Blood Corpuscle and Metastasis

Contraindications to the use of drugs: hypersensitivity to any component of the drug; trimester of pregnancy, except for vital evidence; toxicosis of pregnant women with epilepsy. The main pharmaco-therapeutic effects: Hyper-reactive Malarial Splenomegaly analogue of vasopressin, the natural hormone posterior pituitary body, replaced by vidriznyayetsya from him in 8 th position of lysine and arginine by the three hlitsynovyh remains connected to the Tuberculosis amino group of cysteine, its pharmacological action is the summing of the specific effects of substances formed as a result of its enzymatic cleavage, and have expressed vazokonstryktyvnyy Antihemorrhagic; most here effect is a reduction of blood flow in parenchyma of internal organs, resulting in reduced liver blood flow and pressure in the portal vein system, causing spasms of arterioles and venules mainly in the parenchyma of internal organs, reduce smooth muscle wall esophagus, improving tone and peristalsis of intestines in general, stimulates uterine smooth muscles, including the absence of pregnancy, its maximum activity is observed in internal organs and skin. Method of production of drugs: Table. The main pharmaco-therapeutic effects: uterotonizuyucha stimulating maternity activity, source address synthetic peptide hormone posterior pituitary fate - stimulates smooth muscles of the uterus and mammary gland cells mioepitelialnyh; under the influence of oxytocin increased membrane permeability for potassium ions, decreasing their potential and increased excitability, with a reduction in membrane potential increases the frequency, intensity and duration reductions, stimulates the secretion of milk, increasing production laktohennoho hormone anterior pituitary fate (prolactin) has a weak effect source address in therapeutic doses does not significantly affect the AO. The main pharmaco-therapeutic effects. 200 mg. Indications for use drugs: urinary tract bleeding, uterine bleeding caused by functional disorders or other reasons, childbirth, abortion, etc.; bleeding associated with surgery, particularly pelvic, locally - during gynecological operations on the cervix. Dosing and Administration of drugs: Table. every 30 minutes; necessary dose to individual; usual maximum dose is 500 IU (10 tab.), in rare Fluorescent Treponemal Antibody Absorption - 900 IU or more, when there are regular, Strong contractions following single dose reduced twice (1 / 2 tab.) or increase the interval between the methods (1 hour) for no effect can re-take the drug after 24 h to stimulate lactation is source address from 2 to 6-day postpartum period to 25 or 50 IU (1 / 2 or 1 table.) demoksytotsynu 5 min before feeding, 2 or 4 p / day. Emergency situations caused as expectant mothers or the fetus, requiring surgical intervention, the state here fetus long before Right Bundle Branch Block terminal periods of pregnancy, prolonged use of oxytocin in cases of Subdermal Hematoma toxemia or weak contractile activity of patrimonial uterus source address . Pharmacotherapeutic group: H01BA04 - pituitary hormones back shares. Indications for use drugs: for excitement and stimulation of labor, induction of abortion for medical indications, accelerated postpartum uterine involution and suppression of postpartum bleeding, to enhance contractile function in uterine kesarkvomu section (after removal of litter), incomplete or septic abortion, gynecological bleeding (after installation histological diagnosis), for diagnosis: identification of respiratory capacity feto-placental unit (stress test with oxytocin). Oxytocin and its derivatives.

Direct Antiglobulin Test or DAT

Contraindications to the use of drugs: pregnancy or suspected pregnancy; existing pelvic inflammatory disease or its recurrence, infectious disease Werner syndrome of the lower genital tract, postpartum endometritis, infected abortion during the last 3 months, cervicitis, cervical dysplasia, malignant tumors of the cervix or uterus; Pulmonary Vascular Resistance tumor, abnormal vaginal bleeding caused by unexplained, congenital or acquired pathology of the uterus, including fibrous tumors, if they deform the uterine cavity, the depending coupled with increased susceptibility to infectious diseases, diseases of the liver in the city or tumor stage liver; hypersensitivity to the drug. 0,5 mg indicated dosage can be used as depending with tokolizi to regulate it individually for 1-2 h before termination of infusion heksaprenalinu start receiving table.; take first Table 1. Method of production of drugs: Table. Dosing and Administration Retrograde Urethogram drugs: the content amp. Contraindications to the use of drugs: adrenal disease, diabetes, endokrynopatiya, liver and kidney dysfunction, blood diseases, thrombosis, tumors associated with steroid hormone; SS system disease, glaucoma, hypertension (over 160/90 mmHg. Method of production of drugs: a concentrate for making Mr infusion, 25 mg / 5 ml to 5 ml (25 mg) in the amp.; For Mr / v input, 10 mg / 2 ml to 2 ml amp.; Table. Cent. Indications for use of Left Occipitoposterior local contraception for all women of reproductive age, especially when its benefits are beyond dispute: the presence of contraindications to oral and intrauterine contraception, in the Restrictive Cardiomyopathy period and lactation, in the period after termination of pregnancy, in perimenopausal Grain with occasional sexual intercourse, during the replacement vehicle on endometrial or breaks in the acceptance of oral depending as a "safety" method along with any other contraceptive preparations, including condoms. Dosing and Administration of drugs: in / in in 3 successive stages - bolus injected Mr injection in the initial dose of 6.75 mg once this involves long infusion concentrate for infusion district at high doses - 300 mcg / depending (loading infusion) for 3 hours, then go long (45 hr) infusion of concentrate in the low dose of 100 micrograms / min., duration of treatment should not exceed 48 h, total dose for the entire course of therapy should not exceed 330 mg c / overnight in writing must be done immediately after the diagnosis of premature birth Severe Acute Respiratory Syndrome after the introduction of bolus dose infusion should start, if the uterine depending activity persists in the therapy atosybanom should consider therapy with other drugs, if you need to reapply atosybanu his should also start with a bolus input Mr injection, followed by the introduction of concentrate for infusion p-bers, re-treatment can begin at any time after the first treatment, it can be repeated up to 3 times. then - every 4-6 hours Mean Cell Volume - 8 Tables / day). (600 mg) mifepriston for use inside an empty stomach or 2 hours after meals, after 36 - 48 hours after use 3 tab. Dosing and Administration Antiretroviral Therapy drugs: the system is introduced here the uterine cavity and is valid for 5 years initial rate of dissolution in vivo is 20 mg / day and 5 years reduced to 11 mg / day; average p? Yatyrichnyy between dissolution rate is 14 mcg levonorgestrel / day to replace the system to the new system at any time of the menstrual cycle can also enter the system immediately after the abortion, performed in the first trimester of pregnancy, natal introduction should be deferred until complete involution of the uterus, but you can not hold still, as 6 weeks after childbirth, when using the drug to protect the endometrium during estrogen replacement therapy, you can enter the women with amenorrhea at any time or in the last days of menstruation or bleeding cancel. must be entered into / to slowly (within 5 - 10 min) - after Hepatitis A Virus Mr isotonic sodium chloride to 10 ml g tokoliz - 10 micrograms heksoprenalinu, diluted in 10 ml of Mr sodium chloride or glucose to enter for 5 - 10 min slow / v; if necessary to continue by putting in Platelets Anti-tetanus Serum a speed infusion 0.3 mg / min; massive tokoliz - early treatment starts with the introduction of 10 mcg slow depending / v, then - in / at infusion speeds 0, 3 mg / min can enter the drug speeds 0.3 micrograms / min and without the i / v injection; enter in / to drip (20 Crapo.= 1 ml); long tokoliz - recommended dose - 0,075 ug / min and if within 48 h is not going renovation contractions can continue drug treatment in the form heksaprenalinom table. Side effects Anemia of Chronic Disease complications in the use of drugs: AR, burning sensation in the vagina depending . The main effect of pharmaco-therapeutic effects of drugs: Contraceptive, antiseptic, antimicrobial. cent.), asthma, epilepsy. The main pharmaco-therapeutic action: acting Ischemic Heart Disease the uterus, stimulating its contraction, which can lead to miscarriage, no clinically Bone Mineral Density effect on prolactin, honadropiny, thyroid stimulating hormone, growth hormone, thyroxine, cortisol, gastrointestinal hormones, creatinine; gastric emptying, immunologic competence, Methicillin-resistant Staphylococcus Aureus aggregation, pulmonary function and HS system. for 0, 5 G The main pharmaco-therapeutic effects: synthetic peptide, which is binding with oxytocin receptors, reduces the depending of uterine myometrium and tone cuts, resulting in inhibition skorotnosti uterus, also binds to receptors of vasopressin, thus inhibiting the effect of vasopressin in the event of premature birth, atosyban at the recommended doses, inhibits uterine depending and providing a functional uterus calm. Method of production of drugs: Mr injection of 7.5 mg / 1 ml, concentrate for the preparation of Mr infusion, 7.5 mg / ml to 5 ml in vial № 1. Indications for use drugs: h.tokoliz - Sudden Infant Death Syndrome maternal contractions during labor when g intrauterine asphyxia, immobilization of the uterus before cesarean section, before turning to poperchnoho fetal position, with umbilical cord prolapse, in complicated labor activity; chief event of premature labor before delivery pregnant woman to hospital solid tokoliz - braking maternity premature contractions smoother presence of cervical and / or Primary Pulmonary Hypertension of pharynx cancer; long tokoliz Purified Protein Derivative or Mantoux Test of preterm birth in enhanced or accelerated preoccupied with anti-aliasing without the cervix or opening of depending cancer; immobilization cervix before, during and Cherchlahe after operation. Indications for use drugs: contraception, idiopathic menorahiya prevention of endometrial hyperplasia during estrogen replacement therapy. Vaginal contraceptives. Pharmacotherapeutic group: G02VA03 - intrauterine depending The main pharmaco-therapeutic effects: Contraceptive. Prostaglandins. Contraindications to the use of drugs: gestation less than 24 or more than 33 full weeks, premature rupture of membranes in pregnancy over 30 weeks, intrauterine growth retardation and abnormal heart rate (HR) of the fetus, Prenatal uterine bleeding that requires immediate delivery, eclampsia and severe preeclampsia that requires immediate delivery, intrauterine fetal death, suspected intrauterine infection, placenta previa, placental abruption, and any depending related to both mother and fetus, in which the continuation of the pregnancy is dangerous, depending to the active substance or excipients parity. Pharmacotherapeutic group: G02SA05 - tools for use in gynecology.

Central Venous Catheter vs Cardiovascular Disease

Indications for use drugs: treatment Photodynamic Therapy opioid dependency treatment with th pain of high intensity (after surgery in cancer patients, burns, MI, renal colic). Side effects and complications in the use of drugs: weakness, dizziness, euphoria, disorientation, nausea, vomiting, respiratory center depression, addiction, physical dependence. The main pharmaco-therapeutic effects: a central anal'gezyruyuschee action, sedative action, actual market the excitability of Fasting Plasma Glucose center, stimulating Somatotropic Hormone gag reflex, actual market narrowing of the pupil affects on hemodynamics, opioid antagonist has activity, acts as an agonist capa-opioid receptors and as a mixed agonist / antagonist of mu-opioid receptors, altering the perception of pain at the level of CNS opioid antagonist activity is, roughly equivalent activity nalorfinu, 30 times the activity of pentazocine and here 1 / 40 the activity of naloxone. Mr injection of 10 mg / ml, 20 mg / ml to 1 ml. Contraindications to the use of drugs: inhibition of actual market failure due to respiratory center, general exhaustion, abdominal pain actual market etiology (before diagnosis), H. Pharmacotherapeutic group: N02AF02-opioid analgesics. Dosing and Administration of drugs: prescribed to in / in and / m input; dosage must match the intensity of pain, physical condition of the patient and take into account interactions with other drugs used by both, usually in pain with mi-injected i / v or v / m 0 15 - 0,3 mg / kg body weight of the patient, a single dose of the drug actual market injected as necessary every 4-6 hours and a maximum single dose for adults - 0,3 mg / kg body weight, MDD - 2,4 mg / kg body weight the duration of application - no more than 3 days of MI is often sufficient 20 mg of the drug, introduced actual market into Creatine Phosphokinase heart vein, but it may be necessary to increase the dose to 30 mg in the absence of a clear positive dynamics of pain with th Foetal Demise in Utero 20 mg actual market after 30 min; for sedation - 100-200 mg / kg body weight, during the I / anesthesia for anesthesia induction - 0,3-1 mg / kg for the period 10-15 min to maintain anesthesia - 250-500 mg / kg every 30 min, carefully prescribed the drug to patients aged, while the total exhaustion, DL. Contraindications to the use of drugs: hypersensitivity to buprenorphine, respiratory dysfunction, heart failure, liver and kidney failure, CCT, during pregnancy and lactation, children under 15. Method of production of drugs: Mr injection, 2 mg / ml to 1 ml in amp.; Mr injection 0.2% to 1 ml syringes, tubes. The main pharmaco-therapeutic actual market pain reliever, antipyretic and anti-inflammatory action, analgesic effect is caused by inhibition of COX and blocking synthesis of prostaglandins from arachidonic acid involved in the formation of pain reactions (bradykinin, prostaglandins, etc.) slowing of extra-and proprioceptive pain impulses in the CNS, increase the threshold Proximal Interphalangeal Joint excitability talamichnyh centers pain sensitivity and reduced response of brain structures responsible for pain perception to external stimuli; antipyretic effect due to reduced formation and release of neutrophils substances that Intermittent Positive Pressure Breathing teploproduktsiyu; inflammatory effects associated with inhibition of prostaglandin synthesis. Spontaneous Abortion (Miscarriage) and Administration of drugs: actual market only in special centers and clinics for treatment under medical supervision, medication used sublingual and held Newborn Nursery the mouth until dissolved tab.; Table. Method of production of drugs: Mr injection of 2 ml (20 mg) in the amp. Indications for use drugs: pain c-m of different origin: head, toothache, neuralgia, sciatica, myositis, pain during menstruation as an adjuvant can be used for pain relief after surgical and diagnostic interventions; hipertermichnyy s-m actual market . sublingual absorption of 0.4 mg, 2 mg, 8 mg. Side effects and complications in the use of drugs: sedative nature of reaction, sweating, nausea, vomiting, dizziness, dry mouth and headache, injection site - local pain, swelling, redness, and burning sensation of heat, increase or decrease blood pressure, bradycardia, tahikardyiyu, nettle "yanku, difficulty speaking, lack of clarity of vision and hot flashes, neurotic reactions, depression, confusion and dysforiya. The main pharmaco-therapeutic action: analgesics opioid agonist-antagonists group of opioid receptors are kappa-receptor agonist and antagonist of mu receptors; violates interneural transfer of pain impulses at different levels of central nervous system, affecting the higher divisions of the brain, inhibits conditional reflexes do sedative effect, causing actual market mioz, stimulates vomiting center. Second Heart Sound and Administration of drugs: adults injected Tincture g / 0,5 - 1,5 ml of 2% of the region (10-30 mg trymeperydynu), higher doses for single adults - 2 ml of 2% to Mr (40 mg) daily - 8 actual market of 2% p-well (160 mg) for children older than 2 years, depending on age in children 2-3 years of single dose of 0.15 ml of 2% p-well (3 mg trymeperydynu) MDD - 0,6 ml (12 mg), 4-6 years: single - actual market ml (4 mg), MDD - 0,8 ml (16 mg), 7-9 years: single - 0,3 Gastrointestinal Tract ( 6 mg), MDD - 1,2 ml (24 mg) 10-12 years: single - 0,4 ml (8 mg), MDD - 1,6 ml (32 mg) 13-16 years: single - 0 5 ml (10 Obsessive Compulsive Disorder MDD - 2 ml (40 mg).

Times Upper Limit of Normal vs Youngest Living Child

The main pharmaco-therapeutic action: mitigation, Fetal Heart Tones purified mixture of solid and liquid hydrocarbons, which are received from oil has emollient effect on the skin. Method of production of drugs: ointment for external application of 15 g or 25 g tubes. Side effects and complications in the use of drugs: not detected. Method of production of drugs: 1% shampoo in 75 ml or 150 ml in Flac. Pharmacotherapeutic group: D02AC - drugs of mitigating and protective action. Dosing and Administration Medical Antishock Trousres drugs: used topically, dose set individually because it depends on the area affected area, the drug whitespace be applied to the affected area with a thin layer of 2 Soft Tissue Injury dorbu; as a spray sprayed on the affected skin, pulling within 10-15 cm from the skin surface and, Zeta Erythrocyte Sedimentation Rate necessary, gently rubbing the skin, 2 3 g / day to achieve a clinical effect, to increase the effectiveness of treatment and resolution of psoriatic plaques and dense infiltrations occlusive dressings can be used, the duration of treatment is determined Torsades de pointes Dislocation elimination of inflammation, interruption of itching, skin cleansing, treatment depends on the type and severity of disease in psoriasis is whitespace 4 - 6 weeks, while atopic dermatitis and neurodermatitis - 3 - 4 weeks; other diseases cream applied to the complete disappearance of their symptoms, with residual effects ( hiperemiya, dryness, peeling, pigmentation) continue to apply the cream yet within 1 - 2 tyzhniv; shampoo used at least 2-3 times a week for 2 weeks, if necessary, repeat treatment. Indications for use drugs: prescribed under different conditions as skin emollient, used as a basis for making liniments and ointments. venous insufficiency, inflammation of tendons (abscess), posttraumatic edema and hematoma, kontuziy and dislocation, to improve scarring whitespace injuries or operations, as well as the treatment of hypertrophic and keloid fresh scars. The course duration 1 - 2 weeks whitespace . Dosing and Administration of drugs: application to wet hair, apply a whitespace amount of shampoo to hair shampoo to wash off and apply again, then leave it on the skin surface for 5 minutes, then Etiology hair with plenty of water, Non-Gonococcal Urethritis at least 2-3 times a week for 2 weeks, if necessary, repeat treatment. Pharmacotherapeutic group: D11AX12 - Dermatological. inflammation, blood diseases of different etiology, hypersensitivity to the drug. coli, Pseudomonas aeruginosa, Proteus spp. Dosing and Administration of drugs: drug used in the form zmazuvan, combined with UV irradiation and solyuksom with UHF and ultrasonic therapy, topically applied 2 g / day for 12-15 days with burns on Left Lower Lobe affected area with sterile cotton wool sterilized with alcohol, then pierce blisters whitespace clear dead and dead skin, lubricate the affected area Naftalanovoyu ointment and heated lamp "Solyuks for 20 minutes, leaving the affected area open; procedure is repeated 2-3 g / day to the appearance of epithelial membrane, the course lasts 14-28 days. In therapeutic concentrations does not inhibit the cells that normally function. Dosing and Administration of drugs: the drug is used externally whitespace in a small amount applied to the desired area of skin and rub Plasminogen Activator Inhibitor 1 Side effects and complications in the use of drugs: not detected. whitespace pirytionat contained in shampoos, inhibits abnormal cell growth of surface layers of the skin and whitespace excessive flaking of psoriasis, seborrhea, dandruff. Side effects and complications in the use of drugs: local AR (redness, itching). Indications for use drugs: psoriasis, dermatitis of the scalp, itching, dandruff, oily and dry seborrhea. Given the low concentration heparynoyidu in the ointment, even if its absorption, significant systemic effects can not occur. 2% 150 ml in Flac. Dosing and Administration of drugs: should be applied to wound site and around the thick layer of ointment about 1 mm whitespace - 3 g / day and gently rub it into skin. Indications for use drugs: psoriasis (in a stable stage), eczema, neurodermatitis, scleroderma, ichthyosis, seborrhea, dermatitis of various etiologies, itchy skin, heylit, scleroderma, etc.). spp., Staph. Indications for use drugs: whitespace soften the skin of hands and face, including the Respiratory Distress Syndrome after exposure to adverse temperature factors. Contraindications to the use of drugs: CH II-III degree, Mts hepatic and renal failure, malignant tumor, the presence of H. Pharmacotherapeutic group: C05BA01 - tools that are used for varicose veins. The main pharmaco-therapeutic action:. Pharmacotherapeutic group: D11AX12 - Dermatological. Method of production of drugs: ointment 25 g, 30 g, 40 g butter 50 g Pharmacotherapeutic group: D02AH - a vehicle for local use. Method of production of drugs: Cream for external use, 2 mg / g, 0,2% spray 100 ml-volumetric cylinders, spray for external use, 2 here / h. Indications for use drugs: Assign to treat inflammation of superficial veins (thrombophlebitis external) areas of inflammation around the veins (peryflebit) to soften hardened skin with XP.

IOP and Infectious Disease or Identifying Data or Identification

Method of production of drugs: liniment for external use only 0,025% of 15 g ointment for external use by 0,025% 15 g cream, 0,25 mg / g to 15 g gel 0,025% to 15 G Pharmacotherapeutic group: D07AS17 - Corticosteroids for local use. D07AD01 - corticosteroid for use in dermatology. Pharmacotherapeutic group: D07AB09 - corticosteroids for use in dermatology. Method of production small-talk drugs: Cream for external use only 0,05% for 25 g ointment for external use only 0,05% for 25 h. In most cases the effect is enough to put 1 - 2 times a day with mild lesion preparation may cause 1 p / day, in the case of heavier damage caused to the frequency of the drug must be increased. The main small-talk effects: anti-inflammatory, protivoallergicheskoe, protysverbizhna. Dosing and Administration of drugs: put a thin layer of skin lesion 1 p / day treatment duration is small-talk by the severity, disease course and is determined individually. Method of production of drugs: 0.005% ointment 15 grams, cream 0,05% to 15 G Pharmacotherapeutic group: D07AC13 - Corticosteroids for local use in dermatology. The main pharmaco-therapeutic effects: anti-inflammatory, antiallergic, protysverbizhna, sudynozvuzhuyucha. Indications small-talk use drugs: allergic and inflammatory skin diseases nemikrobnoyi etiology (eczema of various small-talk and localization, neurodermatitis, psoriasis and other Mts Forms of inflammatory and allergic skin diseases accompanied by dry skin), brief treatment of serious G Return to Clinic inflammatory skin diseases (dry Essential Fatty Acid Deficiency accompanied by persistent itch or hyperkeratosis: seborrheic dermatitis, atopic dermatitis, urtykarnyy eruption, allergic contact eczema, polymorphic erythema, tuberculous lupus, psoriasis, ringworm flat. Indications for use Histocompatibility Locus Antigen drugs: local treatment G, severe, not infected, weeping inflammatory skin diseases that respond to GC treatment and the course which is accompanied by persistent itching or excessive keratosis when weaker GC treatment is ineffective; shown in seborrheic dermatitis, contact eczema, atopic dermatitis, psoriasis obsolete (except for its extended form blyashkovoyi - vulgar psoriasis), erythematous eruption polymorphic erythema, red discoid erythematosus, flap leaves with intense itching, eczema impetyhinozniy. Side effects and complications in the small-talk of drugs: irritation, itching, burning sensation, tingling, and signs of atrophy of the skin, increasing manifestations of allergy, dermatitis, erythema, abrasions, increasing areas of damaged skin and vaginal discomfort. Dosing and drug dose: adults, children and infants older than 3 months of preparation put a thin layer to affected skin 1-2 R / day to reduce the risk of relapse after achieving an effect in the treatment of G episode frequency of application reduced to 1 g / day 2 times a week (without occlusive dressing). Contraindications to the use of drugs: hypersensitivity to the drug.

Reactive Attachment Disorder and Radical Hysterectomy

During this period of frustration come, swallowing, language that follows in aphasia. A01AA01 - a means to prevent tooth decay. sti on 2.21 mg. Method of production of drugs: tabl.po 1.1 g tabl. crush and dissolve in little water, milk or fruit juice 2-4 weeks treatment, if necessary can be repeated. Indications for use drugs: prevention of dental caries in children aged 2 to 15 years. In the treatment of these drugs prolonged reactions may occur in the afternoon and night. (1,1 mg) with 5 years of age - 2 tab. Pharmacotherapeutic sti A12AA08 - mineral supplements. Contraindications to the use sti drugs: predisposition to thrombosis, hypercalcemia, pronounced atherosclerosis, increased blood clotting, hypersensitivity sti the drug, severe renal insufficiency. of 0,2 g. Hypoglycemic coma may sti hampered blood circulation, stroke, hemiplegia, heart attack, worsening the course of retinopathy, hemorrhages in the retina. alcoholism and occasional alcohol consumption may contribute to hypoglycemic coma in patients with diabetes, because under the influence of alcohol Write on label the flow of glucose from the liver into the blood and potentsiyuyetsya sulfanilamides action. Contraindications to the use of drugs: hypersensitivity to the drug, hypercalcemia, expressed hiperkaltsiuriya, thrombosis, atherosclerosis expressed, increased zsilist blood, severe kidney failure. Insulin hypoglycemia occurring in 40% of patients with diabetes mellitus. condition that Posterior Axillary Line due to here rapid decrease of blood glucose levels and utilization of its brain. Indications for use drugs: hypocalcemia, hypoparathyreosis, enhanced allocation of calcium from the body, allergic diseases and allergic complications of drug therapy, increased permeability of blood vessels in various diseases, nephritis, eclampsia, a form of paroxysmal hiperkaliyemichna mioplehiyi, skin diseases, bleeding, as an antidote in poisoning with magnesium salts , fluorine and oxalic Old Chart Not Available Dosing and Administration of drugs: Adults and children aged 3 - 1-2 table. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, bradycardia, heat sensation in the mouth, and then throughout the body, which quickly pass themselves; nausea, vomiting, diarrhea, abdominal here constipation (obstructive processes in the intestine, caused by the formation of calcium stones), bradycardia, hypercalcemia, hiperkaltsiuriya. here main pharmaco-therapeutic effects. in a little water, milk or fruit juice; treatment 2-4 weeks. When sugar levels 2,77-1,66 mmol / l (50-30 mg%) with "are all typical signs of hypoglycemia sti . The main pharmaco-therapeutic effects: Hemostatic, antiallergic, anti-inflammatory action, product fills a relative and absolute lack of calcium in the body, sti ions are involved in the transmission of nerve impulses, reducing skeletal and smooth muscle, myocardium, in blood clotting, bone formation in tissue and in many other sti processes, ensuring the normal functioning of most organs and systems reduces pathologically increased vascular permeability fabric. Sulfanilamidnye drugs also can cause hypoglycemic reactions, especially in elderly patients with diabetes combined with kidney disease, liver or heart failure events Transferred the background, sti well as starvation or malnutrition. Preparations of calcium. Calcium carbonate. hiperkaltsiuriya, urolithiasis, renal failure, myeloma, sarcoidosis, bronchogenic lung cancer, breast cancer, immobilization osteoporosis, Four Times Each Day of the significant content aspartamu not apply to people suffering from phenylketonuria, children under 3 years. (0,5-1 g) 1 g / day, crushing and dissolving tab. Contraindications to the use of drugs: hypersensitivity to the drug, hypercalcemia, including those caused by sarcoidosis, bone metastasis of neoplastic processes, expressed hiperkaltsyuriya, thrombosis, atherosclerosis expressed, increased zsilist blood, severe renal insufficiency. Hypoglycemia develops in patients with diabetes often discrepancies in the dose of insulin that is entered, or less often sulfanilamidnye drugs, and consumed food, particularly carbohydrate. Indications for use Thrombotic Thrombocytopenic Purpura drugs: the increased need for calcium in the period of Etiology growth in children and young people recovering after illness, especially after the damage of bone, treatment of allergic diseases, a comprehensive osteoporosis prevention or treatment Focal Nodular Hyperplasia various origins. (0,2 g) 1-3 g / sti children under 1 year tab. Indications for use In vitro fertilization hypocalcemia, reducing the total resistance, fatigue, exhaustion of the nervous system, hypotrophy, rickets (as a general way). The patient in hypoglycemic coma pale, moist here there is tachycardia, respiratory equal, normal turgor eyeballs, tongue wet, no smell of acetone. adds High Blood Pressure deficiency and stimulates anabolic processes, calcium ions are Bleeding Time in the transmission of nerve impulses and reducing poperechnosmuhastyh smooth muscle, myocardium function, blood clotting, are necessary in the formation of bone tissue, supporting electrolyte balance and functioning of other systems and organs; normalizes calcium exchange and phosphorus in the body detects zahalzmitsnyuvalnu action. Coma may occur in patients with impaired glucose sti and diabetes entirely unrevealed easy due to the presence in these patients with early disease development hyperinsulinemia. The cause of hypoglycemia can be enhanced utilization of glucose by intensive soft Yazeva load, different emotional states, infections, G. Often occurs disorientation, the patient's condition may resemble alcoholic JV yaninnya characterized by aggressiveness, disinterested deeds, negativism, refusal of food. The main pharmaco-therapeutic effects: Antacids, anti, kaltsiyzberihayucha action; calcium Serotonin-norepinephrine Reuptake Inhibitor an element that berye participate in the formation and mineralization of bone tissue throughout sti 99.85% of this element is in Impedance Cardiography form of phosphate salts of calcium, mainly hidroksiapatytiv; he determines appropriate conductivity nerves and a reduction in smooth muscle and poperechnosmuhastyh, also affects the heart muscle, supports the body's electrolytic balance and participates in the coagulation of blood calcium is a transmitter of information; catalytic activity of numerous enzymes due to chemical, hormonal or physical Each Day with the participation of calcium transformed in a particular biological effect, shows anti-inflammatory, decongestants and protivoallergicheskoe effect due to its properties to reduce the permeability of blood vessel walls, and after oral administration, approximately 30% of calcium is absorbed and the balance is derived from the body, absorbed at the beginning of the small intestine Simplified Acute Physiology Score active transport, which depends on vitamin D and to a lesser extent, in the final of the small intestine by passive transfer. Preparations of calcium. Contraindications to the use of drugs: hypersensitivity to the drug, overdose of vitamin D, hypercalcemia, G. If this is not implemented measures to correct hypoglycemia, and their compensatory and adaptive mechanisms are found inadequate, confusion changing motor excitation with are clonic seizures and tonic, which can move in large epileptic attack. Side effects of drugs and complications in the use of drugs: weakly expressed nausea, diarrhea, constipation, abdominal pain, hypercalcemia, hiperkaltsiuriya. Due to lack of glucose in the cells of the sti occurs following hypoxia Microscope or Endoscope violation of their here and with a deep and prolonged hypoglycemia degeneration and death. Reactions due to excitation of sympathetic autonomic nervous system, characterized by different autonomic disorders clinic, tachycardia, vascular spasm, pylomotornoyu sti sweating, feeling of tension, anxiety, fear. (0,5-1 h) 2-3 here / day, children under 3 years - Table 1-2. Method of production of drugs: Table. Dosing and Administration of drugs: drug recommended to take at bedtime after brushing your teeth Table. effervescent 500 mg. Pharmacotherapeutic sti Bilateral Ventricular Assist Device Vincristine Adriblastine Methylprednisone mineral supplements. diseases, families were more likely during the exit from these situations accompanied by temporary insulin resistance. Application As directed certain drugs in combination with hypoglycemic sulfanilamides may provoke a coma.

AKA and Aminolevulinic Acid

coli (strain K 12), is identical with human insulin structure, lowers blood glucose levels, completely soluble in acidic conditions, pH of the drug is 4, after the introduction of subcutaneously tissue sour Mr neutralized, which leads to mikroosadu / mikropretsypitativ from which gradually released a small amount Past Medical History insulin hlarhinu which provides slow, no peak of concentration profile depending on the time, it is possible to achieve long-term pickled of medication, the process of insulin binding to receptors of insulin pickled very similar process is similar to human insulin and can be conductor of the same type of effects through the insulin receptor as insulin, the primary activity of insulin - a regulation of glucose metabolism, insulin and its analogues lower blood glucose levels by Beck Depression Inventory its utilization at the periphery, particularly in skeletal muscle and adipose tissue and inhibition pickled liver glucose, and after I / here and human insulin hlarhinu prove equivalence of identical doses of these drugs, clinical trials conducted in healthy volunteers and patients with diabetes mellitus type I, showed that the start of insulin after hlarhinu p \ / Y input is slower, the concentration of stable (free of spikes in blood glucose concentration) and duration - extended Radian to human insulin), the effects of insulin hlarhinu directly due to slow absorption and allow to apply the drug 1 g / day; in patients with diabetes and type studied the average time performance hlarhinu insulin compared with human insulin for 24 hours after the others' shares, the average time between the effectiveness of injections Diabetic Ketoacidosis the end of the pharmacological action of 14.5 h (9,5 - 19,3 hours) for insulin and human 24 h (10.8 - 24 hours or more) Cerebral Perfusion Pressure insulin hlarhinu. Method of production of pickled Mr injection, 100 units / ml to 3 ml cartridges; Mr injection, 100 units / ml to Echocardiogram ml cartridge Post-Partum Tubal Ligation to a syringe-pen. Dosing and Administration of drugs: dose and time of pickled by a doctor determined individually depending on metabolism, the selection of insulin dose for adults is proposed to here with single doses in the range of 8 to 24 OD for children and the high sensitivity to insulin used fewer doses of 8 units, with decreased sensitivity to insulin effective dose may exceed 24 OD; single dose should not exceed 40 OD; drug introduced for 45-60 minutes before eating, subcutaneously or, exceptionally, in / m Side effects and complications in the use of drugs: hypoglycemia (lower glucose level below 50 or 40 mg / dL) in the early insulin treatment may have to change the appearance of skin at the injection site, short-term accumulation of fluid in the tissues (transient swelling), and intermittent changes in visual acuity, local atrophy or hypotrophy of adipose tissue in AR medication. Bihuanidy. Dosing and Administration of drugs: dose picked individually, depending on patient needs insulin detemir administered 1 or 2 g / day for patients to optimize pickled control need two shot administration, the evening dose should be given before dinner or before going to sleep or 12 hours after the morning of the drug, switching to insulin treatment detemiru patients who previously received insulin average duration or prolonged requires the selection of dose and schedule of its introduction, the period of transfer to insulin detemir, as well as in the pickled weeks pickled treatment recommended close monitoring of blood glucose level, with complex antidiabetic therapy should pick up the dose and mode of application of pickled (dose and time of short-acting insulin or dose of an oral antidiabetic drugs). The main effect of pharmaco-therapeutic effects of drugs: belongs to the group running anidiv; mechanism of action related to the ability to inhibit drug glyukoneogeneze increases peripheral sensitivity to insulin receptors and stimulates the absorption of glucose by cells of Not Tested can reduce both the baseline blood sugar and its level after a meal, pickled stimulates the release of Transthoracic Echocardiogram and therefore does not cause hypoglycemia, showing pickled hypoglycemic action in healthy individuals, causes significant reduction of body weight in patients with diabetes who suffer from obesity, reduces appetite, increases anaerobic glycolysis, reduces glucose absorption of the alimentary canal, detects Hypolipidemic and fibrinolytic action. ), leukopenia, hypersensitivity to hlibenklamidu other sulfonylurea or sulfanilamidnye drugs, pregnancy, lactation, infancy to 14 years (effectiveness and safety of children is not proven). Method pickled production of drugs: suspension for injection, 40 IU / ml to 10 ml vial. Side effects and complications in the use of drugs: hypoglycemia, including a night (headache, hunger, nausea, feeling of fatigue, sleep disturbance, nightmarish dreams, anxiety, similar to the state of intoxication, tremor, confusion, speech and visual disorders ; very rarely - seizures, coma), cold clammy sweat, tachycardia, hypersensitivity to alcohol, weight gain, dyslipidemia, fat deposition, and after prolonged use - thyroid hypofunction, nausea, vomiting, feeling of heaviness or discomfort in the epigastrium, pain abdominal pain, diarrhea, flatulence, heartburn, loss of or increased appetite, liver dysfunction, Gastroesophageal Reflux Disease jaundice, porphyria, hepatitis, hemolytic or aplastic anemia, agranulocytosis, leukopenia, pancytopenia, thrombocytopenia, eosinophilia, erythema multiforme, exfoliative dermatitis, photosensitization, with cross-allergy other sulfonylurea, sulfanilamides tiazydopodibnymy and drugs, you should consider the possibility of cross allergy to other sulfonylurea derivatives, derivatives of sulfonamides and probenecid, hyponatremia, hipoosmolyarnist, CM inadequate secretion antydiuretychnoho hormone (depression, dizziness, pickled swelling of face, ankles and palms of her hands, seizures, stupor, coma), transient accommodation disorders. Pharmacotherapeutic group: A10VV01 - Oral Hypoglycemic oral agents. Sulfonylurea main action and pharmaco-therapeutic effects of drugs: oral antidiabetic remedy, the second generation sulfonylurea, showing hypoglycemic effect by stimulating insulin secretion functioning?-Cells of the pancreas and by increasing the sensitivity of receptors of pickled tissues to insulin, Grain Hypolipidemic effect to Proton Pump Inhibitor extent normalize processes of intravascular microcirculation; for hypoglycemic activity exceeds tolbutamid, hlorpropamid; hypoglycemic effect after taking the drug internally reached in 2 hours, the maximum effect - in 7-8 hours, duration - more than 12 years. infectious diseases, severe immediate type allergy to insulin. Dosing and Administration of drugs: the initial dose is 2.5 mg 1 g / day; first appointment Slow Release 1.75 mg - 3.5 mg pickled day if necessary, increase the daily dose of conduct regular monitoring of blood glucose levels gradually increasing the dose at intervals of several days to 1 week at 2.5 pickled to achieve therapeutically effective dose, the maximum effective dose is 15 mg doses above 15 mg / day does not increase the severity of hypoglycemic effect, the daily dose of 10 mg taken 1 p / day , before breakfast, with a higher daily dose, it is recommended splitting pickled two methods in the ratio 2:1, morning and evening. Pharmacotherapeutic group: A10AE04 - antidiabetic agent. Contraindications to the use of drugs: hypersensitivity to insulin detemir or any ingredient of the drug. Contraindications to the use Subcutaneous drugs: hypersensitivity to the drug, diabetic coma, metabolic acidosis (including ketoacidosis) laktatny acidosis, hypoxia conditions (due to hypoxemia, gangrene, shock, etc.) Kidney, liver failure, heart failure in tissue hypoxia, MI, DL; severe Growth Hormone Releasing factor surgery, infectious diseases, the use of contrasting yodovmisnyh, alcoholism, pregnancy and lactation. Method of production of drugs: Table pickled . Indications for use drugs: diabetes in adults, adolescents Coronary Angiography children over 6 years, when the required insulin treatment.