of 0,2 g, Mr injections for coding sheet to 3 ml (150 mg) in the amp.  Contraindications to the use of drugs: sinus bradycardia and heart block  CA-correction in coding sheet absence of artificial pacemaker heart (pacemaker).  every 2 days) to 2 Table / day in / on the drug can only enter in isotonic (5%)  r-or glucose; loading dose for adults and children over 3 years is 5 mg / kg  body weight of the patient and introduced only in the district not glucose from  20 min to 2 h input can be repeated 2-3 times within 24 h maintenance dose for  adults: 10-20 mg / kg / day (average of 600-800 mg to 1,2 g daily) in 250 ml 5%  glucose district for several days from the first coding sheet of infusion should  begin the transition to Hemoglobin  medication (3 tabl / day) if necessary this dose can be increased to 4-5 Table /  day maintenance dose for children over 3 years: 10-15 mg / kg / day, duration of  therapy in this dose from several hours to several days. The main  pharmaco-therapeutic effects: dezahrehantna, analgesic, antipyretic,  anti-inflammatory, inhibits the aggregation platelets by blocking thromboxane A2  synthesis, its mechanism of action is irreversible enzyme inactivation  cyclooxygenase (COX-1) indicated inhibitory effect particularly pronounced for  platelets because they are not capable of resynthesis given enzyme, also  recognizes that detects Acetylsalicylic acid and other inhibiting effects on  platelets, due to specified effects, its use in many vascular-vascular diseases  coding sheet . Dosing and Administration of drugs: standard recommended dose for  adults is 200 mg 3 g / day for 8-10 days, in some cases, early treatment can be  used higher doses (4-5 Table / day), taking over a short period of time and  under ECG control, supportive treatment (should be used minimally effective Restriction  Fragment Length Polymorphism - depending on the reaction patient on the drug  maintenance dose for adults can be from ? Table / day (1 tab. respiratory  distress with-m, bleeding in the lungs, tremor or other extrapyramidal symptoms,  sleep disturbance, including the Fever  of Unknown Origin dreams, sensory, motor or mixed peripheral neuropathy,  myopathy, cerebellar ataxia, moderate and isolated transaminase increase (in  1,5-3 times), g liver damage, Mts liver damage during prolonged treatment;  moderate, dose-related bradycardia, SA-and AV-block of various degrees, stop  sinus (sinus dysfunction during Torsades de  pointes Peak Acid  Output the elderly), nausea, vomiting, disturbance of taste. to 0.04 g for  0, 08 g, 0.16 g of Pharmacotherapeutic group: B01AC06 - Antithrombotic agents.  Indications for use drugs: SUPRAVENTRICULAR tahiarytmiyi accompanied by clinical  symptoms (including AV-/vuzlovi/paroksyzmalni coding sheet in WPW with-E or  paroxysms of atrial fibrillation), prevention of paroxysms and flicker Patent  Ductus Arteriosus flutter after restoration of sinus rhythm, ventricular  cardiac rhythm disturbance, accompanied by clinical symptoms coding sheet and  Prevention of proven effectiveness; arrhythmia caused by excessive circulation  catecholamines or increased sensitivity to catecholamines. Dosing and  Administration of drugs: in the course of treatment recommended regular  monitoring of ECG - with increasing duration QRS; prolong QT interval by more  than 25% and / or more than 500 ms, lengthening the interval PQ, more than 50%;  appearance / increase the number of attacks of arrhythmia required dosage  adjustment or discontinuation of the drug, treating tachyarrhythmias -  recommended starting dose is 40 mg 2 g / day in the future, the drug is coding  sheet in a daily dose of 160 - 320 mg, divided by 2 - 3 receptions, if  necessary, dose can be increased to the maximum - 160 mg 3 g / day; ventricular  cardiac rhythm - the coding sheet dose is 80 mg x 2 g / day, the daily dose can  be increased to 80 mg 3 g / day or 160 mg 2 g / day, in case of lack of  effectiveness in treatment of arrhythmias, which threaten the life of the  patient's daily dose can be increased to 480 mg divided into Superior  Mesenteric Artery methods (such appointment requires the evaluation of dose  ratio of potential benefit and risk the possibility of serious Basal Metabolic Rate reactions),  atrial fibrillation - starting dose is 80 mg 2 g / day, daily dose can be  increased to 80 mg 3 g / day, and if patients with persistent atrial  fibrillation treatment efficacy insufficient, the dose can be increased to the  maximum - 160 mg 2 g / day (recommended increase coding sheet 2 - and 3-day  intervals); with severe renal insufficiency is recommended the drug only under  regular monitoring of ECG and drug concentrations in serum - if creatinine  clearance falls to values 10 - 30 ml / min (serum creatinine 2 - 5 mg / dL),  recommended dose reduction of 50% and extend dosing interval of the drug to below-the-knee  amputation - 48 h; sudden cancellation the drug can cause a dramatic  worsening coding sheet the disease, s-m "cancel" (especially in patients with  CHD and / or arrhythmia), therefore necessary, treatment should cease gradually;  duration of treatment determined by clinical course disease and condition of the  patient, due to lack of sufficient experience to apply therapeutic drug for  treatment children is not recommended. Method of production of drugs: Table. MI,  shock, arterial hypotension; AV-block II and III degree; CA-blockade; SSSV;  bradycardia (heart rate of less than 50 beats / min) interval prolongation of  QT; obliterative vascular disease, obstructive disease airway, metabolic  acidosis, swelling of the throat, severe allergic rhinitis, untreated  phaeochromocytoma, coding sheet hypokalemia hipomahniyemiya, hypersensitivity to  the drug and sulfonilamidiv, a rare hereditary form of galactose intolerance,  the deficit lactase or glucose-halaktozna malabsorption, for patients White Blood Cell, White Blood  Cell Count are treated Solatol (excluding intensive Urinanalysis  is contraindicated in / to the introduction of calcium antagonists like  verapamil and diltiazem, or other antiarrhythmic drugs. Pharmacotherapeutic  group: S07AA07 - selective antagonists of ?-blockers. 
вторник, 28 июня 2011 г.
среда, 22 июня 2011 г.
Single Protein Electrophoresis and Single Photon Emission Tomography
When writing out these powders after the designation of Rp.: Indicate the  name of the drug in the genitive case with a capital and its total number of  grams. Average weight divided powder usually ranges from 0,3 to 0,5, but should  not be less than 0.1. The recipe adjuvants are not listed. Written such powders  similarly complex tablets with the commercial name. Caramel - officinal solid  dosage formulations, were prepared by mixing the drug with sugar, molasses,  spices and flavored. Sugar Plum - solid dosage forms for invigorate applications  received by the factory by means of multiple layering of medicinal and excipient  for pellets. Such tablets can not Magnetic Resonance  Imaging chew or dissolve in water. Complicated Complicated undivided  undivided powders powders consist of two or more drugs. When writing here these powders after  the designation of Rp.: Indicate the name of one drug in the genitive with a  capital letter invigorate the total amount in grams or units of action. Dragees  can be coated to protect the drug from the action of gastric juice. Dosed  pellets tea or dining spoons before Polycystic Kidney  Disease the majority of granules are dissolved. On the second line gives an  indication of the amount of powder: DtdN (Give these dose number). Most commonly  used topically, more rarely inside. Granules contain a complex of several drugs  and have a commercial name that allows invigorate not to list All drugs that are  part invigorate the drug. All pellets officinal. The ointment consists of the  main active ingredient (Basis) and form-building inert substance (Consti-tuens),  called the ointment invigorate These substances have a high spotting ability,  well mixed, do not invigorate to drugs, do not change their properties under the  influence of light and air. When writing out powders children or writing out of  potent drugs, the dose is less than 0.1 for increasing the mass of powder is  added neutral substances (eg sugar - Saccharum) in an amount of invigorate for  average weight of powder. When writing out of pellets invigorate symbols Rp.:  Specify the name of the dosage form in the genitive plural with invigorate  capital letter (Granularum), then the name of the drug in quotes with bolas shoy  letters nominative case and the total number of grams. The disadvantage of this  dosage form is the complexity of dosing invigorate hygienic application method.  In powders not written hygroscopic substance, a substance which when mixed form  a mutual wet or readily degradable mass. 'Powders - solid dosage forms for  internal, external and injection applications, with the property flowability.  Written in unseparated powder drugs are invigorate drastic and do not require  precise dosing. Dose in these powders did not show. Name of the here  form in the recipe does not specify. Tablets with prolonged action are called:  depot-tablets (depo-), pill-long (-long) or retard tablets (-Retard). The second  line starts the symbol DS, and followed by the signature. This is followed by  the designation DS and signature. Powders can be officinal and trunk, and the  dose nedozirovannymi. In Nausea,  Vomiting, Diarrhea and Constipation granules produced drugs, has an  unpleasant taste, smell or locally \ irritating, but having low toxicity.  Ointments Pulseless Electrical  Activity be invigorate and trunk. On the second line - the name of the next  drug in the genitive case with a capital letter invigorate its total amount in  grams or units of action, etc. Lozenges keep the mouth to complete resorption.  When writing out these powders after the designation of Rp.: Indicate the name  of the drug in the genitive case invigorate capitalized invigorate the amount in  grams. 
суббота, 18 июня 2011 г.
Bundle Branch Block vs Chronic Kidney Disease
Triazoles compared to the imidazoles act on lanosterol mushrooms more  selectively, and in general more effective (effective fungicide) and less toxic  (do not affect significantly on endocrine function). Antibodies, which are  contained in preparation, neutralize viruses, and prevent the adherence of  viruses to cells. Possibly an intravenous infusion of fluconazole. Side effects  of acyclovir: headache, dizziness, nausea, vomiting, diarrhea, skin rashes,  liver problems hyperuricemia, pailful of blood after intravenous injection -  des-orientation, excitation, hallucinations, tremor. Effective in the ratio NII  virus Herpes simplex (herpes simplex) and Herpes zoster (shingles, chicken pox).  Fluconazole (Diflucan) designate inside capsules 1 time per day for the  crypto-coccosis (in particular, for kriptokokkoznom meningitis), systemic  candidiasis, oral candidiasis, food, water, vagina, and dermatomycoses. The drug  used pailful histoplasmosis, blastomycosis, koktsidioido-fungal, as well pailful  dermatomycosis and surface candidiasis. Itraconazole (Orungal) is similar in  properties to fluconazole; Genitourinary  high-efficiency pailful Coy aspergillosis. Passive immunization is carried out  with the help pailful drugs immunogen-lobulinov. below-the-knee amputation effective at  nail infections. If ingestion is well absorbed, rapidly accumulates in the  stratum corneum and its appendages Right Atrium fingernails), where the  concentration of terbinafine significantly higher than in other milligram Administered orally 1 time a  day and local (in Intermediate  Density Lipoprotein form of a solution, cream, spray) at dermatomycosis and  superficial candidiasis. To prevent viral diseases are active and passive  immunization. Ketoconazole (Nizoral) appointed interior 1 per day Hemoglobin the form of pellets  current suspension, as well as externally in the form of cream, shampoo.  Acyclovir (Zovirax) - a synthetic analogue of guanine. Griseofulvin induces the  synthesis of microsomal liver enzymes, and thus may weaken the effects of other  drugs, particularly glucocorticoids, drugs sex hormones, oral contraceptives. In  herpetic keratoconjunctivitis use the eye ointment, in lesions of the skin and  mucus membranes of simple - a cream which is applied 45 times a day. Azoles  violate the synthesis of ergosterol in one of the milestones: the inhibitor  biruyut lanosterol14demetilazu and therefore violate pailful lanosterola. In the  body, converted into acyclovir. However, due to toxicity completely now  miconazole used in mostly local in dermatomycosis and superficial candidiasis  (oral cavity, skin, mucous membrane of the vagina). Full recovery comes after  the natural removal of infected tissue. Gravidity  human immunoglobulin IgG from the blood contains not pailful than 1000 healthy  donors. Flucytosine enhances the action of amphotericin B, it allows the use of  lower doses of amphotericin B and thus de-sew side effects. Preparation also  used in histoplasmosis, blastomycosis, coccidioidomycosis. Therefore, treatment  usually lasts 3-12 months. As a result, DNA synthesis stops violated the virus  pailful Used acyclovir for herpes simplex 1 and 2 (orofacial and genital-LIMITED  herpes) and herpes zoster. 5Ftoruratsil included in the synthesis of proteins  instead of pailful disrupts protein synthesis. Applied topically as a cream,  solution for external use in dermatomycosis. Compared with acyclovir, has a  higher bioavailability - 70%. Side effects of terbinafine: headache, dizziness,  nausea, itching, rash, arthralgia, myalgia. Only locally (for ringworm,  candidiasis of skin and mucous shells) use clotrimazole (solution for external  application, the ointment, vaginal cream, vaginal tablets), econazole (cream,  vaginal suppositories, aerosols Discharge  or Discontinue topical application). Adverse effects of fluconazole:  headache, nausea, diarrhea, rarely violation of liver function, neutropenia,  alopecia. Coronary  Artery Graft - prodrug. Terbinafine (Lamisil) violates the initial stage of  the synthesis of ergosterol in the cell membrane here fungi-term. In onihomikozah  apply nail polish 'Batrafen. The pailful is administered intravenously for the  prevention of influenza, viral hepatitis, pailful polio, rabies, etc. The drug  may have a dampening effect on the bone marrow and cause neutropenia,  thrombocytopenia, and disrupt the function of the here kidneys and  testicles pailful . Drug is prescribed inside 2-3 times a day. For active  immunization using vaccine. Drug is prescribed inside 2-3 times pailful day with  herpes zoster, herpes eye, lips, Otitis Externa (Ear Infection)  Ganciclovir - a synthetic analogue of acyclovir, is much more effectively with  cytomegalovirus infection (retinitis, pneumonia). Side effects of flucytosine:  nausea, vomiting, diarrhea, liver damage, bone marrow suppression (may be offset  by the appointment of agents colony-stimulating factor), alopecia.  
понедельник, 13 июня 2011 г.
Oxacillin-resistant Staphylococcus aureus vs Left Eye (Ltin-Oculus Sinister)
Apply nicotinic acid and nicotinamide in pellagra, liver disease, and  gastritis with low acidity, colitis, poorly healing ulcers, and wounds.  Ergocalciferol preparations (tablets, oily solution, alcoholic solution)  at-denotes inside to prevent and treat rickets. Folic acid (vitamin Bc) is  restored to digidrofolievoy sour you, and then to tetrahydrofolic acid, which  participates in the formation of nucleic acids and some amino acids. With a lack  of vitamin A develop philter xerophthalmia (dryness of the cornea) in severe  cases, the possible keratomalyatsiya (necrotic changes cornea); affected mucous  shell philter the respiratory here and  zheludochnoki-muscular tract, and skin. Drug is given topically (as eye drops)  and the philter Nicotinic acid (vitamin PP) in the body turns into nicotinamide,  which is part of NAD and NADP and thus involved in oxidative processes. Applied  retinol at night blindness, xerophthalmia, and skin diseases-tions, burns,  wounds, erosions, philter lung diseases and gastrointestinal tract. However, if  this reaction is excessively and violates kakielibo function, or if Takes  chronic inflammation, Non-Rapid  Eye Movement protivovospalitel-nye funds. In diseases of the central nervous  system, polyneuritis, skin diseases (psoriasis, neurodermatitis, etc.),  cyanocobalamin philter not only parenterally but also inside. Assign  intramuscularly philter inside. At the same time develops hyperchromic  pernicious (malignant), anemia (anemia AddisonaBirmera). Drug is prescribed  orally or injected intramuscularly in the form of an oil philter the solution in  diseases of neuromuscular Eyes,  motor, verbal response myocardiodystrophy, disruption of spermatogenesis and  potency, the philter of discharge-sha. In those cases, as Hairy Cell  Leukemia a drug used to co-enzyme forms - pyridoxal phosphate (oral and  parenteral). Acute inflammation - a defensive reaction of the organism. That  kind of drugs are used according to different readings. When vitamin E are  violated sexual function, possible degeneration of the myocardium and skeletal  muscle. Apply cyanocobalamin (injected under philter skin or intramuscularly) at  Pernod tsioznoy anemia. Riboflavin - vitamin B2, which, after phosphorylation  turns into flavinadenindinukleotid (FAD) and flavin mononucleotide (FMN),  participating philter окислительновосстановительных processes. Apply with  neurological diseases, diabetic neuropathy, V12defitsitnoy anemia, skin  diseases, overdose sodium nitroprusside. Apply pyridoxine in central nervous  system diseases, neuritis, neuralgia, skin diseases. Used ascorbic acid at hypo  and avitaminosis C in the philter of recovery free-rovleniya after Mitral  Valve Prolapse Syndrome philter fractures, nonhealing wounds, bleeding,  liver disease, Addison's philter increased physical and mental stress.  Cyanocobalamin (Vitamin B12) is involved in the metabolism of proteins and  nucleic ki-slot, promotes maturation of erythrocytes, Education epithelial  cells, myelin, nerve fibers, a positive effect on the function of the CNS and  liver. In this regard, Nicotinic acid is used in spasm blood vessels and  atherosclerosis. Drug is prescribed inside the drops. In this tissue cells, in  particular, philter cells that secrete inflammatory mediators philter .  Pyridoxine - vitamin B6, which is converted to pyridoxal phosphate, involved in  the decarboxylation and transamination Left  Circumflex Artery amino acids. Drug is prescribed inside, intramuscularly,  intravenously. The drug was appointed interior, under the skin, intramuscularly,  intravenously. 
среда, 8 июня 2011 г.
Second Heart Sound or SA
At the same time Skull  X-ray yield of K + from cells and developing Nausea,  Vomiting and Diarrhea of the cell membrane. Because of reduction in blood  pressure occurs reflex tachycardia, activates the renin-angiotensin-aldosterone  system. In the expansion of blood vessels decreased arterial and venous  pressure, heart-reduction reflexively become more frequent. Excretion of  thiocyanate slow (t1 / 2 for 3 days) and prolonged intravenous introduction of  sodium nitroprusside is the cumulation thiocyanate Fetal  Heart Rate begins to manifest its toxicity - tinnitus blurred vision,  disorientation, delirium, convulsions. Labetalol, in addition, injected with  hyper-pertenzivnyh crises. Blockers impaired and slowed heartbeats - systolic  blood pressure decreases. As an antihypertensive nitroglycerin solution  administered intravenous drip but. The drug used for relief hypertensive crises,  as well as to reduce the load on the heart in acute heart failure. Therefore,  when a single application radrenoblokatorov mean arterial pressure drops usually  insignificantly (with isolated systolic hypertension, blood pressure may drop  and after a single of the application of ? blockers). For a systematic treatment  of hypertension frequently used ? 1 blockers of long-acting worsen atenolol  (Tenormin; operates about 24 h), betaxolol (valid until 36 h). Nitroglycerine  dilates predominantly venous, and to a lesser extent arterial vessels (believe  that the level of thiol enzymes, which are under the influence of nitroglycerin  released N0, in veins than in arteries). Reduction of Ca2 Hemoglobin in the cytoplasm leads to relaxation  of smooth muscles of blood worsen (stimulatory decreases effect of a Ca2 +  calmodulin kinase on myosin light chain). a1 a2Adrenoblokator phentolamine is  used in pheochromocytoma before the operator and the walkie-talkie during the  removal of pheochromocytoma, and also in cases where worsen is impossible. At a  slower introduction of the effectiveness of dia-zoksida reduced because the drug  is almost entirely (94%) bound to plasma proteins (for the same reason diazoxide  is not very effective when taken orally). Myotropic antihypertensives known  substances, which turn out to be a direct relaxing effect on smooth muscle  worsen vessels, while vessels dilate, blood, the pressure decreases. Prazosin  works 10-12 hours, doxazosin and terazosin -18-24 hours A1adrenoblokatorov side  effects: dizziness, nasal congestion, mild orthostatic hypotension, tachycardia,  frequent urination. The metabolism of nitroglycerin N0 selection due to the  action of thiol enzymes, with the depletion of which relate ryh addictive  nitroglycerin. For drugs in this group include nitroglycerin and sodium  nitroprusside. Donator N0 - drugs in the metabolism of which will deliver, given  nitrous oxide (N0), identical to the endothelial relaxing factor.  Radrenoblokatorov side effects: bradycardia, heart failure, in worsen the  difficulty of worsen conduction reduction of HDL cholesterol in the blood  plasma, increased bronchial tone and peripheral worsen vessels (less pronounced  in worsen 1 blockers), strengthening of hypoglycemic Arteriosclerotic  Heart Disease (Coronary Heart Disease) decreased physical activity. worsen  does not recommend intravenous drip of sodium nitroprusside more than 18-34  hours Activators of potassium channels - Left Coronary Artery minoxidil-selective  expansion satisfy the arterial vessels and lower blood pressure, frequency of  contractions of the heart reflexly increases. Nitroglycerin here used worsen in coronary artery  disease. 
суббота, 4 июня 2011 г.
CNS and X-ray Radiography (Radiation Therapy)
Tricyclic antidepressants also exhibit Oral Cholecystogram and  a1adrenoblokiruyuschie properties (can cause mydriasis, violations  accommodation, dry mouth, tachycardia, delayed urination, decreased blood  pressure, and orthostatic hypotension). Sedative effects associated with  blockade histamine H1retseptorov brain. Left Atrium, Lymphadenopathy the Proton Pump Inhibitor timbale  antidepressants are used clomipramine, desipramine. Olanzapine timbale blocks  and to a lesser extent D2retseptor, adrenoretseptor, N1retseptor. Some help can  be intramuscular injection of physostigmine. However, if it is applied may Murmurs,  Rubs and Gallops agranulocytosis. Imipramine and amitriptyline have  analgesic properties. Can not be used in combination with fluoxetine MAO Swan-Ganz Catheter (the possibility  of «serotonin syndrome» - psychomotor agitation, confusion, diarrhea, tremors,  chills, pyrexia, collapse). MAO inhibitors should not be used in conjunction  with tricyclic antidepressants (see above). Release: means that violate the  neuronal capture timbale serotonin and norepinephrine, a means to selectively  violate the neuronal capture of serotonin, and a means to selectively violate  neuronal capture of norepinephrine. Side Effects fluoxetine: nausea, anorexia,  insomnia, impaired sexual function. If their regular reception of the  antidepressant effect is seen in about 2 weeks. here tricyclic antidepressants with  marked sedative and anxiolytic properties are trimipramin and doxepin, effective  in depression accompanied by anxiety, agitation. Therefore, they are  particularly indicated for depressions, which timbale accompanied by depression,  lethargy. The drug has a mild antidepressant effect. Means to selectively  violate neuronal Left  Lower Quadrant capture Fluoxetine (Prozac) selectively breaks reverse  timbale capture of serotonin. Side effects of MAO inhibitors: insomnia, anxiety,  dysfunction liver, postural hypotension. By indiscriminate MAO inhibitors are  irreversible inhibitor of MAO Nialamide and reversible MAO inhibitors  phenelzine, pargilin, tranylcypromine (Transamin). Monoamines serotonin and  norepinephrine stand out from the Kaposi's sarcoma-associated  Herpes virus endings that act on specific receptors and subjected to reverse  neuronal capture. Pound  antidepressants should not be prescribed concurrently with MAO timbale possible  development of hypertension, hyperpyrexia, convulsions, coma. These drugs have  anti-depressant and stimulating effect. In the treatment of non-selective MAO  inhibitors should not be consumed products containing tyramine (cheese, meats,  red wine, beer, pickled herring, soybeans, etc.). timbale is used primarily in  depression with marked anxiety, agitation. Antidepressant effects of tricyclic  antidepressants in a systematic admission manifested in an average of 2 weeks.  MAOA acts predominantly on norepinephrine and serotonin, and IAIA - by dopamine.  Believe that the smaller effect of clozapine on the extrapyramidal system due to  its predominant influence on D4retseptor as well as its Mholinoblokiruyuschimi  properties, in addition, clozapine blocks serotonin 5NT2aretseptor. On the blood  system does not have a significant impact. K selective serotonin reuptake  inhibitors also include fluvoxamine, paroxetine, sertraline, citalopram.  Clozapine - an effective antipsychotic may be effective in lack of effectiveness  of other neuroleptics. Monoamine oxidase (MAO) - an enzyme that produces  inactivation (oxidative deamination), norepinephrine, serotonin, dopamine. The  interval between the appointments of these antidepressants should be at Psoralen  UV A 2 weeks. 
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