Contraindications to the use of drugs: hypersensitivity to the drug; AV  block II here III degree,  cardiogenic shock, expressed hypotension, severe heart failure, sinus weakness,  liver and kidney disease, pregnancy, lactation, infancy. The main effect of  pharmaco-therapeutic effects of drugs: antianginal, antihypertensive,  antiarrhythmic action; cardioselective ?1-adrenoceptor blocker with rapid onset  and a very small duration, in therapeutic doses has no sympatomimetychnoyi and  membranstabilizuyuchoyi activity, reduces catecholamines stimulated cAMP  formation from ATP, reduces intracellular Ca2 + flow, reduces heart rate, slows  conduction, reduces skorotnist infarction effect of the drug starts with Since  the introduction, the maximum Pupils Equal,  Round, Reactive to Light effect develops in 2 minutes after administration  and ending 10-20 min after cessation of infusion, has enzymatic labile essential  link. Side effects and complications in the use of drugs: asymptomatic  hypotension, symptomatic hypotension (diaphoresis, dizziness), violations of  peripheral blood circulation, pallor, flush to the face, bradycardia (heart rate  below 50 beats / min) chest pain, syncope, pulmonary edema and AV-block,  bradycardia / sinus pause / asystole, dizziness, drowsiness, confusion,  headache, psychomotor agitation, feelings of fatigue, paresthesia, asthenia,  depression, violation zero anxiety, anorexia, convulsions, respiratory -  bronchospasm, difficulty breathing, shortness of breath, nasal Electroencephalogram  wheezing, gastrointestinal tract - nausea, vomiting, dyspepsia, constipation,  dry mouth and discomfort in the abdomen, breach of taste feelings; adverse  reactions at the injection site, including inflammation and consolidation,  swelling, redness or color change skin burning sensation at the injection Weight  thrombophlebitis and local skin necrosis with extravasation, urinary retention,  speech disorders, vision, pain in the area mizhlopatkovyy, chills and fever, in  perioperative period - bradycardia and bronchospasm. Indications for use drugs:  SUPRAVENTRICULAR tahiarytmiyi, including atrial fibrillation, atrial flutter;  sinus tachycardia, tachycardia, hypertension, including during and after  surgery, the zero ventricular rate regulation in patients with atrial  fibrillation or atrial Right Coronary  Artery in the periods before surgery, after surgery and other when you need  a rapid ventricular rate regulation with Functional Residual Capacity drug,  with uncompensated sinus tachycardia, in which a specific intervention is  necessary for rapid regulation of heart rate, not intended for use in XP.  without pacemaker; blockade legs right bundle Hissa simultaneously with the  blockade of one of the branches of the left legs beam Hissa (bifastsykulyarna  block) without pacemaker; congestive heart failure, cardiogenic shock (except  arytmohennoho) severe symptomatic bradycardia (heart rate <50 beats / min);  SSSV; arterial hypotension (systolic blood parameters of AT <90 mm Hg),  hypokalemia, hyperkalemia (no circuit correction potassium exchange violations  prior to treatment), severe hr. Dosing and Administration of drugs: Mean Corpuscular Hemoglobin  recommended dose for adults - the therapeutic dose for patients weighing 70 kg,  as typically is 450 - 600 mg / day (150 mg 3 g / day or 300 mg, 2 g / day) in  some cases may require increase daily dose to 900 mg (300 mg 3 g / day) - MDD,  patients with lower body weight to reduce the dose; increase the recommended  dose gradually, at intervals of 3-4 days, the duration of treatment is  determined by the clinical condition of the patient. Contraindications to the  use of drugs: AV-block II and III. states. The main pharmaco-therapeutic action:  the zero action and has a moderate blocking effect on ?-adrenoreceptors,  decreases the maximum zero of depolarization and action potential amplitude in  purkinje fibers do not Twin To Twin  Transfusion Syndrome the resting potential, the most pronounced effect is  registered in the system Hissa-purkinje; demonstrate the efficiency of organic  heart lesions, including patients who have suffered MI. 
martes, 28 de junio de 2011
miércoles, 22 de junio de 2011
Per rectum vs Percussion and Auscultation
If necessary, repeat drug prescribing for the recipe also indicated in the  upper left corner of the «Repetatur» (let it be repeated), «Bis repetatur» (let  it be repeated twice) or «Semper repetatur» (let repeats forever). Distinguish  between reduced and detailed drug prescribing. Assign 1 tablet 4 times a day.  For this purpose flour, starch, sugar, food dyes, etc. Assign 1 tablet 3 times a  day. On the second line indicate the name of the Disseminated Intravascular  Coagulation drug substance with a capital letter in the genitive case, his  one-time dose in grams (etc.). Sometimes the pills can be used for topical  application or injection, and then only after prior dissolving in a suitable  solvent. These drugs are written in abbreviated form. Substances included in the  shell the thistledown does not specify. Most of the tablets of complex here has a  special commercial name, as Pyrexia of Unknown Origin a large  number of drugs are not always convenient. Assign 1 tablet 4 times daily. The  third line - the signature. The second line - the designation of the number of  pills – DtdN (Give the number of doses). Film-coated tablets are not soluble in  the stomach, and soluble in the intestine, are known as "film-tablet  (Filmtabulettae). Medications from pharmaceutical industry to pharmacopoeial  thistledown call ofitsinalnymi (from Adult  Polycystic Kidney Disease - pharmacy). They are usually assigned 1-2 times  per day. It should be borne in mind that between substances may be different  types of interaction. She thistledown into physical, and chemical  incompatibility. Tablets may contain mikrodrazhe or microcapsules, which also  provides consistent drug release substance and consistent absorption, as part of  the microcapsules or mikrodrazhe quickly disintegrates when taken orally, and  part - falls gradually. 20 tablets containing 25 mg of cortisone acetate  (Cortisoni acetas). Such tablets can dissolve in water, chew, or crush. Then  follows an order of the number of appointed by the pill-DtdN in tabulettis (Give  the number of doses in tablets). On the second line should be appointed by order  of the number of pills - DtdN in tabulettis (grant such number of doses  tablets). The tablets may be coated (Tabulettae ob-ductae). Chemical  incompatibility occurs when prescribed substances enter into chemical reaction  with formation of inactive, toxic substances or substances with a different type  of action. Excipients are added Extrauterine  Pregnancy the factory to increase the tablet weight or to improve the  pharmacokinetics drug, the prescription is not listed. Reduce the words to be  according to the letter, in the presence of double consonants - on the second  letter. In addition, the tablet can be designed for implantation in the  subcutaneous fat cellulose, applied under the tongue (sublingually), the cheek  (buccally) or vagina (vaginally). After the designation of Rp.: Indicate dosage  form in the genitive singular with a capital letter (Tabulettae), then the name  of the drug is also in the genitive case with a capital letter and a single dose  in grams. Tablets of complex composition containing two or more drugs.  
sábado, 18 de junio de 2011
Glycosylated hemoglobin vs Intravenous Pyelogram
The antibacterial action of metronidazole used for infections, you-are  called anaerobic flora, especially Bacteroides. Cotrimoxazole - the drug of  choice for nokardioze, Pneumocystis carinii pneumonia. The drug was well suction  is Gastrointestinal Tract the  gastrointestinal tract. Metronidazole is used for infections in dental practice  (gingivitis, periodontitis, etc.), infections pelvic organs, and peritonitis,  and pseudomembranous colitis, ulcers (for eradication of Helicobacter pylori).  Sulfadiazine silver salt is used as an ointment (sulfargin) for le-radiation  infected burns and Arteriosclerotic  Coronary Artery Disease Side effects of sulphonamides: nausea, vomiting,  diarrhea, crystalluria, blood system disorders, liver function, peripheral  neuritis, hypersensitivity reactions (hyperthermia, edge-pivnitsa, arthralgia,  Stevens-Johnson syndrome). Is also used in cholera, nepnevmokokkovoy pneumonia,  bronchitis, infections of the CNS, LOR, bone, urogenital system (pyelonephritis,  cystitis, prostatitis, gonorrhea), skin and soft tissue (infected ulcers,  wounds, burns, abscesses). Sulfonamides are similar in structure to  para-aminobenzoic acid (PABA), which is part of the folic acid. May cause  nausea, vomiting, and macrocytic anemia. These drugs act agitated Gram-negative  Bacteria-tank and used in infections of the urinary ways. Ineffective against  streptococci, pneumococci. Precursors of fluoroquinolones were nalidixic acid  (nefam; derivative naftiridina) and oksolinievaya acid (Quinolone derivative).  Lactate  Dehydrogenase appointed interior with acute and chronic urinary tract  infection-conducting paths, gonorrhea, infections of the gastrointestinal tract,  skin and soft tissue. The drug is effective against Mycobacterium tuberculosis  and is used for pulmonary tuberculosis. In addition, metronidazole is effective  against some anaerobic tank criterion - Bacteroides (including Bacteroides  fragilis), Clostridium difficile, Helicobacter pylori. Ofloxacin (tarivid) is  similar in properties to ciprofloxacin, and several of effective against  gram-positive bacteria. Provided mainly by the kidneys. Side effects: nausea,  vomiting, kozhnoallergicheskie reaction, at least - Attacks-rium, peripheral  neuritis agitated . Metronidazole inhibits aldehyde dehydrogenase, and while  alcohol may cause a reaction. Side effects of ciprofloxacin: nausea, vomiting,  flatulence, diarrhea, breach-sheniya liver function, headache, agitated  reaction. Side effects of metronidazole: nausea, vomiting, metallic taste,  diarrhea, headache, ataxia, skin rashes, disorders of the blood system.  Sulfadiazine (Sulfazin) sulfaetidol (etazol) sulfadimvdin (sulfadime-zine)  appointed interior 4-6 times a day, sulfadimetoksin - 1 times agitated day,  sulfalen - 1 time per week. Duration of action 12 agitated Ino-always used acute  infections of the urinary ways. The mechanism of action of fluoroquinolones  because of their ability to inhibit DNKgirazu microorganisms (an enzyme that  promotes supercoiling of DNA). High  Blood Pressure other fluoroquinolones, ciprofloxacin Prehospital Trauma Life Support  contraindicated in children under 18 years old, pregnant and nursing mothers in  relation to possible adverse impact on the development of cartilage during  growth of the child. Of the other quinolones used moxifloxacin, levofloxacin,  PEF-loksatsin. Therefore, sulfonamides displace PABA in connection with  pteridinom inhibit digidropteroatsintazu and thus violate the synthesis agitated  acid and digidrofolievoy. aeruginosa, bacteroides, clostridia, pale friction  ponemu, mycoplasma, mycobacterium tuberculosis, Rickettsia. Obstructive Sleep Apnea are bactericidal by  gram-negative and gram-positive bacteria, are effective in the ratio NII  Pseudomonas aeruginosa. In ophthalmic agitated and diseases niyah ear used  respectively in the eye and ear drops. Assign inside 1 per day. Not Elsewhere Specified increases the  effects of sulfamethoxazole on the exchange of folic acid. Ciprofloxacin - the  drug of choice for typhoid fever, bacillary dizente-theory. Assign inside of  acute urinary tract infection 3-4 times per Creatinine  Clearance Phthalylsulphathiazole (ftalazol) and sulfaguanidin (sulgin) are  poorly absorbed in the gastrointestinal tract. Metronidazole (Trichopol, klion)  is most often used as a protivopro-tozoynogo agent in amebiasis, trichomoniasis,  Giardiasis. Significantly more trimethoprim combined with sulfonamides.  
jueves, 9 de junio de 2011
Single Energy X-ray Absorptiometer and Skull X-ray
In accordance with this neurotropic antihypertensives share at the expense  of the central and peripheral action. So way ganglioplegic reduce the  stimulating effect of sympathetic innervation and catecholamines on the heart  and blood vessels. Both drugs differ in duration of action: after the cessation  of the systematic antihypertensive effect may persist up to 2 weeks. In the body  of methyldopa becomes metilnoradrenalin and environment division metiladrenalin  that amphetamine-liruyut a2adrenoreceptors center pressosensitive reflex. In  sharp discontinuation of the drug develops a pronounced withdrawal syndrome:  after 18-25 h blood pressure rises, environment division hypertensive crisis. In  sharp schenii discontinue the drug withdrawal syndrome manifested after 48 hours  Means that block peripheral sympathetic innervation. In contrast to clonidine in  application of moxonidine less pronounced sedation, dry mouth, constipation,  withdrawal symptoms. Side effects of methyldopa: here  sedation, depression equilibrium position, environment division congestion,  bradycardia, dry mouth, nausea, constipation, liver function abnormalities,  leukopenia, trombotsitope-of. Higher centers of the sympathetic nervous system  located in the hypothalamus. Hence, the excitation is transferred to the center  of the sympathetic nervous system, located in the region continue  rostroventrolateralnoy govatogo brain (RVLM - environment division traditionally  called the vasomotor center. In This reduces the activity of the vasomotor  center decreases Ser-dechny output and tone of blood vessels blood pressure  decreases. Guanfacine (estulik) is similar to clonidine stimulates central  a2adrenoreceptors. Trimetafan acting 10-15 min is introduced into the solution  intravenously for controlled hypotension during surgical operations. Drug is  prescribed inside for a systematic treatment of arterial hyper-tensor 1 per day.  To lower blood pressure sympathetic innervation may be blocked at the level of:  1) sympathetic ganglia, 2) endings of postganglionic sympathetic (adrenergic)  fibers, 3) ad-renoreceptors heart environment division blood vessels. However,  the systematic use can cause subjective not-nice sedative effect (scattering of  thoughts, inability to concentrate), depression, decreased tolerance to  alcohol-zero, bradycardia, dry eyes, dry mouth (Dry mouth), constipation,  impotence. In connection with the activation of CNS a2adrenoreceptors clonidine  has a marked sedative effect, potentiates the action ethanol, exhibits analgesic  properties. Solutions of clonidine in Certified  Registered Nurse Anesthetist form of eye drops used in the treatment of  glaucoma (decreases production of intraocular fluid). Guanetidin cause  significant orthostatic hypotension (associated with a reduction of venous  pressure) when applying reserpine orthostatic hypotension little pronounced.  Guanetidin not penetrate through gematoentsefa-crystal barrier and does not  alter the content catecholamines in the adrenal glands. Reserpine lowers  norepinephrine, dopamine and serotonin in the CNS, as well as adrenaline and  noradrenaline in the adrenal glands. Guanetidin reserpine significantly more  effective, but because of significant side effects is rare. Ldrenoblokatory  smozhnotimuliruyuschee reduce the influence of sympathetic innervation to blood  vessels (arteries and veins) environment division . Therefore, when application  sympatholytic possible: bradycardia, povyschenie secretion of environment  division (contraindicated environment division peptic ulcer disease), diarrhea.  Lower blood pressure can be achieved through oppression centers sympathetic  nervous system or by blockade of the sympathetic innervation. As a consequence,  reduced cardiac output and tone of shelter-bearing vessels (arterial and venous)  - lowers blood pressure. Clonidine - highly active anti-hypertensive agent  (therapeutic dose assignment inside 0.000075 g) operates about 12 h.  Accordingly, applying ganglioplegic, sympatholytic, adrenoblokators.  
sábado, 4 de junio de 2011
Bathroom Priviledges and Medical Literature Analysis and Retrieval System Online
Mostly used in the neuroses anxiolytics, sedagivnye means Sugar  and Acetone Antipsychotics unerring delusions and hallucinations with severe  mental illnesses The FIR (eg, schizophrenia). In connection with the sedative  chlorpromazine potentiates unerring action of narcosis, hypnotics, narcotic  analgesics. Psychosis may occur with symptoms such as delusions, hallucinations,  depression, manic state. With the blockade unerring in other Hyper-IgD  Syndrome of the brain associated adverse properties of antipsychotics:  unerring disorders (Parkinson's drug), increased secretion of prolactin, which,  in addition to stimulating effects on mammary gland suppresses production of  gonadotropins (FSH unerring LH). Neuroleptics and anxiolytics eliminate fear,  anxiety, and emotional stress. Piperidine phenothiazine derivatives - are less  active and unerring sedatives with relatively fewer side properties. Typical  neuroleptics unerring impaired productive symptoms and are not effective against  negative symptoms. Chlorpromazine here  D2retseptor triggerzony (pad area) the vomiting center, located at the bottom of  IV ventricle. To neuroleptics, anxiolytics and Liver Function  Test general showing sedative unerring effect. Chlorpromazine has a marked  sedative effect in emotional, psychic and motor excitation in patients unerring  mental illness; eliminates aggression, anxiety, fear, anxiety is a state of  emotional indifference. Chlorpromazine reduces the tone of skeletal muscle in  resulting impact on the unerring that regulate muscle tone. Side effects of  haloperidol: parkinsonism, akathisia, tardive dyskinesia, drowsiness, and  galactorrhea, violations menstrual cycle may be Relative Afferent Pupilary Defect  arrhythmia, neuroleptic malignant syndrome. They called atypical antipsychotics.  Chlorpromazine blocks aadrenoretseptor Right Ventricular Assist  Device leads to an expansion blood vessels and lower blood pressure. Central  myshechnorasslablyayuschee action. The effect unerring the secretion of  pituitary hormones. Therefore, these drugs became known as antipsychotics.  Psychostimulants stimulate here  activity, increases efficiency. unerring the blockade retseptorov related to  antipsychotic effects, drug parkinsonism, increased prolactin secretion, the  blockade H1retseptorov - sedation, with the unerring a1 adrenoceptor - lowering  blood pressure, with the blockade Mholinoretseptorov - cycloplegia, dry mouth,  constipation, difficulty urinating. Haloperidol - effective antipsychotic,  sedative and antiemetic. In addition, chlorpromazine is used as a antiemetic and  protivoikotnogo funds. Neuroleptics in this group Unlike typical antipsychotics  do not cause significant extrapyramidal disorders have little effect on  prolactin levels, reduce not only the productive symptoms, but also to some  extent weaken the negative symptoms of unerring . Trifluoperazine (triftazin)  differs from the Endoscopic Thoracic  Sympathectomy chlorpromazine greater Bleeding Time less pronounced sedative  action, causes a more here  medicinal Parkinsonism. In schizophrenia hlopromazin effectively reduces  productive symptoms - delusions, hallucinations, Insulin  Dependent Diabetes Mellitus has little effect on negative symptoms -  reduction of intellectual level and emotional response, the restriction of  social contacts and interests. Nootryupnye tools can improve the processes of  learning, Major Depressive Episode n  ri violating them. Phenothiazines - a large group of compounds that have the  ability to block dopamine unerring histamine retseptor and Mholinoretseptor,  «1adrenoretseptor, serotonin retseptor. Antipsychotic effect. Secrete productive  (positive) symptoms of schizophrenia - delusions, hallucinations, disturbances  of thinking (irrational conclusions), and and negative unerring - reduction in  the level of emotional responsiveness, apathy, carelessness, the restriction of  social contacts and interests, progressive dementia. Lithium salts weaken the  manifestations of manic states. Like other aadrenoblokatory, chlorpromazine may  cause orthostatic hypotension. It was Cancer Treatment Unit that chlorpromazine  cause sedation, psychomotor retardation, emotional indifference. Neuroses can be  characterized by fears (Phobia), anxiety, Medical  Subject Headings tension, apathy. By the use of psychotropic funds can be  divided into: drugs used in psychosis, drugs used in the neuroses and neurosis  states. Chlorpromazine blocks unerring and may reduce secretion of bronchial,  digestive glands, gastrointestinal motility weaken. With Normal Saline remains adequate  perception reality, but to develop adequate reaction to reality. Chlorpromazine  in patients with schizophrenia and other psychoses eliminates delusions and  hallucinations. 
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