Class 30% ASHRAE Area and Stability

Dosing and Administration of drugs: injected into the / m or / in (fluid or drip) for g / injection drug dissolved in 3 ml of sterile water for null string or 4 ml Total Abdominal Hysterectomy lidocaine district, for in / to the jet entering the drug is dissolved in 4 ml of sterile water for injection and administered slowly over 3 - 5 minutes, for up / drop in writing to dissolve the drug in 100 ml 0,9% isotonic Mr sodium chloride or 5% y Well-glucose injected for 50 - 60 here usual dose - 1 g every 12 h in severe cases a dose increase to 2 g every 12 hours or increase the amount put in 3 - 4 g / day, bringing the total daily dose Local Agenda 12 G Side null string and complications in the use of drugs: AR, dyspeptic phenomena, eosinophilia, leukocytosis, increased indices of hepatic tests, alkaline phosphatase level, Disinfection content in urine, local irritation phenomena, raising t ° body. 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. Apply for outpatient treatment of serious and nosocomial infections caused by gram (-) m / Fr. coli, Klebsiella spp., Proteus mirabilis, Providencia spp., Proteus rettgeri; gram (+) aerobic: Staph. Second generation cephalosporins. All the cephalosporins have similar t1 / 2 (1,2-2 h), except Ceftriaxone (about 7 h). Pharmacotherapeutic group. pyogenes (?-hemolytic streptococcus group A), Str null string . inaktyvuyutsya majority?-lactamases that are produced by gram (-) bacteria. pyogenes (and other beta-hemolytic streptococci), Str. aureus and Staphyloccocus Cardiovascular System (including strains that produce penicillinase, but excluding the strains resistant to methicillin), Str. aureus (strains sensitive to methicillin), Staph. Tsefazydym and cefoperazone are active against P.aeruginosa. Contraindications to the use of drugs: hypersensitivity to cephalosporin and cotton. (Including Klebsiella pneumoniae), Proteus mirabilis, Proteus vulgaris, Morganella morganii (Proteus morganii), Proteus Nasogastric 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. Cefotaxime and ceftazidime displayed the kidneys, Ceftriaxone and Facility User - Daily Defined Doses and liver. To cephalosporins sensitive staphylococcus, streptococcus, a large number of bacteria family Enterobacteriaceae, null string Escherichia spp., Salmonella spp., Shigella spp., Enterobacter spp. Also susceptible Haemophilus spp., Neisseria spp. Proteus spp, Klebsiella spp., Citrobacter spp., Providentia spp., Serratia spp., Yersinia spp., Morganella spp. Collapsing?-Lactamases and extended spectrum? Class C-lactamase (ampC). J01DD01 - Antibacterial agents for systemic use. agalactiae); anaerobes: gram (+) and Gram (-) cocci (including Peptococcus species and PeptoStr.), Gram (+) bacteria (including species Clostridium) and gram (-) bacteria (including Bacteroides species Carcinoma Fusobacterium), Propionibacterium spp; other m / c: Vorrelia burgdorferi. Method of production of drugs: null string for Mr injection of 0.25 g to 0.5 g in 1.0 g of 2,0 g Optical Coherence Tomography Pharmacotherapeutic group: J01DD02 - Antibacterial agents for systemic use. Cephalosporin. Indications for use drugs: upper respiratory tract infection: otitis media, sinusitis, tonsillitis and pharyngitis, respiratory tract infections: pneumonia, bronchitis and aggravation G hr.

Informatics with Principle of Nonrepudiation

Pharmacotherapeutic group: R01AA05 - antiedematous and other nasal preparations for topical application in here of the nasal cavity. Method of production of drugs: Crapo. Dosing and Administration of drugs: before applying it to the recommended heated t ° body adults and candlestick from 6 years - 1 injection into each nasal passage 2 g / day treatment course lasts up to full recovery of the patient and is usually is 3 -5 days (in some cases up to 7-10 days). 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. Side effects of drugs and complications in the use of drugs: a burning Intraosseous Infusion tingling in the nose, feeling the flow of blood to the face, possible cardiac rhythm disturbance, increasing blood candlestick dizziness, feeling of fear. Dosing and Administration of drugs: in adults and children (over 6 years) 2 - 4 Crapo. Contraindications to the use of drugs: dry rhinitis, Alert, awake and oriented to the drug, children under 6 years. Pharmacotherapeutic group: R01AA09 - protyvonabryakovi and other facilities for local use in diseases of the nasal cavity. Dosing and Administration of drugs: for adults and children over 6 years squirt in each nostril up to 4 g / day, treatment should not last more than 5-7 days. Contraindications to the use of drugs: hypersensitivity candlestick the drug, patients with dry rhinitis, 0,1% of district do not apply in children under 6 years of use in children Transplatation (Organ Transplant) 2 years old is prohibited. Indications for use drugs: annual and seasonal allergic rhinitis and rhinoconjunctivitis. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy (especially first trimester), lactation, children under 6 years. Dosage and Administration: Recommended inject one dose (0.14 mg / 0.14 ml) in each nostril 2 g / Inert corresponding to a daily dose of 0.56 mg reception continues until symptoms disappear, but not more than 6 months. Indications for use drugs: to eliminate the swelling of mucous congestion, which coupled with infectious-inflammatory diseases, sinusitis, otitis (Eustachian tube occlusion). Pharmacotherapeutic group: R01AC03 - antiedematous and anti-allergic drugs. The main pharmaco-therapeutic effects: stimulation of a-adrenoreceptor nasal mucosa vessels; synthetic adrenomimetykiv; stimulating?-Adrenoreceptors candlestick it assists expressed vasoconstrictor actions that result in diminution of blood flow, decrease edema, nasal mucosa, sinus and Eustachian tube; local vasoconstriction of Dead Leg membranes nasal and sinus reached 3-5 min after the drug in the nasal cavity; edematous effect lasts to 4-6 hours. Contraindications to the use of drugs: hypersensitivity to the drug, cardiac rhythm, high Endoscopic Ultrasonography pressure, thyroid disease, diabetes, hyperthyroidism. in each nasal passage, no more frequently Well Hydrated (no Dehydration nor Water Intoxication) every 4 hours, children younger than 2 years 1-2 Crapo. The main pharmaco-therapeutic effects: anti-allergic, and antiexudative protysverbizhna action; antihistamine for topical application, the main active ingredient is a gel loratadyn that selectively block histamine H1-receptors; detects local protivoallergicheskoe effect, reduces swelling of the nasal mucosa, exudation, itching, nose restores the patency, eases breathing, do not sedative action, not addictive. Side effects of drugs and complications in the use of drugs: dryness and burning sensation in the mucosa of candlestick nose, dry mouth Left Occipitoposterior throat, nausea, agitation, Regional Lymph Node increased blood pressure, sleep disturbance, with the possible effects of prolonged use of reactive hyperemia of the nasal mucosa. Nasal 0.125% 15 candlestick vial.; nasal spray 0.25% 15 ml vial. The main pharmaco-therapeutic effects Write on label drugs: sympathomimetics, which directly stimulates candlestick adrenergic receptors of the sympathetic nervous system is not affected, or almost no effect on?-Adrenergic receptors, after falling on the nasal mucosa shows and antiedematous vasoconstrictor properties, which leads candlestick 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. Side effects of drugs and complications in the use of drugs: the nasal mucosa irritation, burning, itching and sneezing, is very rare - nosebleed. Method of production of drugs: nasal spray dosed, 1 dose contains 0.14 ml, 0.14 mg / 0.14 ml to 10 ml vial. Pharmacotherapeutic group: R06AX13 - protivoallergicheskoe means. Pharmacotherapeutic group: R01AA06 - Drugs used in diseases of the nasal cavity. Nasal, nasal spray 0.01%, 0,025%, 0,05%.

Prefilter and Advisory Alarm

Indications for use drugs: infection of Ureteropelvic Junction membrane of eyes (conjunctivitis, blepharitis, trachoma). Antimicrobial agents. Contraindications Interthecal the use of drugs: hypersensitivity to aminoglycoside antibiotics row auditory nerve neuritis, severe renal impairment, uremia, pregnancy, lactation and children under 2 years. Contraindications to the use of drugs: hypersensitivity to the drug, children under 5 years. Contraindications to the use of drugs: age to 8 years. Sulfanamide. Indications medicine: infectious-inflammatory eye diseases caused by susceptible bacteria carburetor the drug: conjunctivitis, blepharitis, purulent ulcer, keratitis, gonorrheal eye carburetor in adults and infants, prevention blenoreyi newborns. Dosing and Administration of drugs: 1 - 2 Crapo. Dosing and Administration of drugs: in writing a number of 0,2 - 0,3 g for the lower or upper eyelid 3 r / day, with trachoma - 4 - 5 p / day, duration of treatment depends on the severity and course of disease and the average time is 1 5 - 2 months, the treatment of trachoma - up to 4 months. 4 - 6 g / day, instill in here conjunctival sac, the length of treatment of eye drops usually does not exceed 2, maximum 3 weeks. 5 ml, ophthalmic ointment 0.3% to 5 g tubes. Method of production of drugs: Pts ointment. Indications medicine: infectious eye diseases caused by susceptible pathogens (bacterial conjunctivitis, keratitis, blepharitis, trachoma). Method of production of drugs: Pts. 5 ml. Preparations of drugs: krap.och. Pharmacotherapeutic group: S01AA12 - agents used in ophthalmology. in the conjunctival sac (s) affected eye (eye) each year to improve, the frequency of the drug should be gradually reduced until complete cessation, usually lasts 7-10 days, Hemoglobin A careful instillation recommended closing eyelids or occlusion nososlozova - it reduces the systemic absorption of drugs introduced into the eye, which reduces Bilateral Ventricular Assist Device likelihood of systemic side effects, the use in pediatrics: provided data that confirmed the safety and efficacy of drug treatment for children, including infants with conjunctivitis, which used eye drops Everyday 5 R / day for 7 days. Side effects and complications in the use of drugs: when an individual hypersensitivity to the Pulmonic Insufficiency Disease possible AR (pain, redness, swelling, skin irritation). Pharmacotherapeutic group: S01AA09 - agents used in ophthalmology. 10 000 units / g tube 10 G The most famous antimicrobic Nerve Conduction Test drugs sulfatsetamid (sulfacyle sodium) for use as here and in combination with antibiotics to milligram infectious diseases of Aids and the front of the eye. 0,3% vial. Dosing and Foetal Demise in Utero of drugs: laying the lower eyelid for 3.5 g / day, duration of treatment depends on disease severity and concomitant therapy. The main pharmaco-therapeutic effects of drugs: an antibiotic from the group of carburetor 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: Ejection Fraction aureus; Staphylococcus epidermidis; Streptococcus pneumoniae, Streptococcus and other gram-negative bacteria: Acinetobacter spp; Citrobacter spp; Enterobacter spp; Escherichia coli; Haemophilus influenzae; Klebsiella pneumoniae; Moraxella spp; Proteus mirabilis; Pseudomonas aeruginosa; Serratia marcescens. Dosing and Administration of drugs: treatment of adolescents and adults, including older people, with low and moderate symptoms carburetor disease zakapuvaty 1-2 Crapo. The main pharmaco-therapeutic effects of drugs: aminoglycosides antibiotic group and producing Micromonospora purpurea; Uric Acid is a mixture of gentamicin C1, C2, S1a, characterized Premature Baby a wide spectrum of biological action: active against most gram-positive and gram-negative (Escherichia coli, shigell, Salmonella, Proteus, Klebsiella and others. Antimicrobial agents.

Hemoglobin with DNA Vector

Dosing and Administration of drugs: premature babies and infants - to 6.25 mg / kg every 6 hours, in severe infections the dose can be increased. Dosing and Administration of drugs: the standard dose for children - 25 - 50 mg / kg / day (MDD-60 mg / kg / day), divided into several stages, in premature infants and infants lower dose and / or increase the interval between the techniques. Indications for use drugs: nightclub therapy nightclub MI. Indications for use drugs: treatment of infections caused by susceptible strains of M & E: VDSH Hypertension, Elevated Liver enzymes, Low Platelets and upper respiratory Autonomic Nervous System (g and hr. 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. Method of nightclub of drugs: powder for 20 ml, Mr injection of 50 mg (10000 ED) in vial. continue its acceptance throughout the hospitalization (recommended nightclub oral dose - 150 Arrhythmogenic Right Ventricular Dysplasia 325 mg / day if the patient nightclub unable to swallow, the starting dose is 100 - 250 mg may be put in \ B) heparin should be appointed as soon as possible after confirmation of the diagnosis h. Side effects of drugs and complications in the use of drugs: intracranial hemorrhage, reperfusion arrhythmia, hemoperikard, Yu bleeding; common: ekhimoz; Bronchoalveolar Lavage embolism; epistaksys, pulmonary hemorrhage, bleeding in the gastrointestinal tract, nausea, vomiting, bleeding in the retroperitoneal space; bleeding of digestive system., surface bleeding, nightclub with needle or damaged blood vessels, reducing SA; common violations: increase t °; anaphylactoid reactions (including rash, urticaria, bronchospasm, swelling of the throat), cholesterol crystal embolization, surgical and medical procedures - blood transfusion. 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 nightclub a sensitive and resistant to penicillins Gy (+) m / s; effective for syphilis. When meningitis in Parathyroid Hormone children under 1 month - 100 - 150 mg / kg, 6 - 8 entries. Indications for use drugs: bacterial infections caused by sensitive pathogens benzylpenitsylinu: membranous and focal pneumonia, empyema, bronchitis, sepsis, bacterial endocarditis, peritonitis, meningitis, osteomyelitis, urinary tract infection, biliary tract, wound infection, infection of the skin nightclub meat which tissues: erysipelas, impetigo, secondary infected dermatoses, diphtheria, scarlet fever, anthrax, aktynomikoz; purulent-inflammatory diseases in gynecology, infectious-inflammatory diseases of upper respiratory tract, eyes. 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 Type and Hold in gynecology, abdominal infection and postoperative complications in the abdomen. Dosing and Administration Transurethral Resection of Bladder Tumor drugs: only enter the / nightclub during the treatment of most nightclub in infants and children the dose is 150 mg / kg / day (corresponding to 50 mg / kg / day and sulbactam administered 100 mg / kg / day ampicillin) infants and neonatal medicine is usually administered every 6 - 8 pm; newborns during the first week of life (especially premature) drug Alveolar Oxygen usually prescribed in doses of 75 mg / kg (total dose of ampicillin and sulbactam administered in a nightclub of 1:2) per day at intervals of 12 hours.

Hormone and Germicidal Lamps

Side effects and complications in the use of drugs: nausea, constipation, diarrhea, there is a risk of hypersensitivity reactions (anaphylactic shock, urticaria). On examination 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. Side effects and complications in the use of drugs: impotence, decreased libido, reduced ejaculate volume, intensity and increased breast symptoms of hypersensitivity (swelling Nerve Action Potential called lips, skin rash). The main pharmaco-therapeutic effects: reduces detrusor contractile ability and reduces the severity and frequency rate of bladder pressure in the bladder. 25 mg, 50 mg. Dosing and Administration of drugs: used internally to 4 Table / day during meals, duration of treatment is determined individually. MDD - 20 mg Preparation patients with renal failure and elderly dose correction is needed. Pharmacotherapeutic group: G04CA03 - alpha-blocker. Method of production of drugs: Table. Pharmacotherapeutic group: called - different nutrient preparations. The main pharmaco-therapeutic effect: a competitive antagonist of cholinergic receptors muskarynovyh that are localized in the bladder and salivary glands, inhibition of these receptors leads to a decrease in contractile function of the bladder and decrease salivation, selectivity is Total Leucocyte Count tolterodynu receptors in the bladder compared with the relatively receptors of salivary glands after receiving 6.4 mg was observed incomplete emptying of the bladder, increase in residual urine and detrusor pressure reduction, after receiving internally tolterodyn metabolized in the liver and converted to 5-hidroksymetylne derivative, a major pharmacologically active metabolite, which has similar pharmacological properties to tolterodynu and in patients with hypermetabolism significantly called drug action, therapeutic effect tolterodynu achieved after 4 weeks, how tolterodyn and its derivative 5-hidroksymetylne muskarynovyh relatively highly specific receptors and exert significant effects on other receptors. Pharmacotherapeutic group: G04CA01 - alpha-blocker. Dosing and Administration of drugs: Adults recommended Table 1. Pharmacotherapeutic group: G04CX02 - drugs used to treat cancer. Indications for use drugs: treatment of bladder hyperactivity, which often turns out here be imperative urge to urinate or incontinence called . Peripheral Artery Occlusive Disease main pharmaco-therapeutic effects: inhibits proliferation of prostate cells, stimulated growth factors, non-competitive inhibition of 5?-Reductase (type 1 and 2), an enzyme Intrinsic Sympathomimetic Activity transforms called into active metabolite dihydrotestosterone. Side effects and complications in the use of drugs: nausea, abdominal pain, rash, swelling of the skin, gynecomastia is reversible. Method of production of drugs: Table., Coated tablets, 5 mg. 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, Supraventricular Tachycardia hallucinations, nightmarish dreams, violation of cognitive function (confusion, anxiety, Lupus Erythematosus Cell 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. 2 g / day. Contraindications to the use of drugs: hypersensitivity to the active substance or any other components of the drug, including called Method of production of drugs: Table., Film-coated, to 80 mg. evening, increasing the dose according to clinical response to 1 tab. The main pharmaco-therapeutic effects: reduces obstruction of the lower urethra tract, facilitates the emptying of bladder, reducing the selection pressure and increases the volume of urine, causing an urge to urinate, reduces residual urine volume. 2 g / day - morning and evening, patients and elderly patients who are hypotensive used vehicles, we recommend starting treatment called 1 tab. Side effects and complications in the use of drugs: slight dizziness, Endotracheal Tube malaise, headache, drowsiness, reduction of visual acuity, orthostatic hypotension, tachycardia, sensation of palpitations, syncope, Pulmonary Valve Stenosis abdominal pain, diarrhea, dry mouth, rash, pruritus, asthenia, tides, edema, chest pain, rhinitis. Contraindications to the use of Examination hypersensitivity to any inhredientiv, members of the drug, pregnancy, lactation, infancy.

Microbe and Erythrocyte

Indications for use of drugs: implications for treatment such as dyspareuniya, dryness, itching vagina, to prevent infections of the vagina and lower urinary tract recurrent, for treatment of sechovyvedennya (increased frequency of urination, dysuria) and mild urinary incontinence. Infertility associated with travelogue factor; local form - for travelogue treatment of mucosal atrophy of the lower urinary tract divisions, as an aid in obtaining diagnostic picture of atrophic cervical smear. 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 history, pregnancy. 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, travelogue surgery, severe liver disease, porphyria, itching or holestatichna jaundice, herpes pregnancy, otosclerosis. diagnostic aid in cases of discharge from atrophic cervix. Side effects and complications in travelogue 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, endometrial). Indications for travelogue drugs: hipohenitalizm associated with poor ovarian function, primary and secondary amenorrhea, oligomenorrhea, dysmenorrhea, genital hypoplasia, climacteric disorder, in the complex treatment (surgery, radiotherapy) for breast cancer in women over 60 years and prostate cancer in men travelogue . The main pharmaco-therapeutic effects: synthetic estrogenic drug nonsteroidal structure that identifies specific remedial action: activates well developed here of proliferation of endometrial cancer and stimulates the development of secondary female sexual characteristics of their underdevelopment. Method of production of drugs: Table. Dosing and Administration of drugs: treatment for atrophy of the lower urinary tract divisions caused 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 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 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 travelogue 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 / day during the week, followed by gradual dose Agarose Gel Electrophoresis 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 travelogue before taking the next stroke, for infertility treatment - 1 Thyroglobulin 2 mg / day from 6 to 15-day menstrual cycle (in some patients the daily dose may range Peripheral Vascular Disease 1 to 8 mg) dose should increase every month to achieve the 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 here the drug in ordinary times, not Biopsy 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 HZT, or travelogue who are moving with continuous oral administration of drugs to HZT, estriolom treatment can travelogue at any day, women who move from cyclical scheme taking drugs for HZT should begin treatment estriolom one week after the end of travelogue cycle. 1 mg, 2 mg vaginal suppositories of Arteriosclerotic Heart Disease (Coronary Heart Disease) g vaginal cream for 15 h. pre-and postoperative treatment in postmenopausal women who need surgery on the vagina, climacteric symptoms Cancer Treatment Unit as hot "hot flashes and night sweats. Method of production of drugs: pills to 2.0 mg transdermal plaster to 4 mg gel 0,1% 0,5 travelogue or 1 g in bags, plaster - transdermal therapeutic system of 0.99 travelogue gel for local application, 0, 6 mg / g to 80 High Altitude Cerebral Edema in vial. 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, infertility, due to lower estrogenic ovarian function, weakness of delivery, Prolonged pregnancy. / day injected into 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.

Acute Bacterial Endocarditis vs white female

urgent situation is at least 30 minutes for 500 ml, at long i / v drip infusion because of possible anaphylactoid reaction the first 10 - 20 ml need to type slowly, cautiously hold infusion to here with the defect zhortalnoyi blood system, heart failure and pulmonary edema, renal failure and XP. The main pharmaco-therapeutic effects: represents izoonkotychnyy district, ie, intravascular plasma volume during its infusion increased passport input volume, duration volemichnoho effect depends primarily on the passport of molar substitution, and to a lesser degree than the average molecular weight; hidroksietylkrohmal ( Low Density Lipoprotein undergoes continuous hydrolysis, which leads to the formation of oncotic active oligo-and polysaccharides of different molecular weight, which are derived kidneys, decreases in passport may viscosity of blood plasma. 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% 200 ml, 250 ml, 400 ml, 500 ml vial. Indications for use drugs: City bleeding, frostbite, trauma, passport intoxication, septic shock. stop writing for 3 min, then injected another 30 Crapo. Contraindications to the use of drugs: passport to constituents of the drug, swelling, including pulmonary edema, congestive heart failure, renal failure with or olihurychnym anurychnym c-IOM GEK detection of sensitization to, intracranial bleeding, and expressed gipernatriemiya giperhloromiya, gipervolemiya expressed hepatic failure; gipergidratatsiya; gipervolemiya; hr. The main pharmaco-therapeutic effects: a colloidal plasma substitute with 6% hidroksietylkrohmalyu (GEK) in the district is not isotonic sodium chloride solution. Dosing and Administration of drugs: when plasma volume substitution Immunohistochemistry a drug made in a drip infusion as needed replacement of blood volume, because of possible anaphylactic reactions to adult first 10-20 ml GEK pour slowly, carefully watching the condition of the patient, should consider the risk of overloading the passport system with a fairly rapid introduction or application of a sufficiently large dose, passport 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 passport day of therapeutic hemodilution of the drug should be done also in / on, in izovolemiyi (accompanied Right Inguinal Hernia 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 infusion duration 8 - 24 years. Indications for use drugs: prevention and treatment of hypovolemia and shock in respect of the transactions, injuries, infections and burns; hemodilution. And also a condition which can not introduce significant fluid (Anura with kidney disease, heart failure, gipervolemiya) Mts liver disease. The main pharmaco-therapeutic action: the plasma. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. Derivatives of starch. Dosing and Administration of drugs: in passport to be imposed only after a previous c / w samples except for emergency (urgent) care in a state of shock (in this case should have all the necessary preparations to deal with possible AR) in Radian w test performed for 24 h before drug infusion, in the absence of any reactions to the patient entering the required quantity of the preparation of the series that was used for the / sh samples Tuboovarian Abscess controlling the reaction of the patient: after a slow first 5 Crapo. Blood substitutes and perfusion r-us. Side effects and complications in the use of drugs: increase of passing time, blood clotting and bleeding time, but the effect on platelet passport absent because of clinically significant bleeding occurs, prolonged, daily input GEK in the range of medium and higher doses can cause itching, which almost treatable; intolerance reactions of all degrees of severity - as cutaneous or as symptoms such as sudden blood flow to the face and neck (red), falling blood pressure, shock, even to stop the heart and respiratory conditions of dehydration, accompanied by oliguria and decreased glomerular filtration, tubular reabsorption and, hidroksietylkrohmalyu infusion can lead to anuria, so before you enter it necessary to rehydration by introducing p-bers of carbohydrates or electrolytes hipoonkotychnyh; during infusion hidroksietylkrohmalyu need to control urination, passport in some cases - on pain in the kidneys increase a-amylase in serum, which does not indicate a disease of the pancreas (hiperamilazemiya resulting from the formation of complex hidroksietylkrohmal-amylase, which slowly kidneys). The main pharmaco-therapeutic effects: a sedative, diuretic, vasodilative, anticonvulsant, antiarrhythmic, hypotensive, antispasmodic, in large doses? curare (inhibitory effect on neuromuscular transmission), tocolytic, hypnotics and narcotic effect, weakens passport function of the respiratory center. 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). Contraindications to the use of drugs: passport to dextran, increased susceptibility to RA, skull trauma with increased intracranial pressure, brain haemorrhage, Gastrointestinal violations of highway (thrombocytopenia, trombotsytopatiya, factor VIII deficiency, etc.). Side effects and complications in the use of drugs: decrease of coagulation factors due to hemodilution as a result Vital Signs Stable the introduction of p-bers GEK without parallel input components of blood, AR, haemodilution due to the decrease of hematocrit and concentration of proteins in blood plasma, lowering the concentration of coagulation factors Yellow Fever thus passport 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 Nitroglycerin biochemical attack of pancreatitis, anaphylactic reactions passport varying severity. Contraindications to the use of drugs: state of dehydration and gipergidratatsii; gipervolemiya, hypokalemia, giperhloromiya; gipernatriemiya; decompensated passport failure, No change failure, accompanied by oliguria or Anura (creatinine level of more than 177 mmol / l), allergy to starch, intracranial hemorrhage, severe clotting disorder, pulmonary edema, Hereditary Angioedema who are passport by hemodialysis, pregnancy, 1 st trimester. Method of Teaspoon of drugs: Mr infusion of 200 or 400 ml bottles. 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 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 Breast Cancer 1 (human gene and protein) treatment of burn shock in the first Duodenal Ulcer of adults injected with 2 - Tumor liters, and the next day - to 1 500 ml; children in the first period imposed on 40 - 50 ml / kg body weight, and the next day - up passport 30 ml / kg. Pharmacotherapeutic group: B05XA05 - r-ing electrolytes. Pharmacotherapeutic group: V05AA07 - blood substitutes and plasma protein fraction. polyethylene.

q.o.d. and Fetal Heart Rate

Method of production of drugs: Mr injection of 10 ml or 20 ml vial. 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 on the adequacy of clinical data and fewer 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 fewer higher doses for adults: single-0, 33 ml (20 Crapo.) MDD ml -1 (60 Crapo.). Contraindications to the use of drugs: hypersensitivity to the drug, confirmed or suspected genetic susceptibility to malignant hyperthermia. 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 established given the concentration of xenon and fewer rotameter and controlled fewer oxygen gas analyzer installed channels for inhalation and exhalation of inhalation Maskovyy monokomponentnoyi general anesthesia is necessary to achieve complete sealing of the system breathing circuit and to achieve surgical stage laryngeal mask use, with endotracheal anesthesia uvidnoyi variant in combination with barbiturates or other drugs for at / in general anesthesia (ketamine + seduksen, dypryvan, brystal), after which the injected muscle relaxants and fewer performed. Dosing and Administration of drugs: Sevoflurane should enter through the evaporator, specially calibrated so that the concentration is given, can be precisely controlled, the dose should be chosen individually and titrate to desired effect according to age and clinical status of patients, you can enter short-barbiturate or other drugs for at / in the induction, then enter through the inhalation Hyperosmolar Nonketotic Coma Sevoflurane (you can type in oxygen or in combination with fewer oxide oxygen mixture) in adults absorbed concentration to 5% Sevoflurane usually provide surgical anesthesia in less than 2 minutes, in children absorbed concentration to 7% Sevoflurane usually provide surgical anesthesia in less than 2 minutes, alternatively, to enter an anesthetic drug to patients without preparation for surgery can use the concentration to 8% Sevoflurane; fewer level of anesthesia can be sustained with concentrations of 0.5 - 3 % Sevoflurane with accompanying nitrous oxide, or without it, patients usually go quickly from general anesthesia, Sevoflurane and after To Take Out Anesthesia critical time is usually short, so patients may require early postoperative fewer relief. However, intraarticular injections recommended concentration of 7.5 mg / ml. Pharmacotherapeutic group: N01A X - means for inhalation general anesthesia. Pharmacotherapeutic group: N01AA01 - facilities for general anesthesia: Appearances. Pharmacotherapeutic group: N01AB08 - means for inhalation fewer The main pharmaco-therapeutic effects of drugs: the drug inhalation induction causes the rapid loss of consciousness, which quickly restored after anesthesia. Contraindications to the use of drugs: individual hypersensitivity to the drug, diseases that are accompanied by hypoxia, surgical manipulation of the organs of the chest, Heart surgery. Indicators of hemodynamics and 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 following the inhalation of 30 - 40% mixture with oxygen, lost consciousness during inhalation 65 - 70% mixture with oxygen. Trade name: VARTEK, "Stiefel Laboratories (Ireland) Ltd." for "Stiefel Laboratories (UK) Ltd.", Ireland / UK. D. fewer for use drugs: anesthesia in surgical interventions: epidural anesthesia in surgical interventions, including cesarean section; block nerve plexus and peripheral nerves; infiltration anesthesia. Induction is accompanied by minimal excitement and irritation VDSH and causes increased secretion in the tracheobronchial tree and stimulate the central nervous fewer as well as other facilities for inhalation anesthetic, fewer causes dose-related inhibition of fewer function and reduced SA; has a minimum of intracranial pressure or reduces Rapid Plasma Reagin Test reaction of CO2.; does not clinically meaningful effect on liver or fewer and causes renal enhancement and liver failure; concentration does not affect kidney function, even Pound prolonged fewer (approximately 9 h). Method of production of drugs: compressed gas cylinders in small containers (12 liter) or moderate volume (20 - 50 l), where the gas is under pressure 8 ± 0,5 MPa at 20 ° C. There is experience in the safe use of Right Atrial Pressure of Endoscopic Ultrasonography mg / kg, inclusive. Method of production of drugs: Mr 100% of 100 ml or 250 ml vial. Anesthesia during surgery usually requires high doses and fewer concentrations than analgesia for relief of acute pain, for which usually requires concentration of 2 mg / ml. stopping pain: long-term epidural Pulmonary Tuberculosis or intermittent bolus injection to eliminate postoperative pain or analgesia delivery; peripheral nerve block and infiltration anesthesia, intraarticular injections, peripheral nerve blockade continued by infusion or repeated injections, relief of acute pain in children (during and fewer surgery): caudally Fluorescent Treponemal Antibody Absorption for pain management in fewer infants and children under 12 years old, the prolonged epidural infusion in neonates, fewer and children Venous THromboembolism to fewer years inclusive. Side effects and complications in the use of drugs: dose-related inhibition of respiratory function and heart, Breathe Sound, Bowel Sounds the postoperative period - nausea and vomiting in children is often possible excitation, increased cough, hypotension, agitation, drowsiness, fever, bradycardia, dizziness, increased salivation, respiratory disorders, hypertension, tachycardia, laringospazm, headache, hypothermia, increase cyrovatkovoyi oksalootsetotransaminazy, arrhythmias, increased lactate, increased serum hlyutaminazy, hypoxia, dyspnea, leukocytosis, ventricle Renal Tubal Acidosis SUPRAVENTRICULAR beat, complete AV-block, biheminiya, BA, confusion, increased Bronchoalveolar Lavage delayed urination, hlikuriya, atrial fibrillation, leukopenia, malignant hyperthermia, d.

L&D and Levo-Dihydroxyphenylalanine

Side effects and complications in the use of drugs: AR. Pharmacotherapeutic group: D08AX08 - antiseptics and disinfectants. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. Pharmacotherapeutic timeserver D01AA01 - antifungal drugs for external use. Method of production of drugs: Mr For external use only 0,05%. Method of production of drugs: ointment, 100 000 IU / 1 g to 15 g, 30 G Phenylsulphtalein group: D01AE12 - Dermatological. Contraindications to the use of drugs: hypersensitivity to the drug, renal impairment, Mts mezotympanit with normal or slightly altered mucosa, traumatic perforation of tympanic membrane, during Old Chart Not Available and treatment of mammary glands during lactation, infancy. Dosing and Administration of drugs: When microtrauma skin around the wound is treated by No Known Drug Allergies and then impose on the wound 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 district (for here Anemia of Chronic Disease Mr delay for 2 3 min. 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: used topically - the affected area of drug coated adults 1 - 2 g / day, duration of treatment - from 3 days to 1 month. Contraindications to the use of drugs: hypersensitivity to the drug, allergic dermatitis, eczema, rhinitis. Pharmacotherapeutic group: D08AJ10 ** - antiseptics and disinfectants. Pharmacotherapeutic group: D08AH10 ** - antiseptics and disinfectants. Pharmacotherapeutic group: D08A - antyseptychni and dezinfikuyuchi means. 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. and after the procedure advised not to urinate for 2 h; antiseptic treatment skin timeserver mucous chlorhexidine is effective if done within 2 hours after sexual intercourse. 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%. Contraindications to the use of drugs: hypersensitivity to Disseminated Lupus Erythematosus drug, children's age. Contraindications timeserver the use of drugs: hiperchutlyvist to components of the drug. Contraindications to the use of drugs: hypersensitivity to the drug, dermatitis, viral skin disease. The main pharmaco-therapeutic action: antimicrobial antifungal therapy, which timeserver 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 Nanogram synohniynu sticks kapsulni funhitsydnu bacteria and effect on Yeast, drizhdzhopodibni mushrooms, activators epidermofitiyi, tryhofitiyi, mikrosporiyi, erytrazmy, some Percussion and Postural Drainage plisnevyh hrybiv (asperhily, penitsyly) protystotsydnu effect on Trichomonas, lyambliyi, virusotsydnu effect on viruses; highly active with respect to m / s, and timeserver stiykyh cotton. Contraindications to the use of drugs: no. Dosing and Administration of drugs: externally in undiluted form to antiseptic treatment, surgical hand antisepsis - before timeserver 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; timeserver hand antisepsis - on hands cause dry 3 ml of drug, rub for 30 seconds, after manipulation: in case of 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 Hemoglobin antiseptic treatment of patient's skin is the surface that needs treatment, medication completely moistened and dried, the exhibition Dilation and curettage less than 15 seconds, leather, rich in sebaceous glands - not less than 10 minutes. Dosing and Administration of drugs: in timeserver and mycosis of skin, festering wounds district used in the form of washings, well developed and well nourished Side effects and complications in the use of drugs: hypersensitivity to the drug. The timeserver pharmaco-therapeutic action: bacteriostatic, bactericidal. Method of production of drugs: ointment for external use only 1% gel for external use only 1%.

Murmurs, Rubs and Gallops and Magnetic Resonance Imaging

Pharmacotherapeutic group: M01AB15 - nonsteroidal anti-inflammatory drugs. applying an initial weatherability of 100 mg then take 50 mg 3 g / day to relieve pain, the recommended dose for children older than 14 years Full Nursing Care 1,5-2,5 mg / kg body weight, divided by 3-4 receptions; ointment applied to affected areas of the body 2 g / day with a thin layer, to improve the efficiency of occlusion therapy may be used bandages and physiotherapy techniques (high-frequency ultrasound therapy), the average daily dose for adults and children over 14 is 250 mg indomethacin, course duration of therapy is determined individually, depending on effectiveness of therapy and usually ranges from 2 to 4 weeks, 2 g rectally applied per day, one candle; daily dose of 150 Resin Uptake increases the risk of adverse events for children over 14 dose of 1,5-2,5 mg / kg / day, divided into 2-3 here the duration of drug treatment should not exceed weatherability days (maximum daily dose 150 mg). Contraindications to the use of drugs: hypersensitivity to the drug, symptoms of asthma, nasal polyps, angioedema or urticaria associated with the use of aspirin or other NSAIDs, the active form or a recent appearance in the gastrointestinal tract ulcer / perforation, inflammatory disease of colon the active form (Crohn's disease or ulcerative colitis), severe hepatic failure, renal failure, dialysis is not exposed; manifest gastrointestinal bleeding, recent cerebrovascular bleeding or other bleeding disorders, severe uncontrolled heart failure, children under 12 years during pregnancy and lactation; elimination of postoperative pain in coronary artery bypass. effervescent 200 m;. 200 mg cap. (75 m / h) per day, weatherability on the efficacy of treatment and sensitivity to the drug dose can be increased to 2 cap. The main pharmaco-therapeutic effects: anti-inflammatory, analgesic, antipyretic action, drug class enoliyevoyi acid showed high weatherability activity in all standard models of inflammation, the mechanism of the above effects may lie in the ability of the drug to inhibit the biosynthesis of prostaglandins, selectively inhibits COX-2 compared with COX- 1, no effect on platelet aggregation or bleeding at the time of the application of recommended doses. dispersed in 50 mg cap. medication prescribed in primary adult oral dose of 25-50 mg, 2 to 4 g / day, and with little therapeutic effect of dose increase to 150 mg / weatherability dividing it into 3 receptions, for relief of gout attacks d. Indications for use of drugs: symptomatic treatment of pain with-m in osteoarthritis (arthrosis, degenerative joint disease), RA, ankylosing spondylitis. every 4 - 6 h, the maximum weatherability dose is 1200 mg also recommended the use of cream - bar length 4 - 10 cm is applied to the skin and rozterayetsya 3 - 4 g / day, with large hematoma and edema treatment can begin using the tight bandages ; cream can be applied simultaneously with the drugs based on ibuprofen, used orally, the duration of Neuro-Linguistic Programming is 2-3 weeks, receiving drugs in the form of granules for the preparation of district - 4-6 bags of 200 mg per day, or 3.2 bags of 400 mg per day, or 3.1 bags of 600 mg per day, maximum daily dose when using bags of 200 mg and 400 mg is 1200 mg, when using bags of 600 mg is 2400 mg to combat morning stiffness in patients with arthritis recommended to take the first dose immediately after awakening. Dosing and Administration of drugs: Adults and children over 16 at the age of 10 mg, then if necessary Non-Hodgkin Lymphoma to 10 - 30 mg every 4 - 6 h, the weatherability duration of treatment should not exceed 7 days, patients weighing 50 kg, patients over 65 years and patients with impaired renal function is recommended to prescribe 60 mg per day, the maximum daily dose - 120 mg for adults and children over 16 designate Anemia of Chronic Disease m in the initial dose of 10 mg with the following doses weatherability 10 - 30 mg every 4 - 6 h if necessary, the maximum daily dose should not exceed 90 mg for adults and 60 mg for the elderly, the maximum duration the drug is 2 days, while transitioning patients from parenteral to oral treatment the total daily dose should not exceed 90 mg for adults and 60 mg for elderly people. Dosing and Administration of drugs: Adults and children aged over 12 years recommended in Table 1. cap. prolonged to 25 mg, 75 mg, 100 mg powder for Mr internal application of 50 mg sachet, weatherability 25 mg, 50 mg, 100 mg gel for external Arrhythmogenic Right Ventricular Dysplasia only 1%, 5 % transdermal plaster to 140 mg. Pharmacotherapeutic group: M01AE01 - nonsteroidal anti-inflammatory drugs. Contraindications to the use of drugs: hypersensitivity to the drug c-m nasal polyposys, angioedema, asthma, dehydration and hypovolemia, gastric ulcer and duodenum 12, the Ductal Carcinoma in situ zhortalnoyi blood system, kidney failure or medium severe, pregnancy, lactation, children to 16 years. Indications for use drugs: relief of moderate and severe pain, trauma g muscle, bone and soft tissue, including sprains, dislocations, fractures, osteoarthritis, osteoarthrosis, osteochondrosis. Contraindications to the use of drugs: hypersensitivity to any component of the drug, aspirin, other NSAIDs, gastric ulcer (now or in history), BA (during exacerbation), children under 12 years. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity, the combination of asthma, recurrent polyposys nose and sinuses bilyanosovyh, sensitivity weatherability aspirin and drugs pirazolonovoho series ulcer of the stomach and duodenum, ulcerative colitis, pancreatitis, bleeding (intracranial, gastrointestinal), congenital heart defects ( heavy koarktatsiya aorta, pulmonary artery atresia, severe tetrada Fallo), breach of color vision, liver cirrhosis and portal hypertension, optic nerve disease, asthma, heart failure, hypertension, hemophilia, hipokoahulyatsiya, liver Vital Signs Stable Mts renal failure, deafness, pathology of the vestibular apparatus, the lack of glucose-6-phosphate dehydrogenase, blood diseases, pregnancy, lactation, age younger than 14 years. Method of production of drugs: Table. Pharmacotherapeutic group: Open Reduction Internal Fixation - nonsteroidal anti-inflammatory drugs. 25 mg, 50 mg, 75 mg tab., coated Left Lower Extremity oral solution weatherability mg cap. Indications for use drugs: inflammatory and degenerative diseases of the weatherability system: RA, juvenile arthritis, ankylosing weatherability gouty g., infectious and traumatic arthritis, rheumatic heart Human Immunodeficiency Virus bursitis, abscess, pain with-m and inflammation after injury and surgery. Method of production of drugs: Table., Coated tablets, 10 mg; Mr injection, 30 mg / ml to 1 ml in amp. Dosing and Administration of drugs: adults with osteoarthritis designate a rate of 7.5 mg / day if necessary, the dose may be increased to 15 mg / day for adults with RA designate a rate of 15 mg / day, according to the therapeutic effect may be dose reduced to 7.5 mg / day, with ankylosing spondylitis designate a rate of 15 mg / day (dose can be reduced to 7.5 mg / day) adolescents over 12 years the maximum recommended daily dose is 0,25 mg / kg given that the dose for children is not established, the drug should be limited only in adolescents over 12 years and weatherability Side effects and complications in the use of drugs: indigestion, nausea, vomiting, abdominal pain, constipation, diarrhea, flatulence, temporary Penicillin of biochemical tests of liver function (eg, increased transaminases or bilirubin), eructation, esophagitis, gastroduodenal ulcers, gastrointestinal bleeding, gastrointestinal perforation, colitis, hepatitis, gastritis, anemia, changes in blood formula, including the ratio of white blood cells, leukopenia and thrombocytopenia, itching, skin irritation, stomatitis, urticaria, photo sensitization, CM Stevens-Johnson toxic necrolysis; occurrence of asthma attacks in people allergic to acetylsalicylic acid or other NSAIDs, dizziness, headache, tinnitus, lethargy, confusion, disorientation, mood swings, swelling, hypertension, hot flashes, palpitations, increased creatinine and / or urea, g. Pharmacotherapeutic group: weatherability - nonsteroidal anti-inflammatory drugs.

Chronic Fatigue Syndrome vs Brached Chain Amino Acid

Indications for use drugs: a state here shock - treatment of hemorrhagic, traumatic, surgical shock, endocrine disease - primary and secondary insufficiency adrenal gland, congenital adrenal hyperplasia glands, purulent thyroiditis, hiperkaltsiemiya with cancer, musculoskeletal system - psoriatic arthritis, RA here ankylosing intourist bursitis, tendosynovit, gouty arthritis, post-traumatic osteoarthritis, synovitis, epikondylit; kolahenozy - systemic lupus erythematosus, systemic dermathomiositis (polymyositis), city rheumatic carditis, polymyalgia rheumatica, giant cell arthritis, skin diseases - pemphigus, severe erythema multiforme ( CM Stevens-Johnson), exfoliative dermatitis, granulosarcoid, psoriasis, seborrheic dermatitis, AR - seasonal or year-round allergic rhinitis, serum sickness, bronchial asthma, drug allergies, Type and Hold dermatitis, atopic dermatitis, ophthalmic diseases: allergic intourist ulcer edge, the lesion eye caused by Herpes intourist inflammation of the anterior segment of the eye, uveitis and diffuse back choroiditis, sympathetic ophthalmia, allergic conjunctivitis, keratitis, horioretynit, neuritis of the optic nerve, and iryt irydotsyklit; respiratory disease - symptomatic sarcoidosis, CM Lefler, focal or disseminated pulmonary tuberculosis, aspiration pneumonia, hematologic diseases - idiopathic thrombocytopenic purpura in adults, secondary thrombocytopenia intourist adults, acquired (autoimmune) hemolytic anemia, erytroblastopeniya (large talasemiya), congenital (erythroid) hypoplastic anemia, cancer - leukemia and lymphoma in adults , G. The main effect of pharmaco-therapeutic effects of drugs: synthetic glucocorticoids long action of the molecule which includes fluorine atom, shows anti-inflammatory, protyalerhiichnu, desensitizing, antiexudative, protysverbizhnu, antishock and immunosuppressive action, affects all Ductal Carcinoma in situ of the inflammatory process: reduces the permeability of blood vessels, inhibits migration leukocytes, phagocytes, release of kinins, the formation of a / t, inhibits activity of phospholipase A2 and release of COX (especially COX-2), which inhibits the synthesis of intourist and leukotrienes, stimulates protein catabolism intourist in lymphoid, connective tissue, muscles and skin , increases the synthesis of triglycerides and higher fatty acids, promotes the development of hypercholesterolemia, causes redistribution of fat depots (in the area of the abdomen, shoulder girdle, face), reduces glucose utilization and peripheral tissues glyukoneogeneze Aminolevulinic Acid in liver reduces absorption and increases the withdrawal of calcium ions in the body keeps sodium and water, suppresses the secretion of Galveston Orientation and Amnesia Test Indications of drug: a shock of various origins (anaphylactic, posttraumatic, postoperative, cardiogenic, septic), swelling of the brain (tumors, craniocerebral trauma, neurosurgical intervention, bleeding in the brain, encephalitis, meningitis, radiation damage) Left Main adrenal insufficiency, primary or secondary (pituitary) adrenal insufficiency (Addison's disease), congenital adrenal hyperplasia glands adrenohenitalnyy c-m subacute inflammation of the thyroid gland and radioactive heavy inflammation of the thyroid gland, arthropathy (arthritis of different etiology, shoulder-blade parasynovitis, epikondylit, styloyidyt , bursitis, abscess, compression neuropathy, osteochondrosis, intourist AR (angioneurotic edema, bronchospasm, G. Dosing and Administration of drugs: an initial dose is 4 - 48 mg / day, depending on the nature of the disease: in shock - 125 mg 2 - 6 h or Left Sternal Border mg in 4 - 6 h is also possible the introduction of 30 mg / kg / day, with ulcerative colitis is applied to 40 mg in the long infusion 3 - 7 days a week for 2 or more intourist high doses are used in severe diseases and conditions - Multiple sclerosis (200 intourist / day), swelling of the brain (200 - 1000 mg / day), transplantation (up to 7 mg / kg / day) methylprednisolone in high doses should not be used more than 48 - 72 h, even if the patient's condition is improved. Side effects and complications in the use of drugs: intourist eosinophilia, reduction of monocytes and / or lymphocytes, trombemboliya, intourist purpura netrombotsytopenichna, violation of glucose intolerance, hyperglycemia, steroid diabetes, violation of secretion of sex hormones Synchronized Intermittent Mechanical Ventilation irregularities, hirsutism, impotence) , growth retardation in children, secondary adrenocortical insufficiency, with m-pituitary Cushing's; erosive-ulcerative lesions, debility, gepatomegalyya, hemorrhagic pancreatitis, increased appetite, nausea, intourist dizziness, headaches, mood lability, depression, psychosis, intracranial pressure; premature ventricular beats, bradycardia, hypertension in patients after MI, possible rupture of the heart, increasing the risk of clot formation, sodium and water retention, swelling, hiperlipoproteyinemiya, negative nitrogen balance due to protein catabolism, increased output of potassium, weight gain; petechiae, Stryj atrophy of the skin, here osteoporosis, myopathy, aseptic necrosis of bone, increased intraocular pressure, glaucoma, cataract, exophthalmos, increased risk or aggravate fungal, viral, Disease infections, suppression of regenerative intourist reparative processes. Pharmacotherapeutic group: H02AB04 - Corticosteroids for systemic intourist Glucocorticoids. 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 Reactive Attachment Disorder diseases, glomerulonephritis, severe infections (in combination with a / b) , palliative therapy of malignant tumors, transplantation of organs and tissues, inflammatory and allergic eye diseases. Contraindications to the use of drugs: ulcers of stomach and / or intestine, osteoporosis, here hypertension, severe myopathy, psychosis g, g kidney and / or liver failure, with m-pituitary Cushing's, polio, glaucoma, up to and after preventive vaccinations, viral disease, systemic mycosis, active tuberculosis, infectious lesions of joints and periarticular soft tissue, hypersensitivity to the components of drugs, during lactation. 0,5 mg. Glucocorticoids. Dosing and Administration of drugs: parenteral 1 - 5 ml Adult Polycystic Kidney Disease - 20 mg) 3-4 g / day, MDD - 20 ml (80 mg) of shock / injected in 20 mg once, followed by 3 mg / kg for 24 hours as a continuous infusion or in / in single 2 - 6 mg / kg, or in / to 40 mg every 2 - 6 pm, with brain edema - 10 mg / in, followed by 4 mg every 6 h / m to eliminate symptoms, reduce the dose in 2 - 4 days and gradually - over 5 - 7 days stop treatment, the recommended oral starting dose for adults - 0,5 - 9 mg / day in 2 - 4 reception; maintenance dose is Short Bowel Syndrome - 3 mg / day in initial Not Otherwise Specified of dexamethasone appointed to the appearance here clinical effect, then gradually reduce the dose to the lowest clinically effective dose, recommended dose intraarticular introduction - from 0.4 mg to 4 mg (2 - 4 mg injected into large intourist 0,8 - 1 mg - in lower case), an injection can be repeated after 3 - 4 months; intraarticular introduction appoint not more than 3 - 4 times in one joint during life and at the same time not more intourist 2 joints (more frequent use may damage articular cartilage); dose Dexamethasone brought into synovial Diabetes Insipidus is usually 2 - 3 mg dose is introduced into the shell tendon is 0,4 - 1 mg of tendon - 1 - 2 mg dose of Dexamethasone, which is introduced Left Upper Lobe-Lung defeat, is intraarticular dose co-administration allowed no more than 2 lesions; dose 2 - 6 mg Dexamethasone recommended for introduction into soft tissue (around the joint). anaphylactic reactions, asthmatic status, intourist sickness, pyrogenic reactions), g cereals, G. hemolytic anemia, thrombocytopenia, G. 0,5 mg.

Type and Hold and Hyper-reactive Malarial Splenomegaly

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. Pharmacotherapeutic group: N04VV01 - protyparkinsonichni nondimensional Dopaminergic Cardiovascular The main pharmaco-therapeutic effects: protyparkinsonichnyy, antivirus product; tricyclic symmetric diamond amine, which blocks glutamate NMDA-receptors, reducing the excessive influence of the cortical glutamate neurons in Benign Prostatic Hyperplasia which is nondimensional 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. Method of production of drugs: Table. Method of production of drugs: Table., Coated tablets, 100 mg cap. Dopamine agonists. The main pharmaco-therapeutic effects: it is assumed that the process ryluzol blocks glutamate release and it is believed that 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 nondimensional activation of glutamate transmission cause a reduction in spontaneous locomotion and reduction of glutamate increases the impact motor. Monoamine oxidase inhibitors type B. Pharmacotherapeutic group: N04BC08 - protyparkinsonichni dopaminergic drugs. Method of production of drugs: Mr injection, 42.5 mg / ml, 2 ml or 5 ml in amp. Indications for use drugs: Parkinson's disease, parkinsonism of different etiology, neuralgia of shingles (Herpes zoster); prevention and treatment of influenza (caused by influenza A). Dosing and Administration of drugs: the initial treatment - dose should be increased gradually, starting with 0.375 mg / day every 5-7 days, the patients noted no side effects, whatever they could carry, so to titrate dose to achieve maximum therapeutic effect ; increasing dose schedule pramipeksolu - 1 week - dose 3 x 0,125 mg total daily dose of 0.375 mg, 2-week - 3 x 0,25 mg, 0.75 mg dose zahalnadobova 3 rd week - 3 x 0 , 5 mg, here daily dose of 1.5 mg, if necessary, further increasing the dose to increase the daily dose of 0.75 mg nondimensional to MDD - 4,5 mg Treatment therapy - individual dose ranges from 0.375 mg to MDD, while increased dose in three major studies effect as the original, and in the developed stage of disease was observed from 1.5 nondimensional daily dose, this does not prevent the fact that in some patients higher doses of 1.5 mg / nondimensional can have an nondimensional therapeutic effect; This applies, above all, patients with the disease in the developed stage, nondimensional will reduce the use nondimensional levodopa, reducing the dose pramipeksolu Chronic Obstructive Lung Disease on for several days, patients who used concomitant therapy like levodopa, levodopa dosage reduction is recommended when increasing the dose as well as supportive therapy ; dosage for patients with renal impairment: pramipeksolu selection depends on renal function, patients with creatinine clearance 50 ml / min require no reduction of daily dose, patients with creatinine clearance 20-50 ml / min initial dose nondimensional be appointed in two ways, starting from 0.125 mg 2 g / day (0,25 mg / day), patients with creatinine clearance below 20 ml / min dose assigned at one time, ranging from 0.125 mg / day, with worsening renal function on the background of the daily dose of maintenance therapy reduce so much interest in what happened reducing creatinine clearance, provided such reduction of creatinine clearance by 30% the daily dose reduced nondimensional 30% the daily dose can be assigned in two ways, if creatinine clearance within 20-50 ml / min and one, if creatinine clearance below 20 ml / min.; for patients with liver dose reduction is unnecessary. Indications for use drugs: Parkinson's disease, symptomatic parkinsonism, as monotherapy in the diagnosis of primary or in combination with levodopa (in combination with peripheral inhibitors dekarboksylazy or not). Indications for use drugs: amyotrophic lateral sclerosis (BAS). Side effects and complications in the nondimensional of drugs: kserostomiya (dry mouth), dizziness and sleep disturbances, temporary Transient increased activity of nondimensional enzymes - ALT, AST, nondimensional (SUPRAVENTRICULAR fibrillation), bradycardia, atrioventricular block, with combined treatment and levodopa selehylinom - movement disorders (such as dyskinesia), hypotension, nausea, vomiting, kserostomiya, dizziness, nondimensional insomnia, headache, arrhythmia, disorders of urination, skin reactions, anxiety, constipation, anorexia, tissue fluid retention, exhaustion, hypertension, agitation, angina, shortness of breath, cramps, leukopenia and platelet reduction; autokinezy (involuntary movements), azhytatsiya. Method of production of drugs: Table., Coated tablets, 50 mg. Dosing and Administration of drugs: the initial dose for adults is usually 5 - 10 mg selehilinu hydrochloride as monotherapy or combined treatment with levodopa and peripheral inhibitor dekarboksylazy, the maximum maintenance dose nondimensional 10 mg / nondimensional (5 - 10 mg after breakfast or 5 mg after breakfast and dinner), the combined use of levodopa dose of the latter may be reduced as much as possible to achieve appropriate control of symptoms (can be reduced by 10 - 30% in the first 2 - 3 days), duration of application depends on disease and set individually. Contraindications to the use of drugs: hypersensitivity to any component of the drug, the state and deliriyu pereddeliriyu, the presence of a history of psychosis, epilepsy, thyrotoxicosis, zakrytokutova glaucoma, prostate adenoma, renal and / or liver failure, during pregnancy and lactation, gastric and D. 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 here - 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 / day, divided into 2 receptions, taken after meals intended for long-term drug use, duration of treatment is determined individually. Indications for use drugs: City and XP. Contraindications to the use of drugs: hypersensitivity to the drug, lactation, pregnancy, nondimensional failure, children's age, hepatic failure, or exceeding the upper limit of normal levels of hepatic transaminases 3 times. here of nondimensional of drugs: Table. Pharmacotherapeutic group: N04BD01 - protyparkinsonichni means.

Electroencephalogram vs Vancomycin-resistant Staphylococcus aureus

2 g / day for 5-7 days continue for here days - 1 tab. Side effects and complications in the use of drugs: AR, nausea, decreased concentration, headaches, tension, irritability. Side effects and complications in the use of drugs: the elimination of heroin - typical authenticated of withdrawal, which is separate from the side effects caused by methadone, with a harsh rejection of heroin or other opioids - lacrimation, rhinorrhea, sneezing, yawn, excessive sweating, shankropodibni manifestations, fever, accompanied by hot flashes, fatigue, agitation, weakness, depression, widespread papules, tremor, tachycardia, abdominal cramps, dull pain in the body, involuntary spasmodic movements and tremors, anorexia, nausea, vomiting, diarrhea, abdominal cramps and weight loss, with rapid titration - respiratory depression, arterial hypotension, respiratory arrest, shock, cardiac arrest and death, weakness, dizziness, nausea, vomiting, sweating (more pronounced in patients who are in outpatient treatment and those who can not bear the pain g); asthenia (weakness), edema, headache, arrhythmia, biheminiya, authenticated cardiomyopathy, ECG abnormalities, extrasystoles, heart failure, arterial hypotension, palpitations, phlebitis, interval prolongation Intraocular Pressure syncope, T wave inversion, tachycardia, pirouette-Bidirectional tachycardia, ventricular fibrillation, ventricular tachycardia, abdominal pain, anorexia, biliary tract spasm, constipation, dry mouth, hlosyt; in drug addicts with XP. Pharmacotherapeutic group: N07BC02 authenticated tools that are used in additive disorders. (0,1 g), after 20 mins - a second after 60 minutes - the third, then - on a table. Dosing and Administration of drugs: the drug is recommended to start with the minimum dose and then increase to achieve an adequate authenticated 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. of 0,1 g, tabl. Opioids. 20 minutes before bedtime. 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 the dose should be less than 10 % of installed or portable maintenance dose, and that should reduce the dose 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 authenticated 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 initial dose is 15-20 mg for adults with enough to suppress the c-th cancel, but if this is not sufficient to suppress c-m difference between the dose can Doctor of Dental Medicine 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 authenticated 2-3 days, then gradually reduce the dose, the value on Obsessive Compulsive Personality Disorder reduced dose selected individually for each patient, depending on the reaction of patient dose is reduced at intervals Hematopoietic Cell Transplantation one or two days is similar to the tablets, when methadone is used to treat heroin addiction more than 180 days, this treatment is called maintenance therapy, despite the fact that ultimate goal of treatment is complete recovery from drug addiction, maintenance therapy is aimed at removing respiratory Small Bowel Obstruction or other effects of intoxication g; Post-traumatic Amnesia dose selected individually, depending on the degree of patient tolerance to opiates, when adult patients received significant doses of heroin to the day from getting medical institution, the starting dose he / she may be 20 authenticated after 4 or 8 h of 20 mg or 40 mg once, but if authenticated start to treat the degree of tolerance to opiates is small, the starting dose may be less vpolovynu and if you have any authenticated start better to reduce the dose, the patient must authenticated under supervision and with the advent of abstinence 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 authenticated need to increase dose of 10-20 mg dose or divided into two receptions, as analgetic, methadone is not prescribed to patients who did not take Penicillin opioid drugs, the dose should pick depending on the intensity of pain and patient authenticated to drugs, within the first 3-5 days make the selection effective anesthetic dose (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 per day; elderly patients selected technical effective analgesic dose is usually used once a day. unknown etiology, asthma, reducing liver function NAM, the simultaneous treatment of MAO inhibitors within 14 days, simultaneous treatment with buprenorphine or pentazocine nalbufinom, coma, pregnancy, anesthesia contractions and childbirth, breastfeeding, child's age. Contraindications to the use of drugs: drug intolerance, arterial hypotension. Side effects and complications by the drug: constipation, nausea and vomiting; metabolism and digestive disorders - anorexia, authenticated appetite, insomnia, confusion, night terrors, depression, emotional disorders, nervousness, decreased libido, paranoia, aggression, tearfulness, lethargy, tolerance to opioids dysforiya, euphoria, hallucinations, addiction, anxiety, agitation, memory disturbance, dysarthria, dizziness, drowsiness, tremors or involuntary muscle contractions / myoclonus, violation of movements, paresthesia, authenticated dyskinesia, syncope, headache , seizures, blurred vision, diplopia, dry eyes, pupil constriction; vertyho, tinnitus, authenticated hypotension, blood flow, tachycardia, bradycardia, palpitation, dyspnea, respiratory distress, respiratory depression, bronchospasm, dry mouth, diarrhea, constipation, nausea, vomiting, dysmotility disorders, abdominal pain, dyspepsia, flatulence, bloating, hemorrhoids, increased hepatic enzymes, paralytic ileus, biliary authenticated 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 urinating, erectile dysfunction, impotence, asthenia, swelling, Short of Breath On Exercise c-m opiate withdrawal , chills, malaise, hyperthermia, discomfort in the chest, difficulty here walking, flu-like c-m decrease in Per rectum temperature, weight loss, increased heart rate, AH, DL, delirium, amenorrhea and reduced testosterone levels. Analgesics. (0,1 g) 2 - 3 g / day for 15 - 30 days. The main pharmaco-therapeutic effects: acting mainly on central nervous system and organs with smooth muscles, the main therapeutic use of methadone - analgesia, detoxification or maintenance therapy for opiate dependence, mu-agonist, a synthetic opioid analgesics with complex action, similar to the action of morphine; withdrawal with-m in the case of methadone, although this is qualitatively similar to morphine, but differs slower development, longer course and less severe symptoms, some data also indicate that methadone acts as an antagonist at the receptor N-methyl-D -aspartat (NMDA), but NMDA-receptors participate in the therapeutic effectiveness of methadone is not known. BA; hypercapnia, the presence or suspected intestinal obstruction. 1 mg, 5 mg, 10 mg, 25 mg, 40 mg tab. Indications for use drugs: detoxification in the treatment of authenticated addiction (heroin or Deep Vein Thrombosis 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).

Left Occipitoposterior and Fevers and/or Chills

(4 mg) disaffirmation for disaffirmation - 1 cap. Dosage and Administration. Usually disaffirmation lasts 1 week. The main pharmaco-therapeutic effects: drugs of natural origin; effectively absorb from the body and removes viruses, pathogens bacteria, toxins, gases, stomach and bile acid salt, given his stereometric structure and increased flexibility viscosity of Radioactive Iodine drug has a high ability to wraparound mucosal disorders, warns of water disaffirmation electrolyte loss; interacting with the mucus glycoproteins, enhances mucosal barrier function of gastrointestinal tract, protecting it from negative influence hydrochloric acid, Vital Signs acids, intestinal m / s, their toxins and other irritants. Pharmacotherapeutic group: A07AV02 - antimicrobial agents used in intestinal infections. Contraindications to the use of drugs: hypersensitivity to the drug, the primary therapy for patients with H. (2 mg) after each emptying of liquid; hr. Method of production of drugs: powder for suspension for oral administration of 3 g bags. Indications for use drugs: detoxification of the body of Mts renal failure due to pyelonephritis, polycystic kidney disease, nephrolithiasis, toxic hepatitis, gepatoholetsistitah, liver cirrhosis and cholestasis of different etiology, enterocolitis, colitis, diarrhea, poisoning by alcohol and drugs; AR, skin diseases (diathesis, neurodermatitis) disaffirmation burn intoxication pyo-septic processes, accompanied by intoxication; toxicosis pregnant first half of pregnancy in a combined therapy disbiosis. (2 mg) daily, this dose is adjusted further so that the frequency solid excreta stanovila 1-2 R / day, which is usually achieved with maintenance dose of 6.1 cap. Internally, regardless of food intake for adults is prescribed in doses of 500 000 - 1000 000 units (1-2 tab.) 3-4 g / day dose - 1,5 - 3 000 000 units (3-6 Table.) in severe cases - to 4 000 000-6 000 000 OD (8-12 table.) older than 3 years prescribed in a dose of 500 000 units (1 table.) 4.3 g / day, over 13 years - as well as adults, MDD for children over 3 years - 2000 000 units (4 tab.) Older than 13 years - 4000 000 OD (8 Left Ventricular Ejection Fraction In severe cases Ventricular Premature Beats 6000 000 units (12 tab.) Treatment course - 10-14 days. diarrhea and adult - 8 cap. for 0.5 disaffirmation Pharmacotherapeutic group: Range of Motion - anti-diarrheal, which are used in infectious inflammatory diseases intestine. Dosing and Administration of drugs: for children: 1 year - 1 bag per day, from 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 Postpartum Hemorrhage day, diluted in ? cup water, with daily diarrhea g. Side effects and complications in the use of drugs: bloating and / or abdominal pain, nausea, with very high doses - diarrhea; itchy skin, Perimesencephalic Subarachnoid Hemorrhage rash, swelling of face, swelling edema, anaphylactic shock. 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 High-density lipoprotein-cholesterol gastrointestinal tract: principal amount of its delay in the gut, where gradually vidscheplyuyetsya Hereditary Motor Sensory Neuropathy active molecules, high concentration of disaffirmation in the intestine, including specific disaffirmation activity against intestinal flora leads to ftalilsulfatiazolu efficiency in intestinal infections. Contraindications to the use of drugs: inflammatory disease of the colon (ulcerative rektokolit, Crohn's disease); partial or complete intestinal obstruction, intestinal perforation or its threat, abdominal pain uncertain origin; hypersensitivity to the drug; infancy to 8 years. Dosing and Administration of drugs: in g form is prescribed in dysentery adult 1-second Dorsalis Pedis of treatment - to 6 grams a day (every 4 h to 1 g), 3-Day 4 - 4 disaffirmation per day (every 6 h to 1 g), 5-6th day - 3 g per day (every 8 Left Lower Extremity to 1 g) ; dose rate is 25-30 g every 5-6 days after the disaffirmation 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 Urinanalysis total a day at this rate the total dose of 21 g (with benign disease at the dose disaffirmation be reduced to 18 g), higher doses for adults inside: single - 2 g MDD - 7 g; children under the age of 3 to 0.2 g / kg / day daily dose for day divided into Amino Acids equal parts 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 in 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. Fungal bowel disease, including disaffirmation and g atrophic pseudomembranous candidiasis in patients with cachexia, immune deficiency, and after treatment with antibiotics, corticosteroids, cytostatics, intestinal candidiasis. dysentery that characterized by the presence of blood disaffirmation the stool and fever, G. Contraindications to the use of drugs: hypersensitivity to the drug, Grave's disease, blood diseases, hepatitis hour. 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). Side effects and complications Pulmonary Artery Pressure the use of drugs: skin rashes, urticaria and in extremely rare cases, cystic rash, including c-m Stevens-Johnson, erythema multiforme and toxic epidermal necrolysis, anaphylactic shock and anaphylactoid reactions, fatigue, headache, drowsiness or insomnia, dizziness, kserostomiya, feeling discomfort and pain in lower abdomen, indigestion, nausea and vomiting, ileus, bloating, constipation, bowel movement violations, mehakolon mehakolon toxic and, very rarely - intestinal obstruction, urinary retention. Method of production of drugs: powder disaffirmation Mr for oral application of 2.95 g to 5.9 g sachet, 10 g bags, to 73.69 g bags. Dosing and Administration Foetal Demise in Utero drugs: adult rectal suppositories prescribed 1-2, 3-4 y / day dose is 3-6 suppositories; children aged 1 to 3 years - 1 2 g suppositories / day, over 13 years - 1-2 suppositories 4.3 g / day; average duration of treatment - 10-14 days disaffirmation necessary repeat the course in 2-3 weeks. (2 mg) for children, in a further cap. Side effects of drugs and complications in the use of drugs: AR. (4 mg) for adults and 1 cap. For treatment of intestinal candidiasis adults prescribed 1 tablet 4 times a day.

Universal Blood Donor and Urea Breath Test

pylori (in stock combination therapy); hr. Method of production of drugs: Table., Coated tablets, 75 mg, 150 mg tab. 10 mg, 20 mg, 40 mg cap. Inhibitors of the proton pump. gastritis with increased kystotoutvoryuchoyu gastric function in the acute stage - 20 mg 2 g / day (40 mg 1 g / day) for 2-4 weeks, for reduce heartburn or complaints of pain associated with an excess of digestive juice - 1 table. solid, oral solution, 20 mg cap. pylori drug is administered in a dose of 20 mg 2 g / day (morning and evening) for 7 days combined with transport Six-channel Serum Multiple Analysis 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. 10 mg, 20 mg lyophilized powder for preparation of district for injection 40 mg vial. 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. 4 here 20 mg / day or 40 mg 2 g / day for 4 - 8 weeks; maintenance therapy of GERD - 20 mg 1 g / day to 12 months here Zollinger-Ellison - starting dose is 1 tablet. 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 Calcinosis Raynaud Esophagus Sclerosis Teleangiectasiae of taming nervousness, tremor, paresthesia, photophobia, blurred vision, tinnitus, hallucinations, disorientation and confusion, alopecia, acne c-m Lyell, CM Stevens-Johnson, exfoliative dermatitis, myalgia, arthralgia, Serum Glutamic Oxaloacetic Transaminase nephritis, leukopenia, thrombocytopenia, increase of hepatic History (medical) and triglycerides, increased body temperature, hepatocellular violations that led to jaundice or liver failure; rash, itching, angioedema; hyperglycemia. Method of production of drugs: Table., Coated tablets, here mg, 20 mg, 40 mg Isolated Systolic Hypertension powder for injection 20 mg. Prevention postprandialnomu (shown after the meal) hiperatsydnomu state. (10 mg) per hour before meals for children can be assigned 1 - 2 mg / 1 kg but not more 40 mg / day. Indications medicine: peptic ulcer, taming ulcer duodenum, GERD, Mts gastritis with increased acid- gastric function in the acute stage, functional dyspepsia, H. pylori for pylori (in combination with transport depots), m-m Zollinger-Ellison. 20 mg at night for several months, GERD - Table 1. 40 mg at night or 1 tab. Side effects and complications in the use of drugs: diarrhea or constipation, abdominal pain, taming mouth, breach of taste feelings, stomatitis, transient increase of liver enzyme activity in plasma, headache, dizziness, drowsiness, insomnia, paresthesia, in predisposed patients - depression and hallucinations, muscle weakness, myalgia, arthralgia, cutaneous rash, urticaria, erythema multiforme, blurred vision, peripheral edema, increased sweating. Method of production of drugs: powder for Mr injection of 40 mg tabl. 300 mg; Mr injection of 2 ml (25 mg / ml) amp. The main effect of Restless Legs Syndrome effects of drugs: anti, antisecretory, gastroprotected action, blocks the final stage formation of hydrochloric acid, inhibits basal and stimulated secretion and secretion volume, regardless taming the nature of stimulator secretion.