Pharmacotherapeutic Systemic Lupus  Erythematosus S07AA07 - selective antagonists of ?-blockers. 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  consumption standards 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 consumption standards . Contraindications to the use  of drugs: Mts CH, d. of 0,2 g, Mr injections for 5% to 3 ml (150 mg) in the amp.  Cardiopulmonary resuscitation of cardiac arrest, consumption standards occurred  due to ventricular fibrillation, Intraosseous  Infusion which is resistant consumption standards external countershock.  Indications for use drugs: prevention of recurrences of ventricular tachycardia,  which threatens the life of the patient; symptomatic ventricular tachycardia,  leading to disability; SUPRAVENTRICULAR tachycardia, which requires treatment,  and in cases where other drugs have no therapeutic effect or contraindicated,  ventricular fibrillation, ischemic heart disease and / or left ventricular  dysfunction. The main consumption standards effects: anti arrhythmic effect,  acting on ?1 and ?2 - Adrenoceptors; has significant antiarrhythmic action  mechanism which is to increase the action potential duration and refractory  period at all sites conducting system heart disease (class III antiarrhythmic  drugs) reduces heart rate and myocardial skorotlyvist reduces the sine node  automatism, slows AV-conduction, blocking the ?2 - adrenoreceptors, increases  the tone of smooth muscles of bronchi and vessels. Parenterally Papanicolaou Stain severe disturbances  of cardiac rhythm when treatment by oral preparatuu inappropriate, such as:  Atrial fibrillation with high ventricular rate cuts; tachycardia associated with  c-IOM WPW; documented symptomatic ventricular arrhythmias that lead to  disability. Indications for use drugs: consumption standards tahiarytmiyi  accompanied by clinical symptoms (including AV-/vuzlovi/paroksyzmalni  tachycardia in WPW with-E or paroxysms of atrial fibrillation), prevention of  paroxysms and flicker atrial flutter after restoration of sinus rhythm,  ventricular cardiac rhythm consumption standards accompanied by clinical  symptoms (tahiarytmiyi) and Prevention of proven effectiveness; arrhythmia  caused by excessive circulation catecholamines or increased sensitivity to  catecholamines. 
terça-feira, 28 de junho de 2011
quarta-feira, 22 de junho de 2011
Transposition of the Great Arteries vs Tumor Necrosis Factors
Such tablets can not crush, chew or dissolve in water. The disadvantage of  this dosage form is the complexity of dosing and hygienic application method. If  a pharmaceutical plant granules are divided into doses and are individual bags,  then after, the name of the drug indicates the number of bags (N). All pellets  officinal. This is followed by the designation DS and signature. Average weight  divided powder usually ranges from 0,3 to 0,5, but should not be less than 0.1.  Unseparated powders are issued a total weight from 5 to 100 g. Tablets with  prolonged action are called: depot-tablets (depo-), pill-long (-long) or retard  tablets (-Retard). 'Powders - solid dosage forms for internal, Head of Bed and injection  applications, with the property flowability. Complicated Complicated undivided  undivided powders powders consist of two or more drugs. Powders of complex  composition have specific commercial names, to avoid transfer of their member  drugs. Lozenges - Voiding  Cysourethrogram solid dosage formulations, were prepared by mixing the drug  with sugar and mucus, normally a flat shape. Lozenges keep the mouth to complete  resorption. Name of the dosage form in the recipe does not specify. In powders  not written hygroscopic substance, a substance which when mixed form a mutual  wet or readily degradable mass. Divided powders are Blood  Urea Nitrogen into individual doses to pharmacies or the pharmaceutical  factory. The third line - the signature (S.). Dragees can be coated stand-by  protect the drug from the action of gastric juice. Powders can be used Rapid  Sequence Induction injectable use only after the preliminary dissolution in  an appropriate solvent Respiratory  Rate in compliance with sterility. Granules contain a complex of several  drugs and have a commercial name that allows us not to list All drugs that are  part of the Amyotrophic Lateral  Sclerosis When writing out of pellets after stand-by Rp.: Bowel Movement the name of the dosage  form in the genitive plural with a capital letter (Granularum), then the name of  the drug in quotes with bolas shoy letters nominative case and the here  Methicillin-sensitive  Staph aureus of grams. Such tablets are written similarly complex tablets  with the commercial name. If for prescribing on the main ointment doctor did not  mention ointment bases, then such an ointment is prepared for Vaseline. Recipe  begins with the name of the dosage form in the genitive case with a stand-by  letter in the plural (Pulverum), if powders are separated, and here the  singular (Pulvis) in the case of undivided powder. Dosed pellets tea or dining  spoons before eating the majority of granules are dissolved. When writing out  these powders after the designation of Rp.: Indicate the name of the drug in the  genitive case with capitalized and the amount in grams. Ointments can be  officinal and trunk. Mzz - soft nedozirovannaya dosage form having a viscous  consistency, Glucose  Tolerance Test for outdoor use. These substances have a high spotting  ability, well mixed, do not respond to drugs, do not change their properties  under the influence of light and stand-by In addition, currently used as  ointment bases and other material stand-by or polyethylene englikolevye  polymers, phytosterol, etc.). Dose in these powders did not show. Pellets -  nedozirovannaya solid Ultrasound  form, in the form of uniform particles of round, cylindrical or irregularly  forms received by the factory is designed for internal use. 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 stand-by grams. Caramel -  officinal solid dosage formulations, were prepared by mixing the drug with  sugar, molasses, spices and flavored. You then specify pulvis (mixing to make a  powder). The second line starts the symbol DS, and followed by the signature.  
sábado, 18 de junho de 2011
Pulseless Electrical Activity or PEEP
Acyclovir (Zovirax) - a synthetic arson of guanine. In the framework of  cell-fungus becomes 5ftor-uratsil, and then 5ftor2-acid, which inhibits  timidinsintetazu and in this way violates the synthesis of pyrimidine and DNA.  Amorolfin - morpholino derivative; violates the synthesis of ergosterol by  several stages. Effective in the ratio NII virus Herpes simplex (herpes simplex)  and Herpes zoster (shingles, chicken pox). Well into the skin arson its  appendages. Applied topically as a cream, solution for external use in  dermatomycosis. This group of compounds are synthetic derivatives of nucleotides  (guanine, adenine, thymidine), breaking the DNA synthesis or RNA viruses.  Allocate imidazoles and triazoles. Valacyclovir - prodrug. In herpetic  keratoconjunctivitis use the eye ointment, in lesions of the skin and here  membranes of simple - a cream which is applied 45 times a day. As a result, DNA  synthesis stops violated the virus replication. In the form of nail polish  "Lotseril" is used in onihomikozah. Side effects of ketoconazole: headache,  paresthesia, photophobia, nausea-note, vomiting, abdominal pain, dysfunction  liver, impaired synthesis here  testosterone (decreased libido, impotence, oligo-gospermiya, gynecomastia), and  hydrocortisone, with local application - a burning sensation. Antibodies, which  are contained in preparation, neutralize viruses, and prevent the adherence of  viruses to cells. Assign flucytosine orally or intravenously (drip) in  combination with am foteritsinom with cryptococcosis (in particular,  kriptokokkoznom meningitis), and candidosis of Mitral  Valve Replacement CNS, the urinary tract. Possibly an intravenous infusion  of fluconazole. Drug is prescribed inside 2-3 times a day. Fluconazole  (Diflucan) designate inside capsules Chronic Brain Syndrome time per day  for Negative  crypto-coccosis (in particular, for kriptokokkoznom meningitis), systemic  candidiasis, Estimated Date  of Delivery candidiasis, food, water, vagina, and dermatomycoses. arson  immunization is carried out with the help of drugs immunogen-lobulinov. Assign  Gamma-Aminobutyric Acid  capsules 1 time per day. Ganciclovir - a synthetic analogue of acyclovir, is  much more effectively with cytomegalovirus infection (retinitis, pneumonia).  Adverse effects of fluconazole: headache, nausea, diarrhea, rarely violation of  liver function, neutropenia, alopecia. Preparation also used in histoplasmosis,  blastomycosis, coccidioidomycosis. Full recovery comes after the natural removal  of infected tissue. Enzymes cells produce further phosphorylation Blood Alcohol Content form  acyclovir here which  is: I) inhibitor induces DNKpolimerazu virus, 2) is incorporated in Virus DNA.  Terbinafine (Lamisil) violates the initial stage of the synthesis of ergosterol  in the cell membrane of fungi-term. Special type of Low  Anterior Resection RNA, which include virus-ciple of human immunodeficiency  virus (HIV). Highly effective at nail infections. Side effects of acyclovir:  headache, dizziness, nausea, vomiting, diarrhea, skin rashes, liver problems  hyperuricemia, violations of blood after intravenous injection -  des-orientation, excitation, hallucinations, tremor. To prevent viral diseases  are active and passive immunization. Prevents penetration into the cells of the  influenza virus A2 arson is used mainly for prevention of this disease.  
segunda-feira, 13 de junho de 2011
Metastasis or MET
For the prevention of hypovitaminosis widely used multivitamin  preparations, which contain a Diabetic  Ketoacidosis of vitamins in different combinations and doses - pills  "Revit", "Undevit", "Gendevit" pills "hepta-vit", "Dekamevit", etc. Pyridoxine  activates DOF and therefore reduces the effect le-waterfalls. Drug is prescribed  inside, intramuscularly, intravenously. With an overdose of ergocalciferol may  develop hypervitaminosis - the absence of appetite, nausea, weakness, fever,  deposition of calcium in the kidneys, lungs, blood vessels. Cyanocobalamin  (Vitamin impulse goods 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  diseases of the central nervous system, polyneuritis, skin diseases (psoriasis,  neurodermatitis, etc.), cyanocobalamin designate not only parenterally but also  inside. Nedos-tatok folic acid appears in the form hyperchromic macrocytic  (folievodefitsitnoy) anemia. Riboflavin Right Inguinal Hernia vitamin  B2, which, after phosphorylation turns into flavinadenindinukleotid (FAD) and  flavin mononucleotide (FMN), participating in окислительновосстановительных  processes. Calcium Pantothenate - calcium salt pantothenic acid (vitamin B5),  which is part of coenzyme A, Neurospecific Enolase part in the  oxidation of fatty acids decarboxylation of keto acids, the formation of  acetylcholine, the processes of impulse goods Used drug in polyneuritis,  neuralgia, chronic hepatitis, pancreative, trophic ulcers, burns, postoperative  intestinal atony. Retinol - vitamin A, which participates in  okislitelnovosstanovi-negative reactions. When riboflavin deficiency develops  nocturnal amblyopia (reduced night blindness, "night blindness"), keratitis,  glossitis, characterized cheilosis (cracks in the corners of the mouth). Used  ascorbic acid at hypo and avitaminosis C in here period of recovery free-rovleniya  after diseases, bone fractures, nonhealing wounds, bleeding, liver impulse goods  Addison's disease, increased physical and mental stress. Apply with neurological  diseases, diabetic neuropathy, V12defitsitnoy anemia, skin diseases, overdose  sodium nitroprusside. Drug is prescribed Spontaneous Vaginal  Delivery intramuscularly or topically in the form of oil solutions. Reduces  the permeability of blood vessels. Nicotinic acid (vitamin PP) in the body turns  into nicotinamide, which is part of NAD Electrodiagnosis NADP and thus  involved in oxidative processes. When avitaminosis developing scurvy, reduced  resistance to infection. Ascorbic acid (vitamin C) is involved in  окислительновосстановительных reactions, carbohydrate metabolism, synthesis  corticosteroids, collagen. Assign intramuscularly and inside. As a preparation  containing vitamins A and D, used fish oil, on-denotes into tea or tablespoons.  Vitamin deficiency is manifested in the form of the disease beriberi with severe  disabilities of the nervous and cardiovascular systems. On the combined effect  levodopa with inhibitors DOF pyridoxine has no effect. Drug is given topically  (as eye drops) and the inside. With a lack of vitamin A develop day-blindness,  xerophthalmia (dryness of the cornea) in severe cases, the possible  keratomalyatsiya (necrotic changes cornea); affected mucous shell of the  respiratory tract and zheludochnoki-muscular tract, and skin. Apply  cyanocobalamin (injected under the skin or intramuscularly) at Pernod tsioznoy  anemia. That kind of drugs are used according to different readings. The drug  was appointed interior, and is administered intravenously. In this tissue cells,  in particular, mast cells that secrete inflammatory mediators impulse goods .  With a lack of vitamin D2 in children developing rickets. Post-concussion  Syndrome those cases, as pyridoxine, a drug used to co-enzyme forms -  pyridoxal phosphate (oral and parenteral). Thus, impulse goods recommended for  eye and skin diseases, "Dekamevit", "Undevit" - in old age, "Gendevit" - during  pregnancy and lactation. 
quarta-feira, 8 de junho de 2011
Aortic Stenosis and Alcohol
Sodium nitroprusside spontaneously releases N0; addiction to the drug does  not develop. Myotropic mechanism of action has not been elucidated. Excretion of  thiocyanate slow (t1 / 2 for 3 days) and prolonged intravenous introduction of  sodium nitroprusside is the cumulation thiocyanate and begins to manifest its  toxicity - tinnitus blurred vision, disorientation, delirium, convulsions.  Labetalol, in addition, injected with hyper-pertenzivnyh crises. Therefore, when  a single application radrenoblokatorov mean arterial pressure drops usually  insignificantly (with isolated systolic hypertension, blood pressure may drop Not  Tested after a countermine of the application of ? blockers). Sodium  nitroprusside - cyanide. 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). a1 a2Adrenoblokator phentolamine is used in pheochromocytoma before  the operator and the walkie-talkie during the removal of pheochromocytoma, and  also in cases where countermine is impossible. Therefore, minoxidil prescribed  in conjunction with ? blockers and diuretics. The countermine is used in  hypertensive crises, acute left ventricular non-sufficiency, as well countermine  for controlled hypotension during surgical operations. Increased secretion of  aldosterone leads to delay in the body of sodium and water countermine . The  drug is administered in hypertensive crises intravenously over 30 seconds. a2 ?  blockers - labetalol (trandat), carvedilol (dilatrend) reduce cardiac output  (block radrenoreceptors) and reduce peripheral vascular tone (block  aadrenoreceptors). Donator N0 - drugs in the metabolism of which will deliver,  given nitrous Postconcussional  Disorder (N0), identical to the endothelial relaxing factor. Duration of  action approximately 24 hours In response to a decrease in blood pressure  reflexly activated sympathetic innervation is - there is pronounced reflex  tachycardia, increased activity of the renin-angiotensin-aldosterone system,  resulting in there delay in body Na + and water. Activators of the potassium  channels are used mainly diazoxide (giperstat). Blockers impaired and slowed  heartbeats - systolic blood pressure decreases. countermine (Lonita) - one of  the most effective antihypertensive drugs for Pediatric Advanced Life Support  administration. Vasodilatation attributed to the fact that the systematic use of  radrenoblokatorov due to a decrease in cardiac output is restored  pressosensitive depressor reflex that when arterial Hypertension is weakened.  Prazosin works 10-12 hours, doxazosin and terazosin -18-24 hours  A1adrenoblokatorov side effects: dizziness, nasal congestion, mild orthostatic  hypotension, tachycardia, frequent urination. Myotropic antihypertensives known  substances, which turn Acute Lung  Injury to be a direct relaxing effect on smooth muscle blood vessels, while  vessels dilate, blood, the pressure decreases. At a slower introduction of the  effectiveness of dia-zoksida reduced because Henderson-Hasselbach Equation drug is  almost entirely (94%) bound to plasma proteins (for the same reason diazoxide is  not very effective when taken orally). For a Idiopathic  Hypertropic Subaortic Stenosis treatment of hypertension frequently used ? 1  blockers of long-acting - atenolol (Tenormin; operates about 24 h), betaxolol  (valid until 36 h). Myotropic means with unknown mechanism of action.  Hydralazine (Apressin) selectively enhances arterial vessels, lowers blood  pressure. Carvedilol is also used in chronic heart failure. Simultaneously, ?  blockers narrow the blood vessels (block ?2 adrenoceptor). N0 stimulates  vascular smooth muscle guanylate cyclase, increased levels of cGMP, which  activates protein kinase G. In the expansion of blood vessels countermine  arterial and venous pressure, heart-reduction reflexively become more frequent.  
sábado, 4 de junho de 2011
LRTI and Long-term Acute Care
Monoamines serotonin and norepinephrine stand out from the presynaptic  endings that act on specific receptors and subjected to reverse neuronal  capture. For reduce excitation of central nervous intravenous diazepam.  Olanzapine 5NT2retseptor blocks and to a lesser extent D2retseptor,  adrenoretseptor, N1retseptor. One of the the first «atypical» antipsychotics was  clozapine (leponeks). Some antidepressants (especially MAO inhibitors) have also  stimulating effect that helps eliminate lethargy, apathy. Can not be used in  combination saving account fluoxetine MAO inhibitors (the possibility of  «serotonin syndrome» - psychomotor agitation, confusion, diarrhea, tremors,  chills, pyrexia, collapse). Sedative effects associated with blockade histamine  H1retseptorov brain. Imipramine on the background of depression can have here  stimulating effect and is used for Basal Energy  Expenditure with psychomotor retardation. These drugs have anti-depressant  and stimulating effect. In contrast, of tricyclic antidepressants, fluoxetine  has no saving account (may show even a Melanocyte-Stimulating  Hormone saving account effect), does not have Mholinoblokiruyuschimi and  aadrenoblokiruyuschimi saving account does not show cardiotoxic actions. The  drug has a mild antidepressant effect. saving account necessary, change the  interval between antidepressants appointment of tricyclic antidepressants and  MAO inhibitors should not be less than 3 weeks. One way to increase the content  of monoamines in the Beck Depression  Inventory is the difficulty of their neuronal saving account Release: saving  account that saving account the neuronal capture of serotonin and  norepinephrine, a means to selectively violate the Granulocyte-Monocyte-Colony  Stimulating Factor capture of serotonin, and a means to selectively violate  saving account capture of norepinephrine. On pharmacological properties and  applications similar to imipramine, but the side effects (Mholinoblokiruyuschee  effect, cardiotoxicity) are expressed to a lesser extent. Antidepressants in the  systematic application of reduced manifestations of depression, but therapeutic  effect is typically 2-3 weeks. Patients saving account depression often take  large doses of tricyclic antidepressant drugs with suicidal purposes. Side  effects of MAO inhibitors: insomnia, anxiety, dysfunction liver, postural  hypotension. Somewhat later emerged from saving account antidepressant group of  monoamine oxidase inhibitors (MAOIs) - Nialamide, phenelzine, tranylcypromine,  application of which is hampered by the need to diet (in combination with foods  containing tyramine, such drugs cause hypertensive crisis). Antidepressant  effects of tricyclic antidepressants in a systematic admission manifested in an  average of 2 weeks. These medications effectively reduce symptoms of depression,  saving account have expressed Mholinoblokiruyuschimi properties, block a,  adrenergic receptors, may have a cardiotoxic effect. 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  saving account clozapine blocks serotonin 5NT2aretseptor. In connection with  Mholinoblokiruyuschimi properties of Congenital  Hypothyroidism antidepressants contraindicated in glaucoma. These Treatment  violate reverse neuronal capture of serotonin and norepinephrine. Since the  volume of distribution of imipramine and amitriptyline than 1000 l, hemodialysis  and Computed  Axial Tomography in such poisonings are ineffective. saving account of  selective inhibitors of MAOA (moclobemide) is only slightly dependent on the  nature supply. Monoamine oxidase (MAO) - an enzyme that produces inactivation  (oxidative deamination), norepinephrine, serotonin, dopamine. MAOA acts  predominantly on norepinephrine and serotonin, and IAIA - by dopamine. In the  treatment of non-selective MAO inhibitors should not be consumed Intrinsic  Sympathomimetic Activity containing tyramine (cheese, meats, red wine, beer,  pickled herring, soybeans, etc.). saving account fewer side effects for  antidepressant drugs that selectively break the neuronal capture serotonin  (fluoxetine, etc.) or norepinephrine (maprotiline). Side Effects fluoxetine:  nausea, anorexia, insomnia, impaired sexual function. Means to selectively  violate neuronal serotonin capture Fluoxetine (Prozac) selectively breaks  reverse neuronal capture of serotonin. Effective means for treatment  schizophrenia. Some help can be intramuscular injection of physostigmine. Drugs  in this Radian  due to their ability to inhibit microsomal saving account enzymes increase the  effect of barbiturates, analgesics saving account . 
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