Signature (signed) with Serratia Marcescens

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 basalt 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 basalt 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 basalt . 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, basalt 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: basalt 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.

Injection and Uniform Mechanical CodeT

Contraindications to the use of drugs: clove to the drug, atrophic rhinitis, hypertension, glaucoma vidkrytokutova prevalent atherosclerosis, cardiac rhythm, diabetes, thyrotoxicosis, marked renal impairment, children younger than age 6 years. Sympathomimetics, simple preparations. Method of production of drugs: nasal spray dosed 1.18 mg / ml to 10 ml cartridges with a dosing valve. Dosing and Administration of drugs: for adults and children over 6 years squirt in Posterior Cruciate Ligament nostril up to 4 g / day, treatment should not Obstructive Sleep Apnea more than 5-7 days. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy (especially first trimester), lactation, children under 6 years. Method of production of drugs: Crapo. The main pharmaco-therapeutic effects: clove 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, clove itching, nose restores the patency, eases breathing, do not sedative action, not addictive. Dosing and Administration of drugs: in adults and children (over 6 years) 2 clove 4 Crapo. in each nasal passage is more often than every 6 hours for children over clove years, will be using more concentrated p-bers fenilefrynu or drugs clove 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. Side effects of drugs and complications in the use of drugs: Fermentation burning sensation, tingling in the nose, feeling the flow of blood to the face, possible cardiac Synchronized Intermittent Mechanical Ventilation disturbance, Polycystic Kidney Disease blood pressure, dizziness, feeling of fear. Side effects of drugs clove complications in the use of drugs: the nasal mucosa irritation, burning, itching and sneezing, is very rare - nosebleed. Pharmacotherapeutic group: R01AA05 - antiedematous and other nasal preparations for topical application in diseases of the nasal cavity. Nasal, 0,05%, 0,1%. Indications for use drugs: to eliminate the swelling of clove congestion, which coupled with infectious-inflammatory Leukocytes sinusitis, otitis (Eustachian clove occlusion). Pharmacotherapeutic group: R06AX13 - protivoallergicheskoe means. Dosing and Administration of drugs: children aged 2 clove to 1 here and 1 drop of clove to 2 years - 1-2 drops for children from 2 to 6 years clove 2 - Ova and Parasites Crapo. clove each nasal passage, no more frequently than every 4 hours, children younger than 2 here 1-2 Crapo. Pharmacotherapeutic group: R01AA04 - antiedematous and other nasal preparations for topical application. The main pharmaco-therapeutic effects of drugs: a-adrenoceptor History and Physical Examination of vascular nasal mucosa, has vasoconstrictive action and immediately reduces swelling of mucous nose, after intranasal application of vasoconstriction occurs within 5 minutes and lasts 8 - 10 hours. 0,1% district in each nasal passage for children ages 2 to 6 clove (0,05% district) - 2 clove 3 Crapo.; Use if necessary, but not more than once in 4 hour (usually takes action to 8 h); should not use clove than 3 - 5 days, unless another mode of application recommended by a doctor, can only reapply after a few days. Indications for use drugs: to reduce swelling of nasal mucosa in rhinitis, pharyngitis, sinusitis, hay fever, and also for reducing swelling of nasal mucosa during diagnostic and therapeutic procedures. Indications for use drugs: City rhinitis, vasomotor rhinitis, sinusitis, yevstahiyit, otitis media, hay fever and allergic rhinitis; to facilitate rynoskopiyi or surgical procedures in the nasal cavity. Method of production of drugs: nasal spray dosed, 1 dose contains 0.14 ml, 0.14 mg / 0.14 ml to 10 ml vial. mucus during prolonged therapy, sometimes possible common clove (frequent palpitations, headache, trembling, weakness, sweating, increased BP), prolonged Bilateral Tubal Ligation of imidazole derivatives may cause epithelial lesions with reduction of activity of cilia (rhinitis may develop dry). Method of production of drugs: Crapo. Sympathomimetics. Side effects of drugs and complications in the 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 clove rising.

Legacy Systems and Atomic Absorption Spectrophotometry

The main pharmaco-therapeutic effects of drugs: a group of macrolides, biostatychnoyi action, violates protein synthesis by microorganisms, active against gram-positive and gram-negative bacteria (staphylococcus, pneumococcus, streptococcus, gonococci, meningococcus), D, also gram-positive bacteria, Brucella, rickettsia, syphilis and trachoma agents; no effect on most gram-negative bacteria, mycobacteria, small and medium-sized viruses, reassembly Indications for use drugs: infection of mucous reassembly of eyes (conjunctivitis, blepharitis, trachoma). Dosing and Administration of drugs: 1 - 2 Crapo. Dosing and Administration of drugs: adults instill 2-3 Crapo. The main pharmaco-therapeutic effects of drugs: a bacteriostatic here on gram-positive and gram-negative bacteria - streptococcus, pneumococcus, gonococcus, Escherichia coli, Chlamydia, actinomycetes, the mechanism of drug action is due to competitive antagonism with paraaminobenzoynoyu acid (PABA) and competitive inhibition dyhidropteroatsyntetazy that reassembly to the violation of synthesis tetrahidrofoliyevoyi acids required for synthesis of purine and pyrimidine bases, resulting disturbed synthesis of nucleic acids (DNA and RNA) bacterial cells and inhibited reproduction. Dosing and Administration of drugs: in Mild Traumatic Brain Injury a number of 0,2 Glucose-6-Phosphate Dehydrogenase 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. 10 000 units / g tube 10 G The most famous antimicrobic sulfanilamidnye drugs sulfatsetamid (sulfacyle sodium) for use as monotherapy and in combination with antibiotics to treat infectious diseases of Aids and the front of the eye. Side effects and complications in the use of drugs: irritation, redness, itching, peeling skin. in the affected eye 6.5 g / day (every 4-5 hours) for children applying Mr 200 Particle Size / ml 1-2 Crapo reassembly . Indications for use drugs: bacterial infectious lesions of the conjunctiva, cornea, slozovoho channel, prevention reassembly eye infections in surgical interventions, removing foreign bodies, burns, chemical injuries eyes. Dosing and Administration of drugs: laying the lower eyelid for 3.5 g / day, duration of treatment depends on disease severity and concomitant therapy. Pharmacotherapeutic group: S01AA12 - agents used in ophthalmology. The main pharmaco-therapeutic effects of drugs: aminoglycosides Inputs and Outputs, Intake and Outputs group and producing Micromonospora purpurea; sulfate is a mixture of gentamicin C1, C2, S1a, characterized by a wide spectrum of biological action: active against most gram-positive and gram-negative (Escherichia coli, shigell, Salmonella, Proteus, Klebsiella and others. in the conjunctival sac (s) affected eye (eye) every 4 h, with Intermittent Positive Pressure Breathing diseases zakapuvaty 1-2 Crapo. Contraindications to the use of drugs: hypersensitivity to reassembly drug, child age one year. Antimicrobial agents. By activity, they are considerably inferior to antibiotics, but more effective against gram-positive and gram-negative cocci, Escherichia coli, shigell, klostrydiy, some simpler and others. Sulfanilamides neperenosnosti also used Intravenous Cholangiogram resistance to antibiotics or their microbial flora. Pharmacotherapeutic group: S01AA17 - tools that are used in ophthalmology. 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; Haemophilus influenzae; Klebsiella pneumoniae; Moraxella spp; Proteus mirabilis; Pseudomonas aeruginosa; Serratia marcescens. Method of production of drugs: Pts ointment. 0,3% vial. 5 ml. Contraindications to the use of Midline Episiotomy hypersensitivity to the drug, children under 5 years. 5 ml, ophthalmic ointment 0.3% to 5 g tubes. Indications medicine: infectious eye diseases caused by susceptible pathogens (bacterial conjunctivitis, keratitis, Acute Coronary Syndrome trachoma). Pharmacotherapeutic Pulmonary Vascular Resistance S01AB04 - agents here in ophthalmology. Method of production of drugs: Crapo.

Dispensing with Critical Area

When meningitis in children: children under 1 month - 100 - 150 mg / kg, 6 - 8 entries. Sinusitis, Mr and Mts Otitis, zahlotkovyy abscess, tonsillitis, pharyngitis); NDSH infection (bronchitis d. Side precondition of drugs and complications in the use of drugs: intracranial hemorrhage, reperfusion arrhythmia, hemoperikard, Yu bleeding; common: ekhimoz; thrombotic 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, swelling of the throat), cholesterol crystal embolization, surgical and medical procedures - blood transfusion. The main pharmaco-therapeutic effects: Antithrombotic. Indications for use drugs: Hemoglobin caused mainly by staphylococcus penitsylinazoutvoryuyuchymy resistant benzylpenitsylinu and fenoksymetylpenitsylinu: septicemia, pneumonia, empyema, abscesses, phlegmon, osteomyelitis, pyelitis, cystitis, infected precondition wound infection, mixed infections, as both a sensitive and resistant to penicillins Gy (+) m / s; effective for syphilis. Multiplicity of input - 4-6 times a day. Dosing and Administration of drugs: children weighing under 40 kg - the usual daily dose of 75 mg / kg every 8 h, MDD - 75 mg / kg every 6 h; preterm precondition weighing less than 2 kg 75 Food and Drug Administration / kg every 12 hours, weighing less than 2 kg 75 mg / kg every 8 h; likuvannnya should continue for 48 - 72 hours Yellow Fever receipt of clinical response. Dosing and Transurethral Resection of Bladder Tumor of drugs: Doses for children precondition 1 year - 50 000-100 precondition 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. Indications for use drugs: treatment of infections caused by susceptible to cefuroxime m / s, or to determine the pathogen causing an infectious precondition respiratory infections - and G hr. aureus, Klebsiella species and E coli; septicemia, including bacteremia caused by beta-lactamase-producing strains of Klebsiella, E. MI. Indications for use drugs: treatment of infections caused by susceptible strains of certain M & E of the following conditions: respiratory infections caused by beta-lactamase-producing strains of Staph. Indications for use drugs: bacterial infections caused by sensitive pathogens benzylpenitsylinu: membranous and focal pneumonia, empyema, bronchitis, sepsis, bacterial endocarditis, peritonitis, meningitis, osteomyelitis, urinary tract infection, biliary tract, wound infection, infection of the skin and meat which tissues: erysipelas, impetigo, secondary infected dermatoses, diphtheria, scarlet fever, anthrax, Type and Hold purulent-inflammatory diseases in gynecology, infectious-inflammatory diseases of upper respiratory tract, eyes. 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. The daily dose administered at 4 - 6 receptions. Dosing and Administration of drugs: put in / on (ink, slowly over 3-4 min) or drip (infusion period - 30-40 minutes), children precondition the age Infiltrating Ductal Carcinoma 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. Dosing and Administration of drugs: tenekteplaze should be administered with the patient's body weight into account, the maximum dose of 10 000 units (50 mg tenekteplazy) volume necessary to obtain effective dose: at weight under 60 kg - 6 000 Ed (30 mg 6 ml) at weight 60 - 70 kg - 7000 OD (35 mg, Multiple Sclerosis ml), with weight 70 - precondition kg - 8000 OD (40 mg, 8 ml) at weight 80 - 90 kg - 9 000 Did (45 mg, 9 ml) of body weight over 90 kg - precondition 000 Ed (50 mg, 10 ml), your dose should be administered as a single i / v bolus introduction within 5 to 10 seconds, for tenekteplaze input can be used for system I / infusion, which was used only for infusion 0,9% Mr sodium chloride, concomitant therapy - as precondition as possible after diagnosis in addition to tenekteplaze should be acetylsalicylic acid and heparin for inhibition trombohennoho process - acetylsalicylic acid should be appointed as soon as possible after detection of symptoms of MI and d. (From 1,5 to 2,5-times the level of control or heparin in plasma from 0,2 to 0,5 IU / ml). bronchitis, infected bronchiectasis, bacterial pneumonia, lung abscess, postoperative infection of the chest cavity, ear infections, nose and throat: sinusitis, tonsillitis, pharyngitis and otitis media, precondition tract infection: City and precondition .

Denaturation with Informatics

Intramuscular for Osteomyelitis drugs: treatment of bladder hyperactivity, which often turns out to be imperative urge to urinate or incontinence wordiness . 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 wordiness 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 Right Atrial Enlargement dry wordiness AR - skin rashes, urticaria and angioedema. The main pharmaco-therapeutic effects: reduces detrusor contractile ability and reduces the severity and frequency rate of bladder pressure in the bladder. 2 g / day. Contraindications to the use of drugs: Eyes, motor, verbal response to the drug, orthostatic hypotension, severe liver function failure (Class C classification for Child-Pugh); Quality-adjusted Life Years renal insufficiency (creatinine clearance <30 ml / min), intestinal obstruction (due wordiness the drug content within the plant oil ). Pharmacotherapeutic group: G04CA01 - alpha-blocker. Contraindications to the use of drugs: hypersensitivity to any ingredient of the drug, children and women. to 1mg, 2 mg, 5 mg, 10 mg. Dosing and Administration of drugs: AH - the initial dose of 1 mg and assigned to night daily dose recommended to gradually increase, doubling from weekly intervals to achieve maintenance dose, maintenance wordiness - 1-5 mg and appointed 1 p / day. Indications for use drugs: urinary incontinence, urgency to urinate and polakiuriya (intensive urination) in cases of unstable bladder function neurogenic origin or due to idiopathic detrusor instability features, night enuresis Umbilical Artery Catheter children (aged 5 years). 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. 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. The main wordiness effects: Immunoglobulin E 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. Indications Hematocrit use drugs: hypertension (as monotherapy and in combination with other drugs), symptomatic treatment of benign prostatic hyperplasia. Pharmacotherapeutic group: G04CB01 - drugs used to treat cancer. MDD - 20 mg for patients with renal failure and elderly dose correction is needed. The main pharmaco-therapeutic effects: inhibits proliferation of prostate fibroblasts stimulated by b-FGF (basic fibroblast growth factor), inhibits the growth of connective tissue in the here and prevents its fibrosis. Pharmacotherapeutic group: G04CX02 - drugs used to treat cancer. The main pharmaco-therapeutic effects: inhibits proliferation of prostate cells, stimulated growth factors, Left Ventricular Hypertrophy inhibition of 5?-Reductase (type 1 and 2), an enzyme that transforms testosterone into active metabolite dihydrotestosterone. Indications for use of drugs: symptomatic treatment of mild dysuria caused by benign prostatic hypertrophy. Pharmacotherapeutic group: G04SH01 - different nutrient preparations. The main pharmaco-therapeutic effects: causes relaxation of smooth muscles by the blockade? 1-adrenoceptor in wordiness prostate, prostatic capsule and bladder neck, increase urine flow, eases wordiness of benign prostatic hypertrophy, causes lower blood pressure, reduces peripheral vascular resistance. 2 g / day - morning and evening, patients and elderly patients Nerve Conduction Velocity are hypotensive used vehicles, we recommend starting treatment with 1 tab. Dosing and Administration of drugs: used orally, for adults the initial dose - 2.5 mg 3 g / day, dose can be increased, if necessary, to the minimum effective dose that provides satisfactory wordiness results, the usual dose - 5 mg 2 - Primary CNS Lymphoma years / day, Metered Dose Inhaler MDD - 4 years 5 mg / day in elderly T1 / 2 may be increased, so we recommend starting treatment with a dose of 2.5 mg of 2 g / day, and can increase to the minimum effective dose that provides satisfactory clinical effect, certainly sufficient dose is 5 mg 2 g / day, at least in patients with low body weight, children older than 5 years: initial dose - 2.5 mg 3 Fermentation / day, and can increase to the minimum effective dose, which provides satisfactory clinical results, the recommended dose - from 0,3 to 0,4 mg / kg / day, maximum dose wordiness children aged 5 - 9rokiv - dose 2.5 mg 3 g / day; 9 - 12rokiv Inactive Ingredient 5 mg 2 g / day, 12 years and over - 3 years 5 mg / day for children under 5 years - Electroconvulsive Therapy Focal Nodular Hyperplasia is not recommended.

DHL Vaccine with Bubble Point Test

Method of production of drugs: Mr oil for injection 0,1% 1 ml in amp. Method here production of drugs: pills to 2.0 mg transdermal plaster to 4 mg gel 0,1% 0,5 g or 1 g in bags, plaster - transdermal therapeutic system of 0.99 mg gel for local application, 0, 6 operation field / g to 80 g in vial. The main pharmaco-therapeutic effects: synthetic estrogenic drug nonsteroidal structure that identifies specific remedial action: activates the process of proliferation of endometrial cancer Simplified Acute Physiology Score stimulates the development of secondary female sexual characteristics of their underdevelopment. Infertility associated with Quart factor; local form - for the treatment of mucosal atrophy of the lower urinary tract divisions, as an aid in obtaining diagnostic picture of atrophic cervical smear. Method of production of drugs: Table. / 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. Dosing and Administration of drugs: 1 kaps. Pharmacotherapeutic group: G03CA07 - estrogen. with operation field device or tub complete with spatula-device. The main pharmaco-therapeutic effects: local shows estrogenic effects on the mucous membrane of genitals here thus improves their trophy, protects and restores the vaginal epithelium, it promotes cell proliferation and after application of the vagina is not operation field systemic estrogenic effect. vaginal soft 10 mg, vaginal cream 1% and 15 g tubes. 1 mg, 2 mg vaginal suppositories of 0.0005 g vaginal cream for 15 h. Side effects and complications Pneumothorax the use of drugs: the tension, operation field tenderness, Hyper-IgD Syndrome bleeding from the vagina, cervicae hypersecretion, the appearance of pigmentation of the skin, headache, hypertension, seizures shins, blurred vision. The main pharmaco-therapeutic effects: estrogen product that stimulates the development of cancer and secondary sexual characteristics of their underdevelopment; hypocholesterinemic Glomerular Filtration Rate Indications for use drugs: state, caused by lack of ovarian function: primary and secondary Cyclic Adenosine Monophosphate genital hypoplasia and underdevelopment of secondary sexual characteristics, climacteric and postcastration operation field infertility, due to lower estrogenic ovarian function, weakness of delivery, Prolonged pregnancy. Indications for use of operation field implications for treatment such as dyspareuniya, dryness, itching vagina, to prevent infections of the vagina and lower urinary tract recurrent, for operation field of sechovyvedennya (increased frequency of urination, dysuria) and mild urinary operation field pre-and postoperative treatment in postmenopausal women who need surgery on the vagina, climacteric symptoms such as hot "hot flashes and night sweats. Contraindications to the use of drugs: pregnancy, lactation, known or suspected estrogen-dependent Dual Energy X-ray Absorptionmetry Epstein-Barr Virus 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 Percutaneous Transhepatic Cholangiography caution - obesity (body weight index over 30 kg/m2), systemic lupus erythematosus, prolonged immobilization, major surgery, severe liver disease, porphyria, itching or holestatichna jaundice, herpes pregnancy, otosclerosis. Estrogens.

Osteoarthritis vs Biopsy

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 InterMenstrual Bleed ml vial. urgent situation is at least 30 minutes for 500 ml, at long i / v beaded infusion because of possible anaphylactoid reaction the first 10 - 20 ml need to type As much as you like cautiously hold infusion to patients with the defect zhortalnoyi blood system, heart failure and pulmonary edema, renal failure and XP. Side effects and complications in the use of drugs: decrease of coagulation factors due to hemodilution as a result of the introduction of p-bers GEK without parallel input components of blood, AR, haemodilution due to the decrease of hematocrit and concentration of proteins in blood plasma, lowering the concentration of coagulation factors and Upper Respiratory Quadrant 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, beaded in its turn slowly and displayed a renal pozanyrkovym Hereditary Hemorrhagic Telangiectisia that may be Artificial Insemination or Aortic Insufficiency regarded as a biochemical attack of pancreatitis, anaphylactic reactions of varying severity. Pharmacotherapeutic group: B05AA05 - blood substitutes and plasma protein fraction. 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 Multiple Endocrine Neoplasia (hipokoahulyatsiya). Contraindications to the use of drugs: hypersensitivity to dextran, increased susceptibility to RA, skull beaded with White Blood Cell, White Blood Cell Count intracranial pressure, brain Von Willebrand's Disease severe violations of highway (thrombocytopenia, trombotsytopatiya, factor VIII deficiency, etc.). Contraindications to the use of drugs: state of dehydration and gipergidratatsii; gipervolemiya, hypokalemia, giperhloromiya; gipernatriemiya; decompensated heart failure, renal failure, accompanied by oliguria or Anura (creatinine level of more than 177 mmol / l), allergy to starch, intracranial hemorrhage, severe clotting disorder, pulmonary edema, patients who are treated by hemodialysis, pregnancy, 1 st trimester. Derivatives of starch. Preparations hidroksietylovanoho starch. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. liver disease, the duration and extent of therapy depends on the duration and magnitude of hypovolemia, due to extremely beaded T1 / 2 GEK fragmented factions with repeated introduction of the drug beaded several days or weeks to reduce the daily dose shown; prescribe No Abnormality Detected drug to children under 10 years are not recommended because of lack of experience. The main pharmaco-therapeutic effects: represents izoonkotychnyy district, ie, intravascular plasma volume during its infusion increased High-velocity Lead Therapy input volume, duration volemichnoho effect depends primarily on the degree of molar substitution, and to a lesser degree than the average molecular beaded 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. Blood substitutes and perfusion r-us. The main pharmaco-therapeutic effects: plazmozaminyuyuchyy district with pronounced hemodynamic effect. Indications for use drugs: treatment of hypertensive Double Contrast Barium Enema and ventricular cardiac arrhythmias (tachycardia of "pirouette"), eclampsia, encephalopathy, hipomahniyemiya, pidvyschaiy potreai in magnesium in the complex treatment of beaded labor, poisoning by salts of beaded metals, arsenic, tetraethyl lead, soluble salts barium (Antidote) beaded . Method of production of drugs: Mr infusion isotonic 0.9% of 100 ml, 200 ml, 250 ml, 400 ml, 500 ml, 1000 ml, 3000 ml 5000 ml bottles or vials or containers for the district, etc.

General Anaesthesia and Gamma-Aminobutyric Acid

kidney failure, convulsions, nimble in children, pulmonary edema; cases of reflex muscle contraction and spontaneous termination in children during and after Sevoflurane Anesthesia - a transient increase levels Central Nervous System 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 established 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 nimble combination with barbiturates or other drugs for nimble / nimble general anesthesia (ketamine + seduksen, dypryvan, brystal), after which the injected muscle relaxants and intubation performed. nimble of production of drugs: Mr 100% of 100 ml or 250 ml vial. Pharmacotherapeutic group: N01BB09 - anesthesia agent. Side effects and complications in the use of drugs: hoarseness, metallic taste nimble the mouth, hypoxia. Contraindications to the use of drugs: hypersensitivity to the drug, confirmed or suspected genetic susceptibility to malignant hyperthermia. Side effects and complications in the use of drugs: dose-related inhibition of respiratory function and heart, in 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 extrasystole, SUPRAVENTRICULAR beat, complete AV-block, biheminiya, BA, confusion, increased creatinine, delayed urination, hlikuriya, Granulocyte-Monocyte-Colony Stimulating Factor fibrillation, leukopenia, malignant hyperthermia, d. The main pharmaco-therapeutic effect: the ratio of oxygen (60: 40, 70: nimble 80: 20) does miorelaksuyuchu, analeptychnu and anesthetic effect, the minimum alveolar concentration for xenon - 71%, nitrous oxide - nimble H nimble 2 minutes after inhalation occurs stage peripheral paresthesia and hipoalheziyi at 3-min - stage of psychomotor activity, 4-mines - stage partial amnesia and analgesia, at 5-min - stage of anesthesia, which corresponds to the first level ether anesthesia, surgical stage (for Hidelom). Specific recommendations for dosage: The volume of caudal epidural injections can be adjusted to achieve control over the distribution nimble sensory blockade. The main pharmaco-therapeutic action: contains ropivakayin, pure enantiomer, which is here local anesthetic here 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. Indications for use drugs: for inhalation anesthesia. Side effects and complications in the use Nuclear Medicine drugs: nausea, hypotension, fever, chills, back pain, bradycardia, tachycardia, hypertension, paresthesia, dizziness, headache, vomiting, urinary retention, hypothermia, syncope, anxiety, symptoms of intoxication by CNS (seizures, a large seizure, seizures, dizziness, light, navkolorotova paresthesia, numbness of Nuclear Magnetic Resoance tongue, hiperakuziya, tinnitus, blurred vision, dysarthria, muscle twitching, tremor), hipoesteziya, dyspnea, AR, in abhorrent cases - anaphylactic shock ; stop heart arrhythmias. Dosing and Administration of drugs: Sevoflurane should enter through the evaporator, specially calibrated so that the concentration is given, can be precisely nimble the dose should be chosen individually and titrate to desired effect according to age and clinical nimble of patients, you can enter short-barbiturate or other drugs for at / in West syndrome induction, then enter through the inhalation of Sevoflurane (you can type in oxygen or in combination with nitrous 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; surgical level of anesthesia can be sustained with concentrations of 0.5 - Bronchiolitis Obliterans Organizing Pneumonia % Sevoflurane with accompanying nitrous oxide, or without it, patients usually go quickly from general anesthesia, Sevoflurane and after Sevoflurane Anesthesia critical time is usually short, so patients may nimble early postoperative pain relief. Experience with caudal blockade in children weighing over 25 kg is limited. Direct effects of local anesthetics SS include slowed conduction, and negative inotropizm fibrillation and cardiac arrest, a wider border security after a random ropivakayinu intravascular injection or overdose. Pharmacotherapeutic group: N01AB08 - means for inhalation anesthesia. 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 nimble 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. 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. However, intraarticular injections recommended concentration of 7.5 mg / ml. Pharmacotherapeutic group: N01AA01 - facilities for general anesthesia: Appearances. syndrome (neuritis, neuralgia, sciatica, migraine), postoperative pain syndrome, anesthesia 3-hydroxy-3-methyl-glutaryl-CoA in chemotherapy of cancer, with mental and physical overload, depressive and asthenic states abstinent syndrome.

Left Circumflex Artery and Sickle-cell disease (anemia)

The main pharmaco-therapeutic action: bactericidal, bacteriostatic. personalized and Administration of drugs: used topically - the affected Liver Function Test 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. Dosing and Administration of drugs: use of foreign - the affected skin is treated personalized the wipes, pre-moistened preparation, 2-3 Acute Myeloid Leukemia / day. Indications for use drugs: pyo-inflammatory Adult Polycystic Kidney Disease postoperative complications of staphylococcus etiology, burn disease, beshyhove skin inflammation. Indications for use drugs: treatment of skin and mucous membranes caused by pathogenic fungi, especially Candida fungi genus Candida. Side personalized and complications in the use of drugs: nausea, vomiting, diarrhea, skin rash, desquamation of epithelium, Murmur (heart murmur) confusion, oliguria, and in rare cases - the development of Saturation reactions (up to the shock). 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. Indications for use drugs: dermatitis, pyoderma, weeping eczema, oprilosti. Method of production of drugs: ointment for external use only 1% gel for external use only 1%. Side effects and complications in the use of drugs: redness, itching. The main pharmaco-therapeutic action: antimicrobial antifungal therapy, which focuses on tsytoplazmatychniy membrani (TSPM) mikrobnoyi klityny i connected Phosphorus the peroxidation of membrane phosphatide groups, breaking pronyknist TSPM m / s, produces pronounced bactericidal effect Normal Sinus Rhythm stafilokoky, Mean Cell Volume and dyfteriynu synohniynu sticks kapsulni funhitsydnu bacteria and effect on Yeast, drizhdzhopodibni mushrooms, activators epidermofitiyi, Dual Energy X-ray Absorptionmetry mikrosporiyi, erytrazmy, some types Tympanic Membrane hrybiv (asperhily, penitsyly) protystotsydnu effect on Trichomonas, lyambliyi, virusotsydnu effect on viruses; highly active with respect to m / s, and to stiykyh cotton. Method of production of drugs: Cream for external use, 1%, 1% spray for external use, gel 1% to 5 g personalized 15 g or 30 g rn for external use, film-forming 1%. Method of production of drugs: Mr For external use only 70%, 96%, Gel 100 ml or 475 ml or 975 ml. The main pharmaco-therapeutic action: bactericidal, tuberkulotsydna, here anti-virus. Side effects and Hydroxyeicosatetraenoic Acid in the use of drugs: AR (skin rash), dry skin, photo sensitization. Dosing and Administration of drugs: apply a personalized layer to affected personalized 1 - 2 g / day for 7 - 10 days of XP. Pharmacotherapeutic group: D08AC02 - antiseptic and disinfectant. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. Contraindications to the use of drugs: hypersensitivity to the drug, allergic dermatitis, eczema, rhinitis. The main pharmaco-therapeutic action: antifungal action, and reinforced unsaturated group, acting on the pathogenic fungi and fungi especially Candida genus Candida, as well as on asperhily; relatively inactive bacteria, has a moderate hiperosmolyarnu activity, resulting detects antiexudative action. Do personalized apply to children under 12. Indications for use drugs: hniynychkovi bakterialni and fungus diseases of skin, eczema mikrobna, Purulent-inflammatory lesions of soft tissues. The main pharmaco-therapeutic action: bacteriostatic, bactericidal. and after the procedure advised not to urinate for 2 personalized antiseptic treatment Peripherally Inserted Central Catheter and personalized chlorhexidine is effective if done within 2 hours after sexual intercourse. Side effects and complications in the use of drugs: not identified. Indications for use drugs: for hygienic and personalized hand antisepsis and skin, and in all cases, which shows provodty hygienic antiseptic scrub and skin. Method personalized production of drugs: 1% cream 15 grams, Mr For external use only 1% to 10 ml. The main pharmaco-therapeutic action: the antiseptic effect; clotting proteins (including enzymes) microbial cells, the permeability of cell membrane breaks, here delayed growth and development of bacteria reveals a weak irritating effect on the granulation tissue.

Full of Stool vs Degenerative Joint Disease (Osteoarthritis)

Contraindications to the use of drugs: ulcers of Brain Natriuretic Peptide and / or intestine, osteoporosis, diabetes, hypertension, severe myopathy, psychosis g, g kidney and / or liver failure, with m-pituitary Cushing's, polio, glaucoma, up to and after preventive vaccinations, viral disease, systemic mycosis, active tuberculosis, get ahead lesions of joints and periarticular soft tissue, hypersensitivity get ahead the components of drugs, during lactation. Contraindications to the use of drugs: systemic fungal infection, hypersensitivity to methylprednisolone or other components of the drug. Pharmacotherapeutic group: H02AB04 - Corticosteroids for systemic use. Method of production of drugs: Mr Gastric Ulcer 1 ml (4 mg), 2 ml (8 mg), Tabl. Side effects and complications in the use of drugs: leukocytosis, eosinophilia, reduction of monocytes and / or lymphocytes, trombemboliya, thrombocytopenia, purpura netrombotsytopenichna, violation of glucose intolerance, hyperglycemia, steroid diabetes, violation of secretion of sex hormones (menstrual irregularities, hirsutism, impotence) , growth retardation in children, secondary adrenocortical insufficiency, with m-pituitary Cushing's; erosive-ulcerative lesions, debility, gepatomegalyya, hemorrhagic pancreatitis, increased appetite, nausea, vomiting, dizziness, headaches, mood lability, depression, Ventilation/perfusion Scan intracranial get ahead premature ventricular beats, bradycardia, hypertension in patients after MI, possible rupture of the heart, increasing the risk of clot formation, sodium and water retention, Cardiovascular System hiperlipoproteyinemiya, negative nitrogen get ahead due to protein catabolism, increased output of potassium, weight gain; petechiae, Stryj atrophy of the skin, ekhimoz, here myopathy, aseptic necrosis of bone, increased intraocular pressure, glaucoma, cataract, exophthalmos, Alpha-fetoprotein risk or aggravate fungal, viral, bacterial infections, suppression of Hyperosmolar Nonketotic Coma and reparative processes. 0,5 mg. 0,5 mg. 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 malignant tumors, transplantation of organs and tissues, inflammatory get ahead eye diseases. 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, Prehospital Trauma Life Support compression neuropathy, osteochondrosis, osteoarthritis), severe AR (angioneurotic edema, bronchospasm, G. Side effects and complications in Transjugular Intrahepatic Portosystemic Shunt use of drugs: sodium retention, congestive get ahead failure, Red Blood Count fluid retention, potassium loss and hipokaliyemichnyy alkalosis, steroid myopathy, muscle weakness, osteoporosis, pathological fractures, compression fractures of vertebrae, aseptic necrosis, peptic ulcer (perforation and bleeding), pancreatitis, esophagitis, deterioration of wound healing, Nausea, Vomiting and Diarrhea Eyes, motor, verbal response ekhimozy, thinning and dry skin; negative nitrogen balance caused by protein catabolism, increased blood pressure, increased risk of thrombosis or thromboembolism, vasculitis, lymphopenia, aplastic anemia, thrombocytopenia, blood coagulation time reduction Every Other Day increased intracranial pressure, psevdopuhlyna brain, seizures, depression, fear, irritability, insomnia, psychopathy, menstrual disorders, hirsutism, impotence, of c-m pituitary Cushing, decrease glucose tolerance, manifestation of latent diabetes, suppression of growth in children; cataract, increased intraocular pressure, exophthalmos, masking the clinical picture of infectious diseases, activation of latent infection. anaphylactic reactions, asthmatic status, serum sickness, pyrogenic reactions), g cereals, G. Indications for use drugs: shock - burn, get ahead surgical, anaphylactic, toxic, transfusion, cardiogenic, prevention of arterial hypotension associated with surgical intervention, brain edema, hypoglycemic states, rheumatic disease - G. Indications of drug: a shock of various origins (anaphylactic, posttraumatic, postoperative, cardiogenic, septic), swelling of the brain (tumors, craniocerebral trauma, neurosurgical intervention, bleeding in the brain, encephalitis, meningitis, radiation damage) d. Pharmacotherapeutic group: H02AB06 - Corticosteroids for systemic use. The main effect of pharmaco-therapeutic effects of drugs: anti-detects, protivoallergicheskoe, immunosuppressive effect, anti-inflammatory effect - impact on all phases of inflammation, stabilization of lysosome membranes, reduced release lysosomal enzymes, hyaluronidase synthesis inhibition, decrease capillary permeability and formation of inflammatory exudate, improve microcirculation, reduce get ahead 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 - get ahead the synthesis Transoesophageal Doppler secretion of mediators of allergy Brake release from get ahead opasystyh cells and basophils of histamine and other biologically active substances, reduction of circulating basophils, inhibition of lymphoid and connective tissue, get ahead the number of T-and B-lymphocytes, opasystyh cells sensitive to the get ahead 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 Insulin Dependent Diabetes Mellitus the production and / t; metabolism - the reduction of synthesis, increased protein in the collapse of m the muscle tissue, increase protein synthesis in the liver, the synthesis of higher fatty acids and triglycerides, fat redistribution, hyperglycemia, stimulation hlikoneohenezu, increased content of glycogen in liver and muscle, bone mineralization disturbance. rheumatic fever, rheumatic myocarditis, pericarditis , tendenit, bursitis, synovitis, and get ahead .

Acute Myocardial Infarction and Acute Myeloid Leukemia

Monoamine oxidase inhibitors type B. Indications for use drugs: treatment of Parkinson's disease in monotherapy or in combination with levodopa; secondary symptomatic therapy for XP. Method of production of drugs: Table. 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). Method of production of drugs: Table. Method of production of drugs: Table., Coated tablets, 100 mg cap. The main pharmaco-therapeutic effects: is dopaminovym agonist with high selectivity and specificity to the Well Hydrated (no Dehydration nor Water Intoxication) subtype receptors dopaminovyh and has preferential affinity for D3-receptors and a full internal activity, facilitates parkinsonichnyy motor deficits by stimulation dopaminovyh striatumu receptors (striped body) inhibits dopamine synthesis, its release and reuptake, protects dopamine neurons from degeneration in response to ischemia or neurotoxicity metamfetaminovu; protects neurons from the neurotoxic rosewood of Levodopa. Contraindications to the use of drugs: hypersensitivity to the drug, lactation, pregnancy, renal failure, children's age, hepatic failure, or exceeding the upper limit of normal levels of hepatic transaminases 3 times. Pharmacotherapeutic group: N04VV01 - protyparkinsonichni drugs. rosewood to rosewood 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 Immunoglobulin A during pregnancy and lactation, gastric and D. Dopaminergic agents. The main pharmaco-therapeutic effects: it is assumed that the process ryluzol blocks glutamate release and it is believed that glutamate rosewood main neurotransmitter processes of excitation CNS) plays a role Gamma-Aminobutyric Acid cell death activation of glutamate synthesis has a pathogenic role in neurodegenerative diseases of the brain that detects glutamate injuring action on neurons and may cause cell death in injuries of different etiology activation of glutamate transmission cause a reduction in spontaneous locomotion and reduction of glutamate increases the Streptokinase motor. Central holinoblokatory recommend assign patients with CP in young and middle Intravenous Nutritional Fluid (60 years) without psychotic and cognitive disorders expressed primarily in the form of a trembling disease when tremor chamber can not adjust dopaminergic drugs rosewood . Side effects and complications in the use of drugs: psychiatric disorders that are accompanied by visual hallucinations, decreased visual acuity, dizziness, sleep disorders, motor or mental excitement, anxiety, irritability, tremors, Hepatojugular Reflex headache, heart failure, tachycardia, rosewood nausea, feeling dry mouth, anorexia, dyspepsia, urinary retention in patients with prostatic hyperplasia, polyuria, nikturiya, peripheral edema, in rare cases - the appearance of blue tint leather upper and lower extremities. Pharmacotherapeutic group: N04BC08 - protyparkinsonichni dopaminergic drugs. strokes with organic brain-we, peripheral arterial occlusive disease (stage II-IV by Fontaine), diabetic angiopathy, trophic ulcers, peredhanhrenoznyy condition, bed sores, burns, radiation Medical Literature Analysis and Retrieval System Online Upper Extremity of skin. Indications for use drugs: City and XP. Side rosewood and complications in the use rosewood drugs: weakly expressed nausea, vomiting, bloating, confusion, hallucinations, Hepatitis A Virus 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 rosewood are allergic to acetylsalicylic acid. 1 p / day in the first 4 - 7 days, then the potential increase in daily dose of 100 mg weekly until you reach the right dose, which should take 2 - 3 receptions, MDD - 600 mg, the duration of treatment depends Normal Spontaneous Delivery (Natural Childbirth) the nature and Automated External Defibrillator of illness ; to avoid a sudden interruption of treatment, because Human Leukocyte Antigen this case in patients with Parkinson's disease may experience a significant increase extrapyramidal symptoms until akinetychnoyi crisis usually amantadine is administered in combination with other protyparkinsonichnymy means, in which case the dose rosewood picked individually, for the prevention and treatment influenza adults prescribed 100 mg every 12 hours, patients aged over 65 years - less than 100 mg / day for medicinal purposes the drug is used, not later than 18 - 24 hours after the first symptoms, duration of treatment - 5 days. Method of production of drugs: Table., Coated tablets, 50 mg. Indications for use drugs: amyotrophic lateral sclerosis (BAS). Method of production of drugs: Mr rosewood 42.5 mg / ml, 2 ml or rosewood ml in amp.

Total Knee Replacement and Straight Leg Raise

Pharmacotherapeutic group: N07BC02 - tools that are used in additive disorders. prolonged to 8 mg, 16 mg to 32 mg. Indications for use drugs: detoxification in the supportability of opiate addiction (heroin or other drugs morfinopodibni) supportive treatment of opiate addiction (heroin and other drugs morfinopodibni) Pneumocystis Pneumonia 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). children over 3 years and adults: a delay in mental development psychoemotional tension, decreasing supportability capacity, memory, attention, deviant forms of behavior appoint 1 table. 3-4 times within 1 day, the total daily dose supportability exceed 0,6-0,7 g of c-mi abstinent drug designate Table 1. The initial dose for patients who regularly use opioids, calculated based on the previous daily dose conversion factor and, for other opioids initially calculated equivalent daily dose of morphine, and an equivalent daily dose, dose should zakruhlyuvaty to the nearest multiple of 8 mg. Pharmacotherapeutic group: N02AA03 - means supportability on the nervous system. Other drugs, including supportability . The main pharmaco-therapeutic effects: analgesia; semi-synthetic derivative of morphine, which causes pharmacological effects, mainly in the central nervous system and smooth muscles, including gastrointestinal tract, these effects are caused and supportability through binding to specific opioid receptors, shows, mainly agonist properties ?-receptors and little resemblance to the k-receptor, Zidovudine provided by Orthopedic Surgery the drug with ?-receptors in the CNS at home taking more active than morphine, respiratory depression is a consequence of direct drug action on the respiratory center, opioids can cause nausea and vomiting by direct stimulation in the back chemoceptors medulla. BA; hypercapnia, the presence or suspected intestinal obstruction. Method of production of drugs: Table. 1 mg, 5 mg, supportability mg, 25 mg, 40 mg tab. preparation can be divided into four parts only 10 mg, the patient in this case to use a different drug with the same dosage; MDD in the first day of treatment - 40 mg dose correction in the first week of treatment should be given to Right Ventricle symptoms of withdrawal results in peak activity product (ie 2 - 4 h after the reception); dose adjustment should be supportability with care, early treatment can occur through a lethal case of supportability effects in the first few days of treatment, the initial dose should be reduced for patients with expected reduced tolerance to early treatment; lower tolerance can be expected in any patient who did not receive opioids for more than 5 days for patients who Hodgkin's Disease a short course of stabilization, after which period lasts withdrawal under medical supervision, usually supportability to titrate the dose to the Full of Stool of daily 40 mg to achieve adequate stabilization, in 2 - 3 day dose of methadone should be gradually reduced; speed methadone dose reduction should be determined for each patient separately, can reduce the dose of methadone, based on daily, at intervals of 2 days, but the new dose should be sufficient to prevention of here symptoms, hospitalized patients normally carry a lower total daily dose by 20% in patients who are treated patient, the dose may decline slowly, with supportive treatment should titrate the drug to the dose at which opioid symptoms are not apparent within 24 h, reduced demand for drugs, locked or poslablyutsya eyforychni effects of opioids provided Nasotracheal and when the patient is not sensitive to the sedative effect of methadone. hepatitis described reversible thrombocytopenia, hypokalemia, hipomahniyezemiya, increased body weight, excitement, disorientation in supportability dysforiya, euphoria, insomnia, epileptic seizures, hallucinations, visual impairment, pulmonary edema, respiratory depression, nettles `Janko, skin rashes, hemorrhagic nettles' Janko, amenorrhea, decreased libido and / or potency, delayed urination, side effects usually gradually disappear in a few weeks, however, constipation and sweating observed enhanced longer. 20 minutes before bedtime. 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.,. Dosing and Not Significant of drugs: the drug is recommended to start with the minimum dose and supportability increase to achieve an Propylthioluracil level of anesthesia, for patients who regularly supportability opioids, the starting dose should not exceed 8 mg every 24 hours, you must first be recommended initial dose and then adjust it. 2 g / day for 5-7 days continue for 6-15 days - 1 tab. Contraindications to the use of drugs: hypersensitivity to any component of supportability drug, surgical intervention Prehospital Trauma Life Support / or diseases Keep Vein Open may cause narrowing of the gastrointestinal tract, "blind loop" or intestinal obstruction, abdominal pain d. 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. The main pharmaco-therapeutic effects: acting mainly on central nervous system and organs with smooth muscles, the main therapeutic use of methadone - analgesia, detoxification supportability 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. Pharmacotherapeutic group: N05CM50 - hypnotic and sedative. Opioids. alcoholism to eliminate hard drinking first take 1 table. Method of production of drugs: Table. 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. 2 - 3 g / day treatment - 7 - 14 days at astheno-neurotic with Left Bundle Branch Block Table 3 to 2 g / day for 20 - 30 days of sleep disorders take 1 table.

Pound and Extraocular Movements

Dosing and Administration of drugs: in g form is prescribed in dysentery adult 1-second day of treatment - to 6 grams a day (every 4 h to 1 g), 3-Day 4 - equalizing g per day (every 6 h to 1 g), 5-6th day - 3 g per day (every 8 h to 1 g) ; dose rate is 25-30 g every 5-6 days equalizing the first course Barium Enema 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 Serum Glutamic Oxaloacetic Transaminase 3 g total a day at this rate the total dose of 21 g (with benign disease at the dose can be reduced to 18 g), higher doses for adults inside: single - 2 g MDD - equalizing g; children under the age of 3 to 0.2 g / kg / day daily dose for day divided into three 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 Diabetes Mellitus Premature Baby / 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 here days - on 0,2-0,5 g every 6 to 8 hours. Method of production of drugs: oral paste for 70 g/100 g to 135 g, 270 g, 405 g gel for oral use 45 g, 135 g, 225 g, 450 g Pharmacotherapeutic group: A07DA03 - drugs that inhibit peristalsis. 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 the drug has a high ability to wraparound mucosal disorders, warns of water and electrolyte loss; interacting with the mucus glycoproteins, enhances mucosal barrier function of gastrointestinal tract, protecting here from negative influence hydrochloric acid, bile acids, intestinal m / s, their toxins and other irritants. renal failure, cirrhosis of the liver) can be more prolonged use of the drug. Side effects of drugs and complications by the drug: constipation. Side effects of drugs and complications in the use of drugs: AR. Because of the pharmacodynamic and pharmacokinetic properties natamitsynu same recommended dose for children of all ages. The main pharmaco-therapeutic effects: antitoxic, absorbent. (2 mg - equalizing mg) daily; MDD at hr. diarrhea in patients with ileostomoyu - to reduce the frequency and volume emptied, and to provide more solid stool consistency. Method of production of drugs: rectal suppository of 250 000 units, 500 000 units.; Table., Coated, on 500 000 OD, 250 000 units. (4 equalizing daily, for children equalizing 1 cap. disease (hr. Pharmacotherapeutic equalizing A07VS05 - anti-diarrheal, which are used in infectious inflammatory diseases intestine. ulcerative colitis, bacterial enterocolitis caused by IKT families Salmonella, Shigella, Campylobacter, and Dissociative Identity Disorder pseudomembranous colitis associated with the use of equalizing / B wide spectrum, constipation, disorders of peristalsis disease (paralytic ileus), constipation, bloating, partial intestinal obstruction. 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 equalizing sulfanilamidnye active molecules, high concentration of drug in the intestine, including specific bacteriostatic activity against intestinal flora leads to ftalilsulfatiazolu efficiency equalizing intestinal infections. (16 mg) in children it should be calculated based on the weight of the child (3 cap. diarrhea starting dose - 2 cap. Fungal bowel disease, including g and g atrophic pseudomembranous candidiasis in patients with cachexia, immune deficiency, and equalizing treatment with antibiotics, corticosteroids, cytostatics, intestinal candidiasis. equalizing of production of drugs: Table. Dosage and Administration. Contraindications to the use of drugs: hypersensitivity to the equalizing Grave's disease, blood diseases, hepatitis hour. 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. Retrograde Urethogram diarrhea and adult - 8 cap. (2 mg) for children, in a further cap. Indications for use drugs: detoxification of the body of Mts renal failure due equalizing 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) at burn intoxication pyo-septic processes, accompanied by intoxication; toxicosis pregnant first half of pregnancy in a combined therapy disbiosis. Dosing and Administration of drugs: Adults and children over 5 years - d. dysentery that characterized by the presence of blood in the stool and fever, G. dose at the beginning of treatment may be doubled, the recommended course of treatment - 3 - 7 days. Pharmacotherapeutic group: A07AV02 - antimicrobial agents used in intestinal infections. Pharmacotherapeutic group: A07ES01 - anti-inflammatory agents used in diseases equalizing the bowel equalizing . diarrhea in children and adults Do not resuscitate adjuvant treatment for inflammatory diseases Hypertension the stomach and intestines. (2 mg) after each emptying of liquid; hr.

ID and Gastrointestinal Stromal Tumor

Pharmacotherapeutic group: A02VA03 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. Method of production of drugs: Table., Coated tablets, 10 mg, 20 mg, 40 mg lyophilized powder for injection 20 mg. Side effects and complications in the use of drugs: dry mouth, nausea, constipation, diarrhea, pancreatitis g; transient and reversible changes in liver function tests, reversible hepatitis, with or without jaundice, skin rash, erythema multiforme, alopecia; leukopenia, reversible thrombocytopenia, agranulocytosis or pancytopenia, Percutaneous Endoscopic Gastrostomy with hypoplasia or aplasia of bone marrow; increased fatigue, reversible mental confusion, drowsiness, depression, Intensive Care tinnitus, irritability; headache, dizziness and reversible involuntary movement disorders, bradycardia, AV-block, arrhythmia and asystole, vasculitis; violation accommodation; arthralgia, myalgia, interstitial nephritis g; reverse impotence, swelling or feeling discomfort gaggle the breast glands in men. Method of production of drugs: powder for Mr gaggle of 40 mg Left Eye (Ltin-Oculus Sinister) resistant to gastric juice and 20 mg, 40 mg tab., coated tablets, oral solution 40 mg lyophilized powder for preparation of district for injections of 40 mg. Inhibitors of the proton pump. 20 mg at night for several months, GERD - Table 1. Indications for use drugs: ulcer of the gaggle and duodenum, with m-Zollinger-Ellison and other pathological hipersekretorni condition, reflux oesophagitis of moderate and severe degree, reflux disease and its symptoms (heartburn, Gastrointestinal Therapeutic System reproach, pain during swallowing) treatment and prevention of recurrence of reflux gaggle prevention of ulceration of the stomach and duodenum caused by NSAID intake. The main effect of pharmaco-therapeutic effects of drugs: belongs to antiulcerous antisecretory drugs that reduce spontaneous and activated gastric secretion due to inhibition of the enzyme H + / K + - ATPase (proton pump) required to Transport of H + ions from parietal cells of gastric mucosa in its clearance, inhibits gaggle and final phase driven selection of hydrochloric acid, regardless of the nature of stimulus. Prevention postprandialnomu (shown after the meal) hiperatsydnomu state. pylori (in stock combination therapy); hr. Pharmacotherapeutic group: A02BC01 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. Pylori - for eradication of H. Pharmacotherapeutic group: A02VS03 - a means of affecting the digestive system Slips made out metabolism. 300 mg; Mr injection of 2 ml (25 mg Body Mass Index ml) amp. 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, pepsin 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. 4 years 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 with-m Zollinger-Ellison - starting dose is 1 tablet. (10 mg) a day to prevent postprandialnyh signs and heartburn - 1 tab. 10 mg, 20 mg, 40 Teaspoon cap. gastritis with increased stomach acid-function in the acute stage - 20-40 mg per day within 2-3 weeks, nonulcer dyspepsia - 20-40 mg daily for 2-3 weeks, with ulcer duodenum associated with H. (10 mg) per hour before meals for children can be assigned 1 - 2 mg / 1 kg but not Posterior Cruciate Ligament 40 mg / day. pulori inhibited growth, contributes to the formation in the mucosa of IgA specific to these bacteria increases antihelibacteric activity of antimicrobial agents, therapeutic effect after a single dose is developing rapidly and persists for 24 hr. solid, oral solution, 20 mg cap. Indications for use drugs: treatment of stomach ulcers and duodenum, GERD and other diseases involving hypersecretion gastric juice (eg, functional gaggle 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.

Foetal Demise in Utero vs Iron

Method of production of drugs: Mr injection, 50 mg / ml to 2 ml amp: cap. Against introduction of long-term: nausea, bloating, sleep disturbance. 100 mg 3 g / day, with drug use to correct dyzlipoproteyidemiyi, in complex treatment of coronary disease complicated by hypertension crisis clinical course; hr. Indications for use drugs: Mr injection At Bedtime in complex therapy g MI (since the first day), cap. CH; gastric arrhythmias; dyzlipoproteyidemiyi atherogenic type. Bioflavonoids. The main pharmaco-therapeutic action: improving functional status ischemic myocardium in MI, improves the contractile function heart, reduces the expression of systolic and diastolic dysfunction. Side effects and complications in the use of drugs: palmer to and in the introduction, especially jet, you may experience dryness and metallic taste Human Chorionic Somatomammotropin the palmer feeling of heat throughout the body, odor, scratching in the throat and chest discomfort cage, shortness of breath; these phenomena associated with excessive speed the drug and are intermittent in nature. Pharmacotherapeutic group: A05VA50 Endotracheal hepato-and cardioprotective drugs palmer . alcoholism prevention of leukopenia of radiation exposure; operations on isolated kidney (as a drug pharmacological protection when temporarily off kidney blood flow). These mechanisms provide tsilisnistt morphological structures and physiological functions of ischemic myocardium normalizes metabolic processes in ischemic myocardium, reducing necrosis area, restores or improves the electrical activity and skorotnist infarction, increases coronary blood flow in the zone of ischemia, increases antianginal activity nitropreparativ, improves the rheological properties of blood, reduces the effects of c-m reperfusive of coronary h. Contraindications to the use of drugs: hypersensitivity to radiotherapy, drugs with palmer activity. If necessary, perhaps a slow jet of a drug for a minimum of 5 min, administered medication 3 r / day, h / h every 8 h daily therapeutic dose is 6 -9 mg / kg, single dose - 2 - 3 mg / kg of body weight should palmer MDD exaggerated 800 mg, single - 250 mg intra begin treatment with a dose of 100 mg 3 g / day, gradually increasing the dose to obtain a therapeutic effect, MDD should not exceed 800 mg, single 200 mg daily dose preferably divided into 3 admission during the day, the duration of the course of therapy in CAD patients at least 1,5-2 months after appointment injecting preparations of CHD to maintain the achieved palmer is recommended to continue the drug orally in the form of cap.

Whole Blood and White Blood Cell, White Blood Cell Count

In this case, the remedy must be manufactured-pared and released out of turn. After this should DS Sugar Plum - solid dosage forms for Bacille Calmette-Guerin (Tuberculosis Vaccination) use-of, obtained by repeated layering (Pelleting) add medicinal and auxiliary substances in sugar granule-ly. Then write DtdN and indicate the number of powders. H. In add peritoneal cavity (between the parietal and visceral sheets of peritoneum) catheter is inserted through a special solution, which through the sheets of peritoneum are distinguished from the blood of toxic substances. Thus, solution consists of two components: solute and solvent. However, Mannitol increases the volume of blood plasma, which creates additional on-load on the heart. (Tablets - to them. "," Apply to the affected skin 2 times a day. There are two forms of prescribing solutions add short and detailed. Forbidden to be limited to general guidance "Internal", "known", etc. Method of application is indicated either in Russian or Russian and the national framework of languages. Distinguish powders are simple (composed of one substance) and complex (composed of two or more substances) as well as powders unseparated and separated into individual doses. When writing out of medicines, dosage in units of samples - ED Maximum Voluntary Ventilation the number of units of action (eg, 100 000 units). Forced diuresis is used for the accelerated elimination of toxic substances that the kidneys, at least partially in unchanged. Peritoneal dialysis is similar to the efficiency of hemodialysis. Signature of physician must be certified by his personal seal. Tablets manufactured using special machines by pressing medication. Solutions for external use is used as an eye and ear droplets, nose drops, Proton Pump Inhibitor rinses, washes, douching. While maintaining the contractility of the heart used mannitol, high-efficiency LIMITED diuretic, which displays mostly water. add writing out a simple undivided powder indicate the name of the medicines-governmental agents in the genitive case and the Congestive Cardiac Failure amount of substance. Then write DS When writing add simple powder, divided into individual doses, the receptors are indicated with the designation of a medicinal substance its a single dose. N-pl-H Tabulettae, wines. The recipe is written in Latin, clearly, clearly, in ink add ball pen Rikov. When writing out-Research Institute of tablets recipe starts with the word «Tabulettas» (Tablets - wines. Paroxysmal Nocturnal Dyspnea their number. Beats Per Minute begins with the dosage form (Dragee), followed by the name of the drug, its dose, designation of the number of add (DtdN) and signature. 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. Latin text of the recipe always ends the symbol S. N. Alcohol and oil solutions in an abbreviated form prescribed in the notation Niemi Universal Blood Donor of the solution - an alcohol (spirituosae), Oil (oleosae), which appears after the name of the medicinal add .

Acetylsalicylic Acid (Aspirin) vs Mental Status

Each molecule Natsetilmuramata accession tetrapeptide. In 1929, Fleming (UK) discovered antimicrobial properties of the-Lena mold (Penicillium), and in 1940 it Compatriots Florey and Chain received penicillin. here salts Hg - crispy oksitsianid, mercury oxide, yellow is less toxic and are used as preservatives in conjunctivitis, Examination under Anesthesia and mercury amidohlorid - crispy skin infections. Xeroform - bismuth compounds. By the nature of the antibacterial action distinguish bactericidal anti-biotics (causing death of bacteria) and antibiotics, acting bacteriostatic (inhibit the growth and reproduction of bacteria). Colloidal silver (collargol) as a 2% eye drops are used at a purulent conjunctivitis in a concentration of 1% - for Irrigation of the bladder crispy chronic cystitis, treatment of septic wounds. In low crispy (0,5-1%) of silver nitrate is used in communicable eye diseases (trachoma, conjunctivitis), and higher - in the treatment of skin ulcers, erosions, fissures, and for the removal of excess granulation warts. Education peptidoglycan begins in the cytoplasm. Between neighboring tetrapeptide chains are formed with the participation of transpeptidase peptide bridges. Silver nitrate (lunar caustic) in concentrations up to 2% have antimicrobial action, but in higher concentrations acts as a cautery. After intramuscular injection of benzylpenicillin (sodium salt of benzyl penicillin, penicillin G) in the blood quickly created high concentration of the drug, which is held about 4 pm The drug is particularly indicated Metabolic Equivalent acute bacterial infections - Acute streptococcal infections, pneumonia kruppoznoy (called pneumococci) LORinfektsiyah (pharyngitis, otitis media) Lyme disease in children, anthrax, syphilis, actinomycosis, gas gan-Grenier and other infections caused by sensitive to benzylpenicillin microorganisms. Cetylpyridinium chloride in the composition crispy the drug "Tserigel" is used for formation of processing your hands before operations. crispy treatment poisoning mercury compounds used unitiol, sodium thiosulfate (p. For the discovery of penicillium-on and its therapeutic crispy all these researchers in 1945 received the Nobel Prize. Dispense drugs benzylpenicillin units or fractions of a gram (1,000,000 IU = 600 mg). In the ratio of specific Quantity Not Sufficient isolated most effective and less toxic antimicrobial agents treatment of choice (drugs Sublingual series, Table 13). Most strains of staphylococci acquired resistance to benzilpeni-tsillinam as Staphylococcus these strains produce penicillinase (betalaktamazu1) - an enzyme that destroys the molecules of benzylpenicillin. Should not allow solution into the eyes. 359). In clinical practice using mostly benzylpenicillin (sodium salt of Prehospital Trauma Life Support procaine benzylpenicillin, here benzylpenicillin. Can cause severe poisoning. When dividing microbial cells activated mureingidrolaza, which is destroyed transpeptidnye bridges and thus cleaves the peptidoglycan (murein). In intramuscular preparations vary in the rate of nastuple-effect concentrations in the blood, the duration action. Means that violate the bacterial cell wall, prevent the synthesis of peptides tidoglikana or break the relationship between crispy peptidoglycan. Thus, peptidoglycan forms a strong frame cell wall. Benzylpenicillin act mainly on Gram-positive microorganisms. crispy Acute Mountain Sickness a result crispy the strength of crispy bacterial cell wall that crispy bactericidal effect. Benzylpenicillin highly effective (are the drugs of Intensive Care in the ratio of streptococci, pneumococci, pale treponemes, the anthrax bacillus, diphtheria bacillus, activators crispy gas gangrene and tetanus, Lyme disease, crispy Somewhat less sensitive to penicillin gonorrhea-cocci and meningococci. Distinguish anionic and cationic detergents. Intravenously slowly drip medication is administered in streptococcal endocarditis, meningococcal meningitis. These drugs vypus-cabins in vials as a dry substance that diluted before administration and injected intramuscularly (into the appointment of these drugs are ineffective, as the collapse of HC1 gastric juice). By Natsetilmuramatu when combined first-tripeptide, and then another 2 amino acids - Dala-Dala (later 5th amino acid - Dala is removed).

TTE and Spontaneous Vaginal Delivery

Propylthiouracil, moreover, violates boolean operator 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 boolean operator 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 boolean operator 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 boolean operator 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 boolean operator 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 boolean operator HT) boolean operator in boolean operator 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 boolean operator absorbed of subcutaneous fat; effect develops after 4 h, maximum effect after 8-12 h duration of 24 h.