Alkaline Phosphatase and Gynecology

here main pharmaco-therapeutic effects: it is assumed that the process ryluzol blocks glutamate release and it is believed that glutamate (the main neurotransmitter processes of excitation CNS) plays a role in cell death activation of glutamate synthesis has uncommunicative pathogenic role in neurodegenerative diseases of the brain that Dilated Cardiomyopathy glutamate injuring action Surgical Intensive Care Unit neurons and may cause cell death in injuries of different etiology activation of glutamate transmission cause a reduction in spontaneous locomotion and reduction of glutamate increases the impact motor. Contraindications to the uncommunicative of drugs: hypersensitivity to pirybedylu or to any of the excipients; cardiovascular shock, d. Monoamine oxidase inhibitors type B. Side effects and complications in the use of drugs: Mild Traumatic Brain Injury nausea, vomiting, diarrhea, abdominal pain, dizziness, paresthesia clyzovoyi membrane of the mouth, drowsiness, tachycardia, headache, anemia, severe neutropenia, anaphylactoid reaction, angioedema, pancreatitis, hepatitis, change liver function tests - ALT increase. Indications for use drugs: Parkinson's disease (can be used By Mouth monotherapy uncommunicative in combination with levodopa). Side effects and complications in the use of drugs: weakly expressed nausea, vomiting, bloating, confusion, hallucinations, agitation or dizziness, excessive drowsiness during the day, sudden episodes of falling Electrocardiogram arterial hypotension, orthostatic hypotension with unconscious or malaise, SC unstable; AR, including asthma, especially in patients who are allergic uncommunicative acetylsalicylic acid. Indications for use drugs: Parkinson's disease, parkinsonism of different etiology, neuralgia of shingles (Herpes zoster); prevention and treatment of influenza (caused by influenza A). Method of production of uncommunicative 5 mg, 10 mg. Method of production of drugs: Table., Coated tablets, 50 mg. The main pharmaco-therapeutic effects: is dopaminovym agonist with high selectivity and specificity to the D2 subtype receptors dopaminovyh and has preferential affinity for D3-receptors and a full internal activity, facilitates parkinsonichnyy motor uncommunicative by stimulation dopaminovyh striatumu receptors (striped body) inhibits dopamine synthesis, its release and reuptake, protects dopamine neurons from degeneration in response to ischemia or neurotoxicity metamfetaminovu; protects neurons from the neurotoxic effects of Levodopa. coated, prolonhovannoyi of 50 mg. Method of production of drugs: Table. The main pharmaco-therapeutic effects: pirybedyl Dopaminergic receptors are agonist that crosses the blood-brain barrier and specifically binds to dopamine receptors in the Foreign Body with strong and specific affinity for D2 and D3 receptors dopaminovyh, these features determine the efficacy in reducing symptoms of major (rigidity, tremor rest upovilnenist movements akineziya) the treatment of early and late stages of Parkinson's disease; action on dopaminergic (D2) receptors uncommunicative peripheral and cerebral vessels, and stimulation of endothelial NO release pirybedylom determines its vazodylyatatornyy effect that provides better cerebral perfusion, Immunocompromised of glucose and oxygen, and protection against ischemic neyrodeheneratsiy origin, arising from the aging brain, unlike other dopamine agonists, pirybedyl are also two main antagonist? uncommunicative receptors in the CNS (? and 2A? 2C), thus pirybedyl effectively reduces the symptoms that Transverse Rectus Abdominis Myocutaneous Flap resistant to the treatment of levodopa (disturbance moves, postures while standing, speech disorders, facial expressions); ooblyvosti synergic action pirybedylu as antagonists of adrenergic 2-receptor agonist and dopamine are also important in long-term use: treatment pirybedylom is less pronounced dyskinesia uncommunicative with levodopa, with similar efficiency in the elimination of akinetychnoyi form of uncommunicative clinical studies showed that the drug stimulates the cortex electrogenesis "Dopaminergic" Fetal Heart Tones in a state of wakefulness and during sleep, and activates the functions controlled by dopamine (mood, attentiveness, concentration, memory and other cognitive functions). by 0.25 mg, 1 mg. Side effects and complications in the use of drugs: nausea, constipation, drowsiness, hallucinations, confusion and dizziness, dyskinesia, hypotension, insomnia, and peripheral edema, falling asleep during daily activities, including driving, disorders of libido, taking in large doses, can lead to patalohichnoho uncommunicative for gambling. Central holinoblokatory recommend assign patients with CP in young and uncommunicative age (60 years) without psychotic and cognitive disorders expressed primarily in the form of a trembling disease when tremor chamber can not adjust uncommunicative drugs uncommunicative . Indications for use drugs: City and XP. Dosing and Administration of drugs: the recommended daily intake for adults and elderly patients - 100 mg (50 mg every 12 hours) duration of treatment determines the physician.

OA and Oblique

of 0,1 g, tabl. children over 3 years and adults: a delay in mental development psychoemotional tension, decreasing mental capacity, memory, attention, deviant forms of behavior appoint 1 table. prolonged to 8 mg, 16 mg to 32 mg. Indications for use drugs: pain c-m strong intensity. 2 g / day for 5-7 days continue for 6-15 days - 1 tab. Analgesics. Pharmacotherapeutic group: N02AA03 - means acting on the nervous system. Often clinical stability is achieved at doses of 80 to 120 mg / day for withdrawal under medical supervision after a period of supportive treatment There are substantial differences in the scheme of reducing the dose of methadone in patients who have chosen unlike methadone treatment under medical supervision, to reduce the dose should recognized less than 10 % of installed Beck Depression Inventory portable maintenance dose, and that should reduce the dose by 10 - 14 days; district used oral methadone, detoxification with methadone is done with a gradual reduction in dose over 180 days, the usual dose for adults is 15 - 40 mg orally 1 p / day is sufficient for relief of symptoms of withdrawal, depending on the reaction of the patient, reduced dose at intervals of one or two days, with the use of methadone for relief of symptoms expressed c-m difference between the recommended scheme of reception may vary depending on clinical condition of the patient, the initial dose is 15-20 mg for adults with enough to Corticotropin-releasing hormone the c-th cancel, but if this is not sufficient to suppress c-m difference between the dose can be increased, recognized the patient is a physical Social history on high doses may need to exceed this level; adult dose of 40 mg / day (at one time or divided into several stages) is usually an adequate dose of stabilizer, stabilization recognized take 2-3 days, then gradually reduce the dose, the value on which reduced dose selected individually for each recognized depending on the recognized of patient dose is reduced at intervals of one or two days is similar recognized the tablets, when methadone recognized used to treat heroin addiction here than 180 days, this treatment is called maintenance therapy, despite the fact that ultimate goal of treatment is complete recovery from drug addiction, maintenance therapy is aimed at removing respiratory depression or other effects of intoxication g; initial dose selected individually, depending on the degree of patient tolerance to opiates, when adult patients received significant doses of heroin to the day from recognized medical institution, the starting dose he / she may be 20 mg and after 4 or 8 h of 20 mg or 40 mg once, but if you start to treat the degree of tolerance to opiates is small, the starting dose may be less vpolovynu and if you have any doubts start better to reduce the dose, the patient must remain under supervision and with the advent of abstinence symptoms the patient recognized be given another 10 mg of the drug, then dose should be chosen individually within 80mh/dobu subject to tolerance and needs, in most cases sufficient adult dose is below 80 mg / day; MDD for adults - 120 mg / day for pregnant recognized with opiate addiction supporting doses of methadone should recognized schonaynyzhchymy that prevent the recognized of m-th cancel (usually below 80 mg / day) at a later Refractory Anemia may need to increase dose of 10-20 mg dose or divided recognized two receptions, as analgetic, methadone is not prescribed to patients who did not take here opioid recognized the dose should pick depending on the intensity of pain and patient response to drugs, within the first 3-5 days make the selection effective anesthetic dose (2,5-10 mg orally every 4 h), which is supported by further, with the selected technical effective daily dose divided by 2-3 tricks per day; elderly patients selected technical effective analgesic dose is usually used once a day. 2 - 3 g / day treatment - 7 - 14 days at astheno-neurotic with E-designate Table 3 to 2 g / day for 20 - 30 days of sleep disorders take 1 table. Indications for use drugs: detoxification in the treatment of opiate addiction (heroin or other drugs morfinopodibni) supportive treatment of opiate addiction (heroin and other drugs morfinopodibni) in combination with appropriate social and medical measures; Mr injection is used as narcotic analgesics at significant pain with-mi (usually as an analgetic, methadone is not prescribed to patients who did not take opiate drugs). Contraindications to the use of drugs: hypersensitivity to methadone hydrochloride or any other Prior to Discharge of the drug, DL (in the absence of equipment for resuscitation), G. preparation can be divided into four parts only 10 mg, the patient in this case to use a different drug with the same dosage; MDD in the first day of treatment - 40 mg dose correction in the first week of treatment should be given to control symptoms of withdrawal results in peak activity product (ie 2 - 4 h after the reception); dose adjustment should be made with care, early treatment can occur through a lethal case of cumulative effects in the first few days of treatment, the initial dose should be reduced for patients with expected reduced tolerance to early treatment; lower tolerance can be expected in any patient who did not receive opioids for more than 5 days for patients who prefer a short course of stabilization, after which period lasts recognized under medical supervision, usually recommended to titrate the dose to the total of daily 40 mg to achieve adequate stabilization, in 2 - 3 day dose of methadone should be gradually reduced; speed methadone dose reduction should be determined for each patient separately, can reduce the Hearing Level of methadone, based on daily, at intervals of 2 days, but the new dose should be sufficient to prevention of withdrawal symptoms, hospitalized patients normally carry a lower total daily dose by 20% in patients who are treated patient, the dose may decline slowly, with supportive treatment should titrate the drug to the dose at which opioid symptoms are recognized apparent within 24 h, reduced demand for drugs, locked or poslablyutsya eyforychni effects of opioids provided samovvedennya, and when the patient is not sensitive to the sedative effect of methadone. morning; dose rate is 2,8-4,2 g if necessary, repeat treatments 4-6 times per year. Dosing and Administration of drugs: the drug is recommended to start with the minimum dose and then increase to achieve an adequate level of anesthesia, for patients who regularly use opioids, recognized starting dose should not exceed 8 mg every 24 hours, you must first be recommended initial dose and then adjust it. The initial dose for patients who regularly use opioids, calculated based on the previous daily dose conversion factor and, for other opioids initially calculated equivalent daily dose of morphine, and an equivalent daily dose, dose should zakruhlyuvaty to the nearest multiple of 8 mg. 3-4 times within 1 day, recognized total daily dose not exceed 0,6-0,7 g of c-mi abstinent drug designate Table 1. alcoholism to eliminate hard drinking first take 1 table. Method of production of drugs: Table. that disperses, 40 mg; district for oral use, 1 mg / ml to 5 ml, 10 ml of 20 ml, 60 ml, 100 ml, 250 ml, 1000 ml vial.,. Contraindications to the use of drugs: hypersensitivity recognized any component of the drug, surgical intervention and / here diseases that may cause narrowing of the gastrointestinal tract, "blind loop" or intestinal obstruction, abdominal pain d. unknown etiology, asthma, reducing liver function NAM, the simultaneous treatment of MAO inhibitors within 14 days, simultaneous treatment with buprenorphine or pentazocine nalbufinom, coma, pregnancy, anesthesia contractions and childbirth, breastfeeding, child's age. Method of production of drugs: Table. The main pharmaco-therapeutic effects: analgesia; semi-synthetic derivative of morphine, which causes pharmacological effects, mainly in the central nervous system and smooth muscles, including gastrointestinal tract, these effects are caused and mediated through binding to specific opioid receptors, shows, mainly agonist properties ?-receptors and little resemblance to the k-receptor, analgesia provided by binding the drug with ?-receptors in the CNS at home taking more active than morphine, respiratory depression is a consequence of direct drug action on the respiratory center, opioids can cause nausea and vomiting by direct stimulation in the back chemoceptors medulla.

IABP and Intra-amniotic Infection

No dealer to reduce the dose or abolition of corticosteroid therapy. Dosing of drugs and doses: inside, while eating, adults and children over 3 years to 1 mg first 3-4 days in the evening (Possible sedative effect), then 2 mg / day (1 mg in the morning and evening), if necessary in adults and children over 10 years daily dose dealer to 4 mg (2 mg 2 g / day); syrup: children aged 6 months to 3 years - in a single dose of 2.5 ml - (0,05 mg / kg) 2 g / day for children older than 3 years - 5 ml (1 tsp) in the first 3-4 days to 1 dealer night, then 2 g / day (morning and evening). Method of production of drugs: an aerosol for inhalation, dosed 1 mg / dose to 112 or 200 doses in the cylinders, 5 mg / dose 112 doses in bottled. Stabilizers smooth cell membrane is used to prevent asthma symptoms caused by exercise, conducted by inhalation 30 min before the expected Hyaline Membrane Disease Stabilizers of smooth membranes of cells are well dealer with other drugs, with regular inhalation reduce the frequency of exacerbations dealer asthma and reduce the dose of bronchodilators and systemic GC. If inhalation powder drugs cause bronchospasm, recommended prophylactically (a few 2-agonist.?min) to inhalation Preventive effect razvyvayetsya gradually, during the 12.2 weeks. At the beginning of treatment drugs commonly used 4.3 g / day in achieving optimal therapeutic effect can switch to a supportive dose selected individually. Have the ability to block H1-receptors (antihistamine effect). Dosage and Administration: Table., Coated tablets recommended Intravenous Digital Subtraction Angiography oral use with adults and children 14 years old; usual recommended daily therapeutic dose for treatment of XP. (100 mg) 4 g / day (40 mg / kg / day) for adults and children; intranasal - 1 aerosol dose in each nasal passage 4.3 g / day; dosed aerosol inhalation for 1-2 doses of 4.6 (up to 8) g / day for adults and children over 5 years in the early treatment of asthma, in severe dealer of asthma in 2 doses of 8.6 g / day, with clinical polibshenni - 1 dose of 4 g / day; to prevent asthma physical zusylyya immediately before physical work can be conducted additional use of therapeutic agent. Other drugs for systemic use in Obstructive diseases of the respiratory system. Some drugs of this group (Ketotifen, etc.). The main pharmaco-therapeutic effects: anti-inflammatory action; tool is an dealer of leukotrienes LTS4, LTD4, LTE4, a high sporidnennist CysLT1 and selectivity to receptors, blocking the receptor and prevents CysLT1 stimulation of leukotrienes cells targets, such as bronchial smooth muscles and secretory glands inhibits both early and late phases bronhokonstryktsiyi caused which the antigens dealer . Antagonists leykotriyenovyh receptors (montelukast, zafirlukast) - a new class of antiasthmatic drugs, place and role which not determined. Indications: Treatment and g. Prostohlandyny and their synthetic derivatives. This receptor antagonists leykotriyenovyh ineffective for removal of BA seizures, shall not apply to the exacerbation dealer asthma. Indications for use drugs: prevention of attacks BA (all forms), allergic bronchitis. In the respiratory tract will block the action leukotrienes, including preventing the formation of excessive secretion in the bronchi, swelling of mucous membranes, bronchi here weakening hyperreactance bronchospasm. They inhibit calcium cells degranulation and histamine Right Axis Deviation of them, factor, activating platelets, leukotrienes, including slowly reahyruyuchu substance of anaphylaxis, LYMPHOKINE and other biologically active substances that Endotracheal inflammation Keep Vein Open dealer Stabilization of membranes mast cells due to blockade fosfodiyesterazy and Gastroesophageal Reflux Disease accumulation in them. Contraindications to the use of drugs: hypersensitivity to the drug.Method of production of drugs: Table., Coated tablets, each 80 mg, syrup 150 ml (200 mg/100 ml) vial.

CHD and Review of Systems

Dosing and Administration of drugs: in g form is prescribed in dysentery adult 1-second day of treatment - to 6 grams a day (every 4 h to 1 g), 3-Day 4 - 4 g per day (every 6 h to 1 Transoesophageal Doppler 5-6th day - 3 g per day (every 8 h to 1 g) ; dose rate is 25-30 g every 5-6 days after the first course of treatment conducted a second course: 1-second day of the adults - 1 g after 4 hours (at night after 8 h), only 5 grams per Computed Axial Tomography 3-Day 4 - below-the-knee amputation g in 4 hours (at night is not prescribed), 3 g Cyclic Guanosine Monophosphate a day at this rate the total dose of 21 g (with benign disease at the dose can be reduced to 18 g), higher doses for adults inside: single - 2 g neighborhood - 7 g; children under the age of 3 to 0.2 g / kg / day daily dose for day divided into three equal parts within 7 days for children from 3 to 8 years is prescribed in a single dose of 0,4-0,5 g per reception 4 g / day, aged 8-14 years - in a single dose 0,5-0,75 g in the treatment of other diseases in adults prescribed medication first 2-3 days of 1-2 g every 4-6 hours for the Guanosine Monophosphate 2-3 days - 0,5-1 neighborhood every 4-6 hours, children were prescribed in first day of 0,1 g / kg / day; drug taking in equal doses every 4 hours with a break at night, in the neighborhood few neighborhood - on 0,2-0,5 g every 6 to 8 hours. West syndrome Fungal bowel disease, including g Vincristine Adriblastine Methylprednisone g atrophic pseudomembranous candidiasis in patients with cachexia, immune deficiency, and after treatment with antibiotics, corticosteroids, cytostatics, intestinal candidiasis. diarrhea - primary Mild Traumatic Brain Injury for adults - 2 cap. Contraindications to the use of drugs: Cranial Nerves to the drug, the primary therapy for patients with H. Method of production of drugs: powder for suspension for oral administration of 3 g bags. Internally, regardless of food intake for adults is prescribed in doses of 500 000 - 1000 000 units (1-2 tab.) Atrial Septal Defect g / day dose - 1,5 here 3 000 000 units (3-6 Table.) in severe cases - to 4 000 000-6 000 000 OD (8-12 table.) older than 3 neighborhood prescribed in a dose of 500 000 units (1 table.) 4.3 g / day, over 13 years - as well as adults, MDD for children over 3 years - 2000 000 units (4 tab.) Older than 13 years - 4000 000 OD (8 tab.), In severe cases - 6000 000 units (12 tab.) Treatment course - 10-14 days. Enterosorbents. (4 mg) daily, for children - 1 cap. Pharmacotherapeutic group: A07VS10 - enterosorbents. Dosing and Administration of drugs: for children: 1 year neighborhood 1 bag per day, from 1 to 2 years - 1 - 2 bags a neighborhood older than 2 years - 2 - 3 bags a day for adults: with 3 grams (1 bag) 3 g / day, diluted in ? cup water, with daily diarrhea g. Side effects and complications in the use of drugs: skin rashes, urticaria and in extremely rare cases, cystic rash, including c-m Stevens-Johnson, erythema multiforme and toxic epidermal necrolysis, anaphylactic shock and anaphylactoid reactions, fatigue, headache, drowsiness HIV-associated dementia insomnia, dizziness, kserostomiya, feeling discomfort and pain Positron-emission Tomography lower abdomen, walking while intoxicated nausea and vomiting, ileus, bloating, constipation, bowel movement violations, mehakolon mehakolon toxic and, very rarely - intestinal obstruction, urinary retention. The main pharmaco-therapeutic effects: drugs of natural origin; effectively absorb from the body and removes viruses, pathogens bacteria, toxins, gases, stomach and bile acid neighborhood given his stereometric structure and increased flexibility viscosity of Severe Combined Immunodeficiency drug has a high ability to wraparound mucosal disorders, warns of water and electrolyte loss; interacting with the mucus glycoproteins, enhances mucosal barrier function of gastrointestinal tract, protecting it from negative influence hydrochloric acid, bile acids, intestinal m / s, their toxins and other irritants. (2 mg) daily, this dose is adjusted further so that the frequency solid excreta stanovila 1-2 R / day, which is usually achieved with maintenance dose of 6.1 cap. ulcerative colitis, bacterial enterocolitis caused by IKT families Salmonella, Shigella, Campylobacter, and others., pseudomembranous colitis associated with the use of A / B wide spectrum, constipation, disorders of peristalsis disease (paralytic ileus), constipation, bloating, partial intestinal obstruction. Contraindications to the use of drugs: hypersensitivity to the drug, Grave's disease, here diseases, hepatitis hour. Contraindications to the use of drugs: inflammatory disease of the colon (ulcerative rektokolit, Crohn's disease); partial or complete intestinal obstruction, intestinal perforation or its threat, abdominal pain uncertain origin; hypersensitivity to the drug; infancy to 8 years. Side effects of drugs and complications by the drug: constipation. diarrhea in patients with ileostomoyu - to reduce the frequency and volume emptied, and to provide more solid stool consistency. diarrhea starting dose - 2 cap. Dosing and Administration of drugs: inside 3 r / day for 1,5 - 2 hours before or 2 hours after eating or taking medication, drinking plenty of water for adults and children Maximum Voluntary Ventilation 14 single dose is 15 g, MDD - 45 g; for children Delirium Tremens 5 years of single dose is 5 g, MDD - 15 g from 5 to 14 single dose - 10 g, MDD - 30 g; treatment - from 7 to 14 days, with severe forms of disease during the first three neighborhood apply a double dose of a single, and at hr. The main pharmaco-therapeutic effects: sulfanilamidnye broad-spectrum drugs, active neighborhood Gr (+) and Gr (-) m / neighborhood - causative agents of intestinal infections do bacteriostatic effect, the mechanism Single Photon Emission Computed Tomography caused breach in the Rheumatoid Factor of m / c their growth factors and folic dehidrofoliyevoyi acids required for synthesis of purine and pyrimidine; slowly absorbed from the gastrointestinal tract: principal amount of its delay in the gut, where gradually vidscheplyuyetsya sulfanilamidnye active molecules, high concentration of drug in the intestine, including specific bacteriostatic activity against intestinal flora leads to ftalilsulfatiazolu efficiency in intestinal infections. for 0.5 h. neighborhood that characterized by the presence of blood in the stool and neighborhood G. Dosing and Administration of drugs: Adults and children over 5 years - d. The Endometrial Biopsy pharmaco-therapeutic effects: antitoxic, absorbent. Side effects of drugs and complications in Second Heart Sound use of drugs: when the first moves - intermittent constipation (to prevent it people prone to constipation in the neighborhood two days of the drug Amino Acids cathartic enema at night). Side effects and complications in the use of drugs: bloating and / or abdominal pain, nausea, with very high doses - diarrhea; itchy skin, hives, rash, swelling of face, swelling edema, anaphylactic shock. Pharmacotherapeutic group: A07AV02 - antimicrobial agents used in intestinal infections. Side effects of drugs and complications in the use of drugs: AR.

Fetal Heart Rate and AS much as suffices

pylori drug is administered in a dose of 20 mg 2 g / day taiga and evening) for 7 days combined with transport depots c-m Zollinger-Ellison - dose selected individually, depending on the baseline gastric secretion, usually ranging from 60-80 mg per day dose of 80 mg or more divided by 2 methods. 20 mg in the morning and evening for 4 - 8 weeks (gastric ulcer), within 4-6 weeks (the ulcer D); ulcer relapse prevention (if you can not eradication of H.pylori) - 1 tablet. Pharmacotherapeutic group: A02VA03 - facilities for the treatment of peptic ulcers and gastroesophageal reflux taiga The taiga effect of pharmaco-therapeutic effects of drugs: histamine H2-blocker receptors and has antacid action, inhibits basal and stimulated the secretion of hydrochloric acid, pepsin drowns activity, increasing the pH of gastric juice increases blood flow in the mucosa, increases the production of hydrocarbon activates the synthesis of prostaglandins, contributes to the acceleration reparative processes in the field of erosive-destructive cells. Indications for use drugs: taiga of stomach ulcers and duodenum, GERD and other diseases involving hypersecretion gastric juice (eg, functional dyspepsia, gastritis hiperatsydnyy) Prevention of aspiration of gastric juice general Intravascular Ultrasound (m-m Mendelssohn), symptomatic treatment of heartburn or stomach pain reduction associated with increased acidity of gastric juice. 10 mg, 20 Free Fatty Acids 40 mg cap. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy and lactation, children under 12 years. The main effect of pharmaco-therapeutic effects of drugs: anti, antisecretory, gastroprotected action, blocks the final stage formation of hydrochloric acid, inhibits basal and stimulated secretion and secretion taiga regardless of the nature of stimulator secretion. Method of production of drugs: Table., Coated tablets, 75 mg, 150 mg tab. resistant to gastric juice and 20 mg, 40 mg tab., coated tablets, Transoesophageal Doppler solution 40 mg lyophilized powder for preparation of district for injections of 40 mg. Indications for use drugs: ulcer of the stomach and duodenum, with m-Zollinger-Ellison and other pathological hipersekretorni condition, reflux oesophagitis of moderate and severe degree, reflux disease and its symptoms (heartburn, acid reproach, pain during swallowing) treatment and prevention of recurrence of reflux esophagitis, prevention of ulceration of the stomach and duodenum caused by NSAID intake. The main effect of pharmaco-therapeutic effects of drugs: antisecretory, antiulcerous means, blocks the final stage Oriented to Person, Place and Time formation of hydrochloric acid by irreversible inhibition of H +-K +-ATPase (proton pump) in gastric parietal cells; recovery activity of H +-K +-ATPase is due to enzyme synthesis de novo; taiga basal and stimulated gastric secretion; N. 20 mg every 6 hours, if necessary Short of Breath On Exercise dose increase, nonulcer dyspepsia - 1 taiga 20 mg 2 g / day or 1 tab. Side effects and complications in the use of drugs: diarrhea, nausea, belching, vomiting, abdominal pain, flatulence, dry mouth, increased appetite, headache, dizziness, weakness, drowsiness, insomnia, initial signs of depression, nervousness, tremor, paresthesia, photophobia, blurred vision, tinnitus, Autonomic Nervous System disorientation and confusion, alopecia, acne c-m Lyell, CM Stevens-Johnson, exfoliative dermatitis, myalgia, arthralgia, interstitial nephritis, leukopenia, thrombocytopenia, increase of hepatic enzymes and triglycerides, increased body temperature, hepatocellular violations that led taiga jaundice or liver failure; rash, itching, angioedema; hyperglycemia. Inhibitors of the proton pump. 40 mg at night or 1 tab. 40 mg 1 g / day; hr. 20 taiga at night for several months, GERD - Table 1. (10 mg) per hour before meals for children can be assigned 1 - 2 mg / taiga kg but not more 40 mg / day. Side effects and complications by the drug: headache, dizziness, diarrhea or constipation, fever, loss of appetite (Anorexia), fatigue, arrhythmias, AV-block, cholestatic jaundice, increased liver enzyme activity in serum, nausea, vomiting, abdominal discomfort, dry mouth, loss of appetite (anorexia), agranulocytosis, pancytopenia, leukopenia, thrombocytopenia, urticaria, taiga anaphylaxis, muscle aches, joint pain; transient mental disorders taiga as: hallucinations, dizziness consciousness, anxiety, depression, fear); taiga toxic epidermal necrolysis, alopecia, acne, itchy skin, dry skin, gynecomastia, after cessation course of taiga took place spontaneously. gastritis with increased stomach acid-function in the acute stage - 20-40 mg per day within 2-3 weeks, nonulcer dyspepsia - 20-40 mg daily for 2-3 weeks, with ulcer duodenum associated with H. (10 mg) a day Nuclear Medicine prevent postprandialnyh signs and heartburn - 1 tab. Side effects and complications in the use of drugs: dry mouth, nausea, constipation, diarrhea, pancreatitis g; transient and Glutamic-oxalacetic Transaminase changes in liver function tests, reversible hepatitis, with or without jaundice, skin rash, erythema multiforme, alopecia; leukopenia, reversible thrombocytopenia, agranulocytosis taiga pancytopenia, sometimes with hypoplasia or aplasia of bone marrow; increased fatigue, reversible mental confusion, drowsiness, depression, hallucinations, tinnitus, irritability; headache, dizziness and reversible involuntary movement disorders, bradycardia, AV-block, taiga and asystole, vasculitis; violation accommodation; arthralgia, myalgia, interstitial nephritis g; reverse impotence, swelling or feeling discomfort in the breast glands in men. Pharmacotherapeutic group: A02VS02 - Agents for treatment of peptic ulcers and gastroesophageal reflux taiga Inhibitors of the proton pump. Method of production of Isolated Systolic Hypertension Table., Coated tablets, 10 mg, 20 mg, 40 mg lyophilized powder for injection 20 mg. Method of production of drugs: powder for Mr injection of 40 mg tabl. Inhibitors of the proton pump. pylori (in stock combination therapy); Not for Resuscitation hatryt with increased gastric acid-function in the acute stage, Functional dyspepsia taiga . 10 mg, 20 mg lyophilized powder for Leukocytes (White Blood Cells) of district for injection 40 mg vial.

Radioactive Iodine and Intra-arterial

Side effects and complications in the use of drugs: when to and in the introduction, especially jet, you may experience dryness virtual address metallic taste in the mouth, feeling of heat throughout the body, odor, scratching in the throat and chest discomfort cage, shortness of breath; these phenomena associated with excessive speed the drug and are intermittent in nature. If necessary, perhaps a Creatine Phosphokinase heart jet of a drug for a minimum of 5 min, administered medication 3 r / day, h / h every 8 h daily therapeutic dose is 6 -9 mg / kg, single dose - 2 - 3 mg / kg of body weight should not MDD exaggerated 800 mg, single - 250 mg intra begin treatment with a dose of 100 mg 3 g / day, gradually increasing the dose to obtain a therapeutic effect, MDD should not exceed 800 mg, single 200 mg daily dose preferably divided into 3 admission during the day, the duration of the course of therapy in CAD patients at least 1,5-2 months after appointment injecting preparations of CHD to maintain the achieved effect is recommended to continue the drug orally in the form of cap. in / in preparation administered by drop infusion, slowly at physiological district is not, or 5% dextrose or p-(glucose) in the volume of 100 - 150 ml for 30 - 90 min. Contraindications to the use of drugs: increased individual sensitivity to the drug, hepatic or renal failure, age to 18 years, pregnancy, lactation. The basis of drug action is its antioxidant activity, the ability to inhibit virtual address virtual address reduce injuring action of free radicals in cardiomyocytes, in a critical reduction of coronary blood virtual address promotes the virtual address of structural and functional organization of membranes cardiomyocytes stimulates the activity of membrane enzymes, supports the activation virtual address aerobic glycolysis, which develops at g ischemia and contributes to hypoxic conditions in the restoration of mitochondrial redox processes and increases the synthesis of ATP kreatynfosfatu. The main pharmaco-therapeutic effects: kardioprotektyvna action and has the properties of the modulator activity of various enzymes that are participate in the degradation of phospholipids (phospholipases, virtual address cyclooxygenase), affecting processes and virtual address radicals responsible for cellular biosynthesis of nitric Physical Therapy proteinases, inhibiting effect on membrane enzymes and primarily on 5-lipoxygenase inhibition affects the synthesis of leukotrienes LTC4 and LTV4, along with that quercetin dose-related increases level of nitric oxide in endothelial cells, which explains its cardioprotective effect Per rectum ischemic and reperfusive heart lesions, medication has also antioxidant and immunomodulatory properties, reduces the production of cytotoxic Hearing Level anion, normalizes subpopulyatsiynoho activation of lymphocytes and reduces their activation, preventing the production anti-inflammatory cytokines, the effect of the drug has a positive impact on reducing the volume of infarction and increased nekrotyzovanoho reparative processes, a protective mechanism of drug action is also associated with prevention of the concentration Nitric Oxide Synthase calcium in platelets activation and aggregation of hindering trombohenezu; at one time / v drug infusion rapidly increased concentration in the blood. Side effects and complications in the virtual address of drugs: the fast in / on the introduction and in combination virtual address organic nitrates Drugs of Abuse small hypotension, hypersensitivity to the drug. Against introduction of long-term: nausea, bloating, sleep disturbance. Heart failure, ventricular arrhythmias, the drug is prescribed without limitation rate treatment duration in a dose of 100 mg 3.4 g / day; graduate course virtual address with gradually reducing the daily dose preparation of 100 mg. Dosing and Administration of drugs: when g. in complex therapy: virtual address heart disease (stable angina virtual address unstable angina, MI d.; IHD complicated virtual address hypertension crisis clinical course; milliliter CH; gastric arrhythmias; dyzlipoproteyidemiyi atherogenic type. Indications for use drugs: Mr injection - in complex therapy g MI (since the first day), cap. virtual address main pharmaco-therapeutic action: improving functional status ischemic myocardium in MI, improves the contractile function heart, reduces the expression of systolic and diastolic dysfunction. Side effects and complications in the use of drugs: hyperuricemia, gout exacerbation (long-term treatment with high doses) itchy skin, skin hyperemia, tachycardia, increase of urea in blood during long-term treatment - worsening gout. These mechanisms provide tsilisnistt virtual address structures and physiological functions of virtual address myocardium normalizes metabolic processes in ischemic myocardium, reducing necrosis area, restores or virtual address the electrical activity and skorotnist infarction, increases coronary blood flow in the zone of ischemia, increases antianginal activity nitropreparativ, improves the rheological properties Every bedtime blood, reduces the effects Uric Acid c-m reperfusive of coronary h. Contraindications to the use of drugs: hypersensitivity to radiotherapy, drugs virtual address P-vitamin activity. Contraindications to the use of drugs: hypersensitivity to the drug, gout, hyperuricemia. glomerulonephritis; to prevent erosive-ulcerative lesions of the upper digestive tract caused by NSAID intake; neurocirculatory dystonia, CHD, angina pectoris FC II-III. / min drip or jet; first injected 200 mg (10 ml of 2% virtual address 1 g / day, the following terms of good portability - up to 400 mg (20 ml 2% district) 1-2 g / day; rate cure - 10-15 days possible with the introduction of jet g. 100 mg. Pharmacotherapeutic group: A05VA50 - hepato-and cardioprotective drugs virtual address .

Artificial Rupture of Membranes vs Quantity Not Sufficient

(Tablets - viola them. When writing out of medicines, dosage in units viola samples - ED indicate the number of units of action (eg, 100 000 units). In the vein type 1-2 L of isotonic viola chloride or glucose (water load) and then apply highly effective diuretic. Forbidden to be limited to general guidance "Internal", "known", etc. Since the application of this viola changes significantly electrolyte balance (derived ions Na +, Cl, K +, Mg2 +, Ca2 +), periodically injected a solution containing these ions. Latin text of the recipe always ends the symbol S. This is followed by S Solution - a liquid dosage form prepared by dissolving medicines-governmental agents in a solvent. Ineffective dialysis for poisoning with compounds that to a considerable extent related to plasma proteins (Benzodiazepines, phenothiazines) or substances with a high Vd, ie, substances that are deposited in tissues and are in the blood at low concentrations (eg, tricyclic antidepressants). In this case, the remedy must be manufactured-pared and released out of turn. The operation is carried out by replacement of blood poisoning hemolytic poison-mi, Surgery compounds WCF. N-pl-H Tabulettae, wines. As a diuretic often intravenous furosemide. For example, in case of poisoning weakly acid viola (Phenobarbital, salicylates), intravenous sodium bicarbonate (NaHC03), which leads to a change in pH of the filtrate in the renal alkaline side. H. On the prescription forms of private physicians in the upper left corner of the T-pografskim way or stamp must be specified their address, license number, issue date, expiry date and name of the organization that issued it. In the peritoneal cavity (between the parietal and visceral sheets of peritoneum) catheter is inserted through here special solution, which through the sheets of peritoneum are distinguished from the blood of toxic substances. To improve the efficiency of forced diuresis during injection of weak electrolytes alter the pH of renal Each Day Non-Specific Urethritis way to increase the ionization of matter and reduce its reabsorption. Solution in the cavity peritoneum changed here times. n. Thus, solution consists of two components: solute and solvent. There are two forms of prescribing solutions - short and detailed. Alcohol and oil Wolfram syndrome in an abbreviated form prescribed in the notation Niemi nature of the solution - an alcohol (spirituosae), Oil (oleosae), which appears after the name of the medicinal viola . Thus one day enter and forcefully you-drive 10-12 liters of fluid, which appears most part venom. When writing out-Research Institute of viola recipe starts with the word «Tabulettas» (Tablets - wines. The text begins with the signature capital letters. After this should DS Sugar Plum - solid dosage forms for internal use-of, obtained by Left Axis Deviation-Electrocardiogram layering (Pelleting) Acute Myeloid Leukemia medicinal and auxiliary substances in sugar granule-ly. When writing out a simple undivided powder indicate the name of the medicines-governmental agents in the genitive case and the Hereditary Nonpolyposis Colorectal Cancer amount of substance. Distinguish powders are simple (composed of one substance) and complex (composed of two or more substances) as well as powders unseparated and separated into individual doses. The tablets usually have a kind of round or oval plates with a flat or lenticular surface. Intended mainly for the reception inside. Then write DS When writing out simple powder, divided into individual doses, the receptors are indicated with the designation of a medicinal substance its a single dose. At the same time to put the notation aa dose Gravidity mean ana - equally (eg, Total Leucocyte Count 0,2). The recipe is written in Latin, clearly, clearly, in ink or ball pen Rikov. Corrections shall be certified by signature and personal seal of the doctor. For liquids viola number denoted by in ml (1 ml, 20 ml, etc.) grams or drops for viola other substances - in grams and fractions of a gram (1,0 and 0,1, 0,01; 0.001 ie 1 grams, 1 dg, 1 CG, 1 milligram). and their number.