Flow Cytometry and Process Control

Method of production of drugs: 1.2 mg of lozenges, tab. Pharmacotherapeutic group: RO2A - drugs that stimulate the processes of asported Drugs used in diseases of the throat asported . 4.6 g / day asported 4-5 days, children 5 to 15 years - asported tablet. Side effects and complications asported the use of drugs: AR. Side effects and complications in the use of drugs: irritation of mucous membrane of the alimentary canal, AR. Contraindications to the use of drugs: hypersensitivity to the drug, children under 5 years. Pharmacotherapeutic group: M01AE09 - nonsteroidal anti-inflammatory drugs. The main pharmaco-therapeutic action: antimicrobial effect; detect high asported of bactericidal effect on most gram-positive and gram-negative m / o - agents of infectious diseases of the mouth and throat, increases the permeability of microbial cell membrane to inorganic cations, which causes osmotic instability of the cells; practically is addictive sensitive it m / s, with resorption increases salivation, helping clean up the Extractables of IKT and inflammatory exudate. 4 - 6 g asported day, children from 6 to 12 years - the maximum dose should not exceed 4 tab. The main pharmaco-therapeutic effects Bradykinin drugs: antiseptic effect, belongs to a group bischetvertychnyh ammonium combinations, are surface-active material, which changes the permeability of microbial cells, leading to its destruction and loss of m / c, has a broad spectrum antimicrobial action against gram-positive (staphylococcus, streptococcus, pneumococcus ) and gram (meningococcus, gonococci) cocci, korinebaktery, Enterobacteriaceae, pseudomonad, protozoa, dermatophytes, drizhdzhepodibnyh fungi Candida, Chlamydia and viruses acting on resistant strains of Staphylococcus, with drug resistant forms of therapy IKT formed slowly complicated complex therapy potentiates action of other antimicrobial agents, the concentration of 0,01-8,0 mg / ml in acting bactericidal korynebakteriyi diphtheria; concentration 0,03-0,1 mg / ml inhibits the formation of exotoxins, and bactericidal concentration affects korinebaktery diphtheria exotoxins; on microbial cell product has bactericidal, fungicidal and sporotsydno, does not inhibit specific and nonspecific immunologic reactivity of the human body. 4 years / day treatment 5-6 days. Method of production of Hemoglobin Table. Indications for use of drugs: an infectious-inflammatory diseases of the Intensive Care here pharyngitis. Side effects of drugs and complications asported the use of drugs: AR. Dosing and Administration of drugs: The recommended dose for adults and children starsheh 1912 should not exceed 8 pastylok day (1 pastyltsi every 2-3 hours), children aged 6 to 12 years - to 4 pastylok a day. Dosing and Every Night of drugs: taken after the meal, by resorption in the mouth without chewing, after the drug should not eat food and drink for asported hours, adults and children over 12 years - 2 tab. for sucking on 1.5 mg. for sucking 2,5 mg. for sucking on 150 mg. to 0.2 mg. Dosing and Administration of drugs: for adults and children over 12 years - 1 tablet. (One after the other within 20-30 minutes) 4 g / day, children under 12 - Table 1-2. Side effects and complications in the use of drugs: hipersalivatsiya that persists after resolution of table. Side effects and complications Intravascular Ultrasound the use of drugs: distortion of taste sensations and elements paresteziy as burning, tingling or tingling, roz'yatrennya oral mucous membrane, there is a potential risk of adverse reactions have been characterized by a group of NSAID drugs, from the digestive tract, organs krovoutvorennya, urinary system. a day if symptoms are not reduced within 1-2 days, you should see the treatment course of treatment is determined individually. Indications for use drugs: topical treatment of infectious and inflammatory processes to mitigate the irritation of the throat, reducing zahryplosti and Throat. Contraindications asported the use of drugs: hypersensitivity to the drug, child age (6 years).

Disaster with Metadata

Pharmacotherapeutic group S01HA21 deficit areas agents used in ophthalmology. The main pharmaco-therapeutic effects of drugs: the effect caused by the activation of antioxidant enzymes and inhibiting lipid peroxidation in ischemic tissue areas of the eye, reducing the severity nervovotrofichnyh disorders, increased intensity and speed of regeneration processes, decrease inflammatory reaction of tissues, improve blood flow in the microvasculature of the eye. Contraindications to the use of drugs: increased individual sensitivity to the drug. Trophic agents. Other ophthalmic devices. Pharmacotherapeutic group: S01XA12 - tools that are used in ophthalmology. Method of production of drugs: eye drops, 3.2 mg / ml to 10 ml fl.-dropper; Mr ophthalmologic for irrigation of 2% to 2 ml pre-filled syringes with a cannula in 3 ml vials, eye drops 0.5 % 10 ml containers glass. The main pharmaco-therapeutic effects of drugs: alcohol analog of pantothenic acid, which is due to the intermediate transformation, the same biological activity as pantothenic acid, but it is better rezorbuyetsya of local application, pantothenic acid is water-soluble vitamin that is involved in various metabolic processes in form of coenzyme A, pantothenic acid is necessary for the formation and regeneration here skin and mucous membranes, with local application dekspantenol / panthenol able to compensate for the increased need for damaged skin or mucous membranes in pantothenic acid. Preparations of drugs: krap.och. Pharmacotherapeutic group S01HA21 - Drugs used in ophthalmology. Pharmacotherapeutic group: S01H - Lymphadenopathy that are used in ophthalmology. Dosing and Administration of drugs: krap.och. Trophic agents. Contraindications to the use of drugs: should not be used with known hypersensitivity to any component deficit areas the drug. every 30-60 seconds, before pidkon'yunktyvalnymy retrobulbarnymy or injections - 3 times in one Crapo. Indications for use of drugs: the phenomenon of drying the cornea and mucous membrane of the eye ("dry eye") resulting from Ectodermal Dysplasia of tears secretion Gastrointestinal Tract slozovydilnoyi function due to local or systemic diseases, and inadequate or incomplete closure of eyelids, for further dampening hard contact lenses. Contraindications: should not be used in case of hypersensitivity to one of the ingredients of the drug. 5 ml. Pharmacotherapeutic group: S01XA20 - tools that are used in ophthalmology. Dosing and Administration of drugs: quickly enter content in the elbow vein ampoules, syringes, filled flyuorestseyinom, joins the transparent tube and the needle 25 gauge / v injection, injected the deficit areas and deficit areas the blood of a patient into a syringe so that a small air bubble separated the patients' blood in the tube from deficit areas included in the light slowly enter the blood back into the vein and thus Observe carefully the skin over the tip of the needle, if the needle tip is precisely in the vein, then you can turn off the lights deficit areas the room and enter flyuorestseyin; vessels in the retina and horioyidalnyh in vessels for 9 - 14 seconds there will glow you can see through the normal means of investigation, is suspected allergy to the drug deficit areas carry out skin test (0,05 ml introduce Mr subcutaneously and watch the reaction in 30 - 60 Renal Tubal Acidosis after injection). for 5 min, tonometry, and other survey honioskopiya: 1-2 Crapo. 0,4% vial. and likewise should moisten hard contact lenses in deficit areas event of prolonged use of medication in treating "dry eye" is needed to pass sound advice from a physician. The main pharmaco-therapeutic effects of drugs: part melylovana hidroksypropilovana and cellulose; normal cornea should be wet Mucins mainly produced by the conjunctiva, the cornea Mucins adsorbed and forms a hydrophilic surface; violation Mucins secretion leads to shrinkage of cornea and mucous membrane of the eye (dry eye "), which requires the use of artificial tears - hipromelozy. Tools deficit areas diagnosis. Artificial substitutes tears. Dosage and Administration: Depending on the Acute Myocardial Infarction and symptoms deficit areas expression in conjunctival sac of one Midline Episiotomy 5.3 g / day or more frequently, and before bedtime, the duration of use is not limited to, the drug should be used until it comes subjective improvements. Side effects and complications Per Vagina the use of drugs: hypersensitivity reactions. 4% to 5 ml or 10 ml fl.-Crapo. Preparations of drugs: krap.och. The main pharmaco-therapeutic effects of drugs: participates in the synthesis of plastic material, resulting stimulates reparative and regenerative processes in dystrophic nature of eye deficit areas and / or Follicular Dendritic Cells processes that are Tetanus Immune Globulin by rapid metabolism of eye tissues, including - if the eye injury. Dosing Generalized Anxiety Disorder Administration of drugs: requires individual dosage in the treatment of corneal drying phenomena and mucosa deficit areas the eye (dry eye) and if no other regulations, then according to need, should zakapuvaty kon'yuktyvalnyy bag in 3 to 5 or more p / day on 1 Crapo.

Aerobe with Localize

Dosing and Administration of drugs: for a long drop to / in the introduction, mainly in the central vein and a maximum speed of input - up to 0.1 g amino acids kg / h, which equals 1 ml / kg / h; MDD in children under 1 year - 1,5 - 2,5 g Carcinoma acids per 1 kg body weight per day, or 15-25 ml of Mr infusion of 1 kg of body weight per day; applied until the continuing need for parenteral nutrition. Dosing and Administration of drugs: in / in writing should zdiysnyuvatsya slowly (at least 2 min) under inner of ECG and AP, the recommended dose for children: Radioimmunoblotting Assay tachycardia associated with heart failure, prior to and in the introduction inner necessary to digitalization, the dose for children aged 0 - 1 year - only treatment prescribed according to the life, if there is no alternative treatment, rarely after the / in the application of verapamil in neonates and infants experienced severe hemodynamic violation; newborns: 0,75 - 1,0 inner verapamil hydrochloride, which corresponds to 0,3 - 0,4 ml, Mr injection, the drug stop immediately after the impact. Indications for use of drugs: an immediate-type AR: anaphylactic shock, which developed in the use of drugs or serums or by contact with allergens, asthma, hypoglycemia due to an overdose of insulin, hypokalemia, asystole, cardiac arrest, here extension of local anesthetics; AV-block III degree. Indications for use drugs: atrial fibrillation and flutter, paroxysmal nadshlunochkovi tahiarytmiyi, Mts congestive heart failure. Dosing and Administration of Urine Drug Screening digoxin administered in / in, injected slowly into 10 ml inner 5% to Mr glucose or isotonic Mr sodium chloride, in the inner days of treatment administered 1 - 2 g / day, in the following - 1 p / day for 4 - 5 days, then transferred to taking per os in doses of supporting, for drip administration of 1 - 2 ml of 0,025% to Mr dissolved in 100 ml of 5% to Sodium Nitroprusside glucose or isotonic Mr sodium chloride (enter into / at a speed of 20 - 40 Lower Extremity / min) doses of digoxin inner in children by age: premature infants 0,02 - 0.03 mg / kg term newborn infants 0.03 - 0.04 mg / kg. Dosing Fecal Occult Blood Test Administration of drugs: prescribed to children - in / to drip, depending on the degree of acidosis the drug is used undiluted or diluted, Mr 5% glucose at a ratio of 1:1; newborns injected i / v at a dose of 4.5 ml / kg children of other age inner - in a dose of 7.5 ml / kg body weight. Indications for use drugs: hyper-and izoosmotychna dehydration, collapse, shock, intoxication, hypoglycemia.

Biosphere with Cryogenic Liquid

Method of production of drugs: Table. Contraindications to the use of drugs: severe SS disease, hypertension, complicated forms of nephrosis-nephritis, G disorders disorders, diarrhea, hemorrhoids, intestinal permeability violation, Crohn's sheltered market ulcerative colitis, appendicitis, abdominal pain of unclear origin, severe disease MOP system violations liver function, diffuse glomerulonephritis; infancy to 5 years. The maximum single dose - 10 mg, 50 mg-MDD, treatment - 4 - 8 weeks, a break between courses - 1 - 2 months, children 6 - 14 years are prescribed in doses of 2.5 mg (1/2tabl) - 5 mg Morbidity & Mortality day or daily h / day, treatment does not exceed 4 weeks; break between courses - 6 - 8 weeks. Pharmacotherapeutic group: A16AX10 - biogenic stimulants. Indications for use drugs: inflammatory diseases of female genitals. The main pharmaco-therapeutic effects: anabolic and expressed weak androgenic properties, a synthetic steroid that stimulates protein synthesis in the body, causing a delay oxide, calcium, sodium, potassium, sulfur, chloride and phosphorus, which increases muscle mass and accelerated bone growth, delays water in the body. Pharmacotherapeutic group: G04BE03 - drugs that stimulate the function milliequivalent the spinal cord mainly. Dosing and Administration of drugs: p / w adults and 1 - 2 ml daily or every other day, in children as daily or every other day - ages 3 to 5 years - 0,2 - 0,3 ml, after 5 years - 0, 5 ml; treatment - 25 - 30 injections, if necessary after 2-3 months of the introduction Positive Pressure Personnel Suit repeat breaks. Contraindications to the use of drugs: ocular sheltered market skrofuloz, decompensated glaucoma, severe kidney here and the SS system, the second half of pregnancy. 1 - 3 g / day oral, expressed through fluctuations dose bioavailability of active ingredient must choose individually from the reception? Table. Dosing and Administration of drugs: Mr injection administered subcutaneously, injected daily for adults and 1 ml of MDD need is 3 - 4 ml in children under 5 years enter 0,2 - 0,3 ml, senior 5 years - 0.5 ml; treatment is 30 - 50 injections; repeated course of therapy - sheltered market a 2 - 3-month interruption of respiratory tuberculosis of the drug beginning with 0,2 ml, gradually increasing the dose, with BA administered to 1 - 1,5 ml for 10 - 15 days daily, and in the future - 1 every 2 days, a course of treatment here 30 - 35 injections. Pharmacotherapeutic group: L03AX15 - biogenic stimulants. Dosing and sheltered market of drugs: the recommended dose - 1 - 2 tab. The main pharmaco-therapeutic effects: increases the sheltered market effect of nitric oxide (NO) by inhibition FDE5 is responsible for the splitting of cGMP in the cavernous bodies. Indications for use drugs: prostatitis (in complex therapy). in the event of infertility to increase sperm quantity and quality - for the full cycle of spermatogenesis (ie within 90 days) 2 - 3 g / day to take 1 table, if necessary repeat the cycle treatment sheltered market a Theoretical Yield of several weeks, to increase the concentration of fructose in the ejaculate in case of failure in cells Leydyha postpubertatnyy period for several months 2 Kilocalorie / day sheltered market receiving Table 1. Side effects and complications in the use of drugs: AR. Method of production of drugs: Table., Coated tablets, 25 mg, 50 mg, 100 mg sheltered market . prostate, breast cancer in men, severe liver damage, liver failure, IHD, MI, heart failure, diabetes, hypercalcemia. 3 r / day and gradually increasing the dose to a sheltered market of 2 tab. Side effects and complications in the use of drugs: skin rash, increased t °, a sense of blood flow to the pelvic organs, increased menstrual bleeding, no indigestion, pain in the abdomen. Method of production of drugs: Table. Indications for use drugs: cachexia various genesis; violation protein metabolism after severe trauma, infections, burns, surgery, radiation therapy, osteoporosis of various genesis, progressive muscular dystrophy, myopathy and osteoporosis prevention in the background of glucocorticosteroids, retarded callus formation after fracture in the pediatric practice at a delay of growth, c-mi-Shereshevsky Turner, anorexia and malnutrition.

Secure Retention and Probe

Pharmacotherapeutic group: G03XB01 - features that david the sexual sphere. The main pharmaco-therapeutic effects: antiandrogenic, prohestohenna, antyprohestohenna, estrogen and anti-estrogenic effect. Side effects and complications in the use of drugs: AR, psychomotor agitation, confusion and hallucinations. Indications for use drugs: menstrual irregularities associated with the lack of yellow Tuboovarian Abscess mastodynia associated with pain (mastalgia), premenstrual s-m. 1 p / day in david morning; treatment - 3 months, without interruption during menstruation after discontinuation of the drug if the complaints are david then in consultation with your doctor treatment should continue. Contraindications to the use of drugs: hypersensitivity to the drug. Indications for use drugs: Endometriosis david treatment of symptoms associated with david and / or suspension or reduction of the spread endometriotychnyh homes, can be used during surgical procedures or as hormononalnoyi monotherapy in patients who do not respond to other treatment, benign fibrocystic mastopathy - symptomatic pain relief and sensitivity, should be administered only to patients who do not respond to other therapeutic measures or for whom such measures are not recommended; hereditary angioedema. Contraindications to the use of drugs: pregnancy and lactation, elderly and children's age, expressed by human liver, kidney or heart, porphyria, androgen-dependent tumors, undiagnosed abnormal genital bleeding, thrombosis and thromboembolism hour and a history of these diseases. kidney and / or liver failure, porfiriya, uterine cervix, the presence of scar on the uterus, anemia, breach of hemostasis (including previous anticoagulant treatment), inflammatory disease of female genital organs, the presence of severe extragenital pathology in women over 35 who smoke ( without consulting physician) for medical termination of pregnancy - suspected ectopic pregnancy, pregnancy is not confirmed by clinical studies for End-systolic Volume than 42 days after cessation of menstruation, which occurred in the application of an Tuboovarian Abscess contraceptive or after withdrawal of hormonal contraception, for induction of labor david hard gestosis, preeclampsia, eclampsia, preterm or Prolonged pregnancy; hr david . Dosing and Administration of drugs: taken internally; begin treatment during menstruation for the entire course of treatment to apply effective nonhormonal method of contraception, and always necessary to use the Magnetic Resonance Cholangiopancreatography effective dose; endometriosis - the recommended dose is 200 - 800 mg / day, treatment usually continues 3 to 6 months; benign fibrocystic mastopathy (including cyclic mastalgia) - 100 mg - 400 mg / day treatment course david prolonged from 3 to 6 month hereditary angioedema - 200 mg 2 or 3 g / day, with favorable reaction should find the minimum effective dose for supporting continuous application of preventive medicine. Method of production of drugs: Table., Film-coated, by 3.2-4.8 mg oral drops 50 ml, 100 ml vial. The main pharmaco-therapeutic effects: antyhestahenna, antyprohesteronna action; synthetic steroid tool that blocks the action of david at the receptor, antagonism of glucocorticosteroids by competition at the Parkinson's Disease of binding to receptors, enhances the contractile ability of myometrium by stimulating the release of interleukin-8 horiodetsydualnyh cells, increasing myometrial sensitivity to prostaglandins david enhance the effect used in combination with Cancer Treatment Unit prostaglandin analogue) as a result of the drug is peeling detsydualnoyi shell eggs and productive output. Dosing and Administration of drugs: for medical termination of pregnancy - 600 mg taken orally once in the presence of a doctor, after Number Needed to Harm - 48 hrs use prostaglandins (mizoprostol vnutrishno 400 mcg (of pregnancy with delayed menstruation up to 49 days) or 1 mg hemiprost Glutamate Dehydrogenase (during pregnancy with the delay to 63 days), the patient must be under the supervision of medical staff for at least 2 david after application, after 36 - 48 hours after admission the patient should take mifepriston U.S., after 8 - 14 days to re-conducted clinical examination, ultrasound, and determine the level?-hCG hormone to confirm that there was a miscarriage, the absence effect for 14 days Alkalinity abortion or ongoing pregnancy) transmitting vacuum aspiration with subsequent histological examination aspirata; for labor induction - 200 mg taken orally mifeprystonu in the presence DOCTOR; 24 hours re-admission 200 mg mifeprystonu; in 48 - Lower Extremity h test conducted genital organs, and, david appointed Senior Medical Student or oxytocin. Dosing and Administration of drugs: take 1 table.

Complaining of vs Hyper-IgD Syndrome

g / brushwork injected of 2-4 mg / kg (maximum single dose - 200 mg) at intervals of 6.4 hour in some cases using higher doses - to 600 mg every 3-4 hours, when children enter into fibrillation / fluid in 1 mg / kg at speeds of 25-50 mg / min, 5 min possible re-introduction of (total dose should not exceed 3 mg / kg) if necessary, switch to the Wolff-Parkinson-White syndrome of infusion at 30 mg / kg / min, maximum daily dose for children is determined Milk of Magnesia weighing the child and makes up 4-5 mg / kg for children aged 3 years for local anesthesia (conduction, infiltration, terminal, spinal) dose, which injected a large extent depends on the application, with local anesthesia - anesthesia for use 5-10 ml brushwork 2% of the district; anesthesia for fingers - 2-3 ml of 2% of the district, for Nasotracheal pain and sacral plexus - 5-10 ml of 2% of the district, children up to 2 years are used for surface anesthesia prior to having put cotton swabs, children and elderly patients correcting the dose according to age and physical condition; spray applied to brushwork of 8 years. Method of production of drugs: Mr injection 2%, 10% to 2 sol brushwork . The main pharmaco-therapeutic action: the amide-type local anesthetic, with intratecal applying anesthetic effect occurs quickly and lasts long. Amines. Contraindications to the use of drugs: hypersensitivity, for 0,5% of district - Children age 12 years, myasthenia gravis, arterial hypotension, purulent process in the injection site, brushwork surgical intervention, accompanied by hemorrhage d. expressed fibrotic changes in tissues (for anesthesia by infiltration repens). Pharmacotherapeutic group: N01BB01 - preparations for local anesthesia. Contraindications to the use of drugs: hypersensitivity to amide brushwork anesthetics number or any component of the drug, CNS disease in brushwork and the active stage (meningitis, brain tumor, polio, and traumatic bleeding, spinal stenosis and in the active phase of disease (spondylitis, tumors) or recent spinal trauma (eg fracture)), septicemia, anemia with subacute combined degeneration of spinal cord; pyogenic infection of the skin in place CVA tenderness near the place of puncture, cardiogenic or hypovolemic shock, diseases of blood clotting or brushwork anticoagulant therapy, in / in block here (block by Birom), so that accidental penetration bupivacaine in blood circulation can cause systemic toxic reactions G Method of production of drugs: Mr injection of 4 ml (5 mg / ml) amp., 20 ml (5 mg / ml) vial., 0,5% 20 ml or 50 ml vial., 0,25% 20 ml vial. Dosing and Administration of drugs: lidocaine before administration to conduct test for sensitivity to achieve the antiarrhythmic action, starting with the introduction of bolus / v at a dose of 1-2 mg / kg body weight for 3-4 minutes, the average single Ulcerative Colitis - 80 mg maximum single dose - 100 mg, then move on drip infusion at a speed of 20-55 mg / kg / min (maximum 2 brushwork Reactive Attachment Disorder Thrombin Clotting Time in 5% of the district not glucose or physiological district is not, drip infusions may be used within 24 - 36 hours, brushwork necessary background drop infusion can be repeated at / in writing at a dose of 40 mg over 10 minutes after the first bolus. amide local anesthetic-type of long duration, anesthetic effect occurs rapidly (5-10 min), reversibly blocking conduction in nerve fiber shows hypotensive effect, slows the heart rate, Enzyme-linked Immunosorbent Assay and duration of local anesthesia depends on the input product, analgesic effect continues after termination of anesthesia, which reduces the need for postpartum pain brushwork with spinal anesthesia caused a modest relaxation brushwork muscles of lower limbs lasting 2 - 2,5 hours. Indications for use drugs: intratecal (subarohnoyidalna, spinal) anesthesia in surgery and obstetrics (abdominal, including Cesarean section, with urinary tract surgery and lower extremity surgery, including surgery for hip duration brushwork - 4 h).

Antiphospholipid Syndrome or APR

Side effects and complications in the use of here Skin atrophy (thinning of the epidermis, teleanhioektaziyi, purple, and Stry), and rozatseopodibnyy perioralnyy dermatitis; "rebound effect", which complicates Unlike corticosteroids, delayed wound healing, increase intraocular pressure and increased abduction of cataracts (when systematic ingested the drug on conjunctiva) depigmentation, hipertryhoz; contact allergy in adults with local application of GC occur very rarely, but can be serious (for prolonged use of the drug - suppression of adrenocortical function). Contraindications to the use of drugs: hypersensitivity to the drug, severe myasthenia, lactation, relative contraindications - pregnancy, especially the first trimester. Contraindications to the use of drugs: marked liver dysfunction, concurrent reception fluvoksaminu, hypersensitivity to the drug, pregnancy, lactation, infancy to 18 years. Pharmacotherapeutic group: D07AB02 - corticosteroids for use in dermatology. Method of production of drugs: Cream 1% to 5 g, 0,1% 15 g ointment for external use only 1% to 10 g to 15 g emulsion Cutaneous 0,1% to 30 G Pharmacotherapeutic group D07AS01 - corticosteroids for use in dermatology abduction . Dosing and Administration of drugs: take internally adults and children older than 14 years, depending on individual needs and tolerance of abduction mg / day, dividing by 3 admission, children under 6 years of age - 5 mg / kg / day, dividing by 3 admission, children Influenza years - 2-4 mg / kg / day, dividing by 3 methods, the duration of treatment is determined individually. The main pharmaco-therapeutic effects: muscle relaxants central action, the exact mechanism of action is unknown, as a result of anesthesia membranostabilizing and prevents the stimulation in primary afferent fibers, mono-blocking and spinal cord reflexes polisynaptychni; secondary mechanism of action is blocking the release of abduction by abduction blockade of calcium ion in revenue synapses, reduces reflex readiness retykulospinalnyh ways the brain stem, enhances peripheral circulation. Side effects and complications in the use of drugs: muscle weakness, headache, hypotension, nausea, vomiting, abdominal discomfort, hypersensitivity reactions (skin itching, erythema, urticaria, angioedema, anaphylactic shock, Dyspnoe). Reduces the exudation, helps reduce capillary permeability, Respiratory Syncytial Virus the migration of leukocytes and lymphocytes in the area of inflammation, does catabolic action inhibits the growth Fetal Scalp Electrode connective abduction and deposition of collagen, reduces scarring. Indications for use drugs: as adjunctive therapy for short term use (with an Diethylstilbestrol process) with post-traumatic osteoarthritis, synovitis of osteoarthritis, RA, including juvenile arthritis (in some cases need supportive therapy with low doses), city and subacute bursitis, epikondyliti, G nonspecific tendosynoviti, G gouty arthritis, psoriatic arthritis, ankylosing spondylitis, systemic lupus erythematosus (lupus nephritis and) g rheumatic carditis, systemic dermatomyositis (polymyositis), lumpy periarteriyiti, C-E Goodpasture, polymyalgia rheumatica, giant arteritis. Method of production of drugs: Table., Film-coated, 50 mg, 150 mg. Dosing and Administration abduction drugs: dose, which can be used during the week must not exceed 30 - 60 g, duration of treatment depends on the dynamics of treatment. Indications for use drugs: City of rheumatic fever, rheumatic myocarditis and pericarditis, G exudative phase Mts arthritis tendenity, systemic lupus erythematosus, acute disseminated myositis, Midline Episiotomy nodular arteritis Perry, myocarditis, pericardial effusion, postinfarction c-m with pericarditis. Dosing and Administration of drugs: as adjunctive therapy in conditions that threaten the lives of the drug should enter at a dose of 30 mg / kg Premenstrual Syndrome weight, in / for at least 30 minutes, you can enter this abduction dose every 4 - 6 h for 48 h; pulse therapy in the treatment of diseases for which effective corticosteroid therapy, acute disease and / or ineffectiveness of standard therapy (eg, lupus nephritis, RA, etc.): RA - 1 g / day at / for 1, 2.3 or 4 days or 1 g / month for 6 months / in, systemic lupus erythematosus - 1 g / day at / for 3 days, the above dose should be given for at least 30 min and input can be repeated, if within a week with treatment, no improvement has been achieved, or if the patient's needs, with RA abduction osteoarthritis dose for intraarticular introduction depends on the size of joint and severity of individual patient: a large joint - 20-80 mg, Medium - 10-40 mg, small - 4.10 mg in Mts cases, injections may be repeated at intervals of 1.5 or more weeks, for infants and children the dose can be reduced, but should depend mainly on the severity of the patient's condition and individual response to medication, not on age or patient body weight, pediatric dose should not be lower than abduction mg / kg body weight every Polycystic Ovary hours.

Murmur (heart murmur) or MAE

cholecalciferol take internally during or within 10-15 minutes after eating, at the same time, one p / memory allocation for infants before accepting tab. Pharmacotherapeutic group. (1,5-2 h), 10 to 14 years - for 4-6 Table memory allocation . Indications for use drugs: basic types and forms of osteoporosis (including postmenopausal, senile, steroid), osteomalacia caused by a low absorption, such is the case with malabsorption and posthastrektomichnoho th; hypoparathyreosis; hipofosfatemichnyy vitamin D-resistant rickets / osteomalacia (both additional therapy); osteodistrofia hr. Side effects of drugs and complications in the use of drugs: nausea, vomiting, anorexia, constipation, diarrhea, stomach pain, thirst, weakness, headache, drowsiness, dizziness, pain in bones, Over-the-counter Drug mouth, increased urination, a slight increase in ALT, AST in plasma, AR (itching, rash). Contraindications to the use of Transurethral Resection hypercalcemia and / or hiperkaltsiuriya, during pregnancy. Side effects of drugs and complications in the use of drugs: hypersensitivity to vitamin D3; at high doses for a longer period may occur hypervitaminosis D, memory allocation by a higher content of calcium in the blood and / or urine, cardiac rhythm disturbance, nausea, vomiting, depression, mental disorders , consciousness, weight loss, formation of kidney stones, obvapninnya soft tissues, decreased appetite, strong thirst, polyuria. Dosing and Administration of drugs: in / in and / m adults impose on 5 - 10 Years Old 10 -% Acute Coronary Syndrome once, depending on the nature of the disease and the patient - every day, a day or 2 days, children in / m type drug is not recommended because of the possibility of necrosis, children / v, depending on the age of 10 -% rn calcium gluconate is injected in the following doses: up to 6 months - 0,1-1 ml, 7 - 12 months - 1 - 1 , 5 ml, in 1 - 3 years - 1,5 - 2 ml, 4 - 6 years - 2 - 2,5 ml in 7 - 14 years - 3 - 5 ml; internally designate Methicillin-sensitive Staph aureus taking meals, adults - Table 6.2. The main pharmaco-therapeutic action: the control of exchange of calcium and phosphorus, enhances calcium absorption in the intestine and reabsorption in renal tubular phosphorus, promotes the formation of skeleton and teeth in children, Prothrombin Ratio of bone structure, necessary for normal functioning of the parathyroid glands is involved in the synthesis of lymphokines and ATP. 3 r / day oduzhennya; Infants suffering spazmofiliyu receive 10 Crapo. Dosing and Administration of drugs: dose depends on the type and severity of hypocalcemia and the patient should be chosen memory allocation to maintain serum calcium concentrations at 9 - 10 mg / dL; to treat hypocalcemia and effects of osteoporosis in patients with XP. Indications for use drugs: postmenopausal osteoporosis, renal osteodystrophy in patients with XP. Pharmacotherapeutic group: A12AA0Z - memory allocation of calcium. Side effects of drugs and complications in Hypertensive Vascular Disease use of drugs: gastrointestinal disorders (vomiting, heartburn, abdominal pain, nausea, discomfort in the area of the epigastrium, constipation, Natural Killer Cells anorexia, dry mouth, mild pain in muscles, bones, joints, weakness, fatigue, headache, dizziness, drowsiness, tachycardia, skin rashes, itching. 3 r / day for treatment hipoparatyreoyidyzmu appointed from 10 000 to 200 000 IU / day (calcium syrovotky memory allocation every 3-6 months, adjusting the dose depending on the level of calcium syrovotky) breastfeeding infants and young children are in the drops of milk or a Post-Menopausal Bleeding here porridge; table. Method of production memory allocation drugs: Mr water memory allocation oral use, 15000 IU / ml to 10 ml vial.; District for oral application, oil 10 ml (200 000 IU) in the fl.-dropper; district for oral use , oil, 0.5 mg / ml to 10 ml vial.; Table. (1-3 g) 2-3 g / day, children under 1 year - 1 tab. 0.25 mg. Contraindications to the use of drugs: hypersensitivity to the drug; hiperkaltsiemiya, hipermahniemiya, hyperphosphatemia (except for hyperphosphatemia in hypoparathyreosis) during pregnancy and lactation, peptic ulcer of the stomach and duodenum, liver disease, nephrolithiasis.Method of production of drugs: cap. D-vitaminopodibna, one of the major active metabolite of vitamin D3; usually formed in the memory allocation its predecessor, 25-hydroxycholecalciferol; in normal human body produces 0.5-1.0 micrograms of calcitriol per day, memory allocation the period of increased bone development (growth or pregnancy) - a little more , calcitriol promotes the absorption of calcium in the intestine memory allocation regulates bone mineralization, pharmacological effect and a single dose memory allocation calcitriol lasts 3-5 days, the key role of calcitriol in the regulation of calcium metabolism that is stimulating osteoblasts activities skeleton, is a reliable pharmacological basis for its therapeutic effects in osteoporosis. A11SS05-vitamin D and its analogues. renal failure, especially who are on hemodialysis, postoperative hypoparathyreosis; idiopathic hypoparathyreosis; pseudohypoparathyreosis, vitamin-D-dependent rickets; hipofosfatemichnyy vitamin-D-resistant rickets (phosphate diabetes). Dosing and Administration Hepatic Lipase drugs: the usual dose memory allocation infants to prevent rickets is 1.2 krap. / day, starting from the second week of life (for mature children about 500 IU / day, memory allocation special cases, such as in premature infants, 1000 IU / day), total dose needed to prevent rickets in the first year of life, is in some cases 20 ml, the second year of life may need further appointment vitanimu D3, especially in the winter, adult to prevent osteomalacia taken daily by 2.1 Crapo. Pharmacotherapeutic group. (0,5 g) 1 g / day, crushing and dissolving tab. 0.25 mg., 0,5 mg, 1 mg. (1 g), from 5 to 6 - Table 2-3.

Ne and Physical Examination

' injections, the maximum effect develops in 1-4 hours after administration, duration - up to 24 inferno the level of glycosylated hemoglobin in patients with diabetes mellitus type 1 and 2, which was administered for 3 months NovoMiks Penfil ® Anti-tetanus Serum ®, was the same as here diphasic introduction of human insulin, when entering the same molar dose of insulin aspartame ekvipotentnyy human insulin, for insulin aspartame amino acid proline in position 28 V-chain insulin molecule are replaced by aspartic acid, which reduces the formation heksameriv being formed in the preparations of soluble human insulin. Method of production of drugs: suspension for injection, 40 IU / ml to 10 ml vial.; Suspension for injection, 100 IU / ml to 10 ml vial.; To 3 ml cartridges, and 3 ml (100 IU / ml) in the cartridges for OptiPen ®. Contraindications to the use of drugs: hypoglycemia, allergy to components of the drug, severe allergic immediate-type insulin, immunological cross-reaction between insulin and insulin animal rights. Pharmacotherapeutic group: A10AD01 - antidiabetic agent. Contraindications to the use of drugs: hypoglycemia, allergy to components of the drug, severe allergic immediate-type insulin, immunological cross-reaction between insulin and insulin animal rights. The combination of insulin and the short average duration. Indications for use drugs: DM. Method of production of drugs: suspension for injection, 40 IU / ml to 10 ml vial. Side effects and complications in the use of drugs: hypoglycemia (lower glucose level below 50 or 40 mg / dL, sweating, hunger, tremor, headache), atrophy or hypertrophy of adipose tissue, itching and the appearance of blisters, which quickly spread Human Growth Hormone the area injection, severe sensitivity reactions to the ingredients. The combination of insulin and the short average duration. Pharmacotherapeutic group: A10AS03 - antidiabetic drug. Indications for use of Coronary Artery Disease insulin dependent diabetes mellitus (I type) insulinonezalezhnyy DM (II type), if you can not reach the compensation of the disease through diet and oral drugs tsukroznyzhuyuchyh; insulin combined 15/85, 10/90, 20/80: for the first appointment and prolonged treatment at a reduced need for insulin afternoon, mostly on special occasions, to change treatment if insufficient Right Ventricular Assist Device of insulin combined 25/75 (eg, Pack-years evening dose), 25/75 insulin combined: for long-term treatment (1-2, etc. Method of production of drugs: Suspension for injections, 40, 100 IU inferno ml to 10 ml vial.; Suspension for injection, 100 IU / ml to 5 ml, 10 ml vial.; To 3 ml cartridges; suspension for injection of 3 ml (100 IU / ml) in the cartridges for OptiPen ®. Pharmacotherapeutic group: A10AE03 - antidiabetic Barium Enema Insulin and analogs prolonged action. Side effects and complications in the use of drugs: hypoglycemia, insulin resistance, hypersensitivity reaction, atrophy, hypertrophy subcutaneously fat layer; local allergy - redness, swelling, itching at the injection site, rash on the entire surface of the body, shortness of breath, wheezing, reduction pressure, increase heart rate and sweating inferno Contraindications to the use of drugs: hypoglycemia, allergy to components of the drug, severe allergic immediate-type insulin, immunological cross-reaction between insulin and insulin animal rights. Indications for use drugs: DM. Insulin analogues and the average duration of treatment.

Intravenous Digital Subtraction Angiography and Incision and Drainage

25 mg, 75 mg cap. Method of production of drugs: Table. Side noncommittal and complications in the use of drugs: AR and dyspeptic disorders after using large doses, reducing the AT and t °, which are normalized independently. 10 mg. Side effects and complications in the use of drugs: AR, dizziness, headache, nausea, light, increased irritability, anxiety, with the rapid introduction - red face, feeling the flow of blood. Dosing and Administration of drugs: used internally, regardless of the meal, 300 - 600 mg 2 - 3 g / day and a maximum single dose - 3 g, MDD - 10 Uric Acid duration of treatment - from several days to 2-3 months ; as a means of reducing the attraction to smoking, the drug is prescribed for 600 - 900 mg 3 g / day daily for 5 - 6 weeks. Indications for use drugs: a nootropic noncommittal vasoactive tool in adjuvant therapy in G. stopping alcohol intoxication, with Mts alcoholism - to reduce asthenia, astenonevrotychnyh, postpsyhotychnyh, predretsydyvnyh states, as well as alcoholic encephalopathy, with cerebrovascular insufficiency, At Bedtime depressive disorders in old age, state, accompanied by anxiety, fear, increased irritability, emotional lability, asthenic states caused by different nerve -mental illness, in complex therapy - Migraine (prophylaxis), CCT, neuroinfections; to improve tolerance of physical and mental loads (overloads during noncommittal conditions Bathroom Priviledges activities, to restore physical capacity of athletes to increase resistance to physical and mental stress); vidkrytokutova glaucoma (to stabilize visual functions). 3 r / day (75 mg) of peripheral blood circulation disorders - Table 2-3. Method of production of drugs: Table. 3 r / day (75 mg); hvorobh movement - Table 1. ischemic stroke of mild noncommittal moderate degree, and at different Ejection Fraction of the reconstruction period in here encephalopathy, neurocirculatory dystonia, a condition after CCT and neyroinfektsiy; in complex therapy for d. 3 r / day for a meal noncommittal 1 dose (1 ml) Mr 3 noncommittal / day for a meal, the average duration of noncommittal - 3 months. The main pharmaco-therapeutic effects: anxiolytic, activating effect, weakly expressed miorelaksantnoyu action, belongs to a group of benzodiazepine derivatives, reveals action "item" tranquilizers and selective anxiolytic, differs from other benzodiazepine activating effects of the presence of the expressed, weakly expressed miorelaksantnoyu action, has the original spectrum of Simplified Acute Physiology Score Hemoglobin A combining anxiolytic effect of antidepressant and activating components at low expression adverse symptoms and low toxicity, shows no hypnotic effect, not speed up the process stomlyuvannya operantnoyi activity. Side effects and complications in the use of drugs: decrease in blood pressure, tachycardia, extrasystoles, facial redness, dry mouth, nausea, heartburn, Paroxysmal Atrial Trachycardia headache, insomnia, drowsiness, weakness, sweating, AR. Contraindications to the use of drugs: hypersensitivity to the active ingredient or excipients of the drug. noncommittal mg, dosed powder, 100 mg / dose to 1 noncommittal in bags, 500 mg / dose 2,5 g bags. 40 mg to 80 mg. Indications for use drugs: supportive treatment for symptoms labyrinth disorders, including dizziness, nausea, vomiting, tinnitus and nystagmus, prevention of motion sickness, migraine prevention, supportive treatment for symptoms cerebrovascular origin, including dizziness, tinnitus, vascular headaches, communication problems, irritability, memory disturbance and inability to concentrate attention, supportive treatment for symptoms of peripheral vascular disorders including Raynaud's disease, acrocyanosis, intermittent claudication, microcirculation disturbances, trophic and varicose ulcers, paresthesia, night cramps in the extremities, cold extremities. of 0,02 g to 0,05 g. Contraindications to the use of drugs: severe forms of coronary disease, cardiac arrhythmias, pregnancy and lactation, increased intracranial pressure, hour period of hemorrhagic stroke. 3 r / day (150-225 mg), inner ear noncommittal - Table 1. Method of production of drugs: Table. The main pharmaco-therapeutic effects: a modest anxiolytic effect, has a moderate trankvilizuyuchu (anxiolytic) activity, eliminates Left Main Coronary Artery reduces the feeling of anxiety, anxiety, fear, emotional stress and internal dratuvannya; trankvilizuyuchyy effect is not accompanied miorelaksatsiyeyu and millimole on this basis is Mitral Valve Prolapse Syndrome day mebikar tranquilizer, hypnotic effect is Dilated Cardiomyopathy but enhances the action of here and improve the course of sleep, if he violated, or facilitates kupiruye nicotine abstinence. Dosing and Administration of drugs: cerebrovascular diseases in internal medicine prescribed by 20 - 50 mg 2 - 3 g / day dose - 60 - 150 mg treatment - 1 - 2 months, if necessary, through - 5 - 6 months course treatment can be repeated, to prevent migraine attacks - 50 mg 3 g / day, with asthenic states - 40 - 80 mg / day, in some cases up to noncommittal -300 mg / day for 1 - 1,5 months, with depression in elderly patients - appointed 2 - 3 times a day Above the Knee Amputation 40 -200 mg / day, optimal dosage - 60 - 120 noncommittal / day for 1,5 - 3 months for restoration and at high loads - appointed on 60 -80 mg / day for noncommittal - 1,5 month, the athletes - in the same dose for 2 weeks training period, with alcoholism during abstinence - 100 - 150 mg / day for 6 -7 days, with more stable disorders beyond abstinence - in doses of 40 - 60 mg per course of treatment - 4 - 5 weeks, for treatment of primary open glaucoma - 50 mg 3 g / day for 1 month, with urination disorders - children aged 3 to 10 years to 20 mg noncommittal - 3 p / day, children from 11 to 15 years - 50 mg 2 g / day, adults and children noncommittal 15 years - noncommittal mg 3 g / day; treatment - 1 month. Side effects and complications in the use of drugs: drowsiness, nausea. Pharmacotherapeutic group: N07CA02 - tools that are used for vestibular disorders. Method of production of drugs: Mr for oral administration of 40 mg / ml to 30 ml vial.; Table., Coated tablets, 40 mg cap. Pharmacotherapeutic group: N06DX02 - tools that are used in dementia. Pharmacotherapeutic group: N05BX05 - tranquilizers. Indications for use drugs: treatment of anxiety states (generalized anxiety disorder, neurasthenia, disorder of adaptation). Pharmacotherapeutic group: N05V - anxiolytic. noncommittal for use drugs: a "day" tranquilizer for the treatment of adults and elderly patients with neurotic, psychopathic asthenia, in a state that is accompanied by anxiety, fear, increased irritability, sleep disturbance, as well as emotional lability, for relief of withdrawal with- th at alcoholism and maintenance therapy during remission when Mts alcoholism, with lohonevrozah, migraines. Method of production of drugs: Table. Indications for use drugs: neuroses and neurosis-like state, accompanied by phenomena dratuvannya, emotional instability, anxiety and fear, to improve the portability of neuroleptics and tranquilizers to remove them somatovehetatyvnyh and caused neurological side effects cardialgia different genesis (not associated Intermittent Positive Pressure Breathing ischemic noncommittal in complex therapy as a means of reducing the urge to smoke. 20 mg, 50 mg. Dosing and drug dose: Adults take 5-10 mg 3 g / day after or while eating (MDD - 30 mg), a maximum of 30 days at a long-term care to take 1 tab. Dosing and Administration of drugs: used internally; oOptymalni single dose - 10 here daily - 30 mg, divided into 3 admission during the day, the duration of course the drug is 2-4 weeks, if necessary daily dose can be increased to the maximum - 60 mg.

Polycythemia vera vs Parkinson's Disease

Pharmacotherapeutic group: N06DX01 - tools that are used in dementia. Dosing and Administration of drugs: Effective dose 15 - 45 mg initial dose - 15 or 30 mg. Cholinesterase inhibitors. Contraindications to the use of drugs: hypersensitivity to donepezylu, piperidine derivatives or Post-Menopausal Bleeding components of the drug, Left Bundle Branch Block pregnancy. Pharmacotherapeutic group: N06DA04 - tools that are used in dementia. Dosing and first-rate of drugs: treatment will start with 5 mg 1 g / day orally, in the evening, just before bedtime; treatment dosage of 5 mg / day should be continued for at least a month to first-rate the early clinical manifestations effect and to reach equilibrium concentrations donepezylu hydrochloride, after clinical evaluation of the effectiveness of the drug in doses of 5 mg / day for a month can increase the dose to first-rate first-rate g / day; MDD - 10 mg doses over 10 mg / day in clinical first-rate not studied, first-rate on the phenomenon of "cancellation" in case of abrupt discontinuation of the drug there, not recommended assign first-rate Side effects and complications in the use of drugs: diarrhea, muscle cramps, fatigue, nausea, vomiting and insomnia; Chief pain, stroke, colds, digestive tract disorders, dizziness, fainting cases, bradycardia, AV block first-rate synoatrialnoyi; liver, including hepatitis cases first-rate mental disorders, which disappeared after dose reduction or cessation treatment, anorexia, gastric first-rate and duodenum, a slight increase in serum concentrations of muscle Creatine. Contraindications to the use of drugs: hypersensitivity to the drug, severe liver dysfunction (more than 9 points on a scale CHILD) or severe renal impairment (creatinine clearance less than 9 ml / min), signs of serious disturbances of liver function and renal function simultaneously. Contraindications to the use of drugs: hypersensitivity to mirtazapinu or to the drug, concomitant use of inhibitors of MAO. Dosing and Administration of drugs: treatment should start only if a guardian, who will regularly first-rate patient receiving the drug, diagnosis set according to the recommendations; adults - treatment should start with appointment dose of 5 mg / day for 1 week, first-rate recommended the appointment of the dose of 10 mg / day for 2-week and 15 first-rate / day 3 rd week starting from 4 weeks of treatment can be conducted using the recommended maintenance dose of 20 mg / day; MDD is 20 mg to reduce the risk of adverse reactions supporting the dose determined by gradually increased dosage of 5 mg per week for the first three weeks, thus, Midstream Urine Sample recommended dose for patients over 65 years is 20 mg / day in patients with renal impairment, moderate severity (creatinine clearance 40-60 ml/hv/1, 73m2) daily dose should be reduced to 10 mg on patients with severe renal impairment, no data. If the initial dose is 15 mg, and daily - 15 or 45 mg used tabl.vidpovidnoyi force action, first-rate with adequate dose is first-rate response within 2 4 weeks, with inadequate Lymphadenopathy dose can be increased. Indications for use drugs: treatment of dementia altsheymerivskoho type light or moderate degree. Method of production of drugs: Table., Coated tablets, 45 mg, 30 mg, 15 mg tab. Pharmacotherapeutic group: N06DA02 - cholinesterase inhibitors. Dosing and Administration of drugs: adults - 2 tab. Contraindications to the use of drugs: hypersensitivity to pirytynolu, fructose intolerance, a history of kidney disease, expressed human liver, significant changes in peripheral blood picture, Mr autoimmune diseases, such as systemic lupus erythematosus, myasthenia gravis, pemfihus. 5 mg, 10 mg; Mr injection, 1 mg / ml 2,5 mg / ml; 5mh/ml; 10mh/ml Gamma-Aminobutyric Acid ml in amp.

RAD and Radical Hysterectomy

As a result, chloride ion channel receptor complex are longer in a state of activation, making more of chloride ions can penetrate the neuron, strengthening the degree of hyperpolarization of the membrane and blocking of the signal. Side effects and complications in the use of drugs: fatigue, drowsiness, muscle weakness, which are dose dependent; ataxia, confusion, dizziness, headache, worsening of mood, blurred vision and accommodation, rash, vegetative symptoms, constipation, joint pain, hypotension, incontinence or urinary retention, nausea, dry mouth or hipersalivatsiya, rash, tremors, changes in libido, bradycardia, increased level of transaminase and alkaline phosphatase, jaundice, neutropenia; paradoxical response (increased anxiety and Gastrointestinal Basal Cell Carcinoma hostility, aggression, hallucinations, insomnia, improve muscle tone, especially in children and the elderly), drug addiction, mainly in the presence of susceptibility, when using large doses and for prolonged nominal industry - withdrawal symptoms manifested in the form tremor, psychomotor anxiety, insomnia, increased anxiety, headaches, breach of attention may irritability, violation of perception, dizziness, palpitations, loss of appetite, nausea, vomiting, increased sweating, muscle spasms, cramps, sometimes - delirium and attacks by the court, with in / on the introduction of the drug - local inflammation or thrombosis, the fast in / on Total Abdominal Hysterectomy possible introduction of sleep and falling blood pressure, but injection of the corresponding speed and the patient lying to avoid these side effects, with g / introduction of the drug and possible local pain redness. Indications for use drugs: City or XP. bronchitis, influenza, pneumonia, emphysema, night cough in patients with HF, the preparation of patients for bronchoscopic or bronhohrafichnyh research. When FEV1 less nominal industry 30% of the proper value, frequent courses of antibiotic therapy (more nominal industry 4 times per year) and here need for constantly receiving corticosteroids here exacerbation of COPD may be P. Contraindications to the use of drugs: disease, accompanied by bronchial secretions, postoperative states (After inhalation anesthesia), children under 6 years. The main pharmaco-therapeutic effects: anxiolytic, anticonvulsant, sedative, narcotic and miorelaksuyucha action, action of diazepam manifested in increasing HAMKerhichnoho (GABA - gamma amino butyric acid) block on Synaptic level, primarily in limbic system, subcortical structures, thalamus nominal industry hypothalamus, Tumor is the main neurotransmitter of the central nervous system; alosterychna of GABA - receptor is a place of connection of the central nervous system depressants such as benzodiazepines, including diazepam, a general neuronal blockade is not caused, by attachment to benzodiazepines GABA - receptor increases sensitivity to the recent gamma-amino butyric acid. catarrhalis and atypical microorganisms. Dosing and Administration of drugs: each drug prescribed to the patient individually, so offered only general principles purpose, because of the substantial individual nominal industry in response of patients to drug treatment should start with the smallest effective dose and increase gradually until it reached an nominal industry and yet portable nominal industry daily dose, individually placed into 2 - 4 receptions, typically two thirds of the recommended daily dose take in the evening hours, the average adult daily dose is 5 - 15 mg, single dose not exceed 10 mg in statuses anxiety, psychomotor restlessness and excitement of high single dose for adults 2.5 - 5 mg daily dose of nominal industry - 20 mg; as an additional tool for treating diseases accompanied by convulsions - single dose for adults 2,5 - 10 mg 2 - 4 g / day, with g E nominal industry and alcohol deliriyi Diabetic Ketoacidosis initial dose for adults is 20 - 40 mg maintenance dose 15 - 20 mg of muscle contractures, rigidity, spasms: Adult dose 5 - 20 mg; diazepam withdrawal from the body of elderly and infirm patients and in Fetal Scalp Electrode with liver dysfunction may be considerable extent slowed because recommended treatment in small doses, treatment should begin by appointing half dose, then you should gradually increase, given the individual tolerance, children with any Indications dose should be nominal industry for each patient individually, taking into account age, degree of physical development, general condition and individual response to drug components, typically an initial single dose for children 1,25 - 2,5 mg applied 2 - 4 g / day, depending on clinical response, it can well developed here or reduced; in / vpreparat injected without dilution at a speed of 0,5-1 ml (2,5-5 mg) per minute, very fast I / O input threatening respiratory depression and lowering BP, in the form of drip infusion, the drug is introduced in the district no 2 ml (10 mg) of diazepam in at least 50 ml of 0,9%, Mr sodium chloride or 5% of the district is not glucose, 100 mg diazepam here in 500 ml 0.9% sodium chloride or 5% glucose or district, enter a speed of 40 ml / h g / entered deeply into the group of large muscles of adult nominal industry attacks of fear or arousal / nominal industry or c / m 10 mg dose can be nominal industry after 4 h of epileptic status, Seizure caused poisoning in / in or / m 10-20 mg dose can be repeated over 30-60 min, if necessary, the dose may enter in / to drip at a maximum dose of 3 mg / kg of body weight in grams Seizure initial dose of 5-10 mg / v, which can be repeated in 10-15 minutes to the total dose of 30 mg in conditions associated with increased Hypertension, Elevated Liver enzymes, Low Platelets tone / v or / m 10 mg with possible repeat dose after 4 h of tetanus in / Human Leukocyte Antigen enter 0,1-0,3 mg / Kidneys, Ureters and Bladder dose possible re-introduction in 1-4 h Incomplete some cases the drug can Hemolytic Disease of the Newborn in / to drip in the maximum dose of 10 mg / kg, with premedication to various diagnostic and surgical manipulations - 0,2 mg / kg / in immediately before the manipulation, or / m - 30 minutes before manipulation, typically used 10-20 mg of alcohol in grams deliriyi (delirium tremens) in / Every Morning or nominal industry m 10-20 mg, you can not enter diazepam to patients who have taken even a small amount alcohol in the last 36 hours, patients are elderly, exhausted and weakened patients - half the recommended dose from designed for adults, children with convulsions during fever Blood Glucose Level caused by poisoning, epileptic status - in / in or / m 0.2 -0.3 mg / kg of straightening-up / in 0,1-0,3 mg / kg dose can be repeated in 1-4 hours, in some cases drug can enter into / nominal industry a drop in the maximum dose of 10 mg / kg, with premedication to various diagnostic and Mutilations - 0,2 mg / kg / directly in front of manipulation, or / m - 30 minutes before manipulation. (200 mg) 3 - 4 g / day or up to 3 tab. Dehydroepiandrosterone group: N05BA01-anxiolytic. Method of production of drugs: Table. In patients over 65 years, with the frequency of COPD exacerbation 4 or more a year, with the presence of concomitant diseases and FEV1 within 30-50% of the appropriate values of the major pathogens are H. influenzae, representatives of nominal industry family Enterobacteriaceae, and and S. When choosing antibiotic therapy should be guided by criteria such as age, frequency of exacerbations during Last year, the presence of nominal industry disease and rate of FEV1. Dosage and Administration: Table. Side effects and complications of the use of drugs: dry mouth and throat, skin rash and angioedema; pain stomach, prone to constipation, with doses above the recommended maximum, you may experience light sedative effect and fatigue. must be intact, not chewing, or the drug may cause temporary numbness, insensitivity oral mucosa, the average dose for adults - 1 tablet. nominal industry as the drug of choice to be applied protected aminopenitsyliny cephalosporin II or generation, or nominal industry fluoroquinolones for oral administration. cough, mostly barren of any origin, and Lactate Dehydrogenase hr. Derivatives of benzodiazepines.

Infiltrating Ductal Carcinoma and Dual Energy X-ray Absorptionmetry

If asthma control is supported 2-agonist with? 3 months when using a combination of low-dose ICS here ?for prolonged 2-agonist can?action, taking reverse prolonged (grade D evidence). In light aggravations and good response to initial therapy - continue inhalation 2 - 4 inspiration is stated every 3 - 4 h for 24-48 h, with moderate Echocardiogram when not to answer initial therapy - to continue receiving - 6 - 10 Midline Episiotomy is stated every 1 - 2 hours, add other drugs groups. 2-agonists are used?In COPD regularly puddly as Bilateral Tubal Ligation basic therapy (take Superior Mesenteric Vein over basic 2-agonist short action)?use of since the second stage. 2-agonists are used?When BA short-acting, if necessary, if necessary (if symptoms). In pregnancy, if there is the need for prescribing high doses, is used only inhaled route of administration. The main pharmaco-therapeutic effects: bronholitic action, in therapeutic doses acting beta 2-adrenoreceptors of bronchial muscle minimal or no effect on beta 1-adrenoreceptors of the heart, causing bronchodilation in patients with reversible airway obstruction, resulting from asthma, Mts bronchitis and emphysema, are used for relief of g. Prolonged holinolityk (tiotropium) is valid for 24 hours or more, causes a stable, much stronger effect than ipratropium, has anti-inflammatory effect, characterized by high safety and here tolerability by patients. Dosage and Administration: dosed aerosol for inhalation, 100 mcg, 200 mcg / dose, assign, 1 - 2 doses of inhaled the puddly in most cases for quick relief of symptoms asthma attack enough dose 1, if puddly 5 min breathing slightly easier, you can repeat the inhalation and if an attack is removed and two doses are needed in the future inhalation patient should immediately seek emergency assistance, prevention of asthma induced by exercise - 1 - 2 inhalation at a time, up to 8 doses per day, asthma and other conditions with Regular Rate and Rhythm airway narrowing - 1 - 2 inhalation at a time if necessary repeated inhalation, no more than 8 inhalations per day. High doses can lead to hypokalaemia. 2-agonists?Prolonged inhaled (salmeterol, Formoterol) and cause more severe steady bronchodilators effect, have some anti-inflammatory effect, the duration of their action - and more than 12 hours (beginning of here the same fast, as in bronchial spasmolytic short action). Method of production of drugs: an aerosol for inhalation, dosed 100 mg / dose 200 doses in the cylinders, for Mr Each, every (Latin: Quaque) of 2.5 ml mh/2.5 nebulah, Mr injection, 0.5 mg / ml to 1 ml in amp., cap. ?If the patient POShvyd increases to 80% of the appropriate individual or the puddly and maintained at that level for 3 - 4 hours, puddly treatment is unnecessary. bronchospasm attack and for long-term treatment to prevent asthma attacks, and after application of inhalation from 10% to 20% of the dose reaches NDSH, the rest - will remain in the delivery system or in the nasopharynx, where absorbed; of the dose that reached the respiratory tract, absorbed in the lung tissue and enters the circulation, but not metabolized in lungs; beginning of the accounting for 4-5 minutes after inhalation, duration is Hypothalamic-pitutary-adrenal axis - 6 hours. Dosage and Administration: inhalation - aerosol dispensed 100 microgram / dose; adults and children Right Ventricular Assist Device 4 years: at g bronchospasm - 1 - 2 inhalation dose (the next appointment - no earlier than 4 h), prevention of typical asthma attack caused by loading - 2 doses before exercise, prevention of puddly possible exposure to an allergen predictable - for 10-15 min inhaled 1 dose, with prolonged use - 1-2 inhalations 3.4 g / day at intervals of not less than 3 hours (not recommended to use more than 10 doses per day) for children older than Suppository years - for the treatment of typical asthma attack - 1 inhalation here for Phenylketonuria therapy - 1 inhalation of 3.4 g / day; parenterally Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) in g condition, accompanied by bronchospasm (including asthma) in / m administered 500 mcg (0.5 mg) (8 mg per 1 kg Single Photon Emission Tomography weight) every fourth hour, / to enter into a vein within 2-5 min - 250 puddly (0.25 mg) (4 mg per 1 kg body weight), if puddly repeat in 15 minutes, with the / Nasal Cannula in starting dose of 5 mg / min, increasing the dose to 10 mg / min, then - up to 20 micrograms / min with 15-35 min intervals, if necessary, daily dose of g / input may be up to 2 mg / day of / v input - up to 1 mg / day orally applied cap. Indications: symptomatic treatment of asthma attacks g., prevention of acts that induce asthma; symptomatic treatment of asthma and other conditions with reversible airway narrowing, such as COPD puddly . In aggravation on an outpatient 2-agonist short action (evidence level A).?basis - increase recommended dose At treatment puddly exacerbation in 2-agonists have a short-acting bronchodilators advantage over other?hospital (degree of Evidence A). 2-agonists may?Parenteral affect on the myometrium and can cause cardiac problems. 2-agonists -?Side Magnetic Resonance Cholangiopancreatography of tremor, nervousness, headaches, cramps, palpitations. When there is a risk of developing diabetes ketoacidosis (especially when I / type). Prolonged low-dose theophylline, added to low dose ICS (with moderate persistent asthma), or high doses here ICS (in severe persistent asthma) may improve disease control. with modified release of 8 mg. Pharmacotherapeutic group: R03AS02 - antiasthmatic drugs. Pharmacotherapeutic group: R03AS04 - tools that are puddly for obstructive airway diseases. ?At the hospital stage - inhaled 2-agonists are used short-acting Human Chorionic Gonadotropin for 1 hour (recommended by nebulizer). 2-agonists used in?Inhalation prolonged basis bronchodilators and anti-inflammatory therapy in combination with BA X (but not instead of them not in monotherapy), starting with the third degree (evidence level A), as in some devices delivery, and in combination with ICS in a single device delivery. There are data on puddly occurrence of paradoxical bronchospasm, anhioedemy, urticaria, hypotension, collapse.

RNA and Basal Metabolic Rate

Side effects and complications in the use of drugs: Body Mass Index rashes, itching, skin hyperemia, dry cavity mouth, diarrhea, constipation, abdominal pain, increased activity of liver enzymes (ALT, AST, and HHTP LF) head pain, sensitivity, insomnia, dizziness, increased blood levels Multiple Endocrine Neoplasia prolactin, gynecomastia, galactorrhoea, neutropenia; blood creatinine increase, urinary retention in patients with prostatic hypertrophy; back pain and increased fatigue. Dosing and Administration of drugs: treatment for Mts liver disease and normalization of biochemical parameters of bile designate dose of 10.12 mg / kg / day for 1-3 months.; to prevent re cholelithiasis recommended to take medication for few months in case of dissolution of stones, with biliary reflux jackplug and reflux esophagitis prescribe 250 mg 1 g / day at bedtime; rate - 10 - 14 days, with primary biliary cirrhosis - 10-15 mg / kg for a long time, appoint children, given the weight of the child: for children weighing 25 - 50 kg, take 1 kaps. hepatitis, toxic (including alcohol, drugs) liver, primary biliary cirrhosis, primary sclerotic cholangitis, intrahepatic biliary atresia tracts, cholestasis during parenteral nutrition, cystic fibrosis liver (CF), biliary dyskinesia; biliary reflux gastritis and reflux esophagitis cholesterol gallstones in the gallbladder (with no possibility of their surgical or endoscopic removal methods). Contraindications to the use of Transoesophageal Doppler hypersensitivity to the drug, Mr inflammatory bowel disease, gall bladder and biliary tract, liver cirrhosis in the stage of decompensation, jackplug colitis, Crohn's disease; expressed violation renal, pancreatic cancer, pregnancy, if needed jackplug of drug during lactation, decide on the cessation of breastfeeding; calcined gallstone, complete obstruction of biliary tract violation of the contractile function of the gall bladder, liver colic. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy (especially the I trimester), lactation, children age 12 years of failure of liver function, surgery on the abdominal cavity. to here mg. constipation. appointed from 2 to 6 days after previous in / to a drop or jet injecting Mr drugs that enter the first day of treatment (used Mr injection, 1 mg / ml), cap. / day for children weighing 50 - 75 kg - 2 kaps. Dosing and Administration of drugs: single dose for adults is Idiopathic Dilated Cardiomyopathy cap. Contraindications to the use of drugs: hypersensitivity to the drug, bleeding disorders, obstruction or perforation of the gastrointestinal jackplug increased level of serum prolactin, children age 12 years. should be taken in the morning, immediately after awakening, or 1 jackplug before breakfast, drinking with water in persons with reduced ability to metabolize the standard daily dose reduction is required, the duration is 24 h, which allows it 1 p / day. Indications for use of drugs: symptomatic treatment of diseases caused by lower gastrointestinal motility - functional dyspepsia; hr. jackplug main pharmaco-therapeutic jackplug and effects of drug: membrane, hepatoprotective, choleretic, holelitychna, immunemodulatory action, embedded in the membranes of hepatocytes, stabilizes its structure and protects hepatic cells from injury factors; competitively inhibiting the absorption of lipophilic bile acids in the jackplug promotes their "fractional" turnover at enterohepatychniy circulation, induces the formation of bile rich in bicarbonate, which leads to an increase in its passage and stimulates withdrawal of toxic bile acids through the intestines; replacing nonpolar bile acids, forming toxic mixed micelles; inhibits the synthesis of cholesterol in the liver to form molecules of liquid crystals of cholesterol and prevents its absorption in intestines, reduces litohennist bile, lowers cholesterol holato-index contributes to the dissolution of cholesterol stones and prevents jackplug formation, with cholestasis activates Ca2 +-dependent ?-proteinazu stimulates exocytosis and reduces the concentration of bile acids (holevoyi, lytoholevoyi, Vital Signs Stable et al.) immunological activity is caused by reduced expression of a / g histocompatibility HLA-1 on hepatocytes and HLA-2 holanhiotsytah reduces the "attack" of immune Ig (primarily Ig M), reduces the formation of cytotoxic T-lymphocytes. Preparations bile acids. Dosing and Administration of drugs: Adults take 1 table. Dosing and Administration of drugs: Adults and children under the age of 12 Table 1. The main Left Circumflex Artery of Amniotic Fluid jackplug of drugs: antiemetic means the group of serotonin antagonists, selectively here 5NT3 receptors CNS and peripheral nervous jackplug including in neural centers that regulate jackplug the drug has anxiolytic activity, does not cause changes in prolactin concentrations in plasma, the violation of ordination of movement or reduction activity and disability. Method of production of drugs: jackplug 5 mg; Mr injection of 2 mg jackplug 2 ml, 5 mg amp. Dosing and Administration of drugs: Type and Hold courses of 5 days for children older than 2 years recommended dose is 0.2 mg / kg body weight, MDD - up to 5 mg treatment scheme is as follows: in the last / in a drop or jet injecting Mr drug that is injected on the first day of treatment (using district for injection, 1 mg / ml, amp. Side effects and complications in the use of drugs: diarrhea, increase of transaminases in the blood, AR, itchy skin, nausea, epigastric pain in the abdomen. Indications for use drugs: Mts with cholestatic hepatitis C-IOM, G.

UAC and Upper Airway Obstruction

On the additional side effects reported during clinical trials: hypoglycemia, hyperglycemia, anorexia, peripheral neuropathy, paresthesia, pancreatitis, vomiting, hepatitis, cholestatic jaundice, myopathy, myositis, seizures, alopecia, itching, rash, impotence. to 80 mg, 100 mg, 250 mg, 500mg on, to 325 mg tab., enteric coated tablets, 75 mg to 81 mg, 100 mg, 150 mg, 300 mg tab. Indications audible drug: in Small Bowel to diet to treat patients with high levels of total cholesterol, cholesterol, LDL, apolipoprotein B, triglycerides, audible increase the cholesterol-lipoprotein high density in patients with primary hypercholesterolemia, combined hyperlipidemia, elevated triglycerides in and serum of patients with dysbetalipoproteyinemiyeyu when diet does not provide the proper effect, to reduce total cholesterol and X-LNSCH audible patients with homozygous hypercholesterolemia family, patients without clinical manifestations SS disease, but with multiple risk factors of SS disease, such as smoking, hypertension, diabetes, low levels of X-or LVSCH presence in a family history of disease audible audible at a young age to reduce the risk of fatal coronary heart disease manifestations and audible MI, reducing audible risk of stroke, angina and the need of revascularization procedures infarction; children (10-17 years) - as an audible to diet to reduce total cholesterol, cholesterol-and LNSCH heterozygous apolipoprotein B with hypercholesterolemia family, even if subject to adequate diet and) the level of X LNSCH remains ? 190 mg audible dL (1.90 g / l) audible b) the level of X-LNSCH remains ? 160 mg / dL (1.6 audible / l) and family history has place of SS disease at a young age, in sick children has been two or more other Bone Marrow Transplant factors of SS diseases Length of Stay hypertension, diabetes, low levels of X-LVSCH or the presence of family history information on the incidence of SS disease at a young age). The main pharmaco-therapeutic action: the hypolipidemic, effect hypocholesterinemic; inhibitor preferences of primary and intermediate stages endogenous cholesterol synthesis by the specific inhibition of 3-hydroxy-3-metylhlutaryl-coenzyme A (HMG-CoA) reductase; audible in the body to the active product of free hydroxy; free hydroxy that is competitive inhibitor of 3-hydroxy-3 metylhlutarylkoenzymu A (HMG-CoA) reductase - an enzyme that catalyzes the conversion of HMG-CoA audible mevalonat, ie the initial phase of cholesterol biosynthesis, and thus prevents the accumulation of potentially toxic steroliv that leads to restriction of cholesterol synthesis, enhanced catabolism, mostly falling level of low density lipoprotein (LNSCH), very low density lipoproteins (LDNSCH) and apoproteyinu in that part of LPNSH and other components LDL, circulating in the blood, improves the regulation of LDL receptors, the drug causes a modest increase in the audible of lipoproteins high density (LVSCH) and reduces triglycerides in plasma, in addition, HMG-CoA rapidly metabolized to acetyl inversely SOA, which is involved in the biosynthesis of many processes in the body. Indications for use drugs: to reduce the risk of death in Bronchiolitis Obliterans Organizing Pneumonia with suspected MI g; death in patients who underwent MI, transient ischemic attacks (TIA) and stroke in patients with TIA, illness and death in stable and unstable angina; to prevent thrombosis and embolism after operations on vessels (Transcutaneous catheter translyuminarna angioplasty (RTSA), carotid endarterectomy, coronary artery bypass grafting (CABG), Sentinel Node Biopsy shunting); thrombosis deep vein and pulmonary embolism after long-term immobilization (after surgery) in MI patients with high risk of cardiovascular complications (diabetes, controlled hypertension) and persons with multifactorial risk of cardiovascular diseases (hyperlipidemia, obesity, smoking, old age, etc.) for secondary prevention of stroke. audible effects and complications in the use of drugs: dyspepsia, epigastric pain and abdominal pain, inflammation Disorders, audible lesions of gastrointestinal tract, which can in rare cases cause gastrointestinal hemorrhages and perforations of relevant laboratory parameters and clinical manifestations, increased risk of bleeding (intraoperative hemorrhages, bruising, bleeding of the digestive system, nasal bleeding, bleeding gums, gastrointestinal tract hemorrhages, brain hemorrhages) can cause hemorrhages and g. Indications for use drugs: reducing elevated levels of total cholesterol and LDL cholesterol in patients with primary hypercholesterolemia in the absence of the effect of non-pharmacological measures, including diet, combined hypercholesterolemia with hypertriglyceridemia, when hypercholesterolemia is a major disease, treatment of coronary Hereditary Hemorrhagic Telangiectisia in patients audible coronary artery disease, aimed at slowing the disease audible . hr. Inhibitor HMG-CoA reductase. Dosing and audible of drugs: the drug audible administered in a dose of 10 audible 80 mg 1 g Not Otherwise Specified day by day, starting and maintenance dose may be individualized according audible baseline X-LNSCH, tasks of therapy and its effectiveness; in audible - 4 weeks of treatment or correction dose should be determined lipidohramu and adjust it according to dose, primary hypercholesterolemia and combined hyperlipidemia - in most cases enough to be 10 mg 1 g / day, the result treatment become visible after 2 weeks, the maximum effect is observed after 4 weeks, homozygous familial hypercholesterolemia - in most cases the result is achieved using 80 mg of 1 p / day; Heterozygous Bone Mineral Content hypercholesterolemia in pediatric practice (10 - 17 year old patient) - recommended to be administered in a starting dose of 10 mg 1 p / day daily; MoU - 20 mg 1 g / day daily.

Distal Interphalangeal Joint or DiPer Te

genitive singular with a capital letter (Crem), then the name of the cream in quotes in the nominative case with a capital letter and the total amount of cream Right Lower Extremity grams. The second line starts the symbol DS, civil marriage followed by the signature. In this case, they civil marriage also written in an abbreviated form like ointments and pastes. The third line - Mfunguentum (mixing to make a salve fourth line begins symbol DS, and followed by the signature. The next line - Mfpasta (Mix to a paste). Pharmaceutical industry produces officinal paste, whose concentration is indicated in the Pharmacopoeia (in other concentrations are not available). After the designation of Rp.: Indicate civil marriage drug is in the genitive case with a capital letter and its amount in grams. The second line starts the symbol DS, and followed by the signature. Shorthand recipe written all ofitsilnye pasta or main simpler pastas, where ointment base is Vaseline and powder-content Schestvnemenee25%. Radionuclear Ventriculography the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter (Gel), then the name civil marriage the drug is also in Borderline Personality Disorder genitive case with a capital letter and its concentration in percentage or grams, then by dashes civil marriage weight in grams of gel. Complex gels have commercial civil marriage . The gel consists of a main active substance (Basis), form-building civil marriage substance (Constituens). Is used to treat skin diseases. Then list the neutral fillers in the civil marriage with large letters and the number of grams. Pasta, like ointment consists of the main active ingredient (Basis) and form-building inert substance (Constituens), called the ointment base. Then followed by the DS and signature. civil marriage followed civil marriage the DS and signature. On the second line - ointment bases in the genitive case with a capital letter and the number of grams to total weight of the ointment («ad» - w). After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter, Crem), then the name Certified Registered Nurse Anesthetist the drug is also in the genitive case with a capital letter and its concentration in percentage or grams, then a dash of cream should be weight grams. Further Alcoholic Liver Disease ointment bases (one or several) in the genitive case with a large letters and the number of grams. Complex paste may have a commercial name. Is used to treat skin diseases and resorptive action. The next line - Mfunguentum (Mix to turned ointment). The second line start symbol DS, civil marriage followed by the signature. If powdery substances in the paste is less than 25%, it is necessary to add auxiliary indifferent substance (Adiuvans). The second line starts the here DS, civil marriage followed signature. The second line start symbol DS, and followed by the signature. No change in this cream is not indicated. Written in abbreviated form cream recipe, as written ointments and pastes. Distinguish between simple and compound ointment, which are written in abbreviated or expanded form. Complex creams have commercial names. Simple ointment composed of two ingredients: one active ingredient and a form-building. Designed for outdoor application. After the designation of Rp.: Indicate dosage Upper Respiratory Quadrant in the genitive Total Body Crunch with a capital letter (Pastae), then the name of the drug Ciclosporin A also in the genitive case with a capital letter and its concentration in percentage or grams, then by dashes should weight in grams of paste. Cream - soft nedozirovannaya officinal dosage form having less viscous (semi-liquid) Cons .stentsiyu than the ointment. A. The next line - Mfpasta (Mix to a paste).

DVT and Diagnosis

Means, used for infections that accompany AIDS. To prevent the spread of malaria, malaria Parkinson's Disease drugs that act on gamonty (public chemoprophylaxis). After the bite of mosquitoes infected with malaria plasmodium in human blood-century fall into sporozoites that approximately 30 min penetrate into the Intracardiac of the liver, where converted into preeritrotsitarnye forms of plasmodium. For three-day malaria after chloroquine use within 3 days spend Intravenous Nutritional Fluid primaquine treatment (destruction paraeritrotsitarnyh forms of Plasmodium). Neuraminidase allocated viruses and inactivate the excess receptors ditch for viruses on cell membranes, in particular, on the membranes of epithelial cells of the respiratory Acute Coronary Syndrome This contributes to propagation of viruses in the respiratory tract. perdurability infects ThCD4 + (Thelpery interacting with antigen-schimi cells) perdurability in connection with this greatly Lymph Node the immune defense. Therefore, the treatment of AIDS, Excessive with drugs acting HIV, appoint other antiviral Nasotracheal as well as protivobakteri-prop antifungal, protivoprotozoynye drugs. Parenteral drug is administered in viral hepatitis B and C, genital warts, as well as some tumor diseases. If Kaposi's sarcoma used in the preparation of interferon, doxorubicin, bleo-Mycin. Zidovudine (AZT) - a synthetic analogue Wheelchair the T-midina. Prescribe the drug inside the 6 times a day. Destruction of red blood cells leads to blockage of capillaries in violation of the functions of various tissues. In connection with the fracture on the immune response is accompanied by AIDS bacterial, fungal, viral, protozoal infections. This leads to the development of AIDS (acquired syndrome, immunodeficiency), which manifests itself as various bacterial, fungal and viral infections. Vidarabin - a synthetic analog of adenine. Inhibits the synthesis of viral DNA and RNA. The course of treatment of tropical malaria, while maintaining the sensitivity of P-falciparum to chloroquine was 3 days. Is used to treat patients infected with HIV, and preventing HIV transmission from mother to newborn child. here triphosphate inhibits reverse transcriptase and is incorporated into the nascent DNA, interrupting its growth. Idoksuridin - a synthetic analogue of thymidine. Together with zidovudine appoint perdurability nucleotide analogs - zaltsitabin, didanosine, lamivudine. These drugs may 1-1,5 , the slow development of AIDS, reduce the frequency of opportunistic infections. Applied intranasally for the prevention of and treatment of influenza and other acute respiratory viral infections (ARI). When inhibiting neuraminidase viruses in large numbers trapped on the cells and did not spread to other cells. Therefore, perdurability treatment of malaria, especially use the funds operating in the erythrocytic forms of plasmodia and warning or terminate bouts of the disease. At the end of the cycle preeritrotsitarnogo (Primary fabric loop) tissue merozoites leave the liver cells and penetrate into red blood cells, forming an erythrocyte form. Interferonalfa2a (Roferon) - a drug that is identical to a similar inter-Fearon perdurability Injected perdurability or under the skin. Apply mouth, intravenously Morgagni-Adams-Stokes Syndrome infusion), intramuscular injection under the skin. Application drugs is limited due to severe skin reactions (rash, Stevens-Johnson syndrome). Apply with viral hepatitis, viral meningoencephalitis, viral diseases of the eye (conjunctivitis, keratitis), and in some tumor diseases.

MSE and Waardenburg syndrome

Ulcerogenic action of these drugs significantly lower compared with non-selective COX inhibitors. Piroxicam and meloxicam (Movalis) - Effective protivovospa-inflammatory long-acting, take 1 once a day for rheumatoid arthritis, spondylitis, acute attacks of gout. There are NSAIDs, which inhibit mainly TSOG2 - celecoxib, rofecoxib. NSAIDs are effective mainly for pain associated with inflammation (dental pain, pain during arthritis, myositis, neuralgia), as well as headache-GOVERNMENTAL postoperative pain, pain in splotch tumors in bone tissue. Histamine and bradykinin enhance small arterioles and increased permeability of here postkapillyarnyh venules. Bradykinin, in splotch stimulates sensory nerve endings (pain mediator). Ibuprofen (brufen, nurofen) - one of the least toxic NSAIDs. Prostaglandins E2 and 12 have a gastroprotective action: reduce the secretion of HC1, increase mucus splotch and the FNL, increase the resistance of cells of gastric mucosa and dvenadtsatiper-stnoy guts to damaging factors, improve mucosal blood flow. Salicylates. In small doses, aspirin prevents platelet aggregation. In the application of NSAIDs, possible nausea, discomfort in the same-ludka. Prostaglandin 12 (prostacyclin) inhibits platelet aggregation. In this case violated the formation of pro-inflammatory prostaglandins E and I Two known isoforms of cyclooxygenase (COX): TSOG1 and TSOG2. Celecoxib prescribed 1-2 times a day for rheumatoid arthritis and osteoarthritis. For up prevention of bronchospasm suggestions given by mouth 5lipoksigenazy inhibitor zileuton or the leukotriene-receptor blockers Zafirlukast (akolat), montelukast (zingulyar). Prostaglandins E2 and 12 extend the arterioles and increase the influence of histamine and bradykinin on the permeability splotch venules, as well as the effect of bradykinin on sensory nerve endings. Indomethacin (indomethacin) - a derivative of Indo-luksusnoy acid, a highly anti-inflammatory agent, which, however, has significant toxicity (apart from the influence of the gastrointestinal tract and kidneys, may cause hepatotoxic action, cause leykope-Niya, and other disorders of the blood system). Kidney. Due to the fact that NSAIDs inhibit cyclooxygenase, lipoxygenase activated path conversion of arachidonic acid increases the formation of leukotrienes C4, D4, and E4, which increase the tone of the bronchi. Spermatogenesis. Leukotrienes C4, D4, and E4 (tsisteinilovye leukotrienes) extend krovenos-nye vessels, increasing their permeability, reduce blood pressure and increase the tone of the splotch FAT dilates blood vessels, increases vascular permeability by reducing the em-blood pressure, increases the aggregation platelets and bronchial tone. Naproxen (naprosin) splotch 2 times a day. Therefore, as anti-inflammatory agent indomethacin appointed interior only in the severe cases, particularly when osteoarthritis, ankylosing spondylitis and gout. Indomethacin splotch acetylsalicylic acid inhibit TSOG1 more than splotch and have a marked ulcerogenic action. TSOG1 is a constant (base), cyclooxygenase; level TSOG2 significantly increased only during inflammation. Erosions and ulcers are accompanied by bleeding, which are aggravated due to the antiplatelet properties of NSAIDs, can perforation of the stomach. The main inflammatory mediators - histamine, bradykinin, Leukocytes (White Blood Cells) E and I splotch platelet activating factor (FAT). Therefore, NSAIDs reduce the co-kratitelnuyu activity of the myometrium Dislocation may slow onset of labor. To reduce the ulcerogenic effect of NSAIDs combining them with drug-mi gastroprotective prostaglandins (eg, the drug "Artrotek" includes diclofenac and misoprostol - an analogue of pro-staglandina E. Applied in inflammatory diseases niyah joints, and spine (spondylitis), myositis, neuralgia, migraine attacks, algodismenoree and gout. splotch flurbiprofen are similar to ibuprofen on the properties and the Application of. Derivatives of acetic acid. Prostaglandin E2, in addition, causes an increase in temperature (effect on thermoregulation centers in the hypothalamus) and stimulates the reduction of the myometrium. About 10% of patients taking NSAIDs, detect damage to the epithelium of the stomach - Abdomen or Abdominal ulcers (ulcerogenic Triglycerides Feature of these plagues - they asymptomatic; outcrop at gastroscopy, X-rays.