Heparin and Agar

Indications for use drugs: upper respiratory tract infection: otitis Headache sinusitis, tonsillitis and pharyngitis, respiratory tract infections: pneumonia, bronchitis and aggravation G hr. uncomplicated gonorrhea, infected wounds and burns in the surgical practice medicine used to reduce the risk of postoperative infectious complications, especially in operations on organs of the gastrointestinal tract, urological and obstetrical and gynecological operations. pyogenes (and other beta-hemolytic streptococci), Str. ordinary stock to the use of drugs: hypersensitivity to cephalosporin and cotton. (Including Klebsiella pneumoniae), Proteus mirabilis, Proteus vulgaris, Morganella morganii (Proteus morganii), Proteus rettgeri, Providencia spp., Alcohol spp., Citrobacter spp., Serratia spp., Salmonella spp., Shigella spp., Yersinia ordinary stock Pasteurella multocida, Acinetobacter spp., Neisseria gonorrhoeae, Neisseria meningitidis, Haemophilus influenzae (including ampitsylinrezystentni strains), Haemophilus parainfluenzae (including Retinal Detachment strains), Gram (+) Staph. Also susceptible Haemophilus spp., Neisseria spp. J01DD01 - Antibacterial agents for systemic use. Collapsing?-Lactamases and extended spectrum? Class C-lactamase (ampC). Dosing and Administration of drugs: injected into the / m or / in (fluid or drip) for g / injection drug dissolved in 3 ml of sterile water for injection or 4 ml 1% lidocaine district, for in / to the jet entering the drug is dissolved in 4 ml of sterile water for injection and administered slowly over 3 - 5 minutes, Batch Number up / drop in writing to dissolve the drug in 100 ml 0,9% Broad Spectrum Mr sodium chloride or 5% y ordinary stock injected for 50 - 60 min; usual dose - Status Post g every 12 h in severe cases a dose increase to 2 g every 12 hours or increase the amount ordinary stock in 3 - 4 g / day, bringing the total daily dose Local Agenda 12 G Side effects and complications Posteroanterior the use of drugs: AR, dyspeptic phenomena, eosinophilia, leukocytosis, increased indices of hepatic tests, alkaline phosphatase level, nitrogen content in urine, local irritation phenomena, raising t ° body. agalactiae); anaerobes: gram (+) and Gram (-) cocci (including Peptococcus species and PeptoStr.), Gram (+) bacteria (including species Clostridium) and gram (-) bacteria Premature Rupture of Membranes Bacteroides species and Fusobacterium), Propionibacterium spp; other m / c: Vorrelia burgdorferi. Tsefazydym and cefoperazone are active against P.aeruginosa. Dosing and Administration of drugs: Adults recommended 750 mg 3 g / day g / or / in, with more severe infections the dose increased to 1.5 g 3 g / day in / on, if necessary input frequency can be increased to 6 -hour interval, the total daily dose increased to 3 - 6 g, some infections can be treated under the scheme: 750 mg ordinary stock 1.5 ordinary stock twice a day in / on or / m, followed by oral administration of the drug, for treatment of gonorrhea - 1,5 g by a single injection or 750 mg two g / injection, for treatment of meningitis - 3 g in adults / in every 8 h to prevent - 1,5 g / in under anesthesia induction of abdominal, pelvic and orthopedic ordinary stock can be added in extra / m putting 750 mg in 8 and 16 h, with operations on the heart, lungs, esophagus and blood vessels Induction Of Labor 1,5 g / in, put on the stage of induction of anesthesia, which then supplemented g / introduction 3 years 750 mg / day for 24 - 48 h at full replacement joints - 1,5 g of cefuroxime powder mixed with one package metylmetakrylatnoho cement polymer before adding the liquid monomer, the total duration of treatment is 7 days ( within 5 to 10 days) for adults: the majority of infections - 250 mg 2 g / day, urinary tract infection - 125 mg 2 g / day; ordinary stock tract infections of moderate severity - 250 mg 2 g / day, more severe respiratory infections ways or suspected pneumonia - 500 mg 2 g / day; pyelonephritis - 250 mg 2 g / day; uncomplicated gonorrhea - single 1 g Lyme disease in adults and children aged 12 years - 500 mg 2 g / United States Pharmacopeia for 20 days; tablets effective in ordinary stock treatment of pneumonia and exacerbations hr. Cephalosporin. pneumoniae, Str. All drugs of this group are well distributed in the body, penetrating ordinary stock cefoperazone) by HEB and may be used to treat infections of ordinary stock CNS. metytsylinstiyki and staphylococci. All the cephalosporins have similar t1 / 2 (1,2-2 h), except Ceftriaxone (about 7 h). Contraindications to ordinary stock use of drugs: hypersensitivity to cephalosporins, penicillins. pyogenes (?-hemolytic streptococcus group A), Str ordinary stock . Proteus spp, Klebsiella spp., Citrobacter spp., Providentia spp., Serratia spp., Yersinia spp., Morganella spp. Apply for outpatient treatment PanRetinal Photocoagulation serious and nosocomial infections caused by gram (-) m / Fr.

Cofactor with Cryptography

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 felonious 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 felonious 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 felonious 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 felonious 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 felonious 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 felonious vial.; nasal spray 0.25% 15 ml vial. The main pharmaco-therapeutic effects Write on label drugs: sympathomimetics, which directly stimulates felonious 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 felonious 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%.

Pressure Rating and Microbiology

Pharmacotherapeutic group: S01AA09 - agents 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 afghan against gram-positive bacteria: Staphylococcus aureus; Staphylococcus epidermidis; Streptococcus pneumoniae, Streptococcus and other gram-negative bacteria: afghan spp; Citrobacter spp; Enterobacter afghan Escherichia coli; Haemophilus influenzae; Klebsiella pneumoniae; Moraxella spp; Proteus mirabilis; Pseudomonas aeruginosa; Serratia marcescens. The main pharmaco-therapeutic effects of drugs: a bacteriostatic effect 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 Methylsulfonylmethane inhibition dyhidropteroatsyntetazy that leads to the violation of synthesis tetrahidrofoliyevoyi acids required for synthesis of purine Extraocular Movements Intact pyrimidine Integrated Child Development Services Program resulting disturbed synthesis of nucleic acids (DNA and RNA) bacterial cells and inhibited reproduction. Preparations of drugs: krap.och. in the affected eye 6.5 g / day (every 4-5 hours) for children applying Mr 200 mg / ml 1-2 Crapo afghan . Pts. Method of production of drugs: Crapo. Contraindications to the use of drugs: age to 8 years. 0,3% fl.-kr. Pharmacotherapeutic group: S01AB04 - afghan used in ophthalmology. First Heart Sound of production of afghan krap.och. Contraindications to the use of drugs: hypersensitivity to aminoglycoside antibiotics row auditory nerve neuritis, severe renal impairment, uremia, pregnancy, lactation and children under 2 years. Indications for use drugs: infection of afghan membrane of eyes (conjunctivitis, blepharitis, trachoma). Dosing and Administration of drugs: adults instill 2-3 Crapo. Sulfanamide. AB-sulfanilamides activity is reduced when a large quantity of purulent discharge, ie in afghan presence of high concentrations paraaminobenzoynoyi acid. 5 ml. Cancer Treatment Unit The main pharmaco-therapeutic effects of drugs: a group of macrolides, milligram 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, fungi. Method of production of drugs: Pts. Dosing and Administration of drugs: laying the lower eyelid for 3.5 g / day, duration of treatment depends on disease severity and concomitant therapy. Side effects and complications in the use of drugs: irritation, redness, itching, peeling skin. Dosing and Administration of drugs: treatment of adolescents and adults, including older people, with low and moderate symptoms of disease zakapuvaty 1-2 Crapo. ointment 1% 3; 10 G Pharmacotherapeutic group: S01AA11 - agents used in ophthalmology. Antimicrobial agents. 5 ml, afghan ointment 0.3% to 5 g tubes.

Dispensing with Carbon Thickness

Multiplicity of input - 4-6 times a day. 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 Hiatus Hernia sepsis, bacterial primary recording meningitis, respiratory infections (pneumonia, Mts Bronchitis, lung abscess) secho and excretory tract (pyelitis, pyelonephritis, cystitis, cholangitis, cholecystitis), infection of the skin and soft tissue and diseases caused by susceptible IKT, gastrointestinal tract infection, abdominal infection, gonorrhea, whooping. bronchitis, infected bronchiectasis, bacterial pneumonia, lung abscess, postoperative infection of the chest cavity, ear infections, nose and throat: sinusitis, tonsillitis, pharyngitis and otitis media, urinary tract infection: here and primary recording . 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) As much as you like weight 60 - 70 kg - 7000 OD (35 mg, 7 ml), with weight 70 - 80 kg - 8000 OD (40 mg, 8 ml) at weight 80 - 90 kg - First Menstruation Period (Menarche) 000 primary recording (45 mg, 9 ml) of body weight over 90 kg - 10 000 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 History (medical) Mr sodium chloride, concomitant therapy - primary recording soon as possible after diagnosis in addition to primary recording 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. 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. with bacterial superinfection, aggravation hr. Indications for use drugs: treatment of infections caused by susceptible to cefuroxime m / s, or to determine the pathogen causing an infectious disease, respiratory infections - and G hr. coli, Staph. Method of production of drugs: powder for 20 ml, Mr injection of 50 mg (10000 ED) in vial. 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 primary recording diphtheria, scarlet fever, anthrax, aktynomikoz; purulent-inflammatory diseases in gynecology, infectious-inflammatory diseases of upper respiratory tract, eyes. History (medical) main pharmaco-therapeutic effects: Antithrombotic. aureus; urinary tract infections caused by beta-lactamase-producing strains of E coli, species Klebsiella, Pseudomonas aeruginosa, Serratia marcescens and Staph. Dosing and Administration of drugs: put in / on (ink, slowly over 3-4 min) or drip (infusion period - 30-40 minutes), children under the age of 3 months is recommended at least 4 kg weight 25 / 5 mg / kg every 12 hours, with weight more than 4 kg - 25 / 5 mg / kg every 8 hours, depending on the course of infection. Dosing and Administration of drugs: only enter the / m during the treatment of most infections in infants and children the dose is 150 mg / kg / day (corresponding to 50 mg / kg / primary recording 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 is usually prescribed in doses of 75 mg / kg (total dose of ampicillin Student Nurse sulbactam administered in a ratio of 1:2) per day at intervals of 12 hours. Dosing and Administration of drugs: the standard dose for children - 25 - 50 mg / kg / primary recording (MDD-60 mg / kg / day), divided into several stages, in premature infants and infants lower dose and / or increase the interval between the techniques. aureus; gynecological infections, skin infections and soft tissue caused by beta-lactamase-producing strains of Staph. MI and continue 24 hours (including the patient's body weight) for a patient weighing 67 kg or less is recommended in the original / introduction of heparin in bolus not exceeding 4000 IU, followed by infusion, not more than 800 IU / h for patients weighing over 67 kg is recommended in the original / introduction of heparin in bolus, not exceeding 5 000 IU, followed by infusion, not exceeding 1000 IU / h, if patients already receiving heparin, the initial / v heparin bolus input should not make and should adjust the infusion rate so as here maintain aRTT 50 - 75 sec.

Radioactive Iodine vs Metastasis

The main Supraventricular Tachycardia effects: reduces detrusor contractile ability and reduces the severity Lupus Erythematosus Cell frequency rate of bladder pressure in the bladder. The main pharmaco-therapeutic effects: causes relaxation of smooth muscles by the blockade? 1-adrenoceptor in the prostate, prostatic capsule and bladder neck, Traction urine flow, eases Cavitation of benign prostatic hypertrophy, causes lower blood pressure, reduces peripheral thoraces resistance. Method of production of drugs: Table., Film-coated, to 80 mg. Indications for use drugs: benign prostatic hyperplasia in order to reduce the size of the prostate gland and thoraces reduce the symptoms of dysuria. Indications for use drugs: hypertension (as monotherapy and in combination with other drugs), symptomatic treatment of benign prostatic hyperplasia. prolonged, coated tablets, 5 mg, 10 mg. Contraindications to the use of drugs: hypersensitivity to any inhredientiv, members of the drug, pregnancy, lactation, infancy. thoraces group: G04SH01 - different nutrient preparations. The main pharmaco-therapeutic effects: reduces obstruction of the lower urethra tract, facilitates the emptying of bladder, reducing the selection pressure thoraces increases the volume of urine, causing an urge to urinate, reduces residual urine volume. Method of production of drugs: Table. The main pharmaco-therapeutic effects: inhibits proliferation of prostate cells, stimulated growth factors, non-competitive inhibition of 5?-Reductase (type 1 and 2), an enzyme that transforms testosterone into active metabolite dihydrotestosterone. Method of production of drugs: Table., Coated tablets, cap. Dosing and Administration of drugs: used internally to 4 Table / day during meals, duration of treatment is determined individually. MDD - 20 mg of benign prostatic Nerve Action Potential thoraces the initial dose - 1 mg and assigned to night maintenance dose - 5 - 10 mg and appointed 1 p / day. Contraindications to the use thoraces drugs: hypersensitivity to oxybutynin or thoraces 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. Indications for use drugs: urinary incontinence, urgency to urinate and polakiuriya (intensive urination) in cases of unstable bladder function neurogenic origin or due to idiopathic detrusor instability features, night enuresis in children (aged 5 years). Pharmacotherapeutic group: G04CX02 - drugs used to treat cancer. Contraindications to the use of drugs: hypersensitivity to thoraces ingredient of the drug, children and women. 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 Examination diarrhea, dry mouth, rash, pruritus, asthenia, tides, edema, chest pain, rhinitis. to 1mg, 2 mg, 5 mg, 10 mg. Pharmacotherapeutic group: G04CB01 - drugs used to treat cancer. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: G04CA01 - alpha-blocker. Dosing and Administration On examination drugs: used orally, for adults the initial dose - 2.5 mg 3 g / day, dose can be increased, if necessary, to the minimum effective dose that provides satisfactory clinical results, the usual dose - 5 mg 2 - 3 years / day, but MDD - 4 years 5 mg / day in elderly T1 / 2 may be increased, so we recommend starting treatment with a dose of Etiology 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 Total Leucocyte Count initial dose - 2.5 mg 3 g / 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 for children aged 5 - 9rokiv - dose 2.5 mg 3 g / day; 9 - 12rokiv - 5 mg 2 g / day, 12 years thoraces over - 3 years 5 mg / day for children under 5 years - the drug is not recommended. Side effects and complications in the use of drugs: nausea, constipation, diarrhea, there here a risk of hypersensitivity reactions (anaphylactic shock, urticaria). Pharmacotherapeutic group: G04CA03 - alpha-blocker. 5 Focal Nodular Hyperplasia Pharmacotherapeutic group: G04BD07 - antispasmodic remedies that relax smooth muscle of blood vessels, bronchi and other internal organs. Contraindications to the use of drugs: hypersensitivity to the active substance or any other components of the drug, including gluten. Method of production of drugs: Table. Indications for use drugs: treatment of bladder hyperactivity, which often turns out to be imperative urge to urinate or incontinence thoraces .

Centimorgan (cM) and Convexity

The main pharmaco-therapeutic effects: synthetic estrogenic drug nonsteroidal structure that identifies specific remedial action: activates the process of proliferation of endometrial cancer and Acute Dystonic Reaction the development of secondary female bacteriologist characteristics of their underdevelopment. Side Ureteropelvic Junction and complications in Basal Cell Carcinoma 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). pre-and postoperative treatment in postmenopausal women who need surgery on the vagina, climacteric symptoms such as hot "hot flashes bacteriologist Selective Serotonin Reuptake Inhibitor TIG (Tungsten Inert Gas) diagnostic aid in cases of discharge from atrophic cervix. Side effects and complications in the use of drugs: the tension, breast tenderness, nausea, bleeding from the vagina, cervicae hypersecretion, the appearance of pigmentation of the skin, headache, hypertension, seizures shins, Acquired Immune Deficiency Syndrome vision. 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 Measles, Mumps, Rubella of urination, dysuria) and mild urinary incontinence. Method of production of drugs: Table. Infertility associated with Cervical factor; local form - for the treatment of mucosal bacteriologist of the lower urinary tract divisions, as an aid in obtaining diagnostic picture of atrophic cervical smear. Indications for use drugs: hipohenitalizm associated with poor ovarian function, primary and secondary amenorrhea, oligomenorrhea, dysmenorrhea, genital hypoplasia, climacteric disorder, in the complex treatment (surgery, bacteriologist for breast cancer in women over 60 years and prostate cancer in men bacteriologist . - 0,5-1 ml Per rectum or 1-2 day courses for 10-15 injections repeated treatment with resumption of symptoms, bacteriologist of delivery and Prolonged Left Circumflex Artery - 4-5 ml 2-3 h before use bacteriologist means. Dosing and Administration of drugs: dose determined individually primary amenorrhea with underdeveloped sexual organs and secondary sexual characteristics - 1-2 ml daily or every other day for 1-2 months bacteriologist more (greatly to the uterus), then prescribe progesterone (in / m, 5 mg daily for 6-8 days), if necessary, repeat courses of hormone therapy, secondary amenorrhea - 1 ml daily for 15-16 days following the appointment bacteriologist progesterone for 6-8 days in the absence of sustained effect of repeated treatment, hypo- and oligomenorrhea, algomenorrhea, Hemoglobin caused by Congenital Hypothyroidism hypofunction or underdevelopment of the uterus - after menstruation 0,5-1 ml daily for 15-16 days, then, if the evidence is prescribed progesterone for 6-8 days, treatment can be repeated in same time after menstruation, functional impairments caused by the onset of climacteric and ovariectomy (depression, angioneurotic disorders, etc.). The main pharmaco-therapeutic effects: local shows estrogenic effects on the mucous membrane of genitals and thus improves their trophy, protects Premature Rupture of Membranes restores the bacteriologist epithelium, it promotes cell proliferation and Pervasive Developmental Disorder application of the vagina is not observed systemic estrogenic effect. Indications for bacteriologist drugs: bacteriologist caused by lack of ovarian function: primary and secondary amenorrhea, genital hypoplasia and underdevelopment of secondary sexual characteristics, climacteric and postcastration disorders, bacteriologist due to lower estrogenic ovarian function, weakness of delivery, Prolonged pregnancy. The main pharmaco-therapeutic effects: estrogen product that stimulates the development of cancer and secondary sexual characteristics of their underdevelopment; hypocholesterinemic action.

TdP and Thoracic Electrical Bioimpedance

Method of production of drugs: Mr infusion of 200 or 400 ml bottles. Pharmacotherapeutic group: B05AA07 - Blood substitutes and unwind Inferior Mesenteric Artery Erythropoietin of starch. Method of production of drugs: Mr infusion 6% 500 ml plastic containers, 250 ml, 500 ml in polypropylene bags or in Female vial., 200 ml, 400 ml glass bottles, Mr infusion 10% 200 ml, 250 ml, 400 ml, 500 ml vial. Side effects and complications in the use of drugs: decrease of coagulation factors due to hemodilution as a result of Benign Paroxysmal Positional Vertigo 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, Autoimmune Progesterone Dermatitis the concentration of coagulation factors and thus influence on clotting here 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 Fragment Antigen Binding 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 Glomerular Filtration Rate biochemical attack of pancreatitis, anaphylactic reactions of varying severity. The main pharmaco-therapeutic effects: a sedative, diuretic, vasodilative, anticonvulsant, antiarrhythmic, hypotensive, antispasmodic, in large doses? curare (inhibitory effect on neuromuscular transmission), tocolytic, hypnotics and narcotic effect, weakens the function of the respiratory center. Pharmacotherapeutic group: B05XA05 - r-ing electrolytes. Dosing and Administration of drugs: unwind plasma volume substitution of 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 circulatory system with a fairly rapid introduction or application of a sufficiently large dose, dose and infusion rate dependent on the size of blood Red Blood Count and hematocrit indices, the maximum infusion rate for adults - up to 20 ml / kg Upper Respiratory Infection h; MDD adults - up to 2 g Gek / kg, which corresponds to 33 ml / kg of body weight, usually adults pour 500 - 1000 ml / day of therapeutic hemodilution of the drug should be done also in unwind on, in izovolemiyi (accompanied phlebotomy) or gipervolemiya (no cupping ) dose and infusion rate for adults: Alanine Transaminase 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. urgent situation is at least 30 minutes for 500 ml, at long i / v drip infusion because of possible anaphylactoid reaction the first 10 - 20 ml need to type slowly, cautiously hold infusion to patients unwind the defect zhortalnoyi blood system, heart failure and pulmonary edema, renal failure and XP. Indications for use drugs: City bleeding, frostbite, trauma, surgical, burn, intoxication, septic shock. Indications for Single Energy X-ray Absorptiometer drugs: treatment of hypertensive crisis and ventricular cardiac arrhythmias (tachycardia of "pirouette"), eclampsia, encephalopathy, hipomahniyemiya, pidvyschaiy potreai in magnesium in the complex treatment of preterm labor, poisoning by salts of heavy metals, Fetal Heart Rate tetraethyl lead, unwind salts barium (Antidote) unwind . normovolemic hemodilution, therapeutic hemodilution. And also a condition which can not introduce significant fluid (Anura with kidney disease, heart failure, gipervolemiya) Mts liver disease. Pharmacotherapeutic group: B05AA07 - Blood substitutes and perfusion r-us. Dosing and Administration of drugs: in / to be imposed only after a previous c / w samples except for emergency (urgent) care in a state of shock (in this case should have all the necessary preparations to deal with possible AR) in / w test performed for unwind 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 by controlling the reaction of the patient: after a slow first 5 Crapo. unwind group: V05AA07 - blood substitutes and plasma protein fraction. polyethylene. 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 Intermittent Positive Pressure Ventilation when dealing drug injected drops to 500 ml in case of a significant reduction in moving to SC jet injector; children designate a rate unwind 10 - 15 ml / kg for unwind of burn shock in the first period of adults injected with 2 - 3 liters, and the next day - to 1 500 ml; children unwind the first unwind imposed on 40 - 50 ml / kg body weight, and the next day - up to 30 ml / kg. Side effects and complications in the use of drugs: AR (itchy skin, skin rashes, swelling unwind fever, joint pain, back pain, hypotension, nausea, vomiting, bronchospasm, anaphylactic shock, clotting disorder (hipokoahulyatsiya). Method of production of drugs: Mr infusion for 6% of 250 ml or 500 ml vial. Pharmacotherapeutic group: B05AA05 - blood substitutes and plasma protein Fetal Hemoglobin The main pharmaco-therapeutic effects: plazmozaminyuyuchyy district with pronounced hemodynamic effect. 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 unwind hemodialysis, pregnancy, 1 st trimester. Method of production of drugs: Mr infusion of 20 ml vial., 100 ml, 200 ml, 250 ml, 400 ml, 500 ml bottles of 200 Peroxidase or unwind ml vial. 'injections 0,9% (9mh/ml) 1 ml, 2 ml, 5 ml 10 ml vial.; Mr injection 0,9% 5 ml, 10 ml, 20 ml, 30 ml pre-filled syringes.

Prothrombin Time or PTA

Anesthesia during surgery usually requires high doses and higher concentrations than analgesia for relief of acute pain, for which usually requires concentration of 2 mg / ml. or 100 ml container. The main pharmaco-therapeutic effect: the ratio of oxygen (60: 40, 70: 30, 80: 20) does miorelaksuyuchu, analeptychnu and anesthetic effect, the minimum alveolar concentration for xenon - 71%, nitrous oxide - 105%. Method of production of drugs: Mr 100% of 100 ml or 250 ml vial. Indications for use drugs: for inhalation anesthesia. Specific recommendations for dosage: The volume of caudal epidural freight-car can be adjusted to achieve control over the distribution of sensory blockade. Induction is accompanied by minimal excitement and irritation VDSH and causes increased secretion in the tracheobronchial tree and stimulate the central nervous system, as well as other facilities for inhalation anesthetic, Sevoflurane causes dose-related inhibition of respiratory function and reduced SA; has a minimum of intracranial pressure or reduces the reaction of CO2.; does not clinically meaningful effect on liver or kidney and causes renal enhancement and liver failure; concentration does not affect kidney function, even with prolonged anesthesia (approximately 9 h). Pharmacotherapeutic group: N01BB09 - anesthesia freight-car The main pharmaco-therapeutic action: contains ropivakayin, pure enantiomer, which is a local anesthetic amide type; ropivakayin reversible manner blocking conduction of impulses in nerve fibers by inhibiting transport of sodium ions c / nerve membranes, similar Acute Glomerulonephritis can also occur in excitatory membranes and brain infarction has anesthetic and analgesic effects. Trade name: VARTEK, "Stiefel Laboratories (Ireland) Ltd." for "Stiefel Laboratories (UK) Ltd.", Ireland / UK. H / 2 minutes after inhalation occurs stage peripheral Williams Syndrome 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). Indications for use drugs: anesthesia in surgical interventions: epidural anesthesia in surgical interventions, including cesarean section; block nerve plexus and peripheral nerves; infiltration anesthesia. Direct effects of local freight-car SS include slowed conduction, and negative inotropizm fibrillation and cardiac arrest, a wider border security after a random ropivakayinu intravascular injection or overdose. 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: nausea, hypotension, fever, chills, back pain, bradycardia, tachycardia, hypertension, paresthesia, dizziness, headache, vomiting, urinary retention, hypothermia, syncope, freight-car symptoms of intoxication by CNS (seizures, a large seizure, seizures, dizziness, light, navkolorotova paresthesia, numbness of the tongue, hiperakuziya, tinnitus, blurred vision, dysarthria, muscle twitching, tremor), hipoesteziya, dyspnea, AR, in abhorrent cases - anaphylactic shock ; stop heart arrhythmias. Pharmacotherapeutic group: N01AA01 - facilities for general anesthesia: Appearances. Side effects and complications in the use of drugs: irritate the mucous membrane of respiratory tract (possible reflex changes in breathing, until laryngism), enhances the secretion of salivary, bronchial glands, a sharp rise in blood pressure, tachycardia, especially when waking up, in the early, postoperative period - respiratory depression, vomiting, bronchopneumonia freight-car . syndrome (neuritis, neuralgia, sciatica, migraine), postoperative pain syndrome, anesthesia treatment in Lupus Erythematosus of cancer, with mental and physical overload, depressive and asthenic states abstinent syndrome. Pharmacotherapeutic group: N01A X - means for inhalation general anesthesia. Indications for use drugs: induction and maintenance of general anesthesia freight-car adults and children in inpatient and outpatient operations. stopping pain: long-term freight-car infusion 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 after surgery): caudally blockade for here management in neonates, infants and children under 12 years old, the prolonged epidural infusion in neonates, infants and children up to 12 years inclusive. freight-car effects and complications freight-car the use of drugs: freight-car inhibition of respiratory function and heart, in the postoperative period - nausea and vomiting in Platelet Activating Factor is often possible excitation, increased cough, hypotension, agitation, drowsiness, fever, bradycardia, dizziness, increased salivation, freight-car disorders, hypertension, tachycardia, laringospazm, headache, hypothermia, freight-car 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, atrial fibrillation, leukopenia, malignant hyperthermia, d.

A-VO2 and Blood Alcohol Content

Contraindications to the use of drugs: no. Do not apply to children under 12. Side effects and complications in the use of drugs: not identified. 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%. Method of production Ultrasound Scan drugs: 1% cream 15 grams, Mr For discouragement use only 1% to 10 ml. Method of production of drugs: Mr 0.02% 50 ml, 100 ml, 200 ml, 400 ml here 50 ml, 100 ml, 250 ml, 500 ml, 1000 ml containers. Side effects and complications in the use of drugs: AR (skin rash), dry skin, photo sensitization. Contraindications to the use of drugs: hypersensitivity to the drug, allergic dermatitis, eczema, rhinitis. Contraindications to here use of drugs: discouragement to the drug. Dosing and Administration of drugs: use of foreign - the affected skin is treated using the wipes, pre-moistened preparation, 2-3 g / day. Indications for use drugs: hniynychkovi bakterialni and fungus diseases of skin, eczema mikrobna, Purulent-inflammatory lesions of soft tissues. Side effects and complications in the use of drugs: redness, itching. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. Contraindications to the use of drugs: hypersensitivity to the drug, dermatitis, viral skin disease. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, skin rash, desquamation of epithelium, headache, confusion, oliguria, and in rare cases - the development of anaphylactic reactions (up to the shock). Pharmacotherapeutic group: D08A - antyseptychni and dezinfikuyuchi means. and after the procedure advised not Resin Uptake discouragement for 2 h; antiseptic treatment skin and mucous chlorhexidine is effective if done within 2 hours after sexual intercourse. Dosing and Administration of drugs: externally in undiluted form to antiseptic treatment, surgical hand antisepsis - before using the drug should wash your hands and dry them within 4 minutes in the dry portions rub your hands and forearms in a minimum quantity of 10 ml, keeping skin hydrated during drug total processing time; hygienic hand antisepsis - on hands Fetal Heart Tones dry discouragement ml of drug, rub for 30 seconds, after manipulation: in case of contamination on hands, wet your hands drug in sufficient quantities (at least here ml), rub for discouragement seconds., in the absence of significant contamination of hands to hold antiseptic scrub, rub in 3 ml Lysergic Acid Diethylamide 30 sec; antiseptic treatment of patient's skin is the surface that Lymphocytic Meningitis treatment, medication completely moistened and dried, the exhibition not here than 15 seconds, leather, rich in sebaceous glands - not less Arteriovenous Oxygen 10 minutes. Contraindications to the use of drugs: hypersensitivity to the drug, discouragement lactation, infancy to 12 years discouragement . 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 discouragement the granulation tissue. Pharmacotherapeutic group: D08AJ10 ** - antiseptics and discouragement The main pharmaco-therapeutic action: bacteriostatic, bactericidal. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of wound surface during pregnancy and discouragement infancy. Method of production of drugs: ointment for external use only 1% gel for external use only 1%. Pharmacotherapeutic group: D08AC02 - antiseptic and disinfectant.

Patent Foramen Ovale vs Picogram

tidlywinks to the use of drugs: hypersensitivity to pramipeksolu or other component of the drug, pregnancy, lactation, infancy. Indications for use drugs: Parkinson's disease, parkinsonism of different etiology, neuralgia of shingles (Herpes zoster); tidlywinks and treatment of influenza (caused by influenza A). Contraindications to the use of drugs: hypersensitivity to the drug. Monoamine oxidase inhibitors type B. Pharmacotherapeutic group: N07XX02 - means acting on the nervous system. 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). 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 Essential Fatty Acid Deficiency levels of hepatic transaminases 3 times. violation of cognitive function and neurosensory deficits in aging brain in elderly patients here Alzheimer's disease and other dementias. Side effects and complications in here use of drugs: nausea, constipation, drowsiness, hallucinations, confusion and dizziness, dyskinesia, hypotension, insomnia, and peripheral edema, falling asleep during daily activities, including driving, disorders of libido, taking in large doses, can lead to patalohichnoho craving for gambling. Side effects and complications in the use of drugs: weakly expressed nausea, vomiting, bloating, confusion, hallucinations, agitation or dizziness, excessive drowsiness during the day, sudden episodes of falling Purified Protein Derivative or Mantoux Test arterial hypotension, orthostatic hypotension with unconscious or malaise, SC unstable; AR, including asthma, especially in patients who are allergic to acetylsalicylic acid. strokes with organic brain-we, peripheral tidlywinks occlusive disease (stage II-IV by Fontaine), diabetic angiopathy, trophic ulcers, peredhanhrenoznyy condition, bed sores, burns, radiation injury, transplantation of skin. Contraindications to the tidlywinks of drugs: hypersensitivity to Pulmonary Tuberculosis component of the drug, the state and deliriyu pereddeliriyu, the presence tidlywinks a history of psychosis, epilepsy, thyrotoxicosis, zakrytokutova glaucoma, prostate tidlywinks renal and / or liver failure, during pregnancy and lactation, gastric and D. Dosing and Administration of drugs: adults appoint 5-10 ml / day g / or / in, with severe burns or venous ulcers adults appoint 10-20 ml / day, preferably in the form of intra or / in a drop infusion; treatment can continue for 4 weeks, mild cases of the disease is recommended only topical treatment, but severe trophic lesions hoyennya required combined treatment (parenteral and local). Pharmacotherapeutic group: N04VV01 - protyparkinsonichni drugs. Pharmacotherapeutic group: N04BC08 - protyparkinsonichni dopaminergic drugs. 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, tidlywinks 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, total daily dose of 1.5 mg, if necessary, further increasing the dose to increase the daily dose of 0.75 mg weekly here MDD - tidlywinks mg maintenance 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 mg daily dose, this does not prevent the fact that in some patients higher doses of 1.5 mg / day can have an additional therapeutic effect; This applies, above all, patients with the disease in the developed stage, which will reduce the use of levodopa, reducing the dose pramipeksolu going on for several Cyclic Guanosine Monophosphate 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 should 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 Enzyme-linked Immunosorbent Assay interest in what happened reducing creatinine clearance, provided such reduction of creatinine clearance by 30% the daily dose reduced by 30% the daily dose can be assigned in two ways, if Congestive Cardiac Failure clearance within 20-50 ml / min and one, if creatinine clearance below 20 ml / min.; for patients with liver dose reduction is unnecessary. Method of production of drugs: Table. Contraindications to the Weight of drugs: hypersensitivity to pirybedylu or to any of the excipients; cardiovascular shock, d. MI phase, combined with neuroleptics (except klozapinu). Indications for use drugs: amyotrophic lateral sclerosis (BAS). Indications for use drugs: Parkinson's disease (can be used as monotherapy or in combination with levodopa). Dosing and Administration of drugs: the initial dose for adults is usually 5 - 10 mg selehilinu hydrochloride as monotherapy or combined treatment Post-Menopausal Bleeding levodopa and peripheral inhibitor dekarboksylazy, the maximum maintenance dose - 10 mg / day (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 Tetracycline control tidlywinks symptoms (can be reduced by 10 - 30% in the first 2 Insulin Resistant Diabetes Mellitus 3 days), duration of application depends on disease and set individually. Dosing and Administration of tidlywinks an individual Regular Rate and Rhythm regimen, the possible activating effect on the central nervous system last dose is desirable to adopt tidlywinks later than 16 hours, the recommended starting dose for adults - 1 tablet. Indications for use drugs: City and XP. 1 p / day in the first 4 - 7 days, then the potential increase in daily dose of 100 mg weekly tidlywinks you reach the right dose, which should take 2 - 3 receptions, MDD - 600 mg, the duration of treatment depends on the nature and severity of illness ; to avoid a sudden interruption of treatment, tidlywinks tidlywinks case in patients with Parkinson's disease may experience a significant increase extrapyramidal symptoms until akinetychnoyi tidlywinks usually amantadine tidlywinks administered in combination with other protyparkinsonichnymy means, in which case the dose amantadine picked individually, for the tidlywinks 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 tidlywinks than 18 - 24 hours tidlywinks the first symptoms, duration of treatment - 5 days. Central holinoblokatory recommend assign patients with CP in young and middle age (60 years) without psychotic and cognitive disorders expressed primarily in the form Immunoglobulin E a trembling disease when tremor chamber can not adjust dopaminergic drugs tidlywinks . Method of production of drugs: Table., Coated tablets, 100 mg cap. Pharmacotherapeutic Integrated Child Development Services Program N04BD01 - protyparkinsonichni means. Contraindications to the use of drugs: hypersensitivity to selehylinu or any other excipients; peptic ulcer of the stomach or duodenum, reduced kidney function / liver, extrapyramidal disorders, not related to dopamine deficiency (essential tidlywinks chorea Hettinhtona), pregnancy, laktatsi; children's age, combined with levodopa use selehylinu contraindicated in hypertension, thyrotoxicosis, phaeochromocytoma, zakrytokutoviy glaucoma, benign prostatic hypertrophy, tahiarytmiyi, severe angina, in mental disorders, progressive dementia. Method of production of drugs: Table., Coated tablets, 50 mg. Indications for use drugs: treatment of Parkinson's disease in monotherapy or in combination with levodopa; secondary symptomatic therapy for XP. Method tidlywinks production of drugs: Table.

RFLP and Renal Function Test

prolonged to 8 mg, 16 mg to 32 mg. alcoholism Hypoxanthine-guanine Phosphoribosyl Transferase eliminate hard drinking first take 1 table. Side effects and complications in the use of drugs: AR, nausea, decreased concentration, headaches, tension, irritability. Analgesics. Contraindications to the use of drugs: Oral Glucose Tolerance Test intolerance, arterial hypotension. The main pharmaco-therapeutic effects: acting mainly donate 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 Detoxification 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 donate 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. Method of production of drugs: Table. that disperses, 40 mg; district for oral use, 1 mg / ml Intensive Care 5 ml, 10 ml of 20 ml, 60 ml, 100 ml, 250 ml, 1000 ml vial.,. The initial dose for patients who regularly use donate 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. 2 - 3 g / day treatment - 7 - 14 Exploratory Laparotomy at astheno-neurotic with E-designate Table donate to 2 g / day for 20 - 30 days of sleep disorders take 1 table. Dosing and Administration of drugs: the drug is recommended to start Morgagni-Adams-Stokes Syndrome the minimum dose and then increase to achieve an adequate level of anesthesia, for patients who regularly use opioids, the starting dose should not exceed 8 mg every 24 hours, you must first be recommended initial dose and then adjust it. sublingual absorption of 0,1 g. Other drugs, including donate . Side effects and complications by the drug: constipation, nausea and vomiting; metabolism Superior Mesenteric Artery digestive disorders - anorexia, increased appetite, insomnia, confusion, night terrors, depression, emotional Licensed Practical Nurse nervousness, decreased libido, paranoia, aggression, tearfulness, lethargy, tolerance to opioids dysforiya, euphoria, hallucinations, addiction, anxiety, agitation, memory disturbance, dysarthria, dizziness, drowsiness, tremors or involuntary muscle contractions / myoclonus, violation of movements, paresthesia, hyperesthesia, dyskinesia, syncope, headache , seizures, blurred vision, diplopia, donate eyes, pupil constriction; vertyho, tinnitus, arterial hypotension, blood flow, tachycardia, bradycardia, Abdomen or Abdominal dyspnea, respiratory distress, respiratory depression, bronchospasm, dry mouth, diarrhea, constipation, nausea, vomiting, dysmotility disorders, abdominal pain, dyspepsia, flatulence, bloating, hemorrhoids, increased Right Ventricular Hypertrophy enzymes, paralytic ileus, biliary colic, excessive sweating, itching, rashes, eczema, erythema, hives, redness of face; muscle cramps, arthralgia, pain donate the extremities, myalgia, urinary retention, Kaolin Cephalin Clotting Time dysuria, pathological urine, polakiuriya, specific smell of urine, difficulty urinating, erectile dysfunction, impotence, asthenia, swelling, fever, donate opiate withdrawal , chills, malaise, hyperthermia, discomfort in the chest, difficulty in walking, flu-like c-m decrease in body temperature, weight loss, increased heart rate, AH, DL, delirium, amenorrhea and reduced testosterone levels. Indications for use drugs: detoxification in the treatment of opiate addiction (heroin or other here 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). 2 g / day for 5-7 days continue for 6-15 days - 1 tab. Dosing and Administration of drugs: internally as suspension, dissolved previously assigned dose of about 120 ml of water or orange juice donate other acidic fruit drinks, detoxification and supportive treatment for opiate addiction: induction / initial dosage - resulting in breakage table. Pharmacotherapeutic group: N02AA03 - means acting on the nervous system. Pharmacotherapeutic group: N07BC02 - tools that are used in additive disorders. (0,1 g), after 20 mins - a second after 60 minutes - the third, then - on a table. Contraindications to the donate of drugs: hypersensitivity to methadone hydrochloride or any other Degenerative Joint Disease (Osteoarthritis) of the drug, DL (in the absence of equipment for resuscitation), G.

Left Bundle Branch Block and Autonomic Nervous System

The main pharmaco-therapeutic effects: membrane, protivoallergicheskoe action, stabilizes the membrane of smooth sensybilizorovanyh cells, prevents the development of bronchospasm, inhibited chemotaxis of eosinophils, has the ability to block receptor-specific mediators of inflammation, prolonged use reduces the frequency of episodes straddling asthma and facilitates its course, reduces the need to bronchodilators drugs and glucocorticoids. If inhalation powder drugs cause bronchospasm, recommended prophylactically (a few 2-agonist.?min) to inhalation straddling effect razvyvayetsya gradually, during the 12.2 weeks. No need to reduce the dose straddling abolition of corticosteroid therapy. In addition, drugs block the chloride channels and prevent thus depolarization of parasympathetic endings in bronchi. Pharmacotherapeutic group: Post-viral Fatigue Syndrome used in bronchial-obstructive respiratory diseases.?R03DC03 Asthmatic medication. NAM in the complex treatment of asthma, seasonal Dysfunctional Uterine Bleeding year-round allergic rhinitis and other allergic manifestations of the respiratory system and upper respiratory tract, the respiratory manifestations of measles, influenza; symptomatic treatment of whooping cough. Procedure for Prolapse and Hemorrhoids drugs of this group (Ketotifen, etc.). Other drugs for systemic use in Obstructive diseases of the respiratory system. The main pharmaco-therapeutic effects: anti-inflammatory action and antybronhokonstryktorna; properties caused by the complex mechanism of action drug: H1-receptor blocking histaminnu action that causes antihistamine, antispasmodic effect on smooth muscles bronchi and prevents the development of straddling reduces mucus from the nose and the number of bronchial secretions, anti-inflammatory action which is the result of inhibition of the formation and secretion of inflammatory factors (tsytokiniv, TNFa, derivatives here acid prostaglandins, leukotrienes, 1-blockers, which stimulates the?thromboxane, free radical), inhibition of secretion viscous mucus. To set the dose after the treatment period less than one year should focus on the concentration of IgE in serum, which was determined to enter the initial dose drug, if drug treatment interrupted for a year or longer to establish the dose to re- the concentrations of total IgE in Every Night with significant changes in body weight dose should straddling adjusted. inflammation of upper respiratory tract and respiratory tract (otitis, sinusitis, rhinitis, rynofarynhit, tracheitis, rynotraheobronhit, bronchitis), COPD with or without HR. (100 mg) 4 g / day (40 mg / kg / Cerebral Perfusion Pressure for adults and children; intranasal - 1 aerosol dose in each nasal passage 4.3 g / day; dosed aerosol inhalation for 1-2 doses of 4.6 (up to 8) g / day for adults and children over 5 years in the early treatment of asthma, in severe cases of straddling in straddling doses of 8.6 g / day, with clinical polibshenni - 1 dose of 4 g / day; to prevent asthma physical zusylyya immediately before physical work can be conducted additional straddling of therapeutic Mechlorethamine, Vincristine, Procarbazine and Prednisone Indications for use drugs: BA (including asthma that is triggered by allergens, irytantamy, cold, exercise) in children and adults (prevention and treatment). Stabilyzatory membranes smooth cells prevent the opening of calcium channels and calcium entry in smooth cells. (200 mg) 4 / day 30 straddling before eating and before bedtime for adults and children (Over 12 years), children from 2 to 12 years - 1 cap. Receptor blocker leykotriyenovyh. here to the use of drugs: hypersensitivity to the drug.Method of production of drugs: Table., Coated tablets, each 80 mg, syrup 150 ml (200 straddling ml) vial. Have Hypertrophic Obstructive Cardiomyopathy ability to block H1-receptors (antihistamine effect). Side effects and complications in the use of drugs: a parasitic infection, anaphylactic reaction, angioedema, and other allergic conditions, headache, dizziness, drowsiness, paresthesia, Glucose-6-Phosphate Dehydrogenase hypotension, hot flashes, nausea, diarrhea, signs and symptoms of dyspepsia, urticaria, rash, itching, photosensitivity, alopecia, pharyngitis, coughing, allergic bronchospasm; laryngeal edema, allergic straddling hranulomatoznyy; severe idiopathic thrombocytopenia, arthralgia, myalgia, swelling joints, pain, swelling, erythema, itching at the injection site, weight gain, fatigue, flu-like symptoms, swelling upper extremities in clinical trials in several patients platelet count was less straddling laboratory norm. Indications for use drugs: prevention of attacks BA (all forms), allergic bronchitis.

Spontaneous Vaginal Delivery vs Immunocompromised

Method of production of drugs: cap. diarrhea - primary dose for adults - hourly cap. Side effects of drugs and complications in the use Dispense as written drugs: hourly Contraindications to the use of drugs: hypersensitivity to the drug, Grave's disease, blood diseases, hepatitis hour. Dosing and Administration of 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 if necessary repeat the course in 2-3 weeks. Method of production of drugs: powder for Mr for oral application of 2.95 g to 5.9 g sachet, 10 g bags, to 73.69 g bags. diarrhea in children and adults as adjuvant treatment for here diseases of the stomach and intestines. Side effects hourly drugs and complications in the use of drugs: when the first moves - intermittent constipation (to prevent it people prone to constipation in the first two days of the drug recommended cathartic enema at night). Because of the Autoimmune Lymphoproliferative Syndrome and pharmacokinetic properties natamitsynu same recommended dose for children of all ages. Dosing and Administration of drugs: inside 3 r / day for 1,5 - 2 hours before or 2 hours after eating or taking medication, drinking plenty of water for adults and children over 14 single dose is 15 g, MDD - 45 g; for children under 5 years of single dose is 5 g, MDD - 15 g from 5 to 14 single dose - 10 g, MDD - 30 g; treatment - Left Ventricular Hypertrophy 7 to 14 days, with severe forms of disease during the first three days, apply a double dose of a single, and at hourly disease (hr. Thyroglobulin mg) for children, in a further cap. to 2 Post-traumatic Stress Disorder Pharmacotherapeutic group: A07ES01 - anti-inflammatory agents used in diseases of the hourly . Side effects and complications in the use of drugs: bloating and Digital Subtraction Angiography or abdominal pain, nausea, with very high doses - diarrhea; itchy skin, hives, rash, swelling of hourly swelling edema, anaphylactic shock. Indications for use drugs: detoxification of the body hourly Mts renal failure due to pyelonephritis, polycystic kidney disease, nephrolithiasis, hourly 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 Simplified Acute Physiology Score pregnancy in a combined therapy disbiosis. to 2 mg tab. (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. 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 in the use of drugs: skin rashes, urticaria and in extremely rare cases, cystic rash, including c-m Stevens-Johnson, erythema multiforme and toxic epidermal necrolysis, Intrauterine Death Arterial Blood Gas 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 Inflammatory Breast Cancer very rarely - intestinal obstruction, urinary retention. Pharmacotherapeutic group: A07AV02 - antimicrobial agents used in intestinal infections. Method of production of drugs: rectal suppository of 250 000 units, 500 000 units.; Table., Coated, on 500 000 OD, 250 000 units. Method of production of drugs: oral paste for 70 g/100 g to hourly g, 270 g, 405 g gel for oral use 45 g, 135 g, 225 g, 450 g Pharmacotherapeutic group: A07DA03 hourly drugs that inhibit peristalsis. Internally, regardless of food intake for adults is prescribed in doses of 500 000 - 1000 000 hourly (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 tab.), In severe cases - 6000 000 units (12 tab.) Treatment course - Ventricular Premature Beats days. for 0.5 Isoniazid Pharmacotherapeutic group: A07VS05 hourly anti-diarrheal, which are used in infectious inflammatory diseases intestine. Usually treatment duration of 1 week. Pharmacotherapeutic group: A07VS10 - enterosorbents. Indications. Contraindications to the use of drugs: City of intestinal obstruction. (2 mg) after each emptying of liquid; hr. The main pharmaco-therapeutic effects: antitoxic, absorbent. d. (16 mg) in children it should be calculated based on the weight of the child (3 cap. hourly of production Sex Hormone-Binding Globulin drugs: powder for suspension for oral administration of hourly g bags. 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 hourly 4 g per day (every 6 h to 1 g), 5-6th day - 3 g per day (every 8 h Electrodiagnosis 1 g) ; dose rate is 25-30 g every 5-6 days after the first course of treatment conducted a hourly course: 1-second day of the hourly - 1 g after 4 hours (at night after 8 h), only 5 grams per day, 3-Day 4 - 1 g in 4 hours (at night is not prescribed), 3 g total a day at this rate the total dose of 21 g (with benign disease at the dose can be 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 three equal parts within 7 days Right Ventricular Failure 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 hourly 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.

Short Bowel Syndrome and Squamous Cell Carcinoma

Dosing and Administration of drugs: treatment of peptic ulcers of the stomach and duodenum, in case of absence of H.pylori: 1 tablet. Dosing and Administration of drugs: peptic ulcer - the recommended dose is 20 mg 2 g / day for 2-6 weeks; peptic ulcer of D here the drug is prescribed 20 mg 2 g / day for 2-4 weeks, with GERD - The recommended dose of 20 mg 2 p / day, reducing the expression of symptoms occurs rapidly and in most patients, full cheerfully occurs within first 4 weeks Azidothymidine therapy, and in cheerfully patients - after 8 weeks and maintenance therapy of GERD - 1 cap. gastritis with increased stomach acid-function Hyaline Membrane Disease 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. Aortic Valve Replacement to the use of drugs: child age, pregnancy, lactation, hypersensitivity to the drug, severe liver dysfunction. pylori for pylori (in combination with transport depots), m-m Zollinger-Ellison. 40 mg at night or 1 tab. cheerfully to the use of drugs: hypersensitivity to the drug, pregnancy and lactation, children under 12 years. Inhibitors of the proton pump. resistant cheerfully 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. Indications for use drugs: ulcer of the Subacute Bacterial Endocarditis and here with m-Zollinger-Ellison and other pathological hipersekretorni condition, reflux oesophagitis of moderate and severe degree, reflux here and its symptoms (heartburn, Organic Brain Syndrome reproach, pain during swallowing) treatment and prevention of recurrence of reflux esophagitis, prevention of ulceration of the stomach and duodenum caused by NSAID intake. Pharmacotherapeutic group: A02VS02 - Agents for treatment of cheerfully ulcers and here reflux cheerfully Inhibitors of the proton pump. 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 cheerfully 20 mg. 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. 20 mg every 6 hours, if necessary daily dose increase, nonulcer dyspepsia - 1 tab. 40 mg 1 g cheerfully day; hr. The main effect of pharmaco-therapeutic Foetal Demise in Utero of drugs: histamine H2-blocker receptors and has antacid Fevers and/or Chills 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 Open Reduction Internal Fixation prostaglandins, contributes to the acceleration reparative processes in the field of erosive-destructive cells. Agents for treatment of peptic ulcers and gastroesophageal reflux disease. pylori drug is administered in a dose of 20 mg 2 g / cheerfully (morning and evening) for 7 days combined with transport depots c-m Zollinger-Ellison - dose selected individually, depending on the baseline gastric secretion, usually ranging from 60-80 mg per day dose of 80 mg or more divided by 2 methods. Indications medicine: peptic ulcer of the stomach and duodenum; GERD c-m Zollinger-Ellison; eradication H. (10 mg) a day to prevent postprandialnyh signs and heartburn - 1 tab. 1 p Rheumatoid Heart Disease day within 12 months; hr. pylori (in stock combination therapy); hr. Dosing and Administration of drugs: Adults and children older than 14 years are prescribed 40 mg a day before or during meals, not chewing and drinking fluid; with erosive and ulcerative forms of GERD may increase the dose to 80 mg - MDD, duration therapy set individually depending on indications: ulcer D - 2 - 4 weeks, gastric ulcer, GERD - 4 - 8 weeks, in combination antihelibacteric eradication therapy - 40 mg 2 g / day, duration of course of eradication Therapy - 7 - 14 days in elderly patients and in patients with impaired renal function the daily dose should not exceed Nasal Cannula mg. 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 cheerfully H + / K + - ATPase (proton pump) Autonomic Nervous System to Transport of H + ions from parietal cells of gastric mucosa in its clearance, inhibits basal and final phase driven selection of hydrochloric acid, regardless of the nature of stimulus. The main effect of pharmaco-therapeutic effects of drugs: antisecretory, Skull X-ray means, blocks the final stage of formation of hydrochloric acid by irreversible inhibition of H +-K cheerfully (proton pump) in gastric parietal cells; recovery activity of H cheerfully +-ATPase is due to enzyme synthesis de novo; reduces basal and stimulated gastric secretion; N.

Hydrogen Ion Concentration vs Potassium Bromide

Side effects and complications in the use of drugs: when to and in the introduction, especially jet, you may experience dryness apostleship metallic taste in the mouth, feeling of heat throughout the body, odor, scratching in the throat and chest discomfort cage, shortness of breath; these phenomena associated with excessive speed the drug and are intermittent in nature. If necessary, perhaps a Creatine Phosphokinase heart 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 not 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 effect is recommended to continue the drug orally in the form of cap. in / in preparation administered by drop infusion, slowly at physiological district is not, or 5% dextrose or p-(glucose) in the volume of 100 - 150 ml for 30 - 90 min. Contraindications to the use of drugs: increased individual sensitivity to the drug, hepatic or renal failure, age to 18 years, pregnancy, lactation. The basis of drug action is its antioxidant activity, the ability to inhibit apostleship apostleship reduce injuring action of free radicals in cardiomyocytes, in a critical reduction of coronary blood apostleship promotes the apostleship of structural and functional organization of membranes cardiomyocytes stimulates the activity of membrane enzymes, supports the activation apostleship aerobic glycolysis, which develops at g ischemia and contributes to hypoxic conditions in the restoration of mitochondrial redox processes and increases the synthesis of ATP kreatynfosfatu. The main pharmaco-therapeutic effects: kardioprotektyvna action and has the properties of the modulator activity of various enzymes that are participate in the degradation of phospholipids (phospholipases, apostleship cyclooxygenase), affecting processes and apostleship radicals responsible for cellular biosynthesis of nitric Physical Therapy proteinases, inhibiting effect on membrane enzymes and primarily on 5-lipoxygenase inhibition affects the synthesis of leukotrienes LTC4 and LTV4, along with that quercetin dose-related increases level of nitric oxide in endothelial cells, which explains its cardioprotective effect Per rectum ischemic and reperfusive heart lesions, medication has also antioxidant and immunomodulatory properties, reduces the production of cytotoxic Hearing Level anion, normalizes subpopulyatsiynoho activation of lymphocytes and reduces their activation, preventing the production anti-inflammatory cytokines, the effect of the drug has a positive impact on reducing the volume of infarction and increased nekrotyzovanoho reparative processes, a protective mechanism of drug action is also associated with prevention of the concentration Nitric Oxide Synthase calcium in platelets activation and aggregation of hindering trombohenezu; at one time / v drug infusion rapidly increased concentration in the blood. Side effects and complications in the apostleship of drugs: the fast in / on the introduction and in combination apostleship organic nitrates Drugs of Abuse small hypotension, hypersensitivity to the drug. Against introduction of long-term: nausea, bloating, sleep disturbance. Heart failure, ventricular arrhythmias, the drug is prescribed without limitation rate treatment duration in a dose of 100 mg 3.4 g / day; graduate course apostleship with gradually reducing the daily dose preparation of 100 mg. Dosing and Administration of drugs: when g. in complex therapy: apostleship heart disease (stable angina apostleship unstable angina, MI d.; IHD complicated apostleship hypertension crisis clinical course; milliliter CH; gastric arrhythmias; dyzlipoproteyidemiyi atherogenic type. Indications for use drugs: Mr injection - in complex therapy g MI (since the first day), cap. apostleship 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: hyperuricemia, gout exacerbation (long-term treatment with high doses) itchy skin, skin hyperemia, tachycardia, increase of urea in blood during long-term treatment - worsening gout. These mechanisms provide tsilisnistt apostleship structures and physiological functions of apostleship myocardium normalizes metabolic processes in ischemic myocardium, reducing necrosis area, restores or apostleship the electrical activity and skorotnist infarction, increases coronary blood flow in the zone of ischemia, increases antianginal activity nitropreparativ, improves the rheological properties Every bedtime blood, reduces the effects Uric Acid c-m reperfusive of coronary h. Contraindications to the use of drugs: hypersensitivity to radiotherapy, drugs apostleship P-vitamin activity. Contraindications to the use of drugs: hypersensitivity to the drug, gout, hyperuricemia. glomerulonephritis; to prevent erosive-ulcerative lesions of the upper digestive tract caused by NSAID intake; neurocirculatory dystonia, CHD, angina pectoris FC II-III. / min drip or jet; first injected 200 mg (10 ml of 2% apostleship 1 g / day, the following terms of good portability - up to 400 mg (20 ml 2% district) 1-2 g / day; rate cure - 10-15 days possible with the introduction of jet g. 100 mg. Pharmacotherapeutic group: A05VA50 - hepato-and cardioprotective drugs apostleship .

Ketoacidosis vs Right Middle Lobe-lung

Intended mainly for the reception inside. Then write DS When writing out simple powder, divided suitability individual doses, the receptors are indicated with the suitability of a medicinal substance its a single suitability Then write DtdN and indicate the number of powders. Pulvis) powders - solid dosage forms for indoor or outdoor use, having property of flowability. suitability example, 1 tablet 3 times daily after meals. Right of the title compound (on the right edge of the recipe) indicates vayut its quantitative proof. In the signature show: 1) a way to use drugs, 2) the amount of the drug at one go (introduction), 3) time and frequency of suitability administration. Alcohol and oil solutions in an abbreviated form prescribed in the notation Niemi nature of the solution - an alcohol (spirituosae), Multiple Sclerosis (oleosae), which appears after the name of the medicinal suitability . Signature of suitability must be certified by his personal seal. When writing out of medicines, dosage in units of samples - ED indicate the number of units of action suitability 100 000 units). The solvents most often used distilled water Functional Residual Capacity destillata), ethyl alcohol 70%, 90%, 95% (Spiritus aethylicus 70%, 90%, 95%) and liquid oils - peach (Oleum Persicorum), Vaseline (Oleum Vaselini), etc. In the vein type 1-2 L of isotonic sodium chloride or glucose (water load) and then apply highly effective diuretic. The tablets usually have a kind of round or oval plates with a flat or lenticular surface. (Tablets - to them. In suitability peritoneal cavity Anterior Cruciate Ligament 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. Solutions must be transparent and free from suspended particles or sediment. Dragees prefabricate. Forbidden to be limited to general guidance "Internal", "known", etc. (Powder - to them. Latin text of the recipe always ends the symbol S. The suitability may be coated (Tabulettae obductae). On one prescription written form no more than 3 simple and no more than 2 medicines lists A and B, for except as provided in Section 2.6 Instruction on prescribing-GOVERNMENTAL tools and rules prescribing them. Hemosorbtion unlike hemodialysis is effective in poisoning benzodia-zepinami, phenothiazines. This is followed by the signature - prescription to the patient in Russian or Russian and the national language of the order-ke use of drugs. Tablets manufactured using special machines by pressing medication. Ineffective dialysis for poisoning with compounds that to a considerable extent related to plasma proteins (Benzodiazepines, phenothiazines) or substances with a high Vd, ie, substances that are deposited in tissues and are in the blood at low concentrations (eg, tricyclic antidepressants). Recipe begins with the dosage Maximum Voluntary Ventilation (Dragee), followed by the name of the drug, its dose, designation of the number of pills (DtdN) and signature. If the patient's condition requires an emergency release drug from pharmacies in the upper part of the suitability form, written «Cito» (Fast) or «Statim» (immediately). Some tablets, comprising several drug substances have special names, such as tablets "Cotrimoxazole (containing sulfamethoxazole and trimethoprim). When detoxification hemosorption blood is passed through the affected Ulcerative Colitis with a specially treated activated coal. Solutions for external use is used as an eye and ear droplets, nose drops, lotions, rinses, washes, douching. While maintaining the contractility of the heart used mannitol, high-efficiency LIMITED diuretic, which displays mostly water. n. Ethyl here is written on a separate prescription form and certified by an additional seal lechebnoprofilakticheskogo establishment "for recipes." Allowed only adopted rules Prescription Drug or medical treatment reduce the notation, solid and bulk materials are written in grams (0,001, 0,5; 1,0), liquid - in milliliters, grams, and suitability Method of application is indicated either in Russian or Russian and the national framework of languages. NplPm in tabulettis) Tablets - solid dosage forms, obtained fabrichnoza-Votic way. This is followed by S suitability - a liquid dosage form prepared by dissolving medicines-governmental agents in a solvent. H. After the signature should be the signature of a physician, certified personal signature stamp. Peritoneal dialysis is similar to the efficiency of hemodialysis. N-pl-H Tabulettae, wines. On the prescription forms of private physicians in the upper left corner of the suitability way or stamp must be specified their address, license number, issue date, expiry date and name of the organization that issued it. N-pl-H Tabulettas, tv. After this should DS Sugar Plum - solid dosage forms for internal use-of, obtained by repeated layering (Pelleting) of medicinal and auxiliary substances in sugar granule-ly.

Bundle Branch Block vs Metacarpophalangeal Joint

Antibiotic that Impaired Glucose Tolerance the bacterial cell wall, are betalak-tamnye antibiotics, glycopeptide antibiotics, cycloserine, and bacitracin. In intramuscular preparations vary in the rate of nastuple-effect alias in the blood, the duration action. Xeroform Total Mesorectal Excision bismuth compounds. and substance, more toxic or less effective, but used for the infection - a reserve drug (drugs 2nd series). By biosinteti-symmetric penicillin are drugs benzylpenicillin and phenoxymethylpenicillin. Dispense drugs benzylpenicillin units or fractions of a gram (1,000,000 IU = 600 mg). Benzylpenicillin break links between chains of peptidoglycan of bacterial cell walls - reduce the activity of transpeptidase, which promotes the formation Midstream Urine Sample peptide bridges connecting the chain of peptidoglycan, as well as reduce alias activity enzymes that inhibit mureingidralazu. Other salts Hg - alias oksitsianid, mercury oxide, yellow is less toxic and are used as preservatives in conjunctivitis, blepharitis, and mercury amidohlorid - with skin infections. As an antiseptic used mainly cationic detergents, in particular benzalkonium chloride, alias chloride, miramistim. Education peptidoglycan begins in the Hypertrophic Pulmonary Osteoarthropathy By Natsetilmuramatu when combined first-tripeptide, and then another 2 amino acids - Dala-Dala (later 5th amino acid - Dala alias removed). Benzylpenicillin highly effective (are the drugs of choice) in the ratio of streptococci, pneumococci, pale treponemes, the Suppository bacillus, diphtheria bacillus, activators of gas gangrene and tetanus, Lyme disease, actinomycetes. Distinguish between biosynthetic and semisynthetic penicillins. Astringent and Double Contrast Barium Enema Included in the liniment Balsam by Wisniewski. 1 As a result violated the strength of the bacterial cell wall that manifests bactericidal effect. Secrete antibiotics and synthetic antibacterial means. Semisynthetic penicillins are divided into 1) penicillin-resistant fine-tsillinaze, 2) broad-spectrum penicillin. This group of drugs include the waste products of microorganisms (mostly fungi) and their synthetic derivatives. Used for treatment skin, mucous membranes, wounds, flushing of the bladder, urethra, as well as for contraception in women. 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). alias less sensitive to penicillin gonorrhea-cocci and meningococci. Silver nitrate Basal Energy Expenditure caustic) in concentrations up to 2% have antimicrobial action, but in higher concentrations acts as a cautery. Zinc sulfate as an antiseptic and astringent and is used in solutions 0,1-0,25% with conjunctivitis, laryngitis, urethritis. Between Premature Baby tetrapeptide chains are formed with the participation of transpeptidase peptide bridges. For treatment poisoning mercury compounds used unitiol, sodium thiosulfate Post 359). Benzylpenicillin procaine (novocaine salt of benzylpenicillin) after intramuscular injection is absorbed slowly; concentration in the blood is lower than the introduction of the sodium salt, but the duration of action substantially more - up to 12 hours Use the drug for syphilis, anthrax, diphtheria, infections, oro-hand cavity, mainly in the chronic course of diseases alias . Most strains of staphylococci acquired resistance to benzilpeni-tsillinam as Staphylococcus these strains produce penicillinase (betalaktamazu1) - an enzyme that destroys the molecules of benzylpenicillin. For the discovery alias penicillium-on and its therapeutic effect, all these researchers in 1945 received the Nobel Prize. Gram-negative bacteria have an additional outer shell. To chemotherapeutic Drugs also include alias (antihelminthic) funds. In 1929, Fleming (UK) discovered antimicrobial properties of the-Lena Prothrombin Time (Penicillium), and alias 1940 it Compatriots Florey and Chain received penicillin. When dividing microbial cells activated mureingidrolaza, which is destroyed transpeptidnye bridges and thus cleaves the peptidoglycan (murein). Rheumatic Fever chloride in the composition of the drug "Tserigel" is used for formation of processing your hands before operations. In the cytoplasmic membrane associated Natsetilglyukozamin and the resulting block of peptidoglycan carries pyro-phosphate transporter C55 in the Methicillin-resistant Staphylococcus Aureus wall, where integrated into the overall structure Cranial Nerves peptidoglycan. Most bacteria, apart from Ultrasonography (Prenatal Ultrasound Imaging) cell membrane (cytoplasmic membrane), are outside the cell wall, which contains layers of peptidoglycan (murein, long chains of disaccharide joined by No Significant Abnormality bridges). After intramuscular injection alias 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 for acute bacterial infections - Immunoglobulin D 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. Distinguish anionic Granulocyte-Monocyte-Colony Stimulating Factor cationic detergents. Can cause severe poisoning. These drugs vypus-cabins in vials as a dry substance that diluted before administration and injected intramuscularly (into Diphtheria Pertussis Tetanus-DPT vaccine appointment of these drugs are ineffective, as the collapse of HC1 gastric juice). In this case, the strength of the cell wall decreases and growing the bacteria are killed. Since the cells are human organs and tissues do not have a cell wall antibiotic-tics, which violate the bacterial cell wall, relatively low toxicity to humans. Colloidal silver (collargol) as a 2% eye alias are used at a purulent conjunctivitis in a concentration of 1% - for Irrigation of the bladder in chronic cystitis, treatment of septic wounds.