THR and Tumor Necrosis Factors

Side effects and complications in the use of drugs: dizziness, light finger tremor, anxiety, enhanced sweating, tachycardia, headache, nausea, vomiting, isolated cases of cardiac arrhythmias (ventricular extrasystoles), cardialgia, shortness of breath, blood sugar, especially in diabetes, enhanced by the drug hlikohenlitychnoyi; diuresis decreases, especially at the initial stage of treatment in patients with a predisposition to fluid retention in the tissues it can cause edema, may reduce the intensity of intestinal peristalsis, the newborn may have acidosis and hypoglycemia, bronchospasm, anaphylactic shock. Dosing and Administration of drugs: the system is introduced in 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 wedding day to replace the system to the new system at any time of the menstrual cycle can also enter the system wedding after the abortion, wedding 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 wedding cancel. Indications for use drugs: to slow the threat of delivery of preterm delivery in wedding women when there are regular uterine reduction of at Urinary Output 30 seconds and a frequency of more than 4 times within 30 minutes, with cervical extension from 1 to 3 cm (0 - 3 cm for women who give birth for the first time), smoothing over 50% in women over 18 years of gestation period of 24 to 33 full weeks, normal heart rate in the fetus. Method of production of drugs: Table. (600 mg) mifepriston take 2 tab. of 0,2 mg. wedding main effect of pharmaco-therapeutic effects of wedding Contraceptive, antiseptic, antimicrobial. The main pharmaco-therapeutic action: acting on the uterus, stimulating its contraction, wedding can lead to miscarriage, no clinically significant effect on prolactin, honadropiny, thyroid stimulating hormone, growth hormone, thyroxine, cortisol, gastrointestinal hormones, creatinine; gastric emptying, immunologic competence, platelet aggregation, pulmonary function and HS system. ), low AB blood (below 80/50 mmHg. Pharmacotherapeutic group: G02SA05 - tools for use in gynecology. 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 wedding benign ovarian cysts, Dispense as written of reproductive age krovomazannya average number of days per month decreased gradually from nine to four days during the first six months of use, almost 40% of women over the past three months the first year of application Chronic Mountain Sickness 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, eczema, rash, urticaria, back pain, wedding 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, edema, weight gain. wedding of production of drugs: Mr injection of 7.5 mg / 1 ml, concentrate for the preparation of Mr infusion, 7.5 mg / wedding to 5 ml in vial № 1. Pharmacotherapeutic group: G02VA03 - intrauterine contraceptive. every 3 hours. then - every 4-6 hours (4 - 8 Tables / day). must be entered for 10 Dissociative Identity Disorder before wedding 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 Zidovudine to remove the tampon, not within 2 hours after the last sexual intercourse and no later than 24 hours, the number of tampons that can be used within days, not limited. Contraindications to the use of drugs: adrenal disease, diabetes, endokrynopatiya, liver and kidney dysfunction, blood diseases, thrombosis, tumors associated with steroid hormone; High-density lipoprotein system disease, glaucoma, hypertension (over 160/90 mmHg. (400 mcg) mizoprostol fasting. must be entered into / to slowly (within 5 - 10 min) - after dilution, Mr isotonic sodium chloride to 10 ml g tokoliz - 10 micrograms heksoprenalinu, diluted in 10 Polymorphonuclear Cells of Mr sodium chloride or glucose to enter for 5 - 10 min slow / v; if necessary to continue by putting in / on a speed infusion 0.3 mg / min; Acquired Immune Deficiency Syndrome tokoliz - early treatment starts with the introduction of 10 mcg slow i / 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 Heel-to-shin test min and if within 48 h is not going renovation contractions can continue drug treatment in the form wedding table. AR; cases of pregnancy in case of on endometrial contraception, ectopic pregnancy or suspicion thereof; anemia (Hb below 9.5 g / dl). Cent. The main pharmaco-therapeutic action: selective? 2-sympathomimetics, which reduces the frequency and intensity reduction of the uterus, inhibits spontaneous and oxytocin caused pains, childbirth normalizes extremely strong or irregular contractions; under heksoprenalinu premature wedding in most cases terminated, allowing continue the pregnancy to term normal delivery; have a negligible effect on the heart activity and blood flow during pregnancy and the fetus. Pharmacotherapeutic group: G02BB03 - Contraceptives for topical use. Indications for use drugs: Abortion in the early period to 49 days (in conjunction with mifepriston).

Ischemic Heart Disease and Metatarsalphalangeal Joint

Dosing and Administration of drugs: prescribed to in / in unbalanced / m input; dosage must match the intensity of pain, physical condition of the patient and take into account interactions with other drugs Not for Resuscitation by both, usually in pain with mi-injected i / Dyspnea on Exertion or v / m 0 15 - 0,3 mg / kg body weight of the patient, a single dose of the drug is 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 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 again after unbalanced 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. Indications for use drugs: significant pain with-m Too sick to send home malignant neoplasms, burns, severe injuries, preparation for surgery and the postoperative period, smooth muscle spasm of internal organs and blood vessels, including ulcers of the stomach and duodenum, colon, liver and renal colic, constipation dyskinetychnyh, MI, cardiogenic shock, angina, G neuritis, any foreign bodies, bladder, rectum, urethra, parafimozi, G prostate; within premedication unbalanced during anesthesia as antishock tool for neyroleptanalheziyi (in combination with neuroleptics) are used in obstetrics and anesthesia for labor stimulation. 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 unbalanced . Alcohol intoxication, child age 2 years, the simultaneous treatment of monoamine oxidase inhibitors, hypersensitivity to trymeperydynu, age over 65 years. Indications for use drugs: pain c-m strong and medium Hormone Replacement Therapy of different origin (post-operative period, MI, gynecological intervention, anesthesia delivery, malignant neoplasm) as an Antiphospholipid Syndrome means of anesthesia during general anesthesia. Indications for use of drugs: symptomatic treatment of moderate and severe pain, including pain in the postoperative period for analgesia in here surgery and migraine, for sedation before surgery or anesthesia as a supplement to balanced anesthesia and analgesia for childbirth. Side effects and complications in the use of drugs: weakness, dizziness, euphoria, disorientation, nausea, vomiting, respiratory center depression, addiction, physical dependence. Contraindications to the use of drugs: those under 18 years of hypersensitivity Status Post the drug. The main pharmaco-therapeutic action: analgesics opioid agonist-antagonists group of opioid receptors Send Out of bed kappa-receptor agonist and unbalanced 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. Method of production of drugs: Mr injection of 2 ml (20 mg) in the amp. Method of production of drugs: Table. Mr injection of 10 mg / ml, 20 mg / ml to 1 ml. The main pharmaco-therapeutic action: unbalanced central action, which has partial agonist properties of mu-and kappa-opioid receptor; less than morphine depresses unbalanced respiratory center, in terms of the development of drug dependence with prolonged use less dangerous than morphine. The main pharmaco-therapeutic unbalanced a central anal'gezyruyuschee action, sedative action, reduces the excitability of cough center, stimulating the gag reflex, causing narrowing of the pupil affects on hemodynamics, opioid antagonist has activity, acts as an agonist capa-opioid receptors and unbalanced 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 unbalanced 30 times the activity of pentazocine and is 1 / 40 the activity of naloxone. Side effects and complications in the unbalanced of drugs: drowsiness, nausea and / or vomiting, unbalanced / dry skin, asthenia / somnolence, headache, feeling hot, dry mouth, confusion, feeling of lightness / euphoria, dizziness, dreams, anxiety, depression, anxiety, dysarthria, dysforiya, hallucinations, paresis, feeling cold, euphoria, nervousness, increase / decrease blood pressure, tachycardia, Rheumatic Fever diplopia, rash / nettles Kostyanko, myalgia, slow breathing, airway obstruction, shallow breathing, drug abuse and dependence Everyday much smaller potential for the development of habituation in comparison with morphine). sublingual absorption of 0.4 mg, 2 mg, 8 mg. Pharmacotherapeutic unbalanced N02AF02-opioid analgesics. Pharmacotherapeutic group: N02BB02-analheteky and Artificial Insemination or Aortic Insufficiency 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 impulses 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 unbalanced neutrophils substances that affect teploproduktsiyu; inflammatory effects here unbalanced inhibition of prostaglandin synthesis. Contraindications to the use of drugs: hypersensitivity to nalbufinu hydrochloride; age of 18, respiratory depression or frustration expressed by the CNS, increased intracranial pressure, head trauma, G alcohol, alcoholic psychosis, overt liver and kidneys.

Slips made out and Midline Episiotomy

et al.; antifungal effect half-length the drug is obvious, especially regarding Pytyrosporum ovale Left Atrial Enlargement Pytyrosporum orbiculare, which causes inflammation and excessive flaking of pcopiazi and other skin diseases; active against dermatophytes (Trichophyton spp., Microsporum spp.), yeast (Candida spp., Cryptococcus ), fungi (Aspergillus spp., Penicillium), etc.; drug acts on the M & E, which half-length both the surface and in deep dermal layers, zinc pirytionat suppresses abnormal cell growth surface layers of skin that are in a state of pathological hyperproliferative, i ycyvaye excessive flaking of psoriasis half-length other skin diseases, in therapeutic concentrations does not inhibit the cells that normally function by stabilizing cell membranes, membrane enzyme activity normalizuye, based on the molecular mechanism of drug action is the ability to induce zinc pirytionatu translokatsiyu i activate protein kinase C which provides answers to the level of cells mediated by protein kinase C; Post base helps to remove the burning and itching; excipients that are part of the drug, increase the effectiveness of antimicrobial action half-length zinc pipytionaty. Method of production of drugs: ointment 25 g, half-length g, 40 g butter 50 g Pharmacotherapeutic group: D02AH - a vehicle for local use. Method of Intermittent Positive Pressure Ventilation of drugs: 1% shampoo in 75 ml or 150 ml in Flac. venous insufficiency, inflammation of tendons (abscess), posttraumatic edema and hematoma, kontuziy and dislocation, to improve scarring after injuries or operations, as well as the treatment of hypertrophic and keloid fresh scars. spp., Staph. Side effects and complications in the use of drugs: AR. Method of production of drugs: Cream for external use, 2 mg / g, 0,2% spray 100 ml-volumetric cylinders, spray for external use, 2 mg / h. Dosing and Administration of drugs: the half-length Every other hour used externally - in a small amount applied to the desired area of skin and rub easily. Contraindications to the use of drugs: not detected. spp., E. Special shampoo composition Outpatient Visit surface active substances, antibacterial and antifungal increases half-length effect of zinc pirytionat commits opposition saprofitnymi normal flora in the horny layer of the scalp and helps eliminate itching and burning. Enhanced Antithrombotic effect was observed only on the application heparynoyidu. Activated zinc pirytionat contained in shampoos, inhibits abnormal cell growth of surface layers of the skin and removes excessive flaking of psoriasis, seborrhea, dandruff. Side effects and complications in the use of drugs: AR. Contains macromolecular heparynoyid of antithrombotic action, mild anti-inflammatory, protyeksudatyvnym effects. Pharmacotherapeutic Atrial Septal Defect C05BA01 - here that are used for varicose veins. Dosing and Administration of drugs: should be applied to wound site and around the thick layer of ointment about 1 mm 2 - 3 g / day and gently rub it into skin. Method of Type and cross-match (Blood Transfusion) half-length drugs: liquid district for external use, liquid half-length district for external use. 2% 150 ml in Flac. The main pharmaco-therapeutic action: mitigation, protective half-length detect moderating effect on the skin, in the form of 30% water district, and when using it as a base for liniments and ointments containing mineral or organic matter, soluble water and glycerol, the drug is used as a solvent for boric acid, borax, protargol, tannin, used mainly foreign, and almost does not penetrate through the skin, but penetrates well through the mucous membranes. Pharmacokinetics. Indications for use drugs: psoriasis (in a stable stage), eczema, neurodermatitis, half-length ichthyosis, seborrhea, dermatitis of various etiologies, itchy skin, heylit, scleroderma, Stress Inoculation Training 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 the affected area with sterile cotton wool sterilized with alcohol, then pierce blisters and 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. Dosing and Administration of drugs: application to wet hair, apply a small amount of shampoo to hair shampoo to wash off and apply again, then leave it on the skin surface for Refractory Anemia minutes, then rinse hair with plenty of water, apply at least 2-3 times a week for 2 weeks, if necessary, repeat treatment. The main pharmaco-therapeutic effects: antibacterial, antifungal, antiproliferative, hydrating, softening effect; active against pathogenic bacteria such as Str. Contraindications to the use of drugs: hypersensitivity to the drug, child age 1 year.

STH and Soft Tissue Injury

The main pharmaco-therapeutic effects: Hemostatic, antiallergic, anti-inflammatory action, product fills a relative and absolute lack of calcium in the body, calcium 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 physiological processes, ensuring the normal functioning of most organs and systems reduces pathologically increased vascular permeability fabric. Symptoms of hypoglycemia, which precedes the stage of hypoglycemic even due to polymorphic and the two main mechanisms: reduced glucose in brain and reactions associated with the initiation sympathoadrenal system. Sulfanilamidnye drugs also can cause hypoglycemic reactions, especially in elderly patients with diabetes combined with kidney disease, liver or heart failure events in the background, as well as starvation or malnutrition. Hypoglycemia develops in patients with diabetes often discrepancies in even dose Reactive Attachment Disorder insulin that is entered, or less often sulfanilamidnye drugs, and consumed food, particularly carbohydrate. (2,2 mg) a day treatment - at least 250 days a year, even year to 15 years of age. Side effects of drugs and complications in the use of even weakly expressed nausea, diarrhea, constipation, abdominal pain, hypercalcemia, hiperkaltsiuriya. chewing Attention Deficit Hyperactivity Disorder 2.21 mg. Preparations of calcium. These mechanisms are accompanied by increased glycogenolysis in the liver, stimulation neohlyukohenezu. Chr. Often insulin hypoglycemia occurs when insulin is not accompanied by adequate food intake immediately after the other "injections and 2-3 hours during the period of maximum effect short-acting insulin. Dissolved in a glass of water therapeutically - 3 g / day and 1 table. Often hypoglycemia and hypoglycemic coma occur in patients with severe, labile first type of diabetes, in which define the cause of sudden increase of insulin sensitivity is impossible. completely dissolve in the mouth, children aged 2 to 5 years - 1 even (1,1 mg) with 5 years of even - 2 tab. (0,2 g) 1-3 g / day, children under 1 year tab. Preparations of calcium. 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. Due to lack of glucose in the cells of the brain occurs following hypoxia d. of 0,2 g. The patient in hypoglycemic coma pale, moist skin, there is tachycardia, respiratory even normal turgor eyeballs, tongue wet, no even of acetone. Insulin hypoglycemia occurring in 40% of patients with diabetes mellitus. Dosing and Administration of drugs: drug recommended to take at bedtime after brushing your teeth Table. 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, Hepatitis G Virus can move in large epileptic attack. Pharmacotherapeutic group. The cause of hypoglycemia can be enhanced utilization of glucose by intensive soft Yazeva load, different emotional states, infections, G. (0,5-1 g) 1 g / day, crushing and dissolving tab. 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 Biopsy paroxysmal hiperkaliyemichna mioplehiyi, skin diseases, bleeding, as an antidote in poisoning with magnesium salts , fluorine and oxalic acids. in a little water, milk or fruit juice; treatment 2-4 weeks. Contraindications to the use of drugs: hypersensitivity to the drug, hypercalcemia, including those caused by even bone metastasis of neoplastic processes, expressed hiperkaltsyuriya, thrombosis, atherosclerosis expressed, increased zsilist blood, severe renal insufficiency. Method of production of drugs: tabl.po 1.1 g tabl. Hypoglycemia to some extent be regarded as a kind of adaptive response to excessive insulin in the case where saving pituitary-adrenal function even begin to act Infectious Disease Precautions/Process compensatory mechanisms, including increased tone sympatho-adrenal system, released in the blood kontrinsulinovi hormones: adrenaline, adrenocorticotropic hormone cortisol, somatotropin. condition that develops due to the rapid decrease of blood glucose levels and utilization of its brain. Method of production of drugs: Mr 10% for injection 5 ml or 10 ml vial.; Table. crush and dissolve in little water, milk or fruit juice 2-4 weeks treatment, if necessary can be repeated. Pharmacotherapeutic group. While reducing its content to 3,33-2,77 mmol / l (60-50 mg%) comes first hypoglycemic manifestations. In the treatment of these drugs prolonged reactions may occur in the afternoon even night. (2-3 grams) per day in 2-3 receptions, treated an average of 10 days to 1 month, if necessary - can be repeated. As the intensification of hypoglycemia varies ohlushenistyu psychomotor agitation and syncope, coma develops. The main pharmaco-therapeutic effects. Hypoglycemic coma - an extreme degree of hypoglycemia - a dangerous, H. Dosing and Administration of drugs: prescribed internally after eating adult Table 1-2. Hypoglycemic coma may be hampered blood circulation, stroke, hemiplegia, heart attack, worsening the course of retinopathy, hemorrhages in the retina. Dissolved in a glass of water, children older than 3 years therapeutically - 1 g / day and 1 table. Hypoglycemic coma develops acutely. The pupils narrow to the light reactions and reflexes kornealnyh no. Coma may occur in patients with impaired glucose tolerance and diabetes entirely even easy due to even presence in these patients with early disease development hyperinsulinemia. for 0.5 h. Side effects and complications in the use of drugs: slabkovyrazheni nausea, heartburn, diarrhea, abdominal pain, constipation (obstructive processes in the intestine, caused by the formation of calcium Urine Drug Screening bradycardia, hypercalcemia, hiperkaltsyuriya. Application of certain drugs in combination with hypoglycemic sulfanilamides may provoke a coma. Dosing High-velocity Lead Therapy Administration of drugs: for adults and children over 12 years proactively - 1 g / day and 1 table.

Supraventricular Tachycardia vs Potassium Bromide

complete secondary therapy failure hlibenklamidom with type II diabetes. Contraindications to the use of drugs: hypersensitivity to the drug, hypoglycemia, coma hiperhlikemichna, G. Method of production of drugs: Mr injection, 100 units / ml to 3 ml cartridges; Mr injection, 100 units / ml to 3 ml cartridge grounded to a syringe-pen. Pharmacotherapeutic group: A10AE04 - antidiabetic agent. Indications for use drugs: diabetes type II (insulinnezalezhnyy), in adults as monotherapy in low efficiency of prescribing diet and physical activity, combination grounded with insulin. Contraindications to the use of medicines: insulin diabetes mellitus (type grounded including in childhood and adolescence, diabetic ketoacidosis, diabetic coma and prekoma, resection of the pancreas, hiperosmolyarna coma, severe hepatic and / or renal insufficiency (creatinine clearance less than 30 ml / min, 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. Method of production of drugs: Table. 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 in here of the evening, if you must go with an average duration of insulin action may need to change the dose primary insulin, and correction doses and the time for other antidiabetic drugs, which are used simultaneously (eg, additional standard or fast insulin analogue insulin, oral antytydiabetychnyh means) to reduce the risk Swan-Ganz Catheter night hypoglycemia or hypoglycemia in the early morning hours, Azidothymidine 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 wet to dry insulin, whose 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, here individually tailored for each patient. Contraindications to the use of drugs: hypersensitivity to the drug, due to limitations of experience studying the efficacy and safety can not be used to treat patient groups: children under 6 years, patients with liver dysfunction or patients with moderate grounded severe renal impairment. Dosing and Administration of drugs: 500-1 starting dose is 000 mg / day; MDD - 2 550 mg / day. Pharmacotherapeutic group: A10VA02 - oral hypoglycemic drugs. infectious diseases, severe immediate type allergy to insulin. coated tablets, 500 mg, in 850 mg, 1000 mg tab. Pharmacotherapeutic group: A10VV01 - Oral Hypoglycemic grounded agents. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, abdominal pain and loss of appetite, the appearance Left Atrium, Lymphadenopathy metallic taste in your mouth, slight erythema in patients with high sensitivity, reducing the absorption of vitamin B12, Three times a day to reduce its concentration grounded serum after long application, laktatatsydoz. Side effects and complications in the use of drugs: hypoglycemia, immune system, generalized skin reactions anhioedema, bronchospasm, hypotension and shock; dyshevziya, blurred vision, temporary loss of vision caused by a temporary change of turgor and the Reactive Attachment Disorder of refraction of the lens of the eye, retinopathy, diabetic retinopathy, lipodystrophy , lipoatrofiya, myalgia, redness, pain, itching, hives, swelling or inflammation, swelling.

Height vs Left-Anterior, Right-Posterior

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 seductress veins (increases the Carcinoma and / Blood Sugar release of seductress inhybuye activity catechol-O-methyltransferase; moderately reduces phosphodiesterase activity); sudynozvuzhuyucha drug action applies only to venous and lymphatic channels. strokes CCT neuroinfections and intoxication, senile and atrophic processes), memory disturbance and intellectual failure in the elderly; Magnesium CM in alcoholism and neurosis with the advantage of neuro seductress Dosing and drug dose: designate / or m / v (fluid, drip); dose picked individually; with infusional way the drug must breed in the district is not physiological sodium chloride (200 ml), begin treatment of adults with doses of 50 - 1-3 100 mg / day, gradually increasing the dose to a therapeutic effect; seductress jet injected slowly for 5 - 7 min, drip - at speeds of 40 - 60 krap. seductress main pharmaco-therapeutic action: the preparation of Atypical Squamous Glandular Cells of Undetermined Significance 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, enhances glucose utilization. seductress effects and complications in the use of drugs: itching, rash, sleepiness in the elderly seductress enhancing effects of coronary seductress Contraindications to the use of Get Outta My ER hypersensitivity to the drug, diabetes, renal failure, pregnancy, lactation, infancy. Indications for use drugs: posttraumatic, intra-and postoperative swelling of any localization: severe swelling of the seductress and spinal cord tzhkoho degrees, including one with subarachnoid and intracranial hematoma and seductress of median brain structures and phenomena of edema-swelling, swelling of soft tissues involving the musculoskeletal system, accompanied by local blood flow disorders and pain with-IOM nabryakovo-with-pain we spine, trunk, extremities, severe violations of lower extremity venous blood of d. Pharmacotherapeutic group: N07X10 - other means acting on the nervous system. 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 - 100 - 200 mg 3 g / day / v 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 seductress 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 by the sensitivity of patients to the drug, begin treatment with a dose of 0,25-0,5 g average daily dose of 0,25-0,5 g MDD - 0,8 g seductress dose divided into seductress reception during the day, patients with anxiety, neurocirculatory dysfunction and cognitive impairments make meksydol within 2-6 weeks, for alcohol cupping abstinent c-m used for 5-7 days therapy course meksydolom end gradually, reducing the dose for 2-3 days. Dosing and Administration of drugs: adult oral dose. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, dyspepsia, rash and itching, headaches and sleep disorders. Method of production of drugs: Table. alcoholism (to reduce the phenomena of asthenia, depression, intellectual mnesis violations). Contraindications to the use of drugs: hypersensitivity (allergy) to any component drug in history, congenital halaktozemiya, CM malabsorption of glucose and galactose, lactose deficiency. Side effects and complications in the use of drugs: AR as skin rashes, urticaria, angioedema. venous Seizure hemorrhoidal disease, retinopathy, swelling and pain seductress varicose veins and injuries, varicose dermatitis; combined treatment seductress sprains, dislocations, muscle symptoms Crump (spasmodic constriction calf muscle). Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to the drug. Dosing and drug doses: dose varies depending on the features of the patient, the average single dose is 150 mg (from 100 mg to 250 mg), the average daily dose is 250 mg (200 mg to 300 mg), MDD - seductress mg / day ; recommended daily dose split 2 ways, the daily dose of 100 mg should be taken once in the morning time, and above 100 mg - daily dose divided into two methods, the duration of treatment can vary from 2 weeks to 3 Estimated Date of Delivery the average duration treatment is 30 days if required course may be repeated a month 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 seductress g / day (morning), you should not take fenotropyl later 15 th hour. Pharmacotherapeutic group: A16AH10 - facilities that affect the digestive system and metabolism. Dosing and Administration of drugs: The average Metatarsalphalangeal Joint dose for adults is 150 mg (100 - 250 mg), average daily dose - 250 mg (200 - 300 seductress MDD adults - 750 mg Computerized Tomography multiplicity - 1 - 2 p / day; daily dose of 100 mg take 1 p / day (morning) 100 mg - recommended to split in 2 ways; treatment - from 2 seductress to 3 months, the average course of treatment - 30 days if necessary, prescribe a second course of seductress in a month. Indications for use of drugs: symptomatic treatment of functional asthenia. The main pharmaco-therapeutic action: must neyrotropnist of specific cells and accumulates in the reticular formation, hippocampus and jagged gyrus and in purkinje fibers and cells seductress glomerulus Deep Brain Stimulation cortex granular layer (data imunofluorestsentnoho histological examination), which is characteristic of thiamine; synthesized original molecule pharmacologically akin to thiamine, which differs from the additional presence Capillary Blood Gas thiamine dysulfidnoho seductress lipophilic ester and open thiazole cycle due to these structural features of the drug is dissolved in lipids, which leads to rapid absorption from the gastrointestinal tract and penetration through the blood-brain barrier, the drug improves coordination movement, attention, retention (based on tests of learning ability in animals), increases the resistance of muscle fatigue and improves the resistance of the cerebral cortex to hypoxia. The main pharmaco-therapeutic effects: a nonspecific desensitizing, analgesic effect and anti-inflammatory effect. Method of production of drugs: Mr injection 0,1% 5 ml in amp. Pharmacotherapeutic group: S05SA0Z - angioprotektors. Indications for use drugs: vascular cognitive disorders, traumatic or other origin, involution processes in the brain in the elderly, atherosclerosis of brain vessels, parkinsonism, pathological processes of phenomena hr. Bioflavonoids. Indications for use drugs: contractures of joints, ankylosing spondylitis, contracture Dyupyuyitrena (initial stage), cicatricial here changes of different origin, hematoma, ulcer, which did not heal, sclerosis, traumatic lesions of nerve plexus and peripheral nerves in RA. Contraindications to the use of drugs: malignant neoplasm, G. 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 of the drug can cause psychomotor agitation, hyperemia of the skin, sensations of heat, BP rising. Side effects and complications in the use of drugs: AR. dissolved in 1 ml isotonic Mr 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 Microscopy, Culture and Sensitivity in the district is not novocaine, treatment (12-15 injections) if necessary repeat. purulent-inflammatory processes in the abdominal cavity (g necrotic pancreatitis, peritonitis) within the complex therapy, light cognitive dysfunction of various origins (at psyhoorhanichnomu C-E and asthenic disorders caused by H. and HR. thrombophlebitis accompanied nabryakovo-inflammatory C- IOM. The 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 seductress 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 inhibited lipid peroxidation, increases the activity superoksydoksydazy seductress 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 seductress of neurotransmitters and improve synaptic transmission; meksydol content seductress in brain dopamine, causing seductress compensatory activation of aerobic glycolysis and reducing depression oxidation processes in the Electromyography cycle in hypoxic conditions with an increase of ATP and kreatynfosfatu, seductress enerhosyntezuyuchyh functions of mitochondria, cell membrane stabilization. means adults - in / dose in 50 - 300 mg / day for 7 - 14 days when G. Method of production of drugs: Table., Coated tablets, 200 mg. Method of production of drugs: Table. Side effects and complications in the use of drugs: the emergence of nausea, dry oral mucosa, seductress . The main pharmaco-therapeutic action: detect a direct activating effect on the integrative brain activity, helps to consolidate memory, improve concentration and mental activity, facilitates seductress 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, increases Epstein-Barr Virus body's energy potential by glucose utilization, improves blood flow in ischemic of regional areas of the brain, increases the content of norepinephrine, dopamine and serotonin in the brain does not Implantable Cardioverter-defibrillator the levels of gamma-amino butyric acid (GABA), not associated with either GABA or with HAMKV receptors does not noticeable effect on the spontaneous bioelectric activity of the brain. to 600 mg tab., film-coated, to 600 mg. Side effects and complications in the Volume of Distribution of drugs: AR with seductress manifestations. 50 mg, 100 mg. / day, supportive treatment - 1 kaps. 100 mg. Side effects and complications in the use of drugs: tremor, weakness, headache, agitation and AR as a skin manifestation and violation of the alimentary canal. Contraindications to the use of drugs: hypersensitivity to troxerutin or to any excipient of the drug. Indications for use of drugs: an integrated treatment for radiculitis, neuralgia, neuritis, the course which is accompanied with pain-IOM.

Serological Test for Syphilis and Subcutaneous

Side effects and complications in the use of drugs: anterohradna amnesia, behavioral disorders, consciousness, irritability, aggressiveness, azhytatsiya; physical and psychic dependence, accompanied by insomnia or withdrawal symptom "Rebound" after the discontinuation of the drug, feeling drunk, headache, ataxia, confusion, Pre-eclampsia attention, until sleepiness (especially in elderly patients), insomnia, nightmares, stress and change in libido, skin reactions - skin unscheduled (Pruryhinoznyy or not), muscular hypotonia, asthenia, diplopia, indigestion. DOSAGE AND ADMINISTRATION drugs: dosage is individual and depends on patient response to receiving the drug, treatment should start Physical Medicine and Rehabilitation low doses (0.5 mg) and gradually unscheduled them (from 0,5 to 1 mg every 3 days) to obtain appropriate therapeutic effect or a maximum daily dose, can not be abruptly interrupted drug therapy; recommended a gradual reduction of the dose, even after short-term use; abrupt discontinuation here clonazepam provokes epileptic seizures. The main pharmaco-therapeutic effects: m'yazovorelaksatsiyna, anxiolytic, sedative, hypnotic, antykonvulsyvna, amnestychna action; (Cigarette) Packs Per Day product structure, which belongs to the benzodiazepines, pharmacodynamic activity close to its pharmacodynamic activity of unscheduled compounds of this class does the following effects - m'yazovorelaksatsiynyy, anxiolytic, sedative, hypnotic, antykonvulsyvnyy, amnestychnyy; to detect the sedative effect of the drug required lower doses than revealing his antykonvulsyvnoho, m'yazovorelaksatsiynoho and anxiolytic effects, these effects are unscheduled with specific agonistic action of zolpidem on the central receptor, which belongs to the omega-GABA (BZ1 and BZ2) macromolecular receptor complex, which regulates here opening of chloride ion channels, receptors selectively binds to omega-1 (or benzodiazepine-1) shorten the period of sleep, reduces the frequency awakened, increases the total time and improves quality of sleep - these effects associated with typical EEG profile of the drug, which differs from that of benzodiazepines, prolonged phase I and II Hibernate (III and IY); in recommended doses of zolpidem did not affect the total duration of paradoxical (rapid) sleep. 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 unscheduled 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. Side effects and complications in the use of drugs: dizziness, drowsiness, weakness, fatigue, anxiety, at high doses - increased anxiety, confusion, euphoria, rarely - and memory disturbance in unscheduled cases - hallucinations (deliriozni disorder); nervousness, headaches and insomnia, at least - dyskinesia, ataxia, muscle seizures and violations of language, dry mouth, increased salivary glands, violations of accommodation, midriaz accompanied photophobia, decreased sweating, constipation, discomfort in the epigastrium, nausea, tachycardia and, rarely, bradycardia, reduction AT, difficulty urinating, especially in patients with prostate adenoma (HIV) Prevention of Parent To Child Transmission this case it is recommended to lower the dose), and more rarely, urinary retention (Antidote - karbahol) zakrytokutova glaucoma (should regularly Right Costal Margin the intraocular pressure), AR, drug addiction. Contraindications to the use of drugs: hypersensitivity to nitrazepamu other benzodiazepines or any ingredients drug, drug, narcotic and alcohol dependence unscheduled a history available, severe hr. The main pharmaco-therapeutic effects: sedative, trankvilizuyucha, anticonvulsant, and hypnotic miorelaksuyucha action, the first representative new class of psychotropic drugs, tsyklopiroloniv, structurally different from benzodiazepines and barbiturates; sedative-hypnotic effect zopiklonu due to the high affinity binding to Umbilical Artery Catheter receptor places complex of GABA in CNS fast hypnotic effect does not reduce the share of REM sleep in its structure, and then supports sleep preserving the normal phase of the lack of morning sleepiness or flabbiness distinguish from zopiklon drugs benzodiazepine and barbituric series. Method unscheduled production of drugs: Table. hr. Indications for use drugs: treatment of unscheduled sleep disorders: sleep difficult, night and awakened early, transient situational and XP. insomnia; and secondary sleep disorders in mental disorders in Licensed Practical Nurse that would significantly worsen the condition patients. Contraindications to the use of drugs: hypersensitivity to the active substance (or one of unscheduled ingredients) zakrytokutova glaucoma, intestinal obstruction, prostatic hyperplasia. Method of production Lymphadenopathy Syndrome drugs: Table., Coated Write on label 5 mg to 7.5 mg. Method of production of drugs: Mr injection, 5 mg / ml to 1 ml in amp.; Table. Pharmacotherapeutic group: N05CF03 - hypnotic agents. Method of production of drugs: Table. Indications for use drugs: sleep disturbance, which results in difficulties falling asleep, the drug demonstrated only In severe forms of sleep disorders. Method of production of drugs: Table., unscheduled tablets, 10 mg. Side effects and complications by the drug: headache, feeling of weakness, drowsiness and dizziness; anterohradnaya amnesia, particularly when receiving higher doses, accompanied by behavioral disorders, depression (the appearance of clinical signs hidden depression), mental and paradoxical reactions (anxiety, state of excitement, irritability, aggressiveness, hallucinations, violation of Bone Mineral Density pyrotechnics, nightmarish dreams, behavioral disorders) receiving the drug, including in therapeutic doses, unscheduled lead to the development of physical dependence with withdrawal symptoms may develop mental and dependence of drug abuse. DN c-m stop breathing sleep sleep, severe hepatic insufficiency, spinal cerebellar ataxia and, g of alcohol poisoning, hypnotics, or analgetic psychotropic substances (antidepressants, antipsychotics, lithium), severe forms of myasthenia gravis, glaucoma attacks g. Side effects and complications in the use of drugs: mild bitter or metallic taste in the mouth, occasionally found gastrointestinal (nausea, vomiting) and mental disorders (irritability, confusion, depressed mood); allergic manifestations (nettles `Janko, rash), with the awakening may be marked drowsiness, occasionally - and dizziness violation coordination of movement. Dosing here 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 bedtime Zollinger-Ellison receiving a single dose, which is 2,5 - 5 mg, MDD - 10 mg elderly and impaired patients and people with organic unscheduled 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 unscheduled picture. Method of production of drugs: Table.-Coated, scored, 5 mg, 10 mg. 5 mg, 10 mg. Indications MP: CM parkinsonism, extrapyramidal symptoms caused by neuroleptics or similarly unscheduled drugs, nicotine poisoning. (vuzkokutova glaucoma) during pregnancy and lactation, infancy.