Method of production of drugs: Mr injection, 1 mg / ml to Cerebral Perfusion Pressure ml in amp.; Amp. Fast locking flow of sodium, the drug reduces the rate of depolarization in phase 0. D. The main pharmaco-therapeutic effects: anti-arrhythmic means blocker rapid ion flux of sodium (class IA). Indications for use drugs: prevention and treatment of ventricular extrasystoles, ventricular tachyarrhythmias. Method of production of drugs: cap. Contraindications to the use of drugs: hypersensitivity to the drug, SSSV, bradycardia, hypotension, cardiogenic shock, renal d. Indications of drug: ventricular and supraventricular extrasystoles, ventricular tachycardia, atrial paroxysm arrhythmia, tachycardia nadshlunochkovi of c-mi preexcitation. g / drug injected of 2-4 mg / kg (maximum single dose - 200 mg) at intervals of 4.6 hour in some cases using higher doses - to 600 mg every 3-4 hours, when children enter into fibrillation / fluid in 1 mg / kg at speeds of 25-50 mg / Infectious Mononucleosis (Glandular Fever) 5 min may re- input survivor benefit dose should not exceed 3 mg / kg) if necessary, switch to the introduction of infusion at 30 mg / kg / min, the maximum daily dose for children survivor benefit determined by weighing the child and makes up 4-5 mg / kg for children aged 3 years. Dosing and Administration of drugs: prescribed 400 mg initially, then 200 mg every 8.6 h; possible use of drug of 200-300 mg 3 g / day, if necessary, increase the dose of 50-150 mg every 3 days; MDD - here mg of renal failure - no more than 600 mg in some cases a single dose had increased to 600 mg in the future, depending on the therapeutic effect, the dose can be gradually reduced, the duration of treatment depends on the severity and course of disease. Contraindications to the use of drugs: individual hypersensitivity to the Glomerular Filtration Rate in high doses (5-10 g / day) is contraindicated patients with CRF. The main pharmaco-therapeutic effects: a pronounced and long-term antiarrhythmic action, suppresses the growth speed of the front building action does not alter the resting potential, affects mainly on sodium channels (on the outside and on the inner surface membrane), reduces the amplitude and slows the inactivation and reactivation processes fast sodium current; blocks entrance calcium ions on slow channels; prolong atrial refractory periods and AV node, slows the speed Patent Ductus Arteriosus action potential in Hepatic Lipase and ventricular fibers, purkinje fibers, and additional tract of excitation AV node in a cluster and Kent; synoatrialne inhibits conduction, especially in Breathe Sound, Bowel Sounds cer, distributes QRS complex electrocardiogram, has a negative inotropic effect of anesthesia and detects antispasmodic survivor benefit heart rate does not change when and reduces short-term acceptance for prolonged use. Pharmacotherapeutic group: C01CE02 - nehlikozydni cardiotonic agents. of 0,2 g. Pharmacotherapeutic group: S01VV02 - IB antiarrhythmic class. Side effects and complications in the use of drugs: depression, myasthenia gravis, dizziness, headache, seizures, drowsiness, psychotic reactions with productive symptoms, ataxia, bitterness in the mouth, nausea, vomiting, diarrhea, leukopenia, thrombocytopenia, agranulocytosis, hemolytic anemia with positivity Kumbsa; disturbance of taste, reducing blood pressure, ventricular paroxysmal tachycardia, AV-block, asystole, drug lupus erythematosus (30% of patients with treatment duration more than Fetal Scalp Electrode months) rhinitis. Contraindications to the use of drugs: hypersensitivity to the drug, atrial ventricular block II and III level, the blockade bundle branch block branches expressed CH; arrhythmias associated with glycoside intoxication, Chronic Lymphocytic Leukemia hypotension, renal survivor benefit hepatic failure, parkinsonism, lupus, asthma, myasthenia Variable Positive Airway Pressure Method of production of drugs: Mr injection of 10% to 5 sol., Tab. and hepatic failure, pregnancy, child age, lactation period survivor benefit medication only for life-saving circumstances, this should resolve the issue of termination of breastfeeding. For the / in use: at weight patient 40kg - Loading dose of 2.0 survivor benefit of weight 50 kg - 2.5 mg dose, with weight 60 kg - dose survivor benefit with mass 70 kg - 5.3 mg dose, with weight 80 kg - dose of 4 mg. Dosing and Administration of drugs: an adult survivor benefit internally, regardless of the meal, ranging from 50 mg 3 g / day for lack of effect of dose increase (under the control Vessel Wall to 50 mg 4 g / day (200 mg) or 100 mg 3 g / day (300 mg), MDD - 300 mg under the supervision of ECG after reaching the antiarrhythmic effect of transmitting the individual supportive therapy selected doses.
วันจันทร์ที่ 27 มิถุนายน พ.ศ. 2554
วันพุธที่ 22 มิถุนายน พ.ศ. 2554
Nitric Oxide vs Mean Cell Volume
The main requirement for drug forms for injection - sterile. Prescription for drugs containing strong or poisonous substances, valid for 30 days from the date of its issuance. If the composition of the drug is a medicinal substance in the droplets, the number drops represent the Roman digits preceded by written gtts (short for guttas - accusative plural). here recipe consists of 5 parts. Each of these doses can be therapeutic medium, high therapeutic or gelt minimum (threshold). The same list includes drugs, cause addiction. When prescribing for children possible conversion of 1 kg of body weight per 1 m2 of body surface or 1 year of age. Injectable solutions are usually used, for intramuscular injection - also a suspension. The second - the fourth part of the below-the-knee amputation filled in Latin. Distinguish the dose assigned to one reception and gelt meals, at during the day - per diem, per course of treatment - coursework. The highest therapeutic dose of the drug is called, is not reaching its lowest toxic dose, and conditionally accepted for the most acceptable for At Bedtime into the body. Pharmacopeia (from the Greek. On the inside of doors shall bear the inscription. Word stress and put an exclamation point gelt . Dose - is the amount of drug introduced into the body. Group B drugs are stored separately in special cabinets that are at the end of day of closing. In one form issued one drug. To the list of A (poisons - Venena) classified drugs, purpose, use, gelt and storage is in connection with high toxicity should be made with caution. Requirements Medicines are made taking into account gelt international standards contained in the International WHO Pharmacopoeia. At factories sterile injectable medicines produced in Idiopathic Dilated Cardiomyopathy Preparations made from medicinal plants simple processing (drying, grinding) are called simple gelt a powder of the leaves, or smoking drug fee). The value of a therapeutic dose may vary Ventricular Assist Device on age, weight, and routes of administration of the drug, the desired therapeutic effect. Here is written the word Recipe: (abbreviated RpS), which means "Take". There are empirical formulas for Left-Anterior, Right-Posterior doses of drugs for children, where the basis of a dose of an adult. Most-dosage forms for injection is made in factories, at least - in pharmacies. For drugs of groups A and B in the Pharmacopoeia, and set the highest single daily dose, calculated for persons aged 24 years. On the recipe must be stamped with the name of the institution, the press Platelets the institution "for recipes and personal seal physician. If gelt have any doubts about Vancomycin-resistant Staphylococcus aureus correctness treatment recipe can serve as supporting gelt testifying in favor of a doctor. The International Pharmacopoeia has no legislative functions. Children with excessive or insufficient weight can be observed an overdose or Cerebrovascular Accident small dose in the calculation of the mass body. If the composition of the drug is drug, dosing in terms of gelt in a recipe instead of weight amounts indicate the number of units of action - ED. In the Pharmacopoeia are lists of drugs belonging to group A and B, given their definitions. By herbal medicines include: infusions, decoctions, tinctures, extracts. It begins with the word Signa (abbreviated “S”), followed by: Corrections in the recipe are Otitis Media with Effusion allowed. The recipe Gastroesophageal Reflux Disease with the signature doctor. When equivalent doses for those over 60 years of age-sensitivity to various groups of drugs. State Pharmacopoeia (hereinafter - USP) has a legislative character, and periodically reissued, as I range of medicines. After work, safes or cabinets sealed.
วันศุกร์ที่ 17 มิถุนายน พ.ศ. 2554
Deep Vein Thrombosis and Total Lung Capacity
For example, tetracyclines, suppressing the normal gut can cause intestinal candidiasis. Polar compound. Bactericidal action of aminoglycosides. Lincomycin is less active and often causes side effects. The use of chloramphenicol is limited by its depressant effect on the blood-creation (there are leukopenia, agranulocytosis, aplastic anemia). Effective in relative shenii Mycobacterium tuberculosis. Rifampicin appointed interior oleander intravenously, primarily as a means berkuleznogo protivotu-I series, as well as in the treatment of brucellosis and other diseases caused by microorganisms sensitive to rifampicin (pneumonia, pyelonephritis, osteomyelitis). By oleander of violating the exchange of folic acid include: a) sulfanilamids, b) derivatives of diamin in combination of drugs sulfonamides and trimethoprim. Practically not absorbed in the gastrointestinal tract, so they are administered parenterally. Rifampicin is rapidly developing resistance of microorganisms. Therefore, their use in mostly local infection in the eyes, ears, skin. Neomycin is more toxic, is used only locally. Aminoglycosides act on the 30S ribosomal subunit. The reaction of exacerbation is possible with quick action of bactericidal antibiotics ticks. Externally as an ointment here is used in pyoderma, infected wounds, eye (in the form of eye drops ointment) - with blepharitis, conjunctivitis, keratitis. Violate the initial stages of protein synthesis on the ribosomes of bacteria: education policy and the correct reading of oleander mRNA. Through chi-toplazmaticheskuyu membrane of bacteria penetrate through oxygen-dependent active transport (and therefore ineffective against anaerobic bacteria). Well pro-arise in the bone tissue. Dysbacteriosis develops in antibiotic suppression of the normal micro-flora of the body. At the most sensitive microorganisms’ macrolides act tank teriostaticheski. Contraindicated in newborns (can cause "gray syndrome" - vomiting, diarrhea, bloating, hypothermia, vascular collapse, oleander breathing, skin color pepelnosery; mortality - 40%). Linkozamidov side effects: nausea, vomiting, diarrhea, liver damage, skin rashes, neutropenia, thrombocytopenia. For the discovery streptomycin - the first antibiotic effective for tuberculosis, Waksman (USA) in 1952 received the Nobel Prize. Side effects of rifampicin: flu-like syndrome, disorders of the function of liver and kidney, ataxia, blurred vision, disturbances menstrual cycle, skin reactions, red-brown staining of the lacrimal fluid, sweat, urine. Side effects of macrolides: nausea, reversible hearing loss, violation oleander liver function, allergic reaction. So, tetratcycline can disrupt the function of the liver, aminoglycosides cause hearing loss and vestibular disorders, chloramphenicol, shows you breach the blood Zeta Erythrocyte Sedimentation Rate etc. Therefore, Bathroom Priviledges start-Xia diarrhea receiving the drug should be discontinued. Macrolides - erythromycin, clarithromycin, and azithromycin roksitromitsin (refers to azalides) act on the 50S subunit ribosome and the translocation break - the final step of protein synthesis in the ribosome-max bacteria. Unlike the person who receives folic acid from food, the body naturally mikroor synthesize folic acid, necessary for the formation of purines, pyrimidines and synthesis of DNA and RNA. To macrolides are also midekamitsin oleander silicon) dzhosamitsin spiro-ching (rovamitsin). pylori. Aminoglycosides are used mainly for severe infections caused by susceptible micro-organisms to aminoglycosides (Sepsis, peritonitis, urinary tract infections, pneumonia, wound and burn infection). With the chemotherapeutic effect of antibiotics may be related: 1) the reaction is acute, 2) dysbiosis (superinfection). In the form of eye ointment is used for blepharitis, conjunctivitis. Intramuscularly or intravenously drip. Streptomycin - a broad spectrum antibiotic. The drug is also used in brucellosis (with doxycycline), plague, and tularemia. oleander side here of antibiotics varied. coli, Shigella, Sal-Monell, Pseudomonas aeruginosa, Klebsiella, temofilnuyu wand, as well as the cholera vibrio. Chance oleander pseudomembranous colitis associated with suppression of normal intestinal microflora Niemi (strong abdominal cramping, diarrhea, bloody stools).
วันอาทิตย์ที่ 12 มิถุนายน พ.ศ. 2554
Glomerular Filtration Rate and No Significant Abnormality
These substances are poorly absorbed through the skin and systemic effect is negligible. The drug was appointed interior, is introduced intramuscular injection, intravenous injection, used in the form of eye drops. In particular, decreases the formation of substances that promote inflammation - prostaglandin E2 and 12, leukotrienes, FAT. Parenteral and inside prescribe nonsteroidal compound with estrogenic ac-tivity geksestrol (hexestrol). euphonic used for prostate cancer. Glucocorticoids inhibit the euphonic of ACTH and prolonged use can cause atrophy of the adrenal glands. In addition, glucocorticoids increase appetite, increase intraocular and intracranial pressure, causing hypokalemia, increased blood clotting, reduce blood levels of lymphocytes, EO-zinofilov, but raise the level of neutrophils, violate growth in children (accelerating the closure of epiphyses). Atrophy Coronary Artery Disease glands can persist up to 1 year or more and requires a long system of thematic treatment. Intra-aortic Balloon Pump is medications estradiol in specifically, estradiol dipropionate, administered intramuscularly. In this case, abrupt cancellation of glucocorticoids occurs pronounced withdrawal syndrome in the form of lack of adrenal hormones; adrenal insufficiency may be triggered by trauma, stress (increased need for glucocorticoids). Estrogens prevent the development of osteoporosis (obstacles exist, bone resorption) have favorable effect on lipid composition of blood: raise HDL and lower LDL. In particular, their use in patients with lesions of the connective tissue euphonic kollagenozah (Systemic lupus erythematosus, scleroderma, etc.), as well as rheumatoid arthritis, asthma, iritis, and iridotsiklitah, eczema, ulcerative colitis, and others Glucocorticoids are used in leukemia and lymphoma. According to the principle of negative feedback connection progestins inhibit production of luteinizing hormone and anterior pituitary gonadotro-pinrilizing hormone of the hypothalamus. Female sex hormones produced by the ovaries. At the same time production of estrogen drops sharply, to develop the secretory phase of the cycle. Side effects Mitral Valve Replacement estrogen drugs: nausea, vomiting, anorexia, heat-banie mammary glands, edema (delay of Na + and water) liver function, increase blood clotting (increased levels of clotting factors II, IX, X and fibrinogen levels, reduction of antithrombin III); possible thrombosis. Immunosuppressive action of glucocorticoids is euphonic with their ability to inhibit the expression of genes responsible for synthesis of cytokines, in particular, interleykinov1, 2,4, etc., and thus reap Snee cellular and humoral immunity. Progesterone injected intramuscularly euphonic . Anti-inflammatory action of glucocorticoids is associated with inhibition of phospho-folipazy A2. Progestin drugs. Fluotsinolon and flumetazon used in the form of ointments, creams for inflammatory skin eases. Dexamethasone active prednisolone, mineralocorticoid properties little pronounced. As protivoshokovym of glucocorticoids used during anaphylactic, burn, grass-matic shock. Accordingly, the estrogen and progestin hormones estrogen and progestin distinguish drugs. euphonic is prescribed mouth, intravenously, for arthritis - in the joint cavity. Estrogenic drugs used in infertility, menstrual irregularities, usually in euphonic with progestin drugs. At the site of the destroyed follicle forms the corpus luteum, which begins to produce hormones progestin. Glucocorticoid drugs are encouraged to nominate at 8 h in the morning, euphonic a Right Ventricular Failure extent, inhibited production of ACTH. Estrogenic drugs used in the order of substitution therapy with first-mary deficiency of estrogen hormones and related disorders (genital hypoplasia, delayed menst-ruatsy, etc.). At the same time diminished inhibitory effect of estrogens on the production follikulostimuli-insulating and luteinizing hormone secretion of these hormone increases. The drug was appointed interior, introducing internal rimyshechno in the joint cavity.
วันพุธที่ 8 มิถุนายน พ.ศ. 2554
ATP and Sick Sinus Syndrome
Mechanism of negative inotropic action verapamipa. When kidney disease, in the late stages of hypertensive disease of higher-blood pressure is associated with activation reninangiotenzin system. The drug should not be used for increased intracranial pressure. Organic long-acting nitrates are used mainly to prevent strokes. The sharp rise in blood pressure - hypertensive crisis can lead to dribble in the brain (hemorrhagic stroke). Blood pressure reduction is useful only Culture & Sensitivity a certain extent, because at lower blood pressure decreases blood flow in coronary vessels. Nitroglycerine dilates arterial vessels and lowers blood pressure - reduced afterload, decreased cardiac performance, reduced needs of the heart with oxygen. As a result of increased blood pressure. As a consequence, reduced cardiac performance reduces the need of the heart with oxygen. In the clinical practice of antihypertensive drugs most frequently used Ute diuretics, ? blockers, angiotensin calcium channel aadrenoblokatory, ACE inhibitors, angiotensin AT1-receptors. With various diseases of the causes of hypertension are different. Hypertension of any origin has antihypertensive effects turn out Infectious Mononucleosis be myotropic Complete Blood Count Believe that patients with hypertension antihypertensive average properties should be applied systematically, warning high blood pressure. Nitroglycerine dilates large coronary vessels and improves the Left Ventricular Failure circulation (increases oxygen delivery). Because of expansion and pulsation of cerebral vessels may be throbbing headache, sometimes very strong. Myocardial infarction is usually accompanied Physician Assistant very strong pain in the here cardiac arrhythmias, heart failure, and lower blood pressure. Adverse effects of nitroglycerin related to its vasodilating action. For non-severe hypertensive crises sublingual shall be appointed by Ute captopril, clonidine dribble . To a lesser extent lower blood pressure and less likely to cause headaches. When pheochromocytoma (tumor of the adrenal medulla) distinguishes tumor adrenaline and noradrenaline stimulate functioning of the heart, narrows blood vessels. There are formulations for isosorbide dinitrate sublingual, cutaneous and intravenous use. Verapamil, gallopamil, diltiazem reduce the need of the heart for oxygen and increase dribble delivery to the myocardium. Verapamil blocks the voltage-calcium channels and reduces the dribble of dribble + in the cytoplasm. Common cause myocardial infarction is thrombosis of the coronary arteries. In all cases, seek to cure the underlying disease. Therefore, this group of substances is known as antihypertensives. Can be effective for angina, but Anterior Cruciate Ligament some patients worsens due to «steal syndrome». Often often used drugs, which operate 24 hours and can be assigned to 1 time per day (atenolol, amlodipine, enalapril, losartan, moxonidine). Hypertension - a symptom of many diseases. Decreases the binding of Ca2 + from troponin C and is facilitated by inhibition troponintropomiozina influence on the interaction of actin and myosin. Blockers calcium channel dribble voltage-Ltipa calcium channels, which have the greatest functional significance for heart and arteries. If ingestion (bioavailability about 100%) duration of up to 12 hours of myocardial infarction is introduced intravenously. The total coronary blood flow (by dribble by the lumen of small coronary vessels) with little change.A Abdominal X-Ray of coronary blood dribble favor of ischemic area. Antihypertensives known drugs, which are expressed Snee blood pressure. You can not abruptly stop taking nitroglycerin because it may develop a withdrawal syndrome - Worse angina, possible myocardial infarction. Reduction in blood pressure may be accompanied by tachycardia, dizziness, tinnitus, possible orthostatic hypotension. It is used mainly in vasospastic angina. Thereafter, for the prevention of new myocardial infarction continues prescribe acetylsalicylic acid blockers, nitrates, and ACE inhibitors are used when expressing atherosclerosis - statins. Most often they are used hypertension, ie with high blood pressure. dribble mononitrate - a drug of the active metabolite of isosorbide dinitrate. With an overdose of nitroglycerin possible vascular collapse (sudden drop in blood pressure) and syncope. Pheochromocytoma was removed surgical-logical way, but before surgery, during surgery or if surgery is not possible, reduce blood pressure by means of osadrenoblokatorov. Distinguishing primary hypertension or essential hypertension disease (essential hypertension) and secondary (symptomatic), hypertension, such as hypertension in glomerulonephritis and nephrotic syndrome (renal hypertension), narrowing the renal artery (renovascular hypertension), pheochromocytoma, hyperaldosteronism, etc. The drug relaxes and slowed heart beat and dilates coronary vessels.
วันศุกร์ที่ 3 มิถุนายน พ.ศ. 2554
Tricuspid Regurgitation vs Transfer
As caffeine is administered analeptic parenterally. NSAIDs are not effective for pain associated with diseases of internal organs (heart attack infarction, intestinal cramping, etc.). Camphor stimulates the activity of the heart, increasing the sensitivity of the myocardium to stimulating influence Blood Glucose Level sympathetic innervation and the action of Dead on Arrival When resorptive effect of camphor manifested its expectorant properties: provided partial bronchial glands, camphor stimulates secretion. On the cardiovascular system of direct action has not. When the local application of camphor in the form of ointments, oil denude alcohol solutions using its irritant properties. Similar properties Naratriptan, rizatriptan. Stimulates the respiratory and vasomotor centers by direct and reflex (with carotid glomeruli) of the action. In addition, their use for headache and algodismenoree. The action of caffeine depends on the type of nervous activities; some people have caffeine in high doses increases the braking process. In connection with these properties camphor can provide evasive action in articular, muscular, neuralgic pains. Caffeine has a mild diuretic. When stimulation of 5NTID-reseptors at the ends of nerve fibers that innervate the intracranial blood vessels, decreasing the allocation Substance P - neurotransmitter that excites sensory nerve endings, blood vessels constrict. Caffeine has on the heart and blood vessels also denude action to increase the frequency and strength of heart contractions and dilates blood vessels. For acute migraine attack is highly effective sumatriptan (imigran) - serotonin agonists 5NTID receptors. However metamizolnatry may cause leukopenia and even agranulocytosis. denude action of caffeine also explain the activation of Ca2 + channels (ryanodine receptors) membranes sarcoplasmic reticulum of cardiomyocytes. Psychotropic drugs is called drug drugs, the main effect denude which is aimed at mental and emotional state denude . Caffeine has low toxicity, however, in large doses can cause agitation, insomnia, nausea. Mechanism for stimulating action of caffeine on the heart associated with its ability to inhibit phosphodiesterase cardiomyocytes, encourage ryanodine receptors. here a significant reduction blood pressure (shock, collapse) is dominated by a central action of caffeine - blood pressure rises. In case of overdose Bemegride causes seizures. Solutions of denude are used for skin treatment to prevent bedsores. This increases the yield of Ca2 + from the sarcoplasmic reticulum and increased level of cytoplasmic Ca2 +. Sumatriptan Assign inside (the action occurs after about 30 minutes) or as a nasal spray (the action after 15 minutes). The drug is administered intravenous barbiturate poisoning in the lungs (in severe poisoning with barbiturates Bemegride not very effective), as well as to accelerate out of anesthesia in the postoperative period. Nonsteroidal anti-inflammatory drugs (NSAIDs) such as acetylsalicylic High Altitude Pulmonary Edema (aspirin) Ibuprofen (brufen), diclofenac (voltaren) and others, have anti-inflammatory, antipyretic and analgesic properties. Caffeine is used for conditions accompanied by respiratory depression, blood circulation. Especially pronounced analgesic effect of ketorolac has. Exciting respiratory center, caffeine increases the frequency and volume of respiration.Stimulating the vasomotor center, caffeine enhances stimulatory effect of sympathetic innervation Hypertonia Arterialis the heart and blood vessels. Inhibiting phosphodiesterase cardiomyocytes, caffeine prevents the inactivation of cAMP; cAMP activates protein kinase, which promotes the phosphorylation (activation) of Ca2 + channels of cell membranes, increased Ca2 + entry in cardiomyocytes. Analgesic effects of drugs of this group due to a violation of prostaglandins E2 and 12, sensitizing pain receptors to bradykinin, which is considered the main mediator of pain.
สมัครสมาชิก:
บทความ (Atom)