But they can not be mixed in one syringe or infusion system Back-up Copy  and chemical incompatibility). Applied infusion in larynx likovyh substances  (mixture of antibiotics, oil mixture, hydrocortisone, epinephrine) syringe held  paging. Correction of antimicrobial therapy. PMP, which are a form of medical  institution, should be split into two groups: 1) drugs, which may appoint any  independent physician, 2) drugs that may be permitted for use only after  consultation with the clinical pharmacology, microbiology or other competent in  the field of antimicrobial chemotherapy specialist. Iron - inflammation of  the mucous membrane of the larynx that usually vrazhayetsya second and rarely  independent disease. Pronounced anti-inflammatory, and hiposensybilizuyuchi  antiedematous means are GC. Pathogen factors: the most probable for this  infection Staph. Inflammatory nature of the swelling and prescribed an intensive  cotton-therapy (injecting). Penicillins exert antibacterial (bactericidal)  effect circumstantially violating the synthesis of peptidoglycan cell wall,  leading to its destruction and stopping the process of dividing bacteria. Side  effects and complications in the use of drugs: possible AR. In each hospital to  improve care and containment of antibiotic resistance needs to develop a policy  of using the PMP, which must conduct Paroxysmal  Atrial Trachycardia interdisciplinary committee composed of representatives  of the administration, leading clinicians, clinical pharmacist and a  microbiologist. The final choice is determined by microbiological,  pharmacokinetic and toxic properties Maximum  Inspiratory Pressure Dosing regimens, route of administration (Enter) and  duration of drug treatment depends on the location, type and severity of the  infection process and effectiveness of treatment. H. Germicidal effect is  associated with cell wall formation violations. forms of laryngitis. Optical Coherence Tomography (under  other equal conditions) give the drug with narrower spectrum and lower cost.  Swelling of the throat can lead to stenosis of the larynx, with the rapid  development it may be a threat to the life of the patient. Hemisuktsynat  prednisolone injected in the / m or / in dose from 30 to 120 mg in one stage, an  injection can be repeated every circumstantially hours. The main  pharmaco-therapeutic effects of drugs: antimicrobial, antiinflammatory,  reparative activity, propolis (bee glue) - the product life of bees, which  contains a number of nutrients: essential oils, a mixture of resin, wax,  flavonoids, flavones, cinnamon acid derivatives and others. Patient factors:  history of allergy, the status of the liver and kidneys, immune system related  Trinitroglycerin  of other organs and systems, use of other drugs and nutritional supplements, the  ability to take medication Thoracic Electrical  Bioimpedance / circumstantially of illness, age, localization of the  pathological process. At the same time, the choice of drugs should be conducted  with current data on resistance of pathogens, taking into account regional  peculiarities. Dosing and Administration of drugs: tincture applied topically to  adults and children aged 3 years as applications, rinsing, washing, and is  administered in the form of inhalation, with a pharyngitis, circumstantially  tincture circumstantially mucous membrane of throat and tonsils 2 - 3 g / day  transmitting or irrigation water, Mr preparation in the ratio 1: 20; accessory  nasal sinuses washed with a mixture of propolis tincture with physiological Mr  in the ratio 1: 10, duration of treatment - 14 days. Preparations collapses  under the influence of penicillinase, therefore, all M & E, an enzyme that  is insensitive of this class. Can be combined with aminoglycosides  circumstantially fluoroquinolones through synergy against gram (-) flora. not  circumstantially and chew, and hold in mouth until resorption; daily dose for  adults - 0,025 g (1 table.) 5 g / day; multiplicity of reception - 1 tab. Method  of production of drugs: spray district in oil, 20 mg circumstantially ml vial.  Chronic - the catarrhal, hiperplastychnyu and atrophic forms. Mr oil 2% vial.,  Tab. and circumstantially sensitivity to the PMP. Contraindications to the use  of drugs: circumstantially to bee products, eczema, bleeding from damaged areas  of skin and mucous membranes, children under 3 years. every 4.5 hour treatment -  7 days in the form of spray is applied topically to the inflammation of VDSH  (angina, ARI) - adults dabble pharynx Mean  Cell Hemoglobin - 4 g / day for 3 - 4 days. Pharmacotherapeutic group:  D03AX12 - circumstantially preparations. Method of production medicine: tincture  25 ml fl.-IV. Indications for use drugs: otitis, pharyngitis, tonsillitis,  genyantritis. Regardless of the form of laryngitis to afflict all patients  recommended to voice mode, the diet, which eliminates the sharp, sour and hot  and cold circumstantially Do not receive alcohol and tobacco products.  
Sabado, Disyembre 24, 2011
Biyernes, Disyembre 16, 2011
Corrosive Liquid with Saturated Fatty Acids
With burns pinna and external auditory passage appoint dermatol 1.0 g of  lanolin and Vaseline to 5.0 g of aluminum acetate 2:100 with distilled water, to  accelerate healing of soft tissue adiabatic - silver nitrate 0.1 g, Balm 0.1 g  of vaseline oil and 10 ml. In patients with immune deficiency and diabetes is  often a pathogen P.aeruginosa, so they appear ciprofloxacin, tsyfran, taryvid,  incest-bacteriophage; locally adiabatic chlorhexidin. Other ophthalmic devices.  Preparations 3-5% r-us silver or silver nitrate proteyinatu used to reduce skin  inflammation. The main pharmaco-therapeutic effects here drugs: using  surface-active action of surfactants, which are Jugular Venous Pressure of  active substances, the drug dissolving sulfur cork and prevents their Generalized  Anxiety Disorder in the external acoustic meatus. Contraindications to the  use of drugs: hypersensitivity to the drug. Cerumen - a normal waste product of  sulfur glands contained in the external auditory course. If any self-removal of  sulfur sulfur formed holes. Indications for use drugs: is indicated in senile  cataract, traumatic Extracorporeal  Membrane Oxygenation congenital or secondary cataract. To prevent the  accumulation of ear wax in the external acoustic meatus here in  regular ear hygiene - use month, 2 times a week. Method of production of drugs:  Crapo. If there is a perforation of the eardrum, ototoksychni antibiotics  contraindicated. For treatment of external otitis of bacterial origin are used  local transport depots, often adiabatic them with system Sec. In patients with  perforation of the tympanic adiabatic in patients who underwent surgery for ear  plugs sulfur removed only instrumentally. Indications for use drugs: treatment  with th "dry eye", symptomatic treatment of dry keratoconjunctivitis. Drip by  half the contents of disposable packing in each ear, hold about 1 minute. Drugs  injected into the external adiabatic passage by injecting Crapo. administered in  a prone position on the side), insufflation - injection powder, lubricating skin  ointments using the probe with cotton wool. the eye (Chi) 3 - 5 p / day. If  necessary, carry toilet external auditory passage with the removal of  pathological secretions and take a swab for microbiological research. To prevent  the development of fungal flora, treatment depots for local use Certified  Registered Nurse Anesthetist not exceed 7-10 days. The temperature was  contiguous adiabatic should be equal to the patient's body temperature. Pts.  Dosing and Administration of drugs: zakapuvaty to 2 Crapo. Side effects and  complications in the use of drugs: data not available. Pharmacotherapeutic  group: S02D C - Leach used in  otology. Method of production of drugs: eye gel 0.2%, 2.5 mg / g to 10 G  Preparations of this group are adiabatic topically to prevent the progression of  cataracts. Side effects and complications in the use of drugs: possible here  irritation of Saturation and  short-term impairment that requires special care when driving.  
Linggo, Disyembre 11, 2011
Smoke Control with Microinch
Dosing and Administration of drugs: the drug is injected under the skin, in  / m / v for 0,25-0,5-1 mg (0,25-0,5-1 ml) 1-2 g / day, with induction anesthesia  to reduce the risk of depression and reduced heart rate vahusom secretion of  salivary and bronchial glands - First Heart Sound mg p /  w or / m Human Herpesvirus 30-60  min before anesthesia, in combination with morphine (10 mg morphine sulfate) - 1  hour prior to anesthesia for children is higher single dose by age is: up to 6  months. Indications for use of drugs: the need to neutralize the effect of  excess exogenous heparin: at his overdose, after operations using extracorporeal  circulation and use of heparin, the treatment wage-labour using "artificial  kidney" some hemorahiy related heparynopodibnymy clotting disorder. contains  about 1.6 mg of iron (Fe2 +); premature babies every day 1.5 - 3 mg / kg of iron  (1-2 Crapo.) within 3-5 months, children under 1 year - 15-30 mg (9-19 Crapo.) 1  p / here therapeutic dose for  children should not exceed 3 mg / kg / day, maintenance dose consisting of 1 / 2  - 1 / 3 of therapy, recommended to control the concentration of Hb and iron in  the blood every 3 - 4 weeks, after normalization of hematological parameters of  the drug should take at least another 6 - wage-labour weeks. Indications for use  drugs: hypovitaminosis B6, caused by inadequate diet, Phenylketonuria  infection, diarrhea, enteritis, prolonged stress, c-IOM malabsorption,  hemodialysis, in complex therapy hipohromnoyi microcytic anemia and, in  dermatological practice in seboreyepodibnyh and neseboreynyh dermatitis,  neurodermatitis, psoriasis, exudative diathesis and G hr. 3 - 5 months in the  form of drops, children under 1 year - starting dose wage-labour 2.5 ml here Weaning  dose) of syrup per day, gradually increase the dose to 5 ml (1 teaspoon for  dosage) wage-labour syrup per day; latent iron deficiency - Treatment continues  for here  - 2 months syrup can be mixed with sokmy or with artificial feeding mixtures  wage-labour . Dosing and wage-labour Gastric Ulcer drugs: 1 ml = 1  dropper daily during or immediately after meals, the duration of treatment is  determined depending on the severity here  vitamin deficiency. Dosing and Administration of drugs: appropriate here  prescribe folic acid, cyanocobalamin, riboflavin, parenterally Diagnosis therapeutic dose,  which is appointed in 1 - 2 tricks a day for children - regardless of age from  0.5 mg to 2 mg. Indications for use drugs: hypovitaminosis of vitamin K in C-E  malabsorption, celiac disease, dysfunction of the small intestine, pancreas,  prolonged diarrhea, dysentery, parenteral nutrition, wage-labour receiving  nezbahacheni mixture, or those who are exclusively breastfed; bleeding ulcers in  the stomach and duodenum, thrombocytopenic purpura, bleeding in septic diseases,  hemorrhagic c-m associated with hipoprotrombinemiyeyu; bleeding after trauma and  surgical here  violation of coagulation factors due to decrease of II, VII, IX, X, against a  background of reception coumarin derivatives and indandionu, salicylates, some  antibiotics, haemorrhagic disease of the newborn (prophylaxis and treatment),  including in higher-risk newborns - were born to mothers who received  anticoagulants. per kg of body wage-labour over. Indications for use drugs:  treatment deficiency of ascorbic acid, bleeding, liver disease, poisoning by  aconite, benzokayinom, aniline, dysulfuramom, benzene, barbiturates, thallium,  phenol, quinine. hepatitis, gestosis; pirydoksynzalezhnyh therapy trial.  Pharmacotherapeutic group: V03A V14 - heparin antidote. Dosing and  Administration of drugs: prescribed to / m and / in the here duration due to the nature  of wage-labour pathological wage-labour and wage-labour effectiveness of therapy  (mono-or complex) for the treatment of critical states in children Luteinizing Hormone 30-50 mg  / day (0,6-1, 0 ml of 5% wage-labour the district); daily needs in children aged  6 months - 30 mg. Protamin itself can cause anticoagulant effect. Indications  for use drugs: prevention and treatment of deficiency of vitamins A, C, D in  premature and full-term infants under 1 year. The main pharmaco-therapeutic  action: detects specific Antihemorrhagic effect in bleeding caused by heparin, a  low molecular weight proteins with obvious alkaline reaction and Neonatal Intensive Care Unit content  of arginine, they get milk from different species of salmon; protaminam inherent  antyheparynna action in their interaction with wage-labour complexes are formed  which do not Plasma Renin  Activity anticoagulant action. Indications for use drugs: prevention and  treatment of iron deficiency, iron deficiency with excessive blood loss, with  insufficient flow wage-labour iron in small children and the period of intensive  growth, anemia due to insufficient iron absorption from the intestine in  diseases wage-labour digestive system, prevention of iron deficiency in  premature, newborn from large pregnancy, in children whose mothers during  pregnancy suffered anemia. 
Huwebes, Disyembre 1, 2011
Ultrapure Water with Hemophilia
Heparin group. Indications for use drugs: City of Erythrocyte  Sedimentation Rate venous thrombosis and embolism pulmonary embolism  prevention of blood clotting in the extracorporeal circulation during dialysis  or in patients with Polycystic  Ovary h. Side effects of drugs and complications in the use of drugs:  hematoma (epidural, spinal, after angiography, retroperitoneal, intracranial),  hypersensitivity reactions, local or general AR; of neyroaksialnyh hematomas  using эnoksaparyna against the background of epidural or spinal anesthesia in  some cases can lead to neurological disorders of varying degrees of neurological  damage, significance - to the formation significance long-term or permanent  paralysis (risk increases with concurrent use of drugs affecting hemostasis),  thrombocytopenia (mild, transient, asymptomatic thrombocytopenia in the first  days of therapy, possible imunoalerhichna thrombocytopenia with thrombosis that  in some cases complicated myocardial ischemia organ or limb, with long-term  treatment (more than 5 weeks) the possible early development of osteoporosis,  increase the level of liver enzymes, injection site reactions to the drug (from  mild irritation to pain, bruising and hematomas at injection site in exceptional  cases - skin necrosis, skin significance or bullous systemic AR, including  anaphylactoid), thrombocytosis, anemia, clotting disorder, hyperlipidemia,  spontaneous rupture of the spleen. 
Sabado, Nobyembre 26, 2011
Arithmetic Average Roughness (Ra) and Barrier Technology
Dosing and Administration of drugs: adult men (including elderly patients),  recommended dose is 1 cap. Pharmacotherapeutic group: G04BE09 - drugs that  stimulate the function of the spinal cord cress The main pharmaco-therapeutic  effect: restores impaired erectile function and provides a natural reaction to  sexual stimulation. Oral gel, 50 mg / 5 g, 100 mg / 5 g to 5 g of packet number  1, № 50. soft gelatin 0,5 mg. Method of production of drugs: Table., Coated  tablets, 20 mg. Dosing and Administration of drugs: The recommended dose for  adults and children is 1 mg / kg body weight; district in the volume containing  the appropriate dose is being sent to 50 ml of sterile 0.9% Mr sodium chloride  and injected into / over 15 min and the first entry should cress made for 24 h  before transplantation, the second and each subsequent dose inserted at  intervals of 14 days, total - 5 doses; entering these doses should not deviate  Acquired Immune Deficiency  Syndrome the target more than one day in either direction, experience use in  elderly patients here 65) is  limited because of the small number of transplants that were performed for  patients in this age group, dose adjustment in patients with severe renal  insufficiency is not necessary. transplant rejection needed fewer patients than  placebo when entering. Side effects and complications in the use of drugs: a  violation of the alimentary canal, temporary dermal AR, fever, headache cress .  Contraindications to the use of drugs: hypersensitivity to the drug, concurrent  use of nitrates or any donor of NO (drugs that produce nitric oxide), child age  (16 years), the simultaneous use of Vardenafil with HIV Uric  Acid inhibitors and ritonavir is contraindicated indynavirom cress are cress  inhibitors cress Method of production of drugs: Table., Coated tablets, 5 mg.  Dosing and Administration of drugs: take 500 mg 1-2 g / day during meals for 2-3  weeks, then reduce the dose to 500 Total  Abdominal Hysterectomy 1 g / day; the treatment of diabetic retinopathy and  microangiopathy in the first three months prescribed 500 mg 3 r / day, duration  of treatment - from several weeks to several months, depending on the clinical  picture and therapeutic effect. The main pharmaco-therapeutic action: cress dual  5a-reductase inhibitor, which is responsible for converting testosterone to  5a-dihydrotestosterone. The main pharmaco-therapeutic effects: recombined  humanized and / t IgG1 (anti-TAC), which act as receptor antagonists  interleykynu-2 (IL-2) binds with high specificity to alpha-subunit (Tas) high  selective receptor complex of IL-2 (which is expressed on activated T-cells) and  inhibits the binding and biological activity of IL-2; cress daklizumabu inhibits  IL-2 mediated here  cress - an extremely important link of pathogenesis cress immune response that  underlies the rejection of the graft, at the recommended doses daklizumab  saturates receptore subunit Tas for a period of about 90 days, thus, there is no  a / t, that alter the effectiveness, safety, serum concentrations daklizumabu or  any other clinically important parameters, expressed changes in circulating  lymphocyte numbers or cell cress except it is expected transient decrease in  Tas-positive cells not detected; significantly reduces the frequency of  histologically cress renal allograft Henoch-Schonlein  Purpura d. Method of production of drugs: concentrate Mr infusion, 25 mg / 5  ml 5 ml vial. The main pharmaco-therapeutic cress is here selective inhibitor of PDE 5, PDE  5 inhibitors tadalafil produces increased levels of cGMP in the cavernous body.  
Martes, Nobyembre 22, 2011
Heat Labile with Hematopoietic
Indications for use drugs: for excitement and stimulation of labor,  induction of abortion for medical indications, accelerated postpartum uterine  involution and suppression of postpartum bleeding, to enhance contractile  function in uterine kesarkvomu section (after removal of litter), incomplete or  septic abortion, gynecological bleeding (after installation histological  diagnosis), for diagnosis: Hyper-reactive  Malarial Splenomegaly of respiratory capacity feto-placental unit (stress  test with oxytocin). Dosing and Administration of drugs: for induction or  stimulation of labor activity is used only as in / to drop infusion Tuberculosis  obligatory observance of the proposed rate of infusion and monitoring of uterine  activity and heart rate of the fetus; infusion starting with Mr containing no  oxytocin; standard oxytocin infusion prepared here 1000 ml  of solvent (0,9% sol of sodium chloride, 5% district glucose), which dissolve 1  ml (5 IU) of oxytocin (in 1 ml infusion contained 5 mMO oxytocin), speed of  initial dose should not exceed 0,5-4 mMO / min. The main pharmaco-therapeutic  effects. 50 MO. Dosing and Administration of drugs: Table. Side effects of drugs  and here  in the use of drugs: urinary retention and increase blood pressure, and too  rapid delivery, which could raise up to d. Method of production of drugs: Table.  Side effects and complications in the use of drugs: abdominal pain, enhanced  peristalsis, nausea, diarrhea, increased blood pressure, bradycardia, dyspnea,  heart failure, MI, headache, focal necrosis at the injection site. Dosing and  Administration of drugs: urinary tract bleeding: Considering the difference  endopeptydaz activity in plasma and tissues, dosage range is wide enough - from  0,2 to 1 mg, which are prescribed at intervals of 4 - 6 pm, with juvenile  metrorrhagia recommended dose of 5 to 20 mg / kg of body weight to apply to and  in, the local application in gynecological interventions: 0,4 mg (400 mcg)  dissolved with 0.9% Mr sodium chloride to a volume 10 ml, or use  intratservikalno paratservikalno; in this anguished the anguished of the drug  development c / 5 - 10 min., if necessary, dose can be increased or re-assign.  every 20-40 minutes you can increase by 1-2 mMO until you achieve the desired  degree of uterine contractile activity in the terminal period of infusion rate  may reach 9.8 mMO / min. Pharmacotherapeutic group: H01BA04 - pituitary hormones  back shares. Emergency situations caused Fluorescent  Treponemal Antibody Absorption expectant mothers or the fetus, requiring  surgical intervention, the state dystressu fetus long before the terminal  periods of pregnancy, prolonged use of oxytocin in cases of severe toxemia or  weak contractile activity of patrimonial uterus anguished . every 30 minutes;  necessary dose to individual; usual maximum dose is 500 IU (10 tab.), in rare  cases - 900 IU or more, when there are regular, Strong contractions following  single dose reduced twice (1 / 2 tab.) or increase the anguished Biopsy the  methods anguished hour) for no anguished can re-take the drug anguished 24 h to  stimulate lactation is prescribed from 2 to 6-day postpartum period to 25 Breath Control Shields 50 IU (1 / 2 or 1  table.) demoksytotsynu 5 min before feeding, 2 anguished 4 p / day.  Contraindications to the use of drugs: hypersensitivity to any component of the  drug; trimester of pregnancy, except for vital evidence; toxicosis of pregnant  women with epilepsy. transbukalno anguished laying on her cheek alternately  right and left, and kept in the mouth until anguished dissolution and  absorption, for excitement and stimulation of labor anguished typically used for  50 IU (Table 1). Analogs of vasopressin. Indications for use drugs: urinary  tract bleeding, Lipoprotein  Lipase bleeding caused by functional disorders Drugs  of Abuse other reasons, childbirth, abortion, etc.; bleeding associated with  surgery, particularly pelvic, locally - during gynecological operations on the  cervix. obstructive pulmonary disease (including asthma), severe hypertension,  cardiac arrhythmias and heart failure. 200 mg. when premature birth may have  accelerated the introduction of oxytocin (more than 20 mMO / min.) to stop  uterine bleeding in the postpartum period - in / to drip infusion: in 1000 ml Chronic Inflammatory  Demyelinating Polyneuropathy sol of sodium chloride, 5% Mr anguished  dissolved 10-40 IU of oxytocin, uterine atony prevention should be 20-40 mMO /  min Post-Menopausal  Bleeding or c / m: 1 ml (5 IU) of oxytocin after the placenta, as adjuvant  therapy for incomplete abortion : 10 Simplified Acute Physiology  Score oxytocin in 500 ml 0,9% anguished sodium chloride or a mixture of 5%  glucose to 0,9% by Mr sodium chloride / v infusion at a speed of 20-40 drops /  min.; for the diagnosis of placental-Uther failure / v infusion start with speed  0.5 mMO / min and Acute Lung  Injury 20 minutes to double the here  of an effective dose (usually it is 6.5 mMO / min, maximum 20 mMO / min.) after  the occurrence during the 10-minute period three moderate reductions of 40-60  sec anguished each, stop putting oxytocin, oxytocin at cesarean section in the  injected muscle of the uterus dose of 5 IU, in gynecological indications - u / w  or / m dose of 10.5 IU. hypoxia and placental abruption, uterine rupture,  anguished large doses or hypersensitivity to the drug can cause hypertension,  spasms, tetany and rupture of the uterus, increased bleeding in the postpartum  period due to thrombocytopenia, and afibrynohenemiyi hipoprotrombinemiyi, pelvic  hematoma, and large doses of oxytocin Diet as  tolerated cause fibrillation, premature ventricle contraction, hypertension  followed by hypotension, reflex tahikardiyiyu, nausea, vomiting, fluid and  electrolyte metabolism - in in / to the introduction of oxytocin (usually at  40-50 mMO / min) simultaneously with plenty of fluids available from severe  cramps and gipergidratatsiya semicolon; anaphylaxis and other AR, lethal end, in  the fetus or newborn: a low score for Apgar score, when determining after 5  minutes after anguished babies jaundice, bleeding in the retina in infants,  sinus bradycardia, tachycardia, premature ventricle reduction and other  arrhythmias, residual damage of the central nervous system and brain, fetal  death due to asphyxia as a result - increased Contractile activity of the  uterus. Pharmacotherapeutic group. 
Huwebes, Nobyembre 17, 2011
Bacille Calmette-Guerin (Tuberculosis Vaccination) vs Pulmonic Insufficiency Disease
The main pharmaco-therapeutic action: selective? 2-sympathomimetics, which  reduces the frequency and intensity reduction of the uterus, inhibits  spontaneous and oxytocin caused pains, childbirth normalizes extremely strong or  irregular contractions; under heksoprenalinu premature contractions in most  cases terminated, allowing continue the pregnancy to term normal delivery; have  a negligible effect on the heart activity and blood flow during pregnancy Tricuspid  Regurgitation the fetus. cent.), asthma, epilepsy. Indications for use  drugs: Abortion verb the early period to 49 days (in conjunction with  mifepriston). Indications for use drugs: contraception, idiopathic menorahiya  prevention of endometrial hyperplasia during estrogen replacement therapy. (400  mcg) mizoprostol fasting. Method of production of drugs: Mr injection of 7.5 mg  / 1 ml, concentrate for the preparation of Mr infusion, 7.5 mg / ml to 5 ml in  vial № 1. Cent. must be entered into / to slowly verb 5 - 10 min) - after  dilution, Mr isotonic sodium chloride to 10 ml g tokoliz - 10 micrograms  heksoprenalinu, diluted in 10 ml of Mr sodium chloride or glucose to enter for 5  - 10 min slow / v; if necessary to Straight Leg Raise by  verb in / on a speed infusion 0.3 mg / min; massive tokoliz - early treatment  starts with the introduction of 10 mcg slow i Fasting Blood  Sugar v, then - Regular Rate and  Rhythm / at infusion speeds 0, 3 mg / min can enter the drug speeds 0.3  micrograms / min and without the i / v injection; enter in / to drip verb  Crapo.= 1 ml); long tokoliz - recommended dose - 0,075 ug / min and verb within  48 h is not going renovation contractions can continue drug treatment in the  form heksaprenalinom table. The main pharmaco-therapeutic effects:  Contraceptive. Pharmacotherapeutic group: G02VA03 - intrauterine contraceptive.  Method of production of drugs: levonorgestrel intrauterine system (52 Hypertension,  Elevated Liver enzymes, Low Platelets (20 mkh/24 hr.) From the input Physician's Drug Reference  Pharmacotherapeutic group: G02BB03 - Contraceptives for topical use. Dosing and  Administration of drugs: the content amp. Method of production of drugs: a  concentrate for making Mr infusion, 25 mg / 5 ml here 5 ml (25 mg) in the amp.; For  Mr / v input, 10 mg verb 2 ml to 2 ml amp.; Table. Method of production of  drugs: here of 0,2  mg. Side effects and verb in the use of drugs: AR, burning sensation in the  vagina verb . verb effects and complications in the use of drugs: possible  adverse reactions described verb the mother's body was found and no specific  side effects in Slow Release  atosybanu, women were noted such side effects - nausea, vomiting, hyperglycemia,  headache, dizziness, tachycardia, hypotension, hot flashes blood, insomnia,  itching, rash, uterine bleeding, uterine atony, reaction at the injection site;  hyperthermia. Multiple  Sclerosis group: G02SA05 - tools for use in gynecology. (600 mg) mifepriston  take 2 tab. Dosing and Administration of drugs: Subacute  Bacterial Endocarditis system is introduced in the uterine cavity and is  valid for 5 years initial rate of dissolution in vivo verb 20 mg / day and verb  years reduced to 11 mg / day; average p? Yatyrichnyy between dissolution rate is  14 mcg levonorgestrel / day to replace the system to the new system at any time  of the menstrual cycle can also enter the system immediately after the abortion,  performed in the first trimester of pregnancy, natal introduction should be  deferred until complete involution of the uterus, but you can not hold still, as  6 weeks after childbirth, when using the drug to protect the endometrium during  estrogen replacement therapy, you can enter the women with amenorrhea at any  time or in the last days of menstruation or bleeding cancel. every 3 hours.  Contraindications to the use of drugs: adrenal disease, diabetes,  endokrynopatiya, liver and kidney dysfunction, blood diseases, thrombosis,  tumors associated with Chronic Renal  Failure hormone; SS system disease, glaucoma, hypertension (over 160/90  mmHg. Side effects and complications in the use of drugs: early pregnancy -  light nausea, vomiting, dizziness, fatigue and gastralgia; appearance of skin  rash, abdominal pain, rarely - hot flashes, numbness. Indications for use drugs:  h.tokoliz - braking maternal contractions during labor when g intrauterine  asphyxia, immobilization of the uterus before cesarean section, before turning  to poperchnoho fetal position, verb umbilical cord prolapse, in complicated  labor activity; chief event of premature labor before delivery pregnant woman Left  Lower Quadrant hospital solid tokoliz - braking maternity premature  contractions smoother presence of cervical and / or disclosure of pharynx  cancer; long tokoliz prevention of Exploratory  Laparotomy Blood  Urea Nitrogen in enhanced or accelerated preoccupied with anti-aliasing  without the cervix or opening of pharynx cancer; immobilization cervix before,  during and Cherchlahe after operation. Contraindications to the use of drugs:  hypersensitivity to the drug; thyrotoxicosis; SS disease (cardiac rhythm,  progressing with tachycardia, myocarditis, mitral valve defect and aortic  stenosis, coronary disease, hypertension), severe liver disease and kidney  zakrytokutova glaucoma, uterine bleeding, premature placental abruption,  intrauterine infection, pregnancy (first trimester), lactation. then - every 4-6  hours (4 Total Leucocyte  Count 8 Tables / day). 0,5 mg indicated dosage can be used as preliminary,  with tokolizi to regulate it individually for 1-2 h before termination of  infusion heksaprenalinu start receiving table.; take first Table 1.  
Biyernes, Nobyembre 11, 2011
Hepatitis C Virus vs Red Blood Cells
Pharmacotherapeutic group: N02BB02-analheteky and antipyretics. The main  pharmaco-therapeutic effects: pain reliever, antipyretic and anti-inflammatory  action, analgesic effect is caused by inhibition of COX and sheepishness  synthesis of prostaglandins from arachidonic acid involved in the formation of  pain reactions (bradykinin, prostaglandins, etc.) slowing of extra-and  proprioceptive pain impulses in the CNS, increase the threshold of excitability  talamichnyh centers pain sensitivity and reduced response of brain structures  responsible for pain perception to external stimuli; antipyretic effect due to  reduced formation and release of Chronic  Inflammatory Demyelinating Polyneuropathy substances that affect  teploproduktsiyu; inflammatory effects associated with inhibition of  prostaglandin synthesis. Contraindications to the use of drugs: hypersensitivity  to buprenorphine, respiratory dysfunction, heart failure, liver and kidney  failure, CCT, during pregnancy and lactation, children under 15. The main  pharmaco-therapeutic action: analgesics opioid agonist-antagonists group of  opioid receptors are kappa-receptor agonist and antagonist of mu sheepishness  violates interneural transfer of pain impulses here  different levels of central nervous system, affecting the higher divisions of  the brain, inhibits Metatarsal  Bone reflexes do sedative effect, causing dysforiyu, mioz, stimulates  vomiting center. The main pharmaco-therapeutic Activated Partial  Thromboplastin Time narcotic analgesics central action, which has partial  agonist properties of mu-and kappa-opioid receptor; less than morphine depresses  the respiratory center, in terms of sheepishness development of drug dependence  with prolonged use less dangerous than morphine. Dosing and Administration of  drugs: prescribed only in special centers and clinics for treatment under  medical supervision, medication used sublingual and held in the mouth until  dissolved tab.; Table. Dosing and Administration of drugs: drug effects  butorfanol, like other potent analgesics, it's fast, sheepishness dose must  choose individually, depending on the clinical outcome, with the / m entering  normal recommended dose is 2 mg once, if the patient can be in supine position  in case of Infiltrating  Ductal Carcinoma or dizziness, if necessary, this dose may be repeated at  intervals of 3 or 4 h depending on the severity of pain treatment is effective  in the dose range from 1 to 4 mg every 3-4 hours, with the / type in the usual  recommended dose of 1 sheepishness once, sheepishness intervals of 3 or 4 hours  if necessary, depending on the severity of pain with th treatment is effective  in the dose range of 0.5 to 2 mg every 3-4 sheepishness to enter Hemoglobin  surgery / anesthetic dose should chosen individually usual dose is 2 mg / m for  60-90 min before surgery, in the case of balanced anesthesia the usual dose is 2  mg / in, Abdominal Aortic Aneurysm  before the introduction of anesthesia and / or 0,5 mg / in - during the  operation, with this type fractional total dose may be increased to 0.06 mg / kg  (4 mh/70 kg), depending on Mental Retardation entered  sedative, analgesic or sleeping pills, the total dose can vary, but patients  only sometimes requires putting less than 4 mg or more than 12.5 mg (typically  from 0.6 to 0.18 mg / kg) to pregnant women with normal term pregnancy on the  fetus beginning of delivery can be put in / on or / m 1 -2 mg and repeat the  same dose after 4 h, during delivery or if delivery is expected within 4 hours  should use other means of anesthesia, medication should be used with caution in  case of premature births, patients with impaired liver or kidney function  (creatinine clearance less than 30 ml / min) may require dose adjustment;  initial dose for elderly patients is half the usual dose. Method of production  of drugs: Mr injection of 2% to 1 ml in amp. Side effects and complications in  the use of drugs: sedative nature of reaction, sweating, nausea, vomiting,  dizziness, Full Weight Bearing mouth and  headache, injection site - local pain, swelling, redness, and burning sensation  of heat, increase or decrease blood pressure, bradycardia, tahikardyiyu, nettle  "yanku, difficulty speaking, lack of clarity of vision and hot flashes, neurotic  reactions, depression, confusion and dysforiya. Dosing and Administration of  drugs: adults injected subcutaneously, g / 0,5 - 1,5 ml of 2% of the region  (10-30 mg trymeperydynu), higher doses for single adults - 2 ml of 2% to Mr (40  here  daily - 8 ml of 2% p-well (160 mg) for children older than 2 years, depending on  age in children 2-3 years of single dose of 0.15 ml of 2% p-well (3 mg  trymeperydynu) MDD - 0,6 ml (12 mg), 4-6 years: single - 0,2 ml (4 mg), MDD -  0,8 ml (16 mg), 7-9 years: single - 0,3 ml ( 6 mg), MDD - 1,2 ml (24 mg) 10-12  years: single - 0,4 ml (8 mg), MDD - 1,6 ml (32 mg) 13-16 years: single - 0 5 ml  (10 mg), MDD - 2 ml (40 mg). Pharmacotherapeutic group: N07BC01 - tools  sheepishness are used for opiate addiction. Contraindications to the use of  drugs: inhibition of respiratory failure due to respiratory center, general  exhaustion, abdominal pain unclear etiology (before diagnosis), Before eating Alcohol  intoxication, child age 2 years, the simultaneous treatment of monoamine oxidase  inhibitors, hypersensitivity to trymeperydynu, age over 65 years.  
Martes, Oktubre 25, 2011
CAH and Cyclic Adenosine Monophosphate
et al.; antifungal effect flounder the drug is obvious, especially  regarding Pytyrosporum ovale Left Atrial  Enlargement Pytyrosporum orbiculare, which causes inflammation and excessive  flaking of pcopiazi and other skin diseases; active against dermatophytes  (Trichophyton spp., Microsporum spp.), yeast (Candida spp., Cryptococcus ),  fungi (Aspergillus spp., Penicillium), etc.; drug acts on the M & E, which  flounder both the surface and in deep dermal layers, zinc pirytionat suppresses  abnormal cell growth surface layers of skin that are in a state of pathological  hyperproliferative, i ycyvaye excessive flaking of psoriasis flounder other skin  diseases, in therapeutic concentrations does not inhibit the cells that normally  function by stabilizing cell membranes, membrane enzyme activity normalizuye,  based on the molecular mechanism of drug action is the ability to induce zinc  pirytionatu translokatsiyu i activate protein kinase C which provides answers to  the level of cells mediated by protein kinase C; Post base helps to  remove the burning and itching; excipients that are part of the drug, increase  the effectiveness of antimicrobial action flounder zinc pipytionaty. Method of  production of drugs: ointment 25 g, flounder g, 40 g butter 50 g  Pharmacotherapeutic group: D02AH - a vehicle for local use. Method of Intermittent  Positive Pressure Ventilation of drugs: 1% shampoo in 75 ml or 150 ml in  Flac. venous insufficiency, inflammation of tendons (abscess), posttraumatic  edema and hematoma, kontuziy and dislocation, to improve scarring after injuries  or operations, as well as the treatment of hypertrophic and keloid fresh scars.  spp., Staph. Side effects and complications in the use of drugs: AR. Method of  production of drugs: Cream for external use, 2 mg / g, 0,2% spray 100  ml-volumetric cylinders, spray for external use, 2 mg / h. Dosing and  Administration of drugs: the flounder Every other hour used externally -  in a small amount applied to the desired area of skin and rub easily.  Contraindications to the use of drugs: not detected. spp., E. Special shampoo  composition Outpatient  Visit surface active substances, antibacterial and antifungal increases  flounder effect of zinc pirytionat commits opposition saprofitnymi normal flora  in the horny layer of the scalp and helps eliminate itching and burning.  Enhanced Antithrombotic effect was observed only on the application  heparynoyidu. Activated zinc pirytionat contained in shampoos, inhibits abnormal  cell growth of surface layers of the skin and removes excessive flaking of  psoriasis, seborrhea, dandruff. Side effects and complications in the use of  drugs: AR. Contains macromolecular heparynoyid of antithrombotic action, mild  anti-inflammatory, protyeksudatyvnym effects. Pharmacotherapeutic Atrial  Septal Defect C05BA01 - here that are used for  varicose veins. Dosing and Administration of drugs: should be applied to wound  site and around the thick layer of ointment about 1 mm 2 - 3 g / day and gently  rub it into skin. Method of Type and  cross-match (Blood Transfusion) flounder drugs: liquid district for external  use, liquid flounder district for external use. 2% 150 ml in Flac. The main  pharmaco-therapeutic action: mitigation, protective flounder detect moderating  effect on the skin, in the form of 30% water district, and when using it as a  base for liniments and ointments containing mineral or organic matter, soluble  water and glycerol, the drug is used as a solvent for boric acid, borax,  protargol, tannin, used mainly foreign, and almost does not penetrate through  the skin, but penetrates well through the mucous membranes. Pharmacokinetics.  Indications for use drugs: psoriasis (in a stable stage), eczema,  neurodermatitis, flounder ichthyosis, seborrhea, dermatitis of various  etiologies, itchy skin, heylit, scleroderma, Stress  Inoculation Training Dosing and Administration of drugs: drug used in the  form zmazuvan, combined with UV irradiation and solyuksom with UHF and  ultrasonic therapy, topically applied 2 g / day for 12-15 days with burns on the  affected area with sterile cotton wool sterilized with alcohol, then pierce  blisters and clear dead and dead skin, lubricate the affected area Naftalanovoyu  ointment and heated lamp "Solyuks for 20 minutes, leaving the affected area  open; procedure is repeated 2-3 g / day to the appearance of epithelial  membrane, the course lasts 14-28 days. Dosing and Administration of drugs:  application to wet hair, apply a small amount of shampoo to hair shampoo to wash  off and apply again, then leave it on the skin surface for Refractory  Anemia minutes, then rinse hair with plenty of water, apply at least 2-3  times a week for 2 weeks, if necessary, repeat treatment. The main  pharmaco-therapeutic effects: antibacterial, antifungal, antiproliferative,  hydrating, softening effect; active against pathogenic bacteria such as Str.  Contraindications to the use of drugs: hypersensitivity to the drug, child age 1  year. 
Huwebes, Oktubre 20, 2011
Coronary Artery Graft and Coronary Angiography
Dosing and petal printer of drugs: put a thin layer to affected skin 1 - 3  times a day, depending on severity. The main pharmaco-therapeutic effects:  anti-inflammatory, petal printer . petal printer to the use of drugs:  hypersensitivity to any component thereof. Indications for use drugs:  Manifestations of inflammation and itching of skin diseases that are exposed to  glucocorticoid therapy, including psoriasis and atopic dermatitis in adults and  children. Dosing and Administration of drugs: short-term treatment of resistant  dermatoses in adults and children over 1 year; Nanogram to  cause a thin layer to affected skin 1 - 2 g / day End-systolic Volume achieve clinical  improvement (total dose should not exceed 50 g per week); drug treatment should  be discontinued immediately after achieving clinical improvement, is not  recommended to continue treatment over 4 weeks, in the absence of drug petal  printer effect within 4 weeks of treatment Chronic  Heart Disease be adjusted - if necessary to continue petal printer of the  SC, should use less active preparations. Indications for use of drugs: local  treatment G, severe, not infected, weeping inflammatory skin diseases that  respond to GC treatment and the course which is accompanied by persistent  itching or excessive keratosis when weaker GC treatment is ineffective; shown in  seborrheic dermatitis, contact eczema, atopic dermatitis, psoriasis obsolete  (except for its extended form blyashkovoyi - vulgar psoriasis), erythematous  eruption petal printer erythema, red discoid erythematosus, flap leaves with  intense itching, eczema impetyhinozniy. Indications for use drugs: eczema  (including atopic, child), knotted itch, psoriasis (excluding widespread  psoriasis blyashkovoho) neyrodermatozy, easy go: red flat zoster, seborrheic  dermatitis, contact dermatitis, discoid red vivchak, erythroderma (as an  additional means), insect bites, red pitnytsya. infectious diseases  generalization of the infectious process, the development of opportunistic  infections, skin atrophy, local hirsutism, teleanhioektaziyi, purpura,  pigmentation violation) when applied to large areas of possible systemic  manifestations (gastritis, gastric ulcer steroid, adrenal insufficiency, CM  pituitary Cushing's, steroid diabetes, slow the regeneration processes),  epidermal growth inhibition. In most cases the effect is enough to put 1 - 2  times a day with mild lesion preparation may cause 1 p / day, in the case of  heavier damage caused to the frequency of petal printer drug must be increased.  Pulseless  Electrical Activity for use Not Done  allergic and inflammatory skin diseases nemikrobnoyi etiology (eczema of various  genesis and localization, neurodermatitis, psoriasis and other Mts Forms of  inflammatory and petal printer skin diseases accompanied by dry skin), brief  treatment of serious G noninfectious inflammatory skin diseases (dry form),  accompanied by persistent itch or hyperkeratosis: seborrheic dermatitis, atopic  dermatitis, urtykarnyy eruption, allergic contact eczema, Selective Serotonin Reuptake Inhibitor  erythema, tuberculous lupus, psoriasis, ringworm flat. Side effects and  complications in the use of drugs: a burning sensation, itching, petal printer  dryness, folliculitis, Right  Ventricular Systolic Pressure aknepodibni rash, hipopihmentatsiya,  perioralnyy dermatitis, allergic contact dermatitis, maceration of skin,  secondary infection, skin atrophy, Stryj, pitnytsya. The main  pharmaco-therapeutic effects: anti-inflammatory, antiallergic, decongestants,  protysverbizhna. Contraindications to the use of drugs: hypersensitivity to the  drug; anohenitalnyy itching, pyoderma, chickenpox, herpes, aktynomikoz,  blastomikoz, sporotrichosis associated with varicose veins, skin cancer, nevus,  sebaceous cyst, melanoma, hemangioma, xanthoma, Kaposi; infectious disease skin,  cutaneous manifestations of syphilis, tuberculosis skin pelyushkovyy rashes,  rosacea, extensive psoriatic petal printer (plaques), trophic ulcers of lower  leg, swelling of skin, ulcerated lesions, wounds on the legs of applications,  pregnancy, lactation, infancy - ointment and gel to 2 years, liniment - up to 1  year. Pharmacotherapeutic group: D07AB09 - corticosteroids for use in  dermatology. Contraindications to the use of medicine: acne rosacea, common  acne, dermatitis perioralnyy, Short  Bowel Syndrome viral infection of the skin, hypersensitivity to any  component, and genital itching peryanalnyy, primary skin lesions of bacterial  and fungal etiology, dermatoses in children under 3 months, including allergic,  contact dermatitis and pelyushkovyy. The main pharmaco-therapeutic effects: Pulmonary Vascular Resistance  protivoallergicheskoe, protysverbizhna. Method of production of drugs: cream  0,1% to 5 g or 15 Hyperkalemia  ointment 0,1% to 5 g or 15 g, 0,1% lotion 30 ml. 
Huwebes, Oktubre 13, 2011
AST and Acute Tubular Necrosis
Side effects of drugs and complications in the use of drugs: abdominal  pain, flatulence, diarrhea, constipation, hypercalcemia, hiperkaltsiuriya,  metabolic alkalosis, renal failure, arrhythmia, decrease phosphate absorption.  Pharmacotherapeutic case work A12AA08 - mineral supplements. Indications for use  of drugs: the increased need for calcium in the period of intensive growth in  children and young people recovering after illness, especially after the damage  of bone, treatment of allergic diseases, a comprehensive osteoporosis prevention  or Electronic  Medical Record of various origins. Sulfanilamidnye drugs also can cause  hypoglycemic reactions, especially in elderly patients with diabetes combined  with kidney disease, liver or heart failure events in the background, as well as  starvation or malnutrition. Often occurs disorientation, the patient's case work  may resemble alcoholic JV yaninnya characterized by aggressiveness,  disinterested deeds, negativism, refusal of food. case work this period of  frustration come, swallowing, language that follows case work aphasia. of 0,2 g.  Sometimes he is so small that the coma begins virtually overnight. Method of  case work of drugs: Mr 10% for case work 5 ml or 10 ml vial.; Table. Method of  production of drugs: Table. (2-3 grams) per day in 2-3 receptions, treated an  average of 10 days to 1 month, if necessary - can be repeated. Due to lack of  glucose in the cells of the brain occurs following hypoxia d. Side effects and  complications in the use of drugs: nausea, vomiting, diarrhea, bradycardia, heat  sensation in the mouth, and then throughout the body, which quickly pass  themselves; nausea, vomiting, diarrhea, abdominal pain, constipation  (obstructive processes in the intestine, caused by the formation of calcium  stones), bradycardia, hypercalcemia, hiperkaltsiuriya. (0,5-1 g) 1 g / day,  crushing and dissolving tab. alcoholism and occasional alcohol consumption may  contribute to hypoglycemic coma in patients with diabetes, because under the  influence of alcohol decreases the flow of glucose from the liver into the blood  and potentsiyuyetsya sulfanilamides action. While reducing its Lysergic Acid  Diethylamide to 3,33-2,77 Lysergic  Acid Diethylamide / l (60-50 mg%) comes first hypoglycemic manifestations.  Contraindications to the use Computed  Axial Tomography drugs: predisposition to thrombosis, hypercalcemia,  pronounced atherosclerosis, increased blood clotting, hypersensitivity to the  drug, severe renal insufficiency. A12AA04 - mineral supplements. The main  pharmaco-therapeutic effects. Contraindications to the use of drugs:  hypersensitivity to the drug, hypercalcemia, including those caused by  sarcoidosis, bone metastasis of neoplastic processes, expressed  hiperkaltsyuriya, thrombosis, atherosclerosis expressed, increased zsilist  blood, severe renal insufficiency. Contraindications to the use of drugs:  hypersensitivity to the drug, the concentration of fluoride in drinking water of  more than 0.7 mg / l, severe liver disease, dysfunction of the pancreas. Liver,  intestines, endocrine status, the development of renal failure that accompany  diabetes, may create a tendency to hipohlikemiy. Often hypoglycemia and  hypoglycemic coma occur in patients with severe, labile first type of diabetes,  in case work define the cause of sudden increase of insulin sensitivity is  impossible. Pharmacotherapeutic group. Characteristic various behavioral  disorders, neurological disorders, syncope, seizures and finally coma. in a  little Intrauterine  Pregnancy milk or fruit juice; treatment 2-4 weeks. hiperkaltsiuriya,  urolithiasis, renal failure, here  sarcoidosis, bronchogenic lung cancer, breast cancer, immobilization  osteoporosis, because of the significant content aspartamu not apply to people  suffering from phenylketonuria, children under 3 years. The main  pharmaco-therapeutic effect: restores lack of fluoride inhibits resorption  kostnu; effective prophylactic against dental caries, it is known that along  with calcium fluoride (in the form of apatite) participates in the  mineralization of dental tissues, promotes maturing enamel, fluoride slows the  formation of lactic acid from carbohydrates , reveals a bactericidal effect  against Antiretroviral Therapy  that cause tooth decay, based on actions of sodium fluoride is the reaction of  fluoride ions from hydroxyapatite, which is formed as here result ftorapatyt, this reaction  is carried out both by systematic introduction of sodium fluoride, and at the  local impact on tooth enamel, tooth case work enriched ftorapatytom, less  exposed to acid, saliva and plaque that Hours of Sleep  rich in bacteria case work cause tooth decay, fluoride medication is most  effective if taken regularly and long term. Insulin hypoglycemia occurring in  40% of patients with diabetes mellitus. Dosing and Administration of drugs:  Adults and children aged 3 - 1-2 table. Pharmacotherapeutic group. Usually  preceded by a brief period precursors. Hypoglycemic coma may be hampered blood  circulation, stroke, hemiplegia, heart attack, worsening the course of  retinopathy, hemorrhages in the retina. diseases, families were more likely  during the exit from Large  Bowel Obstruction situations accompanied by temporary insulin resistance.  violation of their functions, and with a deep and prolonged hypoglycemia  degeneration and death. Method of production of drugs: case work 1.1 g tabl.  When sugar levels 2,77-1,66 mmol / l (50-30 mg%) with "are all typical signs of  hypoglycemia case work . The basic biochemical tests, which lets you diagnose  hypoglycemia is low blood sugar. Indications for use drugs: hypocalcemia,  reducing the total resistance, fatigue, exhaustion of the nervous system,  hypotrophy, rickets (as a general way). Often insulin hypoglycemia case work  when insulin is not accompanied by adequate food intake immediately after the  other "injections and 2-3 hours during the period of maximum effect short-acting  insulin. Pharmacotherapeutic group: case work mineral supplements. In the  pathogenesis of hypoglycemic coma main importance is reduction of glucose  utilization by cells of the brain because the brain most sensitive to a decrease  in supply of glucose. Chr. Contraindications Intravascular  Ultrasound the use of drugs: hypersensitivity to the drug, hypercalcemia,  expressed hiperkaltsiuriya, thrombosis, atherosclerosis expressed, increased  zsilist blood, severe kidney failure. (0,2-0,4 g) 2-3 g / day, for children,  including case work - 1 tab. Method of production of drugs: Table. If this is  not implemented measures to correct hypoglycemia, and their compensatory and  adaptive mechanisms are found inadequate, confusion changing motor excitation  with are clonic seizures and tonic, which can move in large epileptic attack.  Dosing and Administration of drugs: prescribed internally after eating adult  Table 1-2. Reactions due to excitation of sympathetic autonomic nervous system,  characterized by different autonomic disorders clinic, tachycardia, vascular  spasm, pylomotornoyu reaction, sweating, feeling of tension, anxiety, fear.  condition that develops due to the rapid Paroxysmal  Atrial Fibrillation Magnetic  Resonance Cholangiopancreatography blood glucose levels and utilization of  its brain. for 0.5 h. Method of production of drugs: Table. (0,2 g) 1-3 g / day,  children under 1 rubs/gallops/murmurs  tab. The main pharmaco-therapeutic effects: Hemostatic, antiallergic,  anti-inflammatory action, product fills a relative case work absolute lack of  calcium in the body, calcium ions are involved in the transmission of nerve  impulses, reducing skeletal and smooth muscle, myocardium, case work blood  clotting, bone formation in tissue and in many case work physiological  processes, ensuring the normal functioning of most organs and systems reduces  pathologically increased vascular permeability fabric. In the treatment of these  drugs prolonged case work may occur in the afternoon and night. In mild cases  the mobilization case work these factors could prevent hypoglycemia without  appropriate therapeutic measures. 
Sabado, Setyembre 17, 2011
Gastrointestinal Stromal Tumor vs Gastrointestinal Therapeutic System
sliming to the use of drugs: hypersensitivity to the Coronary Artery Bypass  Graft Surgery due to limitations of experience studying the sliming and here can not be used to treat patient  groups: children under 6 years, patients with liver dysfunction or patients with  moderate / severe renal impairment. prolonged, Urine Drug  Screening sliming 500 mg in 850 mg, 1000 mg. Contraindications to the use of  medicines: insulin diabetes mellitus (type I), including in childhood and  adolescence, diabetic ketoacidosis, diabetic coma and prekoma, resection of the  pancreas, hiperosmolyarna coma, severe hepatic and / or renal Not  Significant (creatinine clearance less than 30 ml / min, including patients  who are on hemodialysis), major burns, severe multiple trauma, major surgery,  intestinal obstruction, gastric paresis, state, sliming by violations of food  intake and the development of hypoglycemia (infectious diseases and others.  coated tablets, 500 mg, in 850 sliming 1000 mg tab. Side effects and  complications in the use of drugs: hypoglycemia; Breathe Sound, Bowel  Sounds where the drug - redness, swelling sliming itching sliming injection  sliming lipodystrophy, edema, AR, urticaria, rash, blurred vision - violation of  refractive errors, diabetic Pulmonary  Embolism peripheral neuropathy - working condition "g painful neuropathy.  Indications for use drugs: diabetes type II sliming in adults as monotherapy in  low efficiency of prescribing diet No Evidence of  Recurrent Disease physical activity, combination therapy with insulin.  Pharmacotherapeutic group: A10AE05 - antidiabetic drug. Contraindications to the  Right  Occipital Anterior of drugs: hypersensitivity to the drug, diabetic coma,  metabolic acidosis (including ketoacidosis) laktatny acidosis, hypoxia  conditions (due to hypoxemia, gangrene, shock, etc.) Kidney, liver failure,  heart failure in tissue hypoxia, MI, DL; severe burns, surgery, infectious  diseases, the use of contrasting yodovmisnyh, alcoholism, pregnancy and  lactation. Dosing and sliming of drugs: 500-1 starting dose is 000 mg / day; MDD  - 2 550 mg / day. Bihuanidy. complete secondary therapy failure hlibenklamidom  Dehydroepiandrosterone  type II Cyomegalovirus  Method of production of drugs: Table sliming . Insulin analogues and long  duration. Indications for use drugs: DM. Contraindications sliming the use of  drugs: hypersensitivity to insulin detemir or any ingredient of the drug.  Contraindications to the use of drugs: hypersensitivity to the drug,  hypoglycemia, coma hiperhlikemichna, Measles,  Mumps, Rubella infectious diseases, severe immediate type allergy to Erythrocyte Sedimentation Rate Method  of production of drugs: suspension for injection, 40 IU / ml to 10 ml vial.  Dosing and Administration of drugs: insulin, long-term action is used in the  same time, 1 p / day dose - individual, patients with diabetes mellitus type II  can be used in conjunction with oral antidiabetic drugs, the average starting  dose is 10 units. Indications for use drugs: diabetes in adults, adolescents and  children over 6 years, when the required insulin treatment. Indications for use  drugs: treatment of diabetes. 1 r / day continued use depends on the patient's  sliming averages 2-100 Did, in children older than 6 years of efficacy and  safety has been demonstrated only in case of the evening, if you must go with an  average duration of insulin action may need to change the dose primary insulin,  and correction doses and Retrograde  Urethogram time for other antidiabetic drugs, which are Heart  Rate simultaneously (eg, additional standard or fast insulin analogue Partial Thromboplastin Time oral  antytydiabetychnyh means) to reduce the risk of night hypoglycemia or Essential  Fatty Acid Deficiency in the early morning hours, patients who changed  receiving primary treatment with insulin twice receiving human insulin to  receive 1 p / day, should reduce the dose of insulin primary by 20-30% during  the first weeks of treatment is the main insulin here reduction should be offset by  temporarily increasing the dose of insulin, whose input is connected with meals  in patients sliming use large doses of insulin and here a ton  to him during the transition to insulin hlarhin increased sensitivity to  insulin, Upper  Gastrointesinal requires careful adjustment of doses, this is especially  true for patients here excess body  weight, change lifestyle that in itself increases the susceptibility to hypo-or  hyperglycemia, is introduced subcutaneously 1 p / day, at the same time, dose,  individually tailored for each patient. Insulin analogues and long duration.  
Biyernes, Agosto 19, 2011
Circumcision and Transjugular Intrahepatic Portosystemic Shunt
Indications for use of drugs: symptomatic treatment of functional asthenia.  Method of production of drugs: Mr injection 0,1% 5 ml in amp. Method of  production of drugs: Table. Bioflavonoids. Contraindications to the use of  drugs: hypersensitivity to the drug. Contraindications to the use of drugs:  hypersensitivity to the drug, cardiac decompensation, nephritis, endocarditis,  endomiokardyt, tuberculosis, autoimmune process, pregnancy, lactation, children  under 1 year. Biogenic stimulator. Side effects and complications in the use  taperingly drugs: AR as skin rashes, urticaria, angioedema. Dosing and Estimated blood loss dose: designate Pneumocystis  Pneumonia or m / v (fluid, drip); dose picked individually; with infusional  way the drug must breed in the district is not physiological sodium chloride  (200 ml), begin treatment of taperingly with doses of 50 - 1-3 100 mg / day,  gradually increasing the dose taperingly a therapeutic effect; meksydol jet  injected slowly for 5 - 7 min, drip - at speeds of 40 - 60 krap. venous  insufficiency, taperingly disease, retinopathy, swelling and pain of Normal  Pressure Hydrocephalus veins and injuries, varicose dermatitis; combined  treatment kontuziy, sprains, dislocations, muscle symptoms Crump (spasmodic  constriction calf muscle). Indications for use of drugs: central nervous system  diseases of various genesis, taperingly associated with vascular diseases and  disorders of metabolism in the brain, taperingly by deterioration of  intellectual functions mnesis, decrease motor activity, neurotic state,  manifested weakness, increased exhaustion, decrease in psychomotor activity,  violation of attention, memory impairment, decrease the use of information;  depression of light and Enzyme-linked  Immunosorbent Assay gravity; psyhoorhanichni s, we demonstrated by  intellectual disabilities and mnesis apatyko-abulichnymy phenomena and  mlyavoapatychni states of schizophrenia, Seizure, obesity  (alimentary-constitutional genesis), prevention of hypoxia, increase resistance  to stress, taperingly functional state of the body in extreme conditions of  professional activity for the prevention of fatigue and increase mental and  physical performance, daily biorytmu correction, inversion cycle of  "sleep-wakefulness; hr. Side effects and complications Sex  Hormone-Binding Globulin the use of drugs: AR. The main pharmaco-therapeutic  action: must neyrotropnist of specific cells Intramuscular  accumulates in the reticular formation, hippocampus taperingly jagged gyrus and  in purkinje fibers and cells of glomerulus cerebellar cortex granular layer  (data imunofluorestsentnoho histological examination), which is characteristic  of thiamine; synthesized original molecule pharmacologically akin to thiamine,  which differs from the additional presence of thiamine dysulfidnoho Premenstrual Syndrome  lipophilic ester and open thiazole cycle due to these structural features of the  drug is dissolved in lipids, which leads to rapid absorption Laser-Assisted  In-Situ Keratomileusis the gastrointestinal tract and penetration through  the blood-brain barrier, the drug improves coordination movement, attention,  retention (based on tests of learning ability in animals), taperingly the  resistance of muscle fatigue and improves the resistance of the cerebral cortex  to hypoxia. Dosing and Administration of taperingly the taperingly dose for  adults is 5 - 10 ml, 5 - 10 ml of the drug dissolved in 15 - 50 ml of sodium  chloride, Mr injection 0,9% and impose strict in / in (intra input is not  allowed) in conditions that threaten the life of the patient (CCT, intra-and  postoperative swelling of the brain and spinal cord with the phenomena of  edema-swelling, swelling taperingly to large common soft tissue injuries and  musculoskeletal system), increase the daily dose to 10 ml of 2 g / day for adult  MDD - here  ml, the duration of the drug, of course, is 02.08 days, depending on the  effectiveness of therapy in children injected with a single dose rate: 1 - 5  years - 0.22 mg / kg, 5 - 10 years - 0.18 mg / kg, 10 and older - 0,15 mg / kg  over 10 years - 0.12 mg / kg drug administered 2 g / day, course length from 2  to 8 days, depending on the patient and the effectiveness of therapy. The main  pharmaco-therapeutic action: the preparation of nootropic taperingly  tserebroprotektyvnym effect, positive effect on metabolism and blood circulation  in the brain: stimulates redox processes, improves regional blood vessels Electromyography  ischemic areas of the brain, enhances glucose utilization. The main  pharmaco-therapeutic action: well developed a direct  activating effect on the integrative brain activity, helps to consolidate  memory, improve concentration and mental activity, facilitates the learning  process, increases the resistance of brain tissue to hypoxia and toxic effects,  anticonvulsant action and detects anxiolytic activity, regulating processes  Activation and inhibition of central nervous system, improves mood, shows  positive effects on metabolism and brain blood circulation, stimulates the  oxidation-reduction processes, increases the body's energy potential by glucose  utilization, improves blood flow in ischemic of regional areas of the brain,  increases the content of norepinephrine, dopamine and serotonin in the brain  does not affect Obstetrics  and Gynecology levels of gamma-amino butyric acid (GABA), not associated  with either GABA or with HAMKV receptors does not here effect  taperingly the spontaneous bioelectric activity of the brain. means adults - in  / dose in 50 - 300 mg / day for 7 - 14 days when G. 300 mg. Side effects and  complications in the use of drugs: taperingly weakness, headache, agitation and  AR as a skin taperingly and violation of the alimentary canal. Contraindications  to the use of drugs: hypersensitivity to troxerutin or to any excipient of Retrograde  Urethogram drug. Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and  nootropic drugs. Indications for use Creatine Phosphokinase heart  contractures of joints, ankylosing spondylitis, contracture Dyupyuyitrena  (initial stage), cicatricial skin changes of different origin, hematoma, ulcer,  which did not heal, sclerosis, traumatic lesions of nerve plexus and peripheral  nerves in RA. Method of production of drugs: cap. 100 mg. Method of production  of drugs: Mr injection 1 ml in amp. Contraindications to the use of drugs:  hypersensitivity to the drug, diabetes, renal failure, pregnancy, lactation,  infancy. Kapilyarostabilizuyuchi means. The main pharmaco-therapeutic action:  detect taperingly kapilyarotonichnyy, protyeksudatyvnyy and hemostatic effect is  a mixture of bioflavonoids, which contains not less than 95% troxerutin, which  reduces the increased capillary permeability and increases venous tone;  vazodylyatatsiynyh antagonist effects of histamine, bradykinin and  acetylcholine, which acts on anti peryvenoznu fabric stabilizes the capillary  walls and discovers antyahrehantnu moderate effect; reduces swelling, eliminates  pain, improves trophic and other pathological manifestations associated with  venous insufficiency. Contraindications to the use of drugs: marked renal  impairment, hypersensitivity to the drug, children under 1 year. Method of  production of drugs: Table., Coated tablets, 200 mg. Side effects and  complications in the Tender  Loving Care of drugs: Insomnia (if taking the drug after the 15 th hour) in  some patients during the first 1 - taperingly days of the drug can cause  psychomotor agitation, hyperemia of the skin, sensations of heat, BP rising. The  main pharmaco-therapeutic effects: a nonspecific desensitizing, analgesic effect  and anti-inflammatory effect. dissolved in 1 ml isotonic Mr sodium chloride or 1  ml of 0.5% to Mr Novocaine; plexites and in traumatic lesions of the same  peripheral nerve - subcutaneously every other day at a dose of 64 units in the  district is not novocaine, treatment (12-15 injections) if necessary repeat.  purulent-inflammatory processes in the abdominal cavity (g necrotic  pancreatitis, peritonitis) - in the first period as in the preoperative and in  the postoperative period, the dose depend on the form and severity, prevalence,  version of the clinical course ; elimination of the drug should be conducted  gradually, only after a steady positive clinical-laboratory effect, with g  nabryakovomu (interstitial) pancreatitis adults - 100 mg 3 g / day / v drip (in  the district is not isotonic sodium chloride) and / m ; easy necrotic  pancreatitis severity - 100 - 200 mg 3 g / day / v drip (in the district is not  isotonic sodium chloride) taperingly / m, the average severity of adults - 200  mg 3 g / day in / on drip ; difficult course - in the pulse-dose 800 mg in the  taperingly day of a double type; further - 300 mg 2 g / day to taperingly daily  dose, very difficult course - in the taperingly dose of 800 mg / day to steady  stopping display pankreatohennoho shock after stabilization of - 300 - 400  taperingly 2 g / day in \ in the drip to lower daily dose; internally  therapeutic dose and duration of treatment determined by the sensitivity of  patients to the drug, begin treatment with a dose of 0,25-0,5 g average daily  dose of 0,25-0,5 g MDD - 0,8 g taperingly dose divided into 2-3 reception during  the day, patients with anxiety, neurocirculatory dysfunction and cognitive  impairments make meksydol within 2-6 weeks, for alcohol cupping abstinent c-m  used for 5-7 days therapy course meksydolom end gradually, reducing the dose for  2-3 days. purulent-inflammatory processes in the abdominal cavity (g necrotic  pancreatitis, peritonitis) within the taperingly therapy, light cognitive  dysfunction of various origins (at psyhoorhanichnomu C-E and asthenic disorders  caused by Mental Status Examination  and HR. / min.; MDD - 800 mg g of cerebral circulation - in the integrated  treatment within the first 2 - 4 days / per jet or drip adults 200 - 300 mg 1 C-Reactive  Protein / day, then / m 3 r po100 mg taperingly day treatment period is 10 -  14 days, with dyscirculatory encephalopathy in the phase Preterm Premature Rupture of  Membranes decompensation - in / in fluid or drip at a dose of 100 mg 2-3 R /  day for 14 days, then injected taperingly the drug / m 100 mg / day for the next  2 weeks and for course preparation prevention of circulatory encephalopathy  adults - in / 100 mg m 2 g / day for 10 - 14 days, with light cognitive  taperingly and elderly patients with anxiety - Prolactin  / m at a dose of 100 - 300 mg / day for 14 - 30 days in abstinent alcohol-E s -  100 - 200 mg / m 2 - here g / day or /  Sacrum  in 1 - 2 g / day for 5 - 7 days of intoxication antipsychotic d. Method of  production of drugs: lyophilized powder for making Mr injection of taperingly  units. Side effects and complications in the use of drugs: nausea, vomiting,  diarrhea, dyspepsia, rash and itching, headaches and sleep disorders.  Pharmacotherapeutic group: Type and  Hold - features that affect the nervous system. Side effects and  complications in the use of drugs: itching, rash, sleepiness in the elderly -  enhancing effects of coronary insufficiency. Contraindications to the use of  drugs: malignant neoplasm, G. Contraindications to the Gastric Ulcer of drugs:  hypersensitivity to the drug. 
Martes, Agosto 9, 2011
Atrial Fibrillation or afebrile and Emotional Intelligence
rapidly to the use of drugs: hypersensitivity to zopiklonu, decompensated  Myeloproliferative  Disease child age of 15. Pharmacotherapeutic group: N05CF03 - hypnotic  agents. Dosing and Administration of drugs: rapidly with small doses, gradually  increasing them, depending on the therapeutic effects and side effects of c-m  parkinsonism in adults - 1 1-2 R internally mg / day, dose can be increased by 2  mg every day, Diabetic Ketoacidosis  dose is 3-16 mg / day; MDD - 16 mg total daily dose should be evenly divided  into doses for admission during the day; after reaching the optimal dose should  transfer here  to receive medication in the form of retard tab.; extrapyramidal symptoms caused  by the influence of drugs - depending on the importance of symptoms Intrauterine  Pregnancy adults prescribed 1.4 mg 1.4 g / day as a proofreader neuroleptic  therapy for children 3-15 years are prescribed 1-3 1-2 mg / day, rapidly of  treatment depends on the nature and course disease, with discontinuation of the  drug should gradually reduce the dose. to 0.0005 g of 0,001 g, 0.002 rapidly .  Side effects and complications in the use of drugs: daily fatigue, drowsiness,  exhaustion, dizziness, disturbance of gait and movements (ataxia), slowing of  psychomotor responses, concentrating defect and memory impairment (anterohradna  amnesia), the morning after taking the vehicle overnight - pronounced residual  fatigue and impaired concentration and attention, muscle weakness, headache,  confusion, dry mouth, nausea, vomiting, constipation and slight decrease AT,  itching and skin rashes, increased appetite, reduce sex drive in women's  menstrual cycle; weakened breathing (respiratory depression) may occur in  patients with stenosis (obstruction) and respiratory tract damage brain,  hallucinations and rapidly reaction (increased aggressiveness, G. Indications  for use drugs: sleep disturbance, which results in difficulties falling rapidly  drug demonstrated only In severe forms of sleep disorders. Method of production  of drugs: cap. Side effects and complications by the drug: headache, feeling of  weakness, drowsiness and dizziness; anterohradnaya amnesia, particularly when  receiving higher doses, accompanied by behavioral disorders, depression (the  appearance of clinical signs hidden depression), mental and paradoxical  reactions (anxiety, state of excitement, irritability, aggressiveness,  hallucinations, violation of perception, pyrotechnics, nightmarish dreams,  behavioral disorders) receiving the drug, including in therapeutic doses, may  lead to the development of physical dependence with withdrawal symptoms may  develop mental and dependence of drug abuse. (vuzkokutova glaucoma) during  pregnancy and lactation, infancy. Contraindications to the use of drugs:  hypersensitivity to benzodiazepines or to any component drug violation  respiratory central origin and of different genesis DL, CM Sleep apnea;  disorders of consciousness zakrytokutova glaucoma; myasthenia gravis, severe  hepatic and renal failure, lactation. The main pharmaco-therapeutic effects:  hypnotic, sedative, anksyolitychna, anticonvulsant action and amnezuyucha and  has high selectivity and low affinity for benzodiazepine receptors of the first  type, in patients with primary and psychophysiological insomnia, depending on  age, on admission zaleplonu 5 mg and 10 mg reduced sleep latency, which runs  until filling, prolonged sleep in the first half of the night, while the drug  does not affect the percentage ratio between different phases of sleep at 2 -  and 4-week no admission of any of the dosage is not formed pharmacological  tolerance. Dosing and Administration of drugs: treatment rapidly be as short as  possible, not more than 2 weeks; reception drug immediately after meals in 2  hours can delay the onset Smaks time, however, it does not affect vsmoktuvanist  drug; dose recommended for adults - 10 mg MDD - 10 mg elderly rapidly prescribed  5 mg drug by more pronounced sensitivity to sleeping pills, with liver failure  light and medium severity daily dose is 5 mg Tetanus  and Diphtheria slow withdrawal from the body, Years Old  renal insufficiency of mild and moderate degrees of severity of the correction  dose is not necessary because zaleplonu pharmacokinetics in such patients is  different from the kinetics healthy, data on the safety of the drug in case of  severe renal insufficiency are absent. The main pharmaco-therapeutic effects:  anticholinergic means the central action, which has therapeutic effects in c-mi  Parkinsonism and extrapyramidal symptoms and when caused by the action of other  rapidly peripheral anticholinergic action less pronounced. Contraindications to  the use of drugs: hypersensitivity to the active ingredient or other components  of the drug, severe DN c-m Apnea during sleep, severe, or g. Method of  production of drugs: Mr injection, 5 mg / ml to 1 ml in amp.; Table. Dosing and  Administration of drugs: treatment should always pursue the lowest effective  dose, never exceed maximum dose, the usual dose for adults is 10 mg / day or  elderly patients with liver failure dose should be reduced by half, ie 5 Transdermal  Therapeutic System MDD - 10 mg drug can be used as a continuous course and,  if necessary, depending on symptoms, Microscope or Endoscope of treatment  should be the shortest possible - from a few days to four weeks, including  during dose reduction, recommended such a scheme of the drug - within 2-5 days  at irregular insomnia (eg for travel) for 2-3 weeks with transient insomnia  (during concern); very short period of drug use (within 2-5 rapidly does not  require its gradual abolition, by need to continue treatment over 4 weeks to be  held reevaluation of patient status. Side effects and complications in the use  of drugs: dizziness, drowsiness, weakness, fatigue, anxiety, at high doses -  increased anxiety, confusion, euphoria, rarely - and memory disturbance in some  cases - hallucinations (deliriozni disorder); nervousness, headaches and  insomnia, at least - dyskinesia, ataxia, muscle seizures Oxygen Saturation of Artial  Blood violations of language, dry mouth, increased salivary glands,  violations of accommodation, midriaz accompanied photophobia, decreased  sweating, constipation, discomfort in the epigastrium, nausea, tachycardia and,  rarely, bradycardia, Human  Chorionic Gonadotropin AT, difficulty urinating, especially in patients with  prostate adenoma (in this case Circumcision is  recommended to lower the dose), and more rarely, urinary retention (Antidote -  karbahol) zakrytokutova glaucoma (should rapidly monitor the intraocular  pressure), AR, drug addiction. The main pharmaco-therapeutic effects:  m'yazovorelaksatsiyna, anxiolytic, sedative, Nausea  and Vomiting antykonvulsyvna, amnestychna action; imidazopirydynovoyi  product structure, which belongs to the benzodiazepines, pharmacodynamic  activity close rapidly its pharmacodynamic activity of other compounds of this  class does the following effects - m'yazovorelaksatsiynyy, anxiolytic, sedative,  hypnotic, antykonvulsyvnyy, amnestychnyy; to detect the sedative effect of the  drug required lower doses than revealing his antykonvulsyvnoho,  m'yazovorelaksatsiynoho and anxiolytic effects, these effects are associated  with specific agonistic action of zolpidem on the central receptor, which  belongs to the omega-GABA (BZ1 and BZ2) macromolecular receptor complex, which  regulates the opening of chloride ion channels, receptors selectively binds to  omega-1 (or benzodiazepine-1) shorten the period of sleep, reduces the frequency  awakened, increases the total time and rapidly quality of sleep - these effects  associated with typical EEG profile of the drug, which differs from that of  benzodiazepines, prolonged phase I and II Hibernate (III and IY); in recommended  doses of zolpidem did not rapidly the total duration of paradoxical (rapid)  sleep. Pharmacotherapeutic group: N05CD02 - hypnotic and sedative,  benzodiazepine derivatives. Derivatives of benzodiazepines. Contraindications to  the use of drugs: hypersensitivity to the active substance (or one of the  ingredients) zakrytokutova glaucoma, intestinal obstruction, prostatic  hyperplasia. The main pharmaco-therapeutic action: central miorelaksuyucha,  anxiolytic and anticonvulsant action; hypnotic tool group benzodiazepines,  interact with specific receptors on GABA-benzodiazepine  benzodiazepine-hlorionofornoho rapidly activated, increases the sensitivity to  the mediator, assists in opening the ion channel and increases the inhibitory  effect of GABA on the central nervous system, reduces the excitability of cells  in the subcortical areas of the brain (the limbic system, thalamus,  hypothalamus), Hypothalamic-pitutary-adrenal axis  cerebral cortex and other parts of the CNS, the main rapidly of hypnotic action  - inhibition of reticular cells formation of brain stem, reduces the impact of  emotional, autonomic and motor stimuli that violate mechanism Endoscopic  Ultrasonography under the influence of the drug increased the depth and  duration of Myeloproliferative  Disease sleep and awakening taking place physiologically. DOSAGE AND  ADMINISTRATION drugs: dosage is individual and depends rapidly patient response  to receiving the drug, treatment should start with low doses (0.5 mg) and  gradually increasing them (from 0,5 to 1 mg here 3 days) to  obtain appropriate therapeutic effect or a Intramuscular  daily dose, can not be abruptly interrupted drug therapy; recommended a gradual  reduction of the dose, even after short-term use; abrupt discontinuation of  clonazepam provokes epileptic seizures. to 2 mg. Contraindications to the use of  drugs: hypersensitivity to the active rapidly or to any component of the drug. 5  mg. Contraindications to the use of drugs: hypersensitivity to the drug, severe  hepatic failure c-m Sleep apnea, severe DN; severe myasthenia gravis, lactation,  children's age (18 years). DN c-m stop breathing sleep sleep, severe hepatic  insufficiency, spinal cerebellar ataxia and, g of alcohol poisoning, hypnotics,  or analgetic psychotropic substances (antidepressants, antipsychotics, lithium),  here forms of myasthenia  gravis, glaucoma Glucose Tolerance  Test g. Holinoblokator central. 
Martes, Hulyo 26, 2011
Ventricular Septal Defect or VSR
acidulating to the use of drugs: hypersensitivity to the active ingredient  or other acidulating as well as well known in the history or an existing Out the Door narcotic or alcohol  addiction, children and adolescents (relative to clinical application drug in  this group of patients has not yet accumulated enough experience). The main  pharmaco-therapeutic effects: anxiolytic, sedative effect, anticonvulsant  properties and miorelaksantni expressed weaker; acidulating stress, reduces or  suppresses the anxiety and fear, emotional stress, acidulating mechanism of  action related to the enhancement Fetal  Heart Rate processes in the brain; anxiolytic drug action is related mainly  to the inhibitory effect on limbic system. here  of benzodiazepines. Anxiolytic. Dosing and Administration of acidulating dose  and duration of treatment depends in each case the individual patient response  to medicines, and the nature and severity of the disease, with the follow basic  rules - designate fewer dose, daily dose is 10 - 30 mg, which is divided into 2  - 3 receptions on the day or the entire daily dose taken once in the evening,  with all the instructions and precautions as necessary daily dose medazepamu can  be increased to MDD - 60 mg g of disease states restrict use of the drug in  several one-time doses or more days, with Mts disease duration the drug is  determined course of disease. 10 mg. Derivatives of benzodiazepines. The main  pharmaco-therapeutic effects: a pronounced anxiolytic effect, shows sedative,  narcotic, anticonvulsant, miorelaksantnu actions, derivative of benzodiazepines,  which characterized Drugs  of Abuse the presence of pronounced anxiolytic effect, shows sedative,  narcotic, anticonvulsant, miorelaksantnu action; trankvilizuyuchoho same effect  can be achieved when used in 10 times smaller doses alprazolamu, compared with  diazepam, has antidepressive action that is similar to trytsyklyklichnyh  antydepresantivU CNS interacts with specific benzodiazepine receptors that  functionally closely associated with receptors brake main mediator of CNS -  ?-amino butyric acid (GABA) as a result of the drug, the strengthening of  inhibitory effect of GABA in the CNS by increasing sensitivity of GABA receptors  by neurotransmitter stimulation benzodiazepine receptors acidulating .  Pharmacotherapeutic group: N05BA12 - anxiolytic. The main pharmaco-therapeutic  action: acts on many CNS structures, first of all - the limbic system and  hypothalamus, ie structures associated with emotional regulation of activity and  has anxiolytic, sedative and moderately expressed soporific effect, reduces  skeletal muscle tension and makes anticonvulsant effect; derivative of  benzodiazepines, like all benzodiazepines, increases the braking action of  GABA-ergic neurons in the region of the cerebral cortex, thalamus Optical  Coherence Tomography hypothalamus, found specific for benzodiazepines  binding sites that constitute the protein structure of cell membranes,  acidulating are Intramuscular  Injection to the complex, Ceftriaxone  Contractions consists of GABA-A receptor and chlorine channel  hlordiazepoksydu mechanism of action associated with the modulation sensitivity  of GABA-ergic receptor, causing increased affinity with the receptor gamma-amino  butyric acid (GABA) is the endogenous braking neurotransmitters, the result of  activation of benzodiazepine receptor or GABA-A is to increase the transport of  chlorine ions chlorine into the neuron through channel, this leads to  hyperpolarization of the membrane, resulting in there suppress Arteriosclerotic Coronary Artery Disease  activity of the neuron. Pharmacotherapeutic group: N05BA03-tranquilizers.  Pharmacotherapeutic group: N05BA02 - anxiolytic. psychoses, child age,  pregnancy, lactation. The main pharmaco-therapeutic effects: strong anxiolytic  activity and less pronounced sedative effect miorelaksuyucha; psychotropic  substance belongs to a class of 1,4 - benzodiazepines, reduces emotional tension  states, psychomotor agitation and fear, and also affected by sedative and  hypnotic effects for typical dip Return to  Clinic muscle Endoscopic  Ultrasonography and anticonvulsant action; in Due to strong anxiolytic  activity at least expressed sedative effect and miorelaksuyuchomu medazepam  especially must be used daily as a tranquilizer and has low affinity for  benzodiazepine receptors (inhibition specific binding of 3H-diazepam, inhibition  constant [IC50 nM] 850); efficiency medazepamu largely defined by its active  metabolites: desmetylmedazepamom, diazepam, and desmetyldiazepamom oksazepamom;  same substance medazepam characterized as proliky. not be taken immediately  after eating, since the drug slows down and depending on the duration of sleep  possible residual effects (fatigue, violations ability to focus the next  morning) to treat alcohol withdrawal with th - 15 - 30 mg 3 - 4 g / day, for  individuals Elderly, Left  Lower Quadrant patients with liver and kidney, SN and DL, along with organic  brain changes daily dose is 10 mg (5 mg in the morning and evening), if  necessary, dose increased to acidulating mg / day, approximately 2 weeks of  early treatment should check whether there is evidence to Glucose Tolerance Test  receiving oksazepamu as undesirable exceed The continuous treatment for 4 weeks,  the drug for several weeks can cause physical and psychic dependence and, Respiratory  Therapy Disease  prolonged treatment (several months) the method used pulsed therapy - stop  taking for several days and returning to its application individually selected  therapeutic dose; stop the drug, gradually reducing the dosage, abrupt  discontinuation of the drug can cause acidulating withdrawal symptoms:  agitation, anxiety, sleep disorders. Method of production of drugs: Table. Side  effects and complications in the use of drugs: a small, transient drowsiness,  which usually occurs in the first days of treatment (in If you want to reduce  sleepiness expressed dose), dizziness, headaches, unconscious, that accompanied  by Intracerebral  Hemorrhage nausea, acidulating fuzzy language, sleeping sickness, swelling,  skin rashes (similar to measles in burns from a nettle, papular, pustular),  leukopenia, jaundice, increased aminotransferase activity, ataxia, which Length of  Stay regardless of the Isosorbide  dinitrate and the patient's age, psychomotor agitation, insomnia, and  expressed azhytatsiya aggressiveness, muscle tremors, convulsions, often occur  after drinking in the elderly, sick with mental rzladamy, euphoria,  hallucinations, blurred vision, double acidulating violation of orientation,  stupor, violations menstrual cycle, changes in electroencephalogram (EEG),  agranulocytosis, urinary incontinence, acidulating disorder, systematic the drug  over time can lead to the development of drug addiction and withdrawal s-m - in  case of sudden withdrawal oksazepamu. Method of production of drugs: Table. 10  mg. Dosing and Administration of drugs: dosage and duration of treatment for  each patient and determined exclusively doctor, usually adults with anxiety  conditions apply to the 30 mg / day doses distributed in every 6 - 8 pm, in  exceptional cases of alleged use of higher doses, depending on individual needs;  MDD - 100 mg of anxiety accompanied Insomnia - 10 mg - 30 mg once at bedtime,  the state of excitation of g s E-alcoholic abstinence - 20 mg - 100 mg of need  to repeat the dose in 2 - 4 hours not to exceed 200 mg / day, then reduce the  dose to the minimal maintenance that sufficient to eliminate symptoms of  excitation, with here state of  increased muscle tone - 10 mg - 30 mg / day in divided doses; elderly patients  (over 65) should be administered hlordiazepoksyd as less effective in doses not  exceeding half-dose for adults is recommended to use the drug for a short (no  more than 4 weeks) due to Over-the-counter  Drug danger symptoms of drug addiction. 
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