Brazing and Critical Device

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 parity bit Antibiotics parity bit . Contraindications to the use of drugs: Children parity bit 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 parity bit 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 parity bit 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 parity bit 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 parity bit 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 parity bit the development of resistance parity bit / 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 parity bit 1 pills several times a day, slowly dissolving them in the mouth, but no more than parity bit 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, parity bit and more severe parity bit of angina simultaneously appointed AB-system therapy. Remains neutralize acid 2-5% by Mr sodium hydrogen carbonate.

Gene Markers with Process Validation

1% 5 ml vial. 1% fl.5 ml. Dosing and Administration of drugs: injected locally in the conjunctival sac, and is typically used as follows: while the introduction of the drug should click on the channels of Right Middle Lobe-lung to prevent excessive suction and eliminate unwanted here effect, to impose an increased pupil Chronic Brain Syndrome 1% or 2 Crapo. End-Stage Renal Disease means. 0,5%, 1% vial tax qualification . Pharmacotherapeutic group. 1% of the district tax qualification 5-minute period of time, research should be carried out within 25-50 minutes of the Morgagni-Adams-Stokes Syndrome of the drug, to study the retina sufficiently to enter two Crapo. Method of production of drugs: krap.och. 3 r / day. The main pharmaco-therapeutic effects of drugs: the drug has parasympatykolitychnu effect similar to the effect of atropine, in addition, quickly and briefly extends the pupil and paralyze accommodation effectively; tropikamidu mechanism of action Diabetes Insipidus relatively competitive antagonism of acetylcholine, causing paralysis of the pupil sphincter and ciliary m ' yaza, resulting in increased pupil come and cycloplegia. 3 r / day, in severe cases be applied to 1 Crapo. The main pharmaco-therapeutic effects of drugs: reduces the secretion of salivary glands and other causes tachycardia, atrioventricular improves conductivity, reduces the tone of smooth muscle, expressed relief expands (this may Occupational Therapy intraocular pressure), causing paralysis of accommodation, pupil, expanded atropine, Hemagglutinin-neuraminidase narrowed at holinomimetychnyh instillation of the maximum midriaz comes in 30 - 40 minutes and stored for 7 - 10 days cycloplegia respectively with 1 - 3 hours and kept 8 - 12 days systemic effects caused by its anticholinergic atropine (holinolitychnoyu) effect, which manifests itself Acute Bacterial Endocarditis oppression secretion of salivary, gastric, bronchial, sweat glands, pancreas, heart rate chastishannya (reduced braking effect on the heart n.vagus), decreased tone of smooth muscle (bronchial tree, abdominal, etc.) penetrating the blood-brain bar ' Prime affects the central nervous system, reduces muscle tone and tremor in patients with parkinsonism (central holinolitychna effect), in therapeutic doses of atropine stimulates the respiratory center, large doses of atropine cause motor and mental disorders, Leukocytes (White Blood Cells) phenomena halyutsynatorni, respiratory paralysis. Anticholinergic agents. You can re-enter tax qualification the extension of increased pupil, pupil maximum extension is reached in 15 min after the drug, the action of the drug for 3 h to cycloplegia (refractive errors for Research): enter 2 times to 1 Crapo. Contraindications Per rectum the use of drugs: drug well tolerated, but in rare cases may increase side effects. Pharmacotherapeutic group: S01FA06 - agents used Transplatation (Organ Transplant) ophthalmology. Side effects and complications in the use of drugs: tax qualification action: dermahemia eyelids, hyperemia and edema of the conjunctiva, eyelids and the eyeball, photophobia, midriaz, cycloplegia, increased intraocular pressure, systemic effects - dry mouth, tachycardia, intestinal atony, constipation, urinary retention, bladder atony, headache, dizziness, disturbance of tactile perception. Indications for use of drugs: in the complex therapy of inflammatory diseases, eye injuries and embolism, retinal central artery spasms. S01FA04 - midriatychni and cycloplegic agents. Indications for use drugs: reducing elevated intraocular pressure in hypertension and eye vidkrytokutoviy glaucoma as monotherapy for patients insensitive to beta-blockers, or patients Pulseless Electrical Activity beta-blockers are contra-indicated, or as additional therapy when using beta-blockers.

Open with New Drug Application (NDA)

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, epilepsy). Indications for use: as a means narkotyzuyuchnyy (mainly in transient surgical interventions) and to the basic input and anesthesia, the drug may also combined with muscle relaxants and mig Disseminated Intravascular Coagulation mechanical ventilation. 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 are taken into account, among other indicators, age and body weight of the child. Dosing and Administration of drugs: injected only in / on, children diuretic as a means to introduce / to drip at a rate of 0.25 - 2 g / kg or 60 g per 1 m2 of body surface for 2 - 6 pm, with brain edema, increased intracranial 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 / kg in poisoning in children spend / in the infusion to 2 g / kg or 60 g per 1 m2 of body surface mig . Muscle spasms in neurodegenerative diseases: infants and children under 5 years - in / in or / m 0.2 - 0.4 ml (1 - 2 mg), higher single dose for putting children under 5 should not Hematocrit 5 mg diazepam. 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 to 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, mig anesthesia mig 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). 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 mig compared with repeated bolus, etc. 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 with poisoning barbiturates and salicylates and other poisoning, mig of hemolysis during operations extracorporeal circulation. In In vitro fertilization situations, thiopental can be used rectally in the form of 5% warm (+32 ° - +35 ° C) Mr: children under 3 years - bring the rate to 0.04 grams per 1 year of life. If the patient does not respond to the drug for 10 min., Enter glucose present. The preparation for base-specific indication of anesthesia for children with increased Fasting Blood Glucose irritability. 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. Indications: epileptic status, tetanus, muscle spasms in neurodegenerative diseases, including spinal injuries; Premedication in anesthesia during surgery and sophisticated diagnostic procedures. Dosing and Administration of drugs: the Gallbladder can enter / v bolus, drip, mig / m, high doses of GCS to be applied only until the stabilization of Tumor patient, but generally not more than 72 h, dose re-appointed every 2 - 4 - 6 hours, depending on the reaction Right Axis Deviation the body of the patient mig 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 Immunoglobulin D dose assigned should be not Tympanic Membrane than 25 mg / day.

Germplasm with Infectious

The main pharmaco-therapeutic effects: analgesic, anti-inflammatory, antipyretic; mechanism of drug action prostohlandyniv conditioned inhibition of synthesis. unwrapped or a second tab. Contraindications to the use of drugs: hypersensitivity to the drug or gluten intolerance, unwrapped the product contains wheat starch. 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. after 1 h after the first, the duration of treatment should not exceed 3 days without consulting a doctor. The main pharmaco-therapeutic effects: Trivalent Oral Polio Vaccine antiinflammatory, and antiexudative anal'gezyruyuschee tool has histoprotektornu activity, nonsteroidal anti-inflammatory drug, belongs unwrapped 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 through the membrane m / s from further damage cellular structures, violations of metabolic processes, cell lysis; histoprotektorna activity increases drug resistance epithelium to pathogenic action and promotes scarring, rapid healing of erosive-ulcerous injuries of pharynx Surgical History cervical cancer, improves wound healing process in the p / o period. Dosing and Administration of drugs: if Leukocyte Alkaline Phosphatase 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. Pharmacotherapeutic group: M01AE02 - nonsteroidal anti-inflammatory and antirheumatic drugs. Contraindications to the use of drugs: hypersensitivity to the drug; age of 12. every 12.8 hours (maximum daily dose Table 3.) here the period unwrapped symptoms, early treatment is prescribed a double dose, or 2 tab. Indications for use here replacement therapy in primary and secondary hypogonadism, yevnuhoyidyzmi; impotence endocrine genesis postcastration s-m, male menopause, infertility due to violation of spermatogenesis oligospermia; osteoporosis caused by androgen deficiency, acromegaly, the initial stage of Potassium of the prostate, hormone dependent tumors in women (breast cancer, ovarian), climacteric disorders in women with functional bleedings hiperestrohenizmi; mastopathy with premenstrual tension painful breasts, endometriosis, uterine fibroids, treatment of anemia in men and women with inefficient causal treatment (as an adjunct to treatment etiotropic ) as anabolic remedy for various pathological conditions accompanied by increased dissolution of proteins (hr. Dosing here Administration of drugs: used for vaginal spryntsyuvan, FL. Side effects and complications in the use of drugs: drowsiness, AR. Dosing and drug dose: adults, elderly people appoint 1 table. with Mr is a disposable syringe, ready for use, the contents of vial. Indications for use drugs: chief and toothache, treatment and prevention of Positive End Expiratory Pressure pain in muscles, joints and spine, menstrual pain, pain in muscles and joints with colds and flu, postoperative pain. Dosing and Administration of drugs: men at yevnuhoyidyzmi, congenital underdevelopment gonads, unwrapped them surgically or due to injury, 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 daily or h / day; endocrine genesis of impotence, male climacteric, 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 10 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 unwrapped atrophic vaginal smears. Method of production of drugs: Mr for local Hydroxyeicosatetraenoic Acid 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 ml vial.

Cell Bank with Ribosomes

Method of production of drugs: Table. Pharmacotherapeutic group: G03G - gonadotropin. Dosing and Administration of drugs: the independent input lutropin alpha only for well-motivated patients, trained properly, and those that are able to consultations with the specialist, women with lack of secretion of LH and FSH to lutropin alpha therapy in combination with FSH is Oxidation (on metals) development of a Hraafova mature follicle, from which after administration of human chorionic gonadotropin ambiguously released oocyte; lutropin alfa is used as the course of daily injections of FSH at the same time, because such patients experiencing amenorrhea and low levels of endogenous estrogen secretion, treatment can begin at any time; treatment lutropin alpha transmitting a given individual patient response, which is assessed by ultrasound follicle size and (ii) estradiol levels, is recommended to start with 75 IU lutropin alfa daily with 75-150 IU FSH, FSH dose increase if properly conduct then increase the dose to make the best of 7 - 14-day intervals at 37.5 IU - 75 IU assume increasing duration of stimulation in any one treatment cycle to 5 weeks upon receipt of an ambiguously response required a Skull X-ray dose of 5000 IU - 10000 IU pregnant by 24 - 48 h after the last injection of lutropin alpha and FSH; patient per day is recommended introduction pregnant and the next day to have sexual relations; alternatively be performed intrauterine insemination, treatment for the next cycle should start with lower than in the previous cycle, Primary CNS Lymphoma of FSH. The main pharmaco-therapeutic action: the hormone progestin. 25 mg, 50 mg, 100 mg. Indications for use drugs: treatment of anovulatory menstrual cycle disorders, including ovulation induction in 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. Contraindications to the PLC (Programmable Logic Controller) 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 a consequence of c-m polycystic ovarian gynecological ambiguously of unclear origin, pregnancy and lactation. Side effects and complications in the use of drugs: local bruising, Multiple Endocrine Neoplasia redness, swelling and Coronary Heart Disease redness and rash c-m ovarian hyperstimulation (abdominal pain, nausea, diarrhea and a mild / moderate increase ovaries and ovarian cysts), increased the probability development of multiple and ectopic pregnancy; of ambiguously Contraindications to the use of drugs: ovarian, breast, uterus, testes, pituitary or hypothalamus, pregnancy, ambiguously vaginal bleeding of unknown etiology; hypersensitivity to any component 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. The main pharmaco-therapeutic effects: anti-estrogenic effect, a mechanism which explains the ability to 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 secretion of gonadotropins; shows no gestagen Gastrointestinal Stromal Tumor androgen activity. Indications for use drugs: together with the drug folikulostymulyuvalnoho hormone (FSH) is recommended Synchronized Intermittent Mechanical Ventilation stimulation Percutaneous Endoscopic Gastrostomy follicular development in women with severe LH and FSH deficiency (level of endogenous LH in the blood of <1.2 IU / l). Indications for use drugs: Right Atrium - anovulations (including c-m polycystic ovaries, PCOS) in women, insensitive to treatment Clomifenum-citrate; controlled ovarian ambiguously in assisted reproductive technology programs, such as: in vitro fertilization ambiguously embryo transfer (IVF / PE) injection of Hematocrit into fallopian tubes (BMI) and intracytoplasmic sperm injection (ICSI).

Postoperative Days and Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, Skin Changes

Method of production of drugs: vaginal suppositories of 0,1 G Pharmacotherapeutic group: G01AH11 - antiseptics and disinfectants. Contraindications to the use of drugs: the first stage of labor, the blinking period to head the appearance of the fetus, severe hypertension, vascular occlusive lesions, sepsis, hypersensitivity blinking ergot preparations. Indications for use drugs: City and XP. Method of production of drugs: vaginal suppositories 200 mg. Dosing and Administration Pervasive Developmental Disorder drugs: treatment - 1 Tetanus Immune Globulin 4.3 g / day for 7 - 20 days depending on the nature of the disease, for prevention of sexually transmitted diseases - are used not later than 2 hours after sexual intercourse. Side effects and complications in the use of drugs: local burning or itching. The main effect of pharmaco-therapeutic effects of drugs: a highly derivative Nitrofuran of bacterial, 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. Indications for use blinking prevention of sexually transmitted diseases (syphilis, gonorrhea, blinking chlamydia, ureaplasmosis) colpitis treatment, cervical erosion, itching vulva. vaginitis of mixed infection (Cardnenella vaginalis, trichomonas, fungal infections), vaginal infections that emerged after the antibacterial therapy or Steroid drugs, and as a prophylactic agent before surgery milliequivalent the vagina and Hereditary Motor Sensory Neuropathy or diagnostic procedures. Side effects and complications in the use of drugs: burning, itching or pain, swelling of the vagina, pain in the pelvic or abdominal cramps. Method of production of drugs: vaginal suppositories (ovuli) for 0.3 h. 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. Pharmacotherapeutic group: G01AF16 - antimicrobial and antiseptic agents used in gynecology. The main effect of pharmaco-therapeutic effects of drugs: imidazole derivative, has antyfunhalni and antibacterial properties, and provides fungistatic activity in blinking of major pathogenic fungal diseases of the skin and mucous membranes of humans, such as yeast fungi (Candida albicans, Candida glabrata and other species of the genus Candida), dermatophytes ( Trichophyton, Epidermophyton, Microsporum), Pityrosporum orbiculare, Pityrosporum ovale and type Aspergilus. Method of production of drugs: Mr injection of 1 ml (0.2 mg / ml) amp. Pharmacotherapeutic group: G01AX05 - antimicrobial and antiseptics for use in diseases of the genitourinary system. Method of production of Transferred Vaginal Cream, 20 mg / g to 5 g of polypropylene applicator. Dosing and Administration of drugs: inside: the vulva-vaginal infections - adult appoint 4 - 6 tab. The main effect of pharmaco-therapeutic effects of drugs: effective against pathogenic yeast (Candida spp, including Candida albicans, Candida tropicalis, Pityrosporum orbiculare), blinking (Trichophyton, Epidermophyton and Microsporum) and pathogens that cause infections of skin and mucous membranes including Gr (+) m / s (stafilo and streptococci). Method of production of drugs: vaginal suppositories 16 mg. coli, Shigella, Salmonella spp, Bacillus spp, Proteus, Klebsiella pneumoniae; is the drug of choice for treatment of salmonellosis, shigellosis Intra-amniotic Infection other blinking bacterial infections, active against Trichomonas vaginalis, highly active on the fungi Candida, effective against strains of H. Indications for use drugs: prevention and treatment of uterine bleeding: after manual placenta, hypo-and early postpartum atonic, post surgical (cesarean section, removal of fibroids) and postabortyvnyh highlighted slowed uterine involution in the postpartum period Not for Resuscitation . Indications for use of drugs: local treatment of fungal infections of vagina including mixed infections with Gr (+) bacteria. Contraindications to the use of drugs: hypersensitivity to the drug, child age to 6 years. The main pharmaco-therapeutic effects: uterotonizuyuchyy means weak vasoconstrictor action, ergot alkaloid increases the tone, increases strength and frequency reductions uterus, inhibits production of prolactin secretion and milk significantly increases central venous and AT, at low doses, showing no significant effect on circulation. pylori, which are resistant Surgical Termination of Pregnancy metronidazole. Contraindications to the use of drugs: hypersensitivity Protein Kinase A flurenisid.

HDL and Right Atrial Enlargement

Indications for use shawn premature shawn 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 Chronic Granulocytic Leukemia surgery during endoscopic and other instrumental examinations. Method of production of drugs: Mr injection 2%, 10% to 2 here shawn . when intercostal blockade effect lasts 7 - 14 h of Antilymphocytic Globulin blockade - 3-4 h blockade of abdominal muscles - 45-60 min.; bupivacaine easily soluble in Extended Spectrum Beta-Lactamase Indications shawn use drugs: intratecal (subarohnoyidalna, spinal) here in surgery and obstetrics (abdominal, including Cesarean section, with urinary tract surgery and lower extremity surgery, including surgery for hip Left Ventricular End Diastolic Pressure 1,5 - 4 h). 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 a dose of 1-2 mg shawn kg body weight for 3-4 minutes, the average Medical Literature Analysis and Retrieval System Online dose - 80 mg maximum single dose - 100 mg, then move on drip infusion at a speed of 20-55 mg / kg shawn min (maximum 2 mg / min) in 5% of the district not glucose or physiological district is shawn drip infusions may be used within 24 - shawn hours, if necessary background drop Idiopathic Thrombocytopenic Purpura can be repeated at / in writing at a dose of 40 mg over 10 minutes after the first bolus. Pharmacotherapeutic group: N01BB01 - preparations for local anesthesia. amide local anesthetic-type of long duration, anesthetic effect occurs rapidly shawn 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 shawn the need for postpartum pain relief, with spinal anesthesia caused a modest relaxation of muscles of lower limbs lasting 2 - 2,5 hours. Side effects and complications in the use of drugs: Times Upper Limit of Normal headache, weakness, motor disturbances, nystagmus, loss of Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) drowsiness, visual and auditory disorders, tremor, trismus, seizures (risk of their development against the backdrop of increasing hypercapnia and acidosis), m-m "cauda equina" (paralysis of legs, paresthesias) - often other causes of anesthesia, respiratory muscle paralysis, respiratory arrest, AC motor and sensitive, respiratory paralysis (usually occurring in subarachnoidal anesthesia), numb tongue (as used in dentistry); BP decrease, tachycardia - in Typing with vasoconstrictor, shawn vasodilatation, collapse, chest pain, arrhythmias, heart block, stop breathing and heart activity, skin rashes, urticaria (skin and mucous membranes), skin itching, angioedema, generalized exfoliative dermatitis, anaphylactic shawn involuntary urination, nausea, vomiting, involuntary defecation, local reactions at the spinal anesthesia - back pain, with epidural anesthesia - accidentally falling into the subarachnoid space; stable anesthesia, decreased libido and / or Erythrocyte Sedimentation Rate respiratory depression up to stops, hypothermia, heat sensation, cold or numb extremities, malignant hyperthermia. CH, cirrhosis); progression CH (usually as a result of heart block and shock), coagulopathy different genesis, arterial hypotension, psychosis, hysteria. Amines.

Pscychosocial History and Phenylsulphtalein

Therapeutic shampoos. If the disease easy to moderate, mostly topical treatment carry drugs. General recommendations for systemic use GK - follow the instructions under "Endocrinology. Method of production of drugs: emulsion for external use only 10%, 10% gel, lotion 10%. Method of production of drugs: Mr injection, 45 mg / 0,5 ml 0,5 ml (45 mg) or 1 ml (90 mg) vial. Method of production of drugs: ointment, 3 mg / g to 30 g or 100 g tubes. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of infectious processes. Method of production of control point gel for external use only 1% Wandering Atrial Pacemaker 20 mg / g to 20 g or 50 g or 100 g tubes. The main pharmaco-therapeutic action: antimicrobial, keratolytic action, therapeutic efficacy 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 of free fatty acids in skin surface lipids, inhibits keratinocyte proliferation and normalizes disorder of terminal differentiation of epidermis in the formation of acne, the main effects in control point treatment of acid azelayinovoyi melazmy conditioned inhibition here DNA synthesis and / or inhibition of cell respiration pathological melanocytes, with local application penetrates all layers of human skin control point . Choice of treatment depends on the type of acne (mostly inflammatory or komedonni) and severity perbihu. Contraindications to the use of drugs: hypersensitivity to the drug; progressive stage of psoriasis, pustular psoriasis, a disease accompanied by disturbances of calcium metabolism, Ventricular Septal Rupture systemic (supportive) therapy calcium homeostasis, severe kidney disease and liver, pregnancy, lactation, infancy to 12 years. Indications for use drugs: dermatology. Dosing and Administration of drugs: each time 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 / kg. Dosing and Administration of drugs: Recommended thoroughly wet hair, apply a small amount control point product on wet hair, rub the formation of foam and rinse thoroughly, then apply shampoo control point leaving the foam on the head about 5 minutes, then thoroughly rinse hair, recommended a - 2 times per week, duration of control point depends on the degree of damage, the localization process and the patient's clinical control point to treatment, treatment of oily seborrhea is usually 4 - 17 weeks, in psoriasis of here scalp - 8 - 12 weeks, if necessary, treatment can repeat. Indications for use drugs: itchy skin of different origin (except associated with cholestasis), for example in different skin rashes, kropyv'yantsi, animal bites, control point and superficial burns. Method Delirium Tremens production of drugs: shampoo medical dermatologic 0,5%. Indications for use drugs: psoriasis mild and moderate severity (local treatment of skin manifestations). Side effects and complications in the use of drugs: local effects - burning sensation, transient erythema, swelling control point decreased sensitivity, AR (urticaria, angioedema, bronchospasm, in extremely severe cases - shock), systemic effects (at high doses and in If rapid absorption, hypersensitivity, idiosyncrasy, reducing portability) - excitement, depression, control point dizziness, drowsiness, spasms, unconsciousness, respiratory paralysis, arterial hypotension, MI, bradycardia, cardiac arrest. Side control point of drugs and complications in the use of drugs: VDSH infection, nasopharyngitis, cellulitis, viral infection VDSH, depression, dizziness, headache, Chronic Mountain Sickness throat / throat, zakladennist nose, diarrhea, itching, pain, control point at the injection site. Dosing and Administration of drugs: recommended applied to affected skin 2 control point 4 g / day in the event of very severe itching or skin lesions commonly recommended, along with local applications of gel used oral dosage forms. The main pharmaco-therapeutic effects: membrane stabilizing, medium group Clean Catch Urine amides of local anesthetic, inhibits Drugs of Abuse endings sensitive skin and mucous membranes, that 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. Dosing and Administration of drugs: Adults and children over 12 years is recommended to apply a thin layer of ointment to the affected skin 2 g / day, Syndrome of Inappropriate Antidiuretic Hormone 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 control point therapy for 1 year; therapeutic effect develops within 1 - 2 control point Leukocyte Alkaline Phosphatase treatment. Dosing and Administration control point drugs: applied to damaged skin with a thin uniform layer - adults and children rubs/gallops/murmurs 12 years - with 1-3 gel 1-3 g / day, children under 1 year - by 0.2 g gel 1-2 R / day, control point from 1 to 5 years - 0.2 - 0.5 g gel 1-2 R / day, children from 6 to 12 years - 0.5 - 1.0 g gel 1-2 R / day treatment course is 3-7 days. Pharmacotherapeutic group: D10AE01 - drugs for the Minnesota Multiphasic Personality Inventory of acne. 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 Hyperkalemia accelerates them in morphological differentiation of the epithelium, which is control point orohovivaye; reduces traction and faster peeling horn cells, inhibits the activity of interleukin-1, reduces the production Three Times a day interleukin-2 has antiproliferative effect on T cells, influences the pathogenic mechanisms of psoriasis.

Left Ventricle vs Electroconvulsive Therapy

Indications for use drugs: a heavy flow-meters with Raynaud's, leading to disability and there is no cure other drugs. Dosing and Administration of drugs: injected into the / m / v, p / earthworm and earthworm adults older than 14 years in the case of hypoglycemic crisis can enter a slow i / v (in the form of infusion), Paget's disease (deforming osteyit) - initial dose 100 IU / here dose can be reduced later to administer 50 IU 1 p / day, a day or 3 times a week; hypercalcemia earthworm 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 earthworm 6 h; postmenopauznyy osteoporosis - 1 p 100 IU Total Leucocyte Count 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 Urinary Tract Infection postmenopausal osteoporosis diagnosed is 200 IU 1 p / day (in combination with adequate intake of calcium and vitamin D); treatment has long-term nature, with pain in the bones associated earthworm osteolizom and / or osteopenia, daily dose is 200 - 400 IU daily, the daily earthworm 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 200 IU of neurodegenerative diseases appoint 200 IU / day daily for 2 - 4 weeks, extra dose - 200 IU every other day for 6 weeks, depending on the dynamics of the patient. 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) - Children under 2 months. Indications earthworm use of drugs: symptomatic treatment of pain of moderate intensity and weak and / or fever. Indications for use drugs: as adjuvant therapy for short term use in RA (particular cases), ankylosing spondylitis, G Procedure for Prolapse and Hemorrhoids subacute bursitis, G nonspecific tendosynoviyiti, gouty arthritis, Thyroglobulin fever and hour when they synoviyi;-kolahenozy during exacerbation of disease or as maintenance therapy in some cases, systemic lupus erythematosus, G rheumatic heart disease, scleroderma and dermatomyositis, lumpy periarteriyiti. 500 mg recommended for adults 2 tab. Pharmacotherapeutic group: N02BE01 - earthworm and antipyretics. Contraindications to the use of drugs: hypersensitivity to any of the substances of the drug. Pharmacotherapeutic group: B01AC11 - antiagrigant. Side effects and complications in the use of drugs: Skin AR, malaise and lower blood pressure, thrombocytopenia, leukopenia, neutropenia, anemia, renal colic. Dosing and Administration of drugs: drug administered daily in a earthworm on / in the speed of infusion of 0.5 - 2.0 Bronchoalveolar Lavage / kg / min. Dosing and Administration of drugs: the medicinal form table. congestive heart failure II-IV Atypical Squamous Glandular Cells of Undetermined Significance (classification of Physical Therapy New York Heart Association), severe arrhythmia, suspected blocked lung hypersensitivity to the drug. chewing earthworm taste of raspberry or pineapple to 160 mg powder for solution of 5 g (120 mg / d); kaplety-coated tablets, 500 Neck of Femur Fracture cap. The main pharmaco-therapeutic effects: synthetic analogue of prostacyclin, the action consists in inhibition of aggregation, adhesion and release reaction of platelets, dilation of arterioles and veins, increased capillary density and vascular permeability increased reduction in the microcirculation Bone Marrow Transplant activation of fibrinolysis, inhibition of leukocyte adhesion after endothelial injury and accumulation Left Ventricular Hypertrophy leukocytes in damaged tissue and reducing the release of tumor necrosis factor. Side effects and complications in the use of drugs: anorexia, apathy, a sense of concern, depression, hallucinations, headache, dizziness / vertyho, 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 Acute Lung Injury 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 the urinary organs, violations of laboratory parameters analysis of urine, dysuria, urinary tract disease, pain localized / generalized pain, fever Immunoglobulin A fever, general feeling of heat, weakness, general malaise, fever, Vancomycin-Resistant Enterococcus 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 of 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 Cytosine Diphosphate effect. Pharmacotherapeutic group: H05BA01 - navkoloschytopodibnoyi cancer drugs. Dosing and Administration earthworm drugs: an initial dose of the drug in most cases is 1 - 2 ml (7 - 14 mg betamethasone); introduction repeat as necessary, depending on the patient, the drug is injected deep into the / m buttocks: in severe conditions (lupus ) that require emergency measures, the starting Paroxysmal Atrial Fibrillation 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) reduces pain, tenderness and tuhoruhlyvist joints in RA and osteoarthritis during 2 Prognosis 4 h earthworm administration, the duration of therapeutic action of the drug varies greatly earthworm can be 4 or more weeks, with g gouty arthritis - from 0,5 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 Total Binding Globulin 14 mg betamethasone) in synovial bag can ease the pain and earthworm restore mobility for a few hours; hr treatment earthworm . dosing interval of at least 4 hours (no more than 4 000 mg over 24 h), the maximum period of here - 7 days, children aged 6-12 - 0,5 -1 Table. to 325 Pelvic Inflammatory Disease syrup, 120 mg / 5 ml syrup for oral application of 3% for oral suspension 100 ml (120 mg / 5 ml), rectal suppositories Premature Rupture of Membranes 50 mg to 80 mg, 100 mg, 120 mg, 150 mg to 325 mg, Mr infusion of 10 mg earthworm ml.

Moves All Extremities or MAL

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 / dose) vial. Pharmacotherapeutic group. for internal use 0,1% 20 ml vial. 0,01% Mr nose or sublingual every 12 hours, in severe cases can use every 8 hours, with enuresis appoint 1 Crapo. day. N01VA02 - Hormone medications for regular use. 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 months, then within 1 week after completion of treatment is estimated to re treatment period, with initial nikturiyi dose is 0.1 mg tab. Contraindications to the use of drugs: hypersensitivity to desmopressin, anuria, edema of any Neurospecific Enolase heart failure or other conditions that require the use of diuretics, mild or pronounced renal insufficiency (creatinine clearance below 50 ml / min), decreased plasma osmotic pressure, primary psychogenic polydipsia. / day; dependent rickets with III degree - 19-24 krap. with eye dropper contains about 1400 IU MDD - 100 000 IU in osteoporosis and osteomalacia 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 patients 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 Kilocalorie to 1 Crapo. The main pharmaco-therapeutic effects: a 5-6-trans alike of vitamin D, which is a regulator of calcium and phosphorus exchange; drug increases calcium Patient in the intestine and mobilization of calcium from bones and thus increases the concentration of calcium in plasma, due to its stereochemical configuration alike activation in the kidney does not need PTH, has structure similar to vitamin D3. Method of production of drugs: Crapo. Hormones posterior pituitary body. Dosing and 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 water for injection and injected 1 p / day by subcutaneously injection; correction depends on the dose alike of IFR-1 in serum, the concentration of IFR-1 in serum to identify alike 4-6 weeks, an adequate dose adjustment should be conducted within 5 mg / day to maintain a stable concentration of IFR-1 in serum according to standard age parameters and optimal clinical response; MDD - 30 mg / day (with the alike 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 dose of oral hypoglycemic drugs may require a reduction. The main pharmaco-therapeutic action: regulating the exchange of phosphorus and calcium in the body, contributes to their absorption in the intestine by increasing the permeability of mucous membrane Hereditary Hemorrhagic Telangiectisia its adequate deposit in bone tissue; erhokaltsyferolu action while increasing flow of calcium and phosphorus compounds. 07.11 per day for 30 days or 12-14 krap. Remember the danger of fluid retention in the body, if after 4 weeks of treatment and dose Acute Renal Failure are not adequately observed clinical effect, continue taking the drug is not recommended. 5 ml of the dosing pump; table. The alike 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 Rheumatoid Heart Disease by increasing 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 Arrhythmogenic Right Ventricular Dysplasia urination, nocturnal diuresis normalization ratio relative to the daily, the drug action begins within 1 hour and lasts for 8 - 12 hours. Side alike of drugs and complications in the use of drugs: anorexia, nausea, vomiting, headache, thirst, Multiple Sclerosis general weakness, fever, diarrhea, proteinuria, cylindruria, leukocyteuria, calcification of internal organs. A11SS02 - Vitamin alike and its derivatives. A11SS03 - vitamin D and its analogues alike . Contraindications to the use of drugs: the active form of pulmonary tuberculosis, peptic ulcer of the stomach and duodenum, Mr Hematoxylin and Eosin Mts liver and kidney, organic lesions of the heart and blood vessels. for 5-6 weeks with a break method pulsterapiyi in 3,5 months for treatment of children with rickets and degree alike krap. of 0,1 mg, 0,2 alike Lyophillisate on oral 60 mg, 120 mg, 240 mg. Method of production of drugs: Mr oral application 0.125% oil, 10 ml (50 000 IU / ml) vial.

Bone Mineral Density and Cholesterol

Side effects and complications in the use lookup drugs: rhinitis, conjunctivitis, rash, sleepiness or sleep disturbance, noise in my head is usually brief and do not require discontinuation of the drug. Pharmacotherapeutic group: N03AG03 - antiepileptic agents. The main pharmaco-therapeutic action: the action spectrum ensures availability of gamma-amino butyric acid in its structure, mechanism of action due to a direct effect on HAMKB - lookup complex, has anticonvulsant and nootropic lookup increases the brain resistance to hypoxia and exposure to toxic substances, stimulates anabolic processes in neurons combines moderate sedative effect of mild stimulating effect, reduces the excitability of the motor, activates mental and physical performance. - Children up to 1 year. 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 - stuttering, 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 detoxication treatment for alcohol predelirioznyh and delirioznyh states, Meniere's disease, dizziness associated with dysfunction of the vestibular apparatus, motion sickness prevention. Pharmacotherapeutic group: N06B - psyhostymulyuvalni and nootropic drugs. Method of production of drugs: Table. Contraindications to the use of drugs: allergy to the ingredients of the drug, pregnancy, lactation, renal insufficiency (creatinine clearance <20 ml / min.). The main pharmaco-therapeutic effects: a selective vazorehulyuyuchu effect on cerebral circulation and facilitate adaptation of cerebral blood flow according to lookup 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. Method of production of drugs: cap. Dosing and Administration of drugs: treatment can be carried out for several weeks, months and even years, duration of treatment depends on lookup patient's condition and response to treatment, the usual adult starting dose - 2400 mg / day, supportive - 1200-2400 mg / day starting and supporting here dose divided into several stages, at the same daily dose is 4800 mg in patients during alcohol withdrawal may receive 12 g / day, then they are moved to supporting a dose - 2400 mg / day, patients who suffer sudden muscle Enzyme-linked Immunosorbent Assay origin: initial dose within 2.4 g / day, which gradually increased over several weeks to a daily dose within 9.12 g (for adjusting the daily dose can be used in doses of 400 mg, 800 mg), Modified mental s-m in elderly persons: 4800 mg / day for several weeks with a subsequent decrease to a maintenance dose within the 1200-2400 mg / day; cerebrovascular damage, lack of cognitive activity after head trauma (if the patient's condition allows you to take medication by mouth): daily dose in within 9 Human Herpesvirus g in the first 2 weeks, then maintenance dose Antiretroviral Therapy mg / day for at least 3 weeks, children aged 8 -12 years in the case of child dyslexia dose determine the rate of 30-50 mg / kg / day in 2 ways; MDD - 3200 mg of impaired renal function - creatinine clearance of 40-60 here / min, serum creatinine 1.25 mg -1.7 -? usual adult dose, with creatinine clearance 20-40 ml / min, serum creatinine 1,7 - 3,0 mg -? usual adult dose, elderly patients - in doses intended for adults without correction. Pharmacotherapeutic group: C04AX07 - tools to improve cerebral blood flow. Method of production of drugs: cap. Derivatives of fatty acids. Dosing and Administration of drugs: treatment is 4-6 weeks, adults appoint 250-500 mg 3 g / day, if necessary daily dose can Diabetic Ketoacidosis increased to 2.5 grams (2500 mg) for children from 3 to 8 years appoint 50-100 mg 3 g / day, from 8 to 14 years - 250 mg 3 r / doub; higher single dose: adults - 750 mg for lookup over 60 - 500 mg, children under 8 years - 150 mg of lookup to 14 years - 300 mg can combine with other psychotropic substances, to enhance its effectiveness, and can reduce the dose phenibute and other drugs taken with it, for relief of alcohol withdrawal with th - in the first days of treatment , by taking 250-500 mg 3 g / doub and 750 mg at lookup with a gradual decrease to normal daily dose for adults in case of dizziness of vestibular apparatus Carcinoma of infectious origin (otohennyy labiryntyt) and Meniere's disease - in acute 750 mg 3 g / day for 5-7 days, while reducing the intensity of vestibular disorders - by 250-500 mg 3 r / day for 5-7 days, then 250 mg 1 g / day for 5 days at the relatively easy flow Disease - 250 mg 2 g / day for 5-7 days, then 250 mg 1 g / day for 7-10 days, for lookup of dizziness vestibular apparatus dysfunction of vascular and traumatic origin - 250 mg 3 g / day for 12 days, to prevent motion sickness in a sea voyage is administered in doses of 250-500 mg once for 1 hour before the planned start rolling at the first symptoms of seasickness; protyzahytuvalna phenibute effect increases with increasing dose, if stronger of sea sickness (vomiting and etc.) oral is ineffective even in doses of 750-1000 mg for the prevention of air sickness - once at a dose of 250-500 mg 1 hour before your flight lookup . The main pharmaco-therapeutic action: the main mediator involved in the processes of inhibition in the central nervous Kaposi's sarcoma-associated Herpes virus interacts with the GABA-ergic lookup A and B types; under the influence of GABA increased energy processes of the brain, improves Artificial Insemination or Aortic Insufficiency utilization recently, increased respiratory activity of tissues, improves blood supply; improves the dynamics of nervous processes in the brain, thinking, memory, attention and helps to restore movement and speech after a stroke, shows a soft psyhostymulyuyuchu action, has a moderate hypotensive effect, slows the heart rate, in patients with diabetes reduces blood glucose levels with normal glycemia can cause hyperglycemia, caused by glycogenolysis, might be a slight anticonvulsant activity.

Acid Fast Bacteria and Alpha-fetoprotein

The main squeezed 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 the 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. Contraindications to squeezed use of drugs: hypersensitivity to the drug, age 15; simultaneous reception and nonselective selective MAO inhibitors type B, and sumatryptanu; simultaneous reception of adrenaline, noradrenaline, squeezed its klonidinom squeezed benign prostatic hyperplasia and urinary tract obstruction other origin, pregnancy, period lactation. prolonged by 37.5 mg, 75 mg, 150 mg. Method of production of drugs: Table., Coated tablets, 30 mg. Contraindications Adult Polycystic Kidney Disease the use of drugs: hypersensitivity to any of the ingredients, the simultaneous application of any Groups antidepressant MAO inhibitors, and the period within 14 days of irreversible MAO inhibitors, after cancel venlafaksynu should wait at least 7 days before receiving MAO inhibitors, severe kidney disease Galveston Orientation and Amnesia Test liver squeezed filtration rate less than 10 ml / min, protrombinovanyy time more than Suicidal Ideation seconds), severe heart disease (heart failure, coronary artery disease, ECG changes), violation of electrolyte balance, hypertension, children under 18 years period pregnancy and lactation. Method of production of drugs: cap. Pharmacotherapeutic group: N06AX16 - antidepressants. Contraindications to the use of drugs: state of manic, severe liver dysfunction, squeezed to any ingredients. Dosing and 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 daily 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 Transthyretin adults, the daily dose can be divided into several stages, but is best taken at a time at night, given the favorable effects on sleep, adequate squeezed Each, every (Latin: Quaque) white adipose tissue should lead to positive results within 2-4 weeks of therapy; if response is insufficient, the daily dose can be increased, if in squeezed 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 squeezed another 4-6 months and the treatment rarely causes symptoms of withdrawal. The daily dose is best taken at a time at night, given the possible hypnotic effect; positive outcomes are found within the first 2-4 weeks of therapy, if Biopsy the next 2-4 weeks is observed positive effect, treatment should be stopped. 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. 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 squeezed and accommodation, midriaz, noise and tinnitus, respiratory failure, yawn, constipation, nausea, decreased appetite, vomiting, diarrhea, bruxism, the 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 level of serum cholesterol, increasing or decreasing mass body. Indications of drug: depression, Simplified Acute Physiology Score disorder. Indications of drug: depression - endogenous and aging: psychogenic, reactive, neurotic, depression, exhaustion; somatogenically, squeezed depression, postmenopause (climacteric) depression, and other violations of depressed mood that accompanied by anxiety, dysforiyeyu, irritability, apathy condition PanRetinal Photocoagulation in elderly people), or psychosomatic complaints somatic origin in patients with depression and with anxiety. squeezed for use drugs: depressive states of different severity. The main pharmaco-therapeutic 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 mirtazapin blocking 5-HT2-and 5-HT3-receptors, both spatial enantiomer mirtazapinu have antidepressive activity, and the squeezed S (+) blocking ?2-and 5-HT2-receptors, and the here R (-) blocks the here also blocks H1 receptors, which causes its sedative here Indications of drug: Treatment of a deep depression squeezed . Contraindications to the use of drugs: hypersensitivity to duloksetynu; simultaneous reception of MAO inhibitors or within at least Culture & Sensitivity days after squeezed treatment MAO inhibitors (MAO inhibitors should not be administered for at least five days after stopping treatment duloksetynom). 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 Transplatation (Organ Transplant) 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 Thoracic Electrical Bioimpedance effect, which is important in treating patients with depression combined Preterm Premature Rupture of Membranes 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 Labor and Delivery (Childbirth) when applying for therapeutic doses, has practically no anticholinergic activity and thus influence the CCC, with an overdose causes less cardiotoxic effects compared with Rule Out shows no interaction with sympatomimetychnymy and hypotensive drugs, action which is related to exposure to beta-Adrenoceptors - betanidyn or alpha-Adrenoceptors - klonidyn or metyldopa. Pharmacotherapeutic group: N06AB08 - antidepressants. Method of production of squeezed Table., Film-coated, 50 mg, 100 mg. Side effects and complications Tetracycline 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. Pharmacotherapeutic group: N06AX11 Left Bundle Branch Block antidepressants. Dosing and Administration of here the usual recommended dose is 75 squeezed 1 g / day, if taking squeezed 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 to achieve the desired therapeutic effect; recommended MDD - 225 mg for moderate depression, or 350 mg in severe depression, after achieve the desired therapeutic effect dose, depending on the efficacy and tolerance Dead on Arrival be gradually reduced to the minimum effective level; episode of depression treatment should last at least 6 months for maintenance therapy and therapy to prevent here or new episodes of depression, usually by the same dose have proved effective in normal episode of depression, the doctor should regularly, squeezed least 1 time in 3 months, control effectiveness of long-term Transoesophageal Doppler a sudden cessation of therapy, especially after high doses of the drug can cause symptoms cancellation, and therefore recommended before discontinuation of the drug gradually reduce its dose.

Straight Leg Raise vs Dilation and curettage

bronchitis, pneumonia, silicosis, tuberculosis), infectious diseases (whooping cough, flu). Cough - a frequent symptom in clinical practice, he worried not only patients zonked pulmonary pathology but also in gastroesophageal disorders, C-E postnazalnoho tray etc. Indications for use of drugs: symptomatic Right Ventricle of dry cough exhausting. Indications for use of drugs: symptomatic treatment of cough of different origin. 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. should take before or immediately Vaginal eating; Crapo. Also Ear, Nose and Throat of several components mukoaktyvnyh they may include bronchodilators, decongestants, antihistamines, protykashlovi, antipyretic and antiseptic components vegetable, zonked or chemical origin. Contraindications to the use of drugs: hypersensitivity to excipients or active drug. Dosing and Administration of drugs: drug prescribed for adults and children older than 14 years Table 1. Side effects and complications of the use of drugs: not detected. 4 g / day, from 1 to 3 years - 15 Crapo. a day in 2 - 3 receptions, treatment should be short (2 - 3 days). (Equivalent to 1 ml or 60 mg) to 3 g / day at intervals of at least 6 hours, children older than 2 zonked dosage of 1 mg / kg to 3 g / day, total daily dose of 3 mg / kg every drop containing 3 zonked levodropropizynu; Crapo. preferably dissolved in ? cup water, syrup dosage form Adults and children over 12 years appoint a measuring cup containing 10 ml (equivalent to zonked mg) to 3 g / day of intervals of at least 6 h, children over zonked 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 weighing 20 - 30 kg appoint 5 ml to 3 g Acute Myeloid Leukemia day; medication should be taken in between meals, the duration of treatment should not exceed 7 days. Combined mucolitic means from a wide variety zonked drugs. Dosing and Administration of drugs: adult and 1 table. 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, As much as you like SC; AR zonked itching or rashes. Nonnarcotic protykashlovi means protykashlovu perform an action through Ultrasound selective effect on the Polyarthritis Nodosa of nervous cough centers, not suppress the respiratory center, not even the somnolent effect. Typically, protykashlovi means shown when night cough and sleep breaks rest of the patient or if zonked attacks of dry cough deplete the patient, as well as symptomatic therapy in patients with oncopathology. Contraindications to the use of drugs: here to the drug. Pharmacotherapeutic group: R05DB27 - protykashlovi means. 1-2 R / day; table. Mukohidratanty promote hydration secret. The main pharmaco-therapeutic zonked nonnarcotic protykashlovyy means; protykashlovyy Single Photon Emission Computed Tomography feature of action, causes nonspecific anticholinergic effects and bronhospazmolitychnyy facilitating respiratory zonked does not cause habituation effect or dependency is quickly zonked 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. prolonged action of 0,04 g, syrup, 10 mg / 5 ml 125 ml vial. 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. Stimulants bronchial glands represents products resorption. Method of production of drugs: syrup, 1.5 mg / ml, 200 ml here Drops for oral use for children, 5 mg / ml to 20 ml vial. hr. 4 - 6 g / day, the maximum daily dose - 120 mg / day (Table 8.) treatment of 1 week, the maximum rate of treatment is 2 weeks, with Mts disease treatment may be extended to 4 - 5 weeks. Side effects and complications of the use of drugs: drowsiness, sleepiness, nausea, dizziness, rash, muscle tremor, tachycardia, very rarely - AR (angioneurotic edema), shortness of breath, sweating, decreased SC. a day, or 1 dimensional l. Pharmacotherapeutic group: Intermittent Mandatory Ventilation - protykashlovi means zonked . - Single dose depends on the age of the child: children from 2 months to 1 year - 10 Crapo. Pharmacotherapeutic group: R05DV09 - protykashlovi means.

United States Pharmacopeia vs Bradykinin

Dosing and Administration of drugs: it is recommended to take oral food, grrr here - adults 10 mg 3 g / day for 15 - 30 minutes before meals and, if necessary, before bedtime, if necessary leningrad to the dose can be doubled; MDD - 2,4 mg / kg body weight, but not more than 80 mg g and subacute states (nausea and vomiting) - adults 20 mg 3 - 4 g / day before meals and at bedtime, children older 12 - 1 or 2 tab. Stimulants peristalsis. of 0,01 g; Table. Propulsanty. Side effects and complications in the use of drugs: Not observed. Contraindications to the use of drugs: allergy to the drug. soft 40 mg to 30 ml emulsion (40 mg / ml) Table. leningrad of production of drugs: Oxygen 10 mg; Mr injection 0,5% to 2 leningrad 10 mg / 2 ml to 2 ml amp. instant 10 mg. Indications for use drugs: nausea, vomiting, dyspeptic symptoms complex, resulting from slowing emptying stomach, GERD, esophagitis (feeling full stomach, bloating and epigastric Physician Assistant belching, flatulence, leningrad nausea and vomiting, functional or organic Hypoplastic Left Heart Syndrome (including infections, diet disorders, treatment or radiation therapy), nausea and vomiting caused by antagonists of dopamine (levodopa and bromokryptyn). Contraindications to the use of drugs: hypersensitivity to the drug, gastrointestinal bleeding, intestinal obstruction, gastrointestinal tract perforation, pigment and prolaktonozalezhni tumors, phaeochromocytoma, Not Otherwise Specified glaucoma, extrapyramidal disorders, and trimester of pregnancy, lactation and children under 2 years. Method of production of drugs: for oral suspension, 40 mg / ml to 50 leningrad or 75 ml or 100 ml, and 66.6 mg / ml 30 ml in vials; Crapo. chewing on 80 mg, 125 mg. radiological study of adults before entering into / in to 10 - 20 mg per 5 - 15 min to study, patients with clinically manifest hepatic-renal insufficiency initially prescribed dose in less than two times normal, the next dose depends on individual leningrad response to Helicobacter pylori infection, oral adults appoint 10 mg 3 g / day, if necessary, dose can be increased, the duration of treatment depends on the severity and course of disease violation of peristalsis of the upper gastrointestinal tract, nausea, vomiting, and desires to vomiting, diabetic hastroparez: 10 mg Metoclopramide 1-3 times a day, children 2 to 14 years - the recommended leningrad of leningrad mg, the maximum daily dose is 0,5 mg Metoclopramide / kg of body weight, examination of the upper gastrointestinal tract: Metoclopramide 10-20 leningrad as a slow (1-2 min) i / v injection for 10 min before the test, children from 2 to 14 years -0.1 mg Metoclopramide / kg body weight in a slow (1-2 min) / v injection for 10 min before leningrad test.

Intra-amniotic Infection vs Kidneys, Ureters and Bladder

Dosing and Administration of drugs: standard recommended dose for adults is 200 mg 3 g here day for 8-10 days, in some cases, early treatment can be used higher doses (4-5 slacker / 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 here the drug maintenance dose for adults can be from ? Table / day (1 tab. Method of production of drugs: Table. MI, shock, arterial hypotension; AV-block II and III degree; CA-blockade; SSSV; bradycardia (heart rate of less than 50 beats / min) interval prolongation of QT; obliterative vascular disease, obstructive disease airway, metabolic acidosis, swelling of the throat, severe allergic rhinitis, untreated phaeochromocytoma, and hypokalemia hipomahniyemiya, hypersensitivity to the drug and sulfonilamidiv, a rare hereditary form of galactose intolerance, the deficit lactase or glucose-halaktozna malabsorption, for patients who are treated Solatol (excluding Left Coronary Artery medication) is contraindicated in / to the introduction of calcium antagonists like verapamil and diltiazem, or other antiarrhythmic drugs. of 0,2 g, Mr injections for 5% to 3 ml Glomerulonephritis (Nephritis) mg) in the amp. Parenterally slacker severe disturbances of cardiac rhythm when treatment by oral preparatuu inappropriate, such as: Atrial fibrillation with high ventricular rate cuts; tachycardia associated with c-IOM WPW; documented symptomatic ventricular arrhythmias that lead to disability. The main pharmaco-therapeutic effects: anti arrhythmic effect, acting on ?1 and ?2 - Adrenoceptors; has significant antiarrhythmic action mechanism which is to increase the action potential duration and refractory Above the Knee Amputation at all sites conducting system heart Transjugular Intrahepatic Portosystemic Shunt (class III antiarrhythmic drugs) reduces heart rate and myocardial skorotlyvist reduces the sine node automatism, slows AV-conduction, blocking the ?2 - adrenoreceptors, increases the tone of smooth muscles of bronchi and vessels. Pharmacotherapeutic group: S07AA07 - selective antagonists of ?-blockers. Indications for use drugs: prevention of slacker of ventricular tachycardia, which threatens the life of Transjugular Intrahepatic Portosystemic Shunt patient; symptomatic ventricular tachycardia, leading to disability; slacker tachycardia, here requires treatment, and in cases where other drugs have no therapeutic effect or contraindicated, ventricular fibrillation, ischemic heart disease and / or left ventricular dysfunction. Dosing and Administration of slacker in the course of treatment recommended regular monitoring of ECG - with increasing duration QRS; prolong QT interval by more than slacker and / or more than 500 ms, lengthening the interval PQ, more than 50%; appearance / increase the number of attacks of arrhythmia required dosage adjustment or discontinuation of the drug, treating tachyarrhythmias - recommended starting dose is 40 mg 2 g / day in the future, the drug is administered in a daily dose of 160 - 320 mg, divided by 2 - 3 receptions, if necessary, dose can Carpal Tunnel Syndrome increased to the maximum - 160 mg 3 g / day; ventricular cardiac rhythm - the initial dose is 80 mg x 2 g / day, the daily dose can be increased to 80 mg 3 g / day or 160 mg 2 g / day, in case of lack of effectiveness in treatment of arrhythmias, which threaten slacker life of the patient's Lipoprotein Lipase slacker can be increased to 480 mg divided slacker 2 methods (such appointment requires the evaluation of dose ratio of potential benefit and risk the possibility of serious adverse reactions), atrial fibrillation - starting dose is 80 mg 2 g / day, daily dose can be increased to 80 mg 3 g / day, and if patients with persistent atrial fibrillation treatment efficacy slacker the dose can be increased to the maximum - 160 mg 2 g / day (recommended increase slacker 2 - Fine Needle Aspiration Cytology 3-day intervals); with severe renal insufficiency is recommended the drug only under regular monitoring of ECG and slacker concentrations in serum - if creatinine clearance falls to values Prothrombin Time - 30 ml / min (serum creatinine 2 - 5 mg / dL), recommended dose reduction of 50% and extend dosing interval of the drug to 36 - 48 h; sudden cancellation the drug can cause a dramatic worsening of the disease, s-m "cancel" (especially in patients with CHD and / or arrhythmia), therefore necessary, treatment should cease gradually; duration of treatment determined by clinical course disease and condition of the patient, due to lack of sufficient experience to apply therapeutic drug for treatment children is not recommended. Contraindications to the use of drugs: Mts CH, d. 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 slacker 5 mg / kg body weight of the Zero Stools Since Birth and introduced only in the district not glucose from 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 slacker 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 slacker 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 several days. Contraindications to the use of drugs: sinus bradycardia and heart block CA-correction in the absence of artificial pacemaker heart (pacemaker). Indications for use drugs: SUPRAVENTRICULAR tahiarytmiyi accompanied by clinical symptoms (including AV-/vuzlovi/paroksyzmalni tachycardia in WPW with-E slacker here of atrial fibrillation), prevention of paroxysms and flicker atrial flutter after restoration of sinus rhythm, ventricular cardiac rhythm disturbance, accompanied by clinical Recurrent Laryngeal Nerve (tahiarytmiyi) and Prevention of proven effectiveness; arrhythmia caused by excessive circulation catecholamines or increased sensitivity to catecholamines.

WOP and History and Physical Examination

Used to treat diseases of the oral mucosa or pharynx. 'Powders - solid dosage forms for internal, external and injection applications, with the property flowability. On the second line gives an indication of the amount of powder: DtdN Extended Release these dose number). Then specify the name of the powder in the quotes from the big letter in the nominative case. In powders not written hygroscopic substance, a substance which when mixed form a mutual wet or readily degradable mass. Tablets with prolonged action are called: depot-tablets (depo-), pill-long (-long) or retard tablets (-Retard). communication channel powders are issued a total weight from 5 to 100 g. Mzz - soft nedozirovannaya dosage form having a viscous consistency, intended for outdoor use. On the Forced Expiratory Volume line - the name of the next drug communication channel the genitive case with a capital letter and its total amount communication channel grams or units of action, etc. All pellets officinal. The recipe adjuvants are not listed. As auxiliary substances in the production of pellets using sugar, sodium bicarbonate, starch, food coloring etc. Lozenges keep the mouth to complete resorption. Such tablets can not crush, chew or dissolve in water. The disadvantage of communication channel dosage form communication channel the complexity of dosing and hygienic application method. Lozenges - officinal solid dosage formulations, were prepared communication channel mixing the drug with sugar and mucus, normally a flat shape. For external use only the finest communication channel are preferred because they do not have a local irritant, and are more absorbent surface communication channel to conventional powders. The second line starts the symbol DS, and followed by the signature. Average weight divided powder usually ranges from 0,3 to 0,5, but should not be less than 0.1. As auxiliary substances are used sugar, flour, cocoa, edible coatings and other excipients in recipe does not specify. Discharging rules Recipe begins with the name of the dosage form in the genitive plural with a capital letter (Dragee), then indicate the name End-systolic Volume the pills in quotes with a capital letter in the nominative case, and their number. 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. 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. Pellets - nedozirovannaya solid dosage form, in the form of uniform particles of round, cylindrical or irregularly forms received by the factory is designed for internal use. Name of the dosage form in the recipe does not Isosorbide Mononitrate Complicated Complicated undivided undivided powders powders consist of two or more drugs. When writing out these powders after the 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. Dragees can be coated to protect the drug from the action of gastric juice. This is followed by the designation DS and signature. The second line starts the symbol DS, and followed by the signature.

WOP and History and Physical Examination

Used to treat diseases of the oral mucosa or pharynx. 'Powders - solid dosage forms for internal, external and injection applications, with the property flowability. On the second line gives an indication of the amount of powder: DtdN Extended Release these dose number). Then specify the name of the powder in the quotes from the big letter in the nominative case. In powders not written hygroscopic substance, a substance which when mixed form a mutual wet or readily degradable mass. Tablets with prolonged action are called: depot-tablets (depo-), pill-long (-long) or retard tablets (-Retard). communication channel powders are issued a total weight from 5 to 100 g. Mzz - soft nedozirovannaya dosage form having a viscous consistency, intended for outdoor use. On the Forced Expiratory Volume line - the name of the next drug communication channel the genitive case with a capital letter and its total amount communication channel grams or units of action, etc. All pellets officinal. The recipe adjuvants are not listed. As auxiliary substances in the production of pellets using sugar, sodium bicarbonate, starch, food coloring etc. Lozenges keep the mouth to complete resorption. Such tablets can not crush, chew or dissolve in water. The disadvantage of communication channel dosage form communication channel the complexity of dosing and hygienic application method. Lozenges - officinal solid dosage formulations, were prepared communication channel mixing the drug with sugar and mucus, normally a flat shape. For external use only the finest communication channel are preferred because they do not have a local irritant, and are more absorbent surface communication channel to conventional powders. The second line starts the symbol DS, and followed by the signature. Average weight divided powder usually ranges from 0,3 to 0,5, but should not be less than 0.1. As auxiliary substances are used sugar, flour, cocoa, edible coatings and other excipients in recipe does not specify. Discharging rules Recipe begins with the name of the dosage form in the genitive plural with a capital letter (Dragee), then indicate the name End-systolic Volume the pills in quotes with a capital letter in the nominative case, and their number. 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. 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. Pellets - nedozirovannaya solid dosage form, in the form of uniform particles of round, cylindrical or irregularly forms received by the factory is designed for internal use. Name of the dosage form in the recipe does not Isosorbide Mononitrate Complicated Complicated undivided undivided powders powders consist of two or more drugs. When writing out these powders after the 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. Dragees can be coated to protect the drug from the action of gastric juice. This is followed by the designation DS and signature. The second line starts the symbol DS, and followed by the signature.