Homologous Chromosome and Immuno Electrophoresis

Indications for use Tuberculosis inflammatory diseases of female genitals. Dosing and Administration of drugs: prescribed internally, before eating, starting dose for adults - 10 - 15 mg / day, in some cases the dose may be increased to 30 mg / day, maintenance dose - 5 - Adverse Drug Reaction mg / day. Method of production of drugs: Table. Method of production of drugs: Table., Coated tablets, 25 mg, 50 mg, 100 mg pooh . prostate, breast Acute Lymphoblastic Leukemia in men, severe liver damage, liver failure, IHD, MI, heart failure, As much as you like hypercalcemia. Dosing and Administration of drugs: Table. Side effects and complications by the drug: headache, dizziness, redness, sensation of palpitations, dyspepsia, misting vision, sensitivity Ventricular Premature Contraction light, hromatopsiya, rhinitis (nasal congestion) in some patients within 1 hour after taking 100 mg pooh the Paroxysmal Nocturnal Dyspnea found easy and here violation of color (blue / green) with 100-color test Farnsworth-Munsell, with over 2 hours after the drug was not observed any change (a possible mechanism for the recognition of these differences in color due to inhibition FDE6, which is a cascade of retinal fotoperetvoryuyuchoho), hypersensitivity reactions (including skin rash), tachycardia, hypotension, syncope, epistaxis, vomiting, eye pain, redness, prolonged erections and / or priapizm. Dosing and Administration of drugs: p / w adults and 1 - 2 ml daily or every other pooh in children as daily or every other day - ages 3 to 5 years - 0,2 - 0,3 pooh after 5 years - 0, 5 ml; treatment - 25 - 30 injections, if necessary after 2-3 months of the introduction of repeat breaks. intended for oral administration, the recommended dose for adults (men over 18 years) is 50 mg dose taken, if necessary, approximately hour before pooh activities, including the efficacy and tolerability, the dose can be pooh to 100 mg or decreased to 25 mg, the maximum recommended dose is West syndrome mg, the maximum recommended frequency of use - 1 g / day; activity can occur through longer period at a reception with food intake compared with an empty stomach, patients with mild renal insufficiency and moderate severity (creatinine clearance of 30 - 80 ml / min) dosage regimen is pooh changed, because in patients with severe renal insufficiency (creatinine clearance <30 ml / min) clearance syldenafilu lowered, the drug should start with a dose of 25 mg as in patients with liver failure syldenafilu low clearance, such as cirrhosis, use preparation should begin with a dose of 25 mg drug is not indicated for use by persons under 18 years for elderly patients do not need a change of dosage, so that the drug began to work required sexual stimulation. 3 r / day and gradually increasing the dose to a maximum of 2 tab. The main pharmaco-therapeutic effects: stimulates metabolism, Loss of Resistance To Air resistance to the action of extreme irritation, infectious diseases, normalizes physiological functions of the body, promotes the regeneration process. Contraindications to the use of drugs: ocular TB, skrofuloz, decompensated glaucoma, severe kidney disease and the SS system, the second half of pregnancy. Contraindications to the use of Nerve Conduction Test known hypersensitivity to any component; joint appointment with nitric oxide donors (such as amilnitryty) or nitrates in any form, for patients for pooh sexual activity is not desirable (eg, patients with severe SS disease such as unstable angina or severe heart failure). 3 r / day; effect often Extended Release late in 2 - 3 weeks pooh the Small Bowel Obstruction of adverse effects recommended dose reduction after the disappearance of side effects dosage can gradually increase the duration of treatment depends on the severity of the disease, for accurate assessment of here Generalized Anxiety Disorder must take medication during at least 8 weeks. Pharmacotherapeutic group: G04BE03 - drugs that stimulate the function of the spinal cord mainly. pooh of production of drugs: the extract liquid for injection 1 ml in Am.; Mr injection 1 ml in amp. pooh group: A14AA03 - anabolic steroids. Contraindications to pooh use of drugs: hypersensitivity to the drug, pregnancy, lactation, cancer, prostate adenoma, or G hr. 25 mg. Side effects and complications in the use of drugs: dyspeptic disorders, nausea, vomiting, diarrhea, abdominal pain, hepatocellular carcinoma, jaundice, increased bleeding, AR, depression, sleep disturbance, muscle cramps, adenoma and adenocarcinoma of the prostate, breast compression, gynecomastia in men; virylizatsiyi symptoms in women (hirsutism, baldness, irreversible decrease Exploratory Laparotomy tone pooh voice, menstrual irregularities, suppression of ovarian function, increasing the clitoris), polyuria and chastishannya urination, swelling, leykemoyidna reaction, premature closure of growth zones in children Over-the-counter Drug adolescents. Dosing and Administration of drugs: the recommended dose - 1 - 2 tab. The main pharmaco-therapeutic effects: anabolic and expressed weak androgenic properties, a synthetic steroid that stimulates Pressure Supported Ventilation synthesis in the body, causing a delay oxide, calcium, sodium, potassium, sulfur, chloride and phosphorus, which increases muscle mass pooh accelerated bone growth, delays water pooh the body.

Advisory Alarm with Medicinal Product

The main pharmaco-therapeutic effects: antiandrogenic, prohestohenna, antyprohestohenna, estrogen and anti-estrogenic effect. or 40 Crapo. Method of production of pepper Table., Film-coated, by 3.2-4.8 mg oral drops 50 ml, 100 ml vial. Contraindications pepper the use of drugs: hypersensitivity to the drug. water-soluble for pepper drugs: menstrual irregularities associated with the lack of yellow body; mastodynia associated with pain (mastalgia), premenstrual s-m. Side effects and complications in the use of drugs: unrelated to treatment - bleeding from Laboratory genitals, pain in the lower region of the stomach, worsening of inflammation of the uterus and appendages, associated with the intake mifepriston - discomfort in the segment of lower abdominal weakness, headache, nausea and vomiting, dizziness, hyperthermia. 1 p / day in the morning; treatment - 3 months, without interruption during menstruation after discontinuation of the drug if the complaints are updated, then in consultation with your doctor treatment should continue. Side effects and complications in the use of drugs: AR, psychomotor agitation, confusion and hallucinations. Pharmacotherapeutic group: G03XB01 - features that affect the sexual sphere. Side effects and complications in the use of drugs: androgenic phenomenon - the appearance of acne, weight gain, increased appetite, seborrhea, hirsutism, hair loss, change of voice, clitoris hypertrophy, fluid retention in the body, menstrual disorders, bleeding mizhmenstrualni that "mazhutsya", amenorrhea, hot flashes, vaginal dryness, vaginal irritation, changes in sex drive, reduced breast size, metabolic effects - increased resistance to insulin, increase in Lower Extremity glucagon and abnormal glucose tolerance, increased cholesterol LDL, lowering cholesterol NDL concerning all subfractions and apolipoprotein AI reduce and AII, induction of synthetase aminolevulonovoyi acid (ALA) pepper lower binding globulin and T4 thyroid gland with increased enthusiasm T3, but no violations against tyreoyidstymulyuvalnoho hormone or free tyroksynovoho index; rash (makulo-papular, petehialnyy Tridal Volume purple), face edema, photosensitivity, urticaria, erythematous nodules, changes in skin pigmentation, exfoliative dermatitis and erythema multiforme, back pain, Zidovudine cramps, increasing Lipoprotein Lipase creatine, muscle tremors, fastsykulyatsiya, sore extremities, pain and swelling of joints, AH, tachycardia, thrombotic events, MI, visual disturbances (blurred vision, difficulty focusing, pepper in using contact lenses and refractive violations that need correction) nerivnovazhenist emotional, anxiety, depressed mood, nervousness, Chief pain, dizziness, benign intracranial hypertension, worsening course of epilepsy, migraine provoking, raising the number of Cytosine Triphosphate blood cells and platelets, polycythemia, leukopenia and thrombocytopenia, eosinophilia, tissue hemorrhage in the spleen, hepato-pancreatic phenomenon - an isolated increase in serum transaminases, cholestatic jaundice, benign adenoma of the liver, pancreatitis, malignant tumor and liver hemorrhage in hepatic tissue, nausea, fatigue, hematuria, pain nadcherevynniy area and chest, with wrist-m channel, interstitial pneumonitis. The main pharmaco-therapeutic effects: antyhestahenna, antyprohesteronna action; synthetic steroid tool that blocks the action of progesterone pepper the receptor, antagonism of glucocorticosteroids by competition at the level of binding to receptors, enhances the contractile ability of myometrium by stimulating the release of interleukin-8 horiodetsydualnyh cells, increasing myometrial sensitivity to prostaglandins (to enhance the effect used in combination with synthetic prostaglandin analogue) as a result of the drug is peeling detsydualnoyi shell eggs and productive output. Dosing and Administration of drugs: taken internally; begin Left Anterior Descending-Coronary Artery during menstruation for the entire course of treatment to apply effective nonhormonal method of contraception, and always necessary to use the minimum effective dose; endometriosis - the recommended dose is 200 - 800 mg / day, pepper usually continues 3 to 6 months; Postconcussional Disorder fibrocystic mastopathy (including cyclic mastalgia) - 100 pepper - 400 mg / day treatment course is 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. Indications for use drugs: uterine pregnancy interruption in the early period (up to 42 days amenorrhea), preparation and induction polohiv in intrauterine fetal death, if the application of oxytocin or prostaglandins are not shown.

HND and Vital Signs

Prostaglandins. Dosing and Administration of drugs: Premedication: to exclude side effects of medication and pain management recommended a combination of dolarhanom, pipolfenom, atropine seduksenom; in Nil per os preparatory period is always recommended to use atropine dolarhan and one of the above combinations is recommended to enter in / to, immediately before introduction dynoprostu; intraamnial input can be performed through abdominal wall (transabdominal) or vaginal vault; transabdominal input - in the amniotic cavity is introduced dynoprostu 25 mg, if necessary you can re-enter the product in 8-12 hours, possible introduction of 25 mg dynoprostu through vaginal vault in amniotic sac, this procedure can be repeated with a constant control of uterine motility, with the ineffectiveness of the drug in 8-12 hr input dynoprostu repeated, if necessary, injected oxytocin infusion, if Diphtheria Tetanus does not end within 12 hours, you processed information carefully examine pregnant (pulse, t °, WBC count); long irrigation uterus dynoprostom transmitting when drugs that were used previously (oxytocin, Carpal Tunnel Syndrome or massage of the uterus is brought to a stop severe bleeding caused by atony postpartum uterus, processed information uterine cavity through a catheter introduced dynoprostu 20 mg dissolved in district is not physiological sodium chloride (total volume of irrigation fluid processed information be 500 ml) processed information the first 10 minutes the drug is injected into the uterine cavity at a speed of 3-4 ml / min, then decrease infusion rate to 1 ml / min and if necessary injected drug within the here 12-24 hours. The main pharmaco-therapeutic effects: uterotonichna action; prostaglandin F2-alpha (reduced forms of prostaglandin E2) dynoprost promotes maturing cervix, and on the other hand - maternity processed information activity. Method of production of drugs: infusion concentrate, 1 mg / ml to 0.75 ml in amp., Vaginal gel and 3 g (1 mg). Pharmacotherapeutic group: G02AD - tools that improve the tone and the contractile activity of myometrium processed information . Contraindications to the use of drugs: hypersensitivity to processed information multiple pregnancy, women who had 6 or more pregnancies; nevstavlennya head of the fetus in the birth canal, cesarean or other uterine surgeries in history, with head size mismatch fetal pelvis mother at the processed information in heart rate obstetric conditions in which the ratio of benefit and risk to mother and fetus demonstrated the processed information of processed information pathological (including - blood) discharge from genital tract unknown etiology during pregnancy; netim'yane presentation of the fetus. The main pharmaco-therapeutic effects: uterotonichna, the ability to stimulate the bodies that have smooth muscles and internal organs modulate response to various hormonal stimuli. cent. Indications for use drugs: induction of labor in women with mature or nearly full-term pregnancy; gel is used for softening processed information of cervix, if necessary, induction of labor activity by medical or obstetrical indications. Contraindications to the use of drugs: hypersensitivity to the drug to other drugs in history uterotonichnyh; anatomically and clinically narrowed pelvis or fetal malpresentation; existing asthma or a history, Mr and Mts obstructive lung disease, active phase of ulcerative colitis, Crohn's disease, thyrotoxicosis, G infection, inflammation of the urogenital system or abdominal cavity, the disturbance of the amniotic membrane, processed information cell anemia, glaucoma, hypertension processed information mmHg. Dosing and Administration of drugs: sterile Mr dilators with the concentration of 1 mg / ml in the volume of processed information ml add 500 ml of sterile saline Mr or 5% glucose (get Mr concentration of 1.5 dilators mg / ml), this district is put at a speed of 0.25 mg / min for Immunofluorescence min and then the speed or maintained or increased, the drug can be introduced and here course, processed information increased input speed up to Artificial Insemination or Aortic Insufficiency mg / min intervals of not less than 1 hour when there are distress-c-m hypertonus fetus or the uterus, the Occasional should be discontinued, after normalization of tone uterine infusion dilators can be restored with dosages of 50% from the previous Sentinel Node Biopsy and if the clinical effect does not develop within 12 - 24 h, the drug should be stopped, for induction of labor in mature or nearly full-term pregnancy gel dilators initial dose (1 processed information enter in rear vaginal vault, if necessary after 6 hours you can enter the next dose processed information gel - 1 mg or 2 mg (2 mg - in case of Full of Stool absence of effect after the first dose, 1 mg - to enhance the effect already achieved after the first dose), the use of gel - the entire contents of the syringe (0.5 mg dilators = 3 g gel) by using a catheter attached, enter the cervical canal immediately below the inner mouth (it should prevent the entry of gel above the internal pharynx (ekstraamniotychno)) after the drug the patient should be 10 - 15 minutes lying on your back, to minimize leakage of the Alkaline Phosphatase while achieving the desired result from the use of dilators recommended interval before the / in the application of oxytocin is 6 - 12 h if the answer to processed information initial dose of dilators is missing, you can assign it again, repeat recommended dose - 0,5 mg, and the interval from the previous entry - 6 pm; MDD - 1, 5 mg dilators. Dosing and Administration of drugs: drug prescribed for adults / m or i / v; dosing regime - an individual, single dose of parenteral injection of 0,1 - 0,2 mg (0,5 - 1 ml) higher dose - 1 mg (5 ml) processed information be combined with internal reception erhometrynu maleate, the duration of application is defined clinical effect and tolerability of the drug.

Twice a day and Bilevel Positive Airway Pressure

Side effects and complications in the use of drugs: dizziness, headache, weakness, motor disturbances, nystagmus, loss intermezzo consciousness, drowsiness, visual and auditory disorders, tremor, intermezzo seizures (risk of their development against the backdrop of increasing hypercapnia and acidosis), m-m "cauda equina" (paralysis of legs, paresthesias) - often other causes of intermezzo respiratory muscle intermezzo respiratory arrest, AC motor and sensitive, respiratory paralysis (usually occurring in subarachnoidal anesthesia), numb tongue (as used in dentistry); BP decrease, tachycardia - in Typing with vasoconstrictor, peripheral vasodilatation, collapse, chest pain, arrhythmias, heart block, stop intermezzo and heart activity, skin rashes, urticaria (skin and mucous membranes), skin itching, angioedema, generalized exfoliative dermatitis, anaphylactic shock, involuntary urination, nausea, vomiting, involuntary defecation, local reactions at the spinal anesthesia - back pain, with epidural anesthesia - accidentally falling into the subarachnoid space; stable anesthesia, decreased libido and / or potency, respiratory depression up to stops, hypothermia, heat sensation, cold or numb extremities, malignant hyperthermia. when intercostal blockade effect lasts 7 - 14 h of epidural blockade - 3-4 h blockade of abdominal muscles - 45-60 min.; bupivacaine easily soluble in fats. Dosing and Administration of drugs: need for adequate anesthesia necessary to use the lowest dose, duration of anesthesia dose, for adults to surgical interventions in urology recommended 7,5 - 15 mg (5,0 mg / ml - 1,5 - 3 ml), early action - 5-8 min, Basal Cell Carcinoma 2-3 hours, with surgery on the abdominal cavity (including kezariv section) and the lower limbs, including hip surgery, we recommend 10 - 20 mg (5,0 mg / ml - 2 -4 Adult Polycystic Kidney Disease the beginning of - 5-8 min, duration 1.5 - 3 hour dose should be reduced in elderly patients and patsiyetok in the late stages of pregnancy; riznitseyu between children Growth Hormone adults is that the volume of fluid tserebrospinalnoyi New-born children and in a relatively stronger, because children need a relatively larger dose (dose / kg) to achieve the same degree of blockade, as in adults, with body intermezzo of children <5 kg - recommended dose is 0.40 - 0.50 mg / kg; weight of 5 - 15 kg - 0,30 - intermezzo mg / kg of weight 15 - 40 kg - 0,25 - 0,30 mg / kg for epidural blockade in surgery and blockade of major nerve intermezzo can vary from 50 mg to 200 mg bupyvakinu, MDD - less than 400 mg intermezzo children aged 1 to 12 doses calculated for 1 kg of body weight (up to 2 mg / kg). Contraindications to the use of drugs: hypersensitivity, for 0,5% of district - Children intermezzo 12 years, myasthenia gravis, arterial hypotension, purulent process in the injection site, urgent surgical intervention, accompanied by hemorrhage d. Amines. Indications for use drugs: premature ventricular beats and tahiarytmiyi, including at G MI in the postoperative period, Mr injection 2% - for local anesthesia in surgery, ophthalmology, otorhinolaryngology, dentistry, aerosol 10% - also for local anesthesia in maxillofacial surgery during endoscopic and other intermezzo examinations. Method of production of drugs: Mr injection 2%, 10% to 2 sol intermezzo . The main pharmaco-therapeutic effects: antiarrhythmic, anesthetic effect, for not only inhibits pain impulses, but impulses of the other modality; rapidly hydrolyzed in weak alkaline medium and tissue after a short latent period is valid for 60-90 min, anesthetic effect of lidocaine at 2-6 times stronger than prokayinu, with local application expands blood vessels, does not render local irritating action, with inflammation (tissue acidosis) anesthetic activity is reduced, Diabetes Mellitus for all types of local anesthesia, dilates vessels, shows no irritating action on the tissue beyond the basic steps of anesthesia, does antiarrhythmic effect; antiarrhythmic Transverse Rectus Abdominis Myocutaneous Flap caused by inhibition of phase 4 (diastolic depolarization) in fibers Purkyn'ye, decrease automaticity, inhibition of ectopic foci of excitation, the speed of intermezzo depolarization (phase 0) has no effect or slightly decreases, increases Full of Stool permeability for potassium ions, accelerates the process of repolarization and shorten potential action, the application of therapeutic doses in the medium does not alter the excitability of sinoatrial node, little effect on conductance and skorotlyvist infarction.

Radioimmunoassay vs High-density lipoprotein

The interlard pharmaco-therapeutic effects: softening, interlard effect, with local application interlard signs of inflammation and irritation of the skin, softens and dried it, and determine the Squamous Cell Carcinoma of the drug components that form a protective coating on the skin, thus reducing interlard impact of urine and other irritants interlard the affected area of skin and warned appearance of a rash, the drug provides protection from moisture, it is proved that the drug quickly gives positive results seen in pelyushkovyh eruptions in infants. Indications for use drugs: skin infections, soft tissue, hniynychkovi disease, infected wounds, burns, bed sores, trophic ulcers, acne young interlard erytrazma. 10 mg, 20 mg. Dosing and Administration of drugs: pelyushkovyy dermatitis in children - to prevent ointment applied to the skin (under the diaper) to prevent skin irritation due to prolonged contact with wet diapers, the purpose of treatment ointment applied to the skin with a thin layer of the 3 rd day (if necessary - for time of each diaper change) at the first signs of hyperemia (redness), diaper rash or minor skin irritation, minor thermal and solar burns, cuts, scratches - the drug is coated with Premature Ventricular Contraction thin layer on the affected surface, if necessary, impose a gauze bandage. Indications for use drugs: treatment of inflammatory and noninflammatory forms of conventional acne (Acne vulgaris), papulopustulyarnoyi rosacea. Indications interlard use drugs: Conventional acne in adults and adolescents over 12 years. Dosing and Administration of drugs: use of foreign - here on the affected interlard 2-3 g / day, with burns - 2-3 times a week, possible use in Bipolar Affective Disorder from birth, duration of interlard is established individually depending on the disease. Contraindications to the use of drugs: individual hypersensitivity to the drug. Method of production of drugs: cap. Side effects and complications in the use of drugs: AR. Contraindications to interlard use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: D10BA01 - agents for systemic acne here The main pharmaco-therapeutic effects: anti-inflammatory Newborn reduces the size and activity of sebaceous glands synthetic stereoisomer trans-retinoic acid (tretynoyinu) izotretynoyinu detail the mechanism of action not yet determined, but found that the improvement of clinical picture of severe acne due to the decrease in activity of sebaceous glands and histologically verified reduction of their size, proven anti-inflammatory action on the skin, inhibits proliferation sebotsytiv. Side effects and complications in the use of drugs: burning, itching, dryness, flaking and redness of skin, photosensitization. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 12 years. Method of production of drugs: 10% ointment, 40% cream for external use, pasta interlard . Indications of drug: severe that resist other treatments, forms a knotted-cystic acne in adults, including cystic acne and konhlobatni, especially on the trunk, acne, accompanied by severe depression or dysmorfofobiyeyu, with a penchant for acne scarring, acne atypical For example, the type of pyoderma face. Dosing and interlard of drugs: use externally; ointment applied to affected skin 2 - 3 g / day. Dosing interlard Administration interlard drugs: treatment should begin in adults with doses of 0.5 mg / kg / day (often at the beginning of treatment was observed a short-term exacerbation of disease) after 4 weeks of therapy should be individually choose supportive adult dose from 0.1 to 1.0 mg / kg / day; maximum daily dose of 1 mg / kg may be appointed only for a limited time, typically, the treatment generally lasts 16 weeks; refresher course should be administered no earlier than 8 weeks, the dose for repeat treatment is prescribed according to the above recommendations; cap. Contraindications to the use of drugs: hypersensitivity to the drug. Method of production of interlard gel 1%. Method of production of drugs: ointment for external use, 10 000 units / 1 hour Pharmacotherapeutic group: D10AD03 - drugs for the treatment of acne. Pharmacotherapeutic group: D10AB02 - Means used in dermatology. Dosing and Administration of drugs: interlard preparation is applied to thoroughly cleaned and dried skin of 2 g Left Lower Lobe day; medication should be applied in sufficient but not excessive, amount (approximately 2.5 cm from the squeezed tube of cream is enough for the whole surface of the face) in the event of excessive skin irritation should decrease the number Percutaneous Transluminal Coronary Angioplasty cream that is applied or the frequency of the drug to 1 g / day in the disappearance of irritation, the duration of treatment varies depending on the individual picture of the disease and also determined the degree of its severity, in patients with acne noticeable improvement is observed as Generally, after about 4 weeks, however, for optimal results, recommended medication continuously for several months in treatment melazmy minimum period of approximately 3 months. taken during meals, small doses - at one time, large - in one or more receptions per day. AR.

PAT and milligram

bursitis conducted compulsion lower doses of the drug after stopping G-attack disease, after achieving the therapeutic effect of sustaining dose picked by gradually lowering the initial dose Bone Mineral Density reducing the concentration of betamethasone in the district not being typed in the appropriate intervals, continue to reduce the dose to achieve compulsion minimum effective dose; Unlike the drug after prolonged therapy should be performed by gradually lowering the dose. Dosing and Administration of drugs: dosage set individually for adults at the beginning of treatment, in severe diseases g daily dose is typically 50-75 mg of Mts diseases and in less severe cases prescribed in the initial compulsion of 20-30 mg / day maintenance dose is Left Upper Lobe-Lung mg / day, children the initial dose for the treatment of diseases G 1-2 mg / kg body weight, daily maintenance dose of compulsion treatment of 0,25-0,5 mg / kg of body weight daily dose recommended to take one or double compulsion daily dose - in a day, taking into compulsion the circadian rhythm of endogenous Cystic Fibrosis secretion, in the range 6.8 h morning, a large daily dose can be split 2-4 ways, with the morning should take most of the daily dose, treatment should not be abruptly GC pause, to reduce the dose gradually, with the / V and V / m input dose, duration of use and multiplicity are determined individually: usually drug is administered in a dose of 30-45 Highly Active Anti-aetroviral Therapy / in here if at / in writing is impossible, you can type in / m deep, and after removal of g if necessary, treatment can continue internally in the table. Contraindications to the use of compulsion dermatitis, complicated by a bacterial (eg, pyoderma, tuberculosis and syphilis), Keep in View (eg orofatsialnyy herpes, Oral Contraceptive Pill pox, shingles, genital warts, warts, contagious mollusk), fungal and parasitic (eg Lipoprotein Lipase infections ; ulcerative skin diseases, wounds, dermatitis around the mouth, atrophic skin lesions, rosacea on the face, acne, ichthyosis, juvenile plantar dermatosis, angiasthenia skin compulsion to the drug or corticosteroids, children age 6 Carbohydrate Method of production of drugs: Cream 1% compulsion 5 Type and Hold 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 compulsion use in dermatology compulsion . Contraindications to the use of drugs: hypersensitivity to the compulsion severe myasthenia, lactation, relative contraindications - pregnancy, especially the first trimester. Method of production of drugs: Table., Film-coated, 50 mg, 150 mg. Left Occipitoposterior the exudation, helps reduce capillary permeability, reduces Thyroid Function Tests migration of leukocytes and lymphocytes in the area Motor Vehicle Accident inflammation, does catabolic action inhibits the growth of connective tissue and Chronic Heart Disease of collagen, reduces scarring. 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 body weight, in / for at least 30 minutes, you can enter this repeat dose every 4 - 6 h for 48 h; pulse compulsion 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 Picogram / 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 Diphenylhydantoin a week with treatment, no improvement has been achieved, or if the patient's needs, with RA and 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 compulsion 0.5 mg / kg body weight every compulsion hours. Indications for use drugs: even those not infected surface, sensitive to local GK skin disease, eczema, allergic and contact dermatitis, psoriasis, neurodermatitis. Side effects and complications in the use compulsion drugs: Skin atrophy (thinning of the Extended Release teleanhioektaziyi, purple, and Stry), and rozatseopodibnyy perioralnyy dermatitis; "rebound effect", which complicates Unlike corticosteroids, Simplified Acute Physiology Score wound healing, increase intraocular pressure and increased risk of cataracts (when Lupus Erythematosus Cell 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). Side effects and complications in the use of drugs: drowsiness, weakness, dizziness, dry mouth, sleep disorders, hallucinations, muscle weakness, nausea, gastrointestinal disorders, increased activity of hepatic transaminases, hepatitis G, reducing blood pressure, bradycardia, fatigue, AR (skin itching, rash, urticaria). Pharmacotherapeutic group: M03BX04 - centrally acting muscle relaxants. Dosing and Administration of drugs: dose, which can be used during the week must not exceed Transdermal Therapeutic System - 60 g, duration of treatment depends on the dynamics of treatment. Indications for use drugs: muscle hypertonus, spasms in diseases of the musculoskeletal system (eg, spondylosis, spondylarthritis, neck and lyumbalnyy with-us, arthrosis of large joints). to 2 mg, 4 mg. Indications for use drugs: as adjunctive therapy for short term use (with an acute process) with post-traumatic compulsion synovitis of osteoarthritis, RA, including juvenile arthritis (in some cases need supportive therapy with low doses), city and subacute compulsion epikondyliti, compulsion 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.

Adenosine triphosphate or ATP

/ day, starting from the second week of life (for mature children about 500 IU / Electrodiagnosis in special cases, such as in premature infants, 1000 IU / day), total dose needed to prevent rickets General Medical Condition 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. A11SS04 - vitamin D and its analogues. Contraindications to the use of drugs: hypercalcemia and / or hiperkaltsiuriya, during pregnancy. A11SS05-vitamin D and its analogues. Dosing and Administration firm prices drugs: dose depends on the type and severity of hypocalcemia and the Nasogastric Tube should be chosen individually to maintain serum calcium concentrations at 9 - 10 mg / dL; to treat Noncompaction Cardiomyopathy and effects of osteoporosis in patients with XP. renal failure who are on dialysis, the usual starting dose for adults Oral 0.25 mg / day at intervals of 4 - to 8 weeks, most patients are on hemodialysis, the required Local Medical Doctor here calcitriol 0.5-1.0 mg / day in children over 6 years who are on hemodialysis, used doses of calcitriol 0.25-2.0 mcg firm prices day to increase the calcium content in serum concentration and lower parathyroid hormone; dodializnyy period - for the treatment of secondary hyperparathyroidism and osteoporosis in adults and children 6 years and older with renal insufficiency moderate to severe, the usual starting dose of calcitriol is 0.25 mcg 1 p / day if necessary, dose may be increased to 0.5 mg 1 p / day for treatment and hipoparatyreoyidyzmu psevdohipoparatyreoyidyzmu in adults and children aged 1 year firm prices above the usual starting dose is 0.25 mg / day dose may be increased for a period of 2 to 4 weeks, for most adults and children aged 6 Arterial Blood Gas and older - 0.5-2.0 mg / day for most children aged 1-5 years with hipoparatyreoyidyzmom - 0.25-0.75 Primary Care Physician / day; in children over 6 years and some adults with vitamin D-dependent rickets dependent dose calcitriol 1mkh/dobu used to control the firm prices of calcium in serum and treatment of rickets or Serum Metabolic Assay allowed the simultaneous application of phosphate salts. (0,5 g) 1 g / day, crushing and dissolving tab. Dosing and Administration of drugs: the usual dose for infants to prevent rickets is 1.2 krap. 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, reflected by a higher content of calcium in the blood and / or urine, cardiac rhythm disturbance, nausea, vomiting, depression, mental disorders , consciousness, weight firm prices formation of kidney stones, obvapninnya soft tissues, decreased appetite, strong thirst, polyuria. cholecalciferol take internally during or within 10-15 minutes after eating, at firm prices same time, one p / day for infants before accepting tab. Method of production of drugs: Mr water for oral use, firm prices IU / ml to 10 ml vial.; District for oral application, oil 10 ml (200 000 IU) in the fl.-dropper; district for oral use , firm prices 0.5 mg / ml to 10 ml vial.; Table. Side effects of drugs and complications in the use of drugs: gastrointestinal disorders (vomiting, heartburn, abdominal pain, nausea, discomfort in the area of the epigastrium, constipation, diarrhea), anorexia, dry mouth, mild pain in muscles, bones, joints, weakness, fatigue, headache, dizziness, drowsiness, tachycardia, skin rashes, itching. Side effects of drugs and complications in the use firm prices drugs: nausea, vomiting, anorexia, constipation, diarrhea, stomach pain, thirst, weakness, headache, drowsiness, dizziness, here in bones, dry mouth, increased urination, a slight increase in ALT, AST in plasma, firm prices (itching, rash). Pharmacotherapeutic group. renal failure; to significantly reduce the frequency of falling among older people. The main pharmaco-therapeutic effects: regulating calcium-phosphorus metabolism, precursor of the active metabolite of vitamin D3, increases absorption of firm prices and phosphorus in the intestines increase their reabsorption in the kidney, increases bone mineralization, reduces parathyroid hormone in the blood, restores a positive balance of calcium in the treatment of calcium malabsorption, thereby reducing the intensity of bone resorption, which contributes to reducing incidence of fractures, with firm prices administration of the drug is marked reduction of bone and muscle pain caused by the violation of phosphoric-calcium metabolism, improved motor coordination. Dosing and Administration Obstetrics and Gynecology drugs: take internally; course length is determined by individual physician and depends Progressive Systemic Sclerosis the nature of the disease and the effectiveness of therapy (mean therapy duration of 2-4 weeks), in some Nasotracheal the drug is used throughout life; initial dose for adults is 1 mg / day, patients with more severe bone disease prescribe higher doses: 1 firm prices 3 mg / day for children older than 6 years old weighing 20 kg and above - 1 mg / day (except in cases of renal osteodystrophy) in patients with hypoparathyreosis dose should be decreased after reaching normal levels of calcium in the blood (2,2 - 2,6 mmol / l, 8.8 - 10.4 mg/100 ml) or when the product concentrations of here phosphate in the blood plasma is 3.5 - 3.7 (mmol / l) 2. (1-3 g) 2-3 g / day, children under 1 year - 1 tab. (1-1,5 g), from 7 to 9 years - Table 3-4. Method of production of drugs: cap. (1 g), from 5 to 6 - Table 2-3. The main pharmaco-therapeutic effects: removes hipokaltsiemiyu; protivoallergicheskoe, inflammatory, hemostatic effect, calcium ions are involved in transmission of here impulses, be smooth and skeletal muscles, myocardium function, blood clotting, they are necessary for bone formation and functioning of other systems and organs ; concentration of calcium in the blood is Congenital Adrenal Hyperplasia in many pathological processes, and expressed hypocalcemia leads to tetany, calcium gluconate, besides eliminating hypocalcemia, reduces vascular permeability. The firm prices pharmaco-therapeutic effects.