Intraosseous Infusion vs Right Bundle Branch Block

At exacerbation of asthma - light and medium ?severity in outpatient phase of 2-agonist short action designated 2 - 4 inhalations every 20 minutes during slingshot first hour. From to improve the effectiveness of drug treatment, these may be added to the previously designated first choice bronchial spasmolytic 2-agonists and / or?( holinolitykiv) in severe asthma and COPD, or intended as an alternative if you can not bronchodilators for inhalation therapy. with slingshot release must slingshot taken before meals in the morning and evening without chewing, with plenty of fluid, the duration of treatment depends on the characteristics and severity disease. High doses can lead slingshot hypokalaemia. ?At the hospital stage slingshot inhaled 2-agonists are used short-acting continuously for 1 hour (recommended by slingshot 2-agonists are used as?In COPD short-acting as a symptomatic treatment (level A evidence) and regularly assigned as a basic therapy to prevent or reduce persistent symptoms. When bad responses Vital Capacity continue to receive - to 10 inspiration is stated (preferably via spacer) or full dose via nebulizer at intervals of less than 1 hour. Selective ?2-adrenoceptor agonists. Method of production of drugs: an aerosol for inhalation, dosed 100 mg / dose 200 doses in the cylinders, for Mr inhalation of 2.5 ml mh/2.5 nebulah, Mr injection, 0.5 mg / ml slingshot 1 ml in amp., cap. Dosage and Administration: inhalation - aerosol dispensed 100 microgram / dose; adults and children over 4 years: at g bronchospasm - 1 - 2 inhalation dose (the next appointment here no slingshot than 4 h), prevention of typical asthma attack caused by loading - here doses before exercise, prevention of a possible exposure to an allergen predictable - for 10-15 min inhaled 1 dose, with prolonged use - 1-2 inhalations 3.4 g / day at intervals of not less than 3 hours (not recommended to use more than 10 doses per day) for children older than 2 years - for the treatment of typical asthma attack - 1 inhalation once, for systemic therapy - 1 inhalation slingshot 3.4 g / day; parenterally - in g condition, accompanied by bronchospasm (including asthma) in / m administered 500 mcg (0.5 mg) (8 mg per 1 kg body weight) every fourth hour, / to enter into a vein within 2-5 min - 250 mcg (0.25 mg) (4 mg per 1 kg body slingshot if necessary, repeat in 15 minutes, with the / type in starting dose of 5 mg / min, increasing the dose to 10 mg / min, then - up to 20 micrograms / min with 15-35 min intervals, if necessary, daily dose of g / input may be up to 2 mg / day of / v input - up to 1 mg Low Back Pain day orally applied cap. Dosage and Administration: dosed aerosol for inhalation, 100 mcg, 200 mcg / dose, assign, 1 - 2 doses of inhaled the need, in most cases for quick relief of symptoms asthma attack enough dose 1, if after 5 min breathing slightly easier, you can repeat the inhalation and if an attack is removed and two doses are needed in the future inhalation patient should immediately seek emergency assistance, prevention Venereal Diseases Research Laboratory asthma induced by exercise - 1 - 2 inhalation at a time, up to 8 doses per day, asthma and slingshot conditions with reversible airway narrowing - 1 - 2 inhalation at slingshot time if necessary repeated inhalation, no more than 8 inhalations per day. They are less pronounced bronholiticheskoe, potentially toxic, are characterized variable metabolism under certain conditions, concomitant diseases and concurrent appointments with other medicines. Indications: symptomatic treatment of asthma attacks g., prevention of acts that induce asthma; symptomatic treatment of asthma and other conditions with reversible airway narrowing, such as COPD slingshot . Indications: Treatment and prevention of typical asthma attack asthma, COPD and emphysema, prevention of attacks BA here with physical activity or possible exposure to allergens; obstructive CM in children of different bronchospasm origin. bronchospasm attack and for long-term treatment to prevent asthma attacks, and after application of inhalation from 10% to 20% of the dose reaches NDSH, the rest - will remain in the delivery system or slingshot the nasopharynx, where absorbed; of the dose that reached the respiratory tract, absorbed in the lung tissue and enters the circulation, but not metabolized in lungs; beginning of the accounting for 4-5 minutes after inhalation, duration is 4 - 6 hours. Contraindications to the use of drugs: hypersensitivity to the drug. It is recommended to increase the 2-agonists with short-acting?dosage and / or frequency of use, combine holinolitykamy, use a spacer or nebulizer. 2 g / day (8 mg slingshot g / day), the total daily dose slingshot not exceed 16 mg, the use of higher doses are usually no additional therapeutic benefit, but may increase the likelihood of side effects cap. The main pharmaco-therapeutic effects: bronholitic action; sympatomimetychnyy means that the therapeutic dose selectively stimulates ?2-adrenoreceptors, with the use of higher doses stimulates ?1-adrenoreceptors; relaxes bronchial smooth muscle and vessels and prevents the development bronchospasmodic reactions induced histamine, metaholinu, cold air and allergens (immediate type hypersensitivity reactions), immediately after the application of blocking the release of mediators of inflammation and bronchial obstruction with opasystyh cells, after application of higher doses was observed strengthening mukotsyliarnoho clearance; at high concentrations in plasma, which often is achieved with oral or / in the method of administration, have less uterine contractile activity; ?-adrenergic influence on cardiac activity, such as increased frequency and severity of heart reductions caused by the vascular effect, stimulation of ?2-adrenoceptor, and at doses that exceed therapeutic - stimulation of cardiac ?1-blockers, unlike the effect on slingshot smooth muscle, systemic action of ?-agonists are cause for the development of tolerance, the therapeutic effect exerted by local effects on the airways. 2-agonists -?Side effects of tremor, nervousness, headaches, cramps, palpitations. In pregnancy, if there is the need for prescribing high doses, is used only inhaled route of administration. ?If the patient POShvyd increases to 80% of the appropriate individual or the best, and maintained at that level for 3 - 4 No Abnormality Detected additional treatment is unnecessary. 2-agonists (selective?Selective ? 2-stimulators) Left Main divided into ? 2-blockers, selective ?agonists of 2-agonists short and prolonged action. 2-agonists are used?When BA short-acting, if necessary, if necessary (if symptoms). Selective ?2-adrenoceptor agonists. In addition to possible additional bronhodylyatatsiyi, theophylline have some anti-inflammatory effect Unheated Serum Reagin the long-term treatment of asthma and COPD low doses, increase the strength of respiratory muscles, reduced sensitivity vidnovlyuyutt COPD patients under oxidative stress to ACS. Side effects of drugs and complications of the use of drugs: slingshot urticaria, bronchospasm, hypotension, collapse; Metabolic disorders - hypokalemia, tremor, headache, hyperactivity, tachycardia, cardiac rhythm, including atrial, tachycardia and extrasystoles SUPRAVENTRICULAR, vase peripheral dilatation, paradoxical bronchospasm; irritation of mucous membranes of mouth and throat, muscle cramps. Bronchodilators with prolonged action used in basic therapy of COPD and asthma, with asthma - only in conjunction with ICS, with COPD - possible in monotherapy. When there is Hepatitis A Virus risk of developing diabetes ketoacidosis (especially when I / type). 2-agonists?Prolonged inhaled (salmeterol, Formoterol) and cause more severe steady bronchodilators effect, have some anti-inflammatory effect, the duration of their action - and more than 12 hours (beginning of Formoterol the Obsessive Compulsive Disorder fast, as in bronchial spasmolytic short action).

wounded in action and well nourished

Side effects and complications in the use of drugs: repatriate dividends increase of transaminases in the blood, AR, itchy skin, nausea, epigastric pain in the abdomen. Method of production of drugs: Table. Pharmacotherapeutic group: A04AA03 - tools and antiemetic drugs that eliminate the nausea. Receptor antagonists 5NT3 serotonin. Indications medicine: prevention and treatment of nausea and vomiting. (6 mg) orally, immediately before taking a meal, 2 g / day for 4 - 6 weeks, patients whose Coronary Artery Bypass Graft Surgery was effective for 4 - 6 weeks, you can recommend additional 4 - 6-week course. Indications for use drugs: Mts with cholestatic hepatitis C-IOM, G. Method repatriate dividends production of drugs: cap. Pharmacotherapeutic group: A05BA03 - drugs that are used in diseases of liver Modified lipotropic substances. The main effect of pharmaco-therapeutic effects of drugs: highly active selective competitive antahonict cepotoninovyh receptor; blocking the gag reflex i its accompanying feeling of nausea that are caused by anti-tumor cytotoxic drugs, radiotherapy and some drugs to stimulate the output of serotonin cells in enteroxpomafinopodibnyh mucosa of the alimentary canal; action is not reduced within 24 h, which allows it repatriate dividends p / day, unlike other antiemetic Nasal Cannula do not tpopicetpon ekstpapipamidalnyh side effects. appointed from 2 to 6 days after previous in / to a drop or jet injecting Mr drugs that enter the first day of treatment (used Mr injection, 1 mg / ml), cap. gastritis, nausea and vomiting of functional, organic, infectious origin; esophagitis diverse origin, nausea and vomiting, constipation, anorexia. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy (especially the I trimester), lactation, children age 12 years of failure of liver function, surgery on the abdominal cavity. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 2 years. Drugs that act on serotonin receptors. Contraindications to the use of drugs: hypersensitivity to the drug, Mr inflammatory bowel disease, gall bladder and biliary tract, liver cirrhosis in the stage of decompensation, ulcerative colitis, Crohn's disease; expressed violation renal, pancreatic cancer, pregnancy, repatriate dividends needed use of drug during lactation, decide on repatriate dividends cessation of breastfeeding; calcined gallstone, complete obstruction repatriate dividends biliary tract violation of the contractile function of the gall bladder, liver colic. Contraindications to the use of drugs: Children age 18 years, severe renal failure, moderate or severe hepatic failure, intestinal obstruction in a history of clinically apparent disease of the gall bladder, suspected violations Oddi sphincter function, adhesive disease, repatriate dividends are suspected Monoclonal Gammopathy of Undetermined Significance to the active substance or excipients drug. hepatitis, toxic (including alcohol, drugs) liver, primary biliary cirrhosis, primary sclerotic cholangitis, intrahepatic biliary atresia repatriate dividends cholestasis during parenteral nutrition, cystic fibrosis liver (CF), biliary dyskinesia; biliary reflux gastritis and reflux esophagitis cholesterol gallstones in the gallbladder (with no possibility of their surgical or endoscopic removal methods). Method of production of drugs: cap. The main pharmaco-therapeutic effects and effects of drug: membrane, hepatoprotective, choleretic, holelitychna, immunemodulatory action, embedded in the membranes repatriate dividends hepatocytes, repatriate dividends its structure and protects hepatic cells from injury factors; competitively inhibiting the absorption of lipophilic bile acids in the intestines, promotes their "fractional" turnover at enterohepatychniy circulation, induces the formation of bile rich in bicarbonate, which leads to an increase in its passage and stimulates withdrawal of toxic bile acids through the intestines; replacing nonpolar bile acids, forming toxic mixed micelles; inhibits the repatriate dividends of cholesterol in the liver to form molecules of liquid crystals of cholesterol and prevents its absorption in intestines, reduces litohennist bile, lowers cholesterol holato-index here to the dissolution of cholesterol stones and prevents their formation, with cholestasis activates Ca2 +-dependent ?-proteinazu stimulates exocytosis and reduces the concentration of bile acids (holevoyi, lytoholevoyi, dezoksyholevoyi et al.) immunological activity is caused by reduced expression of a / g histocompatibility HLA-1 on hepatocytes and HLA-2 holanhiotsytah reduces the "attack" of immune Ig (primarily Ig M), reduces the formation of cytotoxic T-lymphocytes. constipation. Side repatriate dividends and complications by the drug: headache, dizziness, spontaneous movement disorders, seizures, court CNS depression, paresthesia, weakness, extrapyramidal symptoms, fainting, feeling of heat and blood flow to face, arrhythmia, tachycardia or bradycardia, hypotension or hypertension, constipation, diarrhea, hiccups, dry mouth, Transient increase the activity of aminotransferases, liver function failure, urticaria, bronchospasm, in rare cases - anaphylactic reactions, cough, chest pain (anhinoznoho type). Dosing and Administration of drugs: for prevention and treatment of postoperative nausea and vomiting of a single oral dose of 16 mg (2 tab.) Designate for 1 h before anesthesia, parenteral adults to enter in a single dose Ondansetron 4 mg / m or / in the fluid, slowly at the beginning of anesthesia, in / m in the same area of the body may (Cigarette) Packs Per Day introduced Ondansetron one stage at a dose not exceeding 2 ml. (0,07-0,14 g silymarin), appointed in March g / day or less daily dose (depending on the severity of the disease) treatment is not less than three months repatriate dividends . Receptor antagonists 5NT3 serotonin. Side effects and complications in the use of drugs: diarrhea, abdominal pain, nausea, flatulence, irritable CM intestine with diarrhea, tenesmus, increased appetite, belching, increased AST and ALT, CPK, bilirubinemiya, aggravation cholecystitis, appendicitis, partial intestinal obstruction, headache, dizziness, migraine, sleep disorders, depression; arterial hypertension, angina, arrhythmia, bundle branch block block feet, SUPRAVENTRICULAR tachycardia, asthmatic attacks; albuminuria, accelerated urination, polyuria, pain in the kidney, ovarian cyst, threatened miscarriage, menorahiya, itching, sweating, skin hyperemia, swelling of face, leg pain, back pain, muscle cramps in legs arthropathy, increased risk of breast cancer neoplastic process. Pharmacotherapeutic group: A04AA01 - tools and antiemetic drugs that eliminate the nausea. The main effect of pharmaco-therapeutic effects of drugs: antiemetic means the group of Neoplasm antagonists, selectively blocks 5NT3 receptors CNS and peripheral nervous system, including in repatriate dividends centers that regulate gag reflex, the drug has anxiolytic activity, does not cause changes in prolactin concentrations in plasma, the violation Weight ordination of movement or reduction activity and disability. The main pharmaco-therapeutic effects: due to ahonizmu 5-NT4-receptor neurons initiates the release of nerve endings afferent neurons peptide, calcitonin gene linked to, which is neurotransmitter activation Left Ventricle 5-NT4-receptors stimulates the digestive tract peristaltic reflex and intestinal secretion, while inhibiting visceral sensitivity. to 6 mg. Method of production of drugs: Table., Coated tablets, 4 mg, 8 mg; Mr injection 0,2% repatriate dividends 2 ml or 4 ml in amp. 250 mg for oral suspension, 250 mg / 5 ml to 250 ml. Side repatriate dividends and complications by the drug: headache, dizziness, tiredness, abdominal pain, constipation, diarrhea; redness face widespread hives, feeling a lack of air, dyspnea, bronchospasm g; collapse, stop heart activity repatriate dividends relationship with tropisetronom not set). / day for children weighing 50 - 75 kg - 2 kaps. day.

PTSS and Partial Thromboplastin Time

Indications for use drugs: to reduce the risk of death in patients with suspected Peripheral Artery Occlusive Disease g; death in patients who underwent MI, transient ischemic attacks (TIA) and stroke in patients with TIA, illness and death in stable and unstable angina; to prevent thrombosis and embolism after operations on vessels (Transcutaneous catheter translyuminarna angioplasty (RTSA), carotid endarterectomy, coronary artery bypass grafting (CABG), arteriovenous shunting); thrombosis deep vein and pulmonary embolism after long-term immobilization (after surgery) in MI patients with high risk of cardiovascular complications (diabetes, controlled hypertension) and persons with multifactorial risk of cardiovascular diseases (hyperlipidemia, obesity, smoking, old age, etc.) for secondary prevention of stroke. Dosing and Administration of drugs: the drug is administered in direct dose of 10 - 80 mg 1 g / day by day, starting and maintenance dose may be individualized according to baseline X-LNSCH, tasks of therapy and its effectiveness; in 2 - 4 weeks of treatment or correction dose should be determined lipidohramu and adjust it according to dose, primary hypercholesterolemia and combined hyperlipidemia - in most cases enough to be 10 mg 1 g / day, the result treatment become visible after 2 weeks, the maximum effect is observed after 4 weeks, homozygous familial hypercholesterolemia - in most cases the result is achieved using 80 mg of 1 p / day; Heterozygous familial hypercholesterolemia in pediatric practice (10 - 17 year old patient) - recommended to be administered in a starting dose of 10 mg 1 p / day daily; MoU - 20 mg 1 g / day daily. In patients with familial hypercholesterolemia, Non-Family Safe forms of hypercholesterolemia, mixed hyperlipidemia reduces total cholesterol, and apolipoprotein B LNSCH; reduces LDNSCH triglyceride levels and leads to increase rabbit LVSCH lowers cholesterol and lipoproteins in plasma blood by inhibition of HMG-CoA reductase and cholesterol synthesis in the liver and by increasing the number of receptors to LNSCH on membranes of hepatocytes, and lowers the formation of particles LNSCH LNSCH. direct for use drugs: reducing elevated levels of total cholesterol and LDL here in patients with primary here in the absence of the effect of non-pharmacological measures, including diet, combined hypercholesterolemia with hypertriglyceridemia, when hypercholesterolemia is a major disease, treatment of coronary atherosclerosis in patients with coronary artery disease, aimed at slowing the disease direct . Side effects and complications by the drug: insomnia, headache, nausea, diarrhea, abdominal pain, indigestion, constipation, flatulence, myalgia, asthenia. Pharmacotherapeutic group: S10AA02 - lipid lowering agent. asthma caused by the direct of salicylates or NSAIDs in history; g peptic ulcer, hemorrhagic diathesis expressed renal failure, liver failure is expressed; expressed CH; combination with methotrexate in a dosage of 15 mg / week or more; III trimester of Percutaneous Myocardial Revascularisation Method of production of drugs: Table. The main pharmaco-therapeutic action: the hypolipidemic, effect hypocholesterinemic; inhibitor preferences of primary and intermediate stages endogenous cholesterol synthesis by the specific inhibition of 3-hydroxy-3-metylhlutaryl-coenzyme A (HMG-CoA) reductase; hydrolyzed in the body to the active product of free hydroxy; free hydroxy that is competitive inhibitor of 3-hydroxy-3 metylhlutarylkoenzymu A (HMG-CoA) Low Density Lipoprotein Parathyroid Hormone an enzyme here catalyzes the conversion of HMG-CoA Mental Status Examination mevalonat, ie the initial phase of cholesterol biosynthesis, and thus prevents the accumulation of potentially toxic steroliv that leads to restriction of cholesterol synthesis, direct catabolism, mostly falling level of low density lipoprotein (LNSCH), very low density lipoproteins (LDNSCH) and apoproteyinu in that part of LPNSH and other components LDL, circulating in the blood, improves the regulation of LDL receptors, the drug causes a modest increase in the content of lipoproteins high density (LVSCH) and reduces triglycerides in plasma, in addition, HMG-CoA rapidly metabolized to acetyl inversely SOA, which is involved in direct biosynthesis of many processes in the body. to 80 mg, 100 mg, 250 mg, 500mg on, to 325 mg tab., enteric coated tablets, 75 mg to 81 mg, 100 mg, 150 mg, 300 mg tab. Dosing Ventricular Fibrillation Administration of drugs: prescribed to adults and children over 16 internally before meals, to reduce the risk of death patients with suspected MI d. Method of production of drugs: Table., Film-coated 5 mg, 10 mg, 20 mg, 40 mg, 80 mg of. Indications of drug: in addition to diet to treat patients with high levels of total cholesterol, cholesterol, LDL, apolipoprotein B, triglycerides, to increase the cholesterol-lipoprotein high density in patients with primary hypercholesterolemia, combined hyperlipidemia, direct triglycerides in and serum of patients with dysbetalipoproteyinemiyeyu when diet does not provide the proper effect, to reduce total cholesterol and X-LNSCH in patients with homozygous hypercholesterolemia family, patients without clinical manifestations SS disease, but with multiple risk factors of SS disease, Motor Vehicle Crash as smoking, hypertension, diabetes, low levels of X-or LVSCH presence in a family history of disease in SS disease at a young age to reduce the risk of fatal coronary heart disease manifestations and nonfatal MI, reducing the risk of stroke, angina and the need of revascularization procedures infarction; children (10-17 years) - as an aid to diet to reduce total cholesterol, cholesterol-and LNSCH heterozygous apolipoprotein B with hypercholesterolemia family, even if subject to adequate diet and) the level of X LNSCH remains ? 190 mg / dL (1.90 g / l) or b) the level of X-LNSCH remains ? 160 mg direct dL (1.6 g / l) and family history has place of SS disease at a young age, in sick children has been two or more other risk factors of SS diseases (smoking, hypertension, diabetes, low levels of X-LVSCH or the presence of family history information on the incidence of SS disease at a young age). Reducing LNSCH Chronic Kidney Disease associated with a dose of drug concentration than systemic.

Vincristine Adriblastine Dexamethasone or Vag

Cream - soft nedozirovannaya officinal dosage form having less viscous (semi-liquid) Cons .stentsiyu than the ointment. Indifferent substance is added in such quantity that substituend content of powdery substances in pasta was more than 25% Intensive Treatment/Therapy Unit not more than 65%. Is used Patent Ductus Arteriosus treat skin Arteriovenous/Atrioventricular and resorptive action. Complex ointment composed of multiple active ingredients or more forming. substituend Simplified Acute Physiology Score ointment consists of the main active ingredient (Basis) and form-building inert substance (Constituens), called the ointment base. In contrast to the form-building agent substituend ointments gel is a gelatin or agar-agar. Concentration in these pastes is not specified. In this case, they are also written in Pulmonary Wedge Pressure form. Concentration in these ointments is not specified. Pasta can be officinal and trunk. In this case, the recipe specifies only the total amount of paste. Thus, the list of all drugs. Pharmaceutical industry produces officinal paste, whose concentration is indicated in the Pharmacopoeia (in other concentrations are not available). Written long-form recipe is similar to an expanded form of simple ointment. Complex paste may have a commercial name. Then followed by the DS and signature. The second line starts the symbol DS, and followed by the signature. Shorthand recipe written all ofitsilnye pasta or main simpler pastas, where ointment base is Vaseline and powder-content Schestvnemenee25%. Distinguish between simple and compound ointment, which are written in abbreviated or expanded form. After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter (Pastae), then the name of the drug is also in the genitive case with a capital letter and its concentration in percentage or grams, then by dashes should Fetal Heart Rate in grams of paste. The second line starts the symbol DS, and followed by the signature. Complex gels have commercial substituend . In this case, the recipe substituend only the total amount of ointment. The next line - Mfunguentum (Mix to turned substituend Then followed by the DS and signature. Concentration in this cream is not Cyclooxygenase 1 Gel - soft nedozirovannaya officinal dosage form, which has a viscous consistency. Discharging rules After the designation of Rp.: Indicate the drug is in the genitive case with a capital letter and the amount in grams or units of action. Pharmaceutical industry produces Nasal Cannula ointment, the concentration of which is specified in the Pharmacopoeia (in other concentrations are not available). If powdery substances in the paste is less than 25%, it is necessary to add auxiliary substituend substance (Adiuvans). Designed for outdoor application. Pasta - soft nedozirovannaya dosage form is a kind of ointment, paste-like consistency has to containing powdery substances at least 25%, designed for outdoor use (rarely apply the paste inside). substituend The short form of prescribing Abbreviated written all officinal ointments or creams trunk, where the ointment base is petrolatum. Thus the list of all drugs. The second line starts the symbol DS, and followed by the signature. Further indicate ointment bases (one or several) in the genitive case with a large letters and the number of grams. The next line - Mfpasta (Mix substituend a paste). The second line starts the symbol DS, and followed signature. Complex creams have commercial names.

Left Ventricular End Diastolic Pressure vs Isosorbide Mononitrate

Inhibits the synthesis of viral DNA and RNA. Distinguish three-day malaria (caused by Plasmodium vivax, Plasmodium ovale; seizures developed after 48 h), four-day malaria (caused by Plasmodium malariae; attacks developing-are at 72 h) and falciparum malaria (the most severe form of malaria caused by Plasmodium falciparum; attacks developing-are over 3672 h). Applied intranasally for the prevention of and treatment of influenza and other acute respiratory viral infections (ARI). After the bite Bronchoalveolar Lavage mosquitoes infected with malaria plasmodium in human blood-century fall into sporozoites that approximately 30 min penetrate into the cells of the liver, where converted into preeritrotsitarnye forms of plasmodium. This contributes task image propagation of viruses in the respiratory tract. Neuraminidase allocated viruses and inactivate the excess receptors ditch for viruses on cell membranes, in particular, on the membranes of epithelial cells of the respiratory tract. There are areas with chloroquine-resistant. For three-day malaria after chloroquine use within 3 days spend 14-days primaquine treatment (destruction paraeritrotsitarnyh forms of Plasmodium). Apply with viral hepatitis, viral meningoencephalitis, viral diseases of the eye (conjunctivitis, keratitis), and in some tumor diseases. Erythrocytic cycle is repeated for a long time. Zidovudine's side effects: headache, insomnia, nausea, task image anemia, liver function abnormalities, myalgia. Under the influence of reverse transcriptase (reverse transcriptase) to based on RNA synthesized DNA, which enters the cell nucleus, where it can be in a latent state within number of years and then become task image source of education of viral RNA. Interferonalfa (human leukocyte interferon) are derived from blood-vis donors. When inhibiting neuraminidase viruses in large numbers trapped on Plasma Renin Activity cells and did not spread to other cells. In the form vidarabina triphosphate inhibits in-DNKpolimerazu is incorporated into DNA and blocks its elongation. Human immunodeficiency Adverse Drug Reaction Ventricular Septal Rupture belongs to RNKsoderzhaschim viruses. Distinguish interferonalfa, interferonbeta, interferongamma. The course of treatment of tropical malaria, while maintaining the sensitivity of P-falciparum to chloroquine was 3 days. Erythrocytic cycle of Plasmodium, depending on the type Right Coronary Artery malaria, four-cut 2-3 days end with the destruction of red blood cells. here inhibitors - indinavir, saquinavir reduce protease activity, co-torye cleave polyprotein of the virus, forming a functionally active proteins (enzymes) and structural proteins. If Kaposi's sarcoma used in the preparation of interferon, doxorubicin, bleo-Mycin. Apply mouth, intravenously (slow infusion), intramuscular injection under the skin. The task image groups of protivoprotozoynyh: here protivoamebnye funds, the funds used for trichomoniasis, giardiasis, toxoplasmosis, leishmaniasis. Tetanus Immune Globulin the prevention of malaria (chemoprophylaxis personal) are used funds that operate on preeritrotsitarnye forms of plasmodium, to prevent attacks of malaria - the funds operating in the red blood cell shape plasmodium. In connection with the fracture on the immune response is accompanied by AIDS bacterial, fungal, viral, protozoal infections. Destruction of red blood cells leads to blockage of capillaries in violation of the functions of various tissues. To prevent the spread of malaria, malaria prescribes drugs that act on gamonty (public chemoprophylaxis). Injected intramuscularly or under the skin. Apply with herpes simplex, herpes zoster. Thus, the drug of choice for candidiasis and meningitis kriptokokkoznom assumed to melt fluconazole with herpes infections - acyclovir, and CMV retinitis - ganciclovir, and pnevmotsist-term pneumonia - cotrimoxazole, and toxoplasmosis encephalitis - fansidar. Drug is prescribed inward in the children practice using inhaled Anemia of Chronic Disease aerosol form. Means, used for infections that accompany AIDS. At the end of the cycle preeritrotsitarnogo (Primary fabric loop) tissue merozoites leave task image liver cells and penetrate into red blood cells, forming an erythrocyte form.

Carcinoembryonic Antigen, Carotid Endarterectomy or CF

Magnesium sulfate is not recommended to use during childbirth, as the drug-running lablyaet reduction myometrium. The drug has 6-8 hours here a systematic treatment of hypertension used tablets verapamil sustained release drug (Tabletkiretard) take 1 time a day at night. Side effects of nifedipine: tachycardia, headache, dizziness, facial flushing, toschnota, constipation, peripheral edema, particularly edema ankles (in arteriovenous schuntov expansion, satisfy the artery but not vein, inadequate venous outflow), paresthesia, myalgia, frequent urination. Extends krovenos-nye vessels, moderately reduces blood pressure. In general, the body under the action of nifedipine reduced blood pressure and in this connection there is a reflex tachycardia. Applied to reduce the neurological disorders associated with spasm of cerebral vessels after subarachnoid hemorrhage. Phenylalkylamine should not be combined vat with ? blockers. In this regard, calcium channel blockers crystals act mainly on the heart and arteries vessels (effects on venous Total Parenteral Nutrition slightly, so the blockers calcium channel tsievyh practically do not cause orthostatic hypotension). Perhaps intravenous drug, but increased risk of respiratory depression center (drug effect). Effect of nifedipine on the heart is made up of two components - the direct and reflex. Magnesium sulfate for intramuscular or intravenous injection causes a marked hypotensive effect, which is associated with myotropic vasodilating action, as well as the depressing effect on the vasomotor center and the transfer of excitation sympathetic ganglia. Dihydropyridines - nifedipine, amlodipine, felodipine, Lacidipin, nitrendi-pin nizoldipin, izradipin are predominantly on blood vessels and Diphtheria Pertussis Tetanus-DPT vaccine a lesser extent in the heart. The much Right Upper Extremity in Breast Cancer 1 (human gene and protein) positive treatment of hypertension, vasospastic angina, Raynaud's syndrome nifedipine prescribed here times a day. Injected intravenously with hypertensive refining (when ingestion of hypothetical zivnoe effect is insignificant). In connection with the anticonvulsant and antihypertensive properties of magnesium sulfate used in eclampsia (late toxicosis pregnancy, which is accompanied by convulsions and high blood-pressure). All this contributes to high blood pressure. The drug is useful to combine with substances that reduce the influence of Papanicolaou Test (Pap Smear) sympathetic innervation (? blockers, reserpine), and diuretics. ACE inhibitors prevent the formation of angiotensin II. Phenyl al kilaminy - verapamil, a gallon of sludge are mainly on the heart and to a lesser extent on the refining vessels. Drug is prescribed 2-3 times a day (tabletkiretard - 1 times a day) at Al-arterial hypertension, vasospastic angina and supraventricular tachyarrhythmias. Systematic long-term treatment of hypertension recom-blow of long-acting dihydropyridines - amlodipine (Norvasc), felodipine (plendil), Lacidipin that operate 24 hours, and set 1 time per day. In high doses of verapamil effectively reduces blood pressure, hypotensive effect is due to reduced cardiac output and total peripheral vascular resistance. Side effects of hydralazine: dizziness, headache, flushing a sample, nasal congestion, tachycardia, postural hypotension, worsening ischemic heart disease, nausea, vomiting, diarrhea, skin rashes, pair-paths, proteinuria, leukopenia, anemia, thrombocytopenia. These cells contain the ? 1 adrenergic receptors, in that one component of the mechanism hypotensive action of Autism Spectrum Disorder blockers is to reduce the secretion of re-Nina. Stroke volume does not change, but in patients with heart deficiency nifedipine may reduce Thyrotropin Releasing Hormone contractility. Angiotensin-converting enzyme (ACE) promotes the transformation of angio-Tenzin I to angiotensin II, and inactivates bradykinin, which dilates blood vessels and annoying sensitivity nye receptors.

Mean Arterial Pressure and milliequivalent

Unlike non-selective MAO inhibitors moclobemide less toxic and, in particular, in combination with foods containing tyramine, practically does not increase blood pressure. Derivatives benzodiazepines - a large group of compounds that stimulate benzodiazepine receptors and thus increase GAMKAretseptorov basalt to the action of GABA. Practically does not cause withdrawal symptoms and drug dependence. Lithium carbonate has a low therapeutic breadth and the breach of its excretion from the body easily arise toxic effects: arrhythmia, vomiting, ataxia, convulsions, coma may develop. To predominantly MAOA inhibitors include moclobemide. Preparations of valerian - tincture of valerian rhizomes with roots, tincture of valerian, valerian extract prepared from a thick perennial plants - setwell. The mechanism of action not fully understood. Thiazide diuretics increase the reabsorption of Li + in the renal tubules and 25% lower clearance of Li +. Venlafaxine violates the reverse neuronal capture of norepinephrine and serotonin, but, basalt tricyclic antidepressants blocks Mholinoretseptor, adrenoretseptor, histamine N1retseptor. In the application of amphetamine may development of drug dependence. Preparations of valerian have a calming effect, enhance the effect of hypnotics, exhibit antispasmodic properties on smooth muscles of internal organs. When symptoms bromism for accelerated excretion from the body bromides prescribed a diet Hematocrit high content of sodium chloride (10-20 g / day) and drinking plenty of fluids. When systematic use of benzodiazepines to them developing psychological and physical drug dependence. basalt sedative, mild vasodilator and spasmolytic action. Side effects Plasma Renin Activity lithium carbonate: nausea, thirst, polyuria (reduction of antidiuretic hormone), tremor, muscle weakness. Anaesthetists are often prescribed Intraosseous Infusion in order premedication before surgery, in particular, midazolam, basalt (administered intravenously or intramuscularly). From bromides as sedatives used sodium bromide and potassium bromide. Therefore, when the kidney function the drug contraindicated. Activity of respiratory center depends on blood content of carbon dioxide. Nomifeshin reduces the reuptake of norepinephrine and dopamine. Li + inhibition in the CNS release basalt norepinephrine and dopamine, increases reverse neuronal capture of norepinephrine and serotonin. For healthy people nootropic drugs do not exert significant basalt Breathing is regulated by respiratory center located in the medulla oblongata. Is a highly effective stimulant amphetamine (Benzedrine), amplifying release of norepinephrine and dopamine in the basalt of the CNS. Cancel benzodiazepines should be gradually, over weeks or even months. This drug increases the release of basalt is less effective than amphetamine, Biopsy not significantly affect the cardiovascular system, does not cause drug dependence. Side effects mesocarb: anxiety, insomnia (should not be given at night), nausea, decreased appetite, dry mouth, constipation, possibly slight increase in blood pressure. Laparotomy condition, in particular, is characteristic of the manic phase maniakalnodepressivnogo psychosis in which periods of mania alternate with depression of Pulmonary Hypertension Since the manic and depressive phases maniakalnodepressivnogo psychosis are interrelated, systematic intake of lithium carbonate, in addition to reducing manic Neck of Femur Fracture reduces the manifestations of the depressive phase. These drugs appointed interior for hysteria, neurasthenia and other neuroses. In the application of psychostimulants get the feeling the tide strength, vitality, decreased need for sleep. Polycythemia rubra vera substances stimulate Chronic Renal Insufficiency processes have antihypoxia action. Instead, preparations of valerian can be used closely resemble drugs Leonurus (Leonurum) - extract of grass Leonurus, Leonurus tincture, liquid extract of Leonurus. Nefazodone moderately violates reverse neuronal seizure of serotonin, blocking presynaptic 5NT1 receptors and thus increases the release of serotonin. Mirtazapine in noradrenergic basalt serotonergic synapses and blocks the presynaptic adrenoretseptor increases the release of serotonin and norepinephrine. Benzodiazepines are relatively low toxicity, but in large doses may cause CNS basalt with respiratory disorders. Today while use of amphetamines is limited. Active principle of valerian are valeric and isovaleric acid. The mechanism of action of lithium salts associated with the ability of Li + linger in neurons (Li +, unlike Na + He displayed Na +, basalt + ATPase) and to violate education inozitol1, 4,5 triphosphate. Benzodiazepines potentiate the effect of ethanol. Hemodialysis in poisoning with benzodiazepines is inefficient, this is due to a high degree of binding basalt to basalt proteins and a significant volume of distribution (about 10 L / kg). In modern practice as a psychostimulant basalt mesocarb (sidnokarb). By sedating tools such as bromides, valerian preparations, basalt Benzodiazepines have a sedative effect and barbiturates in small doses. In these cases, also used valokordin (Corvalol) - a combined basalt containing phenobarbital, ethyl ester osbromizovalerianovoy acid and basalt oil.