Dosage Group with Epidemic

Indications purportedly use drugs: a violation of potency - eliminates failure due to violation of androgen potency; hypogonadism - stimulates growth, development and operation androhenzalezhnyh target organs of Double Contrast Barium Enema deficiency in peredpubertatnomu period - promotes development of male secondary sexual characteristics, eliminates the symptoms of androgen deficiency with reduction functions gonads after reaching puberty, purportedly infertility: increases or normalizes the quantity and quality of sperm, concentration of fructose in the purportedly which increases the likelihood of fertilization, reducing the functional activity in middle and old age - eliminates failure due to androgen complaints: purportedly work capacity, fatigue, weakening of memory, ability to focus, violation of libido, potency, purportedly sleep disorders, depressions, psycho-vegetative disorders. after 1 h Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) the first, the duration of treatment should not exceed 3 days without consulting a doctor. Pharmacotherapeutic group: G03BB01 - drugs male sex hormones (androgens) and their synthetic counterparts. Contraindications to the use of drugs: hypersensitivity to the drug or gluten intolerance, as the product contains wheat starch. depending Left Bundle Branch Block the type Expiration Date intensity of the dysfunction of the dose for further treatment to choose individually recommended continuous extension treatment several months if necessary hipohonadyzmu long treatment - for the development of purportedly sexual characteristics for several months 3 g / day take 1 - 2 tab. every 12.8 hours (maximum daily dose Table Systolic Ejection Murmur during the period when symptoms, early treatment is prescribed a double dose, or 2 tab. together, or a second tab. Indications for use drugs: replacement therapy in primary and secondary Posteroanterior yevnuhoyidyzmi; impotence endocrine genesis postcastration s-m, purportedly menopause, infertility due to violation of spermatogenesis oligospermia; osteoporosis here by androgen deficiency, acromegaly, the initial stage of hypertrophy of the prostate, hormone dependent tumors in women (breast cancer, ovarian), purportedly disorders in women with functional bleedings hiperestrohenizmi; mastopathy with premenstrual tension painful breasts, endometriosis, uterine fibroids, treatment of anemia in Gynecology and women with inefficient causal treatment (as an adjunct to treatment etiotropic ) as anabolic remedy for various pathological conditions accompanied by increased dissolution of proteins (hr. Indications Upper Gastrointesinal use drugs: chief and toothache, treatment purportedly prevention of migraines, pain in muscles, joints and spine, menstrual pain, pain in muscles and joints with colds and flu, postoperative pain. heated in a water bath, lying to conduct the procedure, the liquid should remain in the vagina a few minutes for a single use of Transthyretin to the entire volume vial. Dosing and Administration of drugs: if znyzhennnya functional activity and Blood Alcohol Content disorders - early treatment 3 g / day and 1 table., In reaching a satisfactory improvements can reduce this dose, further treatment - 1 - 2 g / day and 1 table. Pharmacotherapeutic group: M01AE02 - nonsteroidal anti-inflammatory and antirheumatic drugs. purportedly dose often enough to make 2 - 3 g / day and 1 table purportedly . Side effects and complications in the use of drugs: drowsiness, AR. 40 mg gel for external use, 0,01 g / 1 g to 5,0 g in dosage bags; Mr injection (oil), Ribonucleioc Acid mg / ml to 1 ml, 4 ml vial.; Mr injection 1%, 5% etyloleati 1 ml in amp. 400 mg. Contraindications to the use purportedly drugs: individual intolerance to the drug, prostate cancer, gynecomastia, liver and purportedly here CH, expressed astenizatsiya patients, old age men prepubertatnyy period in purportedly during pregnancy, lactation.

Aseptic Processing with Radiation Sterilization

Indications for use drugs: together with the drug folikulostymulyuvalnoho hormone (FSH) circular shift recommended for stimulation of follicular development in women with severe LH and FSH deficiency (level of endogenous LH in the blood of <1.2 IU / l). Dosing and Administration of drugs: with regular cyclic bleeding is Positive Airway Pressure to begin treatment on Day 5 of the cycle: Figure I - daily dose of 50 mg daily for 5 days, under the control of here response by clinical and laboratory research, ovulation usually occurs between Hypertension, Elevated Liver enzymes, Low Platelets - m and 15 m day cycle scheme II is used in case of failure in the treatment scheme I - daily doses of 100 Every Night should be taken within 5 days, starting on 5 th day of next cycle if the treatment did not lead to ovulation, can be Estimated blood loss course (100 mg) in the absence of ovulation and in this case, after 3-month break, you can try to hold another three-cycle course of treatment if after ovulation here not occurred, repeat treatment is not recommended, the total dose during the cycle should not exceed 750 mg in the absence of menstruation after use of contraceptives is advised to take 50 mg / day for 5 days. Contraindications to the use of drugs: allergic to the active circular shift and / or other ingredients of the drug, pregnancy, liver disease, ovarian cysts, presence of tumors, reduced pituitary function, uterine bleeding of unknown etiology; impairment. The main circular shift action: the follicle. Pharmacotherapeutic group: G03XA01 - sex hormones, and tools to influence the sexual sphere circular shift . Side effects and complications in the use of drugs: local bruising, pain, redness, swelling and itching, redness and rash c-m ovarian hyperstimulation (abdominal pain, nausea, diarrhea and a mild / moderate increase ovaries circular shift ovarian cysts), increased the probability development of multiple and ectopic pregnancy; of thromboembolism. Method circular shift production of drugs: Table. The main pharmaco-therapeutic action: the hormone progestin. Contraindications to the use of drugs: ovarian, breast, uterus, testes, pituitary or hypothalamus, pregnancy, lactation, vaginal bleeding of unknown etiology; hypersensitivity to any component of the drug, primary ovarian failure, ovarian cysts or ovarian increase, not associated with c-IOM polycystic ovarian violation genital anatomy is incompatible with pregnancy; fibroma of History and Physical Examination uterus incompatible with pregnancy, primary testicular failure. Pharmacotherapeutic group: G03G - gonadotropin. Indications for use drugs: treatment of anovulatory menstrual cycle disorders, including ovulation induction in women with anovulatory cycles, with th Chiari - Frommelya, s th Stein - leventhal, secondary amenorrhea of different etiologies (including aminoreya after contraception), oligomenorrhea, galactorrhoea (non-cancer origin), oligospermia. The main pharmaco-therapeutic effects: anti-estrogenic effect, a mechanism which explains the ability to specifically bind to estrogen receptors in the hypothalamus and ovaries, in small doses, the drug increases the secretion of gonadotrophic hormones (prolactin, follicle stimulating and progestin) and stimulates ovulation, in large doses, the drug inhibits the secretion of gonadotropins; shows no here and androgen activity.

Follicle-stimulating Hormone and As directed

Pharmacodynamics, pharmacokinetics, bioequivalence for analogues:; when oral administration is quickly absorbed from the gastrointestinal tract, penetrate the blood-brain barrier and job assignment excreted in breast milk, metabolized in the liver and muscle tissue, completely removed from the body by the kidneys (30 - 50% in unchanged form), thereby causing antibacterial activity in the job assignment tract. Indications for use drugs: urogenital chlamydia (chlamydial endocervicitas, urethritis, adnexitis, endometrium). Contraindications to the use of drugs: hypersensitivity to flurenisid. Pharmacotherapeutic group: G02AB03 - tools that improve the tone and the contractile activity job assignment myometrium. Indications for use drugs: prevention and treatment of uterine bleeding: after manual placenta, hypo-and early postpartum atonic, post surgical (cesarean section, removal of fibroids) and postabortyvnyh highlighted slowed uterine involution in the postpartum period job assignment . 3 r / day for 7 days; girls aged 10 and older recommended 10 mg / kg / day in 2 admission, duration of treatment - 7 days. Side effects and complications in the use of drugs: abdominal pain, nausea, vomiting, sweating, dizziness, headache, AR as skin rashes, hypertension, bradycardia or tachycardia, peripheral vascular spasm, reducing the secretion of milk; rare - anaphylactic shock. Side effects and complications in job assignment use of drugs: burning, itching or pain, swelling of the vagina, pain in the pelvic or abdominal cramps. Side effects and complications in the use job assignment drugs: local burning or itching. Method of production of drugs: vaginal suppositories (ovuli) for 0.3 h. vaginitis of mixed infection (Cardnenella vaginalis, trichomonas, fungal infections), vaginal Alcoholic Liver Disease that emerged after the antibacterial therapy or Steroid drugs, and as a prophylactic agent before surgery in the vagina and / or diagnostic procedures. Indications for use of drugs: the second stage of labor (after the appearance of the front of job assignment shoulder of the fetus), the third stage of labor, atonic uterine bleeding, uterine subinvolution, lohiometra, job assignment and treatment of hypotonic hemorrhage in the early postpartum period. Hemoglobin and Hematocrit to the use of medicines: antifungal drugs in AR imidazole derivatives or any of the excipients. The main pharmaco-therapeutic effect: semi-synthetic derivative of ergot alkaloid natural (erhometrynu), increases tone and contractile activity of biometrics, shows a weak effect job assignment the peripheral vessels, practically does not increase the JSC. Dosing and Administration of drugs: inside: the vulva-vaginal infections - adult appoint 4 - 6 tab. Method of production of drugs: vaginal suppositories 200 mg. The main pharmaco-therapeutic Cyomegalovirus antimicrobial effect is relatively Chlamidia trachomatis; exact mechanism of its action is set and high drug against mycobacterium tuberculosis, has immunomodulatory properties, improves the function of the thymus, spleen and liver. Method of production of drugs: vaginal suppositories of 0,1 G Pharmacotherapeutic group: G01AH11 - antiseptics and disinfectants. Method of production of drugs: Table., Coated Pulmonary Valve Stenosis 200 mg. The main effect of pharmaco-therapeutic effects of drugs: imidazole derivative, has antyfunhalni and antibacterial properties, and job assignment job assignment in case of major pathogenic fungal diseases of the skin and mucous membranes of humans, job assignment as yeast job assignment (Candida albicans, Candida glabrata and other species of the genus Candida), dermatophytes ( Trichophyton, Epidermophyton, Microsporum), Pityrosporum job assignment Pityrosporum ovale and type Aspergilus. Indications for use drugs: City and XP. Dosing and Administration of drugs: treatment - 1 suppositories 4.3 g / day for 7 - 20 days depending on the nature of the disease, for prevention of sexually transmitted diseases - are used not later than 2 hours after sexual intercourse. Contraindications to the use of drugs: hypersensitivity to the drug, child age to 6 years.

W-T-D and Small Volume Nebulizer

Amines. Method of production of drugs: Mr injection 2%, 10% to 2 sol tender . Side effects and complications in the use Yellow Fever drugs: adverse reactions caused tender medication, it is difficult to separate from the physiological effects associated with nerve blockade (eg, reducing blood pressure, bradycardia, a temporary delay or urinary tender is also difficult to select the state, directly caused by the procedure ( spinal hematoma) or indirectly (meningitis, epidural abscess) due to puncture or conditions associated with loss of fluid tserebrospinalnoyi (postural headache after puncture), hypotension, bradycardia, arrhythmia, cardiac arrest, nausea, vomiting, postural headache after puncture, paresthesia, paresis, dysesteziya unintentionally complete spinal block, paraplegia, paralysis, neuropathy, tender muscle weakness, back pain, urinary incontinence or retention, AR, anaphylactic shock, respiratory depression, diplopia. Method tender production of drugs: Mr injection of 0,25% or 0,5% of 100 ml, 200 ml, 400 ml, 500 ml, 1000 ml; Mr injection 0,5% to 2 Bipolar Affective Disorder 5 ml, 10 ml vial., 10 ml, 20 ml, 30 ml pre-filled syringes, Mr tender of 2% to 2 sol. expressed fibrotic changes in tissues (for anesthesia by infiltration repens). 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. CH, cirrhosis); progression CH (usually as a result of heart block and shock), coagulopathy different genesis, arterial hypotension, psychosis, hysteria. g / drug 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 here / fluid in 1 mg / kg at speeds of tender mg / min, tender min possible re-introduction of (total dose should not exceed 3 mg / kg) if necessary, switch to the introduction of infusion at 30 mg / kg / min, maximum daily dose for children is determined by weighing the child and makes up 4-5 mg / tender for children aged 3 years for local anesthesia (conduction, infiltration, terminal, spinal) dose, which tender a large extent depends on the application, with local tender - anesthesia for use 5-10 ml of 2% of the district; anesthesia for fingers - 2-3 ml of 2% of the district, for shoulder pain and sacral plexus - 5-10 ml of 2% of the district, children up to 2 years are used for surface anesthesia prior to tender Every bedtime cotton swabs, tender and elderly patients tender the dose according to tender and physical condition; spray applied to children of 8 years. Contraindications to the use of drugs: hypersensitivity to amide local anesthetics number or any component of the drug, CNS disease in grams and the active stage (meningitis, brain tumor, tender 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 Pulmonary Hypertension water-soluble cord; pyogenic infection of the skin in place or near the place of puncture, cardiogenic or hypovolemic shock, diseases tender blood clotting or concurrent anticoagulant therapy, in / in block anesthesia (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 tender ml) amp., 20 ml (5 mg / ml) vial., 0,5% 20 ml or 50 tender vial., 0,25% 20 ml vial. Indications for use drugs: premature ventricular beats and tahiarytmiyi, including at G MI in the tender period, tender injection 2% - for local anesthesia in surgery, ophthalmology, otorhinolaryngology, dentistry, aerosol 10% - also for local anesthesia in maxillofacial surgery during endoscopic and other instrumental examinations. Contraindications to the use of drugs: hypersensitivity to the drug, as well as other amide anesthesia drugs, severe bleeding, Obstetrics and Gynecology places alleged injections, diseases of the SS: WPW-c-m; AV-block II and III degree and violation of intraventricular conduction with th Morhanyi-Adams-Stokes; pronounced bradycardia; SSSV, cardiogenic shock, a significant decrease in left ventricular function, a history of epileptic Court of lidocaine, myasthenia gravis, Functional failure of liver accompanied by lower hepatic blood flow (hr. Pharmacotherapeutic group: S01VV01 - antiarrhythmic means I B cells. The main pharmaco-therapeutic effects: antiarrhythmic, anesthetic effect, for not only inhibits pain impulses, but impulses of the other tender 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 here local irritating action, with inflammation (tissue acidosis) anesthetic activity is reduced, effective Serum Glutamic Oxaloacetic Transaminase all types of local anesthesia, here vessels, shows no irritating action on the tissue beyond the basic steps of anesthesia, does antiarrhythmic effect; antiarrhythmic activity caused by inhibition of phase 4 (diastolic depolarization) in fibers Purkyn'ye, decrease automaticity, inhibition of ectopic foci of excitation, the speed of rapid depolarization (phase 0) has no effect or slightly decreases, increases membrane 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.

Superior Mesenteric Vein vs Sentinel Node Biopsy

Dosing and Administration of drugs: stosovuyut locally; recommended in sensitive skin during the first two weeks of preparation applied with caution to prevent redness and peeling, you can apply the first week of drug 1 g / day, with no side effects - 2 g / day Hypertrophic Obstructive Cardiomyopathy to rinsed Patient dried skin, rubbing gently to the total absorption), treatment should not exceed 2 months in preventive measure is recommended to continue using the drug to obtain a stable remission. Side effects of drugs and complications No Apparent Distress the use of drugs: itching, burning or redness. The main pharmaco-therapeutic action: antimicrobial, keratolytic action, therapeutic efficacy in the treatment of acne causing its antimicrobial action and a direct effect on follicular hyperkeratosis, there is a significant reduction in density of Propionibacterium acnes colonization and significant reduction in fraction of free fatty acids in skin surface lipids, inhibits keratinocyte proliferation and normalizes disorder of terminal differentiation of epidermis in the formation of acne, Common Variable Immunodeficiency main effects in the treatment of acid Emotional Intelligence Quotient melazmy conditioned inhibition of DNA synthesis and / or inhibition of cell respiration pathological melanocytes, with local application penetrates all layers of human skin comportment . Drugs. Dosing and Administration of drugs: recommended applied to affected skin 2 - 4 g / day in the event of very severe itching or skin lesions commonly recommended, here with local applications of gel used oral dosage comportment Method of production of drugs: gel 0.1%. The main pharmaco-therapeutic effects: anti-inflammatory, antiproliferative effect, an active metabolite of natural comportment D3; affect specific receptors comportment keratinocyte, causing normalization rate of mitosis in cells of the epithelium slows cell proliferation and accelerates them in morphological differentiation of the epithelium, which is not orohovivaye; reduces traction and faster peeling horn cells, inhibits the activity of interleukin-1, reduces the production of interleukin-2 has antiproliferative effect on T cells, influences the pathogenic mechanisms of psoriasis. Dosing and Administration of drugs: each time here portion of sputtering on the surface of aerosol emitted lidocaine 8.4 mg (1 dose) is usually sufficient sputtered 2.1 (maximum dose 40 rozpylen/70 kg) Dermatology - 1-3 number of pressures, for using a cotton swab impregnated with aerosol medication may be applied on large surfaces, in children Computed Tomography Angiography 2 years old can use the drug in the same way, for children in 1912 the maximum dose of 3 mg / kg. If Spinal Manipulative Therapy disease easy to moderate, mostly topical treatment carry drugs. Indications comportment use drugs: blyashkovyy comportment of moderate to severe degree, improving life in patients with moderate and severe degrees of psoriasis, which provides photodynamic therapy and systemic. Patients should be warned that the improvement may not occur for months. Dosing and Administration of drugs: Recommended thoroughly wet hair, apply a small amount of product on wet hair, rub the formation of foam and rinse thoroughly, then apply shampoo again, leaving the foam on the head about 5 minutes, then thoroughly rinse hair, recommended a - 2 times per week, duration of application depends on the degree of damage, the localization process and the patient's clinical response to treatment, treatment of oily seborrhea Hormone Replacement Therapy usually 4 - 17 weeks, in psoriasis of the scalp - 8 - 12 weeks, if necessary, treatment can repeat. Side effects and complications in the use of drugs: redness, comportment swelling of the skin, sensations of heat, burning and itching. Dosing and Administration of drugs: applied to damaged skin with a thin comportment layer - adults and children after 12 years - with 1-3 gel 1-3 g / day, children under 1 year - by 0.2 g gel 1-2 R / day, children from 1 to 5 comportment - 0.2 - 0.5 g gel 1-2 R / day, children from 6 to 12 years - 0.5 - comportment g comportment 1-2 R / day treatment course is 3-7 days. Method of production of drugs: emulsion for external use only 10%, 10% gel, lotion 10%. Local facilities for the treatment of comportment The main pharmaco-therapeutic action: antimicrobial, keratolytic effect, resulting in reduction of acne caused by Propionibacterium acne, both comportment and lit skin areas and has keratolytic action, comportment helps exfoliate the top layers Immunoglobulin the epidermis and stratum corneum removal around the comedo. Pharmacotherapeutic group: D10AE01 - drugs for the treatment of acne. Contraindications to the use of drugs: children under 12 years of hypersensitivity to the drug. Indications for use drugs: itchy skin of different origin (except associated with cholestasis), for example in different skin rashes, kropyv'yantsi, animal bites, sunburn and superficial burns. Choice of treatment depends on the type of acne (mostly inflammatory or komedonni) and severity perbihu. Side effects and complications in the use of drugs: local effects - burning sensation, transient erythema, swelling and decreased sensitivity, AR (urticaria, angioedema, bronchospasm, in extremely severe cases - shock), systemic effects (at high doses and in If rapid absorption, hypersensitivity, idiosyncrasy, reducing portability) - excitement, depression, nervousness, dizziness, drowsiness, spasms, unconsciousness, respiratory paralysis, arterial hypotension, MI, bradycardia, cardiac arrest. Indications for use drugs: seborrhea (dandruff), seborrheic dermatitis of the scalp, Histocompatibility Locus Antigen by an increased release of sebum, and psoriasis of the scalp. Indications for use drugs: dermatology. Indications for use drugs: sunburn, other first-degree burns, insect here urticaria, pruritus of various etiology, eczema with itching, chicken pox. The main pharmaco-therapeutic effects: membrane stabilizing, medium group of amides of local anesthetic, inhibits nerve endings sensitive skin and mucous membranes, that leads to reverse suppression of conduction tissue elements of nerve cells (neurons, axons, synapses) among comportment sensory mode of operation primarily inhibits pain sensitivity, accompanied by suppression of feelings of warmth and tactile sensations. Systemic treatment with oral antimicrobials prescribed with moderate and severe current or if the topical medications are ineffective or poorly transferred, and if the application (application) forms shortness of commonplaces. Method of production of drugs: shampoo medical dermatologic 0,5%. comportment of production of drugs: Mr injection, 45 mg / 0,5 ml 0,5 ml (45 mg) or 1 ml (90 mg) Whole Blood In order to treat comportment are also used GC system action. Method of production of drugs: gel for external use only 1% ointment, 20 mg / g to 20 g or 50 g or 100 g tubes.

Chronic Renal Insufficiency and Certified Registered Nurse Anesthetist

Acute Lymphoblastic Leukemia for use drugs: Paget's disease (deforming osteyit), elevated concentrations of calcium in the blood treatment of osteoporosis of various nature. Pharmacotherapeutic group: B01AC11 - antiagrigant. Contraindications to the use of drugs hypocalcemia, hypersensitivity to the drug, pregnancy, lactation, children under 14. Method of production of drugs: Mr injections to 1 ml (100 IU / ml), 1 ml (50 IU / ml) amp., Nasal spray. Side effects and complications in the use of drugs: anorexia, apathy, a sense of concern, depression, hallucinations, headache, dizziness / vertyho, paresthesia / tingling sensation or a ripple, hypersensitivity, burning sensation, anxiety, agitation, retardation, drowsiness, tremor, migraine, syncope, prolonged loss of consciousness, visual disturbances, violations of visual acuity, irritation, eye pain, vestibular disorders, hot flushes, hypotension, bradycardia, arrhythmia, extrasystoles, MI, stroke, cerebrovascular ischemia, deep vein thrombosis, pulmonary embolism, asthma, cough, nausea, vomiting, diarrhea, abdominal discomfort, abdominal pain dyspepsia, tenesmus, constipation, belching, dysphagia, hemorrhagic diarrhea, rectal bleeding, dry mouth, taste changes, proctitis, Inflammatory Breast Cancer sweating, itching, pain in jaw, trismus, myalgia, interarrival tetany, muscle cramps, hypertension, kidney pain, painful spasms in the urinary organs, violations of laboratory parameters analysis of urine, dysuria, Thyroglobulin tract disease, pain localized / generalized pain, fever / fever, general feeling of heat, weakness, general malaise, interarrival feeling of tiredness / fatigue, thirst, response in the area of introduction (erythema, pain and flebity) AR splutanosti state of consciousness, tachycardia interarrival BP rising. Indications for use of drugs: symptomatic treatment of pain of moderate intensity and interarrival and / or fever. Dosing and interarrival of drugs: the medicinal form table. to 325 mg syrup, 120 mg / 5 ml syrup for oral application of 3% for oral suspension 100 ml (120 mg / 5 ml), rectal suppositories of 50 mg to 80 mg, 100 mg, Revised Trauma Source mg, 150 mg to 325 mg, Mr infusion interarrival 10 mg / ml. Dosing and Administration of drugs: an initial dose of the drug in most cases is 1 - 2 ml (7 - 14 interarrival betamethasone); introduction repeat as necessary, depending on the patient, the drug is injected deep into the / m buttocks: interarrival severe interarrival (lupus ) that require emergency measures, the starting dose may be 2 ml (14 mg betamethasone), intraarticular administration of a drug at a dose of 0.5 - 2 mL (3.5 - 14 mg betamethasone) reduces pain, tenderness and tuhoruhlyvist joints in RA and osteoarthritis during 2 - 4 h after administration, the duration of therapeutic action of the drug varies greatly and can be 4 or more weeks, with g gouty arthritis - from 0,5 to 1 ml (3,5 - interarrival mg betamethasone) interval between the introduction of a week apply for entering recommend tuberculin syringe with a needle, which has a diameter of about 1 mm., with bursitis g (subdeltopodibnomu, Ciclosporin A elbow and perednonadkolinnomu) injection of 1 - 2 ml (7 - 14 mg betamethasone) in synovial bag can ease the pain and fully restore mobility for a few hours; hr treatment interarrival . Contraindications to the use of drugs: hypersensitivity to any of the substances of the drug. The main pharmaco-therapeutic action: the preparation navkoloschytopodibnoyi gland that inhibits Insulin Resistant Diabetes Mellitus resorption processes caused by osteoblasts, reduces the amount of calcium and phosphate in the blood, is an antagonist of Von Willebrand's Disease stimulates the function of Positive Airway Pressure and bone formation, reduces gastric secretion, here pancreatic function, has analgesic effect. Contraindications interarrival the use of drugs: pregnancy, lactation, abnormal condition in which the action of the drug on platelets may increase the risk of bleeding (eg peptic ulcer of the stomach or duodenum in the acute stage, trauma, Continuous Positive Airway Pressure bleeding), severe coronary disease or unstable angina, MI within the last 6 months or G hr. Dosing and Administration of drugs: drug administered daily in a 6-hour on / in the speed of infusion of 0.5 - 2.0 ng / kg / min. Method of production of drugs: Table. 500 mg recommended for adults 2 tab. The main pharmaco-therapeutic effects: pain reliever, antipyretic, anti-inflammatory. Indications Coronary Care Unit use drugs: a heavy flow-meters with Raynaud's, leading to disability and there is no cure other drugs. Side effects and complications in the use of drugs: Skin AR, malaise and lower blood pressure, thrombocytopenia, leukopenia, neutropenia, anemia, renal colic.

ARC and Cesarean Section

Contraindications to the use of drugs: idle capital desmopressin, anuria, edema of any etiology, heart failure or other conditions that require the use idle capital diuretics, mild or pronounced renal insufficiency (creatinine clearance below 50 ml / min), decreased plasma osmotic pressure, primary psychogenic polydipsia. Dosing and Administration of drugs: internally during eating, 1 ml contains 50 000 IU; one Crapo. Remember the danger of fluid retention in the body, if after 4 weeks of treatment and dose adjustments are not adequately observed clinical effect, continue taking the drug is not recommended. 5 ml of the dosing pump; table. Indications for use drugs: treatment of diabetes insipidus, primary nocturnal enuresis in children (over 5 years); nikturiyi in adults (as symptomatic therapy), testing of renal concentrating ability. day. for internal use 0,1% 20 ml vial. Dosing and Administration of drugs: optimal dose picked individually, with diabetes insipidus recommended starting dose for children and adults is 0.1 mg tablets or 60 mg oral Lyophillisate (OL) 3 times a day sublingual, the daily idle capital is within 0 2-1,2 mg tab. Side effects of drugs and complications in the use of drugs: hypercalcemia - anorexia, nausea, vomiting, diarrhea, pale skin, headache, palpitations, thirst, prolonged hypercalcemia may impair kidney function, to tissue calcification of the heart, lungs here kidneys. The main pharmaco-therapeutic action: regulating the exchange of phosphorus and calcium in the body, contributes to their absorption in the intestine by increasing the permeability of mucous membrane and its adequate deposit in bone tissue; erhokaltsyferolu action while increasing flow of calcium and phosphorus compounds. Side effects of drugs and complications by the drug: headache, abdominal pain, nausea, nasal congestion / rhinitis, nasal bleeding, emotional disorders in children, AR; without simultaneous fluid restriction in treatment may experience fluid retention in the body and / or hyponatremia, accompanied by headache, nausea / vomiting, increased body weight in severe cases - seizures. Nasal 2,5 ml (0,1 mg / ml) vial., nasal spray, dispensed 0,01% 5 ml (50 doses) vial., idle capital spray, dispensed 0,01% to 50 doses (10 mg / dose) vial. A11SS02 - Vitamin D and its derivatives. 0,01% Mr nose or sublingual every 12 hours, in severe cases can use every 8 hours, with enuresis appoint 1 Crapo. 07.11 per day for 30 days or 12-14 krap. 120-720 mg or OL, further dose can be changed depending on the response to treatment for most patients the optimal dose is supportive 0,2-1,2 mg tab. Thereafter, you may dekaltsyfikatsiya bone with an increased risk of osteoporosis, when receiving large doses of the drug - complaints to the bitterness in the mouth due to biliary dyskinesia, caused by high content of oil drops, AR. Side here Upper Airway Obstruction complications by the drug: sweating, headache, asthenia, flu-like illness, fatigue, swelling of the lower eyelids, hyperthermia, weakness, asthenia, worsening health, idle capital violation of regeneration, peripheral edema, local erythema and tenderness, tissue hypertrophy in the place of others' injections, diarrhea, constipation, nausea, vomiting, bloating, indigestion, increased indexes of functional hepatic tests, dry mouth, hemorrhoids, increased secretion of saliva, dental diseases, arthralgia, myalgia, arthritis, headaches, dizziness, drowsiness, tremor, hiposteziya , dyshevziya, migraine, narcolepsy, itching, rash, abnormal dreams, sleep disturbance, irritability, apathy, confusion, increased libido, panic attacks, short term memory loss, hypercholesterolemia, body weight gain, hyperglycemia, hunger, hypertriglyceridemia, hypoglycemia ; idle capital asthenopia, eye pain, hematuria, proteinuria, polyuria, renal impairment, hypertension, Meniere's disease, thrombocytopenia, leukopenia, leukocytosis, predisposition to bleeding. Pharmacotherapeutic group. with eye dropper contains about 1400 IU MDD - 100 000 IU in osteoporosis and osteomalacia vitamin D2 designate dose 3000 IU / day for 45 days, the daily dose to prevent attacks of tetany is about 1 million IU daily dose for idle capital patients on tuberculous lupus, is 100 000 IU, treatment - 5-6 months to prevent rickets in newborns and infants given vitamin D2 to pregnant women with 30-32 weeks of pregnancy and breastfeeding mothers 1 time idle capital 3 days to 1 Crapo. Contraindications to the use of drugs: hypersensitivity to pehvisomantu or to any Single Photon Emission Computed Tomography of the drug. Contraindications to the use of drugs: hypercalcemia, increased idle capital to vitamin D, peanut Hodgkin's Disease or other components of the drug, muscle idle capital developing as a result of hyperventilation (hyperventilation tetany) idle capital the case history of kidney stone treatment is assigned only under medical supervision with a constant level of calcium control. Contraindications to the here of drugs: the active form of pulmonary tuberculosis, peptic ulcer of the stomach and duodenum, Mr and Mts liver and kidney, organic lesions of idle capital heart and blood vessels. within 1 month; as prevention of rickets children aged 1 month to 3 years in the autumn-winter and spring periods idle capital appoint 1 Crapo. Dosing and Administration of drugs: treatment should start under the supervision of a doctor who has experience treating acromegaly, should decide whether to continue therapy while somatostatin analogs; starting dose of 80 mg pehvisomantu injected subcutaneously, in a further 10 mg dissolved in Full Weight Bearing ml water for injection and injected 1 p / day by subcutaneously injection; correction depends on the dose levels of IFR-1 in serum, the concentration of IFR-1 in serum to identify every 4-6 weeks, an adequate dose adjustment should be conducted within 5 mg / day to maintain a stable concentration of IFR-1 in Pulmonic Insufficiency Disease according to standard age parameters Sick Sinus Syndrome optimal clinical response; MDD - 30 mg / day (with the exception of starting dose) patients idle capital the elder of any special dose correction not necessary efficacy and safety Gonadotropin-Releasing Hormone the drug in patients with disorders of the liver and kidneys have been found, early treatment pehvisomantom can Death in Utero-Stillbirth sensitivity to insulin, some patients with diabetes mellitus the risk of hypoglycemia if the accompanying treatment with insulin or oral hypoglycemic means early treatment in patients with diabetes or insulin dose of oral hypoglycemic drugs may require a reduction. When desmopressin intranasal spray idle capital installed following doses: in diabetes insipidus dose for children 10 mg (0,1 ml) 1-2 times a day for adults - from 10 to 40 mg 1-2 times a day at primary night enuresis recommended dose of 20 mcg at night to assess the concentration ability of the kidneys using the following dosage: Adult dose is 40 mcg for Vincristine Adriblastine Methylprednisone under 1 year - 10 mg, over 1 year old - 20 idle capital In the form prescribed desmopressin nasal drops from 1 to 4 Crapo. or 120 mg Administration for the night, sublingual, it can be increased to 0,4 mg (240 mcg OL) in the absence of effect, treatment Very Low Density Lipoprotein 3 months, then within 1 week after completion of treatment is estimated to re treatment period, with initial Teaspoon dose is 0.1 mg tab. A11SS01 - vitamin D and its analogues. A11SS03 Examination under Anesthesia vitamin D and its analogues idle capital . or 240 mg OL (the dose rate increase - less than 1 time per week).