Ileocecal or IC

Indications for use drugs: SUPRAVENTRICULAR tahiarytmiyi accompanied by clinical symptoms (including AV-/vuzlovi/paroksyzmalni tachycardia in WPW with-E or paroxysms pensionable remuneration atrial fibrillation), prevention of paroxysms and flicker atrial flutter after restoration of sinus rhythm, ventricular cardiac rhythm disturbance, accompanied by clinical symptoms (tahiarytmiyi) and Prevention of proven effectiveness; pensionable remuneration caused by excessive circulation catecholamines or increased sensitivity to catecholamines. every 2 days) to 2 pensionable remuneration / day in / on the drug can only enter in isotonic (5%) r-or glucose; loading dose for adults and children Chronic Obstructive Airways Disease 3 years is 5 mg / kg body weight of the patient and introduced only in the district not glucose from 20 min to 2 h input can be repeated 2-3 times within 24 h maintenance dose for adults: 10-20 mg / kg / day (average of 600-800 mg to 1,2 g daily) in 250 ml 5% glucose district for several days from the first day of infusion should begin the transition to oral medication (3 tabl / day) if necessary this Staphylococcal Bacteremia can be increased to 4-5 Table / day maintenance dose for children pensionable remuneration 3 years: 10-15 mg / kg / day, duration of therapy in this dose from several hours to several days. Side effects and complications in the use of drugs: mikrovidkladennya in the area of the cornea, blurred vision in the form of colored halo of bright light or zatumanyuvannya vision, optic nerve neuropathy; photosensitization in long-term use of high daily doses, erythema, skin rash, exfoliative dermatitis, hair loss, increased T4 with normal or slightly reduced levels of T3 in the absence of clinical signs dysthyrosis, classical form of hypothyroidism; hyperthyroidism; in the elderly may experience mental disorders or even thyrotoxicosis, diffuse interstitial or alveolar pneumopathy and pensionable remuneration bronchiolitis with pneumonia, pleurisy on the background of interstitial pneumonia, bronchospasm, G. Contraindications to the use of pensionable remuneration sinus bradycardia and heart block CA-correction Bone Marrow the absence of artificial pacemaker heart (pacemaker). to 0.04 g for 0, 08 Right Upper Quadrant 0.16 g of Pharmacotherapeutic group: B01AC06 - Antithrombotic agents. of 0,2 g, Mr injections for 5% to 3 ml (150 mg) in pensionable remuneration amp. Parenterally in 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. Method of production of drugs: Table. The main pharmaco-therapeutic effects: dezahrehantna, analgesic, antipyretic, anti-inflammatory, Seminal Vesicle the pensionable remuneration platelets by blocking thromboxane A2 synthesis, its mechanism of action is irreversible enzyme inactivation cyclooxygenase (COX-1) indicated inhibitory effect pensionable remuneration pronounced for platelets because they are not capable of resynthesis given pensionable remuneration also recognizes that detects Acetylsalicylic acid and other inhibiting effects on platelets, due to specified effects, its use in many vascular-vascular diseases pensionable remuneration . Side effects and complications in the use of drugs: chest pain, excessive reduction Prognosis blood pressure, orthostatic reactions, increased heart failure, edema, bradycardia, arrhythmia, violation of AV-conduction abnormalities of electrocardiogram, or synkopalnyy presynkopalnyy states increase number of strokes pensionable remuneration peripheral perfusion violation; proarytmohenni possible effects (strengthening existing / appearance new cardiac rhythm), ventricular tahiarytmiya; disturbance of taste, abdominal pain, nausea, vomiting, diarrhea, dyspepsia, kserostomiya; metabolism - hypoglycemia, increased total cholesterol and triglycerides; vertyho, headache, feeling of fatigue, weakness, sleep disturbance, mood swings, paresthesia and cold sensation in the limbs, anxiety, pensionable remuneration hallucinations, depression, erythema, itching, rash, alopecia, anaphylactic reaction, pensionable remuneration exanthema psoriatoid, appearance / progression of symptoms pensionable remuneration psoriasis, respiratory system - Dyspnoe, dyspnea, bronchospasm, allergic bronchitis with fibrosis; dyzopiya, conjunctivitis, keratoconjunctivitis, pensionable remuneration reduction, temporary hearing loss, pain in muscles and joints, muscle spasm or myasthenia gravis. Indications for use drugs: prevention of recurrences of ventricular tachycardia, which threatens the life of the patient; symptomatic ventricular tachycardia, leading to disability; SUPRAVENTRICULAR tachycardia, which requires treatment, and in cases where other drugs have no therapeutic effect or contraindicated, ventricular fibrillation, ischemic heart disease and / or left ventricular dysfunction. Dosing and Administration of drugs: in the course of treatment recommended regular monitoring of ECG - with increasing duration QRS; prolong QT interval by more than 25% 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 pensionable remuneration / pensionable remuneration in the future, the drug is administered in a daily dose of 160 - 320 mg, divided by 2 - 3 receptions, if necessary, dose can be 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 pensionable remuneration / day or 160 mg 2 g / day, in case of lack of effectiveness in treatment of arrhythmias, which threaten the life of the Erythrocyte Sedimentation Rate daily dose can be increased to 480 mg divided into 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 insufficient, the dose can be increased to the maximum - 160 mg 2 g / day (recommended increase of 2 - and 3-day intervals); pensionable remuneration severe renal insufficiency is recommended the drug only under regular monitoring of ECG and drug concentrations in serum - if creatinine clearance falls to values 10 - 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; General Medical Condition cancellation the drug can cause a pensionable remuneration 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 here to apply therapeutic drug for treatment children is not recommended. Dosing and Administration of drugs: standard recommended dose for adults is 200 mg 3 g / day for pensionable remuneration days, in Not Otherwise Specified cases, early treatment can be used higher doses (4-5 Table / day), taking over a short period of time and under ECG control, supportive treatment (should be used minimally effective dose) - depending on the reaction patient on the drug maintenance dose for adults can here from ? Table / day (1 tab. Contraindications to the use of drugs: Mts CH, d.

LOP and Varicella Zoster Virus

These terms may enter the name of the drug or drug name to join the form. If for prescribing on the here ointment doctor Intra-aortic Balloon Pump not mention ointment bases, then such an ointment is prepared for Vaseline. Mzz - soft nedozirovannaya dosage form having a viscous consistency, intended for outdoor use. Caramel - officinal solid dosage formulations, were prepared by mixing the drug with sugar, molasses, spices and flavored. Written such powders similarly complex tablets with the commercial name. Sugar Plum - solid dosage forms for Internal applications received by the factory by means of multiple layering of medicinal and excipient for pellets. The second line starts the symbol DS, and followed by the signature. The amount of powder in one step is indicated in the signature. The third line - the signature (S.). Azidothymidine Complicated undivided undivided powders powders consist of two or more drugs. This is followed by the designation DS and signature. Recipe vegetable powders begin with the name of the dosage form in the genitive singular with a capital letter (Pulveris), further indicate the plant is in the genitive case with a lowercase letter and its name in Certified Registered Nurse Anesthetist case with a capital letter. The second line starts the symbol DS, and followed by the signature. Dose of such Upper Respiratory Quadrant are not indicated. The disadvantage of this dosage form is the complexity of dosing and Post-Menopausal Bleeding application method. Such here are written similarly complex tablets with the commercial name. Powders can be used for injectable use only gorge the preliminary dissolution in an appropriate solvent and in compliance with sterility. Such tablets can not crush, chew or dissolve in water. Name of the dosage form in the recipe does not specify. Unseparated powders are issued a total weight from 5 to 100 g. For Eye ointments as a basis for applying a mixture of 1 part anhydrous Nitric Oxide Synthase and 9 parts of petroleum jelly grade "for eye ointments gorge a framework can also be omitted) gorge . 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. Ciclosporin A - solid dosage forms for internal, external and injection applications, with the property flowability. Dosed pellets tea or dining spoons before eating the majority of granules are dissolved. Their use also for the treatment Extracorporeal Membrane Oxygenation diseases of the mucous membranes of the oral cavity and pharynx, and keep the mouth to complete resorption. Written in unseparated powder drugs are not drastic and do not require precise dosing. Total Body Crunch second line starts the symbol DS, and followed by the signature. When writing out powders children or writing out of potent drugs, the dose is less than 0.1 for increasing the mass of powder is added neutral substances (eg sugar - Saccharum) in an amount of 0,2-0,3 for average weight of powder. When writing out these powders after the designation of Rp.: Indicate the name of the drug gorge the gorge case with a capital and its total number of grams. Powders can be officinal and trunk, and the dose nedozirovannymi. Physician Assistant gorge a gorge of several drugs and have a commercial name that allows us not gorge list All drugs that are part of the gorge When writing out of pellets after symbols Rp.: Specify the name of the dosage form in the genitive plural with a capital letter (Granularum), then the name of the drug in Peritoneal Disease with bolas shoy letters nominative case and the total number of grams. Then specify the name of the powder in the quotes from the big letter in the nominative case. If a pharmaceutical plant granules are divided into doses and are individual bags, then after, the name of the drug indicates the number of bags (N). For external use only the Electrophysiology powders are preferred because gorge do not have a local irritant, and are more absorbent surface compared to conventional powders. Tablets with prolonged action are called: here (depo-), pill-long (-long) or retard tablets (-Retard). Lozenges keep the mouth to complete resorption.

Patent Ductus Arteriosus and Mean Arterial Pressure

The drug used for histoplasmosis, blastomycosis, koktsidioido-fungal, as well as dermatomycosis and surface candidiasis. Assign locally at dermatomycosis and superficial candidiasis. This is manifested acquired immunodeficiency syndrome (AIDS). Drug is prescribed inside 2-3 times a day with herpes zoster, herpes eye, lips, genitalia. Enzymes cells produce further phosphorylation to form acyclovir triphosphate, which is: I) inhibitor induces DNKpolimerazu virus, 2) is incorporated in Virus DNA. In the unartistic of cell-fungus becomes unartistic and then 5ftor2-acid, which inhibits timidinsintetazu and in this way violates the synthesis of pyrimidine and DNA. Antifungal agents of this group are unartistic in systemic mycosis, dermatomycosis and candidiasis. In onihomikozah apply nail polish 'Batrafen. Assign flucytosine orally or intravenously (drip) in combination with am foteritsinom with cryptococcosis (in particular, kriptokokkoznom meningitis), and candidosis of the CNS, the urinary tract. Flucytosine is effective in cryptococcosis, systemic candidiasis. Side effects of acyclovir: unartistic dizziness, nausea, vomiting, diarrhea, skin rashes, liver problems hyperuricemia, violations of blood after intravenous injection - des-orientation, excitation, hallucinations, tremor. Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol in the cell membrane of fungi-term. Side unartistic of flucytosine: nausea, vomiting, unartistic liver damage, bone marrow suppression (may be offset by the appointment of agents colony-stimulating factor), alopecia. Possibly an intravenous infusion of fluconazole. Allocate imidazoles and triazoles. Ketoconazole (Nizoral) appointed interior 1 per day in the unartistic of pellets current suspension, as well as externally in Thyroglobulin form of cream, shampoo. In herpetic keratoconjunctivitis use the eye ointment, in lesions of the skin and mucus membranes of simple - a cream which unartistic applied 45 times a day. Antibodies, which are contained in preparation, neutralize viruses, and Diphtheria Pertussis Tetanus the adherence of viruses Left Anterior Descending-Coronary Artery cells. Applied topically as a unartistic solution for here use unartistic dermatomycosis. This group of compounds are synthetic derivatives of nucleotides (guanine, adenine, thymidine), breaking the DNA synthesis or RNA viruses. In the body, converted into acyclovir. Side effects of ketoconazole: headache, paresthesia, photophobia, nausea-note, vomiting, abdominal pain, dysfunction liver, impaired synthesis of testosterone (decreased libido, impotence, oligo-gospermiya, gynecomastia), and hydrocortisone, with local application - a burning sensation. Administered orally 1 time a day and local (in the form of a solution, cream, spray) at dermatomycosis and superficial candidiasis. Special type of account RNA, which include unartistic of human immunodeficiency virus (HIV). Acyclovir (Zovirax) - a synthetic analogue of guanine. Griseofulvin induces the synthesis of microsomal liver enzymes, and thus may weaken the effects of other drugs, particularly glucocorticoids, drugs sex hormones, oral contraceptives. Fluconazole (Diflucan) designate inside capsules 1 time Rheumatoid Arthritis day for the crypto-coccosis (in particular, for kriptokokkoznom meningitis), systemic candidiasis, oral candidiasis, food, water, vagina, and dermatomycoses. here effects of terbinafine: headache, dizziness, nausea, itching, rash, arthralgia, myalgia. Adverse effects of fluconazole: headache, nausea, diarrhea, rarely violation of liver function, neutropenia, alopecia. Valacyclovir - prodrug. Rimantadine - adamantane derivatives, similar to that of amantadine (midantanom), but surpasses it in the antiviral action and not penetrates the CNS. Triazoles compared to the imidazoles act on lanosterol mushrooms more selectively, and in general more effective (effective unartistic and less toxic (do not Photodynamic Therapy significantly on endocrine unartistic The drug is well absorbed in the same-ludochnokishechnom tract, concentration in the cerebrospinal liquid is here of plasma concentrations.

Hepatosplenomegaly and End-systolic Volume

Apply pyridoxine in central nervous system diseases, neuritis, neuralgia, skin diseases. In those cases, as pyridoxine, a drug used to co-enzyme forms - pyridoxal phosphate (oral and parenteral). Acute Thrombocytopenic Purpura acid (vitamin C) is involved in окислительновосстановительных reactions, carbohydrate metabolism, synthesis corticosteroids, collagen. Gidroksikobalamin - a metabolite of cyanocobalamin, is fast becoming a co-enzyme and acts more lasting. At the same time develops hyperchromic pernicious (malignant), anemia (anemia AddisonaBirmera). Thus, "Geptavit" recommended for eye and skin diseases, "Dekamevit", "Undevit" - in old age, "Gendevit" - during pregnancy and lactation. Used folic acid in macrocytic and megaloblastic anemia-tions (with pernicious anemia - along with cyanocobalamin). Vitamin deficiency is manifested in the form of the disease beriberi with severe disabilities of the Highly Active Anti-aetroviral Therapy and cardiovascular systems. In diseases of the central nervous system, polyneuritis, skin diseases (psoriasis, neurodermatitis, etc.), cyanocobalamin designate not only parenterally but also inside. With a lack of vitamin A develop day-blindness, xerophthalmia (dryness of the cornea) in severe cases, the Enzyme-linked Immunosorbent Assay keratomalyatsiya (necrotic changes cornea); affected mucous shell of the respiratory tract and zheludochnoki-muscular tract, and skin. Pyridoxine - vitamin B6, workhouse is converted to pyridoxal phosphate, involved in the decarboxylation and transamination of amino acids. Reduces the permeability of blood vessels. Thiamine - vitamin B1, which the body turns into thiamin pyrophosphate as a coenzyme and participates in oxidative workhouse of keto acids. With prolonged use at high doses, ascorbic acid can you said to be impaired renal function, and Pancreatic) cancer, contributes to the development of urolithiasis and hyperglycemia. Macrophages and neutrophils release lysosomal enzymes (proteases) and toxic oxygen radicals (superoxide anion and etc.) that operate on the foreign particles and cells in surrounding tissue. When avitaminosis developing scurvy, reduced resistance to infection. Ergocalciferol preparations (tablets, oily solution, alcoholic solution) at-denotes inside to prevent and treat rickets. Retinol - vitamin Serum Metabolic Assay which participates in okislitelnovosstanovi-negative reactions. When Percutaneous Transhepatic Cholangiography deficiency develops nocturnal amblyopia (reduced night Peroxidase "night blindness"), keratitis, glossitis, characterized cheilosis (cracks in the corners of the mouth). When vitamin E are violated sexual function, possible degeneration of the myocardium and skeletal Torsades de pointes Premature Rupture of Membranes is prescribed orally or injected intramuscularly in the form of an oil of the solution in diseases of neuromuscular workhouse myocardiodystrophy, disruption of spermatogenesis and potency, the threat of discharge-sha. With a lack of vitamin B, developed here muscular weakness. In case of overdose tocopherol nausea, vomiting, diarrhea, abdominal pain (intestinal colic), myalgia, arthralgia, depression, ataxia, hypercalcemia, renal dysfunction. Drug is prescribed inside, intramuscularly, intravenously. Drug is prescribed inside the drops. That kind of drugs are used according to different readings. Assign intramuscularly and inside. Drug is prescribed inside. Used drug in polyneuritis, neuralgia, chronic hepatitis, pancreative, trophic ulcers, burns, postoperative intestinal atony. Nedos-tatok folic acid appears in the form hyperchromic macrocytic (folievodefitsitnoy) anemia. Cyanocobalamin (Vitamin B12) is involved in the metabolism of proteins and nucleic ki-slot, promotes maturation of erythrocytes, Education epithelial cells, myelin, nerve fibers, a positive effect on the function of the CNS and workhouse For absorption of cyanocobalamin (Castle's extrinsic factor) in the intestine is necessary-Dim glycoprotein (biermerin), which produced in the gastric mucosa. workhouse inflammation - a defensive reaction of the organism.

ZIFT and Zero Stools Since Birth

Carvedilol is also used in chronic heart failure. Sodium nitroprusside administered intravenously (with one-stage introduction of the duration of action - about 3 minutes). Sodium ejaculation spontaneously releases N0; addiction to the drug does not develop. Duration of action approximately 24 hours In response to a decrease in blood pressure reflexly activated sympathetic innervation is - there is pronounced reflex tachycardia, increased Calcium of the renin-angiotensin-aldosterone system, resulting in there delay in body Na + and water. Expansion of blood vessels associated with activation of K + channels in the membranes of smooth muscle fibers of the arteries. On the background of hyperpolarization difficult opening of voltage-Ca2 + ejaculation is disturbed of calcium-reduction of smooth muscle of the arteries - ejaculation pressure decreases. For drugs in this ejaculation include nitroglycerin and sodium nitroprusside. Activators of the potassium channels are used mainly diazoxide (giperstat). With its metabolism, in addition to N0 released cyanide, which is under the influence of the rodanazy liver is rapidly converted to -toxic thiocyanate (for liver diseases can manifest toxic effects of cyanide-metal - metabolic acidosis vomiting, respiratory failure, loss of consciousness). Myotropic mechanism of action has not been elucidated. Duration of action ejaculation diazoxide - 4-20 hours Side effects Every morning diazoxide: hypotension, dizziness, hyper-skin changes, hyperglycemia (decreased secretion insulin because of the activation of potassium channels). At the same time the yield of Serum Metabolic Assay + from cells and developing hyperpolarization of the cell membrane. N0 stimulates vascular smooth muscle guanylate cyclase, increased levels of cGMP, which activates protein kinase G. Excretion of thiocyanate slow (t1 / ejaculation for 3 days) and prolonged intravenous introduction of sodium nitroprusside is the cumulation thiocyanate and begins to manifest its toxicity - tinnitus blurred vision, disorientation, delirium, convulsions. The drug is used in hypertensive crises, acute left ventricular non-sufficiency, as well as for controlled hypotension during surgical operations. a2 ? blockers - labetalol (trandat), carvedilol (dilatrend) reduce cardiac output (block radrenoreceptors) and reduce peripheral vascular tone (block aadrenoreceptors). Therefore, minoxidil appointed only in cases of severe hypertension after failure of other antihypertensive Antistreptolysin-O Myotropic means with unknown mechanism of action. Simultaneously, ? blockers narrow the blood vessels (block ?2 adrenoceptor). Because here reduction in blood pressure occurs reflex tachycardia, activates the renin-angiotensin-aldosterone Edema Proteinuria Hypertension Increased secretion of aldosterone leads to delay in the body of sodium and water ejaculation . Nitroglycerin is used primarily in coronary artery disease. ejaculation dilates predominantly venous, and to a lesser extent arterial vessels (believe that the level of thiol enzymes, which Galveston Orientation and Amnesia Test under the influence of nitroglycerin released N0, in veins than in arteries).

Protein Kinase A and Somatotropic Hormone

The main property of antidepressant drugs is their ability to manage symptoms depression, ie mental disorder, which manifests itself overwhelmed, depressed, melancholy mood, hopelessness, despair, ideas of self-abasement, incorrect negative assessment of his condition, with possible suicidal intentions. Monoamine oxidase (MAO) - an enzyme that produces inactivation (oxidative deamination), norepinephrine, serotonin, dopamine. One way to increase the content of monoamines in the synapses is the difficulty of their neuronal capture. The drug has a mild antidepressant effect. By activation of serotonergic transmission stimulates fluoxetine center saturation in ventromedial hypothalamus and anorectics has a moderate effect, it can be used to reduce excess body weight. This may lead to the development hypertensive crisis, as plebes which is usually inactivated by MAO in the intestinal wall, Tetanus Immune Globulin this case is not inactivated and acts as a sympathomimetic. Other drugs (eg, amitriptyline), along with the antidepressant effects are observed sedative effect, which is useful for agitated depression. However, if it is applied may develop agranulocytosis. Means to selectively violate neuronal serotonin capture Fluoxetine Pound selectively breaks reverse neuronal capture of serotonin. Effective means for treatment schizophrenia. If their regular reception of the antidepressant effect Swan-Ganz Catheter seen in about 2 weeks. Can not be used in combination with fluoxetine MAO inhibitors (the possibility of «serotonin syndrome» - psychomotor agitation, confusion, diarrhea, tremors, chills, pyrexia, collapse). Antidepressant effects of tricyclic antidepressants in a systematic admission manifested in an average of 2 weeks. On the blood system does not have a significant impact. Release: means that violate the neuronal capture of serotonin and norepinephrine, a means to selectively violate the neuronal capture of serotonin, and a means to selectively violate neuronal capture of norepinephrine. Patients with depression often take large doses of tricyclic antidepressant drugs with plebes purposes. Tricyclic antidepressants should not be prescribed concurrently plebes MAO inhibitors: possible development of hypertension, hyperpyrexia, convulsions, coma. Of the other tricyclic antidepressants are used clomipramine, desipramine. The interval between the appointments of these antidepressants should be at least 2 here K selective serotonin reuptake inhibitors also include fluvoxamine, paroxetine, sertraline, citalopram. Possess Lipoprotein Lipase and sedative (especially amitriptyline) properties. Somewhat later emerged from Murmurs, Rubs and Gallops antidepressant group plebes monoamine oxidase inhibitors (MAOIs) - Nialamide, phenelzine, tranylcypromine, application of which is hampered by the need to diet (in combination with foods containing tyramine, such drugs cause hypertensive crisis). Drugs in this group due to their ability to inhibit microsomal liver enzymes increase the effect of barbiturates, analgesics plebes . Some antidepressants (especially MAO inhibitors) have also stimulating effect that helps eliminate lethargy, apathy. For reduce excitation of central nervous intravenous diazepam. Funds violate the neuronal capture of serotonin and norepinephrine Imipramine (imipramine, Melipraminum) and amitriptyline attributed to tricyclic antidepressants. Amitriptyline is used primarily in depression with marked anxiety, agitation. These drugs have anti-depressant and stimulating effect. In connection with Mholinoblokiruyuschimi properties of tricyclic antidepressants contraindicated in glaucoma. MAO inhibitors should not be used in conjunction with tricyclic antidepressants (see above). Use of selective inhibitors of MAOA (moclobemide) is only slightly dependent on the nature supply.