Active substancePerindoprilPerindopril
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  • Dosage form: & nbsppills
    Composition:

    Tablets 4 mg

    Active substance: perindopril erbumine 4.00 mg (equivalent to perindopril 3.338 mg);

    Excipients: cellulose microcrystalline 24.93 mg, lactose monohydrate 60.30 mg, silicon dioxide colloid 0.27 mg, magnesium stearate 0.50 mg.

    Tablets 8 mg

    Active substance: perindopril erbumine 8.00 mg (equivalent to perindopril 6.766 mg);

    Excipients: cellulose microcrystalline 49.86 mg, lactose monohydrate 120,60 mg, silicon dioxide colloid 0.54 mg, magnesium stearate 1.00 mg.

    Description:

    Tablets 4 mg:

    Oval, flat, white colored tablets, with a risk on one side, with engraved C53 on the other side.

    Tablets 8 mg:

    Round, flat, white color tablets, with a bevel, with engraving C54 on one side.

    Pharmacotherapeutic group:inhibitor of angiotensin-converting enzyme (ACE).
    ATX: & nbsp

    C.09.A.A.04   Perindopril

    Pharmacodynamics:

    Perindopril - ACE inhibitor, interacts with zinc ions in the ACE molecule and causes its inactivation. Perindopril acts through its active metabolite perindoprilata.Reduces the formation of angiotensin II from angiotensin I, eliminates its vasoconstrictor action. Reduction of angiotensin II leads to a direct decrease in the release of aldosterone. Reduces the degradation of bradykinin and increases the synthesis of vasodilating prostaglandins. Suppresses the release of norepinephrine from the endings of sympathetic nerve fibers and the formation of endothelin in the vessel wall. Reduction in the formation of angiotensin II is accompanied by an increase in renin activity of blood plasma (as a result of inhibition of negative feedback). Suppression of ACE is accompanied by an increase in the activity of both circulating and tissue kallikrein-kinin system, while the system of prostaglandins is activated.

    Helps restore the elasticity of large arterial vessels (reducing the formation of excessive amounts of subendothelial collagen), reduces pressure in the pulmonary capillaries. With prolonged use, the severity of myocardial hypertrophy of the left ventricle and interstitial fibrosis decreases, and normalizes the isozyme profile of myosin. Normalizes the work of the heart.Reduces the overall peripheral vascular resistance, preload and afterload (reduces systolic and diastolic blood pressure in the "lying" and "standing" position), the filling pressure of the left and right ventricles, causes an increase in the minute volume of blood and the cardiac index, does not increase the heart rate (heart rate) , increases regional blood flow in muscles. Perindopril increases renal blood flow, does not change the rate of glomerular filtration.

    After ingestion of a single dose, the maximum antihypertensive effect is achieved in 4-6 hours and persists for 24 hours. Stabilization of the antihypertensive effect is achieved after the first month of therapy and persists for a long time.

    With a sharp withdrawal of the drug, there is no pronounced increase in blood pressure (BP).

    Pharmacokinetics:

    After oral administration perindopril quickly absorbed in the gastrointestinal tract. The maximum concentration of perindopril in the blood serum is achieved after 1 hour. The bioavailability of the drug is 65 - 70%. Taking the drug while eating reduces its bioavailability.

    Approx. 20 % total amount of absorbed perindopril is converted to perindoprilat - an active metabolite. In addition to active perindoprilata, five inactive metabolites are formed from perindopril. The half-life of perindopril is 1 hour. The maximum concentration of perindoprilat in the blood serum is achieved in 3-4 hours.

    Binding perindoprilata with blood plasma proteins is insignificant and depends on the concentration, with ACE - less than 30 %. The intake of the drug during meals is accompanied by a decrease in the conversion of perindopril to perindoprilat (this effect has no clinical significance). The volume of distribution of free perindoprilata is approximately 0.2 l / kg.

    Perindoprilat is excreted from the body through the kidneys. The half-life of the metabolite is approximately 3-5 hours.

    Dissociation of perindoprilat, associated with ACE, is slowed down. As a result, the "effective" half-life is 25 hours. Repeated use of perindopril does not lead to its cumulation, and the half-life of perindoprilat with repeated admission corresponds to the period of its activity, so the equilibrium state is reached after 4 days.

    Pharmacokinetics in specific patient groups

    The excretion of perindoprilat is slowed in elderly patients, as well as in patients with chronic heart failure or renal insufficiency. In renal failure, dose adjustment should be performed depending on the creatinine clearance. The dialytic clearance of perindoprilat is 70 ml / min.

    In patients with cirrhosis, the liver clearance of perindopril is reduced by a factor of 2. However, the total amount of perindoprilate formed does not change, and therefore correction of the dosing regimen is not required.

    Indications:

    - Arterial hypertension (in monotherapy or in combination with other antihypertensive drugs).

    - Chronic heart failure (as part of combination therapy).

    - Stable ischemic heart disease (IHD): reduced risk of cardiovascular complications in patients who had previous myocardial infarction and / or coronary revascularization.

    Contraindications:

    - Hypersensitivity to perindopril, accessory components of the drug or other ACE inhibitors.

    - Angioedema in history,including those associated with the use of ACE inhibitors or idiopathic angioedema.

    - Hereditary angioedema angioedema.

    - Age to 18 years (effectiveness and safety not established).

    - Lactose intolerance, lactase deficiency, glucose-galactose malabsorption.

    - Pregnancy, lactation.

    Carefully:

    Renovascular hypertension, bilateral renal artery stenosis, stenosis of the artery only kidneys - risk of severe hypotension and renal failure; chronic heart failure in the stage of decompensation; arterial hypotension; chronic renal failure (creatinine clearance (CK) less than 60 ml / min); significant hypovolemia and hyponatremia (due to a salt-free diet and / or previous diuretic therapy, dialysis, vomiting, diarrhea); cerebrovascular diseases (including cerebral circulatory insufficiency); ischemic heart disease - the risk of excessive blood pressure lowering; stenosis of the aortic or mitral valve, hypertrophic obstructive cardiomyopathy, hemodialysis using high-flow polyacrylonitrile membranes - riskdevelopment of anaphylactoid reactions; condition after kidney transplantation - there is no clinical experience; before the procedure of apheresis of low density lipoproteins (LDL), simultaneous carrying out

    desensitizing therapy with allergens (for example, venom of Hymenoptera) - the risk of anaphylactoid reactions; connective tissue diseases (including systemic lupus erythematosus (SLE), scleroderma), oppression of bone marrow hematopoiesis with immunosuppressant, allopurinide or procainamide - the risk of agranulocytosis and neutropenia; congenital deficiency of glucose-6-phosphate dehydrogenase - single cases of hemolytic anemia; in representatives of the Negroid race - the risk of developing anaphylactoid reactions; surgical intervention (general anesthesia) - the risk of developing excessive blood pressure lowering; diabetes mellitus (monitoring the concentration of glucose in the blood); hyperkalemia; elderly age.

    Pregnancy and lactation:

    Pregnancy

    The use of Perindopril-Richter during pregnancy is contraindicated. The drug should be stopped immediately if pregnancy is detected during the course of therapy. Perindopril penetrates the placental barrier. Admission of ACE inhibitors in the P and Ip trimester of pregnancy has an adverse effect on the fetus (there may be a marked decrease in blood pressure, renal failure, hyperkalemia, hypoplasia of the skull bones, fetal death). For newborns and infants who have undergone intrauterine exposure to ACE inhibitors, it is recommended to monitor for the timely detection of a marked decrease in blood pressure, oliguria, and hyperkalemia.

    Lactation period

    During treatment with the drug, breastfeeding should be abolished (there is no data on perindopril permeating into breast milk).

    Dosing and Administration:

    Perindopril-Richter is recommended to be taken daily 1 time / day, in the morning, before meals.

    Arterial hypertension:

    Perindopril-Richter can be used in monotherapy or in combination with antihypertensive drugs of another group.

    The recommended initial dose is 4 mg 1 time per day in the morning. If the therapy is ineffective for one month, the dose may be increased to 8 mg once a day.

    In patients taking diuretics, diuretics should be discontinued 2-3 days before starting therapy with Perindopril-Richter.In cases where this is not possible, the initial dose of Perindopril-Richter should not exceed 2 mg / day (1/2 tablet), while it is recommended to provide medical supervision of the patient after taking the first dose, it is possible to develop symptomatic arterial hypotension, as well as control of kidney function and potassium content in blood serum.

    Renovascular hypertension and other conditions associated with increased activity of the renin-angiotensin-aldosterone system. The recommended initial dose is 2 mg / day (1/2 tablet) under careful medical supervision (control of blood pressure, kidney function, potassium content in blood serum). The maintenance dose, continuing strict medical control, should be determined depending on the dynamics of blood pressure.

    Chronic heart failure:

    Treatment with patients with chronic heart failure perindopril in combination with a potassium-sparing diuretic and / or digoxin and / or beta-blocker is recommended to begin under close medical supervision using the drug at an initial dose of 2 mg (1/2 tablet) once a day in the morning .Later, after 1-2 weeks of treatment, the dose of the drug can be increased to a dose of 4 mg 1 time / day.

    Stable ischemic heart disease:

    Use Perindopril-Richter should be started at a dose of 4 mg 1 time / day for the first two weeks, then the dose can be increased to 8 mg 1 time / day with good tolerability and under the control of kidney function.

    In elderly patients, a dose of 2 mg (1/2 tablet) should be administered once a day for one week, which can be gradually increased to 4 mg once a day for the following week, and then, if necessary, to 8 mg 1 time / day under the control of kidney function.

    Renal insufficiency:

    If a patient has a disorder of kidney function, the dose of perindopril should be selected taking into account the degree of renal failure. In such patients it is necessary to regularly monitor the content of potassium and creatinine. The following dosing regimen is recommended:

    clearance of creatinine (ml / min)

    recommended dose

    KK> 60 30 <KK <60 15 <KK <30

    Patients on hemodialysis *, CC <15

    4 mg 1 time / day

    2 mg (1/2 tablet) 1 time / day 2 mg (1/2 tablet) every other day 2 mg (1/2 tablet) per day of dialysis

    * Dialysis clearance of perindoprilata is 70 ml / min. Patients on hemodialysis should take a dose of the medication after dialysis.


    In patients with chronic heart failure, with renal insufficiency and with a tendency to electrolyte disorders (hyponatremia), as well as in patients taking both diuretics and / or vasodilators, treatment with the drug is started under strict medical supervision. In patients with a high risk of developing clinically significant arterial hypotension (eg, taking high doses of diuretics), hypovolemia and electrolyte disturbances should be eliminated as far as possible before starting the Perindopril-Richter preparation. It is recommended to carefully monitor the level of blood pressure, the state of kidney function and the content of potassium ions in the blood serum before and during therapy.

    Liver failure:

    When using the drug in patients with impaired liver function, dose adjustment is not required.

    Side effects:

    The following undesirable effects were observed during treatment with perindopril and evaluated at the following frequency: very often (> / 10); often (> 1/100, <1/10); infrequently (> 1/1000, <1/100); rarely (> 1/10000, <1/1000); very rarely (<1/10000), including individual messages.

    From the central and peripheral nervous system: often - headache, dizziness, paresthesia; infrequently - sleep disturbance, mood lability; very rarely confusion.

    From the cardiovascular system: often - marked decrease in blood pressure and related symptoms; very rarely - arrhythmias, angina pectoris, myocardial infarction and stroke as a result of severe arterial hypotension in high-risk patients. From the digestive system: often - nausea, vomiting, abdominal pain, taste disorder, indigestion, diarrhea, constipation; infrequent - dryness of the oral mucosa; very rarely - pancreatitis, hepatitis (hepatocellular and cholestatic). Allergic reactions: often - skin rash, itching; infrequently - angioedema, swelling of the face, lips, extremities, mucous membranes, tongue, glottis and / or larynx, urticaria; very rarely - angioedema of the small intestine, multi-form exudative erythema.

    From the sense organs: often - impaired vision, tinnitus.

    From the respiratory system: often - dry cough, shortness of breath; infrequently bronchospasm; very rarely - eosinophilic pneumonia, rhinitis.

    From the musculoskeletal system and connective tissue: often - muscle spasms.

    From the genitourinary system: infrequently - impaired renal function, decreased potency; very rarely acute renal failure.

    On the part of the hematopoiesis system: very rarely - a decrease in hemoglobin and hematocrit, thrombocytopenia, leukopenia / neutropenia, pancytopenia, agranulocytosis.

    In patients with congenital deficiency of glucose-6-phosphate dehydrogenase in very rare cases, hemolytic anemia occurs.

    Laboratory indicators: may increase the concentration of urea and creatinine in the blood plasma, as well as hyperkalemia, reversible after discontinuation of the drug, more often in patients with renal insufficiency, severe chronic heart failure and renovascular hypertension. In rare cases, there may be an increase in the activity of "liver" transaminases and bilirubin in the blood serum. General disorders and symptoms: often - asthenia; infrequently - increased sweating.

    Overdose:

    Symptoms: marked decrease in blood pressure, shock, stupor, water-electrolyte balance disorders, renal failure, hyperventilation, tachycardia, palpitation, bradycardia, dizziness, anxiety, cough.

    Treatment: gastric lavage, giving the patient a horizontal position with raised legs, replenishing the volume of circulating blood (bcc) - intravenous injection of 0.9% isotonic sodium chloride solution, plasma-substituting solutions, if possible, infusion of angiotensin II and / or intravenous catecholamines, symptomatic therapy, monitoring the function of the cardiovascular and respiratory systems, bcc, urea, creatinine and electrolytes in blood serum, as well as diuresis. With the development of bradycardia or expressed autonomic disorders apply atropine, an artificial pacemaker may be required Perindopril can be removed from the body by hemodialysis. It is necessary to avoid the use of high-flow polyacrylonitrile membranes.
    Interaction:

    Perindopril can be used in conjunction with acetysacchitic acid (as an antiaggregant in doses greater than 3 g / day), thrombolytic agents, beta-blockers and / or nitrates.


    With the combined use of perindopril with other antihypertensive drugs, there is a mutual enhancement of their action.With simultaneous application with beta-blockers, blockers of "slow" calcium channels, diuretics, nitroglycerin and other nitrates, other vasodilators there is an increase in antihypertensive effect.

    Baclofen

    Perhaps increased antihypertensive effect.

    Tricyclic antidepressants, antipsychotics, aids for general anesthesia

    Joint use with ACE inhibitors can lead to an increase in antihypertensive effect and the development of postural hypotension.

    Diuretics

    With simultaneous use with diuretics, especially in patients with hypovolemia and water-electrolyte balance disorders, at the very beginning of perindopril therapy there may be an excessive decrease in blood pressure, the risk of which can be reduced by eliminating the diuretic drug, intravenous injection of 0.9% sodium chloride solution, as well as the use of an ACE inhibitor at lower doses. Further increase in the dose of the drug should be carried out with caution. Potassium-sparing diuretics or kachs preparations

    With simultaneous use with potassium-sparing diuretics (incl. spironolactone, triamterene, amiloride), potassium preparations, salt substitutes containing potassium - increases the risk of hyperkalemia, especially in patients with impaired renal function. Therefore, it is not recommended to combine perindopril with these drugs. These combinations should be used only in case of hypokalemia, observing the precautionary measures and regularly monitoring the content of potassium ions in the blood serum.

    Lithium preparations

    With simultaneous use with lithium preparations - slowing the excretion of lithium from the body (increased cardiotoxic and neurotoxic action of lithium). In this case, it is necessary to conduct regular monitoring of lithium content in blood serum. Non-steroidal anti-inflammatory drugs (NSAIDs)

    The use of non-steroidal anti-inflammatory drugs (including selective inhibitors of cyclooxygenase-2 (COX-2)) may be accompanied by a weakening of the antihypertensive effect of ACE inhibitors. It is known that NSAIDs and

    ACE inhibitors have an additive effect on the increase in potassium in the blood serum, with the possible deterioration of kidney function.These effects are usually reversible. Rarely, acute renal failure may occur, especially in patients with impaired renal function, in elderly patients or in patients with hypovolemia.

    Hypoglycemic agents

    The combined use of ACE inhibitors, and hypoglycemic agents for ingestion, and insulin can increase the hypoglycemic effect and lead to a decrease in the need for insulin or sulfonylurea preparations. This effect is most likely in the first weeks of combined treatment, as well as in patients with renal insufficiency.

    When used concomitantly with ACE inhibitors allopurinol, immunosuppressants, in t.ch. cytostatic agents and systemic glucocorticosteroids, procainamide may increase the risk of developing leukopenia.

    Sympathomimetics

    Sympathomimetics can weaken the antihypertensive effect of ACE inhibitors. Preparations of gold

    With simultaneous use of ACE inhibitors, including perindopril, and gold injections (sodium aurotomy malate) describes a symptom-complex - facial flushing, hot flashes, nausea, vomiting and hypotension.

    Special instructions:

    Arterial hypotension:

    ACE inhibitors can cause a sharp drop in blood pressure. Symptomatic arterial hypotension rarely develops in patients without concomitant diseases. The risk of a marked decrease in blood pressure is increased in patients with a reduced volume of circulating blood, for example, against a background of diuretic therapy, with strict salt-free diet, hemodialysis, diarrhea, or vomiting. Episodes of marked decrease in blood pressure are observed in patients with severe heart failure, both in the presence of concomitant renal failure and in its absence. Most often, this side effect was observed in patients receiving high doses of loop diuretics, as well as against hyponatremia or with renal dysfunction. In such patients, therapy should begin under careful medical supervision, preferably in a hospital setting. In this case, the drug is used in small doses, followed by a thorough titration of the dose. Similar rules should be followed when using the drug in patients with coronary heart disease, cerebrovascular insufficiency, in which a sharp decrease in blood pressure can lead to myocardial infarction or stroke.

    Transient arterial hypotension is not a contraindication for taking the next dose of the drug.

    Before applying Perindopril-Richter, as well as other ACE inhibitors, and at the time of its administration, the blood pressure level of kidney function and the content of potassium ions in blood serum should be closely monitored.

    To reduce the likelihood of symptomatic arterial hypotension in patients receiving high-dose diuretics, the dose of diuretics should be reduced, if possible, a few days before the application of Perindopril-Richter.

    In the case of development of arterial hypotension the patient should be transferred to a supine position on the back. If necessary, normalize the sodium content and / or replenish the volume of the liquid by administering an intravenously isotonic solution of sodium chloride. Arterial hypotension with the first intake of the drug is not a contraindication for the further use of the drug Perindopril-Richter.

    In some patients with congestive heart failure who have normal or low blood pressure, the use of perindopril may cause an additional reduction in blood pressure. This effect usually does not require the cessation of treatment.If arterial hypotension is accompanied by clinical manifestations, a dose reduction or drug cancellation may be required.

    Stable ischemic seudia:

    In patients with stable coronary heart disease in the event of an episode of unstable angina (significant or not), during the first month of therapy with Perindopril-Richter, the ratio of expected benefit to the possible risk of continuing therapy should be assessed.

    Patients with Renovascular Hypertension:

    The use of ACE inhibitors in patients with renal arterial hypertension, as well as with stenosis of the renal artery, especially bilateral and with a single kidney, and also with hyponatremia is accompanied by an increased risk of severe arterial hypotension and kidney failure. Against the background of taking diuretic drugs, the risk of these complications increases. Impaired renal function may be manifested only by minor changes in serum creatinine. Treatment of such patients begins in a hospital under careful medical supervision with the use of small doses of the drug and further selection of a dose.During the first few weeks of therapy, it is necessary to temporarily stop treatment with diuretics and monitor kidney function.

    Mitral stenosis / aortic stenosis / hypertrophic obstructive cardiomyopathy:

    Perindopril-Richter, like other ACE inhibitors, should be used with caution in patients with obstruction of the left ventricular outflow tract (aortic stenosis, hypertrophic obstructive cardiomyopathy), as well as in patients with mitral stenosis.

    Renal insufficiency:

    Use ACE inhibitors in patients with renal insufficiency with caution, since the drug inhibits the activity of the renin-angiotensin-aldosterone system. In the case of renal insufficiency (creatinine clearance <60 ml / min), the initial dose of perindopril should be matched to the creatinine clearance (see section "Dosage and Administration"). In these cases, it is often necessary to reduce the dose or frequency of taking the drug. The kidney function should be monitored throughout the treatment. There are reports of the development of renal failure against the background of the use of ACE inhibitors,However, this is in most cases typical for patients with severe heart failure or kidney disease, including renal artery stenosis.

    In some patients, concomitant use of diuretics may increase serum urea and creatinine levels. In these cases, a reduction in the dose of an ACE inhibitor and / or discontinuation of diuretics may be required. During the first few weeks of therapy with an ACE inhibitor, dynamic monitoring of renal function is recommended.

    Patients on hemodialysis:

    In patients on hemodialysis using high-flow membranes or receiving apheresis procedures for low-density lipoproteins with dextran sulfate, the use of an ACE inhibitor has been associated with the development of anaphylactic reactions that threaten life. In such cases it is necessary to consider

    the possibility of using another type of membrane for dialysis or another antihypertensive agent.

    Hypersensitivity / Angioedema:

    Angioedema, swelling of the face, extremities, lips, tongue, epiglottis and / or larynx was rare in patients,treated patients with ACE inhibitors, especially during the first few weeks of therapy that may occur during any treatment period. In this case, treatment with Perindopril-Richter should be stopped as soon as possible, and the patient should be monitored until the symptoms regress completely. As a substitute, one should consider the possibility of using drugs of another pharmacological class. In cases where there was only edema of the face and lips, the condition usually passes without treatment, but antihistamines may be used.

    Angioedema with edema of the larynx can lead to death. When swelling of the tongue, epiglottis or larynx, airway obstruction can occur, therefore, appropriate therapy should be performed immediately (0.3-0.5 ml of epinephrine (adrenaline) solution 1: 1000 subcutaneously, administration of glucocorticosteroids, antihistamines) and / or measures to ensure patency of the respiratory tract. The patient must be hospitalized.

    Patients with a history of angioneurotic edema not associated with previous treatment with ACE inhibitors may be at increased risk of developing it during treatment with an ACE inhibitor.

    In some cases, when desensitizing the venom of Hymenoptera (hymenoptera), treatment with ACE inhibitors was accompanied by an anaphylactic reaction. This can be avoided by interrupting the use of an ACE inhibitor.

    Cough:

    With the use of an ACE inhibitor, cough may occur. Cough is dry, prolonged, which disappears after discontinuing treatment with an ACE inhibitor. With a differential diagnosis of cough, one should also consider a cough caused by the use of an ACE inhibitor.

    Chiturgy / General anesthesia:

    When using drugs that reduce blood pressure in patients with extensive surgery or during general anesthesia perindopril can block the formation of angiotensin II. The pronounced decrease in blood pressure, caused by a sharp increase in antihypertensive action, which is considered a consequence of this mechanism, can be eliminated by increasing the volume of circulating blood.

    Before surgery (including dentistry), it is necessary to alert the surgeon / anesthesiologist about the use of ACE inhibitors.

    Use of recommended doses of the drug by patients old age may be accompanied by an increase in the concentration of perindopril in the blood, so the selection of a dose requires special attention and is carried out depending on the function of the kidneys and the patient's blood pressure. However, in elderly and young patients, the antihypertensive effect of perindopril is equally pronounced.

    Hypeokaliemia:

    An increase in potassium in the serum was observed in some patients receiving ACE inhibitors, including perindopril, especially if the patient has renal and / or chronic heart failure. It is usually not recommended to use potassium preparations and potassium-sparing diuretics or other medications that affect the increase in serum potassium (for example, heparin). If taking the above drugs in combination is necessary, they should be used against a background of regular monitoring of potassium in the blood serum.

    Liver failure:

    In rare cases, the use of ACE inhibitors has been associated with the onset of a syndrome that begins with cholestatic jaundice and rapidly progressing necrotic hepatitis, and sometimes fatal. The mechanism of this syndrome is unknown.In patients receiving ACE inhibitors, who have jaundice or a significant increase in liver transaminase activity, it is necessary to cancel the taking of these drugs and carry out medical supervision. Neutropenia / Agranuloietosis / Thrombotopenia / Anemia:

    The risk of developing neutropenia against the background of the administration of ACE inhibitors is dose-dependent, depends on the drug taken and the presence of concomitant diseases. This reaction is very rare in patients without concomitant diseases, but the risk increases in patients with impaired renal function, especially against the background of systemic connective tissue diseases (systemic lupus erythematosus, scleroderma) and treatment with immunosuppressants. The disorders are reversible and pass after the withdrawal of the ACE inhibitor. Anemia can develop in patients after kidney transplantation or in people on hemodialysis.

    A slight decrease in hemoglobin occurs during the first 6 months, then the hemoglobin content remains stable and completely restored after the drug is discontinued.In such patients, treatment can be continued, but haematological analyzes should be carried out regularly.

    In patients with congenital deficiency of glucose-6-phosphate dehydrogenase, single cases of hemolytic anemia are described.

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

    Care should be taken when doing physical exercises, hot weather (the risk of dehydration and excessive blood pressure lowering due to a decrease in the volume of circulating blood).

    Because the potential risk of agranulocytosis can not be ruled out, periodic monitoring of the blood picture is required.

    Paiyents of the Negroid race:

    In patients of the Negroid race, the risk of developing angioedema is higher. Like other ACE inhibitors, perindopril less effective as an antihypertensive agent in patients of the Negroid race. This effect, perhaps, is associated with a marked predominance of low-grade status in patients of the Negroid race with arterial hypertension.

    Lactose:

    The drug Perindopril-Richter contains lactose monohydrate.Patients with rare hereditary lactose intolerance, lactase deficiency, or impaired glucose / galactose absorption should not take this drug.

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

    During treatment with the drug Perindopril-Richter, dizziness and arterial hypotension may develop. ACE inhibitors should be used with caution in patients who drive vehicles and engage in activities that require increased concentration and speed of psychomotor reactions.

    Form release / dosage:Tablets, 4 mg, 8 mg. 10 tablets per blister Al / Al. For 3 blisters in a cardboard box together with instructions for use.
    Packaging:(10) - Blister Al / Al (3) / 10 tablets per blister Al / Al. 3 blisters per cardboard pack together with instructions for use. / - cardboard pack
    Storage conditions:

    Store at a temperature not exceeding 30 ° C.

    Keep out of the reach of children!

    Shelf life:

    3 years.

    Do not use after the expiry date printed on the package.
    Terms of leave from pharmacies:On prescription
    Registration number:LP-001125
    Date of registration:03.11.2011
    The owner of the registration certificate:GEDEON RICHTER, OJSC GEDEON RICHTER, OJSC Hungary
    Manufacturer: & nbsp
    Representation: & nbspGEDEON RICHTER OJSC GEDEON RICHTER OJSC Hungary
    Information update date: & nbsp28.08.2015
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