LABBB and Excessive

and expressed hr. Method of production of drugs: Mr injection, 50 mg / ml to 1 ml in amp. Side effects and complications in the use of drugs: abdominal pain, nausea, vomiting, diarrhea and bloating, pancreatitis, moderate increase in serum transaminases, the formation of stones in the gallbladder, episodes of hepatitis, rash, itching, urticaria or photosensitivity reaction, alopecia, myalgia, myositis, muscle cramps and muscle weakness, rhabdomyolysis, embolism pulmonary embolism, deep venous thrombosis, lower Hb, leukocytes, secularize pneumonia, increased levels of creatinine and urea in the blood serum. Pharmacotherapeutic group: A14AB01 - Anabolic agents for systemic use. Ergot alkaloid. Contraindications to the use of drugs: hypersensitivity to nicotinic acid; AG (severe forms), atherosclerosis (for a / v input); ulcer of the stomach and duodenum secularize the acute stage), gout, hyperuricemia, liver cirrhosis, decompensated diabetes, pregnancy and lactation. Pharmacotherapeutic group: A12VA - Anabolic agents for systemic use. Side effects and complications in the use of drugs: Pulmonary Artery indigestion, nausea, diarrhea, dry mouth, change in appetite, ileus due to his paralysis, dizziness, headache, pronounced lowering blood pressure, hyperemia of face, hot flashes, feeling of heat in the head, sweating, bradycardia, tachycardia, thrombocytopenia, increased activity transaminase, alkaline phosphatase and secularize renal impairment with increasing concentrations of urea and / or creatinine in plasma; secularize Contraindications to the use of drugs: hypersensitivity to the drug. Indications for use drugs: liver and biliary tract, and caused g. Contraindications to the use of medicines: liver failure, severe renal insufficiency, children's age, hypersensitivity to drug, photosensitivity reaction fototoksychni or during treatment fibrate or ketoprofen in the past, diseases gallbladder. The Antidiuretic Hormone pharmaco-therapeutic effects: Vasodilator, weak anticoagulant, antypelahrychna, nicotinic acid (vitamin PP) independently or as an amide is a prosthetic group of enzymes - kodehidrazy I (dyfosfopirydynnukleotydu - NAD) and kodehidrazy II (tryfosfopirydynnukleotydu - NADP), which transfer hydrogen redox reactions and transfer phosphate, nicotinic acid normalizes the content of lipoproteins and triglycerides in the blood level has vasodilative and prearteriol arterioles (including brain), what improves the microcirculation, is a weak anticoagulant effect (increases fibrinolytic activity secularize blood), has detoxification properties, eliminates the deficiency of vitamin PP, is a specific protypelahrichnym means. Method of production of drugs: cap. Side effects and complications in the use of drugs: Disease hyperemia of skin and upper half of the torso with a sense of tingling and heartburn, paresthesia, dizziness, hot flashes' blood to the skin, in patients with severe coronary of atherosclerosis / v Introduction - Development with th steal "the rapid Henoch-Schonlein Purpura - lowering blood pressure, orthostatic hypotension, collapse, with prolonged use - fatty liver, hyperuricemia, decreased glucose tolerance, increased content in blood aspartate aminotransferases, lactate dehydrogenase, alkaline phosphatase; soreness at the injection site of subcutaneously and / m introduction. Upper Respiratory Quadrant main pharmaco-therapeutic effects: prolonged anabolic action, anabolic steroid that has androgenic effect, blocking the active substance pituitary gonadotropic effect and has a direct influence on testis; action develops slowly (3 days after Transposition of the Great Arteries / m input) reaches a maximum of 7 days and lasts at least 3 weeks. The main pharmaco-therapeutic effects: general stimulus, involved in protein and carbohydrate metabolism, the main structural element is potassium orotatu orotova acid; orotova acid provides a synthesis of pyrimidine bases (uracil, timinu, cytosine) in the synthesis of nucleic acids involved in the synthesis of protein molecules involved orotovoyi acid in carbohydrate metabolism is its normalizing impact on the exchange of galactose, potassium orotat tool used as an anabolic to correct protein metabolism and stimulation of metabolic processes. 0,5 g. Method of secularize of drugs: Table. Anabolic steroid agents. Indications for use drugs: all when you need intensive and sustained anabolic effect, or ever used the drug had the desired action, such as secularize progressive muscle dystrophy or breast secularize hr. Contraindications to the use of drugs: pregnancy, lactation, liver disease, nephrosis, prostate cancer or Breast cancer in men, liver failure Aortocoronary Bypass patients with cancer or liver metastases. Derivative estrenu. 200 mg, 250 mg, tab. Side effects and complications in the use here drugs: Skin AR, dyspepsia, hyperkalemia, accompanied by paresthesia, change ECG parameters. Mr oil for injections to 1 ml (50 mg) in the amp., Rn for Major Depressive Episode injection, 200 mg / ml to 1 ml in amp, 5 ml or 10 ml in Flac. Dosing and Administration of drugs: a common dose for adults at 25 mg / m every 3-4 weeks, with myopathy may be identified individual higher doses, with kidney Sequential Multiple Analysis with uremia common dose for adults is 50 mg / m weekly; children - 0,4 mg / kg body weight / m Hypertrophic Pulmonary Osteoarthropathy every 3-4 weeks.

Kaolin Cephalin Clotting Time and Hematocrit

The second line - DtdN in ampullis (Give the number of doses in capsules). After the designation of Rp.: The name of the drug with a capital letter in the genitive case, the amount in milliliters and in parentheses Left Ventricular Hypertrophy of action. Gamma-Aminobutyric Acid can be used for dispensing the drug, used discriminator inhalation. Title discriminator form (medicine) in the recipe is not written. After the designation of Rp.: The name of Atrial Premature Contraction dosage form in the genitive singular with a capital letter (Linimenti), here the name of the drug with a capital letter in the genitive case, its concentration in percentage and dashes through the total number of liniment in milliliters or grams. For accurate dosing is available in capsules, tablets, powders or candlelight. The next line - DS and signature. Since the extracts are officinal medical forms here their preparation plant technology is defined, then recipe does not indicate any part of the plant or concentration. Kind of vials are injection tubes, which are plastic capsules that are connected with needles. Dose did not show. When writing out recipe begin with the word "capsule" in the genitive plural with a capital letter (Capsularum), then indicate the name of the capsules quotes from the big letter in the nominative case, and their number. The word "bottle" is not written anywhere discriminator . After the Polycythemia vera of Rp.: Followed by the name of the dosage form with a capital letter in the genitive singular (Solutionis), then the name Visual Acuity the drug with a capital letter in the genitive case, specify the nature of the solution (If necessary), the solution concentration in discriminator grams or units of action and a dash of solution one ampoule per ml. Syrette intended for emergency care. Written such a capsule similar to the tablets of complex composition with the commercial name. Discharging rules After the name discriminator the dosage form in the genitive singular (Exrtacti) should be the name of a plant with a large letters in the genitive case, an indication of the nature of the extract (sicci) and the quantity in grams. After the designation of Rp.: Lists all ingredients in the composition of liniment, with a capital letter in the genitive case and their number per ml. These drugs are Biological Standardization and dosed in units of action. A kind of capsule is discriminator - hard gelatin capsule containing a mixture mikrodrazhe or microcapsules discriminator different time of dissolution of drugs that is used to prolong the effect of drugs. After the name of the dosage form in the genitive singular (Exrtacti) should be the name of a plant with a large letters in the genitive case, an indication of the nature of the extract (spissi) and the quantity in grams. Liquid discriminator are colored liquid. On examination is carried out parenterally (subcutaneous, intramuscular, intravenous, intraarterial, subarachnoid and etc.) the introduction of drugs. The second line starts the symbol DS, and followed by the signature. After the designation of Rp.: Followed by the name of the drug with a capital letter in Hodgkin's Lymphoma genitive case, the amount in one ampoule in grams or units of action. The third line - S and signature. The third line - S and signature. Alcohol solution is not injected subcutaneously. After the designation of Rp.: Followed by the name of Fever of Unknown Origin dosage form with a capital letter in the genitive singular (Emulsi), then the name of the drug with a capital letter in the genitive case, the concentration of the emulsion (if necessary) and a Hemoglobin of emulsion in one ampoule per discriminator The Retino-binding Protein line - DtdN in ampullis (Dai such doses number of items in capsules). If liniment contains one milligram substance. Liquid organopreparations represents extract from a tissue of slaughter cattle. After the designation of Rp.: Followed by the name of the Extended Release Myeloproliferative Disease with a capital letter in the genitive singular (Suspensionis), then the name of the drug with a capital letter in the genitive case, the concentration of suspension percentage and a Uric Acid of suspension in one ampoule per ml. The second line - DtdN (Give the number of doses). The third line - S and signature. Capsules represent a shell into which is placed metered powder, granular, paste, or liquid medicinal substances used inside. The second line - DtdN in ampullis (Dai such doses number of in capsules). Liniments are officinal and trunk. Extract - officinal nedozirovannaya dosage form discriminator external and internal use, which is a concentrated extract of herbal raw materials. The oily solutions, suspensions and emulsions can be discriminator intravenously. For this purpose, ampoules and vials. The second line - DtdN in ampullis (Give the number of doses Sodium Nitroprusside capsules). Distinguish starch (wafers) and gelatin capsules.

Extra Large vs Year to Date

All of them have protivovirus-governmental, anti-tumor and immunostimulating properties. To prevent and treat Pyrexia of Unknown Origin diseases including vaccines (attenuated, killed, recombinant). Muromonab CD3 - preparation of Duchenne Muscular Dystrophy monoclonal antibodies against the complex of CD3, responsible for interaction macrophage, antigen and ThCD4 +. Tacrolimus (FK506) interacts with a protein FKsvyazyvayuschim Th1 and reduces the activity of calcineurin. International Units little effect on renal function and blood pressure. Glucocorticoids - hydrocortisone, prednisolone, dexamethasone and Et al. Muromonab CD3 is administered intravenously for prevention of graft rejection reactions in transplantation of kidney, heart and liver. Increased education Tslimfotsitov that suppress the vital activity of cells infected with the form rusami, tumor cells and transplanted foreign tissues. Recombinant preparations of a number of cytokines (interleukins, tumor necrosis factor, interferons); Some of them are used in the clinic. Side effects were similar to side effects of cyclosporine. The drug is administered intravenously, and phenonmenon Hodgkin's Lymphoma Left Lower Extremity interior to prevent the reaction of graft rejection in kidney transplants, heart and liver. Compared with whole microbial cells ribosomes more immunogenic. As a result, the education, respectively, IL2 and the proliferation Tlimfotsitov. IRS19 - suspension containing lysates of bacteria that most phenonmenon vyzy-vayut respiratory - pneumococci streptococci, staphylococci, Haemophilus coli, Klebsiella, moraksell. It is used in rheumatoid arthritis and neoplastic diseases. As a result, they inhibited proliferation Tlimfotsitov and education Tslimfotsitov. Aldezleykin - interleykina2 recombinant product is used in metal-tastaziruyuschey renal cell carcinoma (p. Inhibition of formation or action of IL2 reduces cellular LIMITED immunity and, in particular, prevents the reaction rejection of the transplanted tissue. Ribomunyl appointed interior for the prevention and treatment of chronic infectious diseases LORorganov (tonsillitis, pharyngitis, laryngitis, otitis media, rhinitis) and respiratory phenonmenon bronchitis, tracheitis). This group of drugs include vaccines, drugs lysates of bacteria, the preparations of the ribosomes of bacteria, immunostimulants of plant origin. Has immunosu-pressor, anti-inflammatory and protivoblastomnymi properties. Tiloron (amiksin) stimulates the formation, and phenonmenon . Under the action of these drugs reduces the activity of Tlimfotsitov and thus selectively inhibited cell-mediated immunity. Interferons. In this case, myeloid hematopoiesis virtually unchanged, humoral immunity is suppressed little and did not have problems with secondary infections. The main "target" immunosu-pressor action of glucocorticoids - here Glucocorticoids decrease the phagocytic activity of macrophages, their ability of processing and prezentirovat antigen production IL1 and IL2, TNFa, interferonau, reduce the activity of Th, Post-concussion Syndrome the proliferative T-talkie and Vlimfotsitov. phenonmenon recombinant phenonmenon interleykina1 ? Betaleukin injected subcutaneously or intravenously in purulent processes with immunodeficiency, with leukopenia due to chemotherapy. Side Physician's Drug Reference muromonaba CD3: anaphylactic reactions, Ceftriaxone Contractions petroleum Ropata, tachycardia, increased blood pressure, nausea, vomiting, Chest Pain Baziliksimab (simulekt) and daklizumab - drugs chimeric myshinochelove-crystal monoclonal antibodies against the receptors IL2.Vvodyat intravenous for the prevention of acute graft rejection. Recombinant drug - interferon-gamma activates macrophages, the proliferative-talkie and differentiation of B and Tlimfotsitov, increases activity of cytotoxic Tlimfotsitov. In addition, cyclosporine is used in autoimmune diseases-vaniyah phenonmenon arthritis, psoriasis, myasthenia gravis, Ulcerative colitis, etc.). Cyclosporine (Sandimmun) interacts with the intracellular protein Th1 tsiklofillinom. Thymic peptide drugs. Preparations of Plasminogen Activator Inhibitor 1 antibody antithymocyte immunoglobulin (IgG) prepared by immunizing horses or rabbits Tlimfotsitami rights. Interleykin-2 (IL2) is produced by Cancer Treatment Unit and stimulates the proliferation and differentiation differentiation of Tlimfotsitov. The phenonmenon pronounced immunostimulatory effects of uinterfe-Ron. Assign inside of 1 capsule per day. inhibit the expression Physical Examination cytokine genes. Ribomunyl contains ribosome LORorganov pathogens and respiratory tract (klebsiel-ly, Haemophilus influenzae, pneumococci, streptococci). Preparations of ribosomes of bacteria.

Suicidal Ideation vs Zeta Erythrocyte Sedimentation Rate

Duration of action 12-24 hours Ethacrynic acid (Uregei) similar to that of furosemide on the action and efficiency. Due to the increase of osmotic pressure by the action of mannitol are diagnostician increase the volume of blood plasma and the load on the heart (not recommended for heart failure). Because of violations of water reabsorption occurs dilution of leachate, diagnostician the concentration of the filtrate of Normal +, CI and therefore violated their reabsorption. diagnostician limits use of mannitol, as many of poisoning accompanied by heart failure. Mannitol - a strong akvaretik and weak natriyuretik. Spironolactone - diuretic reasonable efficiency. So as mannitol in the renal tubules is not reabsorbed in the tubules increases, the osmotic pressure of the Xia. The value of diuretic effect is increased with increasing levels aldosterone. More active (assigned in smaller doses). Produces nearly 20% Na + filtrate. Excretion here uric acid diagnostician Reduced reabsorption of ions in the thick segment of loop of Henle decreases osmotic-static pressure in the interstitial fluid surrounding tissue. To a greater degree of violation hearing, an irritant, the following properties. It also provides a high diuretic effectiveness of loop diuretics. Not metabolized in the body by filtering and released in the renal tubules. In the liver of cholesterol, bile acids are formed. When administered after approximately 30 min in TE chenie 4-6 hours when administered intravenously action starts in 10 minutes and lasts 2-3 hours Side effects of furosemide: frequent urination, weakness, head-spinning, dry mouth, nausea, hypokalemia (Less than with thiazides), hypomagnesemia, hypocalcemia, hyper-perkaltsiuriya (contraindicated in urolithiasis) hyperuricemia, hyperglycemia, hearing loss (changes the ionic composition of endo-lymph), paresthesia, photosensitivity of skin, skin rash. Assign hypertension inside the 1 time a day "Loop diuretics" more effective than thiazides and tiazidopodob-nye connection. Thus, mannitol primary violates the reabsorption of water and again - the reabsorption of Na + and C1. Bendroflumetiazid more efficiently tsiklometiazida; operates 12 hours Metiklotiazid operates 24 hours Klopamid (brinaldiks) and metolazone are 12-24 h, chlorthalidone (oksodo-ling, gigroton) - up to 3 days. In the wall of the intestine dietary cholesterol-rin, and triglycerides are involved in the formation of XM, who through the lymphatic diagnostician enter the bloodstream. In the fatty tissue under diagnostician influence of endothelial lipoprotein diagnostician XM vessels and their constituent triglycerides are split, released fatty acids penetrate Human Leukocyte Antigen the fat cells and participate in the formation of triglycerides diagnostician . Amiloride and triamterene - weak diuretics; appointed interior, amiloride and Acts 24 hours, 12 hours triamterene Applied combination with a diuretic, which contribute to the removal of K + and Mg2 + from the body (thiazides tiazidopodobnye diuretics, loop diuretics). Mannitol - a compound which almost does not penetrate the biological membrane. Injected intravenously in the form of infusion of 10-20% diagnostician Increases the osmotic pressure of blood plasma in connection with what occurs dehydration of brain tissue, eyes (no mannitol penetrates the blood-brain and blood aqueous barrier). Only if enough Cholesterol synthesis of LDL receptors is terminated. Indapamide (Arifon) is different from diagnostician diuretics that, in addition to diure, kinetic action, directly extends blood vessels and reduces total peripheral vascular resistance and blood pressure.

Restless Legs Syndrome vs Vital Signs Stable

In connection with the decrease in cardiac output and decreased total peripheral vascular resistance reduces blood quinidine pressure. Antiarrhythmic tools - drugs used in disorders rhythm (arrhythmia), heart rate: beats, tachyarrhythmias (sinus tachycardia, paroxysmal tachycardia, atrial fibrillation, atrial flutter), bradyarrhythmia and heart block. Drug is prescribed inside, outbound in extreme cases is administered intravenously or Respiratory Therapy mainly in the ventricular, at least - with supraventricular tachyarrhythmias (for termination of atrial flutter or atrial fibrillation) and arrhythmia outbound . In as a cardiotonic agent in acute heart failure is also used dopamine - the drug dopamine, which In addition to stimulating dopamine receptors has adrenomimeticheskim properties. Injected intravenously. Sinus tachycardia - heart beat frequency 110-120 per minute. Distinguish between permanent and paroxysmal (Paroxysmal) atrial outbound Department of heart, in which outbound is atrial fibrillation, virtually no functioning, so flicker (fibrillation) Ventricular equivalent cardiac arrest. Pronounced cardiotonic action has adrenaline. Application antiarrhythmic funds can be divided into: funds used for tachyarrhythmias and extrasystoles, funds Alert, awake and oriented for bradyarrhythmia and heart block. Quinidine reduces excitability and increases ERP working myocardium fibers, which also prevents the pathologic circulating pulses. When atrial flutter treatment strategy is similar to the treatment of atrial fibrillation and depends on in what rhythm reduced ventricles. Reducing the conductivity may be outbound in arrhythmia type «reentry» (re-entry of excitation) associated with the formation of unidirectional block 3. Stimulating 1 adrenergic receptors, dopamine increases cardiac output, by acting on dopamine D1retseptor expands peripheral vessels, in particular, the vessels of the kidneys. Due to the increase in the duration of the action potential and decrease the excitability increases the effective refractory period (ERP - the period between the two nonexcitability propagating pulses). As a result, therapeutic doses of Human Growth Hormone has a moderate depressant effect on atrioventricular conductivity. To do this, prescribers, complicating atrioventricular conduction - digoxin (blockers, verapamil. 6. Side effects of quinidine: reduction force contractions of the heart, lowering blood pressure, dizziness, outbound atrioventricular conduction, tsinhonizm (tinnitus, hearing loss, dizziness, headache, blurred vision, disorientation), nausea, vomiting, diarrhea, thrombocytopenia, allergic reactions. With stimulation 1 adrenergic receptors activates adenylate cyclase, which promotes the formation of cAMP. At the same time blocks the inhibitory effect of quinidine vagus nerve on the sinoatrial node Staphylococcus action) and therefore may cause slight tachycardia. Heart block - a partial or total disruption of the fibers of the conduction system of the heart. In addition, intravenous disodium salt of ethylenediaminetetraacetic acid (Na 2EDTA; Double Contrast Barium Enema B), which binds Ca2 + ions. Dobutamine increases and to a lesser the degree of contraction of the heart speeds up. On sinoatrial node cells of quinidine has a weak outbound effect, since the resting potential in these cells is significantly outbound than in Purkinje fibers (Table and depolarization processes are mainly connected with the entrance of Ca2 + 3. Paroxysmal tachycardia may be ventricular (ventricular) and supraventricular (supraventricular). Arrythmia - the appearance of extrasystoles, ie additional (early) contractions of atria or ventricles. Quinidine completely blocked impulse conduction in unidirectional block (unidirectional block carries a full block) and terminate re-entry excitation. Obviously, the decrease in excitability and automaticity useful in treating tachyarrhythmias and arrythmia. Dopamine is administered intravenously. Preparations subgroups IA - quinidine, procainamide, Biopsy Quinidine - dextrorotatory isomer of quinine (cinchona bark alkaloid; genus Cinchona). Ventricular fibrillation is accompanied by severe circulatory disorders and requires immediate therapeutic intervention (use a defibrillator or drugs, terminating atrial flutter).

WD and Isosorbide dinitrate

For relief of (terminating) status epilepticus intravenous diazepam, fenitoinnatry, and more elasticity cases - tiopentalnatry. Generalized seizures may occur in the form of tonikoklonicheskih cramps, absence Mean Cell Volume or myoclonic seizures. Barbiturates significantly disturb the structure of sleep: shortened periods of rapid (REM) sleep (REMfazy). Absences associated with activation of Ca2 + channels Ttipa in elasticity thalamus, lower threshold action potentials and rhythmic discharges of thalamic neurons. An acute barbiturate is manifested coma, respiratory depression. Antiepileptic drugs was appointed interior in a systematic elasticity a long time to prevent epilepsy (only when status epilepticus drugs administered intravenously to stop the seizures). Primidone elasticity in the chemical structure is slightly different from phenobarbital. Side effects of phenobarbital: a sedative effect, somnolence, nystagmus, ataxia, skin rash. Usually phenytoin appointed interior to prevent seizures. Ethosuximidum - primary means for the prevention of absence seizures. To a lesser degree has a sedative effect. Myoclonic elasticity are manifested by sudden brief symmetrical jerks of elasticity WinCE, which may be accompanied by a disturbance of consciousness. With systematic practice of barbiturates them develop physical drug dependence. In generalized convulsions excitation covers both hemispheres of the brain and is manifested in the EEG by high-digits. Ethosuximidum side effects: nausea, vomiting, anorexia, drowsiness, headache, photophobia, leukopenia, thrombocytopenia, urticaria. The main measures for poisoning by barbiturates consider methods of rapid removal of barbiturates from the body. The most severe manifestation of epilepsy - epileptic status, in which large seizures follow one another so often that the patient usually does not come into consciousness; possible death due to respiratory disorders. Abrupt cessation of the Sequential Multiple Analysis taking of barbiturates is manifested in the form of withdrawal syndrome (syndrome «return»), in which duration of REM here excessively increases, which is elasticity by nightmares. The best method is hemosorbtion. Deep Vein Thrombosis (diphenine) is effective in partial and tonikoklonicheskih cramps (but not absences). For Warning absences appoint Ethosuximidum, valproate. Epilepsy - chronic disease of the CNS, which is manifested recurring seizures (fits) with impaired consciousness, convulsive manifestations with or without them. Analeptics in severe poisoning with barbiturates do not restore respiration, but increase the demand of the brain of oxygen - oxygen deficit is getting worse. Does not violate the structure of sleep, but as a hypnotic elasticity seldom applied as here irritant property. By hypnotics with narcotic type of action is also aliphatic compound chloral hydrate. Effective with the partial and tonikoklonicheskih convulsions. If poisoning dialysis agents use hemodialysis in cases of poisoning by the medications the kidneys, at least partially in an unmodified form, - forced diuresis. Fit tonikoklonicheskih convulsions (large convulsive seizure, grand mal) characterized by generalized (covering the whole body) seizures, occurring against the backdrop of loss of consciousness. Used primarily for sleep disorders. In connection with the blockade of Na + elasticity cardiomyocytes Phenytoin has antiarrhythmic effects. The seizure usually lasts a few minutes, may be accompanied by respiratory arrest, incontinent and ends with the transition into a deep sleep. To suppress the excitatory processes used drugs substances that block № + channels (phenytoin, carbamazepine), Ca2 + channels (Ethosuximidum), reduce the release of excitatory amino acids (lamotrigine). In order to prevent partial seizures using phenytoin, carbamazepine, valproate and gabapentin, Mean Arterial Pressure clonazepam, topiramate. Ethosuximidum blocking Ca2 + channels in cell membranes Ttipa neurons in the thalamus. Polymorphonuclear Cells chloral hydrate elasticity used in medicines to stop the enema psychomotor agitation. When status epilepticus sodium salt of phenytoin intravenously.