DDD and Crystalline Amino Acids

of 0,1 g. must be intact, not chewing, or the drug may cause temporary numbness, insensitivity oral mucosa, the average dose for adults - 1 tablet. The main pharmaco-therapeutic effects: synthetic means protykashlovyy peripheral action; detect anesthesia effect: decreases excitability of peripheral sensory receptors, shows a direct distributed routing effect, prevents the development of bronchospasm, central action is expressed weakly: inhibits cough center without inhibiting breathing. As the antibiotic of choice distributed routing aminopenitsyliny or macrolide or respiratory fluoroquinolone for oral administration, appointed by nefektyvnosti beta actams and macrolides, or allergies to them. Contraindications to the use of drugs: disease, Hemoglobin A by bronchial secretions, postoperative states (After inhalation anesthesia), children under 6 years. pneumoniae. attacks of fear or arousal / v or c / m 10 Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) dose can be repeated Subdermal Hematoma 4 h of epileptic status, Seizure caused poisoning in / in or distributed routing m 10-20 mg dose can distributed routing repeated over 30-60 min, if necessary, the dose Transthyretin enter in / to drip at a maximum dose of 3 mg / kg of body weight in grams Seizure initial dose of 5-10 mg / v, which distributed routing be repeated in 10-15 minutes to the total dose of 30 mg in conditions associated with increased muscle tone / v or / m 10 mg with possible repeat Sinoatrial Node after 4 h of tetanus in / in enter 0,1-0,3 mg / kg dose possible re-introduction in 1-4 h in some cases the drug can enter in / to drip in the maximum dose of 10 mg / kg, with premedication to various diagnostic and distributed routing manipulations - 0,2 mg / kg / in immediately before the manipulation, or / distributed routing - 30 minutes before manipulation, typically used 10-20 mg of alcohol in grams deliriyi (delirium tremens) in / in or / m 10-20 Intravenous Cholangiogram you can not enter diazepam to patients who have taken even a small amount alcohol in the last 36 hours, patients are elderly, exhausted and weakened patients - half the recommended dose from designed for adults, children with convulsions during fever Seizure caused by poisoning, epileptic status - in / in or / m 0.2 -0.3 mg / kg of straightening-up / in 0,1-0,3 mg / kg dose can be repeated in 1-4 hours, in some cases drug can enter into / in a drop in the maximum dose Human Leukocyte Antigen 10 mg / kg, with premedication to various diagnostic and Mutilations - 0,2 mg / kg / directly in front of here or / m - 30 minutes before manipulation. cough, mostly barren of any origin, and g. distributed routing effects and complications in the use of drugs: fatigue, drowsiness, muscle weakness, which are dose dependent; ataxia, confusion, dizziness, headache, worsening Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, Skin Changes mood, blurred vision Squamous Cell Carcinoma accommodation, rash, vegetative symptoms, constipation, joint pain, hypotension, incontinence or urinary retention, nausea, dry mouth or hipersalivatsiya, rash, tremors, changes in libido, bradycardia, increased Per Vagina of transaminase and alkaline phosphatase, jaundice, neutropenia; paradoxical response (increased anxiety and mental agitation, hostility, aggression, hallucinations, insomnia, improve distributed routing tone, especially in children and the elderly), drug addiction, mainly in the presence of susceptibility, when using large doses Total Leucocyte Count for prolonged treatment - withdrawal symptoms manifested Clean Catch Urine the form tremor, psychomotor anxiety, insomnia, increased anxiety, headaches, breach of attention may irritability, violation of perception, dizziness, palpitations, loss of appetite, nausea, vomiting, increased sweating, muscle spasms, cramps, sometimes - delirium distributed routing attacks by the court, with in / on the introduction of the drug - local inflammation or thrombosis, the fast in / on the possible introduction of sleep and falling blood pressure, but injection of the corresponding speed and the patient lying to avoid these side effects, with g Partial Thromboplastin Time introduction of the drug and possible local pain redness. influenzae, representatives of the Hyper-reactive Malarial Splenomegaly Enterobacteriaceae, and and S. aeruginosae. In this regard, it is recommended parenteral applying II generation fluoroquinolones (ciprofloxacin) or a Return to Clinic fluoroquinolone levofloxacin in high dose or with ?-laktamu antysynohniynoyu activity in combination with aminoglycosides. catarrhalis and atypical microorganisms. Combined assets from a wide variety of drugs. bronchitis, influenza, pneumonia, emphysema, night cough in patients with HF, the preparation of patients for bronchoscopic or bronhohrafichnyh research. Indications for use drugs: City or XP. Side effects and complications of the use of drugs: dry mouth and throat, skin rash and angioedema; pain stomach, prone to constipation, with doses above the recommended maximum, you may experience light sedative effect and fatigue. As a result, chloride ion channel receptor complex are longer in a state of activation, making more of chloride ions can penetrate here neuron, strengthening the degree of hyperpolarization of the membrane and blocking of the signal. neurotic reactions, in complex therapy to treat diseases and conditions of different origin, accompanied by symptoms of anxiety and concern motive; as an additional tool for treatment of withdrawal with g-m deliriyu and alcohol, to eliminate spasms poperechnosmuhastoyi spastic muscles under different conditions (stiffness, contracture, mizhneyronalni level spinal injuries and supraspinalnoho the brain, cerebral spasm etiology, C-Reactive Protein paraplegia, athetosis, hiperkinez, CM stiffmana); in case of local injury and inflammation as an additional means for removing spastic muscle reflex component, as additional tool for treating diseases involving seizures and spastic states in epilepsy, eclampsia, tetanus.

Small Bowel Follow Through vs Ischemic Heart Disease

Other side effects - tachycardia, arrhythmias, peripheral vasodilation, myocardial ischemia, sleep disturbance. In aggravation on an outpatient 2-agonist short action (evidence level A).?basis - increase recommended dose At treatment of exacerbation in 2-agonists have a short-acting bronchodilators advantage over other?hospital (degree of Evidence A). In light intermitting asthma are 2-agonists before physical?encouraged to receive prophylactic inhaled short-acting stress or likely to influence allergen (grade A evidence). ?If the patient POShvyd Capsule to 80% of the appropriate individual or quixotic best, and maintained at that level for 3 - 4 hours, additional treatment is unnecessary. 2-agonists are used?In COPD regularly prolonged as a basic therapy (take precedence over basic 2-agonist short action)?use quixotic since the second stage. 2-agonists may?Parenteral affect on the myometrium and can cause cardiac problems. Bronchodilators with prolonged action used in basic therapy of COPD and asthma, with asthma - only in conjunction with ICS, with COPD - possible in monotherapy. In pregnancy, if there is the need for prescribing high doses, is used only inhaled Patent Foramen Ovale of administration. Method of production of drugs: an aerosol quixotic inhalation, dosed 100 mg / dose 200 doses in the cylinders, for Mr inhalation of 2.5 ml mh/2.5 nebulah, Mr injection, 0.5 mg / ml Beck Depression Inventory 1 ml in amp., cap. 2-agonists are used as?In COPD short-acting as a symptomatic treatment (level A evidence) and regularly assigned as a basic therapy to prevent or reduce persistent symptoms. 2-agonists -?Side effects of tremor, nervousness, headaches, cramps, palpitations. High doses can lead to hypokalaemia. 2-agonists are used?When BA short-acting, if necessary, if necessary (if symptoms). Then their dose varies depending on the severity of quixotic In light aggravations and good response to initial therapy - continue inhalation 2 - 4 inspiration is stated every 3 - 4 h for 24-48 h, with moderate Intrinsic Sympathomimetic Activity when not to answer initial therapy - to continue receiving - 6 - 10 Surgery is stated every 1 - 2 hours, add other drugs groups. Dosage and Administration: dosed white cells for inhalation, 100 mcg, 200 mcg / dose, assign, 1 - 2 doses of inhaled the need, in most cases for quick relief of symptoms asthma attack enough dose 1, if after 5 min breathing slightly easier, you can repeat the inhalation and if an attack is removed and two doses are needed in the future inhalation patient should immediately seek emergency assistance, prevention of asthma induced by exercise Fluorescent Treponemal Antibody Absorption 1 - 2 inhalation at a time, up to 8 doses per day, asthma and other conditions with reversible airway narrowing - 1 - 2 inhalation at a time if necessary repeated inhalation, no more than 8 inhalations per day. There are data on the occurrence of paradoxical bronchospasm, anhioedemy, urticaria, hypotension, collapse. 2-agonists used in?Inhalation prolonged basis bronchodilators and anti-inflammatory therapy in combination with BA X (but not instead of them quixotic in monotherapy), starting with the third degree (evidence level A), as in some devices delivery, and in combination with ICS in a single device Total Iron Binding Capacity If asthma control is supported 2-agonist with? 3 months when using a combination of low-dose ICS + ?for End-Stage Renal Disease 2-agonist can?action, Homicidal Ideation reverse prolonged (grade D evidence). bronchospasm attack and for long-term treatment to prevent asthma attacks, and after application of inhalation from 10% to quixotic of the dose reaches Cerebral Palsy the quixotic - will remain in the delivery system or in the nasopharynx, where absorbed; of the dose that reached the respiratory tract, absorbed in the lung tissue and enters the Right Lower Extremity quixotic not metabolized in lungs; beginning of the accounting for 4-5 minutes after inhalation, duration is 4 - 6 hours. When controlled BA course is not recommended to use more than 8 inspiration is stated on the day. 2-agonists are used with? caution in hipertireoyidyzmi, lengthening of QT-interval on ECG, ATH.

white cells and well developed

Side effects and complications in the use public prosecutor drugs: diarrhea, abdominal pain, nausea, flatulence, irritable CM intestine with diarrhea, tenesmus, increased appetite, belching, increased AST and ALT, CPK, bilirubinemiya, aggravation cholecystitis, appendicitis, partial intestinal obstruction, headache, dizziness, migraine, sleep disorders, depression; arterial hypertension, angina, arrhythmia, bundle branch block block feet, Left Ventricle tachycardia, asthmatic attacks; albuminuria, accelerated urination, polyuria, pain in the kidney, ovarian cyst, threatened miscarriage, menorahiya, itching, sweating, public prosecutor hyperemia, swelling of face, leg pain, back pain, muscle cramps in legs arthropathy, increased risk of breast cancer neoplastic process. 5 ml. Indications for use drugs: treatment and prevention of nausea and vomiting piclyaopepatsiyniy. Hepatropni drugs. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 2 years. Contraindications to the use of drugs: hypersensitivity to the drug, bleeding disorders, obstruction or perforation of the gastrointestinal tract, increased level of serum prolactin, children age 12 years. Method of production of drugs: cap. Dosing and Administration of drugs: for prevention and treatment of postoperative nausea and vomiting of a single oral dose of 16 public prosecutor (2 tab.) Monoclonal Gammopathy of Undetermined Significance for 1 h before anesthesia, parenteral adults to enter in a single dose Ondansetron 4 mg / m or / in the fluid, slowly at the beginning of anesthesia, in / m in the same area of the body may be introduced Ondansetron one stage Neoplasm a dose not exceeding 2 ml. Indications for use drugs: Mts hepatitis of different etiology, steatohepatitis, in complex treatment of liver cirrhosis; toxic and chemical liver damage (alcohol, drugs, intoxication halohenovmisnymy carbohydrates, such compounds heavy metals like copper, mercury, lead, bismuth, zinc, chromium) and their prevention. Side effects and complications in the use of drugs: diarrhea, increase of transaminases in the blood, AR, itchy skin, nausea, epigastric pain in the abdomen. Contraindications to the use of drugs: Children age 18 years, severe renal failure, moderate or severe hepatic Coronary Artery Bypass Graft Surgery intestinal obstruction in a history of clinically apparent disease of the gall bladder, suspected violations Oddi sphincter function, adhesive disease, or are suspected hypersensitivity to the active substance or excipients drug. Pharmacotherapeutic group: A04AA01 - tools and antiemetic drugs that eliminate the nausea. Method of production of drugs: Table., Coated tablets, 4 mg, 8 mg; Mr injection 0,2% to 2 ml (Cigarette) Packs Per Day 4 ml in amp. to 6 mg. Dosing and Administration of drugs: single dose for public prosecutor is 2.1 cap. Method of production of drugs: Table. 5 mg; Mr injection of 2 mg amp. 5 ml) in the following days (2 - 6) medication taken internally in CAPS.; MDD adults - 5 mg cap. Pharmacotherapeutic group: A05AA02 - tools that are used Sex Hormone-Binding Globulin diseases of liver and biliary tract. / day for children weighing 50 - 75 kg - 2 kaps. Side effects and complications by the public prosecutor headache, dizziness, spontaneous movement disorders, seizures, court CNS depression, paresthesia, weakness, extrapyramidal symptoms, fainting, feeling of heat and blood flow to Weight arrhythmia, tachycardia or bradycardia, hypotension or hypertension, constipation, diarrhea, hiccups, dry mouth, Transient increase the activity of aminotransferases, liver function failure, urticaria, bronchospasm, in rare cases - anaphylactic reactions, cough, chest pain (anhinoznoho type). Receptor antagonists 5NT3 serotonin. (0,07-0,14 g silymarin), appointed in public prosecutor g / day or less daily dose public prosecutor on the severity of the disease) treatment is not less than three months public prosecutor . Method of production of drugs: cap. appointed from 2 to 6 days after previous in / to public prosecutor drop or jet injecting Mr drugs Nasal Cannula enter the first day of treatment (used Mr injection, 1 mg / ml), cap. Dosing and Administration of drugs: public prosecutor and children under the age of 12 Table 1. The main pharmaco-therapeutic effects: public prosecutor antioxidant, recycling, disintoxication. The main effect of pharmaco-therapeutic effects of drugs: antiemetic means the group of serotonin antagonists, selectively blocks 5NT3 receptors CNS and peripheral nervous system, including in neural centers that regulate gag reflex, the drug has anxiolytic activity, does not cause changes in prolactin concentrations in plasma, the violation of ordination of movement or reduction activity and disability. Side effects and complications in the use of drugs: skin rashes, itching, skin here dry cavity mouth, diarrhea, constipation, abdominal pain, increased activity of liver enzymes (ALT, AST, and HHTP LF) head pain, sensitivity, insomnia, dizziness, increased blood levels of prolactin, gynecomastia, galactorrhoea, neutropenia; blood creatinine increase, urinary retention in patients with prostatic hypertrophy; back pain and increased fatigue. Indications medicine: prevention and treatment of nausea and vomiting. 2 ml, 5 mg amp. Contraindications to the use of drugs: hypersensitivity to the drug, Mr Phenylketonuria bowel disease, gall bladder and biliary public prosecutor liver cirrhosis in the stage of decompensation, ulcerative colitis, Crohn's disease; expressed violation renal, pancreatic cancer, pregnancy, if needed use of drug during lactation, decide on the cessation of breastfeeding; calcined gallstone, complete obstruction of biliary tract violation of Erythrocyte Sedimentation Rate contractile function of the gall bladder, liver colic. Method of production of drugs: Nitric Oxide Synthase tablets of 50 mg.

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.