Active substanceEnalaprilEnalapril
Similar drugsTo uncover
  • Berlipril® 10
    pills inwards 
  • Berlipril® 20
    pills inwards 
  • Berlipril® 5
    pills inwards 
  • Renipril®
    pills inwards 
  • Renitek®
    pills inwards 
    Merck Sharp and Doum B.V.     Netherlands
  • Ednit®
    pills inwards 
    GEDEON RICHTER, OJSC     Hungary
  • Enalapril
    pills inwards 
  • Enalapril
    pills inwards 
    VALENTA PHARM, PAO     Russia
  • Enalapril
    pills inwards 
  • Enalapril
    pills inwards 
    Mapichem AG     Switzerland
  • Enalapril
    pills inwards 
  • Enalapril
    pills inwards 
    BIOSINTEZ, PAO     Russia
  • Enalapril
    pills inwards 
    VALENTA PHARM, PAO     Russia
  • Enalapril
    pills inwards 
  • Enalapril
    pills inwards 
    ORGANICS, JSC     Russia
  • Enalapril
    pills inwards 
    SYNTHESIS, OJSC     Russia
  • Enalapril
    pills inwards 
  • Enalapril
    pills inwards 
    OZONE, LLC     Russia
  • Enalapril
    pills inwards 
    Hemofarm AD     Serbia
  • Enalapril
    pills inwards 
    UPDATE OF PFC, CJSC     Russia
  • Enalapril
    pills inwards 
  • Enalapril HEXAL
    pills inwards 
    HEXAL AG     Germany
  • Enalapril H
    pills inwards 
  • Enalapril Fort
    pills inwards 
    SYNTHESIS, OJSC     Russia
  • Enalapril-Agio
    pills inwards 
  • Enalapril-Acry®
    pills inwards 
    AKRIKHIN HFK, JSC     Russia
  • Enalapril-TAD
    pills inwards 
    TAD Pharma GmbH     Germany
  • Enalapril Teva
    pills inwards 
  • Enalapril-UBF
    pills inwards 
    URALBIOFARM, OJSC     Russia
  • Enalapril-FPO®
    pills inwards 
  • Enalapril-FPO
    pills inwards 
  • Enam®
    pills inwards 
  • Enap®
    pills inwards 
  • Enafarm®
    pills inwards 
  • Dosage form: & nbsppills
    Composition:

    One tablet contains:

    Active substance: enalapril maleate - 10.00 mg.

    Excipients: lactose monohydrate - 165.75 mg, gelatin - 6.00 mg, magnesium carbonate - 25.00 mg, silicon dioxide colloid - 3.00 mg, sodium carboxymethyl starch - 8.00 mg, magnesium stearate - 2.00 mg, iron dye oxide brown, E 172 0.25 mg
    Description:Round slightly biconvex tablets of light brown color with beveled edges and notch for division on one side, white patches are possible
    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 angiotensin-converting enzyme (ACE) inhibitors. 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 is 1 hour, reaches a maximum after 4-6 hours and lasts up to 24 hours. In some patients, enalapril therapy is required for several weeks to achieve the optimal level of blood pressure.

    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).

    Removed during hemodialysis (rate of administration 62 ml / mn) 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 violation of the function of the left ventricle.

    Contraindications:

    - increased sensitivity to enalapril and other ACE inhibitors or drug components;

    - presence in the anamnesis of an angioedema, against the background of administration of ACE inhibitors;

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

    - hereditary or idiopathic angioedema;

    - pregnancy and the period of breastfeeding;

    - age to 18 years (efficacy 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), liver failure, in patients with a restricted diet Niemi salt or hemodialysis, while the use of immunosuppressants and saluretikami, in patients older than 65 years,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® 10 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® 10 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 of 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® 10, the patient should be informed of the potential risk to the fetus.

    If Berlipril® 10 can not be withdrawn during pregnancy, careful monitoring of neonates whose mothers take Berlipril® 10 to detect a possible reduction in blood pressure, oliguria, and hyperkalemia, and monitoring the renal function and the skull of the newborn with ultrasound should be carefully considered.

    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® 10 are taken irrespective 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 tablets of the drug Berlipril® 10) 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 (2 tablets of the drug Berlipril® 10) once a day with daily use.In the future, careful monitoring of the patient, including mandatory monitoring of the state of kidney function, is necessary.

    Patients who are 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 left ventricular dysfunction, Berlipril® 10 is used in combination therapy 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 to 5 mg every 3-4 days according to the individual patient's reaction to the maximum tolerated dose, but not more than 40 mg / day. in chronic heart failure, and 20 mg / day.- with asymptomatic dysfunction of the left ventricle, 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, it is possible to evaluate the effect completely not 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® 10 are given below in the descending frequency of occurrence: Often (>1/10), often (> or = 1/100, <1/10), infrequently (> or = 1/1000, <1/100), rarely (> or = 1/10000, <1/1000), rarely (< 1/10000), including individual messages.

    Violations from the blood and lymphatic system: infrequently: Anemia (including aplastic and hemolytic), rarely: neutropenia, a decrease in the concentration of hemoglobin and hematocrit in the serum, eosinophilia, thrombocytopenia, an increase in lymph nodes, 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, noise at ears, 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, chest pain, heart rhythm disturbances, 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 - an 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, abdominal pain, change in taste perception, infrequently - intestinal obstruction, pancreatitis, lack of appetite, dryness of the oral mucosa, changes in taste perception, peptic ulcer, rarely - stomatitis / aphthous ulcers, glossitis, 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, alopecia, hypersensitivity reactions / angioedema, swelling of the face, extremities, lips, tongue, vocal cords and / or throat, infrequent: sweating, itching, urticaria, alopecia, rarely - erythema multiforme, Stevens-Johnson syndrome, exfoliative dermatitis, toxic epidermal necrolysis, pemphigus, erythroderma.

    A symptomatic 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, an antinuclear antibody titer, an increase in 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, kidney 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 - hyperkalaemia, increased serum creatinine concentration, infrequently - increased serum urea concentration, hyponatremia, rarely - increased 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 disturbance of cerebral circulation or thromboembolic complications, disturbance of water-electrolyte balance, renal failure, increased respiration, tachycardia, palpitations, bradycardia, dizziness, restlessness , 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 impaired renal function 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 10 and thiazide diuretics, The hypokalemia caused by the ingestion of the latter is usually reduced by the action of enalapril.

    Prior therapy high doses of diuretics can lead to hypovolemia and the risk of developing hypotension at the beginning 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 thiazide number of and ACE inhibitors can lead to hypovolemia and, thus, increase the risk of developing arterial hypotension.

    Simultaneous use of the drug Berlipril® 10 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 application with antipyretic and analgesic means can reduce the effectiveness of the drug.

    Enalapril weakens the effect of drugs containing theophylline.

    The hypotensive effect of enalapril is enhanced by diuretics, as well as by hypotensive drugs from 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 hematotoxicity immunosuppressants, allopurinol, cytostatics.

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

    ACE inhibitors increase bioavailability 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 can enhance the hypotensive effect of enalapril.

    Sympathomimetics can reduce the hypotensive effect of enalapril.

    Simultaneous application antacids, adsorbents can lead to a decrease in the bioavailability of ACE inhibitors by almost 50%, as well as to a slowing and weakening of their hypotensive effect, so the interval between preparations should be kept at least 2 hours.

    Enalapril can be used concomitantly 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 oral administration) may further contribute to reducing blood glucose levels, leading to the development of hypoglycemia. This phenomenon is most often observed during the first weeks of simultaneous use of the above drugs, as well as in patients with renal insufficiency. In patients with diabetes mellitus receiving hypoglycemic agents for ingestion and / or insulin, regular monitoring of blood glucose concentration is necessary, especially careful - during the first month of simultaneous use with ACE inhibitors.

    Special instructions:

    Care should be taken in patients with reduced BCC (including, when used simultaneously 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 initiated under the supervision of a physician, up to the optimum dose adjustment of Berlipril® 10 and / or diuretic. Similar tactics can be applied to patients with ischemic heart disease and cerebrovascular diseases, in which excessive drop in blood pressure can 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 to refrain from their use 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, a reduction in the dose and / or cancellation of enalapril and / or a diuretic may be required.

    There is an increased risk of developing arterial hypotension and renal failure in patients with bilateral renal artery stenosis 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,exact gradual selection of an individual dose and control of serum creatinine concentration.

    The experience of using Berlipril® 10 in patients who have recently undergone kidney transplantation is absent. Therefore, the treatment of such patients with this drug is not recommended.

    The use of Berlipril® 10 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 fulminant liver necrosis. When symptoms of jaundice appear or the activity of liver enzymes increases in patients taking ACE inhibitors, discontinue 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 no 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, as well as a combination of all these factors, especially against the background of existing renal failure. Some of these patients developed severe infections, which in some cases did not respond to intensive antibiotic therapy. If 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 the occurrence of cough in the treatment of ACE inhibitors. Usually the cough is of an unproductive and persistent nature 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.

    The reports of angioneurotic edema (edema of Quincke) of the face, limbs, lips, tongue, glottis and / or larynx have been reported in patients receiving ACE inhibitors, including Berlipril® 10, at different periods of treatment. In such cases, treatment with Berlipril® 10 should be discontinued immediately, proper medical supervision should be performed 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 formation of angiotensin II under the influence of 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 surgery (including dental procedures), the surgeon / anesthesiologist should be warned about the use of Berlipril® 10.

    In rare cases, patients taking ACE inhibitors during apheresis of low-density lipoproteins (LDL) with dextran sulfate, life-threatening anaphylactoid reactions were observed. If applicable LDLapheresis, ACE inhibitors should be temporarily replaced with drugs to treat hypertension or heart failure from other groups.

    In patients on dialysis using high-capacity membranes (for example, AN69 ) on the background of the use of ACE inhibitors, anaphylactoid reactions were observed. 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 drugs that increase the concentration of potassium ions in the blood serum (eg, heparin).If the use of the above medicines against the background of treatment with Berlipril® 10 is 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 than in people of other races, possibly because of 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, 10 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 the instructions for use are placed in a cardboard bundle
    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 stated on the package
    Terms of leave from pharmacies:On prescription
    Registration number:П N015007 / 01-2003
    Date of registration:22.07.2008
    The owner of the registration certificate:Berlin-Chemie / Menarini Pharma, GmbH Berlin-Chemie / Menarini Pharma, GmbH Germany
    Manufacturer: & nbsp
    Information update date: & nbsp21.10.2015
    Illustrated instructions
      Instructions
      Up