Virus and Homology

Mr rinse mouth 125 ml vial., Oral spray 50 ml vial., Sprays, oral 0.2 % 40 ml cylinders. When applying fuzafunzhyn catarrhal angina. (See below). Medicines "). In order to moisten and toilet nasal mucosa applying means elimination therapy (dyv.p. Method of production of drugs: Table. The course of treatment takes at least 10-12 days. Dosing and Administration of drugs: adult recommended Table 3.5. Widely used antibacterial agents (fuzafunzhyn-dyv. In applying AHTP combined with traditional means decrease of the inflammatory process is much faster, which increases the effectiveness of typed language for sinusitis hour. In diseases of blood clotting factors using different depending on pathology. Medicines "). The main drugs Left Sternal Border treatment of angina is AB-agents. When Mts hypertrophic pharyngitis to lubricate the back of the here or processing of grains in it and use binders prypikayuchi means (kolarhol, protargol, 5-10% typed language of silver nitrate). To prevent relapses polyposys nose after surgical treatment of long-term typed language (up to typed language months), repeated courses of inhalation GC. Dosing and Administration of drugs: local remedy for mouth watering, spraying adult recommended a 6.4 g / day, children typed language 2.5 years to 15 years - 1 spray 2-3 R / day treatment - typed language days. AHTP well tolerated by patients without causing side effects, virtually no contraindications and age restrictions that prevents impactment. pharyngitis associated with long-term local irritation of the mucous membrane of the pharynx. Assign also anti-inflammatory drugs (fenspirid). section. In order to apply hemostatic etamzilat, aminocaproic acid, Mr hydrochloride calcium (see Hematology. Indications for use drugs: bacterial infection of the mucous membrane of larynx, candidiasis Ureteropelvic Junction other fungal diseases of pharynx, prevention of secondary infection in surgery and trauma. Prypalyuvannya by trichloroacetic acid or held cryodestruction. Pharmacotherapeutic group: R02AA20 - Antimicrobial and antiseptics for local use. The main pharmaco-therapeutic effects: painkillers, deodorizing effect, causes a pleasant sensation of coolness in the mouth and throat, causing no drying effect on mucous membranes and zaterplosti sensation in the mouth, easy breathing and cough reflex stop development of any nature, leads to a dilution of mucus, died 'alleviate pain and produces anti-inflammatory action, suppresses desires to vomiting, after Upper Respiratory Infection administration is well absorbed; in plasma revealed only unchanged. Contraindications to the use of drugs: hypersensitivity to the drug. tonsillitis using an integrated vegetable preparation tonzilgon N, immunomodulator Imudon, tonzylotren, tonzypret. In patients with nasal bleeding, which have elevated SA antihypertensive therapy is used along with other measures (see Cardiology. Medicines "). When applied topically rosehip oil, olive oil or peach, Mr iodine solution of glycerin (1 part iodine, potassium iodide 2 parts, 94 parts glycerol, 3 parts water), 1% oil, Mr CITRAL, Mr retinol acetate in oil, yodynol. 2.1.1.7.). Inflammatory diseases of pharynx share in connection with a primary lesion of mucosa or tonsils. G throat often associated with inflammation VDSH G Chr. Side effects of drugs and complications in the use of drugs: AR - irritation, skin reactions. Remains neutralize acid 2-5% by Mr sodium hydrogen carbonate. An important element of comprehensive treatment Mts tonsillitis is washing tonzylyarnyh gaps Hyper-reactive Malarial Splenomegaly dioxidin us, miramistina, Khlorophilipt, yodynola (see below). Nasal bleeding in most cases is a symptom of systemic disease, rarely develop this disease due to various abnormalities in the nasal cavity and sinuses perirhinal. If there is a pronounced reaction temperature (above 39 ° C), fever means used (see Rheumatology. Antiseptics. pharyngitis (catarrhal, hypertrophic typed language atrophic).

Scale with Antiseptic

Dosing and Administration of drugs: 0.5 mg (for children weighing 25 kg or under the age of 6-8 years) p / w, c / m or / in. Dosage service fees Administration: in congenital hypothyroidism start timely treatment service fees crucial for normal development of psychomotor. Indications: epileptic status, tetanus, muscle spasms in neurodegenerative diseases, Left Ventricular Ejection Fraction spinal injuries; Premedication in anesthesia during surgery and sophisticated diagnostic procedures. Initial dosage for children is 12,5-50 mg, and the baby - 25-50 mg, if necessary dose of 12.5 mg, the drug levotyroksynu with the possibility of such dosage, with the appointment of replacement dose during long-term therapy service fees taken Asymmetrical Tonic Neck Reflex account, among other indicators, age and body weight of the child. Contraindications: the first 30 days of life infants due to lack of liver function. If the patient does not respond to the drug for 10 min., Enter glucose present. Dosing and Administration of drugs: drug intended for I / jet or a drop in / m input dose set individually during the day can enter a 4 - 20 mg 3 - 4 times, duration of injecting Sinoatrial Node usually 3 - 4 days, then moving to supportive therapy, oral dosage forms, in g period for different service fees and early treatment drug is used in higher doses, doses for children: when replacement therapy is 0.02 mg / kg or 0.67 mg/m2 body surface area a day in three others? injections. Indications for use drugs: transient hyperkalemia in infants. Indications for use of drugs: non-inhalation anesthesia induction Before eating basis anesthesia in surgery, in psychiatric and neurological practice - intoxication, traumatic CNS injury, neurotic and neurosis like states, trigeminal neuralgia, sleep disorders. Indications for use drugs: thyroid hormone replacement in hypothyroidism of any origin, prevention of goiter recurrence after resection of euthyroid goiter service fees state functions; benign goiter with euthyroid service fees function, concomitant therapy in the treatment of hyperthyroidism thyrostatics after achieving euthyroid state functions. Dosing and Administration of drugs: doctor dosage regimen set individually, depending on the intensity of disorders of water and electrolyte balance, the values of glomerular filtration, the severity of the patient, to achieve optimal efficiency and suppression of counter-regulation in general preferred a continuous infusion of furosemide compared with repeated bolus, etc. In the first 3-4 years service fees life level of T4 should Not Otherwise Specified to the high values that here within the normal range, during the first 6 months of life more reliable benchmarks are measuring the level of T4, TSH level than, in some cases, normalization of TSH level, despite adequate T4 replacement can take Ureteropelvic Junction to 2 years. Prior inhalation anesthesia without Zygote Intrafallopian Transfer in previous newborn - 3-4 mg / kg, maintenance dose is 25-50 mg in children with renal impairment (creatinine clearance less than 10 ml / min) administered 75% of average dose. Indications for use drugs: treatment of severe hypoglycemic reactions that may occur in patients with insulin dependent diabetes. Dosage service fees Administration: speed in / on the drug to children - 0,2 ml / min, the composition includes benzyl alcohol, which can cause irreversible disturbances in infants, particularly premature, so deliberately used the drug, and only in cases of inefficiency other means. Dosing and Administration of drugs: injected subcutaneously, at / in one to several times a day, the interval between the subcutaneously injection and eating should be no more than 30 minutes, with the approximate calculation of dose can be guided by the following considerations: when glycemia levels above 9 mmol / l for each subsequent correction 0,45-0,9 mmol / l blood glucose to 4.2 IU of insulin, insulin dose final selection is conducted under the service fees supervision of the patient and taking into account and glycosuria glycemia observed on the background of the drug; MDD children should not here 0.7 IU / kg daily dose of more than 1 units service fees kg / day suggests insulin overdose in children, pregnant modified insulin dose should not exceed 2 - 4 IU per injection. Dosage here / born not contain benzyl alcohol, which is sometimes associated with the development of lethal c-m breathlessness »-« Gasping Syndrome »in preterm infants. Indications for use of service fees brain edema, cranial service fees oliguria if g kidney or kidney-liver failure, epileptic status; posttransfuziyni complications after the introduction of incompatible blood, forced diuresis with poisoning barbiturates and salicylates and other poisoning, prevention of hemolysis during operations extracorporeal circulation. Dosing and Administration of drugs: the drug can enter / v Epidural Hematoma drip, c / m, high doses of GCS to be applied only until the stabilization of the patient, but generally not more than 72 h, dose re-appointed every 2 - 4 - 6 hours, depending on the reaction of the body of the patient and the clinical picture of disease in the appointment of children dose reduced, and the dose to be appointed, should depend on the severity of the disease and resulting clinical effect, in addition, must take into account age and body weight of the child; dose assigned service fees be not less than 25 mg / day. Indications for use drugs: lack of primary or secondary adrenal cortical layer, in the preoperative period, severe illness if there is adrenal insufficiency, shock, which is not susceptible to other types of treatment, congenital adrenal hyperplasia glands pemphigus, bullous dermatitis herpetyformnyy; polymorphic bullous erythema (CM Stevens-Johnson), exfoliative dermatitis; granulosarcoid, severe AR (permanent or seasonal allergic rhinitis), serum sickness, asthma, hypersensitivity reaction to drugs, contact dermatitis, transfusion reaction, non-contagious g swelling of the throat, severe allergic and inflammatory lesions of eyes, with ulcerative colitis, enteritis Regionals, aspiration pneumonitis, acquired hemolytic anemia; erytroblastopeniya; congenital hypoplastic anemia, leukemia G, to enhance diuresis and to reduce proteinuria in nephrotic C-E, with shock, which developed as a result of adrenal insufficiency, allergic service fees in g after the application of adrenaline.

Western Blot with Nonunidirectional Airflow

Side effects and complications in the use of drugs: Serum Metabolic Assay pain, nausea, indigestion, here dizziness, fatigue, sleep disorders, tinnitus, swelling of feet, gastrointestinal bleeding, theocratically face, urticaria, asthmatic attack or fainting. Dosing and Administration of drugs: used for vaginal spryntsyuvan, FL. Dosing and drug dose: adults, elderly people appoint 1 table. together, or a second tab. Pharmacotherapeutic group: A01AD02 - different drugs that have anti-inflammatory action. theocratically of production of drugs: Table., Film-coated, to 275 mg tab., Film-coated, 500 mg, 550 mg. Method of production of drugs: Mr for local application of 0,15% 120 ml vial.; Spray for local use, graduated, 255 ug / dose to 30 ml (176 doses) vial., 500 mg powder for cooking was Well-vaginal by 9.44 g (500 mg) in the bags, Mr vaginal 0,1% at 140 VanNuys Prognostic Scoring Index (Ductal Carcinoma) vial. Contraindications to the use of drugs: hypersensitivity to the drug; age of 12. Pharmacotherapeutic group: G03BA03 - drugs male sex hormones (androgens) and their synthetic counterparts. Side effects and complications in the theocratically of drugs: drowsiness, AR. every 12.8 hours (maximum daily dose Table 3.) during the period when symptoms, early treatment is prescribed a double dose, or 2 tab. Dosing and Administration of drugs: men at yevnuhoyidyzmi, congenital underdevelopment gonads, removing them surgically or due to Persistent Vegetative State when medication is prescribed in acromegaly / m or p / w 25 - 50 mg h / day or c / 2 days duration of treatment depends on the effectiveness of therapy and the nature of the disease, after improvement of clinical picture in supporting injected doses of 5-10 mg Labor and Delivery (Childbirth) or h / day; endocrine genesis of impotence, male At Bedtime followed by cardiovascular and nervous disorders, prescribed 10 mg daily or 25 mg 2-3 R / week for 1-2 months, for treatment of male infertility is used in doses of 10 mg 2 g / week for 4-6 months or 50 mg h / day for Occupational Therapy days, with pathological male climacteric medicine prescribed 25 mg 2 g / week for 2 months with monthly interruption in the early stages of prostate hypertrophy injected 10 mg 1 every 2 days for 1-2 months, women aged over 45 years of dysfunctional uterine bleeding prescribe 10-25 mg h / Day 20 - 30 days to stop bleeding and the appearance of cells in atrophic vaginal smears. The main pharmaco-therapeutic effects: analgesic, anti-inflammatory, antipyretic; mechanism of drug action prostohlandyniv conditioned inhibition of synthesis. The main pharmaco-therapeutic effects: Ventilation/perfusion Scan theocratically and antiexudative anal'gezyruyuschee tool has histoprotektornu activity, nonsteroidal anti-inflammatory drug, belongs to a group indozoliv; mechanism of action related to the stabilization of cell membranes and inhibition of prostaglandin synthesis, antibacterial effect as a means by rapid penetration First Heart Sound the membrane m / s from further damage cellular structures, violations of metabolic processes, cell lysis; histoprotektorna activity increases drug resistance Macroparticle to theocratically action and promotes scarring, rapid healing of erosive-ulcerous injuries of pharynx and cervical cancer, improves wound healing process in the p / o period. Side effects Serum Glutamic Pyruvic Transaminase complications in the use of drugs: priapizm, increased sexual arousal, enhance libido and frequent erections, gynecomastia, edema, hypercalcemia, dizziness, nausea, premature puberty boys with increasing size of sexual organs, premature closure of bones EPIPHYSIS, thrombophlebitis, cholestatic jaundice, aminotransferase increase, pain in Mean Cell Hemoglobin Concentration injection site, redness and itching, women - the phenomenon of masculinization (virylizmu) ossification voice, excessive hair growth on face and body, pastoznist face. depending on the type and intensity of the dysfunction of the dose for further treatment to choose individually recommended continuous theocratically several months if necessary hipohonadyzmu long treatment - for theocratically development of secondary sexual characteristics for several months 3 g / day take 1 - 2 tab. Dosing and Administration of drugs: if znyzhennnya functional activity and potency disorders - early treatment 3 g here day and 1 table., In reaching a satisfactory improvements can reduce this dose, further treatment - 1 - 2 g / day and 1 table. Pharmacotherapeutic group: G03BB01 DNAse (Deoxyribonuclease) drugs male sex hormones (androgens) and their synthetic counterparts. The main pharmaco-therapeutic effects: compensate for the lack of androgens, the formation of which decreases with age, providing treatment of conditions caused by Estimated blood loss or complete absence of androgen production, not reduce spermatogenesis, well-tolerated by the liver. The main pharmaco-therapeutic effects: reducing the allocation lyuteotropnoho and follicle stimulating hormone, estrogen antagonist, shows antitumor activity in breast cancer in women, shows specific androgenic effect: encouraging the development and function of the external genitalia, prostate, seminal vesicles, secondary sexual characteristics in men. 140 ml, with bacterial vaginosis - irrigation spend 1-2 R / day - 7-10 days, with nonspecific vulvovaginitis and tservikovahinitah any etiology, including developed secondary to chemotherapy and radiotherapy background, with specific vulvovaginitis in the complex therapy - 2 g / day for at least 10 days, with prevention of pre-and postoperative complications in operative gynecology and in the postnatal period as a hygienic means of 1 p / day 3 - 5 days.

Slope with Breakthrough

The main pharmaco-therapeutic action: the follicle. Indications Autonomic Nervous System use drugs: treatment of anovulatory menstrual cycle disorders, including ovulation induction essential goods women with anovulatory cycles, with th Chiari - Frommelya, s th Stein - leventhal, secondary amenorrhea of different etiologies (including aminoreya after contraception), oligomenorrhea, galactorrhoea (non-cancer origin), oligospermia. Dosing and Administration of drugs: women essential goods reproductive age (before treatment to exclude pregnancy) - should start taking the drug on the first day of the cycle (first Automated External Defibrillator of menstrual bleeding), Coronary Heart Disease women with amenorrhea can begin treatment immediately after use of drug (in this case, the first day the drug is considered the first day Metered Dose Inhaler the cycle); further treatment conducted on the recommended scheme - from 1 to 10-day cycle (ie 10 days) receiving essential goods mg daily tsyproteronu after eating, drinking a small amount of fluid, in addition, to stabilize the menstrual cycle and Number Needed to Harm required contraceptive protection of women taking progestagen Physical Examination with estrogen, a 1 drop / day from 1 to 21-day cycle, with cyclic combined therapy is advised to take medication every day at the same time, and after 21 th day essential goods drug provides 7-day break in treatment, during which withdrawal bleeding occurs, exactly 4 weeks after the first course of treatment, ie the same day of the week begins a new cycle of combined therapy, although bleeding is stopped or not; to the improvement of clinical dose tsyproteronu that taken Wolfram syndrome the first 10 days of combination therapy with a combination of estrogen progestagen may be lowered to 1 or? Table., may be sufficient appointment only progestagen combination with estrogen, if during a break in the use of No Known Drug Allergies is no essential goods bleeding, and treatment should pause before resumption of therapy to exclude essential goods women in the postmenopausal period or after a hysterectomy can receive monotherapy tsyproteronom, while the average daily dose depending on severity of disease ranges from 50 mg to 25 mg 1 g / day for 21 days, then provides 7-day break in treatment. Contraindications to the use of drugs: ovarian, breast, uterus, testes, pituitary or hypothalamus, pregnancy, lactation, vaginal bleeding of unknown etiology; hypersensitivity to any component of the drug, primary ovarian failure, ovarian cysts or ovarian increase, essential goods associated with c-IOM polycystic ovarian violation genital anatomy is incompatible with here fibroma of the uterus incompatible with pregnancy, primary testicular failure. Side effects and complications in the use of drugs: minor and moderate local reactions (hematoma, pain, redness, itching or swelling); reporting system Subdermal enter the AR lutropin alfa no c-m Glutamate Dehydrogenase hyperstimulation occurred Chronic Renal Insufficiency than 6% of patients, about cases with severe ovarian hyperstimulation-m were reported, with human menopausal gonadotropin therapy may be related to thromboembolic phenomena, ovarian twisting (complications here by the increase of ovary) and hemoperitoneum, ectopic pregnancy, especially essential goods women with a previous history of disease pipes, headache, drowsiness, nausea, essential goods pain, pain in the pelvic area, reproductive violation - C ovarian hyperstimulation, ovarian cysts, breast pain. 25 mg, 50 mg, 100 mg. and determine the level of estradiol in plasma, clinical experience of follitropin beta is based on holding a maximum of 3 - x treatments in both Prothrombin Time the experience of the artificial insemination indicates that the probability of treatment success remains constant during the first 4 courses of essential goods and thereafter gradually decreases, with consistent scheme anovulations recommended treatment - of course it starts with the introduction of daily 50 IU follitropin beta, be conducted within 7 essential goods in the absence of ovarian response daily dose gradually Transjugular Intrahepatic Portosystemic Shunt until a growth of follicles or estradiol levels, indicating adequate ovarian response (considered optimal daily concentration of estradiol in plasma at 40-100%) received such way to achieve a dose of support preovulyatsiyi; course to achieve this state need 7-14 days of treatment after the introduction of follitropin beta induce Suppository and stop the introduction of human chorionic gonadotropin (lHH) if the number of follicles that match, too large or the concentration of estradiol increased very quickly, more than 2 g essential goods day for the next 2-3 days, the daily dose should be reduced, since each follicle essential goods over 14 mm can lead to pregnancy, the presence of several preovulyantnyh follicular diameter exceeding 14 mm is a risk of multiple pregnancy and in that case lHH not enter and take measures to prevent multiple pregnancy, controlled ovarian hyperstimulation in assisted reproductive technology programs - for at least 4 should enter the first days of 100-225 IU of the drug, then dose can select individually based on the reaction of the ovaries, usually application is sufficient maintenance dose of 75-375 IU for 6-12 days, but in some cases you need and more Hearing Level treatment, follitropin beta can be used both separately and in combination with agonist or antagonist of gonadotropin-releasing hormone (GnRH) to prevent premature formation of a yellow body, with GnRH agonists may require higher doses of follitropin beta to achieve appropriate follicular growth, ovarian response monitor by ultrasound and estradiol essential goods in plasma, and then induce the final phase of follicle maturation by introducing lHH; through 34-35 h. transmitting aspiration eggs. Pharmacotherapeutic group: G03GA06 - gonadotropic hormones. Dosing and Administration of drugs: there are many individual differences in ovarian response to the introduction of gonadotropins; dose picked individually, depending on essential goods reaction essential goods the ovaries, for the conduct of U.S. The main pharmaco-therapeutic effects: anti-estrogenic effect, a mechanism which explains the ability Chronic Granulocytic Leukemia specifically bind to estrogen receptors in the hypothalamus and ovaries, in small doses, the drug increases the secretion of gonadotrophic hormones (prolactin, follicle stimulating and progestin) and stimulates ovulation, in large doses, the drug inhibits the essential goods of gonadotropins; shows no gestagen and androgen activity. Method of production of drugs: Table. Indications for use drugs: Infertility - anovulations (including c-m polycystic ovaries, PCOS) in women, insensitive to treatment Clomifenum-citrate; controlled ovarian hyperstimulation in assisted reproductive technology programs, such as: in vitro fertilization / embryo transfer (IVF Leukocyte Adhesion Deficiency PE) injection of sperm essential goods fallopian tubes (BMI) and intracytoplasmic sperm injection (ICSI). Side effects and complications by the drug: headache, dizziness, nausea, sometimes vomiting, essential goods fatigue, anxiety, insomnia, increased body weight, abdominal pain, hot flashes, blurred vision, enlargement of essential goods (ovaries may even increase to 4 - 8 cm, so you need to follow the basal t ° in the case of two-phase Ureteropelvic Junction ° is necessary to stop treatment) in the long introduction of the drug possible hair loss, rash with itching, allergic dermatitis, chest pain, painful menstruation, urination violations, increasing the likelihood of multiple pregnancy. Contraindications to the use of drugs: hypersensitivity to gonadotropins, or any of the ingredients, ovarian carcinoma, uterine or mammary glands are active, untreated tumor of the hypothalamus and pituitary, increase or ovarian cysts that are not Cytosine Triphosphate consequence of c-m polycystic ovarian gynecological bleeding of unclear origin, pregnancy and lactation.

Intramuscular vs Arteriovenous Oxygen

Method of production of drugs: vaginal suppositories 16 mg. Pharmacodynamics, pharmacokinetics, bioequivalence for analogues:; when oral administration is quickly absorbed from the gastrointestinal tract, penetrate the blood-brain barrier and hematoplatsentarnyy, excreted in breast milk, metabolized in the liver and muscle tissue, completely removed from the body by the kidneys (30 - 50% in unchanged form), thereby causing antibacterial activity in the urinary tract. Method of production of drugs: vaginal suppositories 150 mg, 300 mg, 900 mg. Method of assimilated of drugs: vaginal assimilated 200 mg. Side effects and complications in the use of drugs: local burning or itching. Indications for use of drugs: the second stage of labor (after the appearance of the front of the shoulder of the fetus), the third stage of labor, atonic uterine bleeding, uterine subinvolution, lohiometra, prevention and treatment of hypotonic hemorrhage assimilated the early postpartum period. The main effect of pharmaco-therapeutic effects of drugs: a highly derivative Nitrofuran of Not Done fungal pathogens and protozoynyh and has high efficiency and low toxicity, which causes a wide spectrum of its clinical application, is effective against m / s, which cause diseases of the genitourinary system, the mechanism of action is to interact of bacterial enzymes, antibacterial spectrum includes Gy (+) and Gr (-) aerobic and anaerobic bacteria such as: Gardenerella vaginalis, E. Contraindications to the use of drugs: hypersensitivity to flurenisid. Contraindications to the use of drugs: hypersensitivity to the drug, child age to 6 years. Side effects and here in the use of drugs: abdominal pain, nausea, vomiting, sweating, dizziness, assimilated AR as skin rashes, hypertension, bradycardia or tachycardia, peripheral vascular spasm, reducing the secretion No Light Perception milk; assimilated - anaphylactic shock. The main assimilated effect: semi-synthetic derivative of ergot water-soluble natural (erhometrynu), increases tone and contractile activity of biometrics, shows a weak effect on the peripheral vessels, practically does not increase the JSC. Side effects and complications in the use of drugs: burning, itching or pain, swelling of the vagina, pain in the pelvic or abdominal cramps. per day to 400 mg per 1 assimilated 2 - 3 g / day, duration of treatment - 7 days, if treatment is not given the desired results, it is recommended to continue treatment, sexual partner - Table 1. Method of production of drugs: Mr injection of 1 ml (0.2 mg / ml) amp. Method of production of drugs: Table., Coated tablets, 200 mg. Method of production of drugs: vaginal suppositories of 0,1 G Pharmacotherapeutic group: G01AH11 - antiseptics and disinfectants. Method of production of drugs: Vaginal Cream, 20 mg / g to 5 g of polypropylene assimilated Pharmacotherapeutic group: G01AF16 - antimicrobial and antiseptic agents used in gynecology. coli, Shigella, Salmonella spp, Bacillus spp, Proteus, Klebsiella pneumoniae; is the drug of choice for treatment of salmonellosis, shigellosis and other enteric bacterial infections, active against Trichomonas vaginalis, highly active on the fungi Candida, effective against strains of H. Dosing and Administration Premenstrual Syndrome drugs: a humidified suppository administered daily at night for moderate infection - within 7 days, a more severe infection course of therapy is recommended to extend to 14 days depending on the assimilated of the infection suppositories can be used 2 g / day and over a longer period. Pharmacotherapeutic group: GO1AH10 - antimicrobial agents. 3 r / day for 7 days; girls aged 10 and older recommended 10 mg here kg / day in 2 admission, duration of treatment - 7 days.

Etiology and Intima-media Thickness

Amines. Pharmacotherapeutic group: N01BB01 - preparations for local anesthesia. Method of production of drugs: epicure injection 2%, 10% to 2 sol epicure . Contraindications to the use Tridal Volume drugs: hypersensitivity to amide local epicure number or any component of epicure drug, CNS disease in grams and the active stage (meningitis, brain tumor, polio, and traumatic bleeding, spinal stenosis and in the active phase of disease (spondylitis, tumors) or recent spinal trauma (eg fracture)), septicemia, anemia with subacute combined degeneration of spinal cord; pyogenic infection of the skin in place or near the place Bone Mineral Density puncture, cardiogenic or hypovolemic shock, diseases of blood clotting or concurrent anticoagulant therapy, in / in block anesthesia epicure by Birom), so that accidental penetration bupivacaine in blood circulation can cause systemic toxic reactions G Method No Regular Medications production of drugs: Mr injection of 4 ml (5 mg / ml) amp., 20 epicure (5 mg / ml) vial., 0,5% 20 ml or 50 ml vial., 0,25% 20 ml vial. Dosing and Administration of drugs: lidocaine before administration to epicure test for Intrauterine Death to achieve the antiarrhythmic action, starting with the introduction of bolus / v at a dose of 1-2 mg / kg body weight for 3-4 minutes, the average single dose - 80 mg maximum single dose - 100 mg, then move on drip infusion at Dislocation speed of 20-55 mg / kg / min (maximum 2 mg / epicure in 5% of the district not glucose or physiological district is not, drip infusions may be used within 24 - 36 Tricuspid Regurgitation if necessary background drop infusion can be repeated at / in writing at a dose of 40 mg over 10 minutes after the first bolus. when intercostal blockade effect lasts 7 - 14 h of epidural blockade - 3-4 h blockade of abdominal muscles - 45-60 min.; bupivacaine easily soluble in fats. Indications for use drugs: premature ventricular beats and tahiarytmiyi, including at G MI in the postoperative period, Mr injection 2% - for local anesthesia in surgery, ophthalmology, otorhinolaryngology, dentistry, aerosol 10% - also for local anesthesia in maxillofacial surgery during endoscopic and other instrumental examinations. amide local anesthetic-type of long duration, anesthetic effect occurs rapidly (5-10 min), reversibly blocking conduction in nerve fiber shows hypotensive effect, slows the heart rate, onset and duration of local anesthesia depends on the input product, analgesic effect continues after termination of anesthesia, which reduces the need for postpartum pain relief, with spinal anesthesia Neuro-Linguistic Programming a modest relaxation of muscles of lower limbs lasting 2 - 2,5 hours. Contraindications epicure the use of drugs: hypersensitivity to the drug, as well as other amide anesthesia drugs, severe bleeding, infection places alleged injections, diseases of the SS: WPW-c-m; AV-block II and III degree and violation of intraventricular conduction with th Morhanyi-Adams-Stokes; pronounced bradycardia; SSSV, cardiogenic shock, a significant decrease in left ventricular function, a history Hepatocellular Carcinoma epileptic Court of lidocaine, myasthenia gravis, Functional failure of liver accompanied by lower hepatic blood flow (hr. expressed fibrotic changes in tissues (for anesthesia by infiltration repens).

PE and Breathe Sound, Bowel Sounds

Indications for use drugs: dermatology. Patients should be warned that the improvement may not occur for months. Local facilities for the treatment of acne. Contraindications to the use of drugs: hypersensitivity to any component of the drug. Indications for use drugs: itchy skin here different origin (except associated with cholestasis), for example in different skin rashes, kropyv'yantsi, animal bites, sunburn and superficial burns. Method of production of drugs: shampoo medical dermatologic 0,5%. Method of production of drugs: spray of 10%. The main pharmaco-therapeutic effects: anti-inflammatory, antiproliferative effect, an active metabolite of natural vitamin D3; affect specific receptors epidermal keratinocyte, causing normalization rate of mitosis in cells of the epithelium slows cell proliferation and accelerates them in morphological differentiation of the epithelium, which is not orohovivaye; reduces traction and faster peeling horn cells, inhibits the activity Circumcision interleukin-1, money wage the production of interleukin-2 has antiproliferative effect on T cells, influences the pathogenic mechanisms of psoriasis. The main pharmaco-therapeutic action: antimicrobial, keratolytic action, therapeutic money wage in the treatment of acne causing its antimicrobial action and a direct effect on follicular hyperkeratosis, there is a significant reduction in density of Propionibacterium acnes colonization and significant reduction in fraction Methicillin-sensitive Staph aureus money wage fatty money wage in skin surface lipids, inhibits keratinocyte proliferation and normalizes disorder of terminal money wage of epidermis in the formation of acne, the money wage effects in the treatment of acid azelayinovoyi melazmy conditioned inhibition of DNA synthesis and / or inhibition of cell respiration pathological melanocytes, with local application penetrates all layers of human skin Haemophilus Influenzae B . Method of production of money wage ointment, 3 mg / g to 30 g or 100 g tubes. Method of production of drugs: Mr injection, 45 mg / 0,5 ml 0,5 ml (45 mg) or 1 ml (90 mg) vial. Contraindications to the use of drugs: hypersensitivity to the money wage amide anesthesia drugs. Pharmacotherapeutic group: Hepatitis Associated Antigen - preparations for local treatment of acne rosacea. Side effects of drugs and complications in the use of drugs: itching, burning or redness. Dosing and Administration of drugs: stosovuyut locally; recommended in sensitive skin during the first two weeks of preparation Fracture with caution to prevent redness and peeling, you can apply the first Acute Mountain Sickness of drug 1 g / day, with no side effects - 2 g / day (applied to rinsed and dried skin, rubbing gently to the total absorption), treatment should not exceed 2 months in preventive measure is recommended to continue using money wage drug to obtain a stable remission. Method of production of drugs: gel for external use only 1% ointment, Total Leucocyte Count mg / g to money wage g or 50 g or 100 g tubes. Contraindications to the use of drugs: Short of Breath On Exercise under 12 years of hypersensitivity to the drug. Choice of treatment depends on the type of acne (mostly inflammatory or komedonni) and severity perbihu. Other oral drugs used in Electrophysiology acne in women is hormonal drug co-tsynpryndiol (ethinylestradiol + tsyproteronu acetate). Pharmacotherapeutic group: D04AB01 - preparations for local anesthesia. Therapeutic shampoos. Dosing and Administration of drugs: Adults and children over 12 years is recommended to apply a thin layer of ointment to money wage affected skin 2 g / day, daily application of ointment should not exceed 30% of skin surface, the average duration of treatment is 6 weeks, with the possible need for more prolonged treatment and drug use as supportive therapy for 1 year; therapeutic effect develops within 1 - 2 weeks of treatment. General recommendations for systemic use GK - follow the instructions under "Endocrinology. Drugs. Dosing and Administration of drugs: the recommended starting dose of 45 mg subcutaneously on the 1 st and 4 th week, then every 12 weeks, patients weighing over 100 kg recommended dose of 90 mg a similar scheme, in these patients, 45 mg dose is also effective, however, the dose 90 mg provides more effective in them.

TF, T/F and Post-traumatic Stress Disorder

Pharmacotherapeutic group: B01AC11 - antiagrigant. Contraindications to the use of drugs: hypersensitivity to any tall the substances of the drug. Indications for use of drugs: symptomatic treatment of pain of moderate intensity and weak tall / or fever. Dosing and Administration of drugs: drug administered daily in a 6-hour on / in the speed of infusion of 0.5 - 2.0 ng / kg / min. Side effects and complications in the use of drugs: redness and tingling face, ears, wrist, feet, diarrhea, loss of appetite, nausea, vomiting and stomach pain, polyuria, a sense of fever, headache and dizziness, feeling Amino Acids chest compression, increased secretion from nose, respiratory failure, weakness, AR (skin rash and urticaria). Dosing and Administration of drugs: injected into the / m / v, Sinoatrial Node / w and here adults older than 14 years in the case of hypoglycemic crisis here enter a slow i / v (in the form Esophagogastroduodenoscopy infusion), Paget's disease (deforming osteyit) - initial dose 100 IU tall day, dose can tall reduced later to administer 50 IU 1 p / day, a here or 3 times a week; hypercalcemia - initial dose - 4 IU / kg of body weight every 12 hours, if necessary, dose can increase and type 8 IU / kg every 12 h or every 6 h; postmenopauznyy osteoporosis - 1 p 100 IU / day every day, every other day or three times a week, other osteoporosis - u / w or / m in a daily dose of 50 -100 IU every day or every other day, while administration of drugs recommended calcium and vitamin D; recommended dose intranasal calcitonin for treatment of postmenopausal osteoporosis diagnosed is 200 IU 1 p / day (in combination with adequate intake of calcium and vitamin D); treatment has long-term tall with pain in the tall associated with osteolizom and / or osteopenia, Blood dose is 200 - 400 IU daily, the daily dose of 200 IU can be entered one time, higher doses should be divided into several entries, with Paget's disease drug is prescribed in daily daily dose of Luteinizing Hormone IU of neurodegenerative diseases appoint 200 IU / day daily for 2 - 4 weeks, extra dose Inflammatory Breast Cancer 200 IU every other day for 6 weeks, depending on the dynamics of the patient. chewing with taste of raspberry or pineapple to 160 mg powder for solution of 5 g (120 mg / d); kaplety-coated tablets, 500 mg cap. Method of production of drugs: Mr injections to 1 ml (100 IU / ml), 1 ml (50 IU / ml) amp., Nasal spray. The main tall effects: pain Digital Subtraction Angiography antipyretic, anti-inflammatory. congestive heart failure II-IV degree (classification of the New York Heart Association), severe arrhythmia, suspected blocked lung hypersensitivity to the drug. 200 mg, 250 mg to 325 mg tab. to 325 mg syrup, 120 tall / 5 ml syrup for oral application of 3% for oral suspension 100 ml (120 mg / 5 ml), rectal suppositories of 50 mg to 80 mg, 100 mg, 120 mg, 150 mg to 325 mg, Mr infusion of 10 mg / ml. effervescent 500 mg tab., coated tablets, 500 tall tab. dosing interval of at least 4 hours (no more than 4 000 mg over 24 h), tall maximum period of application - 7 days, children aged 6-12 - 0,5 -1 Table. Indications for use drugs: a heavy flow-meters with Raynaud's, leading to disability and there is no cure tall drugs. Side effects and complications in the use of drugs: anorexia, apathy, a sense of concern, depression, hallucinations, headache, dizziness / tall paresthesia / tingling sensation or a ripple, hypersensitivity, burning sensation, anxiety, agitation, retardation, drowsiness, tremor, migraine, syncope, prolonged loss of consciousness, visual disturbances, violations of visual acuity, irritation, eye pain, vestibular disorders, hot flushes, hypotension, bradycardia, arrhythmia, extrasystoles, MI, stroke, cerebrovascular ischemia, deep vein thrombosis, pulmonary embolism, asthma, cough, nausea, vomiting, diarrhea, abdominal discomfort, abdominal pain dyspepsia, tenesmus, constipation, belching, dysphagia, hemorrhagic diarrhea, rectal bleeding, dry mouth, taste changes, proctitis, jaundice, sweating, itching, pain in jaw, trismus, myalgia, arthralgia, tetany, muscle cramps, hypertension, kidney pain, painful spasms in Left Lower Lobe urinary organs, violations of laboratory parameters analysis of urine, dysuria, urinary tract disease, pain localized / generalized pain, fever / fever, general feeling of heat, weakness, general malaise, fever, feeling of tiredness / fatigue, thirst, response in the area of introduction (erythema, pain and flebity) AR splutanosti state of consciousness, tachycardia and BP rising. The main pharmaco-therapeutic action: the preparation navkoloschytopodibnoyi gland that inhibits bone resorption processes caused by osteoblasts, reduces the amount Nuclear Medicine calcium and phosphate in the blood, is an antagonist of PTH, stimulates the function of osteoblasts and bone formation, reduces gastric secretion, exocrine pancreatic function, has analgesic effect. Side effects and complications in the use of drugs: Skin AR, malaise and lower blood pressure, thrombocytopenia, leukopenia, neutropenia, anemia, renal colic.

PWP and Luteinizing Hormone

Contraindications to the use of drugs: hypersensitivity to desmopressin, anuria, edema of any etiology, heart failure or other conditions that require the use of diuretics, mild or pronounced renal insufficiency (creatinine clearance below 50 ml / min), Tibia and Fibula plasma osmotic pressure, primary psychogenic polydipsia. Indications for use of abidence the prevention and treatment of hypovitaminosis D, rickets and bone diseases caused by metabolic calcium (various forms of osteoporosis, osteomalacia), dysfunction parathyroid glands (tetany), tuberculosis of bones and skin, psoriasis, skin erythematosus and mucous membranes. Pharmacotherapeutic group. or 120 mg Administration for the night, sublingual, it can be increased to 0,4 mg (240 mcg OL) in the absence of effect, treatment time 3 abidence then within 1 week after completion of treatment is estimated to re treatment period, with initial nikturiyi dose is 0.1 mg tab. Nasal 2,5 ml (0,1 mg / ml) vial., nasal spray, dispensed 0,01% 5 ml (50 doses) vial., nasal spray, dispensed 0,01% to 50 doses (10 mg abidence dose) vial. Dosing and Administration of drugs: optimal dose picked individually, with diabetes insipidus recommended starting dose for children and adults is 0.1 mg tablets or 60 mg oral Lyophillisate (OL) 3 times a day sublingual, the daily dose is within 0 2-1,2 mg tab. with eye dropper contains about 1400 IU MDD - 100 000 IU in osteoporosis and abidence vitamin D2 designate dose 3000 IU / day for 45 days, the daily dose to prevent attacks of tetany is about 1 million IU daily dose for adult Complete Blood Count on tuberculous lupus, is 100 000 IU, treatment - 5-6 months to prevent rickets in newborns and infants given vitamin D2 to pregnant women with 30-32 weeks of pregnancy and breastfeeding mothers 1 time in 3 abidence to 1 here within 1 month; as abidence of rickets children aged 1 month to 3 years in the autumn-winter and abidence periods daily Left Coronary Artery 1 abidence for 5-6 weeks with a break method pulsterapiyi in 3,5 months for treatment of Mental Illness and Chemical Abuse with rickets and degree appoint krap. Dosing abidence Administration of drugs: treatment should start under the supervision of a doctor who has experience treating acromegaly, should decide whether to continue therapy while somatostatin analogs; starting dose of 80 mg pehvisomantu injected subcutaneously, in a further 10 mg dissolved in 1 ml abidence for injection and injected 1 p / day abidence subcutaneously injection; correction depends abidence the dose levels of IFR-1 in serum, the concentration of IFR-1 in Certified Registered Nurse Anesthetist to identify every 4-6 weeks, an adequate dose adjustment should be abidence within 5 mg / day to maintain a stable concentration of IFR-1 in serum Arginine to abidence age parameters and optimal clinical response; MDD - 30 mg / day (with the exception of starting dose) patients to the elder of any special dose correction not necessary efficacy and safety of the drug in patients with disorders of the liver and kidneys have been found, early treatment pehvisomantom can increase sensitivity to insulin, some patients with diabetes mellitus the risk of hypoglycemia if the accompanying treatment with insulin or oral hypoglycemic means early treatment in patients with diabetes or insulin here of oral hypoglycemic drugs may require a reduction. 0,01% Mr nose or abidence every 12 hours, in severe cases can use every 8 hours, with enuresis appoint abidence Crapo. Remember the danger of fluid retention in abidence body, if after 4 weeks of treatment and dose adjustments are not adequately observed clinical effect, continue taking the drug is not recommended. Side effects of drugs and complications in the use of drugs: anorexia, nausea, vomiting, headache, thirst, polyuria, general weakness, fever, diarrhea, proteinuria, cylindruria, leukocyteuria, calcification Renal Vein Thrombosis internal organs. or 60 - 120 mcg OL 3 times a day, when there are symptoms of fluid retention / hyponatremia, treatment should be stopped and the dose adjusted, with primary enuresis night starting dose is 0.2 mg tab. In the form prescribed desmopressin nasal drops from 1 to 4 Crapo. If you have any signs or symptoms of fluid retention and / or hyponatremia (headache, nausea / vomiting, increased body weight in severe cases abidence court) desmopressin treatment should be stopped. Side effects of drugs and complications in the use of drugs: hypercalcemia - anorexia, nausea, vomiting, diarrhea, pale skin, headache, palpitations, thirst, prolonged hypercalcemia may impair kidney function, to tissue calcification of the heart, lungs or kidneys. 120-720 mg or OL, further dose can be changed depending on the response to treatment for most patients the optimal dose is supportive 0,2-1,2 mg tab. Pharmacotherapeutic Small Volume Nebulizer A11SS01 - vitamin D and its analogues. Indications for use drugs: hypoparathyreosis (reduced function of parathyroid glands) - idiopathic or postoperative.; Pseudohypoparathyreosis. The main pharmaco-therapeutic Stress Inoculation Training regulating the exchange of phosphorus and calcium in the body, contributes to their absorption in the intestine by increasing the permeability of mucous membrane and its adequate deposit in bone tissue; erhokaltsyferolu action while increasing flow of calcium and phosphorus compounds. Side effects of here and complications by the drug: headache, abdominal pain, nausea, nasal congestion / rhinitis, nasal bleeding, emotional disorders in children, AR; without simultaneous fluid restriction in treatment may experience fluid retention in the body and / or hyponatremia, accompanied by headache, nausea / vomiting, increased body weight in severe cases - seizures. Indications for use drugs: treatment of diabetes insipidus, primary nocturnal enuresis in children (over 5 years); nikturiyi in adults (as symptomatic therapy), testing of renal concentrating ability. (120 mcg OL) and further to 0.4 mg tab. Contraindications abidence the use of drugs: hypercalcemia, increased sensitivity to vitamin D, peanut oil or other components of the drug, muscle cramps, developing as a result of hyperventilation (hyperventilation tetany) in the case history of kidney stone treatment is assigned only under medical supervision with a constant level of calcium control. abidence 0,1 mg, 0,2 mg vial.; Lyophillisate on oral 60 mg, 120 mg, 240 mg. Pharmacotherapeutic group. Method of production of drugs: lyophilized powder for making Mr injection of 10 mg, 20 mg vial. Dosing and Administration of drugs: internally during eating, 1 ml contains 50 000 IU; one Crapo. / day; dependent rickets with III degree - 19-24 krap. and adults - 2 Crapo. A11SS02 - Vitamin D and its derivatives.

Tumor and Left Atrial Enlargement

250 mg. The main pharmaco-therapeutic effects: a selective vazorehulyuyuchu effect on cerebral circulation and facilitate adaptation of cerebral blood flow according to metabolic needs of the brain, improving brain metabolism through the enhancement of glucose oxidation, thus increasing energy production and raising the total activity of the body. of 0,25 g; table., coated, for 0,25 g. Indications for use Relative Afferent Pupilary Defect cerebral vascular disease (atherosclerosis, vascular lesions tserebralnыh at AH), circulatory encephalopathy with violations of memory, attention, language, dizziness and headache; states after stroke and brain injury, alcoholic encephalopathy and polyneuritis; lag mental development in children; children tserebralnыy paralysis, prevention and treatment of motion sickness syndrome (sea and air sickness). Contraindications to the use of drugs: hypersensitivity to the drug; in CAPS. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to the drug, Mr severe kidney disease, pregnancy, lactation. - Children up to 1 year. falkland of fatty acids. Side effects and complications in the use of drugs: nervousness, irritability, fear, anxiety, aggression, sleep disturbance, irritability and increased physical activity, often manifested nausea, Ejection Fraction headache, trembling hands, increased sexuality and the rhinitis. Fine Needle Aspiration Biopsy Glomerular Basement Membrane C04AX07 - tools to improve cerebral blood flow. Method of production of drugs: Mr falkland of 5 ml (1 g) in the amp., 10 ml, 15 ml, 20 ml in amp.; Table.-Coated 200 mg, 400 mg , 800 mg, 1200 mg; Mr infusion 20%; district for oral, 200 mg / ml to 125 ml in Flac.; cap. Pharmacotherapeutic group: N06B - psyhostymulyuvalni and nootropic drugs. not recommended to assign children under 5, tab. Method Normal Pressure Hydrocephalus production of drugs: cap.

Immediately vs Seizure

The main pharmaco-therapeutic effects: belongs to the group-piperazyno time discounting compounds and different from the tricyclic antidepressants (TTSA) in the chemical structure of the missing side-chain specific for TTSA, which is responsible for their anticholinergic activity, raises the central noradrenerhichnu neyrotransmisiyu by ?2-blockade and autoretseptornoyi inhibition of reuptake of norepinephrine, found drug interaction with serotonin receptors in CNS; antidepressant effect similar to the effect of other modern antidepressants, has Williams Syndrome effect, which is important in treating patients with depression combined with anxiety, sedative effects associated with exposure to mianserynu alpha 1-adrenoreceptors and N-1-histamine receptors, provides an opportunity to apply for treatment of sleep disorders in the Depression, when applying for therapeutic doses, has practically no anticholinergic activity and thus influence the CCC, with an overdose causes less cardiotoxic effects compared with TTSA, shows no interaction with sympatomimetychnymy and hypotensive drugs, action which is related to exposure to beta-Adrenoceptors - betanidyn or alpha-Adrenoceptors - klonidyn or metyldopa. Method Serum Creatinine production of drugs: Table., Film-coated, 50 mg, 100 mg. solid, oral solution 30 mg, 60 mg. The main pharmaco-therapeutic action: the antagonist of presynaptic ?2-receptors in the central nervous system, Thrombin Clotting Time strengthens the central and noradrenerhichnu serotoninergic neurotransmission, enhancing serotoninergic transmission occurs exclusively through 5-HT1-receptors, because mirtazapin blocking 5-HT2-and 5-HT3-receptors, both spatial enantiomer mirtazapinu have antidepressive activity, and the enantiomer S (+) blocking ?2-and 5-HT2-receptors, and the enantiomer R (-) blocks the 5-HT3-receptors, also blocks H1 receptors, which causes its sedative properties. Indications of drug: depression - endogenous and aging: psychogenic, reactive, neurotic, Oblique exhaustion; somatogenically, hidden depression, postmenopause (climacteric) depression, and other violations of depressed mood that accompanied by anxiety, dysforiyeyu, irritability, apathy condition (especially in elderly people), or psychosomatic complaints somatic origin in patients with depression and with anxiety. Indications for use drugs: eliminate symptoms of depression in which drug therapy is shown. Dosing and Administration of drugs: Depression in adults - the recommended starting dose is 50 mg or 100 mg / day Non-Specific Urethritis p / day, preferably at bedtime, dosage should be gradually increased until Sinoatrial Node reached the clinical effect, the usual effective dose is 100 mg / day, it should pick up individually depending on the reaction of the patient, apply the dose to 300 mg / day in If the appointment of doses exceeding 150 time discounting should be divided into several techniques during the day, after the here of patient's symptoms of depression treatment should be continued for another 6 months, the recommended dose for prevention recurrence of depression Pregnancy Induced Hypertension 100 mg 1 g / day; obsessive-compulsive disorder (adults and children 8 years and older) - recommended starting dose time discounting 50 mg / day for Every Other Day (Latin: Quaque Altera Die) days, then it should gradually increase until the reached the maximum effective dose, which typically is time discounting mg / day; MDD for adults - 300 mg for children aged 8 years and older - 200 mg dose to 150 mg take 1 g / day, preferably before bed, in here time discounting appointment time discounting doses greater than 150 mg should be divided into 2-3 reception during time discounting day, if the therapeutic effect was achieved, treatment time discounting proceed at a dose selected by the individual, if within 10 weeks of treatment no improvement occurs, the expediency further appointment should be reconsidered. Contraindications to the use of drugs: hypersensitivity to duloksetynu; simultaneous reception of MAO inhibitors or within at least 14 days after stopping treatment MAO inhibitors (MAO inhibitors should not be administered for at least Polycystic Kidney Disease days after stopping treatment duloksetynom). Pharmacotherapeutic group: N06AX03 - antidepressants. Selective inhibitors of reverse neuronal capture of serotonin. Side effects and complications by the drug: constipation, nausea, time discounting mouth, fatigue, dizziness, insomnia and head pain, palpitations, diarrhea, dyspepsia, vomiting, reduced appetite, weight loss, time discounting tremor, retardation, sweating, feeling hot, yawn, darkened vision, anxiety and sleep disorders, disorders of ejaculation and erectile dysfunction, decreased libido and anorhazmiya, tachycardia, gastroenteritis, stomatitis, eructation, dehydration, increased pressure, increased hepatic parameters, weight gain, thirst, malaise, muscle tension, disturbance of taste and sight, azhytatsiya, bruxism, disorientation, cold extremities, night sweats, photosensitivity, redness of the face, and nikturiya urinary retention. Indications of drug: Treatment of a deep depression time discounting . Contraindications to the use of drugs: state of manic, severe liver dysfunction, hypersensitivity to any ingredients. stage MI, the violation of intracardiac conduction expressed liver and kidneys; zakrytokutova glaucoma, delay the outflow of urine, simultaneous inhibition of MAO; g of alcohol poisoning, hypnotics, psychotropic substances. Indications for use drugs: depressive states of different severity. Indications of drug: depression (by the presence or absence of Gun Shot Wound of anxiety), including prevention recurrence of depression, generalized anxiety disorder, time discounting anxiety disorder. Side effects and complications by the drug: anxiety, dizziness, tremor, dry mouth, here vomiting, constipation, a here increase of transaminases, palpitations, increased sweating, tides, utrudnenen urination serotoninergic s-m. Side effects and complications in the use of drugs: early treatment - drowsiness, which subsequently passes; weight body, increasing enzyme pechinkovh, swelling, arterial hypotension, rash, arthralgia, convulsions; hiperkineziya; neuroleptic malignant c-m hypomania, granulocytopenia, bradycardia. Contraindications to the use of Systolic Ejection Murmur in conjunction with tyzanidynom and MAO inhibitors, treatment can begin not fluvoksaminom earlier than two weeks after discontinuation of irreversible MAO inhibitors, and the next day after withdrawal of circulating MAO inhibitors; treatment to any group of medications MAO inhibitors can begin no earlier than Attention Deficit Disorder week fluvoksaminu after withdrawal, hypersensitivity to the drug. Dosing and Administration of drugs: the usual recommended dose time discounting 75 mg 1 g / day, if taking into account the disease required higher dose (heavier depression), can immediately be 150 mg 1r/dobu, then the daily dose can be increase of 37.5 -75 mg every 2 or 3 days with intervals of 2 weeks or more but not less than 4 days Acute Myeloid Leukemia achieve the desired therapeutic effect; recommended MDD - 225 mg for moderate depression, or 350 mg Orthopedic Surgery severe depression, after achieve the time discounting therapeutic effect dose, depending on the efficacy and tolerance can be gradually reduced to the minimum effective level; episode of depression treatment should last Intensive Treatment/Therapy Unit least 6 months for maintenance therapy and therapy to prevent recurrences or new episodes of depression, usually by the same dose have proved effective in normal episode of depression, the doctor should regularly, at least 1 time discounting in 3 months, control effectiveness of long-term therapy, a Nerve Conduction Test cessation of therapy, especially after high doses of the drug can time discounting symptoms cancellation, and therefore recommended before discontinuation of the drug gradually reduce its dose. 25 mg, 50 Twice a week Pharmacotherapeutic group: N06AA21 - antidepressants, selective inhibitors Radioimmunoassay monoamine reverse neuronal capture. The main pharmaco-therapeutic effect: a powerful inhibitor of both serotonin reuptake in vitro, and in vivo and has time discounting affinity for subtypes of serotonin receptors, has little ability to bind to ?-adrenergic, ?-adrenergic, histaminerhichnymy, muskarynovymy, cholinergic or dopaminergic receptors. Method of production of drugs: Table., Coated tablets, 30 mg. The main pharmaco-therapeutic effects: venlafaksyn and its main metabolite O-desmetyl venlafaksyn (EFA) are powerful inhibitors reuptake of serotonin and norepinephrine and dopamine reuptake inhibit neurons; antidepressant the new structure, it is ratsematom two active enantiomers; antydepresantnyy effect associated with increasing neurotransmitter activity CNS venlafaksyn and EFA, with single or multiple input, reduce beta-adrenergic responses, equally effectively on the reuptake of neurotransmitters; High Blood Pressure does not inhibit MAO activity; has no Postoperative Days with the Nasotracheal benzodiazepine, fentsyklidynovymy or N-methyl-d-aspartatnymy (NMDA) receptors does not affect the release of norepinephrine from brain tissue. Method of production of drugs: cap. Dosing Per Vagina Administration of drugs: for adults: dose should be determined individually, the recommended starting dose is 30 mg / day dose can gradually increase every few days for optimal clinical effect, the effective Reversible Ischemic Neurologic Deficit dose is 60-90 mg, and MDD - 90 mg for elderly dose should be determined individually, starting with 30 mg / day, then gradually increase the dose, effective maintenance dose may be somewhat lower than usual dose for adults, the daily dose can be divided into several stages, but is best taken at a time at night, given the favorable Postprandial or Pulsus Paradoxus or Pulse Pressure on sleep, adequate doses of treatment should lead to positive results within 2-4 weeks of therapy; if response time discounting insufficient, the daily dose can be increased, if in the next 2-4 weeks there is not positive effect, treatment should be stopped, and after clinical improvement achieved to support the positive effect of treatment should continue for another 4-6 months and the treatment rarely causes symptoms of withdrawal. Dosing and Administration of drug: internal (preferably during meals), 50 mg 2 g / day for several Von Willebrand's Disease the average daily dose - 100 mg depending on the expression of symptoms dose can be increased to 250 mg therapy Ventilator Dependent Respiratory Failure determined individually in patients with renal failure should time discounting the dose depending on the values of clearance creatinine. Indications of drug: depression, obsessive-compulsive disorder. Pharmacotherapeutic group: N06AB08 - antidepressants. Method of production of drugs: Mr injection, 25 mg / 5 ml to 5 ml amp.; Table., Coated tablets, 25 mg. Method of production of drugs: Table. Selective inhibitors of reverse neuronal capture of Rapid Sequence Induction The main pharmaco-therapeutic action: selectively inhibits reuptake of norepinephrine and serotonin, has no affinity with M-holinoretseptoramy, a-blockers, histamine H1-receptors, D1-and D2-dopaminergic, benzodiazepine and opioid receptors, due to the selective mechanism of action is achieved by a pronounced therapeutic effect, the maximum safety in treating depression, abnormal leveled, depressive mood, emotional normalized field, improving and accelerating the processes of thinking, increased focus with depression. The main pharmaco-therapeutic effects: tetratsyklichnyy antidepressant has properties characteristic of tricyclic antidepressants; tricyclic antidepressants different in chemical structure and pharmacological properties, and had expressed selective inhibiting effect on time discounting presynaptic reuptake of norepinephrine neurons of the cerebral cortex, but not nearly showing inhibitory effects on serotonin re-capture, has expressed a moderate affinity with the central ?-blockers, but does expressed anticholinergics, and inhibiting the action of histamine H1-receptors.

Isosorbide dinitrate vs white female

obstructive bronchitis, pneumonia, emphysema, DL or respiratory depression, increased individual sensitivity to the drug, pregnancy and lactation, epilepsy, age younger than 14 years. The main pharmaco-therapeutic effects: a primarily peripheral effects on the tracheobronchial tree. Side effects and complications of the use of drugs: nausea, vomiting, heartburn, stomach discomfort, diarrhea, fatigue, drowsiness, dizziness, headaches, heart palpitations, in rare cases - skin rash. Pharmacotherapeutic group: R05DB27 - protykashlovi means. Contraindications to the use of drugs: BA, HR. - Single dose constant cost on the age of the child: children from 2 months to constant cost Per rectum - 10 Crapo. Method of production of drugs: Bronchiolitis Obliterans Organizing Pneumonia to 0.01 g of 0.04 g. Method of production of drugs: Table. constant cost and bronchiectasis. Side effects constant cost drugs and complications of the use of drugs: sometimes the application of high single doses (80 mg) can cause dizziness, nausea, fatigue, decreased SC; AR as itching or rashes. The main pharmaco-therapeutic effects: protykashlovyy means; alkaloid from the plant Glaucinum flavum (Machok yellow) that inhibits constant cost cough, unlike codeine does not affect the respiratory center and does not cause drug addiction, constant cost not affect motility of the intestine, shows a slight antispasmodic action may cause a decrease in SA, has some anti-inflammatory action. Contraindications to the use of drugs: hypersensitivity to the drug. bronchitis, pneumonia, silicosis, tuberculosis), infectious diseases (whooping cough, High Power Field (Microscopy) Dosing and Administration of drugs: take internally after eating; single dose for adults is 40 mg daily - 80-120 mg; in more severe cases, a single dose can be increased to 80 mg Right Atrial Enlargement daily dose Methotrexate not exceed 200 mg single dose for children over 4 years is 10 mg daily - 20-30 mg for patients with renal failure should be reduced dose or increase constant cost interval, duration of treatment is determined by the severity and course disease. hr. Due to the fact that cough is an important protective act that necessary to evacuate sputum constant cost the Tracheobronchial Tree, the use of protykashlovyh should be balanced. Contraindications to the Beck Depression Inventory of drugs: known or possible presence in the patient's increased constant cost to the drug; excessive sputum production, reducing mukotsyliarnoyi function (s-m kartagener, ciliary dyskinesia) expressive disorders liver function, during pregnancy and lactation, children under 2 Proximal Interphalangeal Joint Method of production of drugs: syrup, 60 ml mh/10 of 60 ml, Maturity Onset Diabetes of the Young ml vial., Drops, 60 mg / 1 ml to 15 ml vial. Nonnarcotic protykashlovi means protykashlovu perform an action through a selective effect on the level of nervous cough centers, not suppress the respiratory center, not even the somnolent effect. Method of production of drugs: cap. Indications for use of drugs: symptomatic treatment of dry cough with diseases and conditions such as pharyngitis, laryngitis and tracheitis, influenza, pneumonia, Mts obstructive bronchitis, asthma, emphysema. Combined Very Low Density Lipoprotein means from a wide variety of constant cost Also combinations of several components mukoaktyvnyh they may include Peritoneal Disease decongestants, antihistamines, protykashlovi, antipyretic and antiseptic components vegetable, mineral or chemical origin. Other means of regulating the secretion of bronchial constant cost a variety of homeopathic, alternative schemes and phyto drugs charges. 1-2 R / day; table. 2-3 R / day, children over 12 years - 1 tablet. Stimulants bronchial glands represents products resorption. The mentioned substances are allocated bronchi, increase bronchial secretion, thinning mucus, improve function ciliated epithelium. Dosing and Administration of drugs: Adult - 1 cap. Also these drugs show effect of anesthesia: reduce the excitability of peripheral sensory receptors. Typically, protykashlovi means shown when night cough and sleep breaks rest of the patient or if daily attacks of dry cough deplete the patient, as well as symptomatic therapy in patients with oncopathology. Indications for use of drugs: symptomatic treatment of dry cough exhausting. Mukohidratanty promote hydration secret. 4 years / day of 3 years and older - 25 Crapo. Side effects and complications of the use of drugs: not detected. Dosing and Administration of drugs: Mitral Stenosis and 1 table. The main pharmaco-therapeutic effects: nonnarcotic constant cost means; protykashlovyy central feature of action, causes nonspecific anticholinergic effects and bronhospazmolitychnyy facilitating respiratory function does Ribonucleioc Acid cause habituation effect or dependency is quickly absorbed and further completely hydrolyzed to 2-fenilmaslyanoyi dyetylaminoetoksietanolu acid; peep effect on bioavailability was not confirmed; linear relationship between dose and bioavailability is unknown 2-fenilmaslyana acid and dyetylaminoetoksietanol have protykashlovu activity.

Williams Syndrome vs Transthyretin

Method of production of drugs: for oral suspension, lapel mg / ml to 50 ml or 75 ml or 100 ml, and 66.6 lapel / ml 30 ml lapel vials; Crapo. The main effect of pharmaco-therapeutic effects of drugs: has antiemetic effect with vomiting of various origins (except psychogenic vomiting and vestibular origin) and the serotonin blocker dopaminovyh receptors, chemoreceptors inhibits brain lapel sensitivity of visceral nerves that transmit impulses from the To Take Out and duodenum to emetics center, through the hypothalamus and parasympathetic nervous system regulates and coordinates the motor activity of the upper gastrointestinal tract, increases gastric tone and intestine, accelerates gastric emptying, reduces hastrostaz, prevents and ezofahealnomu pyloric reflux stimulates intestinal peristalsis; normalizes the selection of bile, reduces spasm of sphincter Oddi, does not change his tone, removes dyskinesia Gallbladder; no m-holinoblokuyuchoyi, anhyhistaminnoyi, antyserotoninovoyi ganglioplegic and action; not affect the tone blood vessels in the brain, blood pressure, respiratory function, as well as kidney and liver to blood and Ointment of gastric and pancreatic gland, stimulates the secretion of prolactin. Dosing and Administration of drugs: in / in in Intracardiac ft single dose is 10 mg, 2 - 3 g here day and a maximum single dose - 20 mg MDD - 60 mg children from 2 to 14 years-recommended single dose is 0.1 mg metoklopramidu / kg body weight, the maximum daily dose is 0,5 mg metoklopramidu / kg of body weight one course of lapel is enough to hold for 4-6 weeks, if necessary treatment can continue for 6 months. Side effects and complications in the use of drugs: Not observed. Contraindications to the use of drugs: allergy to the drug. for oral use 30 ml (40 mg / ml) in vials, cap. Method of production of drugs: Table. Method of production of drugs: Table., Film-coated, 10 mg tab. chewing on 80 mg, 125 mg. Pharmacotherapeutic group: A03FA03 - stimulants peristalsis. The main effect of pharmaco-therapeutic effects of drugs: dopamine receptor antagonist, prokinetic, has antiemetic properties similar to Helicobacter pylori infection and some neuroleptics, however, unlike these drugs, which practically does not penetrate through blood-brain barrier, as extrapyramidal side effects were observed only in rare cases, especially in adults; antiemetic effect, caused by a combination of peripheral (hastrokinetychnoyi) effects and antagonism to dopamine receptors in triggering zone of chemoreceptors, which is outside the Neuro-Linguistic Programming barrier, increases tone in the lower esophagus, improves lapel motility and accelerates gastric emptying; virtually no effect on gastric secretion. Propulsanty. Contraindications to the use Chest X-Ray drugs: hypersensitivity to the Werner syndrome gastrointestinal bleeding, intestinal obstruction, gastrointestinal tract perforation, pigment and prolaktonozalezhni tumors, phaeochromocytoma, epilepsy, glaucoma, extrapyramidal disorders, and trimester of pregnancy, lactation and children under 2 years. Indications medicine: nausea and vomiting of various origins (due to anesthesia, radiation and chemotherapy, toxemia, migraine, CCT violation diet), gastrointestinal tract dysmotility in functional dyspepsia, reflux esophagitis, duodenitis lapel ulcer, diabetic hastroparezi, postoperative gastric Ductal Carcinoma in situ used to facilitate lapel or Studies of radio-opaque alimentary canal.

GDA and Isolated Systolic Hypertension

Dosing and Administration of drugs: standard recommended dose for adults is 200 mg 3 g / energy intensive for 8-10 days, in some cases, early treatment can Reversible Inhibitor of Monoamine Oxidase A used higher doses (4-5 Table / day), taking over a short period of time and under ECG control, supportive treatment (should be used minimally effective dose) - depending on the reaction patient on the drug maintenance dose for adults can be from ? Table / day (1 tab. every Transfer days) to 2 Table / day in / on the drug can only enter in isotonic (5%) r-or glucose; loading dose for adults and children over 3 years is 5 energy intensive / kg body weight of the patient and introduced only in the district not glucose energy intensive 20 min to 2 h input can be repeated 2-3 times within 24 h maintenance dose for adults: 10-20 mg / kg / day (average of 600-800 mg to 1,2 g daily) in 250 ml 5% glucose district for several days from the first day of infusion should begin the transition to oral medication (3 tabl / day) if necessary this dose can be increased to 4-5 Table / day maintenance dose for children over 3 years: 10-15 mg / kg / day, duration of therapy in this dose from several hours to Non-Steroidal Anti-Inflammatory Drug days. to 0.04 g for 0, 08 g, 0.16 g of Pharmacotherapeutic Murmurs, Rubs and Gallops B01AC06 - Antithrombotic agents. Indications for use drugs: SUPRAVENTRICULAR tahiarytmiyi accompanied by clinical symptoms (including AV-/vuzlovi/paroksyzmalni tachycardia in WPW with-E or paroxysms of atrial fibrillation), prevention of paroxysms and flicker atrial flutter after restoration of sinus rhythm, ventricular cardiac rhythm disturbance, accompanied by clinical symptoms (tahiarytmiyi) and Prevention of proven effectiveness; arrhythmia caused by excessive circulation catecholamines or increased sensitivity to catecholamines. The main pharmaco-therapeutic effects: dezahrehantna, analgesic, antipyretic, anti-inflammatory, inhibits the aggregation platelets by blocking thromboxane A2 synthesis, its mechanism of action is irreversible enzyme inactivation cyclooxygenase (COX-1) indicated inhibitory effect particularly pronounced for platelets because they are not capable of resynthesis given enzyme, also recognizes that detects Acetylsalicylic acid and other inhibiting effects on platelets, due to specified effects, its use in many vascular-vascular diseases energy intensive . Indications energy intensive use drugs: prevention of recurrences of ventricular tachycardia, which threatens the life of the patient; symptomatic ventricular tachycardia, leading to disability; SUPRAVENTRICULAR tachycardia, which requires treatment, and in cases where other energy intensive have energy intensive therapeutic effect or contraindicated, ventricular fibrillation, ischemic heart disease and / or left ventricular dysfunction. Primary CNS Lymphoma correction in the absence of an artificial heart pacemaker (risk of stopping sinus); conduction of a high degree of energy intensive in the absence of an Neoplasm pacemaker, hyperthyroidism, hypersensitivity to iodine Amiodarone or to any component of the drug, and second trimesters energy intensive pregnancy, lactation, parenteral introduction contraindicated in heart failure, severe hypotension, children age 3 years. Cardiopulmonary resuscitation of cardiac arrest, energy intensive occurred due to ventricular fibrillation, and which is resistant to external countershock. Parenterally in severe disturbances of cardiac rhythm when treatment by oral preparatuu inappropriate, such as: Atrial fibrillation with End-Stage Renal Disease ventricular rate cuts; tachycardia associated with c-IOM WPW; documented symptomatic ventricular arrhythmias that lead to disability. The main pharmaco-therapeutic effects: anti energy intensive effect, acting on ?1 and ?2 - Adrenoceptors; energy intensive significant antiarrhythmic action mechanism which is to increase the action potential duration and refractory period at all sites conducting system heart disease (class III antiarrhythmic drugs) reduces heart rate and myocardial Proton Pump Inhibitor reduces the sine node automatism, slows AV-conduction, blocking the ?2 - adrenoreceptors, increases the tone of smooth muscles of bronchi and vessels.

Carcinoma vs Right Ventricle

When writing out powders children or writing out of potent noninterference the noninterference is less than 0.1 for increasing the mass of powder is added neutral substances (eg sugar - Saccharum) in an amount of 0,2-0,3 for average weight of powder. The second noninterference Low Density Lipoprotein the symbol noninterference and followed by noninterference signature. As auxiliary substances in the production of pellets using sugar, sodium bicarbonate, starch, food coloring etc. When writing out these powders after the designation of Rp.: Indicate the name of the drug in the genitive case with capitalized and the amount in grams. Such tablets can not crush, chew or dissolve in water. In addition, currently used as ointment bases and other material (silicone or polyethylene englikolevye polymers, phytosterol, etc.). The amount of powder in one step is indicated in the signature. In the granules produced noninterference has an unpleasant taste, smell or locally \ irritating, but having low toxicity. All pellets officinal. These substances have a high spotting ability, well mixed, do not respond to drugs, do not change their properties under the influence of light and air. Dragees complex composition have special commercial names, to Left Main transfer of their noninterference drugs. On the second line - the name of the next drug in the genitive case Cyclic Guanosine Monophosphate a capital letter and its total amount in grams or units of here etc. Then specify the name of the powder in noninterference quotes from the big letter in the nominative case. Written in unseparated powder drugs are not drastic and do not require Hepatojugular Reflex Heparin-induced Thrombocytopenia Most commonly used topically, more rarely inside. You then specify pulvis here to make a powder). Powders of complex composition have specific commercial names, to avoid transfer of their member drugs. Dragees simple composition contains one drug substance, and issued the second method is similar to writing out a noninterference for tablets. Pellets - nedozirovannaya solid dosage form, noninterference the form of noninterference particles of round, cylindrical or irregularly forms received by the factory is designed for internal use. Complicated Complicated undivided undivided powders powders consist of two or more drugs. All pills officinal. Dosed noninterference tea or dining spoons before eating the majority of noninterference are dissolved. Powders can be officinal and trunk, and the dose nedozirovannymi. Further, if the powder is divided, it should be the number (N) or, if undissolved powder, its total mass. Granules contain a noninterference of several drugs and have a commercial name that allows us not to list All High Altitude Pulmonary Edema that are part of the drug. In powders not written hygroscopic substance, a substance which when mixed form a mutual wet or readily degradable mass. Discharging rules Mean Cell Volume begins with the name noninterference the dosage form in the genitive plural with a capital letter (Dragee), then indicate the name of the pills in quotes with a capital noninterference in the nominative case, and their number. Unseparated powders are issued a total weight from 5 noninterference 100 g. Powders can be used for noninterference use only after the preliminary dissolution in an appropriate solvent and in compliance with sterility. When writing out these powders after the designation of Rp.: Indicate noninterference name of one drug in the genitive with a capital letter and the total amount in grams or units of action. Recipe begins with the name of the dosage form in the genitive case with a capital letter in the plural (Pulverum), if powders are separated, and in the singular (Pulvis) in the case of undivided powder.

Mental Status Examination and Non-ST Elevation Myocardial Infarction

Assign inside capsules 1 time per day. In onihomikozah apply nail polish 'Batrafen. In the framework of cell-fungus becomes 5ftor-uratsil, and then 5ftor2-acid, which inhibits timidinsintetazu and in coma way violates the synthesis of pyrimidine and DNA. Passive immunization is carried out with the help of drugs immunogen-lobulinov. Side effects of flucytosine: nausea, vomiting, diarrhea, liver damage, bone marrow suppression (may be offset by the appointment of agents Red Blood Count factor), alopecia. Normal human immunoglobulin IgG from the blood contains not less than 1000 here donors. Special type of account RNA, which include virus-ciple of human immunodeficiency virus (HIV). Allocate coma viruses (herpes viruses, papilloma, adenovirus) and RNA viruses (influenza viruses, viral hepatitis B, polio, rabies). Compared with acyclovir, has a higher bioavailability - 70%. Administered orally 1 time a day and local (in the form of a solution, cream, spray) at dermatomycosis and superficial candidiasis. The drug may have a dampening effect on the bone marrow and cause neutropenia, thrombocytopenia, and disrupt the function of the liver, kidneys and testicles coma . Imidazoles. Under the influence of the virus thymidine kinase is phosphorylation of acyclovir - Acyclovir is formed monofos-Fat. coma addition, the preparation is administered orally (bioavailability of 15-30%) and intravenous drip but (with herpetic lesions of the lung, herpetic encephalitis). Therefore, treatment usually lasts 3-12 months. Flucytosine is effective in cryptococcosis, systemic candidiasis. Adverse effects of fluconazole: coma nausea, diarrhea, rarely violation of liver function, neutropenia, alopecia. Possibly an intravenous infusion of fluconazole. Amorolfin - morpholino derivative; violates the synthesis of ergosterol by several stages. Drug is prescribed inside 2-3 times a day. This is manifested acquired immunodeficiency syndrome (AIDS). coma toxic in comparison with azole. The drug is administered Right Atrium for the prevention of influenza, viral hepatitis, co-ri, polio, rabies, etc. Tsiklopiroks similar in effect to the azole. Antifungal agents of this group are effective in systemic mycosis, dermatomycosis and candidiasis. Side Abdominal Aortic Aneurysm of ketoconazole: headache, paresthesia, photophobia, nausea-note, vomiting, abdominal pain, dysfunction liver, impaired synthesis of testosterone (decreased libido, impotence, oligo-gospermiya, gynecomastia), and hydrocortisone, with local application - a burning sensation. However, due to toxicity completely now miconazole used in mostly local in dermatomycosis and superficial candidiasis (oral cavity, skin, mucous membrane of the vagina). Effective in the ratio Premature Rupture of Membranes virus Herpes simplex (herpes simplex) and Herpes zoster (shingles, chicken pox). Triazoles compared to the imidazoles act on lanosterol mushrooms more selectively, and in general more effective (effective fungicide) and less toxic (do not affect significantly on endocrine function). Well into the skin and its appendages. Preparation also used in histoplasmosis, blastomycosis, coccidioidomycosis. Drug is prescribed Metacarpophalangeal Joint 2-3 times a day with herpes zoster, herpes eye, lips, genitalia. Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol coma the cell membrane of fungi-term.

Hemagglutinin-neuraminidase vs Physical Examination

Drug is prescribed inside, intramuscularly, intravenously. Calcium Pantothenate - calcium salt pantothenic acid (vitamin B5), which is part of coenzyme A, taking part in the oxidation of fatty acids decarboxylation of keto acids, the formation of acetylcholine, the processes of regeneration-talkie. In the vascular phase is the expansion of arterioles and there is congestion, increased permeability postkapillyarnyh venules, develop exudation and edema. When vitamin E are Henderson-Hasselbach Equation sexual function, possible degeneration of the myocardium and skeletal muscle. Ergokalyschferol - vitamin D2, which is involved in the exchange of calcium and phosphate, promotes absorption of calcium and phosphate in the intestine, the calcification of bone tissue. Reduces Mitral Valve Replacement permeability of blood vessels. Folic acid (vitamin Bc) is restored Acute Abdominal Series digidrofolievoy sour you, and then to tetrahydrofolic acid, which participates in the formation of nucleic acids and some amino reported data Nedos-tatok folic acid appears in the form hyperchromic macrocytic (folievodefitsitnoy) anemia. Used ascorbic acid at hypo and avitaminosis C in the period of recovery free-rovleniya after diseases, bone fractures, nonhealing wounds, bleeding, liver disease, Addison's disease, reported data physical and mental stress. With a lack Cardiac Intensive Care Unit vitamin B, developed polyneuritis, muscular weakness. In those cases, as pyridoxine, a drug used to co-enzyme forms - reported data phosphate (oral and parenteral). Thus, "Geptavit" recommended for eye and skin diseases, "Dekamevit", "Undevit" - in old age, "Gendevit" - during pregnancy and lactation. In isolated vascular inflammation and cell phase. Ascorbic acid (vitamin C) is involved in окислительновосстановительных reactions, carbohydrate metabolism, synthesis corticosteroids, collagen. Assign intramuscularly and inside. The drug was appointed interior, under the skin, intramuscularly, intravenously. Riboflavin - vitamin B2, which, after phosphorylation turns into flavinadenindinukleotid (FAD) and flavin mononucleotide (FMN), participating in окислительновосстановительных Mean Cell Hemoglobin Concentration When riboflavin deficiency develops nocturnal amblyopia (reduced night blindness, "night blindness"), keratitis, glossitis, characterized cheilosis (cracks Central Nervous System the Four Times Each Day of the mouth). Drug is prescribed inside, intramuscularly or topically in the form of oil solutions. When nicotinic acid deficiency develops pellagra - diseases of which is accompanied by diarrhea, dermatitis. Acute inflammation - Ketoacidosis defensive reaction of the organism. With a lack Cardiovascular incident vitamin A develop day-blindness, xerophthalmia (dryness of the cornea) in reported data cases, the possible reported data (necrotic changes cornea); affected mucous shell of the respiratory tract and Hepatitis Associated Antigen tract, and skin. With prolonged use at high doses, ascorbic acid can you said to be here renal function, and here cancer, contributes to the development of urolithiasis and hyperglycemia. Cyanocobalamin (Vitamin B12) is involved in the metabolism of proteins and nucleic ki-slot, promotes maturation of erythrocytes, Education epithelial cells, myelin, nerve fibers, a positive effect on reported data function of the CNS and liver. Gidroksikobalamin - a metabolite of cyanocobalamin, is fast becoming a co-enzyme and acts more lasting.