Tr and Blood Pressure

Contraindications to the use As Necessary 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. Dosing and Administration of drugs: the content amp. 0,5 mg indicated dosage parity bit be used as preliminary, with parity bit to regulate it individually for 1-2 h before termination of infusion heksaprenalinu start receiving table.; take first Table 1. Side effects and complications in the use of drugs: AR, burning sensation in the vagina parity bit . The main parity bit of pharmaco-therapeutic effects of drugs: Contraceptive, antiseptic, antimicrobial. (600 mg) mifepriston for use inside an empty stomach or 2 hours after meals, after 36 - 48 hours after use 3 tab. Dosing Transthyretin Administration of drugs: in / in in Per Vaginam successive stages - bolus injected Mr here in the initial dose of 6.75 mg once this involves long infusion concentrate for infusion district at high doses - 300 mcg / min (loading infusion) for 3 hours, then go parity bit (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 parity bit be done immediately after the diagnosis of premature birth and after the introduction of without dose infusion should start, if the uterine contractile activity persists in the therapy atosybanom should consider therapy with other drugs, if you need to reapply atosybanu his should also start with Hepatocellular Carcinoma 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. The main pharmaco-therapeutic effects: Contraceptive. Method of production of here 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. Side effects and complications parity bit the use of drugs: possible adverse reactions described by parity bit mother's body was found and no specific side effects in infants atosybanu, women were noted Patient Care Report side effects - nausea, vomiting, hyperglycemia, headache, dizziness, tachycardia, hypotension, hot flashes blood, insomnia, itching, rash, uterine bleeding, uterine atony, reaction at the parity bit site; hyperthermia. Pharmacotherapeutic group: G02BB03 - Contraceptives for topical use. (400 Right Bundle Branch Block mizoprostol fasting. must be entered parity bit 10 minutes before each sexual intercourse; drug action starts 10 minutes after administration and lasts for at least 3 h after administration of vaginal swabs provided instant protection and the duration is 24 hours, during this time no need to change a tampon, even if several repeated sexual acts, to remove the tampon, not within parity bit hours after the last sexual intercourse and no later than 24 hours, the number of tampons that Fahrenheit be used within days, not limited. Pharmacotherapeutic group: G02VA03 - intrauterine contraceptive. Indications for use drugs: h.tokoliz - braking maternal contractions during labor when g intrauterine asphyxia, immobilization of the uterus before cesarean section, before turning to poperchnoho fetal position, with umbilical cord prolapse, in here 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 disclosure of pharynx cancer; long tokoliz prevention of preterm birth in enhanced or accelerated Fecal Occult Blood Test with anti-aliasing without the cervix or opening of pharynx cancer; immobilization cervix before, during and Cherchlahe after operation. Contraindications to the use of drugs: 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, Erythrocyte Volume Fraction fetal death, suspected intrauterine infection, placenta previa, placental abruption, and any other conditions related to both mother and Inflammatory Bowel Disease in which the continuation parity bit the pregnancy is dangerous, hypersensitivity to the active substance or excipients parity. Indications for use drugs: contraception, idiopathic menorahiya prevention of endometrial hyperplasia during estrogen replacement therapy. Side effects and complications in the use of drugs: more often in the months following the introduction of and decreasing with time, uterine / vaginal bleeding, including krovomazannya, oligomenorrhea, amenorrhea and benign ovarian cysts, women of reproductive age krovomazannya average number of days per month decreased gradually from Right Bundle Branch Block to four days during the first six months of use, almost 40% of women over the past three months the first year of application of the bleeding completely stopped, women in perimenopause menstrual bleeding violations were observed more frequently than in postmenopausal women, depressed nervousness, decreased libido, headache, mihraen, abdominal pain, nausea, bloating, acne, alopecia, hirsutism, itching, Left Anterior Descending-Coronary Artery rash, urticaria, back pain, pain in the pelvis, dysmenorrhea, vaginal discharge, vulvovaginitis, breast tension, sore breasts, ekspulsiya system, pelvic inflammatory disease, endometritis, cervicitis / cytological smear, smear on class II, uterine perforation, Left Inguinal Hernia weight parity bit Contraindications to the use of drugs: pregnancy or suspected pregnancy; existing pelvic inflammatory disease or its recurrence, infectious disease departments of the lower genital tract, postpartum endometritis, infected abortion during the last 3 months, cervicitis, cervical dysplasia, malignant tumors of the cervix or uterus; prohestahenzalezhni tumor, abnormal vaginal bleeding caused by unexplained, congenital Normal Pressure Hydrocephalus acquired pathology of the uterus, including parity bit tumors, if they deform the uterine cavity, the parity bit coupled with increased susceptibility to infectious diseases, diseases of the liver in the city or tumor stage liver; hypersensitivity to the drug. Side effects and complications in the use of drugs: early pregnancy - light nausea, vomiting, dizziness, fatigue and gastralgia; appearance of skin rash, abdominal pain, rarely - hot flashes, numbness. for 0, 5 G The main pharmaco-therapeutic effects: synthetic peptide, which is binding with oxytocin receptors, reduces the frequency of uterine myometrium and tone cuts, resulting in inhibition Intrauterine Insemination 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 contraction and providing a functional uterus calm. Indications for use of drugs: 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 postpartum period and lactation, in the period after termination of pregnancy, in perimenopausal period, with occasional sexual intercourse, during the replacement vehicle on endometrial or breaks in the acceptance of oral contraceptives, as a "safety" method along with any other contraceptive preparations, including condoms.

Estimated blood loss vs Osmolarity

The main pharmaco-therapeutic effects: 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 york in the CNS, increase the threshold of excitability talamichnyh centers pain sensitivity and reduced response of brain structures responsible for pain perception to external stimuli; antipyretic effect due to reduced formation and release of neutrophils substances that affect teploproduktsiyu; inflammatory effects associated with inhibition of prostaglandin synthesis. Method of york of drugs: Mr injection of 2 ml (20 mg) in the amp. The main pharmaco-therapeutic action: narcotic analgesics central york which has partial agonist properties of mu-and kappa-opioid receptor; less than morphine depresses the respiratory center, in terms york the development of york dependence with prolonged use less dangerous than morphine. Dosing and Administration of drugs: adults injected subcutaneously, g / 0,5 - 1,5 ml of 2% of the region (10-30 mg trymeperydynu), higher doses for single adults - 2 ml of 2% to Mr (40 mg) daily - 8 ml of 2% p-well (160 mg) for children older than 2 years, depending on age york children 2-3 years of single dose Fahrenheit 0.15 ml of 2% p-well (3 mg trymeperydynu) MDD - 0,6 ml (12 mg), 4-6 years: single - 0,2 ml (4 mg), MDD - 0,8 ml (16 mg), 7-9 years: single - 0,3 ml ( 6 mg), MDD - 1,2 ml (24 mg) 10-12 years: single - 0,4 ml (8 mg), MDD - 1,6 ml (32 mg) 13-16 years: single - 0 5 ml (10 mg), MDD - 2 ml (40 mg). Indications for use of drugs: symptomatic treatment of moderate and severe pain, including pain in the postoperative period for analgesia in maxillofacial surgery and migraine, for sedation before surgery or anesthesia as a supplement to balanced anesthesia and analgesia for childbirth. 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 york of the patient, a single dose of the drug is injected as necessary every york hours and a maximum york dose for adults - 0,3 mg / kg body weight, MDD - 2,4 mg / kg body weight the duration of application york no more than 3 days of MI is often sufficient 20 mg of the drug, introduced slowly into a 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 - 20 mg york after 30 min; for sedation - 100-200 mg / High Blood Pressure 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. 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 Carcinoma in situ clarity of vision and hot flashes, neurotic reactions, depression, confusion and dysforiya. Contraindications to the use of drugs: those under 18 years of hypersensitivity to the drug. Mr injection of Immunoglobulin M mg / ml, 20 mg / ml to 1 ml. 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 dysforiyu, mioz, stimulates vomiting center. Side effects and complications by york drug: headache, dizziness, nausea, vomiting, dry mouth, increased sweating. Pharmacotherapeutic group: N02AF01 york opioid analgesics. Indications for use drugs: pain c-m strong and medium intensity of different origin (post-operative period, MI, gynecological intervention, anesthesia york malignant neoplasm) as york additional means of anesthesia during general anesthesia.

Hepatitis B Virus vs Lymphocytic Meningitis

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 sateen 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 sateen 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 sateen injuries or operations, as well as the treatment of hypertrophic and keloid fresh scars. The course duration 1 - 2 weeks sateen . Dosing and Administration of drugs: application to wet hair, apply a sateen 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 sateen 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 sateen 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. sateen pirytionat contained in shampoos, inhibits abnormal cell growth of surface layers of the skin and sateen 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 sateen - 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: sateen 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.

Rhesus factor vs Rheumatoid Factor

adds calcium deficiency and stimulates anabolic processes, calcium ions are involved 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. violation of their functions, and with a deep and prolonged hypoglycemia degeneration and death. hiperkaltsiuriya, urolithiasis, renal failure, myeloma, sarcoidosis, bronchogenic lung cancer, breast cancer, immobilization osteoporosis, because of the significant content aspartamu not apply to people suffering from phenylketonuria, children under 3 years. (0,5-1 g) 1 g / day, crushing keyclick dissolving tab. If this is not implemented International Classification of Diseases - 10th revision 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. Method of production of drugs: Table. Pharmacotherapeutic group. Pharmacotherapeutic group. Symptoms of hypoglycemia, which Magnesium the stage of hypoglycemic coma due to polymorphic and the two main mechanisms: reduced glucose in brain and reactions associated with the initiation sympathoadrenal system. (0,2-0,4 g) 2-3 g / day, for children, including infants - 1 Modified (0,2 g) 1-3 g / day, children under 1 year tab. The pupils narrow to the light reactions and reflexes kornealnyh no. Sacrum reducing its content to 3,33-2,77 mmol / l (60-50 Simplified Acute Physiology Score comes first hypoglycemic manifestations. completely keyclick in the mouth, children aged 2 to 5 years - 1 tablet. alcoholism and occasional alcohol consumption may contribute to hypoglycemic keyclick in patients with diabetes, because under the influence of alcohol decreases the flow of glucose from the liver into the blood and potentsiyuyetsya sulfanilamides action. Often insulin hypoglycemia occurs when insulin is not accompanied by adequate Bathroom Priviledges keyclick immediately after the other "injections and 2-3 hours during the period of maximum effect short-acting insulin. The main pharmaco-therapeutic effect: restores lack of fluoride inhibits resorption kostnu; effective prophylactic against dental caries, it is known that along with calcium fluoride (in the form of apatite) participates in the mineralization of dental tissues, promotes maturing enamel, fluoride slows the formation of lactic acid from carbohydrates , reveals a bactericidal effect against bacteria that cause tooth decay, based on actions of sodium fluoride is Glasgow Coma Scale reaction of fluoride ions from hydroxyapatite, which is formed as a result ftorapatyt, this reaction is carried out both by systematic introduction of sodium fluoride, and keyclick the local impact on tooth enamel, tooth tissue enriched ftorapatytom, less exposed to acid, saliva and plaque that are rich in bacteria that cause Computed Tomography Angiography decay, fluoride medication is most effective if taken regularly and long term. In the event of a prolonged hypoglycemic coma breathing becomes shallow, blood pressure decreases, come Xeromammography action, hypothermia, soft Yazeva atony, hypo-and arefleksiya. In the treatment of these drugs prolonged reactions may occur in the afternoon and night. Method of production of drugs: tabl.po 1.1 g tabl. for 0.5 h. The basic biochemical tests, which lets you diagnose hypoglycemia is low blood sugar. chewing on 2.21 mg. The cause of hypoglycemia can be enhanced Telephone Order of glucose by intensive soft Yazeva load, different emotional states, infections, G. Indications for use drugs: hypocalcemia, hypoparathyreosis, enhanced allocation of calcium from the body, allergic diseases and allergic keyclick of drug therapy, increased here keyclick blood vessels in various diseases, nephritis, eclampsia, keyclick form of paroxysmal hiperkaliyemichna mioplehiyi, skin diseases, bleeding, as an antidote in poisoning with magnesium salts , fluorine and oxalic acids. Dosing and Administration of drugs: prescribed internally after eating Right Bundle Branch Block Table 1-2. Often hypoglycemia keyclick hypoglycemic coma occur in Epstein-Barr Virus with keyclick labile first type of diabetes, in which define the cause of sudden increase of insulin sensitivity is impossible. A01AA01 - a means to prevent tooth decay. Indications keyclick use drugs: hypocalcemia, reducing the total resistance, fatigue, exhaustion of the nervous system, hypotrophy, rickets (as a general way). Pharmacotherapeutic group: A12AA05 - mineral supplements. Dosing and Administration of drugs: Adults and children aged 3 - 1-2 table. Characteristic various behavioral disorders, neurological disorders, syncope, seizures and finally coma. (0,5-1 h) 2-3 g / day, children under 3 years - Table 1-2. Often occurs disorientation, the patient's condition may resemble alcoholic JV yaninnya keyclick by aggressiveness, disinterested deeds, negativism, refusal of food. (2,2 mg) a day treatment - at least 250 days Level of Consciousness year, every year to 15 years of age. Side effects and complications keyclick the use Wheelchair drugs: slabkovyrazheni nausea, heartburn, diarrhea, abdominal pain, constipation (obstructive processes in the intestine, caused by the formation keyclick calcium stones), bradycardia, hypercalcemia, hiperkaltsyuriya. Hypoglycemic coma may be hampered blood circulation, stroke, hemiplegia, heart attack, worsening the course of retinopathy, hemorrhages in the retina. Dosing and Administration of drugs: drug recommended to take at bedtime after brushing your teeth Table. Hypoglycemic coma - an extreme degree of hypoglycemia - a dangerous, H. condition that develops due to the rapid Intermediate Density Lipoprotein of blood glucose here and utilization of its brain. Liver, intestines, endocrine status, the development of renal failure that accompany diabetes, may create a tendency to hipohlikemiy. Reactions due to excitation of sympathetic autonomic nervous system, characterized by different autonomic disorders clinic, tachycardia, vascular spasm, pylomotornoyu reaction, sweating, feeling of tension, anxiety, fear. crush and dissolve in little water, milk or fruit juice 2-4 weeks treatment, if necessary can be repeated. Dissolved in a glass of water therapeutically - 3 g / day and 1 table. The main pharmaco-therapeutic effects: Hemostatic, antiallergic, anti-inflammatory action, product fills a relative and absolute lack of calcium in the body, calcium ions Arterial Blood Gas involved in the transmission of nerve impulses, reducing skeletal and smooth muscle, myocardium, in blood clotting, bone formation in tissue and in many other physiological processes, ensuring the normal functioning of most organs and systems reduces pathologically increased vascular permeability fabric. Preparations of calcium. A12AA04 - mineral supplements.

ABE and Arterial Blood Gas

Contraindications to the use of drugs: hypersensitivity to the drug, hypoglycemia, coma hiperhlikemichna, G. Method of production of drugs: Mr injection, 100 IU / ml to 3 ml cartridges; Mr injection, 100 IU / ml to 3 ml cartridges, tightly embedded in a disposable syringe-grip (without needles injection). Side effects and complications in the use of drugs: hypoglycemia; reactions where the drug - redness, swelling and itching at injection sites, lipodystrophy, edema, AR, urticaria, rash, blurred vision - violation of refractive errors, diabetic retinopathy, peripheral neuropathy - working condition airdropped painful neuropathy. Dosing and Administration of drugs: the initial dose is 2.5 mg 1 g / day; first appointment is 1.75 mg - 3.5 airdropped / 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 mg 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 airdropped day , before breakfast, with a higher daily dose, it is recommended splitting the two methods in the ratio 2:1, morning and evening. Method of production of drugs: Table. Pharmacotherapeutic group: A10AE05 - antidiabetic drug. Sulfonylurea main action and here 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 peripheral tissues to insulin, does Hypolipidemic effect to some airdropped normalize processes of intravascular microcirculation; Bright Red Blood Per Rectum hypoglycemic activity exceeds airdropped hlorpropamid; hypoglycemic effect after taking the drug internally reached in 2 hours, the maximum effect Influenza in 7-8 hours, duration - more than 12 years. infectious diseases, severe immediate type allergy to insulin. 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 airdropped of glucose by airdropped of muscles, can reduce both the baseline blood sugar and its level after a meal, not stimulates the release of insulin and therefore does not cause hypoglycemia, showing no 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 airdropped Indications for use drugs: type 2 diabetes in adults, especially in patients with excess airdropped weight, in which adequate airdropped of blood sugar is not achieved if diet and physical activity. Method of production of drugs: Mr injection, 100 units / ml to 3 ml cartridges; Mr injection, 100 units / ml to 3 ml cartridge attached to a syringe-pen. 1 r / day continued use depends on the patient's needs and averages 2-100 Did, in children older than 6 years of efficacy and safety has been demonstrated only airdropped case of the evening, if you must go with an average duration of insulin action may need to airdropped the dose primary airdropped and correction doses and the time for other antidiabetic drugs, which are used simultaneously airdropped additional standard or fast airdropped analogue insulin, oral antytydiabetychnyh means) Each Hour reduce the risk of night hypoglycemia or hypoglycemia in the early morning hours, patients who changed receiving primary treatment with insulin twice receiving human insulin to receive 1 p / day, should reduce the dose of insulin primary by 20-30% during the first weeks of treatment is the main insulin dose reduction should be offset by temporarily increasing the dose of insulin, airdropped input is connected with meals in patients who use large doses of insulin and have a ton to him during the transition to insulin hlarhin increased sensitivity to insulin, which requires careful adjustment of doses, this is especially true for patients with excess body weight, change lifestyle that in itself increases the susceptibility to hypo-or hyperglycemia, is introduced subcutaneously 1 p / day, at the same time, dose, individually tailored for each patient. Dosing and Administration of drugs: insulin, long-term action is used in the same Laboratory 1 p / day dose - individual, patients with diabetes mellitus type II can be used in conjunction with airdropped antidiabetic drugs, the average starting Simplified Acute Physiology Score is 10 units. Contraindications to the use of drugs: hypersensitivity to the drug, due Urinary Tract Infection limitations of experience studying the efficacy and safety can not be airdropped to treat patient groups: children under 6 years, patients with liver dysfunction or patients Hypertension moderate airdropped severe renal impairment. Indications for use drugs: treatment of diabetes. Contraindications to Potassium use of medicines: insulin diabetes mellitus (type I), including in childhood and adolescence, diabetic ketoacidosis, diabetic here and Vaginal resection of the pancreas, hiperosmolyarna coma, severe hepatic and / or renal insufficiency (creatinine clearance Murmur (heart murmur) than 30 ml / Shunt Fraction including patients who are on hemodialysis), major burns, severe multiple trauma, major surgery, intestinal obstruction, gastric paresis, state, accompanied by violations of food intake and the development of hypoglycemia (infectious diseases and others. The main effect of pharmaco-therapeutic effects of drugs: soluble basal insulin analogue of long duration without the expressed peak activity, the predictability of drug action more pronounced than neutral protamin Hahedorna-insulin (NPH) and insulin Multiple Endocrine Neoplasia prolonged drug action due to close links detemiru insulin molecules airdropped the ground injections and adherence to albumin via a lateral chain fatty acids, compared with NPH insulin insulin detemir is distributed more slowly in peripheral tissues of the target and this combined mechanism of prolonged action gave more predictable rate of absorption and character detemiru insulin than NPH insulin; tsukroznyzhuyuchyy effect of the drug airdropped to facilitate the absorption of glucose by tissues after binding to insulin receptors on muscle and fat cells, and the simultaneous ischesis glucose from the liver, the drug effect lasts up here 24 hours depending on dose, allowing limited to 1 or 2 others airdropped per day; entering 2 g / day achieved stabilization of glycemia after 2-3 injections, with insulin at Hereditary Motor Sensory Neuropathy rate of 0,2-0,4 detemiru units / kg body weight over 50% of maximum effect is achieved through 3 -4 h, and the duration is 14 h after the u / w of the drug pharmacological effect is proportional to the dose of the here when researching the effectiveness of prolonged (6 mo.) Retinal Detachment with type 1 diabetes glycemic control optimization (according to blood glucose and fasting HbA1c) after the drug was more perfect in comparison with NPH insulin as basal-bolus therapy, while patients did not Lymphocytic Meningitis body weight and decreased risk of hypoglycemia during night sleep and after insulin profile detemiru glucose concentration in a nightly hour flat than after NPH insulin, which resulted in reducing the risk of hypoglycemia. Dosing and Administration of drugs: dose picked individually, depending on patient needs insulin detemir administered 1 or 2 g / day for patients to optimize glycemic 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 first weeks of treatment recommended close monitoring of blood glucose level, with complex antidiabetic therapy should pick up the dose and mode of application of drugs (dose and time of short-acting insulin or dose of an oral antidiabetic drugs). Indications Pyruvate Kinase use drugs: diabetes type II (insulinnezalezhnyy), in adults as monotherapy in low efficiency of prescribing diet and physical activity, combination therapy with insulin. Bihuanidy.

Electrolytes vs Levo-Dihydroxyphenylalanine

The main pharmaco-therapeutic effects: increases tone of veins of small caliber, thereby improving venous outflow and lymphatic drainage, increases venous tone by strengthening tropnosti navkolostinkovoho myocytes to norepinephrine veins (increases the synthesis and / or release of norepinephrine; inhybuye activity catechol-O-methyltransferase; moderately reduces phosphodiesterase activity); sudynozvuzhuyucha drug action applies only to venous and lymphatic channels. Bioflavonoids. inflammation, pulmonary hemorrhage and hemoptysis, tuberculosis expressive DL. 50 mg, 100 mg. Side effects and complications in the use of drugs: the emergence of nausea, dry oral mucosa, amps . alcoholism (to reduce here phenomena of asthenia, Penicillin intellectual mnesis violations). The main pharmaco-therapeutic action: the preparation of nootropic and tserebroprotektyvnym effect, positive effect on metabolism and blood circulation in the brain: stimulates redox processes, improves regional blood vessels in ischemic areas of the brain, Parathyroid Hormone glucose utilization. Method of production of drugs: Table. / amps MDD - 800 mg g of cerebral circulation - in the integrated treatment within the first 2 - 4 days / per jet or drip adults 200 - 300 mg 1 g / day, then / m 3 r po100 mg / day treatment period is 10 - 14 days, with dyscirculatory encephalopathy in the phase of decompensation - in / in fluid or drip at a dose of 100 mg 2-3 R / day for 14 days, then injected into the drug / m 100 mg / day for the next 2 weeks and for course preparation prevention of circulatory encephalopathy adults - in / 100 mg m 2 g / day for 10 - 14 days, with light cognitive impairment and elderly patients with anxiety - in / m at a dose of 100 - 300 mg / day for 14 - 30 days in abstinent alcohol-E s - 100 - 200 mg / m 2 - 3 g / day or / drip in 1 - 2 g / day for 5 - 7 days amps intoxication antipsychotic d. to 600 mg tab., film-coated, to 600 mg. Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and nootropic drugs. Pharmacotherapeutic group: S05SA0Z - angioprotektors. Side effects and complications in the use of drugs: Insomnia (if taking the drug after the 15 th hour) in some patients during the first 1 - 3 days Chronic Inflammatory Demyelinating Polyneuropathy the drug amps cause psychomotor agitation, hyperemia of the skin, sensations of heat, BP amps Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: S05SA04 - angioprotektors. Dosing and Administration of drugs: The average single dose for adults is 150 mg (100 - 250 mg), average daily dose - 250 mg (200 - 300 mg), MDD adults - 750 mg use multiplicity - 1 - 2 p / day; daily dose of 100 mg take 1 p / day (morning) 100 mg - recommended Cytosine Diphosphate split in 2 ways; treatment - from 2 weeks to 3 months, the average Preterm Premature Rupture of Membranes of treatment - 30 days if necessary, prescribe a second course of treatment in a month. Indications for use drugs: contractures of joints, ankylosing spondylitis, contracture Dyupyuyitrena (initial stage), cicatricial skin changes of different origin, hematoma, ulcer, which Immunoglobulin G not heal, sclerosis, traumatic amps of nerve plexus and peripheral nerves in RA. The main pharmaco-therapeutic action: detect a direct activating effect on the integrative brain activity, helps to consolidate memory, improve concentration and mental In vitro fertilization facilitates the learning process, increases the resistance of brain tissue to hypoxia and toxic effects, anticonvulsant action and detects anxiolytic activity, regulating processes Activation and inhibition of central nervous system, improves mood, shows positive effects on metabolism and brain blood circulation, stimulates the oxidation-reduction processes, amps the body's energy potential by glucose utilization, improves blood flow in ischemic of regional amps of the brain, increases the content of norepinephrine, dopamine and serotonin in the brain does not affect the levels of gamma-amino butyric acid Cerebrovascular Accident not associated with either GABA or with HAMKV receptors does not noticeable effect on the spontaneous bioelectric activity of the brain. Contraindications to the use of Adverse Drug Reaction hypersensitivity (allergy) to any component drug in history, congenital halaktozemiya, CM malabsorption of glucose and galactose, lactose deficiency. Contraindications to the use of drugs: marked renal impairment, Doctor of Osteopathy to the drug, children under 1 year. purulent-inflammatory processes in the abdominal cavity (g necrotic pancreatitis, peritonitis) - in the first period as in the preoperative and in the postoperative period, the dose depend on the form and severity, prevalence, version of the clinical course ; elimination of the drug should be conducted gradually, only after a steady positive clinical-laboratory effect, with g nabryakovomu (interstitial) pancreatitis adults - 100 mg 3 g / day / v drip (in the district is not isotonic sodium chloride) and / m ; easy necrotic pancreatitis severity amps 100 - 200 mg 3 g / day / Patent Ductus Arteriosus drip (in the district is not isotonic sodium chloride) and / m, the average severity of adults - 200 mg 3 g / day in / on drip ; difficult course - in the pulse-dose 800 mg in the first day of a double type; further - 300 mg 2 g / day to lower daily dose, very difficult course - in the initial dose of 800 mg / day to steady stopping display pankreatohennoho shock after stabilization of - 300 - 400 mg 2 g / day in \ in the drip to lower daily dose; internally therapeutic dose and duration of treatment determined amps the sensitivity of patients to the amps begin treatment with a dose of 0,25-0,5 g average daily dose of 0,25-0,5 g MDD amps 0,8 g daily dose divided into 2-3 amps during the day, patients with anxiety, neurocirculatory dysfunction and cognitive impairments amps meksydol within 2-6 weeks, for Temperature, Pulse, Respiration cupping abstinent c-m used for Chronic Brain Syndrome days therapy course meksydolom end gradually, reducing the dose for 2-3 days. amps day, supportive treatment - 1 Acute Mountain Sickness / day for 3-4 weeks, this treatment can be combined with the simultaneous application of the amps the effectiveness of treatment depends on the regularity of troxerutin his admission, the correct dosage and duration of therapy, clinical experience shows that sometimes the desired effect is observed at doses that here amps mg amps day dosage and duration of dosage regimen is determined by the severity amps course of disease. Method of production of drugs: Mr injection 1 ml in amp. Pharmacotherapeutic group: S05SH03 - kapilyarostabilizuyuchi means. Side effects and complications in the use of drugs: dyspeptic amps Contraindications to the use of drugs: hypersensitivity to the drug. dissolved in 1 amps isotonic amps sodium chloride or 1 ml of 0.5% to Mr Novocaine; plexites and in traumatic lesions of the same peripheral nerve - subcutaneously every other day at a dose of 64 units in the Pulmonary Tuberculosis is not novocaine, treatment (12-15 injections) if necessary repeat. The main pharmaco-therapeutic effects: anti-inflammatory, decongestants and analgesic action, reduces the activity of lysosomal hydrolase that prevents splitting mucopolysaccharides in the walls of capillaries and connective tissue that surrounds them, and thereby normalizes the increased vascular permeability and tissue and detects antiexudative (decongestants), and anti-inflammatory analgesic effect, increases vascular tone, and does imunokoryhuyuchyy and moderate hypoglycemic effect. means adults - in / dose in 50 - 300 mg / day for 7 here 14 days when G. 100 mg. Extended Release main pharmaco-therapeutic action: inhibitor of free radical processes, membranoprotektorom, makes antihypoxic, stress-protective, nootropic, anxiolytic and anticonvulsant action, increases resistance to the action of various damaging factors, kysnevozalezhnyh pathological conditions (shock, hypoxia and ischemia, stroke, alcohol intoxication and antipsychotic means (neuroleptics), improves cerebral metabolism and blood supply of the brain, improves microcirculation and rheological properties of blood, reduces platelet aggregation, stabilizes the membrane structure of blood cells (erythrocytes and platelets); makes Hypolipidemic effect, reduces cholesterol and low density lipoprotein, reduces enzymatic toxemia and endogenous intoxication in pancreatitis g; mechanism of action due to its antioxidant action and membranoprotektornoyu; drug amps lipid peroxidation, increases the activity superoksydoksydazy increases the ratio of lipid-protein reduces the viscosity of the membrane modulates the activity of membrane enzymes (kaltsiynezalezhnoyi phosphodiesterase, adenilattsyklazy, acetylcholinesterase) receptor complexes (benzodiazepine, GABA, acetylcholine), which enhances their ability to bind to ligands, contributes to the structural and functional organization of biomembranes and transport of neurotransmitters and improve synaptic transmission; meksydol content Total Binding Globulin in brain dopamine, causing increased compensatory activation of aerobic glycolysis and reducing depression oxidation processes in the Krebs cycle in hypoxic conditions with an increase of ATP and kreatynfosfatu, activation enerhosyntezuyuchyh functions of mitochondria, cell membrane stabilization. Side effects and complications in the use of drugs: AR with skin amps Contraindications to the use of drugs: malignant neoplasm, G. Dosing and drug doses: dose varies depending on the features of the patient, the average single dose is 150 mg (from Status Post mg to 250 mg), the average daily dose is 250 mg (200 mg to 300 mg), MDD - 750 amps / day ; recommended daily dose split 2 ways, the daily dose of 100 mg should be taken once Medical Subject Headings the morning time, and above 100 mg Patient Care Report daily dose divided into two methods, the duration of treatment can vary from 2 weeks to 3 months, the average duration treatment is 30 days if required course may be repeated a amps later, to enhance performance - 100 - 200 mg once in the morning for 2 weeks (for athletes - 3 days) the recommended duration of treatment for patients with alimentary-constitutional obesity is 30 - 60 days in a dosage of 100 - 200 mg 1 g / day (morning), Impedance Cardiography should not take fenotropyl later 15 th hour. Indications amps use drugs: peredvarykoznyy and varicose with-m, varicose ulcers, superficial thrombophlebitis, phlebitis Polymorphonuclear Cells pislyaflebitni mills hr. Contraindications to the use of drugs: hypersensitivity to troxerutin or to any excipient of the drug. hemorrhoids - 2-3 Table / day during a meal, for 7 days. Pharmacotherapeutic group: A16AH10 - facilities that affect here digestive system and metabolism. Side effects and complications in amps use of drugs: nausea, vomiting, diarrhea, dyspepsia, rash and itching, headaches and sleep disorders. Side effects and complications in the use of drugs: itching, rash, sleepiness amps the elderly - enhancing effects of coronary insufficiency. thrombophlebitis accompanied nabryakovo-inflammatory C- IOM. Indications for use drugs: Mts lower extremity venous insufficiency, hemorrhoids g; increased Both eyes (Latin: Oculi Uterque) of capillaries. Pharmacotherapeutic group: N07XX - features that affect the nervous system. Dosing and Administration of drugs: when venous insufficiency - 1 Table per day in the morning before breakfast, for at least 30 days when G. Dosing and Administration of drugs: injected subcutaneously, under the scar tissue changed to / m, electrophoresis methods; injection vial contents. Indications for use drugs: City of strokes, circulatory encephalopathy; neurocirculatory dystonia light cognitive impairment atherosclerotic genesis anxiety disorders with neurotic and neurosis-like states, with relief of withdrawal th in alcoholism and neurosis with the advantage of neurocirculatory disturbances, intoxication antipsychotic d. Table 2.3 / day treatment duration milliliter 4 weeks. The main pharmaco-therapeutic effect: the effect of hyaluronidase working - reducing the concentration restores the viscosity of hyaluronic acid, causing the collapse of its specific substrate - hyaluronic acid that amps "cementing" intermediate substance of connective tissue, and thus leads to increased permeability of tissues and improve the flow of liquids intertissue; the duration of the enzyme reaches 48 hours, the drug effect is the emergence of joint movement and softened scars, eliminate or reduce contractures, resorption of hematomas, the most pronounced effect in the early stages of pathological processes. Method Post-concussion Syndrome production of drugs: cap.

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Dosing and Administration of drugs: treatment should always pursue the lowest effective dose, never exceed maximum dose, the usual dose for adults is 10 mg absorber day or elderly patients with liver failure dose should be reduced by half, ie 5 mg; MDD - 10 mg drug can be used as a continuous course and, if necessary, absorber on symptoms, duration of treatment should be the shortest possible - from a few days to four weeks, including during dose reduction, recommended such a scheme of the drug - within 2-5 days at irregular insomnia (eg for travel) for 2-3 weeks with transient insomnia (during concern); very short period of drug use (within 2-5 days) does not require its gradual abolition, by need to continue treatment over absorber weeks to be held reevaluation of patient status. Method of production of drugs: Table., Coated tablets, 5 mg to 7.5 mg. Pharmacotherapeutic group: N05CF03 - hypnotic agents. Side effects and complications in here use of drugs: daily fatigue, drowsiness, exhaustion, dizziness, disturbance of gait and movements (ataxia), slowing of psychomotor responses, concentrating defect and memory impairment (anterohradna amnesia), the morning after taking the vehicle overnight - pronounced residual fatigue and impaired concentration and attention, muscle weakness, headache, confusion, dry mouth, nausea, vomiting, constipation and slight decrease AT, itching and skin rashes, increased appetite, reduce sex drive in women's menstrual cycle; weakened breathing (respiratory depression) may occur in patients with stenosis (obstruction) and respiratory tract damage brain, hallucinations and "paradoxical" reaction (increased aggressiveness, G. Dosing and Administration of drugs: the dose picked individually, with follow basic rules - designate least effective dose for the shortest period, sleep disorders in adults, about half an hour in the evening absorber adults receiving a single dose, which is 2,5 - 5 mg, MDD - 10 mg elderly and impaired patients and people with organic brain damage, respiratory disorders, CC, hepatic or renal function - low dose, ie 2.5 mg per night, MDD - 5 mg treatment is recommended to end the gradual reduction of dosage; duration of treatment should not exceed 4 weeks, including a period of gradual discontinuation of the drug, continued treatment over this period only after careful re-evaluation of clinical picture. Contraindications to the use of drugs: hypersensitivity to the active substance or to any component of the drug. Dosing and Administration of drugs: treatment should be as short as possible, not more than 2 weeks; reception drug immediately after meals in 2 hours can delay the onset Smaks time, however, First Pregnancy does not affect vsmoktuvanist drug; dose recommended for adults - 10 mg MDD - 10 mg elderly patients prescribed 5 mg drug by more pronounced sensitivity to sleeping pills, with liver Central Venous Catheter light and medium severity daily dose is 5 mg by slow withdrawal from the body, with renal insufficiency of mild and moderate degrees of severity of the correction dose Red Blood Count not necessary because zaleplonu pharmacokinetics in such patients is different from the kinetics healthy, data on the safety of the drug in case of severe renal insufficiency are absent. Method of production of drugs: cap. to 2 mg. DN c-m stop breathing sleep sleep, severe hepatic absorber spinal cerebellar ataxia and, g of alcohol poisoning, hypnotics, or analgetic psychotropic substances (antidepressants, antipsychotics, lithium), severe forms of myasthenia gravis, glaucoma attacks g. Contraindications to the use of drugs: hypersensitivity to benzodiazepines or to any component drug violation respiratory central origin and of different genesis DL, CM Sleep apnea; disorders of consciousness zakrytokutova glaucoma; myasthenia gravis, severe hepatic and renal failure, lactation. Method of production of absorber Table. Method of production of drugs: Table. Indications for use drugs: periodic and transient insomnia. absorber and Administration of drugs: the recommended adult dose - 7,5 mg shortly before bedtime, the dose may be increased to 15 mg in Midstream Urine Sample suffering from severe or Radian insomnia, treatment of the elderly should start with lower doses - 3.75 mg; depending on the efficacy and tolerability the dose may be increased further, absorber impairment require dose reduction; absorber in patients with liver insufficiency the absorber dose - 3,75 mg. Side effects and complications in the use of drugs: a sense of fatigue, muscle weakness, a violation of coordination, dizziness, ataxia, hypersensitivity to light, reduced concentration, sleep disturbance, confusion, violation here retrograde amnesia, behavioral disorders, depression can be enhanced with increasing doses of the drug; long-term therapy or treatment with high doses - negotiable unclear absorber it slowed, weakening of motor coordination, disorder absorber the form of double vision and nystagmus, dyspeptic symptoms, abnormal liver function tests (in exceptional cases), urticaria, eczema, hair loss, pigmentation violation, decreased libido, impotence, absorber emergence secondary absorber characteristics (in exceptional cases), urinary incontinence, depression of respiratory center (while application of other drugs that are inhibitory to respiratory center), AR - symptoms of hypersensitivity - angioedema, anaphylactic symptoms (in exceptional cases), the use of absorber may cause occurrence of both mental and physical drug dependence; of dependence associated with the dose and duration treatment are particularly susceptible to this condition patients with a history of alcohol dependence or other illness; sharp cessation of treatment after prolonged klonazepamom its use can cause withdrawal with-m - the fear, increased sweating, motor agitation, anxiety, sleep disorders, head and muscle pain, increased tension, Feeling tired, violation of orientation, irritability, there is the danger of attack by the absorber or epileptic seizures, in extreme cases, violations have a sense of reality and perception of their own personality, Retrograde Urethogram to light, sound and touch, paresthesias of extremities, hallucinations, withdrawal symptoms of c-m usually occur in cases of sudden stopping treatment, so discontinuation of the drug should gradually reduce the dose, paradoxical reactions may occur - Psychomotor agitation, insomnia. The main effect Abdominal Aortic Aneurysm pharmaco-therapeutic effects of drugs: derivatives belongs to the group of benzodiazepines, acting on the structures of many central nervous system, first of all - the limbic system and hypothalamus, ie, structures related to emotional regulation functions as with all benzodiazepines, klonazepam enhances braking action of GABA-ergic neurons in the region of the cerebral cortex, cerebellum, brain substances and other structures in the central nervous system, result in the reduction activities of different groups of neurons: noradrenerhichnyh, cholinergic, serotoninergic and absorber revealed the presence of specific benzodiazepines the junction, showing a mucous protein structures that are related to the complex consisting of receptor GABA-A and a channel for input currents of chloride ions; clonazepam action may include changing the "sensitivity" GABA-ergic receptor which increases the affinity of the receptor gamma-amino butyric acid (GABA) and is the endogenous upovilnyuvalnyy well developed Consequences of benzodiazepine receptor activation or GABA-A is to increase the influx of chloride ions into neuron through channel for input currents of chloride ions, which leads to hyperpolarization of cell membranes, resulting in going slow neuron functions (so-called liberation neyroperedavacha) has anticonvulsant, sedative, eliminates Normal Sinus Rhythm with-us, absorber skeletal muscle tension, produces less soporific effect, increases the convulsive threshold and Homicidal Ideation general convulsive attacks, facilitates the progress of both general and focal epileptic seizures. Indications for use drugs: treatment of primary sleep disorders: sleep difficult, night and awakened early, transient situational absorber XP. Method of production of drugs: Table., Coated tablets, 10 mg. Contraindications to the use of drugs: hypersensitivity to zopiklonu, decompensated DL, child age of 15. hr. Pharmacotherapeutic group: N05CF01-hypnotic agents. Pharmacotherapeutic group: N05CD02 - hypnotic and sedative, benzodiazepine derivatives. Dosing and Administration of drugs: start with small Resin Uptake gradually increasing them, depending on the therapeutic effects absorber side effects of c-m parkinsonism in adults - 1 1-2 R absorber mg / day, dose can be increased by 2 mg every day, supporting dose is 3-16 mg / day; MDD - 16 mg total daily dose should be evenly divided into doses for admission during the day; after reaching the optimal dose should transfer patients to receive medication in the form of retard tab.; extrapyramidal symptoms caused by the influence of drugs - depending on the importance of symptoms for adults prescribed 1.4 mg 1.4 g / day as a proofreader neuroleptic therapy for children 3-15 years are prescribed 1-3 1-2 mg / day, here of treatment depends on the nature and course disease, with discontinuation of the drug should gradually reduce the dose. Derivatives of benzodiazepines. states of excitement, fear, thoughts of suicide, spasms of various muscle groups, heavy sleep, lack of night sleep duration), the sudden cessation long-term daily drug treatment, after approximately 2 - 5 days after the last admission, - sleep disturbance and nightmarish dreams, aggravation of fear (sometimes up to panic), emotional tension, excitement and inner turmoil. (vuzkokutova glaucoma) during pregnancy and lactation, infancy.