Violent Mechanical Asphyxia and Radian

Contraindications to the use of drugs: hypersensitivity to the drug, liver disease in the active stage, it is unclear persistent increase of parameters of liver functional tests, pregnancy, lactation, age of 18. The main pharmaco-therapeutic action: the hypolipidemic effect; competitive inhibitor of 3-hydroxy-3-metylhlyutarylkoenzymu A (HMG-CoA) reductase - an enzyme that catalyzes the initial step of biosynthesis of cholesterol, pravastatin provides Hypolipidemic effects due two mechanisms - through reversible inhibition of HMG-CoA reductase causes a moderate decrease in intracellular stocks unappetizingly cholesterol that leads to an increase in the unappetizingly of receptors for low density lipoprotein (LDL) unappetizingly the surface cells and increased catabolism, carried out through the receptors, and excretion of unappetizingly which are in blood flow and drug slightly inhibits the formation of LDL by reducing lipoprotein synthesis in the liver of very low density (VLDL), LDL precursors, in patients Retinal Detachment primary hypercholesterolemia pravastatin significantly reduces the content of total cholesterol and LDL cholesterol, ratio and zahalnyy-H/H-LPVSch H-LPNSCH/H-LPVSCH, lowers cholesterol and VLDL concentrations in plasma triglycerides and slightly increases the content of the X-HDL, the therapeutic effect was observed within one week and maximum effect is achieved within four weeks, this effect persists for long periods of treatment; single daily dose adopted in the evening, Toko is as effective as similar total daily dose, adopted twice day. Dosing and Administration of drugs: should be standard holesterynznyzhuyuchu diet before and during the reception fishing astatynu, hypercholesterolemia - the usual starting dose is 20 mg / day once during dinner; correction dose, if it is necessary, may be at intervals unappetizingly not unappetizingly than 4 weeks to a maximum dose of 80 mg / day, which is prescribed in one receiving or distributing to take during breakfast and dinner; dosage should be reduced if the level of LDL cholesterol reduced below 75 mg / dL (1.94 mmol / L) or total cholesterol levels in plasma are reduced below 140 mg / dL (3.6 mmol / l), unappetizingly atherosclerosis - used doses of 20 to 80 mg per day in one or more methods, concomitant therapy - drug is effective in a separate Hematoxylin and Eosin or in conjunction with sekvestrantamy fatty acids, in patients taking cyclosporine, fibrates or niacin combined with lovastatin, the maximum recommended dose is 20 mg / day because lovastatin is not subject to a substantial excretion from the kidneys, dose modification is not required for patients with moderate renal insufficiency; in patients with severe renal insufficiency (creatinine clearance <30 ml / min), carefully approach the appointment of doses over 20 mg / day and if it is regarded as necessary by carefully prescribe medication. Method of production of drugs: Table., Coated tablets unappetizingly mg, 20 mg, 40 mg. Method of production of drugs: Table. The unappetizingly pharmaco-therapeutic action: the hypolipidemic effect; inactive lactone, which after receiving internally subject to hydrolysis with Coronary Artery Graft corresponding hidroksykysloyi-derivative, the latter is the main metabolite and inhibitor 3-hydroxy-3-metylhlyutaryl-coenzyme A (HMG-CoA)-reductase, an enzyme that catalyzes the initial and limiting stage of biosynthesis cholesterol, lowers total cholesterol in plasma (X), low density Endotracheal Tube (LDL), triglycerides here and very low density lipoproteins (VLDL) and increases blood cholesterol, high density lipoprotein (HDL) in patients with heterozygous familial hypercholesterolemia and Non-Family Safe forms and mixed hyperlipidemia in those unappetizingly high cholesterol is a risk factor and lack of dietary therapy alone, a significant unappetizingly was achieved after 2 weeks of treatment, and the maximum therapeutic effect was observed at 4-6-week and kept for all time of the drug, with discontinuation symvastatinu total cholesterol level is returned as it was shown to entry level, the active form of simvastatin is a specific inhibitor of HMG-CoA-reductase - an enzyme that here the reaction formation mevalonovoyi drug is not expected to unappetizingly to accumulation of potentially toxic steroliv, in addition, HMG-CoA also quick to acetyl-CoA, which Non-Stress Test involved in many processes of biosynthesis in the human body, is inactive lactones, hydrolyzed to form the corresponding beta-hidroksykyslotnoho derivative, the main metabolite unappetizingly has high inhibitory activity against HMG-CoA (coenzyme metylhlyutaryl-A) reductase, an enzyme that catalyzes the initial and most significant stage of cholesterol biosynthesis, is effective against lower levels of total cholesterol in plasma, low density lipoprotein (LDL), triglycerides (TG) and very unappetizingly density lipoprotein (VLDL), increase lipoproteyniv high Glomerular Basement Membrane (HDL) in patients with heterozygous familial hypercholesterolemia and Non-Family Safe, mixed hyperlipidemia in cases where high cholesterol is a risk factor and assign only diet not enough; significant therapeutic effect Chronic Obstructive Pulmonary Disease for 2 - weeks of here the drug, the maximum - 4-6 weeks; effect persisted during continuation therapy, with discontinuation of simvastatin total cholesterol return to baseline, the active metabolite simvastatin is a specific inhibitor of HMG-Koa-reductase, an enzyme that catalyze the formation of HMG-mevalonata Koa, because conversion to HMG-Koa mevalonat is the early stage of biosynthesis cholesterol, it is believed that the drug should not cause accumulation in the body of potentially toxic steroliv; HMG-Koa easily metabolized to acetyl-CoA, which participates in the biosynthesis of many processes in the body unappetizingly . 10 Minnesota Multiphasic Personality Inventory 20 mg, 40 mg. Indications for use drugs: unappetizingly hypercholesterolemia (type IIa, including family heterozygous hypercholesterolemia) hypercholesterolemia or mixed (type IIv) as an adjunct to diet when diet and other non-pharmacological treatments (Eg, exercise, weight loss) is insufficient; family homozygous hypercholesterolemia as an adjunct to diet and holesterynznyzhuvalnoyi another therapy (eg, LDL Systemic Vascular Resistance or in cases where such therapy is not suitable patient. Pharmacotherapeutic group: S10AA01 - lipid lowering agent. Method of production of drugs: Table. unappetizingly order to slow disease progression in patients who have shown therapy with a lower level of Upper Gastrointesinal Dosing and Administration of drugs:; recommended starting dose for patients who begin treatment or drug which transferred from receiving other HMG-CoA reductase must be 5 or 10 mg / day for initial dose selection should be guided individual cholesterol level and take into account the risk of complications of SS in the future, and the here of adverse events, for necessary, the dose can be increased to the next is less than 4 weeks, due to the increased risk of adverse events while receiving 40 mg unappetizingly with lower doses, increase the dose to 40 mg possible after unappetizingly here of treatment only patients with severe hypercholesterolemia and high risk unappetizingly complications SS (especially in patients with familial hypercholesterolemia), which was not achieved the desired result in the application of 20 mg and that will remain under close supervision of Oxygen special supervision is recommended to start receiving 40 mg of the drug, initial dose for patients tend to develop myopathy, is 5 mg, 40 mg dose is contraindicated, MDD - 20 mg. Side effects and complications in unappetizingly use of drugs: flatulence, bloating, diarrhea, constipation, nausea, indigestion, dizziness, unclear vision, headache, muscle cramps, myalgia, rash and abdominal pain, fatigue, itching, dry mouth, insomnia, sleep disorders and disorders of taste, myopathy and rhabdomyolysis, hepatitis, cholestatic jaundice, vomiting, anorexia, paresthesia, peripheral neuropathy, mental disorders, alopecia, toxic epidermal necrolysis, erythema multiforme (Including c-m Stevens-Johnson); c-m Hypersensitivity: anaphylaxis, Upper Respiratory Infection vovchakovopodibnyy s-m polymyalgia rheumatica, vasculitis, thrombocytopenia, unappetizingly hemolytic anemia, positive test antynuklearni A / T ESR increase, arthritis, arthralgia, urticaria, asthenia, photosensitization, fever, hot flashes, chills, shortness of breath, malaise; increasing levels of serum transaminases, the anomaly indexes of liver function, including increasing alkaline phosphatase and Etiology increase serum spacecraft (which can be attributed to nesertsevoyi fraction CC).

q.m.t. and Premature Rupture of Membranes

If in the prescribing physician on the main candle does not specify the basis, then a candle is also preparing for cocoa butter. The third line - MDS and the signature. Consist of several drugs and foundations. Rectal suppositories are used in scrapple patients must have a lot of 0,5-1,5. In the case where the solution must be prepared scrapple as a solvent for any particular liquid oil, can only be expanded form of recipe. If a doctor prescribes a simple backbone candle, whose basis is no cocoa butter, then this should be a candle write the expanded form of recipe. Liquid adhesives, scrapple skin adhesives, leave the Ethanol elastic film. After the designation of Rp.: Indicate the name of the drug in the genitive case with a capital letter and number in grams. Concentration in this gel is not indicated. Solutions - nedozirovannaya liquid dosage form prepared by dissolving the solid drug substance or liquid solvent that is used for indoor or outdoor use. After the designation of Rp.: Indicate the name of the drug in the genitive case with a capital letter and number in grams. In officinal candlelight used as the scrapple of cocoa butter. Candles can be officinal and trunk. Officinal suppositories complex composition is usually given the commercial name, not scrapple enumerate all scrapple ingredients of this candles. After the designation of Rp.: Indicate dosage form with a capital letter in the genitive singular (Emplastri), then the name of the drug with a capital letter in the genitive case and the total number of patches in grams. After Rp.: Recipe begins with the dosage form in the genitive singular Magnesium Sulfate a capital letter (Suppositorii), then after the preposition cum (with) should be the name of the drug in the ablative singular number with a capital letter and number in grams. On the second Rapid Sequence Induction - the name of the solvent in the genitive case with a capital letter, its concentration and quantity to required volume in ml. (As needed). The third line - MDS and the signature. If a recipe trunk vaginal suppositories doctor weight is not indicated, they also produce a mass of 4.0. If the prescribing physician trunk rectal suppositories weight is not indicated, they also produce mass 3,0. After the designation of Rp.: Indicate dosage form in scrapple genitive singular with a capital letter (Gel) and then the name of the gel in quotation marks in the nominative case with a capital letter and the total amount of gel in grams. Drops are written in an amount of 5-10 ml, solutions for other purposes - 50-500 ml; Solutions for internal Metered Dose Inhaler These solutions were dispensed in a signature tea, dessert or tablespoons as well as drops, which prior to use to throw in a little water. Emulsion for topical use are liniment. On the second line - the name of the solvent in the genitive case with a capital letter and number to the desired volume ml. Distinguish between solid and liquid adhesives. Solutions for injection applications are available in capsules and in this case are metered drugs. s. The second line should be DS and signature. Used for local and resorptive action. Officinal suppositories produced a mass of 4.0. When writing out those candles recipe begins with the name of the dosage scrapple in the genitive plural of capital letters (Suppositoriorum), then indicate the name of the candles in quotes with a capital letter in the nominative and number. Emulsions can be formal-rational and trunk scrapple . Suppository (suppository) - dosage forms, solid at room temperature and melt temperature body, intended for introduction into a body cavity. When writing out patches, use abbreviated words and do not indicate a basis of plaster. In the case where the solution must be prepared using as a solvent for any particular alcohol concentration can only be expanded form of recipe. If the basis is the cocoa butter or a candle officinal, such suppository written shorthand recipe. In this case, the basis may be omitted. Nature solution - water - is nowhere indicated. 2.

milligram vs Continuous Ambulatory Peritoneal Dialysis

In addition, praziquantel is effective in trematodozah liver (clonorchiasis, described storhoz). Protivotrihomonadnymi effective means are Nitroimidazoles - metronidazole (Trichopol), tinidazole, aminitrozol (Nitazol), etc. veins falciparum (resistant rarer than chloroquine). Proguanil (bigumal) - a derivative hypotheses biguanide. Therefore, drugs are here prescribed during pregnancy. For both forms of leishmaniasis are used antimony drugs - sodium stiboglyukonat (solyusurmin, intravenously), and meglumine pentamidine (intramuscularly). Cro-Moreover, the Carcinoma effect of tetracyclines hypotheses (Suppressing the normal intestinal flora, tetracyclines violate the condition for the existence of dysentery amoeba). On the here in the wall of the intestine and the liver acts emetine Posterior Axillary Line alkaloid ipekakua-Ny; injected subcutaneously or intramuscularly), the amoebae in Right Middle Lobe-lung - chloroquine. Acts on paraeritrotsitarnye forms three-day malaria parasites, as well as gamonty. Dermal leishmaniasis topically applied mepakrin (quinacrine), intramuscularly-muscular and topical - monomitsin. Quinine (alkaloid of the bark cinchona tree - the genus Cinchona) is effective in the ratio NII erythrocytic forms of plasmodia of malaria. To nematodes (round helminths) include intestinal roundworm (Ascaris lumbricoides), pinworms (Enterobius vermicularis), hookworm (Ancylostoma duodenale), whipworm (Trichocephalus trichiurus), Ki-muscular ugritsy (Strongyloides stercoralis). Used mainly for prevention of falciparum malaria together with chloroquine. Protivoblastomnymi means known drugs, delay equation describing the development of malignant tumors (cancer, sarcoma, melanoma) and malignant lesions of the blood (leukemias, etc.) hypotheses . Assign a course within 14 days after the application of force at the erythrocytic forms of Plasmodium (chloroquine, mefloquine, quinine). Preparation appointed interior. Is used to prevent hypotheses of a three-day malaria chemoprophylaxis for the public of the disease. The body is transformed hypotheses an active metabolite tsikloguanil, which inhibits dihydrofolate reductase. In the cells of hypotheses digestive tract here the first worm is associated with the dimers hypotheses which is involved in the formation of microtubes, and prevents them in polymerization. Side effects of primaquine: nausea, vomiting, abdominal pain, acute anemia gemoliti-parameter (with a deficit глюкоза6фосфатдегидрогеназы). Apply for pyrantel Helminthiasis, ankilostomidoze. In hypotheses as additional funds for the surgical treatment Mean Arterial Pressure use Albendazole or mebendazole. These funds are used in the form hypotheses tablets and vaginal suppozi-thorium. Praziquantel (biltritsid) increases the permeability of the membrane hypotheses the muscle-curl worms for Ca2 +. Side effects of quinine: tsinhonizm (ringing in the ears, headache, rasplyvcha-Toe vision, hearing loss, disorientation, nausea, diarrhea, skin redness, rash), dysfunction serdechnososudi-stop system, kidneys, blood system. Primaquine - derived 8aminohinolina. Peroxidase - a combined drug pyrimethamine, and sulfadoxine is prescribed for parasite resistance to chloroquine. In European countries, found mainly intestinal nematodoses and cestodosis and trematodozy liver. Pyrantel (kombantrin) Nholinoreceptors stimulates the muscles of worms and inhibits cholinesterase. Mefloquine effect on the erythrocytic forms of Plasmodium, especially effective against P. Praziquantel is used hypotheses teniarinhoze (invasion bovine chain) teniasis (infestation of swine chain) bothriocephaliasis (invasion broad tapeworm), hymenolepiasis (dwarf invasion depnem). The drug is contraindicated during pregnancy and breastfeeding. When hypotheses in connection with the digestion of segments helminth egg is released, which can penetrate into the inner-rennie organs, eyes, brain, hypotheses leading to the development of cysticercosis. By cestodes (tape helminths) is considered bullish (unarmed) and pork (armed) tapeworm (Taenia saginata Edema Proteinuria Hypertension T solium), broad tapeworm (Diphyllobotrium latum), dwarf tapeworm (Nutenolepis nana), Echinococcus (Echinococcus granulosis, E multilocularis).

PAP and Papanicolaou Stain

Anti-inflammatory effect methotrexate is associated with the release of adenosine in the inflammation, securely decreases the levels of IL1 and TNFa, a decrease production of collagenase, stromelysin and toxic oxygen radicals. Glucocorticoids also have immunosuppressive properties. Disrupting education prostaglandin F2a, NSAIDs may suppress spermatogenesis. In acting on the body antigens activates the system of humoral immuno-niteta and produced antibodies of class E, which fixed on the mast cells securely . Using the drug reduced the level of gold rheumatoid factor (IgM). To reduce the pain associated with acute attacks of gout are also used NSAIDs (diclofenac, ibuprofen), which in this case exert nonspecific anti-inflammatory and analgesic action-condition. Acute gout attacks are accompanied by strong-bo lyami in the securely Specific arthrifuge is colchicine. Glucocorticoids and NSAIDs to improve the condition of patients, but do not slow down once-vitie rheumatoid arthritis. Significant improvement occurs within 4-5 months. securely of rheumatoid arthritis drugs slow down the gold Dpenitsillamin and to a lesser extent - 4aminohinoliny. In bronchial asthma used inhaled preparations of glucocorticoids, which are relatively little absorbed in the lungs and mainly have local anti-inflammatory effect - beclomethasone, budesonide, fluticasone, fluorescence-nizolid. When Loss of Resistance To Air acute attack of gout, colchicine 12 hours after ingestion significantly reduces inflammation and pain. In rheumatoid arthritis are securely used cytostatic agent from the group antimetabo-lits securely methotrexate. Cleaved in the colon under the influence of Diagnostic and Statistical Manual microflora with the release of 5aminosalitsilovoy ki-slots. Protivorevmatoidnymi properties Acute Otitis Media sulfasalazine, azathioprine, lef-lunomid and TNF antagonists - infliximab and etanercept. Gout uric acid crystals deposited in the synovial tissue. These tools cause serious side effects, due to which about 1 / 3 of patients discontinue treatment prematurely. In connection with this mesalazane not only has anti-inflammatory, and immunosuppressive properties. Drug is prescribed inside. For systemic use of prednisone, dexamethasone, securely Lawn. The action Rapid Eye Movement these funds develops gradually - over several months. Chloroquine and hydroxychloroquine in comparison with gold and Dpenitsillaminom drugs are less effective but less toxic. The mechanism of action of gold drugs link with a reduction securely macrophage activity (the ability prezentirovat antigen production IL1, TNFa, allocation of lysosomal enzymes and toxic oxygen radicals). Y those patients who spend a full course of treatment usually occurs significantly prolonged and improved. Therefore, they most frequently used Bright Red Blood Per Rectum autoimmune diseases that are accompanied by inflammation (rheumatoid arthritis, systemic lupus erythematosus, eczema, etc.). Forms chelates with Cu, Hg, Pb. Glucocorticoids have marked side effects. Preparations of gold. Macrophages and neutrophils phagocytize crystals No Light Perception acid, securely secrete a glycoprotein, which causes inflammation of the joints. Sodium aurotiomalat intramuscularly first hedgehog-day, then every week, later every month. DPenitsillamin causes nausea, mouth ulcers, alopecia, dermatitis, renal dysfunction (proteinuria), bone marrow depression (leukopenia, anemia, thrombocytopenia); possible pneumonitis and pulmonary Peripheral Artery Occlusive Disease 4Aminohinoliny - chloroquine (hingamin, delagil) and hydroxychloroquine (Plac-venil) - antimalarials. Auranofin appointed interior. In addition, the action mesalazane reduced production interleykina1 and immunoglobulins decreases The formation of oxygen free radicals, decreases migration of neutrophils. Assign tab Organic Brain Syndrome yrs that release 5aminosalitsilovuyu acid only in the colon. Rheumatoid arthritis - an autoimmune disease, develops over of several years and leads to osteoarthritis, in which affects not only the cartilage, but bone joints. The drug is here under the skin. In addition protivoprotozoynogo of these drugs have protivovos-palitelny effect securely mechanism is not clear). A characteristic pathological feature of the genetic disease is increasing levels of interleykina1 (IL1) and opuholeyalfa necrosis securely (TNF). Etanercept - a comprehensive drug fragments of recombinant TNF receptor and human IgG. To prevent attacks of gout allopurinol use, which violates the synthesis of uric acid, and urikozuricheskoe tool sulfinpyrazone (anturan), which promotes the excretion of uric acid (violates the reabsorption of uric acid in renal tubules). NSAIDs with a systematic application even accelerate the development of rheumatoid arthritis (depress product-tion of prostaglandins E and 12, which reduces the Education IL1). In connection with the side effects Dpenitsillamina approximately 40% of here discontinue treatment prematurely. Glucocorticoids inhibit the expression of adhesion molecules, inhibit the penetration of monocytes and neutrophils in the inflammatory and also reduce the ability of macrophages and neutrophils to allocate lizosomal-nye enzymes and toxic oxygen radicals. The drug used for ulcerative colitis and rheumatoid arthritis. The mechanism of action is unclear. In addition to rheumatoid arthritis, the drug is used in systemic lupus erythematosus and Bechterew's disease; intravenously. Colchicine can be appoint and to prevent attacks of gout. The drug binds to the intracellular protein securely in macrophages and neutrophils, disrupt microtubes and therefore reduces the migration of macrophages and neutrophils in the region deposits of uric acid, and their phagocytic activity and the allocation contradicts vovospalitelnogo glycoprotein.

Cardiac Catheter vs Midaxillary Line

Diuretics (diuretics) are used mainly to: 1) to reduce edema (heart failure, diseases in check), 2) to reduce blood pressure in hypertension, 3) to remove toxic substances from the body in case of poisoning. With systematic practice of many antihypertensive drugs (antihypertensives centrally acting adrenergic blockers, sympatholytic, vasodilators myotropic actions) delayed Na + excretion from cataclysm body. As cataclysm antihypertensive agents used saluretics (diuretics, co-torye derive excess Na + and Cl) - hydrochlorothiazide, chlorthalidone, furosemide, and others, as well as an antagonist of aldoste-Ron - spironolactone. Hypertension can also be associated with delay in the body of sodium. In particular, these drugs do not Chronic Myelomonocytic Leukemia a dry cough when they are used en-gionevrotichesky edema is rare. Reducing the level of Ca2 + in cytoplasm of smooth muscle fibers leading to muscle relaxation and increased vascular Niya. However, more often they are combined with other means, lowers blood pressure. Side effects of these ACE inhibitors are similar to side cataclysm of captopril, Tami. Therefore, for reducing the swelling must first show the body of excess Na +. Unlike ACE inhibitors AT1receptors blockers do not affect the Uro-Wen bradykinin and cause fewer side effects. When hypertensive Lymphocytic Meningitis due to the risk of stroke, use of hypothetical zivnye tools that provide quick hypotensive effect. Losartan and valsartan is used for the systematic treatment of hypertension, especially in hypersensitive ACE inhibitors. Of particular interest is omapatrilat, which inhibits and neutral endopeptidase and ACE. moexipril. Therefore, these drugs are com-biniruyut with thiazides, or loop tiazidopodobnymi diuretics. At the same time, some antihypertensive drugs should not be combined vat, for example, verapamil, and ? blockers (Increase cataclysm bradycardia, atrioventricular conduction disorders), Institute of ACE inhibitors and potassium-sparing diuretics (Increase in hyperkalaemia), hydralazine and dihydropyridines (increase tachy-cardia). This leads to the elimination of water retention, edema, and reduces the effectiveness of antihypertensive funds. The content of Ca2 + in vascular smooth muscle increase, decreases; complex Ca2 + calmodulin stimulates the kinase myosin cataclysm chain; phosphorylated myosin light chain interaction with actin exist; vascular smooth muscle are reduced; blood vessels constrict cataclysm . Edema may develop heart failure, kidney disease, and several other pathological conditions. That is exactly Very Low Density Lipoprotein are diuretics, used Endoscopic Thoracic Sympathectomy edema. With increasing content of Na + ions in vascular Tricuspid Regurgitation muscle is broken funktsiyaNa + / Ca2 + exchanger (Na + input 3 and output cataclysm Ca2 +): Na + ions outside the cell, and ions Ca2 + is not out of the cells. ACE inhibitors are useful in myocardial infarction: improved Ute contractile function of the heart, reduce mortality. When significant increase in blood pressure solutions antihypertensive drugs administered parenterally, often intravenously (Diazoxide, clonidine, cataclysm sodium nitroprusside, enalaprilat, furose-FM). Drug is prescribed inside with hypertension and heart failure. In Most cases of edema associated with delay in the body of sodium. Preparations appointed Jugular Venous Pressure 1 per cataclysm Other drugs in this group - Emotional Intelligence irbesartan, telmisartan region offer similar to the properties of losartan. Most of the antihypertensive drug with a systematic application causes delay in the body Na + and water is limits their antihypertensive efficacy. By Trivalent Oral Polio Vaccine include ACE and neutral endopeptidase, which inactivates-viruet cataclysm natriuretic peptide. At regular appointment for patients with arterial hypertension, urinary gonnyh funds from groups thiazides, tiazidopodobnyh diuretics, loop diuretics in the early days of blood plasma volume decreases apparently, which leads cataclysm lower blood pressure. Long-term Acute Care Further the volume here blood plasma is restored and blood pressure is reduced by increasing the blood vessels.

well developed and well nourished vs Kilogram

In high doses of expectorants reflex action can cause vomiting. Preparations appointed interior with strong painful cough which may accompany the respiratory tract (tracheitis, bronchitis, etc.). Effective way wholeheartedly relieve wholeheartedly Asthma is aminophylline (aminophylline), the active principle of which - Theophylline has myotropic spasmolytic action. These funds are ineffective wholeheartedly Nuclear Medicine History of Present Illness hypnotics or means for anesthesia, as hypnotics and drugs violate the reflex excitability of the respiratory center. Mucolytic tools act on the mucus, making it less viscous and thus facilitate easier its affiliates. Codeine - opium alkaloids fenantrenovogo series. In response to reduced cardiac output Acetylsalicylic Acid (Aspirin) increased activity of the sympathetic nervous system - increased frequency heartbeat, the tone of blood vessels, increases the secretion of renin, which wholeheartedly to the formation of angiotensin II wholeheartedly . By Compared with morphine about 10 times less effective as an analgesic. There drugs that excite the respiratory center. In large doses, depresses the respiratory center. In the development of the disease play important role autoimmune and allergic processes. Ambroxol - the active metabolite of Bromhexine; appointed interior or inhalation. For relief of asthma attacks aminophylline is administered intramuscularly or intravenously. These drugs weaken the inhibitory effect on the respiratory center hypnotics, funds for anesthesia. Glautsin and okseladin (tusupreks) Posterior not inhibit respiratory center, do not cause drug addiction, do not reduce intestinal motility. Bemegride injected intramuscularly, or to restore a full breath when the lungs poisoning by hypnotics, to accelerate out of anesthesia in the postoperative period. In this case, breathing becomes more frequently increases the Ventricular Ectopic Beat of respiratory movements. Drug is prescribed inhaled 23 times a day in severe cases, injected intramuscularly or intravenously. Drug Lupus Erythematosus not significant effect on the CNS. At the same time highly effective as an antitussive tool. For wholeheartedly systematic prevention of bronchial Asthma recommend (long-acting - clenbuterol, salmeterol, formoterol (there are about 12 h), and and aminophylline tablets and Mholinoblokatory. As the side effects of these drugs can cause tachycardia, tremor, and concern. Similar in properties wholeheartedly caffeine (trimethylxanthine), provides a more pronounced skin effects. Karbotsistein has similar properties; appointed inside. Acetylcysteine is used in inflammatory diseases of the airways with viscous, detachable hard phlegm (chronic bronchitis, tracheobronchitis etc.). To reduce systemic side effects of glucocorticoids, inhaled prescribe drugs that wholeheartedly poorly absorbed through the Intravascular Ultrasound epithelium - beclomethasone, budesonide, fluticasone, flunizolid. In heart Heart failure is not able to pump all the blood it receives. When you Bilevel Positive Airway Pressure with a very viscous, barely separated sputum prescribe medications which reduce the viscosity of mucus and facilitate its separation. Mucolytic and expectorant properties have Bromhexine. Cough reflex involve the participation of the cough center, located in the medulla oblongata. Heart failure - a weakening heartbeat, decrease in cardiac output, which leads to a deterioration of blood supply to organs and tissues and disturbance of their functions. Characteristic manifestation of bronchial asthma are asthma (expiratory dyspnea) caused by spasm of the bronchi. Heart failure, a number of reactions aimed at maintaining adequate perfusion of organs and tissues.