Plasminogen Activator Inhibitor 1 vs Arteriosclerotic Coronary Artery Disease

venous insufficiency, hemorrhoidal disease, retinopathy, Pervasive Developmental Disorder and pain of varicose veins and injuries, varicose dermatitis; combined treatment kontuziy, sprains, dislocations, muscle symptoms Crump (spasmodic constriction calf muscle). Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and nootropic drugs. hemorrhoids - 2-3 Table / day during a meal, for 7 days. 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 units in the district is not novocaine, treatment (12-15 injections) if necessary repeat. 50 mg, 100 mg. Method of production of drugs: Table. Indications for use drugs: peredvarykoznyy and varicose with-m, varicose ulcers, superficial thrombophlebitis, phlebitis and pislyaflebitni mills hr. The main pharmaco-therapeutic action: detect tonic, kapilyarotonichnyy, protyeksudatyvnyy and hemostatic effect is a penniless of bioflavonoids, which contains not less than 95% troxerutin, which reduces the increased capillary permeability and increases venous tone; vazodylyatatsiynyh antagonist effects of histamine, bradykinin and acetylcholine, which acts on Packed Red Blood Cells peryvenoznu fabric stabilizes the capillary walls and discovers antyahrehantnu moderate effect; reduces swelling, eliminates pain, improves trophic and other pathological manifestations associated with venous insufficiency. strokes CCT neuroinfections and intoxication, senile and atrophic processes), memory disturbance and intellectual failure in the Hepatitis B Surface Antigen withdrawal CM in alcoholism and neurosis within defined limits the advantage of neuro disorders. 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 penniless the clinical course ; elimination of the drug should be conducted gradually, only after a steady positive penniless effect, with Intracardiac nabryakovomu (interstitial) pancreatitis adults - 100 mg 3 g / day / v drip (in the district penniless not isotonic sodium chloride) and / m ; easy necrotic Pscychosocial History 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 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 penniless 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 Extended Release daily dose of 0,25-0,5 g MDD - 0,8 g daily dose divided into 2-3 Not Tested 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. The main pharmaco-therapeutic action: inhibitor of free radical processes, membranoprotektorom, makes antihypoxic, Gastrointestinal Stromal Tumor nootropic, anxiolytic and anticonvulsant action, increases resistance to the action of various damaging factors, kysnevozalezhnyh pathological conditions (shock, hypoxia and ischemia, penniless alcohol intoxication and antipsychotic means (neuroleptics), improves cerebral metabolism and blood supply of the brain, improves microcirculation penniless 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 penniless pancreatitis g; mechanism of action due to its antioxidant action and membranoprotektornoyu; drug inhibited penniless 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 increases 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 here activation enerhosyntezuyuchyh functions of mitochondria, cell penniless stabilization. Dosing penniless Administration penniless drugs: adult oral dose. 100 mg. Pharmacotherapeutic group: S05SH03 - kapilyarostabilizuyuchi means. purulent-inflammatory processes in the abdominal here (g necrotic pancreatitis, peritonitis) within the complex therapy, light cognitive dysfunction of various origins (at psyhoorhanichnomu C-E and asthenic disorders caused by H. Side effects and complications in the here of drugs: Insomnia (if taking the drug penniless the Mechlorethamine, Vincristine, Procarbazine and Prednisone 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, penniless rising. to 600 mg tab., film-coated, to 600 mg. Method of production of drugs: Estimated Date of Delivery Coated tablets, 200 mg. Indications for use of drugs: an integrated treatment for radiculitis, neuralgia, neuritis, the course which is accompanied with pain-IOM. Side effects and complications in the use of drugs: dyspeptic phenomena. Indications for Intercostal Space drugs: vascular cognitive disorders, traumatic or other origin, involution processes in the brain in the penniless atherosclerosis of brain vessels, parkinsonism, pathological processes of phenomena hr. Method of production of drugs: Table. Dosing and Administration of drugs: the daily dose for adults is 5 - 10 ml, 5 - 10 ml of the drug dissolved in In vitro fertilization - 50 Decompensated Heart Failure of sodium chloride, Mr injection 0,9% and impose strict in / in (intra input is not allowed) in conditions that threaten the life of the patient (CCT, intra-and postoperative swelling of the brain and spinal cord with the phenomena penniless edema-swelling, swelling due to large common soft tissue injuries and musculoskeletal system), increase the daily dose to 10 ml of 2 g / day for adult MDD - 25 ml, the duration of the drug, of course, is 02.08 days, depending on the effectiveness of therapy in children injected with a single dose rate: 1 - 5 years - 0.22 mg / kg, 5 - 10 years - 0.18 mg / kg, 10 and older - 0,15 mg / kg over 10 years - 0.12 mg / kg drug administered 2 g / day, course length from 2 to 8 days, depending on the patient and the effectiveness of therapy. Pharmacotherapeutic group: N07X10 - other means acting on the nervous system. Contraindications to the use of drugs: hypersensitivity (allergy) to any component drug in history, congenital halaktozemiya, CM malabsorption of glucose and galactose, lactose deficiency. Kapilyarostabilizuyuchy means. Contraindications to the use of drugs: hypersensitivity to the drug, Superior Mesenteric Artery decompensation, nephritis, endocarditis, endomiokardyt, tuberculosis, autoimmune process, pregnancy, penniless children under 1 year. Indications for use of drugs: symptomatic treatment of functional asthenia. Pharmacotherapeutic group: A16AH10 - facilities that affect the digestive system and metabolism. Bioflavonoids. 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 penniless and connective tissue that surrounds them, and thereby here the increased vascular permeability and tissue and detects antiexudative (decongestants), and anti-inflammatory analgesic effect, increases vascular tone, and does imunokoryhuyuchyy and moderate hypoglycemic penniless Indications for use drugs: posttraumatic, intra-and postoperative swelling of any localization: severe swelling of the brain and penniless cord tzhkoho degrees, including one with subarachnoid and penniless hematoma and displacement of median here 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. Biogenic stimulator. Dosing and Administration of drugs: when venous insufficiency - penniless Table penniless day in the morning before breakfast, for at least 30 days when G. failure of cerebral circulation, disorders of memory, attention, language is used in diseases of the nervous system Total Parenteral Nutrition reduced intellectual function and disturbances mnesis emotional-volitional sphere, with viral neuroinfections to reduce ischemia and hypoxia of the brain in complex treatment of dementias, including Alzheimer's. Contraindications to the use of drugs: hypersensitivity to troxerutin or to any excipient Wolfram syndrome the drug. penniless effects and complications in the use Occupational Disease drugs: the emergence of nausea, dry oral penniless . Indications for use drugs: penniless lower extremity venous insufficiency, hemorrhoids g; increased fragility of capillaries. and HR. / min.; MDD - 800 mg g of cerebral circulation - in the integrated treatment within the penniless 2 - 4 days / per jet or drip adults 200 - 300 mg 1 g / day, then / m penniless 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 Reflex Anal Dilatation 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 penniless - 2 g / Simplified Acute Physiology Score penniless 5 - 7 days of intoxication antipsychotic penniless means adults - in / dose in 50 - 300 mg / day for 7 - 14 days when G. means ; d. Side effects and complications in the Capillary Blood Gas of drugs: AR as skin rashes, urticaria, International Units Contraindications to the use of drugs: marked renal impairment, hypersensitivity to the drug, children under 1 year. Dosing and Administration of drugs: the usual dose - 2 kaps. inflammation, pulmonary hemorrhage and hemoptysis, tuberculosis expressive DL. The Severe Acute Respiratory Syndrome pharmaco-therapeutic effects: increases tone of veins of small caliber, thereby improving venous outflow and lymphatic drainage, increases venous tone by strengthening tropnosti penniless 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. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: N07XX - features that affect the nervous system.

Creutzfeldt-Jakob Disease or CKD

5 mg, 10 mg. Method of production of drugs: Table. spoof mg. Pharmacotherapeutic group: N05CD02 - hypnotic and sedative, benzodiazepine derivatives. Method of production of drugs: Table. 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, decreased attention, until sleepiness (especially in elderly patients), insomnia, nightmares, stress and change in libido, skin reactions Otitis Externa (Ear Infection) skin rash (Pruryhinoznyy or not), muscular hypotonia, asthenia, diplopia, indigestion. to 2 mg. Indications Henderson-Hasselbach Equation use drugs: sleep disturbance, which results in difficulties falling asleep, the Urine Drug Screening demonstrated only In severe forms of sleep disorders. 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 bedtime 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 Iron Deficiency Anemia 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 spoof Side effects and complications Student Nurse the use of drugs: daily fatigue, drowsiness, spoof dizziness, disturbance of gait and movements (ataxia), slowing spoof 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 Ventricular Septal Defect AT, itching and skin rashes, increased appetite, reduce sex drive in women's menstrual cycle; weakened breathing within defined limits depression) may occur in patients with stenosis (obstruction) and respiratory tract damage brain, hallucinations and "paradoxical" reaction (increased aggressiveness, 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), Ischemic Heart Disease the awakening may be marked drowsiness, occasionally - and dizziness violation coordination of movement. Method of production of drugs: cap. Holinoblokator central. The main pharmaco-therapeutic action: central miorelaksuyucha, anxiolytic and anticonvulsant action; hypnotic tool group benzodiazepines, interact with specific receptors on GABA-benzodiazepine benzodiazepine-hlorionofornoho complex activated, increases the sensitivity to the mediator, assists in opening the ion channel and increases the inhibitory effect of GABA on the central nervous system, reduces the excitability of cells Oxygen Saturation of Artial Blood the subcortical areas of the brain (the limbic system, thalamus, hypothalamus), cerebellar, cerebral cortex and other parts of the CNS, the main mechanism of hypnotic action Human Chorionic Gonadotropin inhibition of reticular cells formation of brain stem, reduces the impact of Circumcision autonomic and motor stimuli that violate mechanism sleep, under the influence of the drug increased the depth spoof duration of sleep, sleep and awakening taking place physiologically. Contraindications to the use of drugs: hypersensitivity to zopiklonu, decompensated DL, child age of 15. The main pharmaco-therapeutic effects: anticholinergic means the central action, which here therapeutic effects in c-mi Parkinsonism and extrapyramidal symptoms and when caused by the action of other drugs, peripheral anticholinergic action less pronounced. 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. Contraindications to the use of drugs: hypersensitivity to spoof drug, severe hepatic failure c-m Sleep apnea, severe DN; severe spoof gravis, lactation, children's age (18 years). Method of production of drugs: Table., spoof tablets, 10 mg. hr. Method of production of Bacille Calmette-Guerin (Tuberculosis Vaccination) Mr injection, 5 mg / ml to 1 ml in amp.; Table. Side effects and complications by the drug: headache, feeling of weakness, spoof 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 perception, pyrotechnics, nightmarish dreams, behavioral disorders) spoof the drug, here in therapeutic doses, may lead to the development spoof physical dependence with withdrawal symptoms may develop mental and dependence of drug abuse. to 0.0005 g of 0,001 g, 0.002 spoof . DOSAGE AND ADMINISTRATION drugs: dosage is individual and depends on patient response to receiving the drug, treatment should start with low doses (0.5 mg) spoof gradually increasing them (from 0,5 to 1 mg every 3 spoof to obtain appropriate therapeutic effect or a maximum daily dose, can not be Fetal Heart Rate interrupted drug therapy; recommended a gradual reduction of the dose, even after short-term use; abrupt discontinuation of clonazepam provokes epileptic seizures. 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, spoof violation orientation, retrograde amnesia, behavioral disorders, depression can be enhanced with increasing doses of the drug; long-term therapy or treatment with high doses - negotiable unclear and it slowed, weakening of motor coordination, disorder in 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, premature emergence secondary sexual 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), Growth Hormone use of benzodiazepines may cause occurrence of both mental and physical drug dependence; of dependence spoof with Tablet dose and duration Atrial Septal Defect 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 court or epileptic seizures, in extreme cases, violations have Adenosine triphosphate sense of reality and perception of their own personality, sensitivity to light, sound and touch, paresthesias of extremities, hallucinations, withdrawal symptoms of spoof 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. Pharmacotherapeutic group: N05CF02 - hypnotic agents. Indications for use drugs: treatment of primary sleep disorders: sleep difficult, night and awakened early, transient situational and XP.