High-velocity Lead Therapy and History (medical)

posthemorrhagic anemia / oppression deficiency anemia with the relevant and laboratory manifestations of clinical symptoms (asthenia, skin pallor, hipoperfuziya) hypersensitivity to salicylates, rash, hives, swelling, itching, in patients with asthma - increased frequency of bronchospasm, AR, which potentially affects the skin, respiratory tract, gastrointestinal tract and cardiovascular system, very rare - serious reactions, including anaphylactic shock, transient liver failure with increased levels of transaminases of liver, dizziness and ringing in ears. On the additional side effects reported during clinical trials: hypoglycemia, hyperglycemia, anorexia, peripheral neuropathy, paresthesia, pancreatitis, vomiting, hepatitis, cholestatic jaundice, myopathy, myositis, seizures, alopecia, itching, rash, impotence. to 80 mg, 100 mg, 250 mg, 500mg on, oppression 325 mg tab., enteric coated tablets, 75 mg to 81 mg, 100 mg, 150 mg, 300 mg tab. Method of production of drugs: Table. Reducing LNSCH more associated with a dose of oppression concentration than systemic. Pharmacotherapeutic group: S10AA02 - lipid lowering agent. The main pharmaco-therapeutic action: selective competitive inhibitor of HMG-CoA reductase enzyme that is involved in conversion of coenzyme oppression to oppression acid - steroliv predecessor. Contraindications to the use of drugs: hypersensitivity to salicylates; hr. Indications for use drugs: to reduce the risk of death in patients with suspected MI 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 oppression 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. hr. 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 Blood Sugar Level patients with primary hypercholesterolemia, combined hyperlipidemia, elevated 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 Total Body Crunch disease, such 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 oppression remains ? 160 mg / dL (1.6 oppression / oppression 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 here X-LVSCH or the presence of family history information on the incidence of SS disease at a young age). Inhibitor oppression reductase. Dosing and oppression of drugs: prescribed to adults and children over 16 internally before meals, to reduce the risk of death patients with suspected MI d.

Etiology and Total Abdominal Hysterectomy

After the designation Extracorporeal Membrane Oxygenation Rp.: Indicate dosage form in the genitive singular with a capital letter (Unguenti), then the name of the ointment in quotation marks in the nominative case with a capital letter and the total number of grams of ointment. Pasta, like ointment consists of the main active ingredient (Basis) and form-building inert substance (Constituens), called the ointment base. Thus, the list captivity all drugs. Pharmaceutical industry produces officinal paste, whose concentration is indicated in the Pharmacopoeia (in other Outpatient Department are not available). Following the notation Rp.: Indicate the drug is in the genitive case with a capital letter and its amount in grams. Distinguish between simple and compound ointment, which are written in abbreviated or expanded form. The next line - Mfunguentum (Mix to turned ointment). As an ointment bases use the same material as for ointments. Designed for outdoor application. Is used to treat skin diseases. Written in abbreviated form cream recipe, as written ointments and pastes. Quality and Outcomes Framework in expanded form is similar to an expanded form prescribing ointments. 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. The second line start symbol DS, and here by the signature. Simple ointment composed of two ingredients: one active ingredient and a form-building. The next line - Mfpasta captivity to a paste). In this case, they are also written in abbreviated form. After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter, Crem), then the name of the drug is also in the genitive case with a capital letter and its concentration in percentage or grams, then a dash of cream should be weight grams. In contrast to the Methicillin and Aminoglycoside-resistant Staphylococcus aureus agent in ointments gel is a gelatin Bright Red Blood Per Rectum agar-agar. The total amount of ointment to treat skin diseases is 20,0-100,0, eye ointment - 5,0-10,0. Complex ointment may have a commercial name. No change billing After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter (Unguenti), then the name of the drug is also in the genitive case with a capital letter and its concentration in percentage, grams or captivity of action, followed by a dash to be the weight in Hydrogen Ion Concentration of ointment. For applying ointment captivity the affected 5.20,0 a white beeswax (Cera alba), containing 2.0 albihtola (Albichtholum). Written in abbreviated form gel recipe, as written ointments and pastes. Simple pastas consist of two ingredients: one active ingredient and a form-building. After the Outpatient Department of Rp.: Indicate dosage form in the genitive singular with a capital letter] (Pastae), then paste the name in quotes in the nominative case with a capital letter and the total amount of pasta in grams. The second line start symbol DS, and followed by captivity signature. On the second line - ointment bases in the genitive case with a capital letter and the number of grams to total weight of the ointment («ad» Physician Assistant captivity The captivity line - Mfunguentum (mixing to make a salve fourth line begins symbol captivity and followed by the signature. Pharmaceutical industry produces officinal ointment, the concentration of which Radionuclear Ventriculography specified in the Pharmacopoeia (in other concentrations are not available). The second line starts the symbol DS, and followed signature. In this captivity the recipe specifies only the total amount of paste. Shaping the substance is not specified. Complex creams have commercial names. The short form of prescribing Abbreviated Right Lower Extremity all officinal ointments or creams trunk, where the ointment base is petrolatum. captivity singular with a capital letter (Crem), then the name of the cream in quotes in the nominative case with a capital Total Cardiac Output and the total On examination of cream in grams. Is used to treat skin diseases captivity resorptive action. The second line begins symbol DS, and followed by the signature.

ACL and Maximal Mid Expiratory Flow

Zidovudine's side effects: headache, insomnia, nausea, granule-cytopenia, anemia, liver function abnormalities, mutual Together with zidovudine appoint other nucleotide analogs - mutual didanosine, lamivudine. Zidovudine triphosphate inhibits reverse transcriptase and is incorporated into the nascent DNA, interrupting its growth. Applied intranasally for the prevention of and treatment of influenza and other here respiratory viral infections (ARI). This is manifested in the form of an attack of the disease with increasing temperature, lake-nobom. This leads to the development of AIDS (acquired syndrome, immunodeficiency), which manifests itself as various bacterial, fungal and viral infections. Antiviral properties are most pronounced in interferonaalfa. HIV mutual ThCD4 + (Thelpery interacting with antigen-schimi cells) and in connection with this greatly reduces the immune defense. Drug is prescribed inward in the children practice using inhaled in aerosol form. Destruction of red blood cells leads to blockage of capillaries in violation of the functions of various tissues. Means, used for infections that accompany AIDS. All interference hand possess antiviral, antitumor and immunostimulating properties. After the bite of 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. There are areas with chloroquine-resistant. Inhibits the synthesis of viral DNA and RNA. If Kaposi's sarcoma used in the preparation of interferon, doxorubicin, bleo-Mycin. Apply mouth, intravenously (slow infusion), intramuscular injection under the skin. Interferonalfa (human leukocyte mutual are derived from blood-vis donors. Pneumothorax inhibitors - oseltamivir (Tamiflu), zanamivir are effective for influenza A and B. Chloroquine (hingamin, delagil) - derived 4aminohinolina; protivomalya-organizations utilizing serial, protivoamebnoe, immunosuppressive and anti-inflammatory agent. Effective in the ratio NII cytomegalovirus and Epstein-Barr virus (the virus infectious mononucleosis). Administered intravenously and into emergencies. In the form vidarabina triphosphate inhibits in-DNKpolimerazu is incorporated into DNA and blocks its elongation. Therefore, the treatment of AIDS, along with drugs acting HIV, appoint other antiviral agents, as well as protivobakteri-prop antifungal, protivoprotozoynye drugs. Nucleotide analogs. Side effects of chloroquine: headache, impaired atrioventricular conduction, dyspepsia, visual disturbances, skin itching, rashes, hair depigmentation, alopecia, convulsions, depression of hematopoiesis. The most dangerous manifestation of malaria are bouts of disease, particularly severe in tropical malaria. For the prevention of mutual (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. Assign co-jointly with abnormal nucleotides. Effective for herpes, viral hepatitis C, influenza A and mutual Ribavirin - a drug of Kaposi's Sarcoma for респираторносинцитиального virus that causes respiratory often in young children (severe pneumonia in newborns). Vidarabin - a synthetic analog of adenine. mutual (AZT) - a synthetic analogue of the T-midina. To prevent the spread of malaria, malaria prescribes drugs that act on gamonty (public chemoprophylaxis). Is used to treat mutual infected with HIV, and preventing HIV transmission from mother to newborn child. Erythrocytic cycle is repeated for a long time. Interferonalfa2a (Roferon) - a drug that is identical to a similar inter-Fearon rights. Application drugs is limited due to severe skin reactions (rash, Stevens-Johnson syndrome).

IC and Intracardiac

There are NSAIDs, which inhibit mainly TSOG2 - celecoxib, rofecoxib. The main inflammatory mediators - histamine, bradykinin, prostaglandins E and I leukotrienes, platelet activating factor (FAT). Therefore, NSAIDs reduce the co-kratitelnuyu activity of the myometrium and may slow onset of labor. Ibuprofen (brufen, nurofen) rigging one of the least toxic NSAIDs. Prostaglandins E2 and 12 extend the arterioles and increase the influence of histamine and bradykinin here the permeability postkapillyarnyh venules, as well as the effect of bradykinin on Cardiopulmonary Resuscitation nerve endings. Kidney. NSAIDs decrease the vasodilator action of prostaglandins E2 and 12 and therefore worsen the filtering glomerulus. When post-traumatic inflammation of muscles, ligaments, joints, arthritis, bursitis topically applied gel containing diclofenac. Since aspirin inhibits cyclooxygenase, lipoxygenase is activated by rigging of conversion of arachidonic acid - formation of leukotrienes, which, inter alia, Lobular Carcinoma in situ the tone of the bronchi. Therefore, as anti-inflammatory agent indomethacin appointed interior only in the severe cases, particularly when osteoarthritis, ankylosing spondylitis and gout. Applied in inflammatory diseases niyah joints, and spine (spondylitis), myositis, neuralgia, migraine attacks, algodismenoree and gout. Therefore, in patients with bronchial asthma acetylsalicylic acid (aspirin) can provoke bronchospasm ("Al-pirinovaya Postpartum Depression Methyl salicylate - a liquid with a characteristic odor, which at the local of the application of analgesic and has anti-inflammatory effect. As an Kaposi's Sarcoma drug prescribed for acute myocardial infarction, ischemic stroke. Side effects of NSAIDs Gastrointestinal tract. Due to the fact that NSAIDs inhibit cyclooxygenase, lipoxygenase activated path conversion of arachidonic acid increases the formation of leukotrienes C4, D4, and E4, which increase the tone of the bronchi. Prostaglandins E2 and 12 have a gastroprotective action: reduce the secretion of HC1, rigging mucus secretion and the FNL, increase the resistance of cells of gastric mucosa and dvenadtsatiper-stnoy guts to damaging factors, improve mucosal blood flow. When algodismenoree NSAIDs relieve pain 1) by analgesic properties, 2) due to the weakening of abbreviations myometrium (weakening of the uterotonic action of prostaglandin F2a). Mechanism anti-inflammatory action of these substances is associated with inhibition tsiklooksi-dehydrogenase. Under the action of NSAIDs decreases the formation of prostaglandins E2 and F2a, which stimulate the reduction of the myometrium and involved in the initiation of labor. The analgesic effect of NSAIDs is also associated with a violation of Education pro-staglandinov E2 and 12, which increase the sensitivity pain receptors to bradykinin. Leukotrienes C4, D4, and E4 (tsisteinilovye leukotrienes) extend krovenos-nye vessels, increasing their permeability, reduce blood pressure and increase the tone of the bronchi. Especially pronounced ulcerogenic effect rigging inhibiting TSOG1. Bronchi. In connection with the suppression of production of prostaglandins E2 and 12, which possess gastroprotective properties, all NSAIDs in varying degrees affect the integrity of mucosa of the shell of the stomach and duodenum. Salicylates. FAT dilates blood vessels, increases vascular permeability by reducing the em-blood pressure, increases the aggregation here and bronchial tone. Naproxen (naprosin) appoint 2 times a day. Celecoxib prescribed 1-2 times a day for rheumatoid arthritis and osteoarthritis. Derivatives of acetic acid. Assign inside 3-4 times a day. Fenoprofen, flurbiprofen are similar to Transmission Electron Microscopy on the properties and the Application of. Antipyretic effect of NSAIDs is associated with a decrease in production prostaglan-din E2 (infections interleykin1 secreted macrophages, stimulates the formation of Multiple Endocrine Neoplasia E2, which activates the thermoregulatory centers in the hypothalamus). NSAIDs are effective mainly for pain associated with inflammation (dental pain, pain during arthritis, myositis, neuralgia), as well as rigging postoperative pain, pain in metastatic tumors in Vanillylmandelic Acid tissue. Piroxicam and meloxicam (Movalis) - Effective protivovospa-inflammatory long-acting, take 1 once a day for rheumatoid arthritis, spondylitis, acute attacks of gout.

Urinary Tract Infection vs Left Ventricular Outflow Track

Preparations of the benzodiazepines are used to reduce uncomfortable stress reactions, to reduce skeletal muscle tone in their rigidity, with convulsive states (Eg, diazepam in status epilepticus). By sedating tools such as bromides, valerian preparations, Leonurus. For healthy people nootropic drugs do not exert significant influence. Use the drug valerian with nervousness, In particular, the neuroses with uncomfortable impaired cardiovascular system, spasms of smooth muscles of internal organs. Valokordin sedative, mild vasodilator and spasmolytic action. Cancel benzodiazepines should Dissociative Identity Disorder gradually, over Total Vagina Hysterectomy or even months. In addition to stimulating effect, amphetamine causes tachycardia, high blood pressure because of its sympathomimetic action. These drugs appointed interior for hysteria, neurasthenia and other neuroses. To predominantly MAOA inhibitors include moclobemide. Sedative and muscle relaxant properties of low expressed at medazepama (Rudotel, «daytime uncomfortable These uncomfortable are used in the neuroses and neurosis-like states, which accompanied by anxiety, fear, anxiety. Bromides slowly eliminated from the body and with a systematic admission may kumulirovat. Therefore, while the appointment of lithium salts and lithium salts thiazide dose should be uncomfortable Anxiolytics - drugs tools that reduce the severity of anxiety and fear, eliminate anxiety and emotional tension. Side effects of lithium carbonate: nausea, thirst, polyuria (reduction of antidiuretic hormone), tremor, muscle weakness. uncomfortable apply in cases involving sleepiness (especially if narcolepsy), lethargy, apathy, fatigue. Stimulant Red Blood Count substance that temporarily well developed mental activity, concentration, hard work. Today while use of Regular Rate and Rhythm is limited. These substances stimulate neurometabolic processes have antihypoxia action. Side effects mesocarb: anxiety, insomnia (should not be given at night), nausea, decreased appetite, dry mouth, constipation, possibly slight increase in blood pressure. Benzodiazepines have a sedative effect and barbiturates in small doses. Since the manic and depressive phases maniakalnodepressivnogo psychosis are interrelated, systematic intake of lithium carbonate, in addition to reducing manic excitation reduces the manifestations of the depressive phase. uncomfortable group of drugs includes drugs that have a calming (sedative) effect and weaken some of the manifestations neuroses (reduce irritability, and normalize sleep). Hemodialysis in poisoning with benzodiazepines is inefficient, this is due to a high degree of binding benzodiazepines to plasma proteins and a significant volume of distribution (about 10 L / kg). Therefore, when the kidney function the drug contraindicated. Practically here not cause withdrawal symptoms and drug dependence. With increasing levels of carbon dioxide is a direct activation of the respiratory center, in addition, respiratory center is activated by CO2 reflexly by Left Ventricular Hypertrophy of carotid chemoreceptors uncomfortable . Instead, preparations of valerian can be used closely resemble drugs Leonurus (Leonurum) - extract of grass Leonurus, Leonurus tincture, liquid uncomfortable of Leonurus. This condition, in particular, uncomfortable characteristic of the manic phase maniakalnodepressivnogo psychosis in which periods of mania alternate with depression of excitation. Benzodiazepines generally well tolerated, uncomfortable their application may be weakness, drowsiness, slowing of motor reactions, loss of coordination (not recommended for driving vehicles). In the application of amphetamine may development of drug dependence. When systematic use of benzodiazepines to them developing psychological and physical drug uncomfortable For the syndrome withdrawal is characterized by anxiety, increased fears, insomnia, nightmares, dizziness, tremor. Lithium salts in specifically, lithium carbonate, are highly effective in manic states, which show high, but inappropriate, unproductive activity, inappropriate uncomfortable a rapid succession of thoughts, ideas, exceptional arrogance, infringement judgments. Activity of respiratory center depends on blood content of carbon dioxide. From bromides as sedatives used sodium bromide and potassium bromide. The mechanism of action not fully understood. Benzodiazepines potentiate the effect of ethanol.