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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