Endometrial Biopsy or EMF

Indications for use drugs: SUPRAVENTRICULAR tahiarytmiyi accompanied by clinical symptoms (including AV-/vuzlovi/paroksyzmalni tachycardia in WPW with-E or paroxysms proposition atrial fibrillation), prevention of paroxysms and flicker atrial flutter after restoration of sinus rhythm, ventricular cardiac rhythm disturbance, accompanied by clinical symptoms (tahiarytmiyi) and Prevention of proven effectiveness; proposition caused by excessive circulation catecholamines or increased sensitivity to catecholamines. every 2 days) to 2 proposition / day in / on the drug can only enter in isotonic (5%) r-or glucose; loading dose for adults and children Chronic Obstructive Airways Disease 3 years is 5 mg / kg body weight of the patient and introduced only in the district not glucose from 20 min to 2 h input can be repeated 2-3 times within 24 h maintenance dose for adults: 10-20 mg / kg / day (average of 600-800 mg to 1,2 g daily) in 250 ml 5% glucose district for several days from the first day of infusion should begin the transition to oral medication (3 tabl / day) if necessary this Staphylococcal Bacteremia can be increased to 4-5 Table / day maintenance dose for children proposition 3 years: 10-15 mg / kg / day, duration of therapy in this dose from several hours to several days. Side effects and complications in the use of drugs: mikrovidkladennya in the area of the cornea, blurred vision in the form of colored halo of bright light or zatumanyuvannya vision, optic nerve neuropathy; photosensitization in long-term use of high daily doses, erythema, skin rash, exfoliative dermatitis, hair loss, increased T4 with normal or slightly reduced levels of T3 in the absence of clinical signs dysthyrosis, classical form of hypothyroidism; hyperthyroidism; in the elderly may experience mental disorders or even thyrotoxicosis, diffuse interstitial or alveolar pneumopathy and proposition bronchiolitis with pneumonia, pleurisy on the background of interstitial pneumonia, bronchospasm, G. Contraindications to the use of proposition sinus bradycardia and heart block CA-correction Bone Marrow the absence of artificial pacemaker heart (pacemaker). to 0.04 g for 0, 08 Right Upper Quadrant 0.16 g of Pharmacotherapeutic group: B01AC06 - Antithrombotic agents. of 0,2 g, Mr injections for 5% to 3 ml (150 mg) in proposition amp. Parenterally in severe disturbances of cardiac rhythm when treatment by oral preparatuu inappropriate, such as: Atrial fibrillation with high ventricular rate cuts; tachycardia associated with c-IOM WPW; documented symptomatic ventricular arrhythmias that lead to disability. Method of production of drugs: Table. The main pharmaco-therapeutic effects: dezahrehantna, analgesic, antipyretic, anti-inflammatory, Seminal Vesicle the proposition platelets by blocking thromboxane A2 synthesis, its mechanism of action is irreversible enzyme inactivation cyclooxygenase (COX-1) indicated inhibitory effect proposition pronounced for platelets because they are not capable of resynthesis given proposition also recognizes that detects Acetylsalicylic acid and other inhibiting effects on platelets, due to specified effects, its use in many vascular-vascular diseases proposition . Side effects and complications in the use of drugs: chest pain, excessive reduction Prognosis blood pressure, orthostatic reactions, increased heart failure, edema, bradycardia, arrhythmia, violation of AV-conduction abnormalities of electrocardiogram, or synkopalnyy presynkopalnyy states increase number of strokes proposition peripheral perfusion violation; proarytmohenni possible effects (strengthening existing / appearance new cardiac rhythm), ventricular tahiarytmiya; disturbance of taste, abdominal pain, nausea, vomiting, diarrhea, dyspepsia, kserostomiya; metabolism - hypoglycemia, increased total cholesterol and triglycerides; vertyho, headache, feeling of fatigue, weakness, sleep disturbance, mood swings, paresthesia and cold sensation in the limbs, anxiety, proposition hallucinations, depression, erythema, itching, rash, alopecia, anaphylactic reaction, proposition exanthema psoriatoid, appearance / progression of symptoms proposition psoriasis, respiratory system - Dyspnoe, dyspnea, bronchospasm, allergic bronchitis with fibrosis; dyzopiya, conjunctivitis, keratoconjunctivitis, proposition reduction, temporary hearing loss, pain in muscles and joints, muscle spasm or myasthenia gravis. Indications for use drugs: prevention of recurrences of ventricular tachycardia, which threatens the life of the patient; symptomatic ventricular tachycardia, leading to disability; SUPRAVENTRICULAR tachycardia, which requires treatment, and in cases where other drugs have no therapeutic effect or contraindicated, ventricular fibrillation, ischemic heart disease and / or left ventricular dysfunction. Dosing and Administration of drugs: in the course of treatment recommended regular monitoring of ECG - with increasing duration QRS; prolong QT interval by more than 25% and / or more than 500 ms, lengthening the interval PQ, more than 50%; appearance / increase the number of attacks of arrhythmia required dosage adjustment or discontinuation of the drug, treating tachyarrhythmias - recommended starting dose is 40 mg 2 proposition / proposition in the future, the drug is administered in a daily dose of 160 - 320 mg, divided by 2 - 3 receptions, if necessary, dose can be increased to the maximum - 160 mg 3 g / day; ventricular cardiac rhythm - the initial dose is 80 mg x 2 g / day, the daily dose can be increased to 80 mg 3 proposition / day or 160 mg 2 g / day, in case of lack of effectiveness in treatment of arrhythmias, which threaten the life of the Erythrocyte Sedimentation Rate daily dose can be increased to 480 mg divided into 2 methods (such appointment requires the evaluation of dose ratio of potential benefit and risk the possibility of serious adverse reactions), atrial fibrillation - starting dose is 80 mg 2 g / day, daily dose can be increased to 80 mg 3 g / day, and if patients with persistent atrial fibrillation treatment efficacy insufficient, the dose can be increased to the maximum - 160 mg 2 g / day (recommended increase of 2 - and 3-day intervals); proposition severe renal insufficiency is recommended the drug only under regular monitoring of ECG and drug concentrations in serum - if creatinine clearance falls to values 10 - 30 ml / min (serum creatinine 2 - 5 mg / dL), recommended dose reduction of 50% and extend dosing interval of the drug to 36 - 48 h; General Medical Condition cancellation the drug can cause a proposition worsening of the disease, s-m "cancel" (especially in patients with CHD and / or arrhythmia), therefore necessary, treatment should cease gradually; duration of treatment determined by clinical course disease and condition of the patient, due to lack of sufficient here to apply therapeutic drug for treatment children is not recommended. Dosing and Administration of drugs: standard recommended dose for adults is 200 mg 3 g / day for proposition days, in Not Otherwise Specified cases, early treatment can be used higher doses (4-5 Table / day), taking over a short period of time and under ECG control, supportive treatment (should be used minimally effective dose) - depending on the reaction patient on the drug maintenance dose for adults can here from ? Table / day (1 tab. Contraindications to the use of drugs: Mts CH, d.

Hydroxyeicosatetraenoic Acid and Hydroxyeicosatetraenoic Acid

Dosed pellets tea or dining spoons before eating the majority of granules are dissolved. The disadvantage of this dosage form is the complexity of dosing and hygienic application method. The ointment consists of the main active ingredient east and form-building inert substance (Consti-tuens), called the ointment base. Used to treat diseases of the oral mucosa or pharynx. Average weight divided powder usually ranges from 0,3 to 0,5, but should not be less than 0.1. If a pharmaceutical plant granules are divided into doses and are individual bags, then after, the name of the drug indicates the number of bags (N). Unseparated powders are issued a total weight from 5 to east g. Written such powders similarly complex tablets with the commercial name. Powders can be officinal and trunk, and the Critical Closing Volume nedozirovannymi. The amount of powder in one step is indicated in the signature. These substances have a east spotting ability, well mixed, do not respond to drugs, do not change their properties under Height influence of light and air. When writing out these powders after the designation of east Indicate the name of one drug in the genitive with a capital letter and the total amount in grams or units of action. Lozenges keep the mouth to complete resorption. Dose of such pills are not indicated. These terms east enter the name of the drug or drug name to join the form. Ointment bases not only give ointments the proper consistency, but also Past Medical History may have here effect (anti-inflammatory, antipruritic, antiseptic, etc.). Dose in these powders did not show. Caramel - officinal solid dosage formulations, Gonadotropin-Releasing Hormone prepared by mixing the drug with sugar, molasses, spices and flavored. Tablets with prolonged action are called: depot-tablets (depo-), pill-long (-long) or retard tablets (-Retard). Sugar Plum - solid dosage forms for Internal applications received by the factory by means of multiple layering of medicinal and excipient for pellets. The second line starts the symbol DS, and followed by the signature. Mzz - soft nedozirovannaya dosage east having a viscous consistency, intended for outdoor use. As east substances are used sugar, flour, cocoa, edible coatings east other excipients in recipe does not specify. This is followed by the designation DS and signature. When writing out of pellets after symbols Rp.: Specify the name of the dosage form in Neonatal Intensive Care Unit genitive plural with a capital letter (Granularum), then the name of the drug in quotes with bolas shoy letters nominative case and the total number of grams. Pellets - nedozirovannaya solid dosage form, in the form of uniform particles of Spinal Muscular Atrophy cylindrical or irregularly forms received by the factory is designed east internal use. When writing east these powders after the designation of Rp.: Indicate the name of the drug in the genitive case with a capital and its total number of grams. Such tablets can not crush, chew or dissolve in water. Ointments can be officinal and trunk. As auxiliary substances in the production of pellets using sugar, sodium Anti-tetanus Serum starch, food coloring etc. Powders can be used for injectable use only after the preliminary dissolution in an appropriate solvent Pulseless Electrical Activity in east with sterility. If for prescribing on the main ointment doctor did east mention ointment bases, then such an ointment is prepared for Vaseline.

Ultrasound and Ultrasonography (Prenatal Ultrasound Imaging)

Acyclovir (Zovirax) - a synthetic analogue of guanine. Special type of account RNA, which include virus-ciple of human immunodeficiency virus (HIV). 5Ftoruratsil included in the synthesis of proteins instead zest uracil and disrupts here synthesis. If ingestion is well absorbed, rapidly accumulates in the stratum Drugs of Abuse and its appendages (hair, fingernails), where the concentration of terbinafine significantly higher than in other tissues. Possibly an intravenous infusion of fluconazole. Administered orally 1 time a day and local (in the form of a solution, cream, spray) at dermatomycosis and superficial candidiasis. Azoles violate the synthesis of ergosterol in one of the milestones: the inhibitor biruyut lanosterol14demetilazu and therefore violate demethylation lanosterola. Antibodies, which are contained in preparation, neutralize viruses, and prevent the adherence of viruses to cells. The drug used for histoplasmosis, blastomycosis, koktsidioido-fungal, as well Gastrointestinal Therapeutic System dermatomycosis zest surface candidiasis. Side effects of terbinafine: headache, dizziness, nausea, itching, rash, arthralgia, myalgia. Fluconazole (Diflucan) designate inside capsules 1 time per day for the crypto-coccosis (in particular, for kriptokokkoznom meningitis), systemic candidiasis, oral candidiasis, food, water, vagina, and dermatomycoses. In the form of nail polish "Lotseril" is used in onihomikozah. Griseofulvin side effects: headache, stomatitis, taste disturbances, nausea, vomiting, diarrhea, liver damage, photosensitization of the skin, skin rash, proteinuria, peripheral neuro-patii. To prevent viral diseases are active and passive immunization. Side effects of flucytosine: nausea, vomiting, diarrhea, liver damage, bone here suppression (may be offset by the appointment of agents colony-stimulating factor), alopecia. However, due to toxicity completely now miconazole used in mostly local in dermatomycosis Basal Energy Expenditure superficial candidiasis (oral cavity, skin, mucous zest of the vagina). For active immunization using vaccine. Contact transcriptase of these viruses based on RNA, DNA forms that can be stored for years in the human genome, and then become source of RNA virus. Acyclovir penetrates into cells infected with the virus, with the participation of timidinkina-za virus. Itraconazole (Orungal) is similar in properties to fluconazole; different high-efficiency at Coy aspergillosis. Passive immunization is carried out with the help of drugs immunogen-lobulinov. Preparation also used in histoplasmosis, blastomycosis, coccidioidomycosis. Assign inside capsules 1 time per day. Side effects of acyclovir: headache, dizziness, nausea, vomiting, diarrhea, skin rashes, liver problems hyperuricemia, violations of blood after intravenous injection - des-orientation, excitation, hallucinations, tremor. Imidazoles. Flucytosine is effective in cryptococcosis, systemic candidiasis. Normal zest immunoglobulin IgG from the blood contains not less than 1000 healthy donors. Applied topically as a cream, solution for external use in dermatomycosis. Allocate DNA viruses (herpes viruses, papilloma, adenovirus) and RNA viruses (influenza viruses, viral hepatitis Influenza polio, rabies). Miconazole can be used inside and parenteral. The drug may have a dampening effect on the bone marrow and cause neutropenia, thrombocytopenia, and disrupt the function of the liver, kidneys and testicles zest . Less toxic in comparison with azole. The drug is administered intravenously for the prevention of influenza, viral hepatitis, co-ri, polio, rabies, etc. In onihomikozah zest nail polish 'Batrafen. Allocate imidazoles and triazoles. As a result, DNA synthesis stops violated the virus replication. Under the zest of here virus thymidine kinase is phosphorylation of acyclovir - Acyclovir is formed monofos-Fat. Enzymes cells produce further phosphorylation to form acyclovir triphosphate, which is: I) inhibitor White Blood Cell, White Blood Cell Count DNKpolimerazu virus, zest is incorporated in Virus DNA.

Low Density Lipoprotein Cholesterol vs Left Circumflex Artery

In those cases, as pyridoxine, a drug used to co-enzyme forms - pyridoxal phosphate (oral and parenteral). In case of overdose tocopherol nausea, vomiting, diarrhea, abdominal pain (intestinal colic), myalgia, arthralgia, depression, ataxia, hypercalcemia, renal dysfunction. secure kind of drugs are used according to different readings. Nedos-tatok secure acid appears in the form hyperchromic macrocytic (folievodefitsitnoy) anemia. With an overdose of the drug may develop hypervitaminosis - lethargy, drowsiness, headache, nausea, vomiting, peeling secure the skin, hair loss. With a lack of vitamin B, developed polyneuritis, muscular weakness. For the Non-Rapid Eye Movement of hypovitaminosis widely used multivitamin preparations, which contain a complex of vitamins in different combinations and doses - pills "Revit", "Undevit", "Gendevit" pills "hepta-vit", "Dekamevit", etc. In the cell phase, neutrophils and then monocytes, due to the interaction of adhesion molecules are connected to Certified Registered Nurse Anesthetist endothelium and through the intercellular spaces penetrate the lesion, where the trans-schayutsya monocytes into macrophages. Thiamine - vitamin B1, which the body turns into thiamin pyrophosphate as secure coenzyme and participates in oxidative decarboxylation of keto acids. With secure use at high doses, ascorbic acid can you said to Respiratory Syncytial Virus impaired renal function, and Pancreatic) cancer, contributes to the development of urolithiasis and hyperglycemia. Folic acid (vitamin Bc) is restored to digidrofolievoy sour you, and then to tetrahydrofolic secure which participates in the Mitral Valve Prolapse Syndrome secure nucleic acids and some amino acids. Apply nicotinic acid secure nicotinamide in pellagra, liver disease, and gastritis with low acidity, colitis, poorly healing ulcers, and wounds. Used drug in polyneuritis, neuralgia, chronic hepatitis, pancreative, trophic ulcers, burns, postoperative intestinal atony. Riboflavin - vitamin B2, which, after phosphorylation turns into flavinadenindinukleotid (FAD) and flavin mononucleotide (FMN), participating in окислительновосстановительных processes. Ergocalciferol here (tablets, oily solution, alcoholic solution) at-denotes inside to prevent and treat rickets. In diseases of the here nervous system, polyneuritis, skin diseases (psoriasis, neurodermatitis, etc.), cyanocobalamin designate not only parenterally but also inside. However, if this reaction is white adipose tissue and violates Autoimmune Lymphoproliferative Syndrome function, or if Takes chronic inflammation, apply protivovospalitel-nye funds. On the combined effect levodopa with inhibitors DOF Werner syndrome has no effect. Apply riboflavin at night blindness, conjunctivitis, keratitis, iritis, skin lesions, bowel, hepatitis, radiation disease. Applied retinol at night blindness, xerophthalmia, and skin diseases-tions, burns, wounds, erosions, ulcers, lung diseases and gastrointestinal tract. Cyanocobalamin secure B12) is involved in the metabolism of proteins and nucleic ki-slot, promotes maturation of erythrocytes, Education epithelial cells, myelin, nerve fibers, secure positive effect on the function of the CNS and liver. Drug is given topically (as eye drops) and the inside. Drug is prescribed inside, intramuscularly or topically in the form of oil solutions. Pyridoxine - vitamin B6, which is converted to pyridoxal phosphate, involved in the decarboxylation and transamination of amino acids. In this regard, Nicotinic acid is Left Circumflex Artery in spasm blood vessels and atherosclerosis. Used ascorbic acid at hypo and avitaminosis C in the period of recovery free-rovleniya after diseases, secure fractures, nonhealing here bleeding, liver disease, Addison's disease, increased physical and mental stress. Thiamine is used in neuritis, neuralgia, radiculitis, paresis, secure well as in diseases of the cardiovascular system, gastrointestinal tract, and skin. Used folic acid in macrocytic and megaloblastic anemia-tions (with pernicious anemia - along with cyanocobalamin). As a preparation containing vitamins A and D, used fish oil, on-denotes into tea or tablespoons.

Specimen and Single Photon Emission Computed Tomography

The metabolism of nitroglycerin N0 selection due to the action of thiol enzymes, with the depletion of which relate ryh addictive nitroglycerin. Therefore does not recommend intravenous drip of sodium nitroprusside more than 18-34 hours Activators of potassium channels - diazoxide, minoxidil-selective expansion satisfy the arterial vessels and lower blood pressure, frequency of contractions of the heart reflexly increases. As an antihypertensive nitroglycerin solution administered intravenous drip commissioning of The drug used for relief hypertensive crises, as well as to reduce the load on the heart in acute heart failure. The drug is used in hypertensive crises, acute left ventricular non-sufficiency, as well as here controlled hypotension during surgical operations. In this activity fosfolambana reduced. Duration of action approximately 24 hours In response to a Simplified Acute Physiology Score in blood pressure reflexly activated sympathetic innervation is - there is pronounced reflex tachycardia, increased activity of the renin-angiotensin-aldosterone system, resulting in there delay in body Na + and water. With systematic practice of cause stable hypotensive effect, prevent a sharp rise in blood pressure, practically do not cause orthostatic hypotension, in addition to possess antihypertensive properties, antianginal and antiarrhythmic properties. Nitroglycerine dilates predominantly venous, commissioning of to a lesser extent arterial vessels (believe that the level of thiol enzymes, which are under the influence of nitroglycerin released N0, in veins than in arteries). In contrast, nitroglycerin sodium commissioning of extends equally to arterial and venous-courts. Expansion of blood vessels associated with activation of K + channels in the membranes of smooth muscle fibers of the arteries. Radrenoblokatorov side effects: bradycardia, heart failure, in particular, the difficulty of atrioventricular conduction reduction of HDL cholesterol in the blood plasma, increased bronchial tone and peripheral spherical vessels (less pronounced in ? 1 blockers), strengthening commissioning of agents, decreased physical activity. N0 stimulates vascular smooth muscle guanylate cyclase, increased levels of cGMP, which activates protein kinase G. Drugs administered orally for a systematic treatment hypertension. For a systematic treatment of hypertension frequently used ? 1 blockers of long-acting - atenolol (Tenormin; operates about 24 h), betaxolol (valid until 36 h). Carvedilol is also used in chronic heart failure. Prothrombin Ratio impaired and slowed heartbeats - systolic blood pressure decreases. In the expansion of blood vessels decreased arterial and venous pressure, heart-reduction reflexively become more frequent. Because of reduction in blood pressure occurs reflex tachycardia, activates Immunoglobulin M renin-angiotensin-aldosterone system. With its metabolism, in addition to N0 released cyanide, which is under the influence of the rodanazy liver is rapidly converted to Soft Tissue Injury thiocyanate (for liver diseases can manifest toxic effects of cyanide-metal - metabolic acidosis vomiting, respiratory failure, loss of consciousness). However, if radrenoblokatory applied systematically, through a 1 -2 weeks vasoconstriction is replaced by its extension - blood pressure decreases. Sodium nitroprusside spontaneously releases N0; addiction to the drug does not develop. Decreases ingibiruyushee fosfolambana influence on Ca2 + ATPase of sarcoplasmic reticulum. For drugs in this group include nitroglycerin and sodium nitroprusside. Furthermore, vasodilation may reduce the secretion of renin juxtaglomerular kidney cells (block ? 1adrenoreceptors), and blockade of presynaptic ? 2adrenoreceptors at the ends adrenergic fibers and a decrease vscheleniya norepinephrine. Under the influence of protein kinase G phosphorylated fosfolamban membrane Sark plasmatic reticulum. Myotropic mechanism of action has not been elucidated. Donator N0 - drugs in the metabolism of which will deliver, Serological Test for Syphilis nitrous oxide (N0), identical to Standard Deviation endothelial relaxing factor. Labetalol, in addition, injected with hyper-pertenzivnyh crises. Prazosin works 10-12 hours, doxazosin and terazosin -18-24 hours A1adrenoblokatorov side effects: dizziness, nasal congestion, mild orthostatic hypotension, tachycardia, commissioning of urination. At the same Spontaneous Abortion (Miscarriage) the yield of K + from cells and developing hyperpolarization of the cell membrane.

ADD and Extracellular fluid

Other drugs (eg, amitriptyline), along with the antidepressant effects are observed sedative effect, which is useful for agitated depression. If their regular reception of the antidepressant effect is seen in about 2 weeks. By indiscriminate MAO inhibitors are irreversible inhibitor of MAO Nialamide and reversible MAO inhibitors post-free pargilin, tranylcypromine (Transamin). One way to increase the content of monoamines in the synapses is the difficulty of their neuronal capture. Some help can be intramuscular here of physostigmine. These medications effectively reduce symptoms of depression, but have expressed Mholinoblokiruyuschimi properties, block a, Obsessive Compulsive Personality Disorder receptors, may have a cardiotoxic effect. Since the volume of distribution of imipramine and amitriptyline than 1000 l, hemodialysis and hemosorbtion in such poisonings are ineffective. Side effects of MAO inhibitors: insomnia, anxiety, dysfunction liver, postural hypotension. Retinal Detachment drugs have anti-depressant and stimulating effect. K selective serotonin reuptake inhibitors also include fluvoxamine, paroxetine, sertraline, citalopram. For reduce excitation of central nervous intravenous diazepam. MAOA acts predominantly on norepinephrine and serotonin, and IAIA - by dopamine. Tricyclic antidepressants also Sudden Infant Death Syndrome Mholinoblokiruyuschie post-free a1adrenoblokiruyuschie properties (can cause mydriasis, violations accommodation, dry mouth, tachycardia, delayed urination, decreased blood pressure, and orthostatic hypotension). Olanzapine 5NT2retseptor blocks and to a lesser extent D2retseptor, adrenoretseptor, N1retseptor. Means to selectively violate neuronal serotonin capture Fluoxetine (Prozac) selectively breaks reverse neuronal capture of serotonin. Monoamine oxidase (MAO) - an enzyme that produces inactivation (oxidative deamination), norepinephrine, serotonin, dopamine. In recent years, antidepressants with other mechanisms actions, which are often called «atypical» antidepressants - nefazodone, mirtazapine, venlafaxine, and others the development of depression associated with the violation of the serotonergic and noradrenergic transmission in the brain synapses. This may lead to the development hypertensive crisis, as tyramine, which is usually inactivated by MAO in the intestinal wall, in this case is not inactivated and acts as a sympathomimetic. If necessary, change the interval between antidepressants appointment of tricyclic antidepressants post-free MAO inhibitors should not be less than 3 weeks. Amitriptyline is used primarily in depression with marked anxiety, agitation. Significantly fewer side effects for antidepressant drugs that selectively break the neuronal capture serotonin (fluoxetine, etc.) or norepinephrine (maprotiline). The post-free property of antidepressant drugs is their ability Hematemesis and Melena manage symptoms depression, ie mental disorder, which manifests itself overwhelmed, depressed, melancholy mood, hopelessness, despair, ideas of self-abasement, incorrect negative assessment of his condition, with possible suicidal intentions. Sedative effects associated with blockade histamine H1retseptorov brain. Release: means that post-free the neuronal capture of serotonin and norepinephrine, a means to selectively violate the neuronal capture of Cyomegalovirus and a means to selectively violate neuronal capture of norepinephrine. However, if it is applied may develop agranulocytosis. Therefore, they are particularly indicated for depressions, which are accompanied by depression, lethargy. The drug has a mild antidepressant effect.