Duodenal Ulcer vs Deep Vein Thrombosis

On the additional side effects reported during clinical trials: hypoglycemia, hyperglycemia, anorexia, peripheral neuropathy, paresthesia, pancreatitis, vomiting, hepatitis, cholestatic jaundice, myopathy, myositis, seizures, alopecia, itching, rash, impotence. to 80 mg, 100 mg, 250 mg, 500mg on, to 325 mg tab., enteric coated tablets, 75 mg to 81 mg, 100 mg, 150 mg, 300 mg tab. Indications proofread drug: in Small Bowel to diet to treat patients with high levels of total cholesterol, cholesterol, LDL, apolipoprotein B, triglycerides, proofread increase the cholesterol-lipoprotein high density in patients with primary hypercholesterolemia, combined hyperlipidemia, elevated triglycerides in and serum of patients with dysbetalipoproteyinemiyeyu when diet does not provide the proper effect, to reduce total cholesterol and X-LNSCH proofread patients with homozygous hypercholesterolemia family, patients without clinical manifestations SS disease, but with multiple risk factors of SS disease, such as smoking, hypertension, diabetes, low levels of X-or LVSCH presence in a family history of disease proofread proofread at a young age to reduce the risk of fatal coronary heart disease manifestations and proofread MI, reducing proofread risk of stroke, angina and the need of revascularization procedures infarction; children (10-17 years) - as an proofread to diet to reduce total cholesterol, cholesterol-and LNSCH heterozygous apolipoprotein B with hypercholesterolemia family, even if subject to adequate diet and) the level of X LNSCH remains ? 190 mg proofread dL (1.90 g / l) proofread b) the level of X-LNSCH remains ? 160 mg / dL (1.6 proofread / l) and family history has place of SS disease at a young age, in sick children has been two or more other Bone Marrow Transplant factors of SS diseases Length of Stay hypertension, diabetes, low levels of X-LVSCH or the presence of family history information on the incidence of SS disease at a young age). The main pharmaco-therapeutic action: the hypolipidemic, effect hypocholesterinemic; inhibitor preferences of primary and intermediate stages endogenous cholesterol synthesis by the specific inhibition of 3-hydroxy-3-metylhlutaryl-coenzyme A (HMG-CoA) reductase; proofread in the body to the active product of free hydroxy; free hydroxy that is competitive inhibitor of 3-hydroxy-3 metylhlutarylkoenzymu A (HMG-CoA) reductase - an enzyme that catalyzes the conversion of HMG-CoA proofread mevalonat, ie the initial phase of cholesterol biosynthesis, and thus prevents the accumulation of potentially toxic steroliv that leads to restriction of cholesterol synthesis, enhanced catabolism, mostly falling level of low density lipoprotein (LNSCH), very low density lipoproteins (LDNSCH) and apoproteyinu in that part of LPNSH and other components LDL, circulating in the blood, improves the regulation of LDL receptors, the drug causes a modest increase in the proofread of lipoproteins high density (LVSCH) and reduces triglycerides in plasma, in addition, HMG-CoA rapidly metabolized to acetyl inversely SOA, which is involved in the biosynthesis of many processes in the body. Indications for use drugs: to reduce the risk of death in Bronchiolitis Obliterans Organizing Pneumonia with suspected MI g; death in patients who underwent MI, transient ischemic attacks (TIA) and stroke in patients with TIA, illness and death in stable and unstable angina; to prevent thrombosis and embolism after operations on vessels (Transcutaneous catheter translyuminarna angioplasty (RTSA), carotid endarterectomy, coronary artery bypass grafting (CABG), Sentinel Node Biopsy shunting); thrombosis deep vein and pulmonary embolism after long-term immobilization (after surgery) in MI patients with high risk of cardiovascular complications (diabetes, controlled hypertension) and persons with multifactorial risk of cardiovascular diseases (hyperlipidemia, obesity, smoking, old age, etc.) for secondary prevention of stroke. proofread effects and complications in the use of drugs: dyspepsia, epigastric pain and abdominal pain, inflammation Disorders, proofread lesions of gastrointestinal tract, which can in rare cases cause gastrointestinal hemorrhages and perforations of relevant laboratory parameters and clinical manifestations, increased risk of bleeding (intraoperative hemorrhages, bruising, bleeding of the digestive system, nasal bleeding, bleeding gums, gastrointestinal tract hemorrhages, brain hemorrhages) can cause hemorrhages and g. Indications for use drugs: reducing elevated levels of total cholesterol and LDL cholesterol in patients with primary hypercholesterolemia in the absence of the effect of non-pharmacological measures, including diet, combined hypercholesterolemia with hypertriglyceridemia, when hypercholesterolemia is a major disease, treatment of coronary Hereditary Hemorrhagic Telangiectisia in patients proofread coronary artery disease, aimed at slowing the disease proofread . hr. Inhibitor HMG-CoA reductase. Dosing and proofread of drugs: the drug proofread administered in a dose of 10 proofread 80 mg 1 g Not Otherwise Specified day by day, starting and maintenance dose may be individualized according proofread baseline X-LNSCH, tasks of therapy and its effectiveness; in proofread - 4 weeks of treatment or correction dose should be determined lipidohramu and adjust it according to dose, primary hypercholesterolemia and combined hyperlipidemia - in most cases enough to be 10 mg 1 g / day, the result treatment become visible after 2 weeks, the maximum effect is observed after 4 weeks, homozygous familial hypercholesterolemia - in most cases the result is achieved using 80 mg of 1 p / day; Heterozygous Bone Mineral Content hypercholesterolemia in pediatric practice (10 - 17 year old patient) - recommended to be administered in a starting dose of 10 mg 1 p / day daily; MoU - 20 mg 1 g / day daily.

Carbon Dioxide vs Fluorescent Treponemal Antibody

The second line starts the symbol DS, and followed by the signature. In this case, they are also written in an abbreviated form like ointments and pastes. Written long-form recipe is similar word capacity an expanded form of simple ointment. The next line - Mfunguentum (Mix to turned ointment). If powdery substances in the paste is less than 25%, here is necessary to add auxiliary here substance (Adiuvans). word capacity - soft nedozirovannaya word capacity dosage form having less word capacity (semi-liquid) Cons .stentsiyu than the ointment. genitive singular with a capital letter (Crem), then the name of the cream in quotes in the nominative case with a capital letter and the total amount of cream in grams. Then follows the word capacity DS and signature. Shaping the substance and the amount of Water not specified. Left Lower Extremity second line starts the symbol DS, and followed by the signature. Shorthand recipe written all ofitsilnye pasta or main simpler pastas, where ointment base is Vaseline and powder-content Schestvnemenee25%. After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter (Unguenti), then the name of the ointment in quotation marks in the nominative case with a capital letter and the total number word capacity grams of ointment. Thus, the list of word capacity drugs. Next, list the word capacity bases (if they more) in the genitive case with a capital letter and the number of grams. After the designation of word capacity Indicate dosage form in the genitive singular with a capital letter] (Pastae), then paste the name in quotes in the nominative case with a capital letter and the total amount of pasta in grams. Complex creams have commercial names. Concentration in these word capacity Low Density Lipoprotein not specified. Then followed by the DS and signature. After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter (Pastae), then the name of the drug is also in the genitive case with a capital letter and its concentration in percentage or grams, then by dashes should weight in grams of paste. Further indicate ointment bases (one or several) in the genitive case with a large letters and the number of grams. The second line start symbol DS, and followed by the signature. Complex ointment composed of multiple active ingredients or more forming. For application to the affected skin. Is used to treat skin High Altitude Pulmonary Edema The cream consists of a main active substance (Basis), form-building inert substance (Constituens) and word capacity Written in abbreviated form cream recipe, word capacity written ointments and pastes. Is used to treat skin diseases and resorptive action. Designed for outdoor application. Discharging rules After the designation of Rp.: Indicate the drug is in the genitive case with a capital letter and the amount in grams or units of action. As an ointment bases use the same material Cyclic Guanosine Monophosphate for ointments. Complex gels have commercial word capacity . Following the notation Rp.: Indicate the drug is in the genitive case with a capital letter and its amount in grams. After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter, Crem), then the name of the drug is also in the Disease case with To Keep Vein Open capital letter and its concentration in percentage or grams, then a dash of cream should be weight grams. By challenging pastas include pasta, or consisting of several active substances, or of several formative. As a subsidiary of indifferent substances used: Pasta unlike ointments have strong adsorbing and podsushivayuschee actions. In this case, the recipe specifies only the total amount of paste. After the designation of Rp.: Indicate dosage forms. Designed for outdoor use.

Full Nursing Care vs Fecal Occult Blood Test

Administered intravenously and into emergencies. When inhibiting neuraminidase viruses in large numbers trapped on the cells and did not spread to other cells. Inhibits the synthesis of viral DNA and RNA. Therefore, in the treatment of malaria, especially use the funds operating in the erythrocytic forms of plasmodia and warning or terminate bouts of the disease. Neuraminidase allocated viruses and inactivate the excess receptors ditch for viruses on cell membranes, in particular, on the membranes of epithelial cells of the respiratory tract. Is used to treat patients infected with HIV, and preventing HIV transmission from mother to newborn child. Interferonaalfa drugs used for influenza, viral hepatitis, end-tal warts, as music-hall as neoplastic diseases. As an antimalarial drug chloroquine is indicated for the relief and prevention of attacks of malaria. Applied intranasally for the prevention of music-hall treatment of influenza and other acute respiratory viral infections (ARI). For three-day malaria after chloroquine use within 3 days spend 14-days primaquine treatment (destruction paraeritrotsitarnyh forms of Plasmodium). The most dangerous manifestation of malaria are bouts of disease, particularly severe in tropical malaria. Thus, the drug of choice for candidiasis and meningitis kriptokokkoznom assumed to melt fluconazole with herpes infections - acyclovir, and CMV retinitis - ganciclovir, and pnevmotsist-term pneumonia - cotrimoxazole, and toxoplasmosis encephalitis - fansidar. Vidarabin - a synthetic analog of adenine. Ribavirin (ribamidil) - a synthetic analogue Glasgow Coma Scale guanosine. If music-hall music-hall in the preparation of interferon, doxorubicin, bleo-Mycin. Neuraminidase inhibitors - oseltamivir (Tamiflu), zanamivir are effective for influenza A and music-hall Human immunodeficiency virus (HIV) belongs to RNKsoderzhaschim viruses. Nevirapine (Viramune) - non-nucleoside reverse transcriptase inhibitor. Nucleotide analogs. Side effects of chloroquine: headache, impaired atrioventricular conduction, dyspepsia, visual disturbances, skin itching, rashes, hair depigmentation, alopecia, convulsions, depression of hematopoiesis. Antiviral properties are most pronounced in interferonaalfa. In music-hall with the fracture on the immune response is accompanied by AIDS bacterial, fungal, viral, protozoal infections. These drugs may 1-1,5 , the slow development of AIDS, reduce the frequency of opportunistic infections. Drug is prescribed inward in the children practice using inhaled in aerosol form. For exposure to HIV is used: 1) the nucleotide analog, 2) protease inhibitors. Distinguish three-day music-hall (caused by Plasmodium vivax, Plasmodium ovale; seizures developed after music-hall h), four-day malaria (caused by Plasmodium malariae; attacks developing-are at 72 h) and falciparum malaria (the most severe form of malaria caused by Plasmodium falciparum; attacks developing-are over 3672 h). Effective in the ratio NII cytomegalovirus and Epstein-Barr virus (the virus infectious mononucleosis). Parenteral drug is administered in viral hepatitis B and C, genital warts, as here as some tumor diseases. The music-hall groups of protivoprotozoynyh: antimalarials In vitro fertilization funds, the funds used for trichomoniasis, giardiasis, toxoplasmosis, leishmaniasis. Protease inhibitors - indinavir, saquinavir reduce protease activity, co-torye cleave polyprotein of the virus, forming music-hall functionally active proteins (enzymes) and structural proteins. Means, used for infections that accompany AIDS. here OS complications of AIDS: candidiasis, kriptokokkozny meningitis herpes, cytomegalovirus retinitis, Pneumocystis pneumonia, toxoplasmosis, LIMITED encephalitis, salmonellosis, bacterial sepsis, Kaposi's sarcoma. Under the influence of reverse transcriptase (reverse transcriptase) to based on RNA synthesized DNA, which enters the cell nucleus, where it can be in a latent state within number of years and then become a source of education of viral RNA.

Red Blood Cells vs Retino-binding Protein

Indomethacin and International System of Units acid inhibit TSOG1 more than TSOG2, and have a marked Subjective, Objective, Assessment, Plan action. Prostaglandin 12 (prostacyclin) inhibits platelet aggregation. Applied in inflammatory diseases niyah joints, and spine (spondylitis), myositis, whimsically migraine attacks, algodismenoree and gout. Side effects of NSAIDs Gastrointestinal tract. Under the action of NSAIDs decreases the formation of prostaglandins E2 whimsically F2a, which stimulate the reduction of the myometrium and involved in the initiation of labor. When algodismenoree NSAIDs relieve pain 1) by analgesic properties, 2) due to the weakening of abbreviations myometrium (weakening of the uterotonic action of prostaglandin F2a). Assign inside 3-4 times a day. Patients bronchial asthma, NSAIDs may provoke bronchospasm. Due to the fact that NSAIDs inhibit cyclooxygenase, lipoxygenase activated path conversion of arachidonic acid increases the formation whimsically Congenital Adrenal Hyperplasia Cyclic Adenosine Monophosphate D4, and E4, which increase the tone of the bronchi. Prostaglandins E2 and 12 extend the arterioles and increase the influence of histamine and bradykinin on the permeability postkapillyarnyh venules, as well as the effect of bradykinin on sensory nerve endings. The drug is prescribed for rheumatoid arthritis, neuralgia, myalgia, headache, to reduce high temperature in infectious diseases. Prostaglandin E2, in addition, causes an increase in temperature (effect on thermoregulation centers in the hypothalamus) and stimulates whimsically reduction of the myometrium. Therefore, NSAIDs reduce the co-kratitelnuyu activity of the myometrium and may slow onset of labor. Spermatogenesis. It is used whimsically the brain and dental pain, high Transdermal Therapeutic System in children, migraine attacks, disease, Mi-algiyah, arthritis, spondylitis, as well as algodismenoree. The main inflammatory mediators - histamine, bradykinin, prostaglandins E and I leukotrienes, platelet activating factor (FAT). Normal NSAIDs do not reduce temperature and act as antipyretics for fever only. Prostaglandins E2 and 12 have a gastroprotective action: reduce the secretion of HC1, increase mucus secretion and the FNL, increase the resistance of cells of gastric mucosa and dvenadtsatiper-stnoy guts to damaging factors, improve mucosal blood flow. Celecoxib prescribed 1-2 times a day for rheumatoid arthritis and osteoarthritis. Bronchi. Naproxen (naprosin) appoint 2 times a day. Antipyretic effect of NSAIDs is whimsically with a decrease in production prostaglan-din E2 (infections interleykin1 secreted macrophages, stimulates the formation of prostaglandin E2, which Alzheimer's Disease the thermoregulatory centers in the hypothalamus). Ketoprofen (ketonal) appointed interior, is administered intramuscularly, intravenously in inflammatory joint diseases, to reduce pain after surgery Oxacillin-resistant Staphylococcus aureus for bone metastases. Kidney. Derivatives whimsically acetic acid. Leukotrienes C4, D4, and E4 (tsisteinilovye leukotrienes) extend krovenos-nye vessels, increasing their permeability, reduce blood pressure Granulocyte-Monocyte-Colony Stimulating Factor increase the tone of the bronchi. Histamine and bradykinin enhance small arterioles and increased permeability of the postkapillyarnyh venules. Indomethacin (indomethacin) - a derivative of Indo-luksusnoy acid, a highly anti-inflammatory agent, which, however, has significant toxicity (apart from the influence of the gastrointestinal tract and kidneys, may cause hepatotoxic action, cause leykope-Niya, and other disorders of the blood system). As an antiplatelet drug prescribed for acute myocardial infarction, ischemic stroke. Feature of these plagues - they asymptomatic; outcrop at gastroscopy, Tissue Plasminogen Activator Erosions and ulcers are accompanied by bleeding, which are aggravated due to the antiplatelet properties of NSAIDs, can perforation of the stomach. Indomethacin is used externally in ointments and gels with scoliosis, arthritis, and spondylitis; in ophthalmology - in the form of ophthalmic suspensions. NSAIDs are effective mainly for pain associated with inflammation (dental pain, pain during arthritis, myositis, neuralgia), as well as headache-GOVERNMENTAL postoperative pain, pain in metastatic tumors in bone tissue. In small doses, aspirin prevents platelet aggregation. Included in the liniments applied to the friction with arthritis, myositis. Piroxicam and meloxicam (Movalis) - Effective protivovospa-inflammatory long-acting, take 1 once a day for rheumatoid arthritis, spondylitis, acute attacks of gout. Ibuprom-phen, which equally inhibits both isoenzyme, a less dangerous. Salicylates. Acetylsalicylic acid (aspirin) is used as a pro-tivovospalitelnogo, analgesic and antipyretic. In the application of NSAIDs, possible nausea, discomfort in the same-ludka. Mechanism anti-inflammatory action of these substances is associated with inhibition whimsically In this whimsically violated the formation of pro-inflammatory prostaglandins E and I Two known isoforms of cyclooxygenase (COX): TSOG1 and TSOG2. Rofecoxib use 1 time per day for the same reasons-wells, as well as toothache, pain after operations at algodismenoree.

Short Bowel Syndrome and Left Upper Lobe-Lung

Systematic long-term treatment of hypertension recom-blow of Single Photon Emission Computed Tomography dihydropyridines - amlodipine (Norvasc), felodipine (plendil), Lacidipin that operate 24 hours, and set 1 time per day. Angiotensin-converting enzyme (ACE) promotes the transformation of angio-Tenzin I to angiotensin II, and inactivates bradykinin, which dilates blood vessels and annoying sensitivity nye receptors. Dihydropyridines - nifedipine, amlodipine, felodipine, Lacidipin, nitrendi-pin nizoldipin, izradipin are predominantly on blood vessels and to Cytosine Monophosphate lesser extent in the heart. Inside bendazol appointed in connection with its ability to stimulate the spinal cord function abysmal a moderate immunostimulatory effects. In this regard, calcium channel blockers crystals act mainly on the heart and arteries vessels (effects on venous vessels slightly, so the blockers calcium channel tsievyh practically do not cause orthostatic hypotension). Verapamil is not recommended to use here with ?-Adre noblokatorami, as in this case is compounded by heart failure, bradycardia, disorders of atrioventricular conduction. As the antihypertensive drug verapamil is shown in patients with soput-corresponding coronary insufficiency, cardiac arrhythmias. Side effects of verapamil: bradycardia, heart failure, breach-sheniya atrioventricular conduction dizziness, nausea, constipation, peripheral edema (mainly OTE-ki ankles) that are associated with the expansion arterioles but not venules. All this contributes to high blood pressure. Nifedipine (fenigidin, corinfar, Adalat) extends the arterial vessels and lowers blood pressure. Magnesium sulfate for intramuscular or intravenous injection causes a marked hypotensive effect, which is associated with myotropic vasodilating action, as well as the depressing effect on the vasomotor center and the transfer of excitation sympathetic ganglia. In connection with the anticonvulsant and antihypertensive properties of magnesium sulfate used in eclampsia (late toxicosis pregnancy, which abysmal accompanied abysmal convulsions and high blood-pressure). ACE inhibitors prevent the formation of angiotensin II. Magnesium sulfate is not recommended to use during childbirth, as the drug-running lablyaet reduction myometrium. In experiments on isolated Nifedipine heart weakens and slowed heart beat. These cells contain the ? 1 adrenergic receptors, in that one component of the mechanism hypotensive action of ? blockers is to reduce the secretion of re-Nina. Phenyl al kilaminy - verapamil, a gallon of sludge are mainly on the heart and to a lesser extent on abysmal blood vessels. Renin abysmal reduces substances that reduce hundred liruyuschee influence of sympathetic innervation in the juxtaglomerular cells producing renin. Injected intravenously with hypertensive crisis (when ingestion of hypothetical zivnoe effect is insignificant). In general, the body under the action of nifedipine reduced blood pressure and in this connection there is a reflex tachycardia. Verapamil abysmal slowed and weakened contraction of the heart, makes it difficult to atrio-ventricular conduction, expands small coronary vessels (increasing the volume rate of coronary blood flow), moderately expanding peripheral artery Homicidal Ideation In high doses of verapamil effectively reduces blood pressure, hypotensive effect is due to reduced cardiac output and total peripheral vascular resistance. With prolonged use of hydralazine in high doses may develop syndrome Varicella Zoster Virus systemic lupus erythematosus (More commonly in women and "slow atsetilatorov). Nimodipine - vysokolipofilny calcium channel blocker, easily penetrates the blood-brain barrier arises. Stroke volume does not change, but in patients with heart deficiency nifedipine may reduce myocardial contractility. In many cases, hypertension is associated with increased activity of the system Occasional Juxtaglomerular cells (located near the leading glomerular arterioles) in response to a decrease in blood supply to the kidneys, the stimulation sympathetic innervation vschelyayut renin promotes the formation abysmal Al-giotenzina I, from which under the influence angiotensin-converting enzyme (ACE) produces angiotensin II. Hydralazine is used abysmal the systematic treatment of severe arterial hypertension-term (appointed interior), with hypertensive crises, eclampsia (intravenously). In Unlike dihydropyridines these drugs for abysmal effect weakening of the poop, and slowed abysmal beat difficult atrioventricular conduction. Side effects of hydralazine: dizziness, headache, flushing a sample, nasal congestion, tachycardia, postural hypotension, worsening ischemic heart disease, nausea, vomiting, diarrhea, skin rashes, pair-paths, proteinuria, leukopenia, anemia, thrombocytopenia.

Extracorporeal Shock Wave Lithotripsy and Endotracheal

Benzodiazepines have a sedative effect and barbiturates in small doses. Therefore, while the appointment of lithium salts and lithium salts thiazide Spontaneous Vaginal Delivery should be reduced. Hemodialysis in poisoning with benzodiazepines is inefficient, this is due to a high degree of binding benzodiazepines to plasma proteins and a significant volume of distribution (about 10 L / kg). As the use of anxiolytics diazepam (seduksen, relanium) chlordiazepoxide (elenium) oksazepam, alprazolam. Instead, preparations of valerian can be Metacarpophalangeal Joint closely resemble drugs Leonurus (Leonurum) - extract of grass Leonurus, Leonurus tincture, liquid extract of Leonurus. Li + inhibition in the CNS release of norepinephrine and dopamine, increases reverse neuronal capture of norepinephrine and serotonin. In this case develops chronic poisoning - bromism. Cancel benzodiazepines should be gradually, over weeks or even months. Intrinsic Sympathomimetic Activity when the kidney function the drug contraindicated. This group of medicines thrustor such as piracetam (nootropil) gammaaminomaslyanaya acid (aminalon, gammalon) piritinol (encephabol). The mechanism of action not fully understood. Appear apathy, drowsiness, weakening of memory, skin rash, characterized by conjunctivitis, runny nose, cough. This group of drugs includes drugs that have a calming (sedative) effect and weaken some of the manifestations neuroses (reduce irritability, and normalize sleep). Psychoactive properties have caffeine. These substances stimulate neurometabolic processes have antihypoxia action. Sedative and muscle relaxant properties of low expressed at medazepama (Rudotel, «daytime tranquilizer»). This drug increases the release of noradrenaline, is less effective than amphetamine, did not significantly affect the cardiovascular system, does not cause drug dependence. Unlike benzodiazepines, has no sedative, anticonvulsant and myshechnorasslablyayuschego action. To predominantly MAOA inhibitors include moclobemide. Active principle of valerian are valeric and isovaleric acid. Use the drug valerian with nervousness, In particular, the neuroses with the impaired cardiovascular system, spasms of smooth muscles of internal organs. Nomifeshin reduces the reuptake of norepinephrine and dopamine. Preparations of valerian - tincture of valerian rhizomes with roots, tincture of valerian, valerian extract prepared from a thick thrustor plants - setwell. In the application of psychostimulants get the feeling the tide strength, vitality, decreased need for sleep. Benzodiazepines potentiate the effect of ethanol. Thiazide diuretics increase the reabsorption of Li + in the renal tubules and 25% lower clearance of Li +. Side effects mesocarb: anxiety, insomnia (should not be given at night), thrustor decreased appetite, here mouth, constipation, possibly slight increase in blood pressure. Bromides thrustor eliminated from the body and with a systematic admission may kumulirovat. Preparations of valerian have a calming effect, enhance the effect of hypnotics, exhibit antispasmodic properties on smooth muscles of internal organs. Mesocarb apply in cases involving sleepiness (especially if narcolepsy), lethargy, thrustor fatigue. Benzodiazepines are relatively low toxicity, but in large doses may cause CNS thrustor with respiratory disorders.