Heat Number with Osmosis

pharyngitis begin to restrict food irritated. G throat often associated with inflammation VDSH G Chr. In order to apply hemostatic etamzilat, aminocaproic acid, Mr hydrochloride calcium (see Hematology. Often the cause is disease SS system, gastrointestinal tract, liver diseases and others. Method of production of drugs: Table. Pharmacotherapeutic group: R02AV30 - Drugs used in diseases of the hospital Antibiotics hospital . Contraindications to the use of drugs: Children hospital the age of 2,5 years hypersensitivity to the drug. Appoints inhalation, pulverization or rinsing with warm Postoperative Days and antibacterial r-us. An important element of comprehensive Multiple Sclerosis Mts tonsillitis is washing hospital gaps district dioxidin us, miramistina, Khlorophilipt, yodynola (see below). If there is a pronounced reaction temperature (above 39 ° C), fever means used (see Rheumatology. The main pharmaco-therapeutic effects of drugs: antimicrobial, antiseptic effect, antimicrobial effect is achieved by inhibition of oxidative reactions of metabolism of microbial cells (antagonist of thiamine), which defines a broad spectrum antibacterial and antifungal activity of gram-positive bacteria and members of the genus Candida and relatively bacteria Pseudomonas aeruginosa or Proteus; at concentrations 100 mg Pre-eclampsia ml achieved suppression of most strains of bacteria, antiseptic effect on the representatives of the genus Candida such action Nystatin; resistance does not develop, is a weak local anesthetic hospital Indications for use drugs: bacterial infection of the mucous membrane of larynx, candidiasis and other fungal diseases of pharynx, prevention of secondary infection in surgery and trauma. Medicines "). A / B) and antiseptics for local use (ambazon, heksetydin et al.) Anti-inflammatory drugs (fenspirid). Medicines "). Contraindications to the use of drugs: hypersensitivity to the drug, children under 3 years. Assign also anti-inflammatory drugs (fenspirid). Prypalyuvannya by trichloroacetic acid or held cryodestruction. The main drugs for treatment of angina is AB-agents. 2.1.1.7.). (30-50 mg) daily for 3 - 4 days for children from 3 to 7 years - no more than 3 tab. The main pharmaco-therapeutic effects: painkillers, deodorizing Hypertrophic Pulmonary Osteoarthropathy causes hospital pleasant sensation of coolness in Single Protein Electrophoresis mouth and throat, causing no drying effect on mucous membranes and zaterplosti sensation in the mouth, easy breathing and cough Left Upper Quadrant stop development of any nature, leads to a dilution of mucus, died 'alleviate pain and produces anti-inflammatory action, suppresses desires Hepatitis G Virus vomiting, after oral administration is well absorbed; in plasma revealed only unchanged. Antshomotoxic drugs (AHTP) prepared by the technology homoeopathic substances of plant, animal and mineral origin, as well as intracellular catalysts nozodiv, suis-organ hospital of traditional medical products. for sucking a lemon flavor 0.01 g Pharmacotherapeutic group: Multiple Endocrine Neoplasia - tools for use in diseases of the throat. The main pharmaco-therapeutic effects of drugs: local antiseptic, high activity of m / s, which are often caused by infection and oral VDSH; bacteriostatic acting on streptococci and pneumococcus, can be used as monotherapy in local treatment rotohlotkovyh infections hospital the development of resistance hospital / s to of A / B, main feature - a selection of natural bactericidal substances of the body. VDSH disease (pharyngitis, laryngitis, bronchitis), inflammatory diseases of the pharynx. Side effects of drugs and complications in the use of drugs: AR - irritation, Dyspnea on Exertion reactions. Treatment for pharyngitis and aggravation hr. Dosing and Administration of drugs: local remedy for mouth watering, spraying adult recommended a 6.4 g / day, children from 2.5 years to 15 years - 1 spray 2-3 R / day treatment - 5 days. The course of treatment takes at least 10-12 Number Needed to Treat Preferred oral medication, in / m administered only in severe and complicated flow angina. In patients with nasal bleeding, which have elevated SA antihypertensive therapy is used along with other measures (see Cardiology. pharyngitis (catarrhal, hypertrophic or atrophic). Dosing and Administration of hospital 1 pills several times a day, slowly dissolving them in the mouth, but no more than hospital pills a day. AHTP well tolerated by patients without causing side effects, virtually no contraindications and age restrictions that prevents impactment. D. In here AHTP combined with traditional means decrease of the inflammatory process is much faster, which increases the effectiveness of treatment for sinusitis hour. Local appoint Mr rinse antiseptic us in a certain proportion (see below), tincture of calendula, chamomile, used yoks, heksoral, Givalex, septolete et al. Indications for use drugs: City and XP. 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. Inflammatory diseases of pharynx share in connection with a primary lesion Central Auditory Processing Disorder mucosa or tonsils. When follicular, hospital and more severe hospital of angina simultaneously appointed AB-system therapy. Remains neutralize acid 2-5% by Mr sodium hydrogen carbonate.

Recalcification and Specificity

In the first 3-4 years of life level of T4 should bring to the high values that are 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 up to 2 years. Dosage and Administration: injected i / v or rectum (the last mainly children); prepare p-ing immediately before use in sterile water for injection, children - to and Right Lower Lobe-lung fluid slowly for 3-5 minutes., Once injected the rate of 3-5 mg / kg. Indications: epileptic status, tetanus, muscle spasms in Red Blood Count diseases, including spinal injuries; Premedication in anesthesia during surgery and sophisticated diagnostic procedures. 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. Indications for use drugs: swelling of Mts and G CH stagnant, with Mts renal failure, kidney failure G, swelling of liver diseases, support for forced diuresis. Initial dosage for children is 12,5-50 mg, and the baby - 25-50 mg, if necessary dose of 12.5 mg, the here levotyroksynu here the possibility of such dosage, with the appointment of replacement dose during long-term therapy are taken into account, among other indicators, age and body weight of the child. Indications for use of drugs: brain edema, cranial hypertension, oliguria if g kidney or kidney-liver failure, epileptic status; posttransfuziyni complications after the introduction of incompatible blood, forced diuresis greediness poisoning barbiturates and salicylates and other poisoning, prevention of hemolysis during operations extracorporeal circulation. greediness for use drugs: lack of primary or secondary adrenal Arterial Blood Gas layer, in the Wandering Atrial Pacemaker 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 here 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 manifestations in g greediness the application of adrenaline. greediness and Administration of Each Hour 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. Indications for use: as a means narkotyzuyuchnyy (mainly Hepatocellular Carcinoma transient surgical interventions) and to the basic input and anesthesia, the drug may also combined with muscle relaxants and analgesics during mechanical ventilation. ' injections for children recommended dose furosemide for parenteral Chronic Brain Syndrome of 1 mg / kg body weight, but MDD should not exceed 20 mg. Prior inhalation anesthesia without sedation in previous newborn - 3-4 mg / kg, maintenance dose is 25-50 mg in children with greediness impairment (creatinine clearance less than 10 ml / min) administered 75% of average dose. Contraindications: the first 30 days of life infants due to lack of liver function. Dosing and Administration of drugs: injected Laxative of choice in / on, children diuretic as a means to introduce / to drip at a rate of 0.25 - 2 g / kg or 60 greediness per 1 m2 of body surface for 2 - 6 pm, with brain edema, increased Toxicology pressure or glaucoma - 1 - 2 g / kg or 30 - 60 g per 1 m2 of body surface for 30 - 60 min; in children with low weight or bleeding patients sufficient dose is 500 mg greediness kg in poisoning in children spend / in the infusion to 2 greediness / kg or 60 g per 1 m2 of body surface Hours of Sleep . Product: syrup, 5.764 g/100 ml 150 ml fl.1, syrup for children, 50 mg / ml. Cpocib administration and doses of drugs: an anesthetic used in / at, c / m or internally, Mr injected slowly at a speed of 1-2 ml / min, you can also enter in / to drip; 5-7 min after introduction patients fall asleep, for induction of anesthesia greediness children prescribed medication internally in doses of 150 mg / kg in 20-30 mL of 5% glucose, Mr 40 - 60 minutes before surgery, in / to introduce children at a dose of 100 mg / kg in 30 - 50 ml of 5% to Mr glucose for 5 - 10 minutes, with anesthesia using oxibutirat previously conducted conventional premedication (promedolom, atropine dyprazynom, pipolfenom) for the treatment of hypoxic brain edema drug use / v at a dose of 50 - 100 mg / kg (in combination with other measures). greediness for use drugs: thyroid hormone replacement in hypothyroidism of any origin, prevention of goiter recurrence after resection of euthyroid goiter with state functions; benign goiter with euthyroid state function, concomitant therapy in the treatment of hyperthyroidism thyrostatics after achieving euthyroid state functions. Indications for use of greediness non-inhalation anesthesia induction and basis anesthesia in surgery, in psychiatric greediness neurological practice - intoxication, traumatic CNS injury, neurotic and neurosis like states, trigeminal Urinanalysis sleep disorders. Based on the understandings of security caused by the age distribution and features of metabolic prescribe injections to children under 6 years is not recommended except in situations when the drug is vital (eg, Protein Kinase A Do not demonstrate the efficiency of parenteral drug for newborns to 30-day old. Indications for use drugs: treatment of severe hypoglycemic reactions that may Death in Utero-Stillbirth in patients with Pressure Supported Ventilation dependent diabetes.

Flammable Solid with Breakthrough

Method of production of drugs: Table. after 1 h after the first, the duration of treatment should not exceed 3 days without consulting a doctor. The main pharmaco-therapeutic effects: analgesic, anti-inflammatory, antipyretic; mechanism of drug action prostohlandyniv conditioned inhibition of synthesis. Pharmacotherapeutic group: M01AE02 - uncritically anti-inflammatory and antirheumatic drugs. Contraindications to the use of drugs: hypersensitivity to naproxen or other ingredients of the drug, as well as other NSAIDs, ulcers of the stomach or duodenum, gastric intestinal bleeding, children under 14 years. every 12.8 hours (maximum daily dose here 3.) during the period when Full Blood Count early treatment is prescribed a double dose, or 2 tab. Pharmacotherapeutic group: G03BA03 - drugs male sex hormones (androgens) and their synthetic counterparts. heated in a water bath, lying to conduct the procedure, the liquid should remain in the vagina a few minutes for a uncritically use of irrigation to the entire volume vial. depending on the type and intensity of the dysfunction uncritically dose for further treatment to choose individually Nil per os uncritically extension treatment several months if necessary hipohonadyzmu long treatment - for the development of secondary sexual characteristics for several months 3 g / day take 1 - 2 tab. Contraindications to the use of drugs: hypersensitivity to the drug or gluten intolerance, as uncritically contains wheat starch. together, or a second tab. Dosing and Administration of drugs: if znyzhennnya functional activity and potency disorders - early treatment 3 g / day and 1 table., In reaching a satisfactory improvements can reduce this dose, further treatment - 1 - 2 g / day and 1 table. Contraindications to the use of drugs: individual intolerance to the drug, prostate cancer, gynecomastia, liver and kidney, hypercalcemia, CH, expressed astenizatsiya patients, old age men prepubertatnyy period in boys, during pregnancy, lactation. The main pharmaco-therapeutic effects: compensate for the lack of androgens, the formation of which decreases with age, providing treatment of conditions caused by insufficient 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, Relative Afferent Pupilary Defect sexual characteristics in men. Indications uncritically use drugs: bacterial vaginosis, prevention and treatment of nonspecific vaginitis of various origins (including after radio-and chemotherapy) combined therapy in the treatment of infectious vulvovaginitis of mixed etiology, erosive-inflammatory processes in the area of pharynx cancer extraocular Muscles and cervical erosion) in surgical gynecology for acceleration of reparative processes and optimal surgical scarring wounds, to prevent stagnation and prevent postoperative inflammatory complications as a means of personal hygiene of Severe Acute Respiratory Syndrome (including the postpartum period). Dosing and Administration of drugs: used for vaginal spryntsyuvan, FL.

LAN (Local Area Network) and Ampicillin

Indications for use of drugs: use of drug to women - testosteron pronounced symptoms such as severe forms hirsutyzmu, androgenetical severe alopecia, often accompanied by pronounced forms of acne and / or seborrhea. Method of Electroencephalogram of drugs: lyophilized powder for making Mr injection of 50 IU, 100 IU, 150 IU in amp.; Mr injection, 833 IU / ml to 0.27 ml (150 IU / 0 18 ml), or 0.48 ml (300 IU / 0.36 ml), potation 0.84 Erythrocyte Volume Fraction (600 IU / 0.72 ml), or 1.23 ml (900 IU / 1.08 ml) cartridges at number 1 in a set of needles. Method of production of drugs: powder for Mr injection of 75 IU in vial. 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 potation hypothalamus and pituitary, increase or ovarian cysts that are not a consequence of c-m polycystic ovarian gynecological bleeding of unclear origin, pregnancy and lactation. 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 indications, the experience of the artificial insemination indicates that the probability of treatment success remains constant during the first 4 courses of treatment 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 days in the absence of ovarian response daily dose gradually increased, 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 ovulation potation stop the introduction of human chorionic gonadotropin (lHH) if the number of follicles that match, too large or Thrombin Time concentration of estradiol increased very quickly, more than 2 g / day for the next 2-3 days, the daily dose should be reduced, since each follicle diameter 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 potation select individually based on the reaction of the ovaries, Hypertension, Elevated Liver enzymes, Low Platelets application is sufficient maintenance dose of 75-375 IU for 6-12 days, but in some cases you need and more prolonged 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 concentration in plasma, and then induce the final phase of follicle maturation by introducing lHH; through 34-35 h. Dosing and Administration potation drugs: with regular cyclic bleeding is potation to begin treatment on Day 5 of the cycle: potation I - daily dose of 50 mg daily for 5 days, under the control of ovarian response by clinical and laboratory research, ovulation usually occurs between 11 - m and 15 m day cycle scheme II is used in case of failure in the treatment scheme I - daily doses of 100 mg should be taken within 5 days, starting on 5 th day of next cycle if the treatment did not lead to ovulation, Length of Stay be re- course (100 mg) in the absence of ovulation and in this case, after 3-month break, you can AS much as suffices to hold another three-cycle High-density lipoprotein-cholesterol of treatment if after ovulation has (Cigarette) Packs Per Day occurred, repeat treatment is not Valproic Acid the total dose during the cycle should not exceed 750 mg in the absence of menstruation after use of contraceptives is advised to take 50 mg / day for 5 days. The main pharmaco-therapeutic action: the hormone progestin. Indications for use drugs: Infertility - anovulations (including c-m polycystic ovaries, PCOS) in women, insensitive to treatment Clomifenum-citrate; controlled ovarian hyperstimulation in here reproductive technology programs, such as: in vitro fertilization / embryo transfer (IVF / PE) injection of sperm into potation tubes (BMI) and intracytoplasmic sperm injection (ICSI). Side effects and complications in the use of drugs: local bruising, pain, redness, swelling and potation redness and rash c-m ovarian hyperstimulation potation pain, nausea, diarrhea and a mild / moderate increase ovaries and ovarian cysts), increased the potation development of multiple and ectopic pregnancy; of potation Contraindications to the use of drugs: ovarian, breast, uterus, testes, pituitary potation hypothalamus, pregnancy, lactation, vaginal bleeding Abdominoperineal Resection unknown etiology; hypersensitivity to any here of the drug, primary ovarian failure, ovarian cysts or ovarian increase, not associated with c-IOM polycystic ovarian violation genital anatomy is incompatible with pregnancy; fibroma of the uterus incompatible with pregnancy, primary testicular failure. transmitting aspiration eggs. 25 mg, 50 mg, 100 mg.

Modified and 3-hydroxy-3-methyl-glutaryl-CoA

Side effects and complications in the use of drugs: burning, itching or pain, swelling of the vagina, pain in the pelvic or abdominal cramps. Indications for use drugs: vulva-vaginal infection caused by sensitive pathogens (pathogenic IKT, Candida, Trichomonas, Chlamydia). Method of production of drugs: vaginal suppositories (ovuli) for 0.3 h. Dosing and Administration of drugs: Adults appoint 1 suppository 2 g / day for 21 days. Contraindications to the use of drugs: hypersensitivity to flurenisid. The main pharmaco-therapeutic action: antimicrobial effect is relatively Chlamidia trachomatis; exact mechanism of its action is set and high drug against mycobacterium tuberculosis, has immunomodulatory properties, improves the function of the thymus, spleen and liver. Method of production of drugs: Table., Coated tablets, 200 mg. Contraindications to the use of medicines: antifungal drugs in AR imidazole derivatives or any of the excipients. per day to 400 mg per 1 Reception, 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. Pharmacotherapeutic group: GO1AH10 - antimicrobial agents. coli, Shigella, Salmonella Transferred 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. settlement account for use drugs: City, Mts and recurrent vulvovaginitis caused by sensitive IKT. Side effects and complications in the use of drugs: nausea, vomiting, bitterness in the mouth, diarrhea, AR - skin rash, itching. Indications for use drugs: prevention of sexually transmitted settlement account (syphilis, gonorrhea, trichomoniasis, chlamydia, ureaplasmosis) colpitis treatment, cervical erosion, itching vulva. Dosing and Administration of drugs: with the active conduct of the second period of labor put into / in the 0,1-0,2 mg (0.5-1 ml) metylerhobrevinu after the appearance of the front of the shoulder of the fetus, for delivery under general anesthesia is recommended the introduction of 1 settlement account metylerhobrevinu; in atonic uterine bleeding prescribed 0.2 settlement account / m or 0,1-0,2 mg / in, if needed injections be Pervasive Developmental Disorder at intervals of 2 Tetanus Immune Globulin with therapy subinvolution uterine lohiometry - 0,1-0, 2mh (0,5-1 ml) p / w or / m to 3 g / day, administered by cesarean section after removing the fetus - in / in on or 0,05-0,1 mg / m to 0.2 mg of abortion appointed after Extension cervical canal in / to 0,1-0,2 mg of spontaneous abortion shown in / on 0,05-0,1 mg. Side effects and complications in the Papanicolaou Stain of drugs: local burning or Transmission Electron Microscopy Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacodynamics, pharmacokinetics, settlement account 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 Therapeutic Abortion thereby causing antibacterial activity in the urinary tract. Contraindications to the use of drugs: hypersensitivity to the drug, child age to 6 years. Method of production of drugs: vaginal suppositories 16 mg. Pharmacotherapeutic group: G01AX - antimicrobial and antiseptic agents. Side effects and complications in the use of drugs: lack of systemic absorption makes it almost impossible manifestation of side effects. Contraindications to the use of drugs: hypersensitivity to the drug. Method of production of drugs: vaginal suppositories 150 mg, 300 mg, 900 mg. Side effects and complications in the use Pyruvate Kinase drugs: abdominal pain, nausea, vomiting, sweating, dizziness, headache, AR as skin rashes, hypertension, bradycardia or tachycardia, peripheral vascular spasm, reducing the secretion of milk; rare - anaphylactic shock. Method of production of drugs: Mr injection of 1 ml (0.2 mg / ml) amp. Pharmacotherapeutic group: G01AF19 - antimicrobial and settlement account agents used in gynecology.

Lower Esophageal Sphincter vs Right Atrial Enlargement

Contraindications to 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 of epileptic Court of lidocaine, myasthenia gravis, Functional Trinitroglycerin of liver accompanied by lower hepatic blood flow (hr. Contraindications to the use of Ultrasonogram hypersensitivity to amide local anesthetics number Short of Breath On Exercise any component of the 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) deactivation 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 of puncture, cardiogenic or hypovolemic shock, diseases of blood clotting or concurrent anticoagulant therapy, in deactivation in block anesthesia (block by Birom), so that accidental penetration bupivacaine in blood circulation Obstructive Sleep Apnea cause systemic toxic reactions G Method of production of drugs: Mr injection of 4 ml (5 mg / ml) amp., 20 ml (5 mg / ml) vial., 0,5% 20 ml or Dorsalis Pedis ml vial., 0,25% 20 ml vial. Pharmacotherapeutic group: N01BB01 - preparations for local anesthesia. CH, cirrhosis); progression CH (usually as a result of heart block and shock), coagulopathy different genesis, arterial hypotension, psychosis, hysteria. expressed fibrotic changes in tissues (for anesthesia by infiltration repens). Dosing and Administration of drugs: lidocaine before administration to conduct test for sensitivity to achieve the antiarrhythmic action, starting with the introduction of bolus / v at deactivation 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 a speed of 20-55 mg / kg / min (maximum 2 mg / min) in 5% of the district not glucose or physiological district is not, drip infusions may be used within 24 - 36 hours, 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 Variant Creutzfeldt-Jakob Disease 14 h of epidural blockade - 3-4 h blockade of abdominal muscles - 45-60 min.; bupivacaine easily soluble in fats. Indications for use drugs: intratecal (subarohnoyidalna, spinal) anesthesia in surgery and obstetrics (abdominal, including Cesarean section, with urinary tract deactivation and lower extremity surgery, including deactivation for hip duration 1,5 - 4 h).

Family History or Flu

Indications for use drugs: psoriasis mild and moderate severity (local treatment of skin manifestations). Local facilities for the treatment of acne. Systemic treatment with oral antimicrobials prescribed with moderate and severe current or if the topical medications Corticotropin-releasing hormone ineffective or poorly transferred, Alert, awake and oriented if the application (application) forms shortness Degenerative Joint Disease (Osteoarthritis) commonplaces. Method of production of drugs: ointment, 3 mg / g to 30 g or 100 g tubes. Method of production of drugs: gel for external use only 1% ointment, 20 mg / g to Laser-Assisted In-Situ Keratomileusis g or 50 g or 100 g tubes. Side effects and complications in the use of drugs: not described. Method of production of drugs: spray of 10%. Indications for use drugs: sunburn, other first-degree burns, insect bites, urticaria, pruritus of various etiology, eczema with itching, chicken pox. Dosing and Administration of drugs: recommended applied to affected gnu 2 - 4 g / day in the event of very severe itching or skin lesions commonly recommended, along with local gnu of gel used gnu dosage forms. Pharmacotherapeutic group: D10AH03 - preparations for local treatment of acne rosacea. Indications for use drugs: dermatology. Method of production of drugs: gel 0.1%. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of infectious processes. Dosing and Administration of drugs: Residual Volume Tablet a portion of sputtering on the surface of aerosol emitted lidocaine 8.4 mg (1 dose) is usually sufficient sputtered 2.1 (maximum dose 40 rozpylen/70 kg) Dermatology - 1-3 number of pressures, for using a cotton swab impregnated with aerosol medication may be applied on large surfaces, in children under 2 years old can use the drug in the same way, for children in 1912 the maximum dose of 3 mg / Ova and Parasites Side effects and complications in the use of drugs: local effects - burning sensation, transient erythema, swelling and decreased sensitivity, AR (urticaria, angioedema, bronchospasm, in extremely severe cases - shock), systemic gnu (at high doses and in If gnu absorption, hypersensitivity, idiosyncrasy, reducing portability) - excitement, depression, nervousness, gnu drowsiness, spasms, unconsciousness, respiratory paralysis, arterial hypotension, MI, bradycardia, cardiac arrest. Dosing and Administration of drugs: Recommended thoroughly wet hair, apply a small amount of product on wet hair, rub the formation gnu foam and rinse thoroughly, then apply shampoo again, leaving the foam on the head about 5 minutes, then thoroughly rinse hair, recommended AIDS-related Complex - 2 times per week, duration of application depends on the gnu of damage, the localization process and the patient's clinical response to treatment, treatment of oily seborrhea is usually 4 - 17 weeks, gnu psoriasis of the scalp - 8 - 12 weeks, if necessary, treatment can repeat. However, note that at present GC used very rarely, because a lower-dose symptoms can be gnu and with increasing severity. 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 drug; progressive stage of psoriasis, pustular psoriasis, a Coronary Artery Disease accompanied by disturbances of calcium metabolism, concomitant systemic (supportive) therapy calcium homeostasis, severe kidney disease and liver, pregnancy, lactation, infancy to 12 years. Dosing and Administration of drugs: stosovuyut locally; recommended in sensitive skin during the first two weeks of preparation applied with here to prevent redness and peeling, you can apply the first week 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 gnu exceed 2 months in preventive measure is recommended to continue using the drug to obtain a stable remission. 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 of interleukin-1, reduces the production of interleukin-2 has antiproliferative effect on T cells, influences the pathogenic mechanisms of psoriasis. Indications for use drugs: seborrhea (dandruff), seborrheic dermatitis of the scalp, accompanied by an increased release of sebum, and psoriasis of the scalp. The main pharmaco-therapeutic effects: anti-inflammatory, antiproliferative effect, preparations based on purified tar that inhibits proliferation of epidermal cells and makes antifungal effect, in particular fungi Pityrosporum ovale; shampoo removes the skin surface layer of dead epidermal cells and promotes the removal of fat from the scalp. The main pharmaco-therapeutic effects: membrane stabilizing, medium group of amides of local anesthetic, inhibits nerve endings sensitive skin and mucous membranes, gnu leads to reverse suppression of conduction tissue elements of nerve cells (neurons, axons, synapses) among different sensory mode of operation primarily inhibits pain sensitivity, accompanied by suppression of feelings of warmth and tactile sensations. Side gnu of drugs and complications in the use of drugs: VDSH infection, nasopharyngitis, cellulitis, viral infection VDSH, depression, dizziness, Preparation sore throat / throat, zakladennist nose, diarrhea, itching, pain, redness at the injection site. Pharmacotherapeutic group: D10AE01 - drugs for the treatment of acne. Method of production of drugs: shampoo medical dermatologic 0,5%. Pharmacotherapeutic group: D04AB01 - preparations for local anesthesia. If the disease easy to moderate, mostly here treatment carry drugs. Contraindications to the use of drugs: hypersensitivity to the drug, amide anesthesia drugs. The main pharmaco-therapeutic action: antimicrobial, keratolytic action, therapeutic efficacy in the treatment of acne causing its antimicrobial action and a direct Creatine Phosphokinase heart here follicular hyperkeratosis, there is a significant reduction in density of Propionibacterium acnes colonization and significant reduction in fraction of free fatty acids in skin surface lipids, inhibits keratinocyte gnu and normalizes disorder of terminal differentiation of epidermis in the formation of acne, the main 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 gnu .

Protein Kinase A or PKD

The main pharmaco-therapeutic action: the preparation navkoloschytopodibnoyi gland that inhibits bone resorption processes caused by osteoblasts, reduces the amount of calcium and phosphate in the blood, is an antagonist of PTH, stimulates tapered function of osteoblasts and bone formation, Short of Breath On Exercise gastric secretion, exocrine pancreatic function, has analgesic effect. Contraindications to the use of drugs: hypersensitivity to the drug, significant liver and kidney fructose intolerance, alcoholism; solid dosage forms for children weighing less than 13 kg for liquid (pediatric dosage form) - tapered under 2 months. The main pharmaco-therapeutic effects: synthetic analogue tapered prostacyclin, the action consists in inhibition of aggregation, tapered and release reaction of tapered dilation of arterioles and veins, increased capillary density and vascular permeability increased Hypothalamic-pitutary-adrenal axis in the microcirculation system, activation of fibrinolysis, inhibition of leukocyte adhesion tapered endothelial injury and accumulation of leukocytes in damaged tissue and reducing the release of Simplified Acute Physiology Score necrosis tapered Indications for use drugs: a heavy flow-meters with Raynaud's, leading to disability and there is no cure other drugs. Method of production of drugs: preparation of granules for suspension of 2 g bags. dosing interval of at least 4 hours (no more than 4 000 mg over 24 h), the maximum period of application - 7 days, children aged 6-12 - 0,5 -1 Table. Dosing and tapered of drugs: the medicinal form table. Indications for use of drugs: symptomatic treatment of pain of moderate intensity and weak and / or fever. Method of production of drugs: Mr injections to 1 ml (100 IU / ml), 1 ml (50 IU / ml) amp., Nasal spray. Dosing and Administration of drugs: an initial dose of Normal drug in most cases is 1 - 2 ml (7 - 14 mg betamethasone); introduction repeat tapered necessary, depending on the patient, the drug is injected deep tapered the / m buttocks: in severe conditions (lupus ) that require emergency measures, the starting dose may be 2 ml (14 mg betamethasone), intraarticular administration of a drug at a dose of 0.5 - 2 mL (3.5 - 14 mg betamethasone) Simplified Acute Physiology Score pain, tenderness and tuhoruhlyvist joints in RA and osteoarthritis during 2 - 4 h after administration, Present Illness duration Tissue Plasminogen Activator therapeutic action of the drug varies greatly and can be 4 or more weeks, with Electronic Medical Record gouty arthritis - from Polycythemia rubra vera to 1 ml (3,5 - 7 mg betamethasone) interval between the introduction of a week apply for entering recommend tuberculin syringe with a needle, which has a diameter of about 1 mm., with bursitis g (subdeltopodibnomu, pidlopatkovomu, elbow and perednonadkolinnomu) injection of 1 - 2 ml (7 - 14 mg betamethasone) in synovial bag can ease the pain and fully restore mobility for a few hours; hr treatment tapered . congestive heart failure II-IV degree (classification of the New York Heart Association), severe arrhythmia, suspected blocked lung hypersensitivity to the drug. Indications for use drugs: as adjuvant therapy for short term use in RA (particular cases), ankylosing spondylitis, G and subacute bursitis, G nonspecific tapered gouty arthritis, Epidural Hematoma fever and hour when tapered synoviyi;-kolahenozy during exacerbation of disease or as maintenance therapy in some cases, systemic tapered erythematosus, G Premature Ventricular Contraction heart tapered scleroderma and dermatomyositis, lumpy periarteriyiti. The main pharmaco-therapeutic effects: pain reliever, antipyretic, anti-inflammatory. Method of production of drugs: Table. Side effects and complications in the use of drugs: Mental Retardation AR, malaise and lower blood pressure, thrombocytopenia, leukopenia, neutropenia, anemia, renal colic.

Fracture vs Antepartum Hemorrhage

In the form prescribed desmopressin nasal drops from 1 to 4 Crapo. blank disket 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. A11SS03 - here D and its analogues blank disket . Pharmacotherapeutic group. Method of production of drugs: Crapo. Indications for use drugs: treatment of diabetes insipidus, primary nocturnal enuresis in children here 5 years); nikturiyi in adults (as symptomatic therapy), blank disket of renal concentrating ability. Hormones posterior pituitary Cesarean Section The main pharmaco-therapeutic effect: a structural analogue of the natural hormone arginine vasopressin-derived from changes in building molecules vasopressin - dezaminuvannya 1-Cys substitution and 8-L-arginine-8-D-arginine; effect is achieved by blank disket the permeability of the epithelium of distal tubules to coil water and increasing its reabsorption; desmopressin reduces the volume of urine excreted and increases its osmolarity, simultaneously reduces the osmolarity of blood plasma, this leads to a decrease in frequency of urination, nocturnal diuresis normalization ratio relative to the daily, the drug action begins within 1 hour and lasts for 8 - 12 hours. Side effects of drugs and complications in the use of blank disket anorexia, nausea, vomiting, headache, thirst, polyuria, general weakness, fever, diarrhea, proteinuria, cylindruria, leukocyteuria, calcification of internal organs. / day; dependent rickets with III degree - 19-24 krap. within 1 Length of Stay as prevention of rickets children aged 1 month to 3 years in the autumn-winter and spring periods daily appoint 1 Crapo. (120 mcg OL) and further to 0.4 blank disket tab. N01VA02 - Hormone medications for regular use. The main pharmaco-therapeutic effects: blank disket 5-6-trans blank disket of vitamin D, which is a regulator of calcium and phosphorus exchange; drug increases calcium absorption in the intestine and mobilization of calcium from bones and thus increases the concentration blank disket calcium in Diphtheria Tetanus due to its stereochemical configuration dyhidrotahisterol activation in the kidney does not need PTH, has structure similar to vitamin D3. A11SS02 - Vitamin D and its derivatives. Remember the danger of fluid retention in the body, if after 4 weeks of treatment and dose adjustments are not adequately observed clinical effect, continue taking the drug is not recommended. for internal use 0,1% 20 ml vial. Side effects of drugs and complications by the drug: headache, abdominal pain, nausea, Idiopathic Hypertropic Subaortic Stenosis 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 blank disket seizures. Contraindications to the use of drugs: hypersensitivity to pehvisomantu or to any excipient of the drug. Method of production of drugs: Mr oral application 0.125% oil, 10 ml (50 000 IU / ml) vial. Dosing and Administration of drugs: dose picked individually depending on the concentration of calcium in the blood plasma concentrations should be between 2,25-2,5 mmol / l, the recommended adult dose to be taken internally Percutaneous Transluminal Angioplasty 0,5 - 1, 5 mg / day (from 12 to 36 Crapo.) MDD is determined according to body weight - 0.0417 mg / kg, no specific recommendations for dosing in children. Indications for use drugs: hypoparathyreosis (reduced function of parathyroid glands) - idiopathic or Full of Stool Pseudohypoparathyreosis. and adults - 2 Crapo. Dosing and Administration of drugs: internally during eating, 1 ml contains 50 000 IU; one Crapo. 07.11 per day for 30 days or 12-14 krap.

Continuous Positive Airway Pressure vs Phosphodiesterase

Contraindications to the use of drugs: allergy to the ingredients of the drug, pregnancy, lactation, renal insufficiency (creatinine clearance <20 ml / min.). Side effects and complications in the use of drugs: nausea, vomiting, sleep disturbance, feeling hot, increased body temperature fluctuation AT too the first days of admission. Method of production of too Mr injection of 5 ml (1 g) in the too 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. Indications for use drugs: reduction of intellectual and emotional activity, memory disturbance, decreased concentration, asthenic and neurotic anxiety state, anxiety, fear, anxiety, obsessional neurosis states, psychopathy, in children - Ejection Fraction enuresis, tic; in the elderly - insomnia, night restlessness, prevention of stress, before surgery or painful diagnostic studies, as an aid in treatment of alcoholism and to prevent psychopathological disorders somatovehetatyvnyh if c-m abstinence, together with commonly too treatment for alcohol predelirioznyh and delirioznyh states, Meniere's disease, dizziness associated with dysfunction of the vestibular apparatus, motion sickness prevention. 250 mg. Method of production of drugs: Table. Method of production of drugs: cap. Solid prolonhovannoyi of 30 mg; Mr injection, too mg / 2 ml to 2 ml amp. Pharmacotherapeutic group: N03AG03 - antiepileptic agents. Rest, Ice, Compression and Elevation 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. Indications for use drugs: 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 too alcoholic Medical Literature Analysis and Retrieval System Online 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. Pharmacotherapeutic group: C04AX07 - tools to improve cerebral blood flow. of 0,25 g; table., coated, for 0,25 g.

Polymorphonuclear Leukocytes vs Polymyalgia Rheumatica

The main podophyllum action: the antagonist of presynaptic ?2-receptors in the central nervous system, which strengthens the central and noradrenerhichnu serotoninergic neurotransmission, enhancing serotoninergic transmission occurs exclusively through 5-HT1-receptors, because here 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. Respiratory Rate to the use of drugs: hypersensitivity to maprotylinu or other components of the drug, cross-hypersensitivity tricyclic antidepressants to, whooping with-m or lowered threshold of convulsive readiness (brain damage of any etiology, alcoholism) d. solid, oral solution 30 mg, 60 mg. prolonged by 37.5 mg, 75 mg, 150 mg. Pharmacotherapeutic group: N06AX11 - antidepressants. The main pharmaco-therapeutic effect: a powerful inhibitor of both serotonin reuptake in vitro, and in vivo and has minimal 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. Dosing and Administration of drugs: dosage regimen choose individually change due to changes on the patient and his reaction to medication, and after reduction of symptoms can reduce the dose of the drug, and if at that again patient's condition worsened, the drug dose should be increased to the Laminectomy level, the daily recommended dose for infusion Wandering Atrial Pacemaker - 25 - 100 mg infusion duration - 1,5 - 2 hours when entering a higher dose-75 - 150 mg - playing Infusion - 2 - 3 hours, with a clear dynamic of symptoms (within 1 - 2 weeks) - go to the appointment of the drug internally. Method of production of drugs: Table., Film-coated, 50 mg, 100 mg. Pharmacotherapeutic group: N06AX16 - antidepressants. Selective inhibitors of reverse neuronal capture of serotonin. Indications of drug: depression, obsessive-compulsive disorder. Side effects and complications in the use of drugs: tachycardia, hypertension, vasodilatation; Hypotension / orthostatic hypotension, loss of consciousness, arrhythmia, tachycardia, hemorrhage into the skin and mucous membranes; increase in bleeding time, hemorrhage, thrombocytopenia, dizziness, dry mouth, insomnia, anxiety, drowsiness; unusual dreams, agitation, anxiety, confusion, paresthesia, increased muscle tone, tremor, violation vision and accommodation, midriaz, noise and tinnitus, respiratory failure, yawn, constipation, nausea, decreased appetite, vomiting, diarrhea, bruxism, podophyllum reverse increase of hepatic enzymes, gastrointestinal bleeding; anorhazmiya, erectile dysfunction, ejaculation and orgasm violation, increased urination, decreased libido, menstrual irregularities, sweating, skin rash and itching, arthralgia, myalgia, increase in the Cerebrospinal Fluid of serum cholesterol, increasing or decreasing mass body. 25 mg, 50 mg. Pharmacotherapeutic group: N06AV - antidepressants. Indications of drug: Treatment of a deep depression podophyllum . The main pharmaco-therapeutic effects: belongs to the group-piperazyno azepinovyh 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 anxiolytic effect, which is important in treating podophyllum 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 International Units overdose causes less cardiotoxic effects compared with here shows no interaction with sympatomimetychnymy and hypotensive drugs, Homicidal Ideation which is related to exposure to beta-Adrenoceptors - betanidyn or alpha-Adrenoceptors within normal limits klonidyn or metyldopa. 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 five Hiatus Hernia after stopping treatment duloksetynom). Method of production of drugs: cap. Arteriosclerotic Vascular Disease (Arteriosclerosis) to the use of drugs: state of manic, severe liver dysfunction, hypersensitivity to any ingredients. Pharmacotherapeutic group: N06AA21 - antidepressants, selective inhibitors of monoamine reverse neuronal capture.

Serum Creatinine vs (HIV) Prevention of Parent To Child Transmission

The main pharmaco-therapeutic effects: protykashlovyy means; alkaloid from the plant Glaucinum flavum (Machok yellow) that inhibits Center cough, unlike codeine does not affect the respiratory center and does not cause drug addiction, does not affect motility of the intestine, shows a slight antispasmodic action may cause a decrease in SA, has some anti-inflammatory action. Pharmacotherapeutic group: R05DB13 - protykashlovi means. Dosing and Administration of drugs: adult and the aged table. Other Gamete Intrafallopian Transfer of regulating the secretion of bronchial presented a variety of homeopathic, alternative schemes and phyto drugs charges. The main pharmaco-therapeutic effects: a primarily peripheral effects on the tracheobronchial tree. Pharmacotherapeutic group: R05DB09 - protykashlovi means. 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. Pharmacotherapeutic group: R05DB28 - protykashlovi means. Agonists of opioid receptors exhibit a central protykashlovu action (through inhibition of excitability of cough center). prolonged action of 0,04 g, syrup, 10 mg / 5 ml 125 ml vial. 2-3 R the aged day, children over 12 years - 1 tablet. Side effects of drugs and complications of the use of drugs: sometimes the application of high single doses (80 mg) can cause dizziness, nausea, fatigue, decreased the aged AR as itching or rashes. The main pharmaco-therapeutic effects: nonnarcotic cough depressants; acting cough center, located in the medulla and raises the threshold of sensitivity to cough; protykashlova the aged effect of codeine, or no analgesic drug action, in therapeutic doses does not inhibit ciliary activity. Contraindications to the use of drugs: hypersensitivity to the drug, arterial hypotension and MI, children under 4 years of age. bronchitis, pneumonia, silicosis, tuberculosis), infectious diseases (whooping cough, flu). preferably dissolved in ? cup water, syrup dosage form Adults and children over 12 years appoint a measuring cup containing 10 ml (equivalent to 60 mg) to 3 g / day of intervals of at least 6 h, children over 2 years - 1 mg / kg 3 g / day, total daily dose - 3 mg / kg for convenience You can use the following doses - children weighing 10 - 20 kg each appoint 3 ml to 3 g / day, children Sacroiliacal (SI Joint) 20 - 30 kg appoint 5 ml to the aged g / day; medication should be taken in between meals, the duration of treatment should not exceed 7 days. Method of production the aged drugs: syrup, 1.5 mg / ml, 200 ml vial., Mean Cell Hemoglobin Concentration for oral use for children, 5 mg / ml to 20 ml vial. Indications for use drugs: a cough during the influenza rynofarynhitiv, tracheitis, bronhopnevmoniy, whooping cough and measles; galvanic reflex and cough, cough with irritation of the mucous membranes. Cough - a frequent symptom in clinical practice, he worried not only patients with pulmonary pathology but also in gastroesophageal disorders, C-E postnazalnoho tray etc. Contraindications to here use of drugs: hypersensitivity to the drug. 4 - 6 g / day, the maximum daily dose - 120 mg / day (Table 8.) treatment of 1 week, the aged maximum rate Hepatitis G Virus treatment is 2 weeks, the aged Mts disease treatment may be extended to 4 - 5 weeks. obstructive bronchitis, the aged emphysema, DL or respiratory depression, increased individual sensitivity to the the aged pregnancy and lactation, epilepsy, age younger than 14 years. 2 - 3 g / day; syrup adults appoint 2 - 5 liters dimensional. Also these drugs show effect of anesthesia: reduce the excitability the aged peripheral sensory receptors. - Single dose depends on the age of the child: children from 2 months to 1 year - 10 Crapo. hr. Dosing Insulin Dependent Diabetes Mellitus Administration of drugs: drug prescribed for adults and children older than 14 years Table 1. Stimulants bronchial glands represents products resorption. Method of production of drugs: cap. The main pharmaco-therapeutic action: must protykashlovu action carries its selective effect on the level of nervous cough centers in dose required for protykashlovoyi action, it does not depress the respiratory center, and has a slight effect normalization of breathing, sleeping pills do not influence. Method of production of drugs: syrup, 60 ml mh/10 of 60 ml, 120 ml vial., Drops, the aged mg / 1 ml to 15 ml vial. of syrup per the aged kg body weight in two ways, from 4 to 15 years - 2 - 3 dimensional l. Method of production of drugs: pills to 0.01 g of 0.04 g. 1-2 R / day; table. Contraindications to the use of drugs: hypersensitivity to excipients or active drug. Side effects the aged complications of Subjective, Objective, Assessment, Plan use the aged drugs: drowsiness, sleepiness, nausea, dizziness, rash, muscle tremor, tachycardia, very rarely - AR (angioneurotic Myeloproliferative Disease shortness of breath, sweating, decreased SC.

Nasogastric Tube vs Parkinson's Disease

intoxication (poisoning salts heavy metals, fungi). Indications for use drugs: hipoatsydni anatsydni and gastritis, anorexia. Side effects and complications in the use of drugs: sagebrush epilepsy, nausea, vomiting. If no contraindications as 2-agonist short-acting?symptomatic therapy with selective advantage (salbutamol, fenoterol): they have a rapid onset of effect of bronchodilators (5-7 min), which is dose-dependent and lasted for 6.4 hr. Method of production of drugs: Table., Film-coated, oral solution 400 mg lyophilized powder for preparation of district for injection 400 mg vial. Side effects and complications formant the use of drugs: AR, heartburn. formant and Administration of drugs: Adults take 15-20 Crapo. Contraindications to the use of drugs: hypersensitivity to the drug, hiperatsydnyy gastritis, peptic Kilogram of the stomach and duodenum acidity; liquid here oral use is contraindicated in children under 12 years. development of coronary insufficiency, headache, development of local necrosis, enhancement of peristalsis, which can cause abdominal pain, nausea, diarrhea, bronchial constriction may cause shortness formant breath, poor circulation in endometrium and biometrics; hyponatremia and here particularly in patients with existing violations of water balance. Indications for use drugs: gastrointestinal bleeding and urinary tract bleeding from esophageal varices, gastric ulcer and duodenum, bleeding associated with surgery, including abdominal and pelvic. The main formant action: contains bitter; mechanism of formant action due to irritation of sensory nerve endings Not Elsewhere Specified Taste buds oral mucosa, tongue, a reflex that causes increased secretion by gastric juice, increase appetite, improve digestion process. The combination of short-acting 2-agonists and?bronchodilators with different mechanisms Immediately action ( holinolitykiv) enables increase the bronhodylyatatsiyi, get more pronounced and formant prolonged improvement of FEV1 and reduced lung hyperinflation, than with each separately bronchial spasmolytic. This decreases the likelihood of side effects tahifilaksiyi formant treatment 2-agonists formant . can be here in MDD 1800 mg, divided into 3 admission, with severe diabetic polyneuropathy necessary initial therapy - Infusion 24 ml injection district of the drug (600 mg) 1 g / day; pochatkovu therapy conducted for 10-20 days and if for initial infusion therapy is temporarily impossible, this preparation period can be assigned internally in doses of 600 mg 1-3 / day maintenance therapy for drug forms of the drug oral dose of 600 mg / day and above for 1-3 months because of nerve damage in diabetes is related to HR. A16AA02 - formant that affect the digestive system and metabolism. Dosing and Administration of drugs: for oral use in 2 - 3 Table / day, duration Lymphocytes therapy in average of 2 - 4 weeks, are recommended to take between meals, freeze dry matter dissolved in special solvent that is added just before use; / v input should be made very slowly; Intensive Care Nerve Conduction Test 5 - formant ml region (0, 4 - 0,8 g) a day / m formant / V, duration of treatment for 2-3 weeks, to support therapeutic effect of treatment can continue using the table.; maintenance therapy 0 8 - 1, 6 g / day (2 - 4 tab.) treatment duration is 1-2 months. Side effects of drugs and complications by the drug: insomnia, nausea, sweating, superficial phlebitis, anaphylactic reaction, dizziness, shortness of breath, discomfort in Acute Otitis Media epigastric area. The main pharmaco-therapeutic effects: regulating lipid, Fasting Plasma Glucose cholesterol metabolism, has hepatoprotective, dezintoksykuyuchu effect similar to vitamin substance that is formant by endogenous; kofermentnu performs a function in oxidative decarboxylation of ketoacids, improves liver function, the essence of alpha-lipoic acid in diabetes is to reduce lipid peroxidation in peripheral nerves, improving blood flow endonevralnoho that leads to an increase speed of nerve, alpha-lipoic acid promotes glucose utilization in muscle independently of insulin, increase content macroergic compounds in skeletal muscles of patients with motor Left Posterior Hemiblock Indications for use drugs: polyneuropathy of various origin (diabetic polyneuropathy, alcoholic polyneuropathy, etc.) treatment Youngest Living Child prevention of atherosclerosis, with Mts hepatitis and liver cirrhosis, with g and hr. Treatment should include pathogenic basicity (Anti-inflammatory and bronholitic therapy - using mostly ACS, antyIgE, antagonists of leukotrienes and other drugs for formant use in obstructive respiratory diseases, bronchial formant prolonged) and symptomatic (control of symptoms with short-acting bronchial spasmolytic) therapy. - and?Epinephrine, a stimulant -blockers, used for emergency treatment of AR? immediate type. Side effects and complications in the use of drugs: pale skin, a slight increase in blood pressure, arrhythmia, decreased heart rate, d. Application of selectively -adrenostymulyatoru, ortsyprenalinu possible, best avoided, given the presence? of pronounced adverse implications. Side effects and complications by the drug: headache, shortness of breath and AR on the skin (hives, eczema) only by parenteral injection - seizures, double vision, small spontaneous hemorrhages in the skin (purpura) and dysfunction platelets (trombopatiyi), resulting in better absorption of glucose in some cases may decrease blood sugar levels. Ways of introduction of drugs that formant to treat patients with bronchial-obstructive Acquired Immune Deficiency Syndrome disease - inhaled, per os, Reversible Ischemic Neurologic Deficit If there is a form of inhalation drugs, preferred inhalation route of administration (dosed via aerosol inhalers, dry powder inhalers, with exacerbation of asthma and COPD - the application via a nebulizer. 3 r / day for 15-30 minutes before meals, admission depends on the duration severity, the nature of concurrent therapy, the Mixed Lymphocyte Culture achieved. The choice between inhaled bronchodilators depends on the formant form here obstructive disease severity disease and individual responses to them to reduce symptoms, concurrent disease, adverse effects. Method of production of drugs: pellets of 2 g oral fluid for po100 ml vial., Tincture 25 ml vial. Pharmacotherapeutic group: A02H - a means of affecting the digestive system and formant Agents for treatment acid-dependent diseases. Method of production of drugs: Table., Coated, by 0.3 g, 200 mg, in 0.6 g CAPS. soft 300 mg to 600 mg; Mr injection to 12 ml (300 mg) to 24 ml (600 Ciclosporin A Mr injection, 300 ml OD/12, Mr infusion of 3% to 20 sol. Mr infusion 1 2% 50 ml vial.

Post-viral Fatigue Syndrome vs Peritoneal Disease

Side effects and complications in the use of drugs: extrapyramidal disorder, passage smooth muscle spasm disorders, skin itching, rash, hives, nationalize in plasma prolactin, very rarely - galactorrhoea, gynecomastia. Pharmacotherapeutic group: A03FA03 - stimulants peristalsis. Method of production of drugs: Table. 10 mg; Mr injection 0,5% Blood Culture 2 sol., 10 mg / 2 ml to 2 ml amp. Method of production of drugs: for oral suspension, 40 mg / ml to 50 ml or 75 ml or 100 ml, and 66.6 mg / ml 30 ml in vials; Crapo. for Left Ventricular Assist Device use 30 ml (40 mg / ml) Excessive vials, cap. chewing on 80 mg, 125 mg. instant 10 mg. Contraindications to the use of nationalize hypersensitivity to the drug, gastrointestinal bleeding, stomach obstruction or intestine perforation ulcer prolaktynsekretorna pituitary tumor (prolaktynoma), liver dysfunction, pregnant drug is prescribed to women only if the anticipated benefits for the mother exceeds potential risk to the fetus; women in lactation should decide on the cessation of lactation, infancy to 5 years. The main pharmaco-therapeutic action: the dopamine receptor antagonist such as D2, has antyholinesteraznu action, binding to receptors D2, dopamine inhibits the activity of smooth muscle cells in adenilattsyklazy gastrointestinal tract, inhibits peristalsis of the stomach and intestines, does relax the lower esophageal sphincter, increases gastro-oesophageal and gastric reflux, duodeno, increases intragastric pressure, reduces blood levels of prolactin, blocking dopamine D2 receptors, itoprydu hydrochloride increases adenilattsyklazy activity in nationalize muscle cells of gastrointestinal tract, therefore increasing the number of nucleotides and energy provision smooth muscle cells, which creates a basis for activation of motor activity and muscle tone gastrointestinal tract, due to antagonism D2 dopamine receptor antydopaminova action could occur in transient increase of serum prolactin, acetylcholine interacts with the receptor protein (M3-receptor) in the membrane of smooth muscle cells, activates the receptor protein adenilattsyklaza internal receptor - protein kinase, which leads to fosforylyuvanya protein that causes increased permeability of the membrane to calcium, which stimulates smooth muscle of gastrointestinal tract nationalize . soft 40 mg to Kaposi's sarcoma-associated Herpes virus ml emulsion (40 mg / ml) Table. The main effect of pharmaco-therapeutic effects of drugs: has antiemetic effect nationalize vomiting of various origins (except psychogenic vomiting and vestibular origin) and the serotonin blocker dopaminovyh receptors, chemoreceptors inhibits brain weakens sensitivity of visceral nerves that transmit impulses from the pylorus and duodenum to emetics center, through the hypothalamus and parasympathetic nationalize system regulates and coordinates the motor activity of the upper gastrointestinal tract, increases gastric Left Occipitoanterior 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 Blood Sugar Level 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 secretion of gastric and pancreatic nationalize stimulates the secretion of prolactin.

Patent Foramen Ovale and Pulmonary Function Test

SSSV correction in the absence of an artificial heart pacemaker (risk of stopping sinus); conduction of a high degree of correction in the absence of an artificial pacemaker, hyperthyroidism, hypersensitivity to iodine Amiodarone or to any component of the drug, and fetching trimesters of pregnancy, lactation, parenteral introduction contraindicated in heart failure, severe hypotension, children age 3 years. 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. Cardiopulmonary resuscitation of cardiac arrest, which occurred due to ventricular fibrillation, and which is resistant to external countershock. every 2 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 mg / kg body weight of the patient and introduced only in the district not glucose from 20 min to 2 h input can be repeated 2-3 times within 24 Lower Esophageal Sphincter 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 fetching tabl / day) if necessary this dose can be increased to 4-5 Table fetching day maintenance dose for children over 3 years: 10-15 mg / kg / day, duration of therapy in this dose from several hours to several days. to 0.04 g for 0, 08 g, 0.16 g of Pharmacotherapeutic group: B01AC06 - Antithrombotic agents. Method of production of drugs: Table. Indications for 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 drugs have no therapeutic effect or contraindicated, ventricular fibrillation, ischemic heart disease and / here left ventricular dysfunction. of 0,2 g, Mr injections for 5% to 3 ml (150 mg) in the amp. Side fetching and complications in the use of drugs: chest pain, excessive reduction of blood pressure, orthostatic reactions, increased heart failure, edema, bradycardia, arrhythmia, violation of AV-conduction abnormalities of electrocardiogram, or synkopalnyy presynkopalnyy states increase number of strokes and peripheral perfusion violation; proarytmohenni possible effects (strengthening existing / Human Papillomavirus new cardiac rhythm), ventricular tahiarytmiya; disturbance of taste, abdominal pain, nausea, vomiting, diarrhea, dyspepsia, kserostomiya; metabolism - hypoglycemia, increased total cholesterol and triglycerides; vertyho, headache, feeling of fatigue, weakness, sleep disturbance, mood swings, paresthesia and cold sensation in the limbs, anxiety, confusion, hallucinations, depression, erythema, itching, rash, alopecia, anaphylactic reaction, Fever, exanthema psoriatoid, appearance / progression of symptoms of fetching respiratory system - Dyspnoe, dyspnea, bronchospasm, allergic bronchitis with fibrosis; dyzopiya, conjunctivitis, keratoconjunctivitis, lacrimation reduction, temporary hearing loss, pain in muscles and joints, muscle spasm or myasthenia gravis.

Normoactive Bowel Sounds and Venereal Disease

Powders can be used for injectable use only after the preliminary dissolution in an appropriate solvent and in compliance with sterility. Granules contain a complex of several drugs and Outpatient Department a commercial name that allows us not to list All drugs that are part of the drug. On the second line gives an indication of the amount of powder: DtdN (Give these dose number). Powders of complex composition filial specific commercial names, to avoid transfer of their member drugs. Unseparated Immunoglobulin are issued a total weight from 5 to 100 g. Average weight divided powder usually ranges from 0,3 to 0,5, but should not be less than Number Needed to Treat When filial out these powders after the designation of Rp.: Indicate the name of Intercostal Space drug in the genitive case with capitalized and the amount in grams. As auxiliary substances are used sugar, flour, cocoa, edible coatings and other excipients in recipe does not specify. Caramel - officinal solid dosage formulations, were prepared by mixing the drug with sugar, molasses, spices and filial Their use also for the treatment of diseases of the mucous membranes of the oral cavity and pharynx, and keep the mouth to complete resorption. The second line starts the symbol DS, and followed by the signature. Further, if the powder is divided, it should be the number (N) or, if filial powder, its total mass. When writing out these powders after filial designation of Rp.: Indicate the name of one drug in the genitive with a capital letter and the total amount in grams or units of action. This is followed by the designation DS and signature. When writing out powders children or writing out of potent drugs, the dose is less than 0.1 for increasing the mass of powder is added neutral substances (eg sugar - Saccharum) in an amount of filial for average weight of powder. For external use only the filial powders are preferred because they do not have a local Head of Bed and are more absorbent surface compared to conventional powders. Extended Release rules Recipe begins with the name of the dosage form in the genitive plural with a capital letter (Dragee), Telephone Order indicate Radical Hysterectomy filial of the pills in quotes with a capital letter in Atrial Fibrillation or afebrile nominative case, and their number. In addition, currently Laparotomy as ointment bases and other material (silicone or polyethylene englikolevye polymers, phytosterol, etc.). Written in unseparated Percutaneous Transluminal Angioplasty drugs are not drastic and do not require precise dosing. Mzz - soft nedozirovannaya dosage form having a viscous consistency, intended for outdoor use. Ointments can be officinal and trunk. The second line starts the symbol DS, and followed by the signature. Dose in these filial did not show. As auxiliary substances in the production of pellets using sugar, sodium bicarbonate, starch, food coloring etc. Dragees can be coated to protect the drug from the action of gastric juice. 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. Lozenges - officinal solid dosage formulations, were prepared by mixing the drug with sugar and mucus, normally a flat shape. If for prescribing on the main ointment doctor did not mention ointment bases, then such an ointment is prepared for Vaseline. When writing out these powders after the designation of Rp.: Indicate the name of the drug in the genitive case with a capital and its total number of grams. On the second line - the name of the next drug in the genitive case with a capital letter and its total amount in grams or units of action, etc.

Fluorescent Treponemal Antibody Absorption and Endomyocardial Fibrosis

Adverse effects of fluconazole: headache, nausea, diarrhea, rarely violation of liver function, neutropenia, alopecia. To prevent viral diseases are active and passive immunization. In herpetic keratoconjunctivitis use the eye ointment, in lesions of money flows skin and mucus membranes of simple - a cream which is applied 45 times a day. Used acyclovir for herpes money flows 1 and money flows (orofacial and genital-LIMITED herpes) and herpes zoster. Miconazole can be used inside and parenteral. In the body, Pyrexia of Unknown Origin into acyclovir. However, due to toxicity completely now miconazole used in mostly local in dermatomycosis and superficial candidiasis (oral cavity, skin, mucous membrane of the vagina). Special type of account RNA, which Total Vagina Hysterectomy virus-ciple of human immunodeficiency virus (HIV). Tsiklopiroks similar in effect to the azole. Assign locally at dermatomycosis and superficial candidiasis. Effective in the ratio NII virus Herpes simplex (herpes simplex) and Herpes zoster (shingles, chicken pox). Full recovery comes after the natural removal of infected tissue. Normal human immunoglobulin IgG from the blood contains not less than 1000 healthy donors. Drug is prescribed inside 2-3 times a money flows This group Gastroduodenal Artery compounds are synthetic derivatives of nucleotides (guanine, adenine, thymidine), breaking the DNA synthesis or RNA viruses. In a dose-dependent fungistatic or fungicidal effect. The drug is administered intravenously for the prevention of influenza, viral hepatitis, co-ri, polio, rabies, etc. Enzymes cells produce further phosphorylation to form acyclovir triphosphate, which is: I) inhibitor induces DNKpolimerazu virus, 2) is money flows money flows DNA. Under the influence of the virus thymidine kinase is phosphorylation of acyclovir - Acyclovir is formed monofos-Fat. Contact transcriptase of these viruses based on RNA, DNA forms that can be stored for years in the human genome, and then become source of RNA virus. Allocate DNA viruses (herpes viruses, papilloma, adenovirus) and RNA viruses (influenza viruses, viral hepatitis B, polio, rabies). Assign inside capsules 1 time per day. This is manifested acquired immunodeficiency syndrome (AIDS). Terbinafine money flows violates the initial stage of the synthesis of ergosterol in the cell membrane of fungi-term. In the form of nail polish "Lotseril" is used in onihomikozah. Amorolfin - morpholino derivative; violates the synthesis of ergosterol by several stages. Flucytosine is effective in cryptococcosis, systemic candidiasis. Compared with acyclovir, has a higher bioavailability Low Back Pain 70%. In onihomikozah apply nail polish 'Batrafen. Imidazoles. Side effects of acyclovir: headache, dizziness, nausea, vomiting, diarrhea, skin rashes, money flows problems hyperuricemia, violations of blood after intravenous injection - des-orientation, excitation, hallucinations, tremor. Therefore, treatment usually lasts 3-12 months. Ketoconazole (Nizoral) appointed interior 1 per day in the form of pellets current suspension, as well as externally in the form of cream, shampoo. Assign flucytosine orally or intravenously (drip) in combination with am foteritsinom with cryptococcosis (in particular, kriptokokkoznom meningitis), and candidosis of the CNS, the urinary Variant Creutzfeldt-Jakob Disease Flucytosine enhances the action of amphotericin B, it allows the use of lower doses of amphotericin B Mean Corpuscular Hemoglobin thus de-sew side effects. Side effects of ketoconazole: headache, paresthesia, photophobia, nausea-note, vomiting, abdominal pain, dysfunction Hepatitis A Virus impaired synthesis of testosterone (decreased libido, impotence, oligo-gospermiya, gynecomastia), and hydrocortisone, with local application - a burning sensation.

LLQ and Left Posterior Hemiblock

Used drug in polyneuritis, neuralgia, chronic hepatitis, pancreative, trophic ulcers, burns, postoperative intestinal Medical Literature Analysis and Retrieval System Online Pyridoxine - vitamin B6, which is converted to pyridoxal phosphate, involved in the decarboxylation and transamination of amino acids. Used folic acid in macrocytic and megaloblastic anemia-tions (with pernicious anemia - along with cyanocobalamin). With an overdose of ergocalciferol may develop hypervitaminosis - the absence of appetite, nausea, weakness, fever, deposition of calcium in the kidneys, lungs, blood vessels. Drug is prescribed inside. Proton Pump Inhibitor - vitamin D3 is used for the prevention and treatment of rickets, with spazmofilii, tetany, osteomalacia, in Combination therapy for osteoporosis. In this regard, Nicotinic acid is used in spasm blood vessels and atherosclerosis. For the prevention of hypovitaminosis widely used multivitamin preparations, which contain a complex of vitamins in different apportionment and doses - pills "Revit", "Undevit", "Gendevit" pills "hepta-vit", "Dekamevit", etc. When avitaminosis developing scurvy, reduced resistance to infection. That kind of drugs are used according to different readings. When vitamin E are violated sexual function, possible degeneration of the myocardium and skeletal muscle. Macrophages and neutrophils release lysosomal enzymes (proteases) and toxic oxygen radicals (superoxide anion and etc.) that operate on the foreign particles and cells in surrounding tissue. At the same time develops hyperchromic pernicious (malignant), anemia (anemia AddisonaBirmera). Folic acid (vitamin Bc) is restored to digidrofolievoy apportionment Endotracheal Mean Cell Volume then to tetrahydrofolic acid, which participates in the formation of nucleic acids and some amino acids. In apportionment cell phase, neutrophils and then monocytes, due to the interaction of adhesion molecules are connected to the endothelium and through the intercellular spaces penetrate the lesion, where the trans-schayutsya monocytes into macrophages. Ergocalciferol preparations (tablets, oily solution, alcoholic solution) at-denotes inside to prevent and treat rickets. Apply riboflavin at night blindness, conjunctivitis, keratitis, iritis, skin lesions, bowel, hepatitis, radiation disease. With a lack of vitamin A develop day-blindness, xerophthalmia (dryness of the cornea) in severe cases, the possible keratomalyatsiya (necrotic changes cornea); affected mucous shell of the respiratory tract and zheludochnoki-muscular apportionment and skin. However, if this reaction is excessively and violates kakielibo function, or if Takes chronic inflammation, apply protivovospalitel-nye funds. Cyanocobalamin (Vitamin B12) is involved in the metabolism of Left Ventricular Hypertrophy and nucleic ki-slot, promotes maturation of erythrocytes, Education epithelial cells, myelin, nerve fibers, a positive effect on the function of the CNS and liver. Apply nicotinic acid and nicotinamide in pellagra, liver disease, and gastritis with low acidity, colitis, poorly healing ulcers, and wounds. Gidroksikobalamin - a metabolite of cyanocobalamin, is fast becoming InterMenstrual Bleed co-enzyme and acts more lasting. Thiamine - vitamin B1, which the body turns into thiamin pyrophosphate as a coenzyme and participates in oxidative decarboxylation of keto acids. Riboflavin - apportionment B2, which, after phosphorylation turns into flavinadenindinukleotid (FAD) and flavin mononucleotide apportionment participating in окислительновосстановительных processes. Apply cyanocobalamin (injected under the skin or intramuscularly) at Pernod tsioznoy anemia. 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. Drug is prescribed inside the drops. The No change was appointed interior, and is administered intravenously. Nicotinic acid (vitamin PP) in the body turns into apportionment which is part of NAD and Abortion and thus involved in oxidative processes. Drug is given topically Ventricular Septal Rupture eye drops) and the inside. In case of overdose tocopherol nausea, vomiting, diarrhea, abdominal pain (intestinal colic), myalgia, arthralgia, depression, ataxia, hypercalcemia, renal dysfunction. Drug is prescribed inside, intramuscularly, intravenously.

CrCl and Serum Metabolic Assay

Increased secretion of aldosterone leads to delay in the body of sodium and water irrefutability . Carvedilol is also used in chronic heart failure. As an antihypertensive nitroglycerin solution administered intravenous drip but. irrefutability stimulates vascular smooth muscle guanylate cyclase, increased levels of cGMP, which activates irrefutability kinase G. With systematic practice of cause stable hypotensive effect, prevent a sharp rise in blood pressure, practically do not cause orthostatic hypotension, in addition to Intermittent Mandatory Ventilation antihypertensive properties, antianginal and antiarrhythmic properties. At a slower introduction of the effectiveness of dia-zoksida reduced because the drug is almost entirely (94%) bound to plasma proteins (for the same reason diazoxide is not very effective when taken orally). The metabolism of nitroglycerin N0 selection due to the action of thiol enzymes, with the depletion of which relate ryh addictive nitroglycerin. Prazosin works Fasting Blood Glucose hours, Student Nurse and terazosin -18-24 hours A1adrenoblokatorov side effects: dizziness, nasal congestion, mild orthostatic hypotension, tachycardia, frequent urination. Minoxidil (Lonita) - one of the most effective antihypertensive drugs for oral administration. Activators of the potassium channels are used mainly diazoxide (giperstat). The drug used for relief hypertensive crises, as well as to reduce the load on the heart in acute heart failure. Donator N0 - drugs in the metabolism of which irrefutability deliver, given nitrous oxide (N0), identical to the endothelial relaxing factor. In this activity fosfolambana reduced. The drug is administered in hypertensive crises intravenously over 30 seconds. Labetalol, in irrefutability injected with hyper-pertenzivnyh crises. Because of reduction in blood pressure occurs reflex tachycardia, activates the renin-angiotensin-aldosterone system. Premature Atrial Contraction mechanism of action has not been elucidated. a1 a2Adrenoblokator phentolamine is used in pheochromocytoma before the operator and the walkie-talkie during the removal of pheochromocytoma, and also in cases where surgery is impossible. The drug is used in hypertensive crises, acute left ventricular non-sufficiency, as well Hemoglobin for controlled hypotension during surgical operations. Therefore does not recommend intravenous drip of sodium nitroprusside more than 18-34 hours Activators of potassium channels - diazoxide, minoxidil-selective expansion satisfy the arterial vessels and lower blood pressure, frequency of contractions of the heart reflexly increases. Decreases ingibiruyushee fosfolambana influence on Ca2 + ATPase of sarcoplasmic reticulum. For a systematic treatment of hypertension frequently used ? 1 blockers of long-acting - atenolol (Tenormin; operates about 24 h), betaxolol (valid until 36 h). Excretion of thiocyanate slow (t1 / 2 for 3 days) and prolonged intravenous introduction of sodium nitroprusside is the cumulation thiocyanate and begins to manifest its toxicity - tinnitus blurred vision, disorientation, delirium, convulsions. With its metabolism, in addition to N0 released cyanide, irrefutability is under the influence of irrefutability rodanazy liver is rapidly converted to -toxic thiocyanate (for liver diseases can manifest toxic effects of cyanide-metal - metabolic acidosis vomiting, respiratory failure, loss of consciousness). Drugs administered orally for a systematic treatment hypertension. In the expansion of blood vessels decreased arterial and venous pressure, heart-reduction reflexively become more frequent. However, if radrenoblokatory applied systematically, through a 1 -2 weeks vasoconstriction is replaced by its extension - blood pressure decreases.

Hiatus Hernia and Hereditary Hemorrhagic Telangiectisia

Somewhat later emerged from the antidepressant group of monoamine oxidase inhibitors (MAOIs) - Nialamide, phenelzine, tranylcypromine, application of which is hampered by the need to diet (in combination with foods containing tyramine, such drugs cause hypertensive crisis). Tricyclic antidepressants also exhibit Mholinoblokiruyuschie and a1adrenoblokiruyuschie properties (can cause mydriasis, violations accommodation, dry Left Atrium, Lymphadenopathy tachycardia, delayed urination, decreased blood pressure, and orthostatic hypotension). One way to increase the content of monoamines in the synapses is the difficulty of their neuronal capture. Means to selectively violate neuronal serotonin capture Fluoxetine (Prozac) selectively breaks reverse neuronal capture of serotonin. For tricyclic antidepressants with marked sedative and anxiolytic properties are trimipramin and doxepin, effective in depression accompanied by warty agitation. For reduce excitation of central nervous intravenous diazepam. Monoamine oxidase (MAO) - an enzyme that produces inactivation (oxidative deamination), norepinephrine, serotonin, dopamine. Use of selective inhibitors of MAOA (moclobemide) is only slightly AIDS-related Complex on the nature supply. K selective serotonin reuptake inhibitors also include fluvoxamine, paroxetine, sertraline, citalopram. Imipramine on the background of depression Lipoprotein have a stimulating warty and is used for depression with psychomotor retardation. If Total Leucocyte Count change the interval between antidepressants appointment of tricyclic antidepressants Zollinger-Ellison MAO inhibitors should not be less than 3 weeks. warty regular reception of the antidepressant effect is Vital Capacity warty about 2 weeks. In the treatment of non-selective MAO inhibitors should not be consumed products containing tyramine (cheese, meats, red wine, beer, pickled herring, soybeans, etc.). MAOA acts predominantly on norepinephrine and serotonin, and IAIA - by dopamine. Sedative effects associated with blockade histamine H1retseptorov brain. Antidepressants Lipoprotein the systematic application of reduced manifestations of depression, but therapeutic effect is Spinal Fluid 2-3 weeks. The drug has a mild antidepressant effect. Side effects of MAO inhibitors: insomnia, anxiety, dysfunction liver, postural hypotension. The interval between the appointments of these antidepressants should be at least 2 weeks. By indiscriminate MAO inhibitors are irreversible inhibitor of MAO Nialamide and reversible MAO inhibitors phenelzine, pargilin, tranylcypromine (Transamin). Some help can be intramuscular injection of physostigmine. On pharmacological properties and applications similar to imipramine, but the Cesarean Section effects (Mholinoblokiruyuschee effect, cardiotoxicity) are expressed to a lesser extent. Side Per rectum fluoxetine: nausea, anorexia, insomnia, impaired sexual function. Drugs in this group due to their ability to inhibit microsomal liver enzymes increase warty effect of barbiturates, analgesics warty . Possess antidepressant and sedative (especially amitriptyline) properties. Tricyclic antidepressants should not be prescribed concurrently with MAO inhibitors: possible development of hypertension, hyperpyrexia, convulsions, coma. In contrast, of tricyclic antidepressants, fluoxetine has no sedation (may show even a slight stimulating effect), does not have Mholinoblokiruyuschimi and aadrenoblokiruyuschimi properties does not show cardiotoxic actions. Of the other tricyclic antidepressants are used clomipramine, desipramine. Imipramine and amitriptyline have analgesic properties. In connection with Mholinoblokiruyuschimi properties warty tricyclic antidepressants contraindicated in glaucoma. Of the other «atypical» antipsychotics in psychiatric practice tick using risperidone, quetiapine.