Active substanceEnalaprilEnalapril
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  • Dosage form: & nbsppills
    Composition:

    One tablet contains:

    Active substance: enalapril maleate - 20.00 mg.

    Excipients: lactose monohydrate 155.75 mg, gelatin 6.00 mg, magnesium carbonate 25.00 mg, silicon colloidal dioxide 3.00 mg, sodium carboxymethyl starch 8.00 mg, magnesium stearate 2.00 mg, an iron dye oxide red, E 172 0.25 mg.

    Description:round, slightly biconcave tablets of pale pink color, with bevelled edges and a notch for division on one side, white and dark pink color may be impregnated
    Pharmacotherapeutic group:Angiotensin-converting enzyme inhibitor
    ATX: & nbsp

    C.09.A.A.02   Enalapril

    Pharmacodynamics:

    Enalapril maleate is an antihypertensive agent from the group of inhibitors angiotensin-converting enzyme (ACE). Enalapril maleate is a salt of maleic acid and enalapril, a derivative of L-alanine and L-proline. Enalapril is a prodrug: as a result of its hydrolysis, a enalaprilate, which directly inhibits ACE. The mechanism of its action is associated with a decrease in the formation of angiotensin II from angiotensin I, a decrease in its content leads to a direct decrease in the release of aldosterone. At the same time, the overall peripheral vascular resistance decreases, systolic and diastolic blood pressure (BP), post- and preload on the myocardium.

    Enalapril extends the arteries more than the veins, with a reflex increase in heart rate (heart rate) is not noted. Reduces the degradation of bradykinin, increases the synthesis of prostaglandins.

    The hypotensive effect of enalapril is more pronounced with a high concentration of renin in the blood plasma than with normal or reduced. Decrease in blood pressure within the therapeutic limits does not affect cerebral circulation, blood flow in the vessels of the brain is maintained at a sufficient level and against a background of low blood pressure.,

    Enalapril improves coronary and renal blood flow.

    With prolonged use enalapril reduces myocardial hypertrophy of the left ventricle and myocyte walls of arteries of a resistive type, prevents the progression of heart failure and slows the development of dilatation of the left ventricle.

    Improves the blood supply of the ischemic myocardium.

    Has a weakly expressed diuretic effect.

    The time of onset of an antihypertensive effect with ingestion - 1 hour, reaches a maximum. in 4-6 hours and persists up to 24 hours. In some patients, to achieve the optimal level of blood pressure, enalapril therapy is necessary for several weeks.In chronic heart failure, a significant clinical effect is observed with long-term treatment with enalapril - 6 months or more.

    Pharmacokinetics:

    After ingestion, 60% enalapril is absorbed. Food intake does not affect its absorption. Enalapril quickly metabolized in the liver with the formation of an active metabolite - enalaprilata. Connection with blood plasma proteins up to 60%.

    The maximum concentration of enalapril in the blood plasma is achieved after 1 hour, enalaprilata - after 3-4 hours. Enalaprilat easily passes through the histohematological barriers, excluding the blood-brain barrier, a small amount of it penetrates the placenta and into the breast milk. The half-life of enalaprilata is about 11 hours. enalapril mainly kidneys - 60% (20% - in the form of enalapril, and 40% - in the form of enalaprilata), through the intestine - 33% (6% in the form of enalapril and 27% in the form of enalaprilate).

    Udalis at a hemodialysis (the rate of excretion is 62 ml / min) and peritoneal dialysis.

    Indications:

    - arterial hypertension (including renovascular hypertension);

    - chronic heart failure;

    - prevention of the development of clinically significant heart failure in patients with asymptomatic dysfunction of the left ventricle.

    Contraindications:

    - Hypersensitivity to enalapril and other ACE inhibitors or components of the drug;

    - presence in the anamnesis of an angioedema along with the administration of ACE inhibitors;

    - lactose intolerance, lactase deficiency, glucose-galactose malabsorption;

    - hereditary or idiopathic angioedema;

    - pregnancy and the period of breastfeeding;

    - age under 18 years (efficiency and safety not established).

    Carefully:

    Primary hyperaldosteronism, bilateral stenosis of the renal arteries, stenosis of the single kidney artery, condition after kidney transplantation, hyperkalemia, aortic stenosis, mitral stenosis (with violation of hemodynamics), idiopathic hypertrophic subaortic stenosis, systemic connective tissue diseases, coronary heart disease, cerebrovascular diseases, sugar diabetes, kidney failure (creatinine clearance <80 mg / min), hepatic insufficiency, in patients; observing a diet with restriction of table salt or being on hemodialysis, with simultaneous use with immunosuppressants and saluretic, in patients over 65 years of age,when oppression of bone marrow hematopoiesis; conditions, accompanied by a decrease in the volume of circulating blood (BCC), including diarrhea, vomiting.

    Pregnancy and lactation:

    The use of Berlipril® 20 during pregnancy is contraindicated.

    Patients planning pregnancy should be transferred to alternative treatment with a confirmed safety profile for use in pregnant women.

    When pregnancy is confirmed, the use of Berlipril® 20 should be discontinued immediately and, if necessary, alternative therapy should be initiated. The use of ACE inhibitors during the II and III trimesters of pregnancy was accompanied by a negative effect on the fetus, including the development of arterial hypotension, renal failure, hyperkalemia and / or hypoplasia of the skull bones in a newborn. Perhaps the development of oligohydramnion, apparently due to a decrease in the function of the kidneys, the fetus. This complication can lead to limb contracture, deformation of the bones of the skull, including its facial part, and lung hypoplasia. When using the drug Berlipril® 20, the patient should be informed of the potential risk to the fetus.

    If it is not possible to cancel Berlipril® 20 during pregnancy, careful monitoring of newborns whose mothers take Berlipril® 20 to detect possible lowering of blood pressure, oliguria and hyperkalemia, monitoring the state of renal function, and the skull of the newborn with ultrasound is necessary.

    Enalapril and enalaprilate are excreted in breast milk in trace amounts, but their safety has not been studied. If you need to use the drug during lactation, breastfeeding should be discontinued.

    Enalapril can be removed from the bloodstream of a newborn with peritoneal dialysis; theoretically - through exchange blood transfusion.

    Dosing and Administration:

    Inside. The tablets of the drug Berlipril® 20 are taken regardless of the time of ingestion, without chewing, squeezed with enough liquid.

    To select the appropriate dosage regimen, it is advisable to use the most suitable dosage of the drug - 5 mg, 10 mg or 20 mg (Berlipril® 5, Berlipril® 10 or Berlipril 20, respectively). The drug is used as a monotherapy, and in combination with other antihypertensive drugs;

    Arterial hypertension

    The initial dose is from 5 mg to 20 mg of enalapril maleate once a day, depending on the severity of the arterial hypertension.

    With mild hypertension, the recommended maintenance dose is 5-10 mg of enalapril maleate (1/2 - 1 tablet of Berlipril® 10) once a day, with moderate arterial hypertension of 10-20 mg of enalapril maleate (1 / 2- 1 pill of Berlipril® 20) once a day.

    With more severe arterial hypertension, the recommended maintenance daily dose of enalapril maleate is 20 mg (1 tablet of Berlipril® 20) once a day. Dosage is selected individually for each patient, but should not exceed 40 mg per day. The maximum daily dose of the drug is 40 mg once or twice.

    Renovascular hypertension

    The initial dose is 5 mg of enalapril maleate (1/2 tablet of Berlipril® 10) once a day. After taking the first dose of the drug, careful monitoring of blood pressure is necessary. Then the dose is selected in accordance with the therapeutic effect. The maximum daily dose is 20 mg (1 tablet of the drug Berlipril® 20) once a day with daily administration. In the future, careful monitoring of the patient, including mandatory monitoring of the state of kidney function, is necessary.

    Patients taking diuretics at the same time should temporarily stop diuretic therapy 2-3 days before the drug is prescribed. In case this is not possible, the initial dose of enalapril maleate should not exceed 5 mg / day. The drug is recommended to be administered with caution, as in such patients there may be a deficiency of fluid and / or hyponatremia, in the future the dosage is selected individually.

    In chronic heart failure and asymptomatic dysfunction of the left The ventricle preparation Berlipril® 20 is used as part of combination therapy concomitantly with diuretics, and, if necessary, cardiac glycosides or beta-blockers. The initial minimum dose of the drug is 2.5 mg (1/2 tablet of the drug Berlipril ® 5) once a day, treatment should be started under the close supervision of the doctor. An increase in the dose of enalapril maleate should be carried out gradually, usually 2.5-5 mg every 3-4 days according to the patient's individual response to the maximum tolerated doses,but not more than 40 mg / day for chronic heart failure and 20 mg / day for asymptomatic left ventricular dysfunction, once or twice. Selection of maintenance dose is carried out for 2-4 weeks.

    Treatment with enalapril for a long time, with chronic heart failure and asymptomatic left ventricular dysfunction to assess the effect is completely possible no earlier than 6 months after the initiation of therapy. In cases of too pronounced decrease in blood pressure, the maintenance dose of the drug is gradually reduced.

    In elderly patients, the more pronounced hypotensive effect and the lengthening of the action time of the drug are more often, which is associated with a decrease in the rate of enalapril excretion, so the recommended initial dose of enalapril maleate for elderly patients is no more than 2.5 mg (1/2 tablet of the drug Berlipril® 5). The maintenance daily dose should be selected depending on the concentration of serum creatinine.

    Side effects:

    Possible side effects with Berlipril® 20 are given below on the descending frequency of occurrence: very often (> 1/10), often (> or = 1/100, <1/10), infrequently (> or = 1/1000, <1/100), rarely (> or = 1 / 10000, <1/1000), very rarely (<1/10000), including individual messages.

    Disorders from the blood and lymphatic system: infrequently: anemia (including aplastic and hemolytic), rarely: neutropenia, a decrease in hemoglobin and hematocrit in the serum, eosinophilia, thrombocytopenia, lymph node enlargement, pancytopenia, agranulocytosis, oppression of bone marrow hematopoiesis, autoimmune diseases.

    Disorders from the metabolism and nutrition: infrequently - hypoglycemia.

    From the side of the central nervous system: often: headache, depression, infrequently confusion, insomnia, increased excitability, paresthesia, vertigo, tinnitus, rarely - a change in the nature of dreams, sleep disorders.

    From the side of the organ of vision: rarely - blurred vision.

    From the cardiovascular system: very, often - dizziness, often - hypotension (including orthostatic hypotension), syncope, pain, in the chest, heart rhythm disorders, angina pectoris, infrequently orthostatic hypotension, palpitations, myocardial infarction or cerebral stroke possibly due to a sharp drop in blood pressure in patients at high risk , rarely - Raynaud's syndrome.

    From the respiratory system: very often - unproductive dry cough, infrequently - rhinorrhea, sore throat and hoarseness, bronchospasm, bronchial asthma, rarely - dyspnea, rhinitis, pulmonary infiltrates, allergic alveolitis, eosinophilic pneumonia.

    From the digestive system: very often - nausea, often - diarrhea, pain in the stomach, change in taste perception, infrequent - intestinal obstruction, pancreatitis, lack of appetite, dryness of the oral mucosa, change in taste perception, peptic ulcer, rarely - stomatitis, aphthous ulcers, glossitis, very rarely - angioedema of the intestine.

    From the liver and bile ducts: rarely - liver failure, hepatitis - hepatocellular or cholestatic, including hepatic necrosis, cholestasis (including jaundice).

    From the skin and subcutaneous tissues: often - skin rash, hives, hypersensitivity reactions, angioedema, facial edema, extremities, lips, tongue, vocal cords and / or throat, infrequent: sweating, itchy skin / urticaria, alopecia, rarely erythema multiforme, Stevens-Johnson syndrome, exfoliative dermatitis, toxic epidermal necrolysis, pemphigus, erythroderma.

    A symptom complex has been reported that may be accompanied by some and / or all of the following side effects: fever, serositis, vasculitis, myalgia / myositis, arthralgia / arthritis,yshtitration of antinuclear antibodies, increased erythrocyte sedimentation rate, eosinophilia, and leukocytosis. There may be a skin rash, photosensitivity or other skin manifestations.

    From the side of the kidneys and urinary tract: infrequently - a violation of kidney function, proteinuria, renal failure, rarely - oliguria.

    From the genitals and mammary glands: infrequently - erectile dysfunction, rarely - gynecomastia.

    General disorders: very often - asthenia, often - fatigue, infrequently - muscle cramps, flushes to the face, tinnitus, fever.

    Laboratory indicators: often - hyperkalemia, increased serum creatinine concentration, infrequently - increase, serum urea concentration, hyponatremia, rarely - increase in activity of "hepatic" enzymes / hyperbilirubinemia.

    In rare cases with simultaneous use of ACE inhibitors (including enalapril) and intravenous administration of gold preparations (sodium aurotomy malate) describes a symptom complex that includes reddening of the facial skin, nausea, vomiting and arterial hypotension.

    Overdose:

    Symptoms: approximately 6 hours after ingestion, a marked decrease in blood pressure, up to the development of collapse, myocardial infarction, acute impairment of cerebral circulation or thromboembolic complications, disturbance of water-electrolyte balance, renal failure, increased respiration, tachycardia, palpitations, bradycardia, dizziness , anxiety, a sense of fear, muscle cramps, coughing, stupor. Concentration in blood plasma enalaprilata 100-200 times higher than after the application of therapeutic doses, was observed after ingestion respectively 300 mg and 440 mg enalapril maleate.

    Treatment: the drug should be discontinued immediately; therapeutic measures should be aimed at eliminating enalapril and enalaprilat and correcting arterial hypotension. The patient is transferred to a horizontal position with a low headboard. In mild cases, gastric lavage and activated charcoal are shown,in more severe cases - intravenous infusion of physiological solution, plasma substitutes, if necessary - the introduction of angiotensin II or catecholamines; Hemodialysis (the rate of excretion of enalaprilate is 62 ml / min).

    Patients with a bradycardia that is resistant to therapy are shown staging the pacemaker.

    Interaction:

    When used simultaneously with non-steroidal anti-inflammatory drugs (NSAIDs), including selective inhibitors of cyclooxygenase-2 (COX-2 inhibitors), it is possible to reduce the hypotensive effect of ACE inhibitors, including enalapril.

    In some patients with impaired renal function, simultaneous use of NSAIDs and ACE inhibitors may lead to further impairment of renal function.

    These changes are usually reversible.

    The use of potassium-containing food additives, potassium-containing salt substitutes - and / or the use of potassium-sparing diuretics, as well as heparin, can lead to a significant increase in the concentration of potassium ions in the blood serum, especially in patients with renal dysfunction and / or diabetes mellitus. If it is necessary to use concomitant with enalapril, the above drugs should be regularly monitored by the concentration of potassium ions in the blood serum.

    With the simultaneous use of the drug Berlipril® 20 and thiazide diuretics, hypokalemia caused by the administration of the latter is usually reduced by the action of enalapril.

    Prior therapy with high doses of diuretics can lead to hypovolemia and the risk of developing hypotension, during the initiation of enalapril therapy. Excessive hypotensive effects of enalapril can be reduced either by abolishing the diuretic, either by increasing the bcc or drinking common salt, as well as starting treatment with enalapril at a low dose. Simultaneous application diuretics of the thiazide series and ACE inhibitors can lead to hypovolemia and, thus, increase the risk of developing arterial hypotension.

    The simultaneous use of the drug Berlipril® 20 and lithium preparations is not recommended because of the risk of developing lithium intoxication. If this combination is necessary, careful monitoring of the concentration of lithium in the blood serum is necessary.

    Simultaneous use with antipyretic and analgesic agents can reduce the effectiveness of the drug.

    Enalapril weakens the effect of drugs containing theophylline.

    The hypotensive effect of enalaryl enhances diuretics, and also, hypotensive preparations of other groups, including beta-blockers, methyldopa, nitroglycerine and other nitrates, blockers of "slow" calcium channels, hydralazine, prazozin, as well as some drugs for anesthesia, ethanol, tricyclic antidepressants, antipsychotic drugs.

    ACE inhibitors can increase the hematotoxicity of immunosuppressants, allopurinol, cytostatics.

    Drugs that cause oppression of bone marrow hematopoies, increase the risk of developing neutropenia and agranulocytosis.

    ACE inhibitors increase the bioavailability of digoxin, increasing its concentration in the blood. In this regard, with the simultaneous administration of ACE inhibitors and cardiac glycosides, the dose of the latter should be somewhat reduced to avoid the development of unwanted effects or the effect of a relative overdose.

    Neuroleptics may increase the hypotensive effect of enalapril.

    Sympathomimetics can weaken the hypotensive effect of enalapril.

    Simultaneous use of antacids, adsorbents can lead to a decrease in the bioavailability of ACE inhibitors by almost 50%as well as to slowing down and weakening their hypotensive effect, so you should observe the interval between doses of drugs, at least 2 hours.

    Enalapril can be used simultaneously with acetylsalicylic acid (in cardiac doses less than 300 mg / day), thrombolytics and beta-blockers.

    Epidemiological studies have shown that simultaneous use of ACE inhibitors and hypoglycemic agents (insulin, hypoglycemic agents for admission inside) can additionally withto help reduce blood glucose levels, leading to the development of hypoglycemia. This phenomenon is most often observed during the first weeks of simultaneous application of the above drugs, and also the patients with renal insufficiency. In patients with diabetes, receiving hypoglycemic agents for ingestion and / or insulin, a regular monitoring the concentration of blood glucose, especially careful - during the first month - concurrent use with ACE inhibitors.

    Special instructions:

    Care must be taken in patients with reduced BCC (including,with simultaneous use with diuretics, in conditions of restriction of consumption of table salt, in hemodialysis, diarrhea, vomiting), in which a sudden and pronounced decrease in blood pressure may develop in response to the use of an ACE inhibitor. In patients with chronic heart failure of mild degree, with or without chronic renal insufficiency, symptomatic arterial hypotension is usually not observed. The development of arterial hypotension is most likely in patients with a more severe degree of chronic heart failure due to the use of high doses of diuretics, hyponatremia or functional renal failure. In these patients, treatment should be started under the supervision of a physician, up to an optimal dose adjustment of Berlipril® 20 and / or a diuretic. Similar tactics can be applied to patients with coronary heart disease and cerebrovascular diseases, in which excessive drop in blood pressure, may lead to myocardial infarction or stroke.

    In the case of development of severe arterial hypotension, the patient should be placed in a horizontal position and, if necessary, intravenous infusion of physiological solution should be started.

    Transient arterial hypotension is not a contraindication for the continuation of enalapril treatment after BP stabilization. In the case of a re-expressed decrease in blood pressure should reduce the dose or cancel the drug. Before and during the treatment with ACE inhibitors, a dynamic control of blood pressure, certain biochemical and electrolyte blood indices (hemoglobin concentration, potassium ions, sodium ions, creatinine, urea, "liver" enzymes in blood serum) and urine for the presence of protein is necessary.

    Like all vasodilators, ACE inhibitors should be administered with caution to patients with left ventricular hypertrophy and valvular obstruction and refrain from their application in cases of cardiogenic shock and hemodynamically significant obstruction.

    In cases of impaired renal function (creatinine clearance <80 ml / min), careful monitoring of serum potassium and serum creatinine concentration is necessary.

    In patients with renal insufficiency, it may be necessary to reduce the dose and / or frequency of the drug. In some patients with bilateral stenosis of the renal arteries or stenosis of the artery of a single kidney, there was an increase in the concentration of urea and creatinine in the serum.Changes were usually reversible and returned to normal after discontinuation of treatment.

    In some patients who did not have renal disease before treatment, there was a slight and transient increase in serum urea and creatinine levels when enalapril was used concomitantly with diuretics.

    In such cases, it may be necessary to reduce the dose and / or withdrawal of enalapril and / or diuretic

    There is ayshThe risk of developing arterial hypotension and renal failure in patients with bilateral stenosis of the renal arteries or stenosis of the artery of a single kidney that are on therapy with ACE inhibitors. Only modest changes in the serum creatinine concentration can indicate a decrease in renal function. In these patients, treatment should begin with small doses under close medical supervision, precise gradual selection, individual dose and control of serum creatinine concentration.

    The experience of using Berlipril® 20 in patients who have recently undergone kidney transplantation is not available. Therefore, the treatment of such patients with this drug is not recommended.

    The use of Berlipril® 20 in patients with hepatic insufficiency usually does not require dose adjustment. Rarely, the administration of ACE inhibitors is associated with a syndrome that begins with the development of cholestatic jaundice until the development of fulminantabout necrosis of the liver. When symptoms of jaundice appear or the activity of liver enzymes increases in patients taking ACE inhibitors; should stop drug therapy and conduct an appropriate examination.

    There are reports of the development of life-threatening anaphylactic reactions in patients receiving ACE inhibitors during desensitisation with Hepaticoptera (Heminoptera) venom. Such reactions can be avoided, if before the beginning of desensitization temporarily stop the intake of an ACE inhibitor. The use of ACE inhibitors in patients receiving immunotherapy with bee venom should be avoided.

    Neutropenia, agranulocytosis, thrombocytopenia, anemia can develop on the background of therapy with ACE inhibitors. With normal kidney function and, in the absence of other complications, neutropenia occurs rarely.

    ACE inhibitors are prescribed only in emergency cases if the patient has systemic connective tissue diseases, during immunosuppressive therapy,in cases of simultaneous use of allopurinol or procainamide, ande with a combination of all these factors, especially against the background of "renal failure." Some of these patients developed severe infections, which in some cases did not respond to intensive antibiotic therapy. enalapril it is still used in such patients, periodic monitoring of the number of white blood cells in the blood formula is recommended, and patients should be instructed accordingly to immediately inform the doctor of any signs of infection.

    It is reported about the occurrence of cough in the treatment of ACE inhibitors: Usually cough, is non-productive.continuous and stops after the drug is discontinued.

    Cough due to treatment with ACE inhibitors should be taken into account in the differential diagnosis of cough.

    Reports of angioedema (edema of the Quincke) of the face, limbs, lips, tongue, glottis and / or larynx have been reported in patients receiving ACE inhibitors, including Berlipril® 20, at different periods of treatment. In such cases, treatment with Berlipril® 20 should be discontinued immediately,should be implemented proper medical supervision until the symptoms disappear completely.

    Even in those cases where there is only difficulty swallowing without difficulty breathing, patients should be under medical supervision for a long time, since therapy with antihistamines and corticosteroids may not be sufficient. Angioedema of the larynx or tongue can be fatal. Swelling of the tongue, glottis or larynx can lead to airway obstruction, appropriate therapy involving subcutaneous administration of 0.1% adrenaline solution (0.3-0.5 ml) and / or measures to ensure airway conduction should be performed in the shortest possible time.

    In patients of the Negroid race, the frequency of angioedema development with ACE inhibitors is higher than in representatives of other races. Like other ACE inhibitors, enalapril, appears to be less effective in lowering blood pressure in patients of the Negroid race than in others, perhaps because of the high prevalence of low renin levels in this population of patients with hypertension.

    During the period of treatment it is not recommended to drink alcoholic beverages. alcohol increases the hypotensive effect of the drug.

    In patients undergoing surgery or general anesthesia with the use of drugs that reduce blood pressure, enalapril can block the increase in the formation of angiotensin II due to the compensatory release of renin. If it is assumed that arterial hypotension develops by this mechanism, it can be corrected by an increase in BCC.

    Before surgical interventions (including dental procedures) It is necessary to alert the surgeon / anesthesiologist about the use of Berlipril® 20.

    In rare cases, life-threatening anaphylactoid reactions have been observed in patients taking ACE inhibitors during low-density lipoprotein (LDL) apheresis with dextran sulfate. If LDL-apheresis is used, ACE inhibitors should be temporarily replaced with drugs to treat arterial hypertension of heart failure from other groups.

    In patients on dialysis using high-capacity membranes (eg AN69®), anaphylactoid reactions were observed with the use of ACE inhibitors.Therefore, for such patients it is recommended either the use of dialysis membranes of a different type, or the use of antihypertensive drugs of another group.

    In patients with diabetes mellitus, who take hypoglycemic agents for ingestion or insulin, it is necessary to carefully monitor the concentration of blood glucose during the first month of enalapril treatment.

    In some patients taking ACE inhibitors, incl. enalapril, an increase in the concentration of potassium ions in serum is observed. The risk group for hyperkalemia includes patients suffering from renal insufficiency or diabetes mellitus, taking potassium-sparing diuretics or potassium-containing salt substitutes, and other medications that receive a concentration of potassium ions in the blood serum (eg, heparin). If the use of the above medicines against the background of treatment with Berlipril ® 20 is recognized as necessary, regular monitoring of the concentration of potassium ions in serum is recommended.

    Like other ACE inhibitors, enalapril may be less effective in lowering blood pressure in representatives of the Negroid race in comparison with persons of other races,due to the low level of renin in patients with hypertension in this population.

    The sudden cessation of enalapril treatment does not lead to the development of the "withdrawal" syndrome (a sharp rise in blood pressure).

    Effect on the ability to drive transp. cf. and fur:

    Care must be taken when driving vehicles and engaging in potentially dangerous activities requiring increased concentration of attention and speed of psychomotor reactions (possibly dizziness due to a sharp decrease in blood pressure, especially after taking the initial dose of enalapril in patients taking diuretics).

    Form release / dosage:

    Tablets, 20 mg.

    Packaging:

    10 tablets per contour cell package (blister) made of laminated film (polyamide / aluminum / PVC) and aluminum foil.

    For 3, 5 or 10 blisters together with instructions for use are placed in a cardboard box.

    Storage conditions:

    Store at a temperature not exceeding 25 ° C.

    Keep the medicinal product out of the reach of children!

    Shelf life:

    3 years.

    Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:П N015000 / 01-2003
    Date of registration:22.07.2008
    Expiration Date:Unlimited
    The owner of the registration certificate:Berlin-Chemie / Menarini Pharma, GmbH Berlin-Chemie / Menarini Pharma, GmbH Germany
    Manufacturer: & nbsp
    Information update date: & nbsp23.01.2017
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