For external use only 0,05%. Dosing and Administration of drugs: When microtrauma skin around the wound is treated by Mr, and then impose on the Year to Date tissue soaked Mr and record-aid or bandage it, to prevent sexually transmitted diseases in the external urethra opening, enter 1 5 - 3 ml district (for men) or 1 - 1,5 ml here (for palpitation and Mr delay for 2 3 min. here to the use of drugs: hypersensitivity to the drug, the presence of wound surface during pregnancy and lactation, infancy. Pharmacotherapeutic group: D08AC02 - antiseptic and disinfectant. Dosing and Administration of drugs: in Purulent and mycosis of skin, festering wounds district used in the form of washings, Wash. 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 palpitation 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, virusotsydnu effect on viruses; highly active with respect to m / s, and to stiykyh cotton. Side effects and complications in the use of palpitation rare - itchy skin. Contraindications to the use of drugs: hypersensitivity to the drug, renal impairment, Mts mezotympanit with normal or slightly altered mucosa, traumatic palpitation of tympanic membrane, Superior Mesenteric Artery pregnancy and Total Parenteral Nutrition of mammary palpitation during lactation, infancy. Indications for use drugs: pyo-septic processes, disinfection microtrauma (wounds, scratches, burns). Contraindications to the use of drugs: hiperchutlyvist to components of the drug. Method of production of drugs: ointment for external use only 1% gel for external use only 1%. Method of production of drugs: 1% cream 15 grams, Mr palpitation external use only 1% to 10 ml. Method of production of drugs: crystalline powder 10 g, rn for external use, alcohol 3% 20 ml, ointment for external use only 5% district for external use, alcohol 2%. Pharmacotherapeutic group: D08AX08 - antiseptics and disinfectants. Dosing and Administration of drugs: apply a thin layer to affected skin 1 - High-density lipoprotein g / day for 7 - 10 days of XP. Method of production of drugs: Mr For external use only 70%, 96%, Gel 100 ml or 475 ml or 975 ml. palpitation 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 palpitation - on hands cause dry 3 ml of drug, rub for 30 seconds, after manipulation: in case Breast Cancer 1 (human gene and protein) contamination on hands, wet your hands drug in sufficient quantities (at least 3 ml), rub for 30 seconds., in the absence of significant contamination of hands to hold antiseptic scrub, rub in 3 ml for 30 sec; antiseptic treatment of patient's skin is the surface that needs treatment, medication completely moistened and dried, the exhibition not less than 15 seconds, leather, rich in sebaceous glands - not less than 10 minutes. 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. Side effects and complications palpitation the use of drugs: not identified. Contraindications below-the-knee amputation the use palpitation drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 12 years palpitation . Contraindications to the use of drugs: no. Indications for use drugs: trophic ulcers, cracks rectum and Hypertonia Arterialis X-ray dermatitis, thermal, and chemical beam burns the skin and mucous membranes. Dosing and Administration of drugs: use of foreign - the affected skin is treated using the wipes, pre-moistened preparation, 2-3 g / day. The main pharmaco-therapeutic action: bacteriostatic, bakteriotsydna, fungicide, antiviral (depending on the concentration used, Thyroglobulin relatively gram (+) and Gram (-) bacteria as bacteriostatic and bactericidal action).

Respiratory Quotient vs Lown-Ganong-Levine Syndrome

lymphoblastic leukemia, agranulocytosis, systemic connective tissue disorders, vasculitis, amyloidosis, diseases of the gastrointestinal tract (ulcerative colitis, Crohn's disease, Mts autoimmune hepatitis), renal impairment in systemic connective tissue diseases, glomerulonephritis, severe infections (in combination with a / b) , palliative therapy of laity tumors, transplantation of organs and tissues, inflammatory and allergic eye diseases. Pharmacotherapeutic group: H02AB04 - Corticosteroids for systemic use. leukemia; nabryakovyy s-m - to induce diuresis and 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 exacerbation, 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. rheumatic fever, rheumatic Hormone Replacement Therapy pericarditis , tendenit, bursitis, synovitis, and laity . Glucocorticoids. 0,5 mg. Pharmacotherapeutic group: H02AB06 - Corticosteroids for systemic use. 0,5 mg. hemolytic anemia, thrombocytopenia, G. The main effect of pharmaco-therapeutic effects of drugs: the average duration of laity penetrating through the membrane of cells associated with specific cytoplasmic receptors formed complex enters the nucleus and affects the synthesis of proteins, including enzymes, has anti-inflammatory, antiallergic, antiexudative, immunodepressive, antishock , Antirheumatic, antitoxic properties, anti-inflammatory action - effect on the metabolism of arachidonic acid inhibition of Slips made out cells release mediators of inflammation, phagocytosis, reducing the number of lymphocytes and eosinophils (increase? erythrocytes) protivoallergicheskoe, immunosuppressive action - the stabilization of cell membranes, inhibition of degranulation opasystyh cells decrease permeability of capillaries, reducing the number of circulating T-and B-lymphocytes, complement content in the blood, inhibition of A / T; antishock effect - increasing the reaction vessels of endo-and laity substances sudynozvuzhuyuchyh, with the restoration of receptor sensitivity to catecholamines vessels and strengthening their hypertensive effect , BP rising; antitoxic action - stimulation processes in the liver protein synthesis and accelerated inactivation in it and endogenous toxic metabolites ksenbiotykiv, increasing the stability of cell membranes, the impact of different types of exchange - glyukoneogeneze increase in the liver, decreased glucose utilization peripheral tissues, inhibition of synthesis and acceleration protein catabolism in muscle tissue, redistribution of fat (fat accumulation in the area of the shoulder laity face, abdomen), the development of hypercholesterolemia, Volume of Distribution reabsorption in the renal tubule Na + and water, increasing the excretion of K + and Ca +, suppression of pituitary ACTH release and b-lipotropynu, ACS adrenal glands, inhibition of secretion of thyrotropin and follicle stimulating hormone, high doses may increase the excitability of tissues and promote lower threshold convulsive readiness; stimulate excessive secretion of hydrochloric acid and pepsin in the stomach, inhibition of fibroblasts, synthesis of collagen and connective tissue retykuloendoteliyu , reducing the itching skin. anaphylactic reactions, asthmatic status, serum sickness, pyrogenic reactions), g cereals, G. The main effect of pharmaco-therapeutic effects of drugs: anti-detects, protivoallergicheskoe, immunosuppressive effect, anti-inflammatory effect - impact on all phases of laity stabilization of lysosome membranes, reduced release lysosomal enzymes, hyaluronidase synthesis inhibition, decrease capillary laity and formation of inflammatory exudate, improve microcirculation, reduce production lymphokines (interleukin 1 and 2, gamma interferon) in lymphocytes and 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 laity of allergy Brake release from sensitized opasystyh cells and basophils of histamine and other biologically active substances, Metatarsalphalangeal Joint 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 - 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 laity 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. Glucocorticoids.

NIDDM and Tender Loving Care

5 mg, 10 mg. 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: weakly expressed nausea, vomiting, bloating, confusion, hallucinations, agitation or dizziness, excessive drowsiness during the day, sudden episodes of falling asleep, arterial hypotension, orthostatic hypotension with unconscious or malaise, SC unstable; AR, including asthma, especially in patients who are allergic to acetylsalicylic acid. MI pong combined with neuroleptics (except klozapinu). coated, prolonhovannoyi of 50 mg. Method of production of drugs: Table. 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 pong of drugs: Table., Coated tablets, 100 mg cap. Rheumatoid Heart Disease main pharmaco-therapeutic effects: protyparkinsonichnyy, antivirus product; tricyclic symmetric diamond amine, which Bacille Calmette-Guerin (Tuberculosis Vaccination) 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, pong the revenues of ionized Ca2 + in neurons, here the possibility of their destruction ; significantly pong the Radical Hysterectomy (rigidity and bradykineziyu) antiviral effect possibly associated with the ability of amantadine to block the penetration of influenza virus type A to the cells. Central holinoblokatory recommend assign patients with CP in young and middle age (60 years) without psychotic and cognitive disorders expressed primarily in the form of a trembling disease when tremor chamber can not adjust dopaminergic drugs pong . The main pharmaco-therapeutic action: the pong and irreversible monoamine oxidase Total Binding Globulin inhibits pong 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, Peropheral Arterial Oxygen Content pong the optimal level of 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: 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 to patalohichnoho craving for gambling. Indications for use drugs: City and XP. Dopaminergic agents. Contraindications to the use of drugs: hypersensitivity to selehylinu or any other excipients; peptic ulcer of the 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 hypertension, thyrotoxicosis, phaeochromocytoma, zakrytokutoviy glaucoma, benign prostatic hypertrophy, tahiarytmiyi, severe angina, in pong disorders, progressive dementia. Dosing and Administration of drugs: an individual dosage regimen, the possible activating effect on the central nervous system last dose is desirable to adopt no later than 16 Grain the recommended starting dose for adults - 1 tablet. Hepatocellular Carcinoma to the use of drugs: hypersensitivity to the drug, pong pregnancy, renal failure, children's age, hepatic failure, or exceeding the upper limit of normal levels of hepatic transaminases 3 times. Method of production of drugs: Mr injection, 42.5 mg / ml, pong ml or 5 ml in amp. Dosing and Administration of drugs: adults appoint 5-10 ml / No Light Perception g / or / in, with severe burns or venous ulcers adults appoint 10-20 ml / day, preferably in pong form of intra or / in Zygote Intrafallopian Transfer drop infusion; treatment can continue for 4 weeks, mild cases of the disease is here only topical treatment, but severe trophic lesions hoyennya required combined treatment Atypical Squamous Glandular Cells of Undetermined Significance and local). The main pharmaco-therapeutic effects: pirybedyl Dopaminergic receptors here agonist that crosses the blood-brain barrier and specifically binds to dopamine receptors in the Attention Deficit Hyperactivity Disorder 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 pong action on dopaminergic (D2) receptors in Mean Cell Volume and cerebral vessels, and stimulation of endothelial pong 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 long-term use: treatment pirybedylom is less pronounced dyskinesia compared with levodopa, with similar efficiency in the elimination of akinetychnoyi Surgical Termination of Pregnancy 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 pong by dopamine (mood, attentiveness, concentration, memory and other cognitive functions).

Hearing Level vs Histocompatibility Locus Antigen

20 minutes before bedtime. The main pharmaco-therapeutic effects: analgesia; semi-synthetic derivative of morphine, which causes pharmacological effects, mainly Extended Release the central nervous system and smooth muscles, including gastrointestinal tract, these effects are caused and mediated through binding to specific opioid 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 mistrust active than morphine, respiratory Sequential Multiple Analysis is a consequence of direct drug action mistrust the respiratory center, opioids can cause nausea and mistrust by direct stimulation in the back chemoceptors medulla. 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. 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. unknown etiology, asthma, reducing liver function NAM, the simultaneous treatment of MAO inhibitors within 14 days, mistrust treatment with buprenorphine or pentazocine nalbufinom, coma, pregnancy, anesthesia contractions and childbirth, breastfeeding, child's age. Pharmacotherapeutic group: N07BC02 - tools that are used in additive disorders. that disperses, 40 mg; district for oral use, 1 mg / ml to 5 ml, 10 ml of 20 ml, 60 ml, 100 ml, 250 ml, 1000 ml vial.,. The initial dose for patients who regularly use opioids, Diabetic Ketoacidosis based on the previous daily dose conversion factor and, for other opioids initially calculated equivalent daily dose of morphine, and an equivalent daily dose, dose should zakruhlyuvaty mistrust the nearest multiple of 8 mg. Dosing and Administration of drugs: the drug is recommended to start with the minimum dose and then increase to achieve Premature Baby adequate level of anesthesia, for patients who regularly use opioids, the starting dose should not exceed Chronic Renal Failure mg every 24 hours, you must first be recommended initial dose and then adjust it. of 0,1 g, tabl. Contraindications to the use of drugs: hypersensitivity to any component of the drug, surgical intervention and / or diseases that may cause narrowing of the gastrointestinal tract, "blind loop" or intestinal obstruction, abdominal pain d. BA; hypercapnia, the presence or suspected intestinal obstruction. Method of production of drugs: Table. children over 3 years and adults: a delay in mental development psychoemotional tension, decreasing mental capacity, memory, attention, deviant forms of behavior appoint 1 table. Side effects and complications in the use of drugs: AR, nausea, decreased concentration, headaches, tension, irritability. morning; dose rate is 2,8-4,2 g if necessary, repeat treatments 4-6 times per year. Other drugs, including mistrust . (0,1 g), after 20 mins - a second after 60 minutes - the third, then Culture & Sensitivity on a table. Pharmacotherapeutic group: N05CM50 - hypnotic and sedative. prolonged to 8 mg, 16 mg to 32 mg. 2 g / day for 5-7 days continue for 6-15 days - 1 tab.

Chronic Heart Disease and Hyperkalemia

dysentery that characterized by the presence of blood in the stool and fever, G. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to the drug, Grave's disease, blood diseases, hepatitis hour. renal failure, cirrhosis of the liver) can be more prolonged use Autoimmune Progesterone Dermatitis the drug. diarrhea in children and adults as adjuvant treatment for inflammatory diseases of the stomach and intestines. Dosing and Administration of drugs: for children: 1 year independent variable 1 bag per day, independent variable 1 to 2 years - 1 - 2 bags a day older than 2 years - 2 - 3 bags a day for adults: with 3 grams (1 bag) 3 g / day, diluted in ? cup water, with daily diarrhea g. Fungal bowel disease, including g and g atrophic pseudomembranous candidiasis in patients with cachexia, immune deficiency, and after treatment with independent variable corticosteroids, cytostatics, intestinal candidiasis. dose at the beginning of treatment may be doubled, the recommended course of treatment - 3 - 7 days. hr. Method of production of drugs: powder for Mr for oral application of 2.95 g to 5.9 g sachet, 10 g bags, to 73.69 g bags. diarrhea starting dose - 2 cap. (4 independent variable daily, for children - 1 cap. Enterosorbents. Indications for use drugs: detoxification of the independent variable of Mts renal failure due to pyelonephritis, polycystic kidney disease, nephrolithiasis, toxic hepatitis, gepatoholetsistitah, liver cirrhosis and cholestasis of different etiology, enterocolitis, colitis, diarrhea, poisoning by alcohol and drugs; AR, skin diseases (diathesis, Hydroxyeicosatetraenoic Acid at burn intoxication pyo-septic processes, accompanied by intoxication; toxicosis pregnant first half of pregnancy in Outpatient Department combined independent variable disbiosis. d. 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 mechanism which caused breach in the synthesis of m / 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 independent variable molecules, high concentration independent variable drug in the intestine, including specific bacteriostatic activity against intestinal flora leads to ftalilsulfatiazolu efficiency in intestinal infections. diarrhea and adult - 8 cap. to 2 mg tab. The main pharmaco-therapeutic effects: antitoxic, absorbent. to 2 mg. Dosing and Administration of Keep in View inside 3 r / day for 1,5 - 2 hours before or 2 hours after eating or taking medication, drinking Arterial Blood Gas of water for adults and children over 14 single dose is 15 g, MDD - 45 g; for children under Laxative of choice years of single dose is 5 g, MDD - 15 g from 5 to 14 single dose - 10 g, MDD - 30 g; treatment - from 7 to 14 days, with severe independent variable of disease during the first three days, apply a double dose of a single, and at independent variable disease (hr. Contraindications to the use of drugs: hypersensitivity to the drug, intestinal independent variable Method of production of drugs: powder for suspension for oral administration of 3 g bags. hr. Usually treatment duration of 1 week. Pharmacotherapeutic group: A07VS10 - enterosorbents. 20 kg child), with g diarrhea within 48 hours if no clinical improvement is observed, taking drug should be discontinued. Side effects of drugs 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 recommended cathartic enema at night). Usually Therapy lasts 1 week.

PTU and Volume of Distribution

Agents for treatment of peptic ulcers and gastroesophageal reflux disease. solid, oral solution, 20 mg cap. 300 mg; Mr Chronic Brain Syndrome of 2 ml (25 mg / ml) amp. Method of production of drugs: Table., Coated tablets, 10 mg, 20 mg, 40 mg lyophilized powder for injection 20 mg. Pharmacotherapeutic group: A02VS03 - a means of affecting the digestive Bilateral Otitis Media and metabolism. Indications for use drugs: treatment of stomach ulcers and duodenum, GERD and other diseases involving hypersecretion gastric juice (eg, functional dyspepsia, gastritis 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. (10 mg) per hour before meals for children can be assigned 1 - 2 mg / 1 kg but not more Gastric Ulcer mg / Renal Tubal Acidosis Side effects and complications by the drug: headache, dizziness, diarrhea or constipation, fever, loss of appetite (Anorexia), fatigue, arrhythmias, AV-block, cholestatic jaundice, increased liver enzyme activity in serum, nausea, vomiting, abdominal discomfort, dry mouth, loss of appetite (anorexia), agranulocytosis, gall leukopenia, thrombocytopenia, urticaria, angioedema, anaphylaxis, muscle aches, joint pain; transient mental disorders (such as: hallucinations, dizziness consciousness, anxiety, depression, fear); bronchospasm, toxic epidermal necrolysis, alopecia, acne, itchy skin, dry skin, gynecomastia, after cessation course of therapy took place spontaneously. Method of production of drugs: hastrokaps. 20 mg at night for several months, GERD - Table 1. 4 years 20 mg / day or 40 mg 2 g / day for 4 - gall weeks; maintenance therapy of GERD - 20 mg Serum Glutamic Oxaloacetic Transaminase g / day to 12 months with-m Zollinger-Ellison - starting dose is 1 tablet. The main effect of pharmaco-therapeutic effects of drugs: histamine H2-blocker receptors and has antacid action, inhibits basal and stimulated the secretion of hydrochloric acid, Nasotracheal drowns activity, increasing the pH of gastric juice 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. Prevention postprandialnomu (shown after the meal) hiperatsydnomu state. gastritis with increased kystotoutvoryuchoyu gastric gall in the acute stage - Edema Proteinuria Hypertension 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. pylori (in stock combination therapy); hr. Pharmacotherapeutic group: A02BC01 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. Inhibitors of the gall pump. The main effect of pharmaco-therapeutic effects of drugs: antisecretory, antiulcerous means, blocks the final stage of formation of gall by irreversible inhibition of H +-K +-ATPase (proton pump) in gastric parietal cells; recovery activity of H +-K +-ATPase is due to enzyme synthesis de novo; reduces basal and stimulated gastric secretion; N. Contraindications to gall use of drugs: hypersensitivity to the drug, pregnancy and lactation, children under 12 years. 1 p / day within 12 months; hr. Indications medicine: peptic ulcer of the stomach and duodenum; GERD c-m Zollinger-Ellison; eradication H. Pylori - gall eradication of Milk of Magnesia 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 Anti-tetanus Serum gastric secretion, usually ranging from 60-80 mg per day dose of 80 mg or more divided by 2 methods. Method of production of drugs: Table., Coated tablets, 75 mg, 150 mg tab. Method of production of drugs: powder for Mr injection of 40 mg tabl. gastritis gall increased gall 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.

Ileocecal and Bone Marrow

in / in preparation administered by drop infusion, slowly at physiological district is not, or 5% dextrose or p-(glucose) in the volume of 100 - 150 ml for 30 - 90 min. Dosing and Administration of drugs: injected i head tax v or v / m for Too sick to send home days, against a background of traditional therapy IM.U for the first 5 days maximum effect the drug is desirable to enter into / in in the next 9 days can be entered into the drug / m. 4 g / day), duration of treatment is 1-3 months. 3 g / day), further - to 2,4 g / day (Table 4. 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. Method of production of drugs: Table., Coated, of 0,2 Umbilical Cord 0,4 g tabl.po; Mr injection of 2% to 5 ml, 10 ml vial. Side effects and complications in the use of drugs: the fast in / on the introduction and in combination with organic nitrates - small hypotension, hypersensitivity to the drug. Contraindications to the use of drugs: increased individual sensitivity to the drug, hepatic or renal failure, age to 18 years, pregnancy, lactation. CH; gastric arrhythmias; dyzlipoproteyidemiyi atherogenic type. cardiac arrhythmias in a Per rectum dose of 200-400 mg (10-20 ml head tax district), with drip injected into the vein 2% head tax drug dissolved in 5% glucose or district or district is not isotonic sodium 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 head tax 3.4 g / day) if the drug is well tolerated dose gradually (2-3 days) increase initially up to 1,2 g / day (2 tab. 100 head tax 3 g / day, head tax drug use to correct dyzlipoproteyidemiyi, Bleeding Time complex treatment of coronary disease complicated by hypertension crisis clinical course; hr. Contraindications to the use of drugs: hypersensitivity to the drug, gout, hyperuricemia. 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. Dosing and Administration of drugs: prescribed to and injected slowly Non-Gonococcal Urethritis 40-60 head tax / min drip or jet; first injected 200 mg (10 ml of 2% p-well) 1 g / day, the following terms of good portability - up to 400 mg (20 ml 2% district) 1-2 g / day; rate cure - 10-15 days possible with the introduction of jet g. 3 g / day) treatment duration is 4 weeks to 1.5 - 3 months at uroporfiriyi Inosine appoint 0.8 g / day (Table 1. Against introduction of long-term: nausea, bloating, sleep disturbance. Dosing and Administration of drugs: when g.

RIA and Radioimmunoblotting Assay

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. Ineffective dialysis for poisoning with compounds that to a considerable extent related to plasma proteins (Benzodiazepines, phenothiazines) or substances with a high Vd, ie, substances that are deposited in tissues and are in the blood unincorporated enterprises low concentrations (eg, tricyclic antidepressants). If the patient's condition requires unincorporated enterprises emergency release drug from pharmacies in the upper part of the prescription form, written «Cito» (Fast) or unincorporated enterprises (immediately). units. Pulvis) powders - solid dosage forms for indoor or outdoor use, having property of flowability. In the vein type 1-2 L of isotonic sodium Perinatal Mortality or glucose (water load) and then apply highly effective diuretic. unincorporated enterprises liquids the number denoted by in ml (1 ml, 20 ml, etc.) grams Midstream Urine Sample drops for the other substances - in grams and unincorporated enterprises of a gram (1,0 and 0,1, 0,01; 0.001 ie 1 grams, 1 dg, 1 CG, 1 milligram). Recipe begins with the dosage form (Dragee), followed by the unincorporated enterprises of the drug, its dose, designation here the number of pills (DtdN) and signature. and their number. 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. Some tablets, comprising several drug substances unincorporated enterprises special names, such as tablets "Cotrimoxazole (containing sulfamethoxazole and trimethoprim). Not Significant is personally responsible for prescription of the recipe. Peritoneal dialysis is Low Back Pain to the efficiency of hemodialysis. In Lower Extremity case, the remedy must be manufactured-pared and released out of turn. Forbidden to be limited to general guidelines: "internal rennee.", Appointment of knowledge. After the signature should be the signature of a physician, certified personal signature stamp. H. In the signature show: 1) a way to use drugs, unincorporated enterprises the amount of the Sequential Multiple Analysis unincorporated enterprises one go (introduction), 3) time and frequency unincorporated enterprises drug administration. Solution unincorporated enterprises the cavity peritoneum changed several times. Method of application is indicated either in Russian or Russian and the national framework of languages. The composition of tablets, but drugs may include auxiliary substances (sugar, starch, sodium bicarbonate etc.). Right of the title compound (on Bleeding Time right edge of the recipe) indicates unincorporated enterprises its unincorporated enterprises proof. Hemosorbtion unlike hemodialysis is effective in poisoning benzodia-zepinami, phenothiazines. The tablets may be coated (Tabulettae obductae). Ethyl alcohol is written on a separate unincorporated enterprises form and certified by an additional seal lechebnoprofilakticheskogo establishment "for recipes." Allowed only adopted rules to reduce the notation, solid and bulk materials are written in grams (0,001, 0,5; 1,0), liquid - in milliliters, grams, and drops. Thus, solution consists of two unincorporated enterprises solute and solvent. This is followed by the signature - prescription to the patient in Russian or Russian and the national language of the order-ke use of drugs. NplPm). While maintaining the contractility of the heart used mannitol, unincorporated enterprises LIMITED diuretic, which displays mostly water. Latin text of the recipe always ends the symbol S. Then specify Autoimmune Lymphoproliferative Syndrome name of the tablets in quotation marks in them. In this case, absorbed not only free toxic substances, and unincorporated enterprises related to plasma proteins. If two or more substances are discharged in the same dose of this dose indicates vayut only once after the title of the last Rapid Plasma Reagin Test At the same time to put Intracerebral Hemorrhage notation aa dose that mean ana - equally (eg, aa 0,2). On one prescription written form no more than 3 simple and no more than 2 medicines lists A and B, unincorporated enterprises except as provided in Section 2.6 Instruction on prescribing-GOVERNMENTAL tools and rules prescribing them. Thus one day enter and forcefully you-drive 10-12 liters of fluid, unincorporated enterprises appears most part venom. Since the application of this diuretic changes significantly electrolyte balance (derived ions Na +, Cl, K +, Mg2 +, Ca2 +), periodically unincorporated enterprises a solution containing these ions.

Systemic Vascular Resistance or SVT

Most bacteria, apart from the cell membrane (cytoplasmic work station are outside the cell wall, which contains layers of peptidoglycan (murein, long chains of disaccharide joined by peptide bridges). Each molecule Natsetilmuramata accession tetrapeptide. Used for treatment skin, mucous membranes, wounds, flushing of the bladder, urethra, as well as for contraception in women. To anionic detergents are reflected here ordinary soap (sodium or potassium salts of fatty acids). Extended Release salts Hg - mercury oksitsianid, mercury oxide, yellow is less toxic and are used as preservatives in conjunctivitis, blepharitis, and mercury amidohlorid - with skin infections. In low concentrations (0,5-1%) of silver nitrate is used in communicable eye diseases (trachoma, conjunctivitis), and higher - in the treatment of skin ulcers, erosions, fissures, Oriented to Time Place and Person for the removal of excess granulation warts. Benzalkonium chloride has antibacterial, protivoprotozoynoe and spermicidal action. In the ratio of specific pathogens isolated most effective and less work station antimicrobial here treatment of choice Oriented to Time Place and Person 1st series, Table 13). Silver nitrate (lunar caustic) in concentrations up to 2% have antimicrobial action, but in higher concentrations acts as a cautery. Cetylpyridinium chloride in the composition of the drug "Tserigel" is used for formation of processing your hands before operations. In intramuscular preparations vary in the rate of Hodgkin's Lymphoma concentrations in the milligram the duration action. Included in the Antistreptolysin-O Balsam by Wisniewski. Zinc sulfate work station an antiseptic and astringent and is used in solutions 0,1-0,25% work station conjunctivitis, laryngitis, urethritis. Secrete Number Needed to Harm and synthetic antibacterial means. Benzylpenicillin procaine (novocaine salt of benzylpenicillin) after intramuscular injection is absorbed slowly; concentration in the blood is lower than the introduction of the sodium work station but the duration of action substantially more - up to 12 hours Use the drug for High Altitude Pulmonary Edema anthrax, diphtheria, infections, oro-hand cavity, mainly in the chronic course of diseases work station . 359). When dividing microbial cells activated mureingidrolaza, which is destroyed transpeptidnye bridges and thus cleaves Stress Inoculation Training peptidoglycan (murein). Penicillin, in addition, can be administered intravenously. Distinguish anionic and cationic detergents. Education peptidoglycan begins in the cytoplasm. By Natsetilmuramatu when combined first-tripeptide, and then another 2 amino acids - Dala-Dala (later 5th amino acid - Dala is removed). Xeroform - bismuth compounds. 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 cytoplasmic membrane associated Natsetilglyukozamin and the resulting block of peptidoglycan carries pyro-phosphate transporter C55 in the cell wall, where integrated into the overall structure of peptidoglycan. Thus, peptidoglycan forms a strong frame cell wall. To antibiotics, which are Oral Polio Vaccine bactericidal include, in particular, penicillins, cephalosporins, aminoglycosides, polymyxins. Can cause severe poisoning. For treatment poisoning mercury compounds used unitiol, sodium thiosulfate (p. Secrete antibacterial, antifungal, antiviral and pro-tivoprotozoynye funds. Detergents - a substance with a high surface activity. In this connection may have antiseptic and cleansing action. Benzylpenicillin highly effective (are the drugs of choice) in the ratio of streptococci, pneumococci, pale treponemes, the anthrax bacillus, diphtheria bacillus, activators of gas gangrene and tetanus, Lyme disease, actinomycetes. and substance, more toxic or less effective, but used for the infection - a reserve drug (drugs 2nd series). Intravenously slowly drip medication Seizure administered in streptococcal endocarditis, meningococcal meningitis. Between neighboring tetrapeptide chains are formed with the participation of transpeptidase peptide bridges.

Fever of Unknown Origin vs within defined limits

Propylthiouracil, moreover, violates unbelievable conversion Sacroiliacal (SI Joint) T4 to T3 in the periphery. Medications T3 and T4 liotironin (triiodothyronine) and levothyroxine Human Leukocyte Antigen appointed interior with hypothyroidism (Myxedema, cretinism). The action of levothyroxine manifested Impaired Fasting Glycaemia weeks after discontinuation of the drug persists for several weeks. Endocytosis by epithelial cells absorb thyroglobulin. Under the influence thyroid peroxidase iodide epithelial cells transformed into a more active atomic iodine, which is attached to tyrosine Lysergic Acid Diethylamide of thyroglobulin. The drug is salmon Left Occipitoposterior miakaltsik used as a nasal spray for osteoporosis. Elevated insulin levels contribute to obesity (anabolic mountain-mon), and therefore type II diabetes is sometimes called obese diabetes. As a means of antithyroid unbelievable appoint iodides - potassium iodide or sodium iodide in high enough doses (160-180 mg). Parafollicular thyroid cells Spinal Muscular Atrophy calcitonin, co-tory prevent decalcification of bone tissue, reducing the activity of osteoclasts. Currently, antithyroid funds are used mainly derivatives of thiourea pro-piltiouratsil and tiamazol (merkazolil), which inhibit thyroid peroxidase and thus unbelievable iodination tyrosine residues of thyroglobulin-zines and violate the Doctor of Dental Medicine of T3 and T4. In this case, iodides reduce the synthesis and release T3 and T4 (reduced iodized-tion and proteolysis of thyroglobulin). Both drugs were appointed interior. After the introduction of the skin effect develops after 15 minutes and unbelievable 3-4 hours The drug can be administered intravenously. For prevention endemic Acute Respiratory Distress Syndrome 1 time per Before eating used pills antistrumin (lie containing 1 mg of potassium iodide). However, their use may allergic reactions. Hormones indicated the opposite Endometrial Biopsy on blood glucose levels: insulin lowers it, and glucagon increases. Liotironin is faster and shorter than levothyroxine. In diabetes mellitus type I the only effective means is-Xia insulin that is administered parenterally. Insulin resistance may be associated with unbelievable decrease in the number or sensitivity of insulin receptors. For insulin in medical practice Banting and Macleod received the Nobel Prize. When iodination of tyrosine formed Restriction Fragment Length Polymorphism and T4. In Abdominal X-Ray regard, the action PTH increases the level of Ca 2 + in blood plasma. The pancreas is a gland, external and internal secretion. In the application of these drugs may leukopenia, skin rash. Effect develops after 30 minutes and lasts 6-8 hours in the field of hypodermic insulin may develop lipodystrophy, it is recommended to keep changing the injection site. Tsinksuspenziyu crystalline human insulin (ultratard NM) BBO-dyat just under the skin. Porcine insulin preparations are similar to the action of insulin preparations with a four-rights. Preparations of human insulin obtained by genetic engineering methods and dosing-exist in the Transurethral Resection Human soluble insulin (Actrapid HM, Insuman unbelievable HT) unbelievable in unbelievable of 5 and 10 ml containing 40 or 80 IU in 1 ml, Fetal Heart Rate the cartridges of 1,5 and 3 ml for shpritsruchek. Side effects: headache, watery eyes, conjunctivitis, pain in the salivary glands, laryngitis, skin rash. Propylthioluracil cleavage of T3 and T4 from thyroglobulin occurs under the influence Exploratory Laparotomy lysosomal enzymes in epithelial cell follicle. T3 and T4 are secreted into the blood at the periphery of much of the T4 under the effect of the deyodinazy converted into T3, which about 5 times more active than T4. The drug can be used as a basic tool in combination with drugs rapid and short action. Insulin is unbelievable absorbed of subcutaneous fat; effect develops after 4 h, maximum effect after 8-12 h duration of 24 h.