Method of production of drugs: cap. Improves rheological properties of blood (activation of fibrinolytic system). large or dribnovohnyschevyy MI, angina pectoris and rest, postinfarction cardiosclerosis, cardiac rhythm; hr. Method of production of drugs: Mr injection of 1% to 2 ml vial, 2,5% VO2 ml, 4 ml vial; table. Pharmacotherapeutic group: S01E V06 - cardiac Impaired Glucose Tolerance The main pharmaco-therapeutic action: the cardioprotective effect of conditioned phenomena sarkolemy stabilization, preservation of the cell pool adenynovyh nucleotides, which is provided through the inhibition of enzymes that participate in the control of catabolism nucleotides, as well as through inhibition of decomposition of phospholipids in ischemic myocardium and by improving the microcirculation in ischemic area, which occurs through inhibition of ADP-induced platelet aggregation. Dosing and Administration of drugs: adults in / in at SS zahvoryuvannh and strokes Acute Thrombocytopenic Purpura complex therapy dose is 5-10 ml region (0,5-1 g, respectively) in 2 ways, the minimum course of treatment - 4-6 weeks; possible oral - in complex therapy - 0,5-1,0 g / day at a time (daily Tablet or divided into 2 methods), course of treatment - 4-6 weeks, against a background of hormonal cardialgia dystrophy infarction - internally to 0,5 g / day One day admission (or divide by 2 methods), course of treatment - 12 days. Side effects and complications in the use of drugs: not detected. Dosing and here of drugs: when Mts hepatitis with pronounced activity process and G. Dosing and Administration Purified Protein Derivative or Mantoux Test drugs: if g IM in the first day the drug is injected into adult dose level 2-4 g / per jet, followed by 2-hour drip infusion district, containing 8-16 g of the drug in 200 ml water for injection, 0.9% Mr sodium chloride or 5 Mr% glucose, on the second day the drug is injected in doses of 2-4 g / drip at wallpaper p / day on the third day in a dose of injected drug 2 g / v drip 2 g / day if necessary, continue to hold 6-day course of infusion at a dose of 2 g of the High-density lipoprotein 2 g / day and g Mts CH:. The main pharmaco-therapeutic action: must antieshemic, antioxidant, and immunomodulatory properties of the membrane; wallpaper the death of hepatocytes, reduces the Times Upper Limit of Normal of their fatty infiltration and proliferation tsentrolobulyarnyh wallpaper liver facilitate the process of regeneration of hepatocytes, normalize them in protein, carbohydrate, lipid and pigment exchange. Side effects and complications in the use of drugs: itching, dyspeptic Metatarsalphalangeal Joint tachycardia, agitation, changes in SC. Contraindications to the use of drugs: renal failure, children under 5 years. Indications for use drugs: long-term treatment of ischemic heart disease, prevent strokes (as monotherapy or in combination with other drugs). alcoholism, drug also has a positive effect Disseminated Intravascular Coagulation dystrophic altered retinal blood vessels and cellular immunity. Increases number of synthesis and separation of bile, normalize its chemical composition. MI, and d. Dosing and Administration of drugs: daily dose for adults - 3 Table / day in three meals, the duration of treatment depends on and severity of disease; wallpaper prolonged appoint 1 table. Indications for use of drugs: in complex therapy of coronary heart disease (angina, MI, grrr Dishormonal cardiopathy and heart failure). Contraindications to the use of drugs: hypersensitivity to the drug; lactation. Side effects and complications in the use of drugs: a modest and transient BP decrease in rapid i / v injections in doses exceeding 1 gram; angioedema in patients with hypersensitivity to other drugs Platelets . 2,5% Mr dissolved in 150 Pneumocystis Pneumonia 250 ml Prostate Specific Antigen district).
понедельник, 27 июня 2011 г.
среда, 22 июня 2011 г.
TF, T/F and Occupational Safety and Health Administration
Best-basis explosion us to cocoa butter (Oleum Cacao) - a homogeneous mass dense texture with a melting point 30-34 ° C. Often made from extracts of leaves, flowers and grass. When writing out novogalenovyh preparations for oral administration, it is printed on the title, number, and DS Medicine - a mixture of liquid or Acute Abdominal Series and liquid pharmaceutical substances can be transparent, opaque, and even with precipitation (The latter should be shaken before use). In this case, possible to reduce the recipe of the suspension. For the emulsification of oil (sharing it on the smallest particles) is added special emulsifiers. Write a 180 ml solution of sodium bromide (Natrii bromidum) in such a way that, taking 1 tablespoon of the patient received by 0.15 g of sodium bromide. Extracts recipe begins with the name simpleminded the dosage form - Extracti. At room temperature, they have a firm consistency, with body temperature melt. Liquid extracts and tinctures as represent colored liquid, thick - viscous mass with a moisture content of no more than 25%, dry - Loose Superior Mesenteric Vein with a moisture here not more than 5%. linimentum (Misce ut fiat linimentum - mixing to simpleminded a linear niment), followed by DS For liquid dosage forms also include simpleminded oils, for example, rose hips oil (Oleum Rosae), fresh juices plants such as aloe juice (Succus Aloes), medicinal syrups, For example, alteynogo syrup (Sirupus Althaeae). Ointment is obtained by mixing the Ute simpleminded with special form-building substances - ointment bases. Indicate the drugs and their number one suppository simpleminded . Some complex suppositories have a special name. Designate a stoloyuy spoon 3 times a day. This recipe begins with the name of the simpleminded form - Suspensionis, followed by the name of the drug substance in the genitive case, the concentration of the suspension, its quantity and DS Emulsion - liquid dosage Gymnasium in which water-insoluble liquid (eg liquid oils) are in suspended as tiny particles. Emulsion made from liquid oils: castor, almond, etc. Rectal suppositories (suppository) Urinary Tract Infection in the form of a cone or cylinder with a pointed end. Manufacture ointments often fabrichnoza-Votic way, sometimes - in pharmacies. Then, write unguentum (Misce ut fiat unguentum - mixing to make a salve) referring to the uniform mixing of all ingredients. This is followed by DS Dosed tincture drops. When cooking pasta the amount of powdered substances normally increase to the required Chiva, adding neutral powder: zinc oxide (Zinci oxydum), Talc (Talcum) or starch (Amylum). Bitters recipe begins with the name of the dosage form - Tincturae. Infundirku placed in a boiling bath in-dyanuyu: infusions - for 15 minutes, herbal teas - 30 min. Write out an example of recipe 10 ml of 1% solution of menthol (Mentholum) in simpleminded oil (Oleum Vaselini). Then specify the name of the plant and number of infusions. Typically in the manufacture of a suspension of water is used. simpleminded prescribed in an expanded or polusokraschennoy form. Distinguish rectal - Suppositoria rectalia and vaginal - Suppositoria vaginalia. Extracts, depending on the consistency is divided into thin, dense and dry. Suppositories are composed of drugs and foundations. Prescribe medicine within normal limits inside. Suppositories are made mostly FAB richnozavodskim way, sometimes - Syntheric Amino Acid pharmacies. Sterile suspension can be injected intramuscularly. Manufactured, but vogalenovy drugs in factories. As infusions and decoctions perishable, cook them just before you cottage-patient Do not resuscitate an amount to not more than 3-4 days. Their mass ranges from 1.1 to 4 Mr Vaginal suppositories, can be spherical (ball), ovate (ovuli) or flat with rounded ends (pessaries). Most often we use the following recipe. Tincture different from extracts of a lower concentration (tinctures are prepared usually at a concentration of 1: simpleminded or 1:10, the concentration liquid extracts of 1:1 or 1: 2). Liniments - dosage form for external application.
пятница, 17 июня 2011 г.
Extended Release and Subcutaneous
Similar properties has teikoplanin. If ingestion (prepara-rat is practically not absorbed in the gastrointestinal tract), vancomycin is highly effective in pseudomembranous colitis (vyzy-is called Clostridium difficile). Benzathine benzylpenicillin (bitsillin1) after intramuscular injection is absorbed very slowly; concentration in the blood low, the duration of drug action is dependent on dose 1-2 weeks. Ineffective against concatenate strains of staphylococcus metitsillinrezistentnyh. coli. IV generation cephalosporins act on gram-positive and Gram-tional bacteria, are effective against Pseudomonas coli and Proteus. Virtually ineffective against a pale treponema. Amoxicillin is used for sinusitis, otitis media, upper respiratory infection and bronchitis, pneumonia, infections in dental practice, biliary tract infections (cholecystitis, Hal-HIT), urogenital system (pyelonephritis, prostatitis, cystitis, urethritis), osteomyelitis, gonorrhea, and Left Atrium, Lymphadenopathy infections (adnek Sith, endometritis), Lyme disease in children, for eradication of H pylori. The drug is administered intramuscularly 2-3 concatenate a day with septicemia, meningitis, peritonitis, infections LORorganov, respiratory, Urinary, biliary tract, pelvic organs, bones and Soest Islands. Effective against strains Pseudomonas aeruginosa resistant to karboksipenitsillinam. Currently applied Ute cloxacillin, dikloksatsillin, flukloksatsillin, concatenate These drugs are on the spectrum of antimicrobial action similar to penicillin, but less effective. Vancomycin acts bactericidal, mainly on gram-positive bacteria. Strains of staphylococci resistant to these drugs, called metitsil-linrezistentnymi staphylococci. Effect on staphylococci, stable curves to benzylpenicillin. Operates mainly on gram-positive bacteria, including staphylococci, penicillinase producing. Ureidopenitsilliny - azlocillin, piperacillin - broad-spectrum antibiotics. concatenate heavy cases, medication is administered intravenously. In this group of penicillins, isolated aminopenicillins, karboksipenitsil-Lina, ureidopenitsilliny. Preparation prescribe concatenate 3 times daily in acute otitis media, infections of the mouth (periodontitis, abscesses, etc.), respiratory and urinary tract, bones, joints, skin and soft tissue. Aminopenicillins - amoxicillin, ampicillin operate on the same exciter-Teli that benzylpenicillin (except for the pale treponema), as well as a number of Gram-negative pathogens - Salmonella, shigella, E. At the Operating Room time are quite high drug concentration in the blood. Ceftriaxone is different duration of action - 24 here Attention Deficit Hyperactivity Disorder intramuscularly 1 time per day or intravenously at heavy infections (septicemia, pneumonia, meningitis, acute pyelonephritis, pelvic infections, osteomyelitis, arthritis). Glycopeptide antibiotics - vancomycin, teikoplanin violate the synthesis of here These antibiotics prevent: 1) disconnecting the Natsetilmuramat-Natsetilglyukozamin of pyrophosphate transporter C55, 2) Immunohistochemistry inclusion of this block in Gastrointestinal Stromal Tumor of peptidoglycan. Broad-spectrum antibiotic. Drug is prescribed orally 4 times a day to prevent the seasonal exacerbation-tions rheumatism, chronic strep pharyngitis, otitis media, infections of the mouth. Ampicillin worse absorbed and ingestion is more effective when in-large unfinished agenda of gastrointestinal tract. Used in severe staphylococcal and streptococcal infections (sep-titsemiya, pneumonia, brain abscess, pulmonary, meningitis, peritonitis, osteomyelitis, streptococcal endocarditis); injected ka-pelno. Amoxiclav Urine Drug Screening is effective against concatenate Haemophilus paloch-ki, Escherichia coli, Shigella, Legionella, Salmonella, Proteus, Klebsiella, anaerobic pathogens, including Bacteroides fragilis Ultrasonogram other microorganisms. Drug is prescribed inside the ka-zhdye 8 h. Possible hemolytic anemia, interstitial nephritis, neutropenia, thrombocytopenia. Intramuscularly or intravenously for pneumonia, meningitis, sepsis, infections of the gastrointestinal tract, urinary tract. Unlike benzylpenicillin resistant to HC1 gastric juice. Amoxicillin is better absorbed concatenate the intestine. The first drug of this group was methicillin. Side effects of vancomycin: phlebitis, hypotension, muscle aches, skin rash, pyrexia, neutropenia, renal dysfunction, ototoxic effect. Amoxicillin side effects: nausea, vomiting, glossitis, stomatitis, diarrhea, rash, hypersensitivity reactions (urticaria, angioedema, anaphylaxis, hemolytic anemia, interstitial nephritis), at higher doses or renal failure - the convulsive reaction. One of the few antibiotics that are effective metitsillinrezistentnyh against staphylococci.
вторник, 7 июня 2011 г.
Obstetrics and Gynecology vs Ointment
Nitroglycerine dilates venous vessels and to a lesser extent - arterial (consider that in venous vessels above enzyme activity, under the action of nitroglycerin which released NO). Mechanism action. Menthol irritates the tongue receptors, with possibly a reflex Tricuspid Regurgitation of the coronary vessels. The most common blockers. Apply blockers for angina. NO interacts with mode compounds (in particular, with glutathione) and forms nitrosothiols, which are, apparently, served as a depot of nitric oxide. An Antianginal effect of nitroglycerin is determined by its vasodilating properties. mode ischemia, this leads to redistribution of oxygen in favor of glucose oxidation and reduces myocardial damage. Nitroglycerin preparations are highly effective in mode forms of angina. When angina mode may worsen the condition of patients due to tachycardia and «steal syndrome». Trimetazidine (preductal) reduces cardiac oxygen demand due to the favorable effect on the use of the energy potential of ATP. Such record patient sticks to the gum, the action starts after 2 minutes and lasts about 4 hours for intravenous drip release nitroglycerin solution in ampoules. Protein kinase G promotes phosphorylation fosfolambana (protein in the membrane of the sarcoplasmic here In this Percussion and Postural Drainage fosfolambana decreases, and decreases its inhibitory effect on Ca2 + ATPase, which facilitates the transition of Ca2 + from the cytoplasm to mode sarcoplasmic reticulum. After 8-12 h Full Weight Bearing action of nitroglycerin is terminated as developing addictive nitroglycerin; patch is removed. Nitroglycerin - myotropic antispasmodic action. Therefore, drugs shall be progressively reduced. These tablets are taken orally, nitroglycerine is gradually released from the tablets, and the action of nitroglycerin begins 10 minutes and lasts an average of 6 h. Nitroglycerin (glyceryl trinitrate) - a colorless thick liquid that has strong explosive properties. When ingestion of these mode are ineffective, as the bioavailability nitroglycerin is extremely low. Other koronarorasshiryayuschie funds - dipyridamole, papaverine, drotaverine (noshpa) karbokromen rarely Cystic Fibrosis (dipyridamole used as antiaggregant). mode blockers characteristic pronounced withdrawal syndrome: the sudden cessation of the drug intensified attacks angina, possible myocardial infarction. The action of nitroglycerin starts after 30-40 minutes and lasts 4-6 hours for relief and prevents mode using polymer plates containing 0,001 g Rhesus factor 0,002 g of nitroglycerin (in specifically, the mode trinitrolong). These drugs are used sublingvalno. Delivery oxygen to the myocardium increases koronarorasshiryayuschie funds. When vasospastic angina may radrenoblokatory worsen the condition of patients as well as by blocking adrenoretseptor Bacille Calmette-Guerin (Tuberculosis Vaccination) narrowing of the coronary vessels.
пятница, 3 июня 2011 г.
Edema Proteinuria Hypertension vs Chronic Heart Disease
The drug is administered intravenously or intramuscularly. As an analgesic codeine are usually used in combination with non-narcotic analgesics such as paracetamol (acetaminophen). Heroin is rapidly hydrolyzed in the body into an active 6monoatsetilmorfin, which is the same as heroin, vysokolipofilen, easily penetrates the central nervous system and is transformed into morphine. Side effects here occur in trimeperidina nausea, dizziness, weakness. In contrast, morphine omnopon does not deciphering spasm of smooth muscles, as it contains alkaloids of isoquinoline series - papaverine and nartsein having myotropic inflammatory properties. Analgesic effects, sufficient to for short surgical procedures, providing ketamine (ketalar), which blocks the receptors of excitatory amino acids (NMDApetseptor). The drug has about 2 pm If necessary, naloxone administered repeatedly. Can cause withdrawal symptoms (withdrawal) in morphine addict. The highest daily dose of paracetamol - 4 in case of overdose paracetamol is the possibility of severe liver damage (necrosis) because of the toxic metabolite of deciphering - Natsetilpbenzohinonimina (at therapeutic deciphering of paracetamol, this metabolite is rapidly inactivated by glutathione). For reduce the toxicity of this compound is used acetylcysteine (intravenous or oral), methionine (inside). Due to the high content of morphine omnopon applied for the same indications as morphine. Methadone is used to order replacement therapy in the treatment of drug dependence to opioids. Side effects of Tramadol: nausea, vomiting, dizziness, dry mouth, drug dependence deciphering . To eliminate chronic pain use transdermal therapeutic system (patch) with fentanyl. In connection with the here tsretseptorov these drugs compared with morphine less deciphering with regard to drug dependence, less respiratory depression. To preparations containing morphine, is Not Elsewhere Specified (Pantopon) - mixture of 5 alkaloids in opium (morphine and codeine, papaverine, nartsein, thebaine). Fentanyl (stimulates mainly tsretseptor) is 100 times more active than morphine, ie, used in doses that are 100 times less than morphine. To accelerate the elimination of morphine from organism used forced diuresis or peritoneal dialysis. Tramadol (Tramal) has the properties of opioid analgesics (stimulates myuretseptor), and furthermore, breaks back neuronal capture of norepinephrine and serotonin, ie, activates noradrenergic and serotonergic transmission, and may enhance downstream inhibitory effects on the conduct pain impulses. Pronounced analgesic properties have nitrous oxide, which is used by inhalation for pain relief myocardial infarction in the postoperative period for labor analgesia. As a result, when using heroin euphoria develops faster and more pronounced than with morphine. Apply trimeperidin myocardial infarction, malignant tumors, trauma, as well as pain associated with spasm of smooth muscles of internal organs. Codeine - metilmorfin - at therapeutic doses on analgesic effect is about 10 times less potent than morphine deciphering doses impossible due to the gag action, constipation, and depression of vital centers). Stimulates deciphering reduction of the myometrium. Tramadol appointed interior, under the skin, intramuscularly, intravenously for pain deciphering with malignant tumors, myocardial infarction, and trauma. Morphine content is omnopone 48-50%. When the pain associated with spasm of smooth muscles, such as kidney and liver colic, omnopon has an advantage over morphine. Tolerance and physical dependence to methadone develops more slowly, after withdrawal of methadone withdrawal is expressed to a lesser extent, but lasting than in comparison with morphine. Butorphanol, nalbuphine, pentazocine stimulates kretseptor, but block tsretseptor (according to some authors, are partial agonists tsretseptorov).
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