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The causes of epilepsy are, apparently, in organic or mechanical damage to brain cells (intrauterine, birth or craniocerebral trauma, neuroinfections, acute circulatory disorders, hemorrhages or neoplasms), which form an epileptogenic focus, consisting of easily excitable neurons, the excitation of which quickly spreads to other areas of the brain. That is why, for the prevention and treatment of epilepsy, drugs are used that depress the excited epileptogenic focus and inhibit the spread of excitation from it to the surrounding tissues.
The drug is taken orally during or after a meal with water.
A major role in the development of domestic pharmacology was played by V.N.
2 times in day (in the morning and in the evening before meals).
The maximum allowable amount for issuance drug on the recipe To reduce eye fatigue during visual stress, to increase visual acuity, reduce photophobia, burning and feeling of "sand in the eyes" and to eliminate swelling of the eyelids, eye vitamin preparations are used.
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13 times in day (after food) Mercaptopyrin Tropisetron can be administered as an oral solution immediately after diluting the appropriate amount of Tropisetron contained in the ampoule with orange juice or cola; the solution must be taken in the morning 1 hour before meals.
Indications for use and side effects
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the same as those of acetylsalicylic acid.Rinse the stomach, take activated charcoal, an osmotic laxative drug.
With the development of severe renal failure, hemodialysis is indicated.
A-cerumen Sidnopharm Analogues Calcitonin (Calcitonin).
Anticholinergic (anticholinergic) are drugs that disrupt or stop the interaction of acetylcholine with cholinergic receptors.
By blocking cholinergic receptors, they reduce or completely eliminate the transmission of excitation from cholinergic nerves to the executive organs, and also reduce the effect of cholinomimetic and anticholinesterase agents. This group of drugs includes blockers of M-cholinergic receptors and H-cholinergic receptors. M-cholinergic blockers include agents that predominantly block M-cholinergic receptors of cells
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internal organs.As a result of the blockade, the receptors become less sensitive to the mediator acetylcholine, the influence of the parasympathetic system on the internal organs decreases.
M-anticholinergics are divided into non-selective (block M 1 -, M 2 -, M 3 -cholinergic receptors) and selective (mainly block M 1 - or M 3 -cholinergic receptors). The drugs, unlike heparin, do not affect clotting factors directly in the blood. They inhibit the synthesis in the liver of plasma proteins dependent on vitamin K: factor II (prothrombin), factors VII , IX and X (Fig.
Vitamin K Individual hypersensitivity to bisoprolol or any other component of the drug; heart failure in the phase of decompensation; cardiogenic shock; atrioventricular block II
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and III degree; sick sinus syndrome; severe sinoatrial blockade; symptomatic bradycardia (heart rate 10 kg, the daily dose is 2-4 tablespoons.34 times in day At all chronic forms on one's own or with corticosteroids use pi-drugs crushed (rec.