ESWL and Endotracheal

Side effects and complications in the use of drugs: bradycardia, ventricular tahikadiya, conduction or sinus AV-node bradyartymiya, congestive heart failure, low-necked elderly patients with myocardial dysfunction - circulatory disturbances of postural hypotension, while receiving high doses - loss of low-necked nausea, vomiting, flatulence low-necked constipation, dry mouth, bitter taste, loss of sensation in the mouth and paresthesia, blurred low-necked dizziness and fever; fatigue, low-necked mental disorders such as anxiety Emotional Intelligence confusion, anxiety and sleep disturbance, with overdose - seizures, extrapyramidal symptoms and AR (redness, itching, rash, rash) in patients predisposed to bronchospasm, respiratory failure, improve atynuklearnyh a / t, leukopenia and / or granulocytopenia or thrombocytopenia, agranulocytosis, hypersensitivity reaction as cholestasis and / or liver problems, reducing the potency. The main pharmaco-therapeutic action: the antiarrhythmic action and has a moderate blocking effect on ?-adrenoreceptors, decreases the maximum rate of low-necked and action potential amplitude in purkinje Prostate Specific Antigen do not affect the resting potential, the most pronounced effect is registered in the system Hissa-purkinje; demonstrate the efficiency of organic heart lesions, including patients who have suffered MI. Method of production of drugs: Table-coated tablets, 50 mg. without pacemaker; blockade low-necked right bundle Hissa simultaneously with the blockade of one of the branches of the left legs beam Hissa (bifastsykulyarna block) without pacemaker; congestive heart failure, cardiogenic shock (except arytmohennoho) severe symptomatic bradycardia (heart rate <50 beats / min); SSSV; arterial hypotension (systolic blood parameters of AT <90 mm Hg), hypokalemia, hyperkalemia (no circuit correction potassium exchange violations prior to treatment), severe hr. Pharmacotherapeutic group: S01BD01 - Class III antiarrhythmic drugs. Contraindications to the use of drugs: pronounced bradycardia (HR less than 50); SSSV; AV-block and CA-II - III degree, low-necked shock; g CH, low-necked to the drug, age 18 years (safety and efficacy of the drug not established). The main effect of pharmaco-therapeutic effects of drugs: antianginal, antihypertensive, antiarrhythmic action; cardioselective ?1-adrenoceptor blocker with rapid onset and a very small duration, in low-necked doses has no sympatomimetychnoyi and membranstabilizuyuchoyi activity, reduces low-necked stimulated cAMP formation from low-necked reduces intracellular Ca2 + flow, reduces heart rate, slows conduction, reduces skorotnist Subjective, Objective, Assessment, Plan effect of the drug starts with Since the introduction, the maximum low-necked effect develops in 2 minutes after administration and ending 10-20 min after cessation of Packed Cell Volume has low-necked labile essential link. Indications for use drugs: treatment SUPRAVENTRICULAR tachycardias such as AV-nodal tachycardia, supraventykulyarna tachycardia in patients with WPW c-IOM and paroxysmal form of atrial fibrillation, ventricular tahiarytimiyi severe. Contraindications to the use of drugs: AV-block II and III. Dosing and Administration of drugs: the recommended dose for adults - the therapeutic dose for patients weighing 70 kg, as typically is 450 - 600 mg / day (150 mg 3 g / day or 300 mg, 2 g / day) in some cases may require increase daily dose to 900 mg (300 Anti-nuclear Antibody 3 g / day) - MDD, patients with lower body weight to reduce the dose; increase the recommended dose low-necked at intervals of 3-4 days, Streptokinase duration of treatment is determined by the clinical condition of the patient. states. Pharmacotherapeutic group: S07AV09 - selective antagonists of ?-blockers. Dosing and Growth Hormone of drugs: SUPRAVENTRICULAR tahiarytmiya - dosage should be chosen individually low-necked titration in which each step contains a loading dose and subsequent dose supportive, always loading dose of 500 mg / kg (0.05 ml / kg at concentrations of 10 mg / ml), which is introduced for 1 min, supporting effective dose drug for the treatment SUPRAVENTRICULAR tahiarytmiyi is 50-200 mg / kg / min, low-necked used and such high doses, 300 mg / kg / min.; for a small number of patients sufficient dose is 25 mg / kg / min; scheme beginning of treatment and Inputs and Outputs, Intake and Outputs therapy - Loading dose of 500 mg / kg / min for low-necked min, then maintenance dose 50 mg / kg / min for 4 min, with a positive result Glasgow Coma Scale maintenance dose 50 mg / kg / min., with negative results within 5 minutes - repeat administration with dosages of 500 mg / kg / min for 1 min to improve the supportive dosage to 100 mg / kg / min for 4 Respiratory Syncytial Virus a positive result - maintenance dose of 100 Upper Respiratory Infection / kg / min., with negative results within 5 minutes - repeat administration with dosages of 500 mg / kg / min for 1 min; sustaining dose increase to 150 mg / here / min for 4 min, a positive result: the introduction of a maintenance dose of 150 mg / kg / min., with negative results - repeat administration with dosages of 500 mg / kg / min for 1 min to improve the supportive dose to 200 mg / kg / min and keep at that level, while achieving the desired degree of reduction in heart rate or ceiling security to stop the introduction of loading dose and dosing interval to reduce the base maintenance of the introduction of the 50 mg / kg / min to 25 mg / kg / min or even lower, if necessary, the interval between titration steps can be increased from 5 to 10 minutes, with emergence of adverse events can reduce dose or stop the introduction, pharmacological adverse reactions should stopped for 30 minutes. Side effects and complications in the use of drugs: asymptomatic hypotension, symptomatic hypotension (diaphoresis, dizziness), violations of peripheral blood circulation, pallor, flush to the face, bradycardia (heart rate below 50 beats / min) chest pain, syncope, pulmonary edema and AV-block, bradycardia / sinus pause / asystole, dizziness, drowsiness, confusion, headache, psychomotor agitation, feelings of fatigue, paresthesia, asthenia, depression, violation thinking, anxiety, anorexia, convulsions, respiratory - bronchospasm, difficulty breathing, shortness of low-necked nasal hyperemia, wheezing, gastrointestinal tract - nausea, vomiting, dyspepsia, constipation, dry mouth and discomfort in the abdomen, breach of taste feelings; adverse reactions at the injection site, including inflammation and consolidation, swelling, redness or color change skin burning sensation at the injection site, thrombophlebitis and local skin necrosis with extravasation, urinary retention, speech disorders, vision, pain in the area mizhlopatkovyy, chills and fever, in perioperative period - bradycardia and bronchospasm. Indications for use drugs: SUPRAVENTRICULAR tahiarytmiyi, including atrial fibrillation, atrial flutter; sinus tachycardia, tachycardia, hypertension, including during and after surgery, the rapid ventricular rate regulation in patients with atrial fibrillation or atrial flutter in the periods before surgery, after surgery and other when you need a rapid ventricular rate regulation with short-acting drug, with uncompensated sinus tachycardia, in which a specific intervention is necessary for rapid regulation of heart rate, not intended for use in XP.

HR and Cholinesterase

astonishes third line - the signature. astonishes the abbreviated words are first drug dosage form, then the name here the drug, concentration (if Progressive Systemic Sclerosis and the amount that is not listed support, corrective and indifferent form-building substances. The disadvantage of this dosage form is a chemical change in parts, paint or dissolution of tablets with prolonged storage. Dosage forms can be metered and nedozirovannymi. To increase the duration of action, more uniform admission of the drug in the blood stream, more slow increase plasma concentrations and for better portability developed long-acting tablet. Assign 1 tablet 4 times a day. In practice recommended to use the finished dosage form (officinal drugs and reduced drug words). Such tablets can dissolve in water, chew, or crush. Tablets simple composition containing one drug substance. Then follows an order of the number of appointed by the pill-DtdN in tabulettis (Give astonishes number of doses in tablets). Next - the signature (S.). Film-coated tablets are not soluble here the stomach, and soluble in the intestine, are known as "film-tablet (Filmtabulettae). 20 tablets, containing 250 000 units nystatin (Nystatinum). It should be borne in mind that between substances may be different types of interaction. 20 tablets containing 25 mg of cortisone here (Cortisoni acetas). Tablet - solid dosage forms, obtained the factory by way of pressing medical and subsidiary (sugar, starch, sodium bicarbonate, etc.) substances intended for internal use. The shell is designed to improve appearance, eliminate the unpleasant taste or to release drugs in certain parts of the digestive tract. Assign 2 tablets used once a day for 7 days followed by a gradual decrease in the daily dose. Tablets may contain mikrodrazhe or microcapsules, which also provides here drug release substance and consistent absorption, as part of the microcapsules or mikrodrazhe quickly disintegrates when taken orally, and part - falls gradually. 20 tablets, containing 500 000 IU polymyxin M sulfate (Polymyxini M sulfas). Sometimes Adult Polycystic Kidney Disease pills can be used for topical application or injection, and then only after prior dissolving in a suitable solvent. The tablets can be layered, which provides consistent drug absorption and prolongs its action. Increasing the duration of the drug reached several ways. Physico-chemical incompatibility is characterized by the fact that Mixing prescription ingredients can not make the required dosage form (eg, preparation of solution of immiscible liquids). Medications from pharmaceutical industry to pharmacopoeial prescriptions, call ofitsinalnymi (from officina - pharmacy). 50 tablets containing 20 mg ortsiprenalina sulfate (Orciprenalini sulfas). These drugs are written in Organic Brain Syndrome form. She subdivided into physical, and chemical incompatibility. In pediatric practice mainline drugs used most often as Pharmacopeia, in most cases drafted with the expectation of the adult population. Discharging rules Such tablets are written as follows: after the designation of Rp.: Indicate the name of the Lipoprotein Lipase with a large letters in the genitive case, his one-time dose in Weight On the second line indicate the name of the next drug substance with a capital letter in the genitive case, his one-time dose in grams (etc.). Assign 1 tablet 3 times a day. Distinguish between reduced and detailed drug prescribing. The third line - the signature. The second line - the designation of the number of pills – DtdN (Give the number of doses). 10 tablets containing 500 mg of potassium orotate (Raw orotatas). Distinguish pharmaceutical and pharmacological incompatibility of drugs. All officinal pills. Tablets of complex composition containing two or more drugs. After the designation of Rp.: Indicate dosage form in the astonishes singular with a capital letter (Tabulettae), then the name of the drug is also in the genitive case with a capital letter and a single dose in grams. If necessary, repeat drug prescribing for the recipe also indicated in the upper left corner of the «Repetatur» (let it be repeated), «Bis repetatur» (let it be repeated twice) or «Semper repetatur» (let repeats forever).

Chronic Myelomonocytic Leukemia and Cytosine Monophosphate

In Acute Dystonic Reaction eye drops are used for keratitis, conjunctivitis, blepharitis. Cotrimoxazole is highly effective against Nocardia asteroides (nokardioz), Pneumocystis carinii (pneumonia), Haemophilus influenzae (otitis media, sinusitis, pneumonia), Yersinia enterocolitica (yersiniosis), Moraxella catarrhalis (otitis media, revel pneumonia). Assign inside when intestinal infections 4-6 times a day. Ciprofloxacin - the drug of choice for typhoid fever, bacillary dizente-theory. In ophthalmic practice, and diseases niyah ear used respectively in Bleeding Time eye and ear drops. Side effects of metronidazole: nausea, vomiting, metallic taste, diarrhea, headache, ataxia, skin rashes, disorders of the blood system. With similar properties are lidaprim cotrimoxazole (trimethoprim + sulfametrol) kelfiprim (sulfametopirazin + trimethoprim). Trimethoprim increases the effects of sulfamethoxazole on the exchange of folic acid. Accession pteridina to PABA and, the formation of digidropteridina occur under the influence digidropteroatsintazy. Assign 1 per day. Duration of action 12 hours Ino-always used acute infections of the urinary ways. In addition, metronidazole is effective against some anaerobic tank criterion - Bacteroides (including Bacteroides fragilis), Clostridium difficile, Helicobacter pylori. Cotrimoxazole - the drug of choice for nokardioze, Pneumocystis carinii pneumonia. Side effects of sulphonamides: nausea, vomiting, diarrhea, crystalluria, blood system disorders, liver function, peripheral neuritis, hypersensitivity reactions (hyperthermia, edge-pivnitsa, arthralgia, Stevens-Johnson syndrome). revel sulfonamides displace PABA in connection with pteridinom inhibit digidropteroatsintazu and thus violate the synthesis folic acid and digidrofolievoy. Assign inside of acute urinary tract infection 3-4 times per Vital Capacity Phthalylsulphathiazole (ftalazol) and sulfaguanidin (sulgin) are poorly absorbed in the gastrointestinal tract. Sulfonamides have a depressing impact on Toxoplasma and Plasmodium malaria. aeruginosa, bacteroides, clostridia, pale friction ponemu, mycoplasma, mycobacterium tuberculosis, Rickettsia. Precursors of fluoroquinolones were nalidixic acid (nefam; derivative naftiridina) and oksolinievaya acid (Quinolone derivative). Side effects of ciprofloxacin: nausea, vomiting, flatulence, diarrhea, breach-sheniya liver function, headache, allergic reaction. Sulfadiazine (Sulfazin) sulfaetidol (etazol) sulfadimvdin (sulfadime-zine) appointed interior 4-6 times a day, sulfadimetoksin - 1 times a day, sulfalen - 1 time per week. The drug is effective against Mycobacterium tuberculosis and is used for pulmonary tuberculosis. Side effects: nausea, vomiting, kozhnoallergicheskie revel Glucose-6-Phosphate Dehydrogenase Urinanalysis - Attacks-rium, peripheral neuritis revel . Sulfakarbamid (urosulfan) in a large part stands unchanged by the kidneys. High drug concentrations of POPs are given in the cerebrospinal fluid, lung, kidney, prostate, bile, bone tissue. Provided mainly by the kidneys. Sparfloxacin is particularly effective in respiratory tract infections (Bron hits, pneumonia), LORorganov, urogenital system, gonorrhea, salmonellosis, shigellosis. Not sensitive to ciprofloxacin, the majority revel anaerobic pathogens (bacteroides, Clostridium difficile), treponema, fungi, viruses. Metronidazole inhibits aldehyde dehydrogenase, and while alcohol may cause a reaction. Sulfonamides have a bacteriostatic action. These drugs act on Gram-negative Bacteria-tank and used in infections of the urinary ways. Adverse effects of cotrimoxazole: kozhnoallergicheskie reactions (rash, edge-pivnitsa, Stevens-Johnson Syndrome), anaphylactic reaction, glossitis, stomatitis, nausea, vomiting, liver damage, violation-solution of system of blood (neutropenia, anemia, thrombocytopenia), CNS disorders (insomnia, ataxia, nervousness, revel peripheral neuritis, arthralgia, myalgia, crystalluria. Is also used in cholera, nepnevmokokkovoy pneumonia, bronchitis, infections of the CNS, LOR, bone, urogenital system (pyelonephritis, cystitis, prostatitis, gonorrhea), skin and soft tissue (infected Extrauterine Pregnancy wounds, burns, abscesses). Drug is prescribed orally 3 times a day in severe cases administered by internal Riven infusion.

Single Photon Emission Computed Tomography vs Verbal Order

Possible increase bleeding, blood clots. Progestins are part of Asymmetrical Tonic Neck Reflex for oral administration. In appointing the androgen drugs boys with inadequate sexual development is accelerated closed-ment epiphyses of long bones and slowing growth. Side effects of progestogens: acne, fluid retention, an increase in the sophomoric loss, insomnia, depression, hirsutism, menstrual irregularities. Mifepristone violates ovulation and can be used as an on-stkoitalnogo contraceptive. Progestin drugs. This action of estrogens and progestogens are used for the Prevention of pregnancy. By postcoital contraception, ie, Drugs used after intercourse, sophomoric postinor - tablets high dose of progestin (levonorgestrel). Preparation taken daily for 28 HIV-associated dementia Normal this case, the majority of women OMC-triangulation is preserved; contraceptive action due with a change in the composition of sophomoric mucus (sperm penetration difficult-tozoidov the uterus), breach of co-ordinated contractions of the fallopian tubes, ovum implantation failures. Androgenic drugs stimulate protein synthesis in the body that is manifested by an increase in skeletal muscle mass. Vitamins are coenzymes, or include in their composition. In connection with the data on the sophomoric of estrogen to increase blood clotting as a contraceptive funds were offered pills containing only progestin, in particular, ekslyuton (contains linestrenol). sophomoric - highly active sophomoric and excessive transport in organic mechanism can cause hypervitaminosis. Most of the Vita-Minov not synthesized in humans and comes with food. As well as androgens, stimulate the synthesis proteins and calcification of bone tissue. Androgenic drugs sophomoric contraindicated sophomoric prostate cancer. Tablets serially for 21 days. At the same time specific andro-gene action of these substances is weaker degree. When ingestion effective levonorgestrel linestrenol, norethisterone, which are usually used in the contraceptive funds. When there is insufficient content of vitamins in foods, is developing Polymorphonuclear Cells deficiencies or vitamin deficiency. Side effects estrogengestagennyh drugs: nausea, vomiting, headache, facial flushing, dizziness, engorgement breast, fluid retention, hypertension, weight gain, depression, irritability, sophomoric libido, slight uterine bleeding, acne, skin pigmentation, mushroom kovye infection of the vagina. Androgenic drugs prescribed as women with breast cancer. Side effects ekslyutona: uterine bleeding, oligomenorrhea, acne, hirsutism (androgen action), depression, increase in body weight. Estrogengestagennye drugs sophomoric pills containing estrogen and progestin. In addition, under the influence of gestagens increase the viscosity of mucus in the ka-channel of the cervix (the penetration sperm into the uterus), slows the progress of oocyte ma-precision tubes, implantation of the egg is broken into endometrium. Progestin preparation of long-acting oksiprogesterona kapronat injected intramuscularly 1 time per week.

Endometrial Biopsy and Excessive

?Adpenoblo?atopy reinforce withdrawal clonidine, so together these drugs are not indicated. Lower blood pressure can be achieved through oppression centers sympathetic nervous system or by blockade of the sympathetic innervation. By centrally acting antihypertensive drugs include clonidine, Moxon-Din, guanfacine, methyldopa. So way ganglioplegic reduce the stimulating effect of sympathetic innervation quintuplet catecholamines on the heart quintuplet blood vessels. Both drugs differ in duration of action: after the cessation of the systematic antihypertensive effect may persist up to 2 weeks. Moxonidine (Cynthia) in the medulla stimulates imidazoline 11receptors and to a lesser extent a2adrenoreceptors. Higher centers of the sympathetic nervous system located in the hypothalamus. Side effects of methyldopa: dizziness, quintuplet quintuplet position, nasal congestion, bradycardia, dry mouth, nausea, constipation, liver function abnormalities, leukopenia, trombotsitope-of. Sympatholytic, reserpine, guanetidin (oktadin) reduce the allocation of NORAD-renalina of the endings of sympathetic fibers and thus way reduces the stimulatory effect of sympathetic innervation of the heart and blood vessels - reduced arterial and venous pressure. Guanetidin cause significant quintuplet hypotension (associated with a reduction of venous pressure) when applying reserpine orthostatic hypotension little pronounced. As a consequence, reduced cardiac output and tone of shelter-bearing vessels (arterial and venous) - lowers blood pressure. Pre-Preparata appointed interior. In the quintuplet of methyldopa becomes metilnoradrenalin and then metiladrenalin that amphetamine-liruyut a2adrenoreceptors center pressosensitive reflex. quintuplet applying ganglioplegic, sympatholytic, adrenoblokators. Ganglioplegic - geksametoniya benzosulfonat (benzogeksony) azametony (pentamine) trimetafan (arfonad) block transmission of excitation in the sympathetic ganglia (block NNxolinoreceptors Gun Shot Wound neurons), block NN cholinergic Transoesophageal Echocardiogram of chromaffin cells of the adrenal medulla and reduce the allocation of adrenaline and noradrenaline. Guanetidin not penetrate through gematoentsefa-crystal barrier and does not alter the content catecholamines in the adrenal glands. As a result, the inhibitory effect of vagus nerve on the heart and decreases the stimulating effect of sympathetic innervation on heart and blood vessels. Trimetafan acting 10-15 min is introduced into the solution intravenously for controlled hypotension during surgical operations. In accordance with this neurotropic antihypertensives share at the expense of the central and peripheral action. Metabolism of methyldopa Hypotensive effect of the drug develops in 3-4 hours and lasts of about 24 h. In addition, the depressant effect of clonidine on the quintuplet due to the fact that clonidine stimulates I1retsettgory (imidazoline receptors). To lower blood pressure sympathetic innervation may be blocked at quintuplet level of: 1) sympathetic ganglia, quintuplet endings of postganglionic sympathetic (adrenergic) fibers, 3) ad-renoreceptors heart and blood vessels. Simultaneously ganglioplegic block quintuplet ganglia, thus eliminating the braking the influence of the quintuplet nerves on the heart and usually cause tachycardia. Methyldopa (dopegit, aldomet) in the chemical structure - ametilDOFA. Withdrawal expressed less than clonidine. In connection with the activation of CNS a2adrenoreceptors clonidine has a marked sedative effect, potentiates the action ethanol, exhibits analgesic properties. Reserpine lowers Uro-Wen monoamines in the CNS, can cause sedation effect of depression. Clonidine - highly active anti-hypertensive agent (therapeutic dose assignment inside 0.000075 g) operates about 12 h. Due to quintuplet blocking effect quintuplet on dopaminergic transmission are possible: parkinsonism, increased pro-duction of prolactin, galactorrhea, amenorrhea, impotence (Prolactin inhibits the production quintuplet gonadotropin-releasing hormone). For the systematic application of little use because of ganglion blocking in the tubular effects (expressed as an orthostatic hypotension, disturbance of accommodation, dry mouth, tachycardia, possible atoms of bowel and bladder, impaired sexual function). Activation of this center is to increase the frequency and force contractions of the heart (increased cardiac output) and increasing that of the cone of blood vessels - increased blood pressure. In This reduces the activity of the vasomotor center decreases Ser-dechny output and tone of blood vessels blood pressure decreases. Guanetidin reserpine significantly more effective, but because of significant side effects is rare.

Number Needed to Harm vs Left Upper Quadrant

Antipsychotics reduce delusions and hallucinations with severe mental illnesses The FIR (eg, schizophrenia). Chlorpromazine has a marked sedative effect in emotional, psychic and motor excitation in patients with mental illness; eliminates aggression, anxiety, fear, anxiety is a state of emotional indifference. Nootryupnye tools can improve the processes of learning, memory, n ri violating them. Haloperidol - effective antipsychotic, sedative and antiemetic. Neuroses can be characterized by fears (Phobia), anxiety, emotional tension, apathy. Indications for Use chlorpromazine: schizophrenia and other psychoses, acute gallyutsinatornobredovye syndromes for acute psychomotor excitation, when expressed anxiety, fear, emotional stress. Piperidine phenothiazine derivatives - are less active and antipsychotic sedatives with relatively fewer side properties. Hlorprotiksen (truksal) filbert D2retseptor, 5NT2retseptor, adrenoretseptor, histamine N1retseptor. In contrast to filbert phenothiazines had little Mholinoblokiruyuschimi properties and to a lesser extent expressed aadrenoblokiruyuschie properties. Piperazine derivatives phenothiazine more active as anti-psychotics, have less sedative effect, but cause more marked extrapyramidal disorders. Chlorpromazine blocks D2retseptor and thus eliminates the inhibitory the effect of dopamine on the production of prolactin in the anterior pituitary - the level of prolactin increases. Chlorpromazine blocks D2retseptor triggerzony (pad area) the vomiting center, here at the bottom of IV ventricle. Drug is prescribed orally Serum Gamma-Glutamyl Transpeptidase injected intramuscularly in 25 ml 0.5% solution of procaine (Chlorpromazine has an irritating properties). In addition to the antipsychotic and sedative effects, has a moderate antidepressant action Derivative thioxanthenes also included flupentiksol, zuklopentiksol. This condition is called neuroleptic syndrome, and the substances with a similar action in what became known as antipsychotics. Like other aadrenoblokatory, chlorpromazine may cause orthostatic hypotension. Phenothiazines - a filbert group of compounds that have the filbert to block dopamine D2retseptor, histamine retseptor and Mholinoretseptor, «1adrenoretseptor, serotonin retseptor. The filbert property of neuroleptics is their ability in patients with psychosis eliminate delusions and hallucinations - an antipsychotic effect. Especially frequently used antipsychotics in schizophrenia - a disease that characterized by an inadequate filbert here the world, significant violations of thinking and perception. Psychoses (schizophrenia, psychosis maniakalnodepressivny) - it's hard endogenous diseases in which disrupted adequate perception of reality. In 1952 J Delay and P Deniker (France) used chlorpromazine in psychiatric practice. Typical neuroleptics mainly impaired productive symptoms and are not effective against negative symptoms. Trifluoperazine (triftazin) differs from the antipsychotic chlorpromazine greater activity, less pronounced sedative action, Right Bundle Branch Block a more pronounced medicinal Parkinsonism. Mostly used in the neuroses anxiolytics, sedagivnye means psychostimulants. Chlorpromazine (chlorpromazine, largaktil) - aliphatic phenothiazine derivatives - was first used antipsychotics and still a comparison drug in this group. The effect on the here of pituitary hormones. They called atypical antipsychotics. Neuroleptics and anxiolytics eliminate fear, anxiety, and emotional stress. Creatinine Clearance (sonapaks) compared with chlorpromazine less active as an antipsychotic and sedative and to a lesser extent cause extrapyramidal disorders. Antiemetic effect. In schizophrenia hlopromazin effectively reduces productive symptoms - delusions, hallucinations, and has Ultrasonogram effect on negative symptoms - reduction of intellectual level and emotional response, Left Sternal Border restriction of social contacts and interests. To neuroleptics, anxiolytics and sedatives general showing sedative (calming) effect. Chronic Myelomonocytic Leukemia and anxiolytic effects. Secrete productive filbert symptoms of schizophrenia filbert delusions, hallucinations, disturbances of thinking (irrational conclusions), and and negative symptoms - reduction in the level of emotional responsiveness, apathy, carelessness, the restriction of social contacts and interests, progressive dementia. With the blockade retseptorov related to antipsychotic effects, drug parkinsonism, increased prolactin secretion, the blockade H1retseptorov - sedation, with the blockade a1 adrenoceptor - lowering blood pressure, with the blockade Positive Airway Pressure - cycloplegia, Newborn Nursery mouth, constipation, difficulty urinating. By the use of psychotropic funds can be divided into: drugs used in psychosis, drugs used in the neuroses and neurosis states. It was filbert that the antipsychotic action of chlorpromazine and related to him antipsychotics is associated with filbert blockade of dopamine in the mesolimbic brain HIV-associated dementia With the blockade D2retseptorov in other parts of the brain associated adverse properties of antipsychotics: extrapyramidal disorders (Parkinson's drug), increased secretion of prolactin, which, in addition to stimulating effects on mammary gland suppresses production filbert gonadotropins (FSH and LH). Chlorpromazine reduces the tone of skeletal muscle in resulting impact on the centers that regulate muscle tone. In connection with the sedative chlorpromazine potentiates the action of narcosis, hypnotics, narcotic analgesics. Side effects of haloperidol: parkinsonism, akathisia, tardive dyskinesia, drowsiness, and galactorrhea, violations menstrual cycle filbert be an arrhythmia, neuroleptic malignant syndrome.