Active substanceAmlodipine + LysinoprilAmlodipine + Lysinopril
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    GEDEON RICHTER, OJSC     Hungary
  • Equator®
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    GEDEON RICHTER, OJSC     Hungary
  • Dosage form: & nbsppills
    Composition:

    Each tablet contains active ingredients: amlodipine besylate 13.88 mg, equivalent to 10.00 mg amlodipine and lisinopril dihydrate 21.76 mg, equivalent to 20.00 mg of lisinopril; auxiliary substances: microcrystalline cellulose 101 181.08 mg, microcrystalline cellulose 12 173.28 mg, sodium carboxymethyl starch 8.00 mg, magnesium stearate 2.00 mg.

    Description:

    Round biconvex tablets white or almost white. On one side engraving CF3.

    Pharmacotherapeutic group:antihypertensive agent combined (angiotensin-converting enzyme inhibitor and blocker of "slow" calcium channels)
    ATX: & nbsp

    C.09.A.A.03   Lisinopril

    C.08.C.A.01   Amlodipine

    Pharmacodynamics:

    Combined drug containing active ingredients: lisinopril and amlodipine.

    Lisinopril refers to angiotensin-converting enzyme (ACE) inhibitors, reduces blood levels of angiotensin II and aldosterone, while increasing the concentration of bradykinin, a vasodilator mediator. Affects the tissue renin-angiotensin system. Reduces the overall peripheral vascular resistance and arterial pressure (BP), pre- and postnagruzku, pressure in the pulmonary capillaries, does not affect the heart rate, while it is possible to increase the minute volume of the heart and increase blood flow in the kidneys. Expands arteries more than veins. Improves the blood supply of the ischemic myocardium. With prolonged use, myocardial hypertrophy and the walls of arteries of resistive type decrease. Increases the tolerance of the myocardium to physical exertion in patients with chronic heart failure. It plays a role in the restoration of endothelial function, damaged as a result of hyperglycemia.

    Increases life expectancy with chronic cardiac insufficiency.Slows the progression of left ventricular dysfunction after myocardial infarction, not complicated by heart failure.

    The hypotensive effect is observed after 1 hour after taking the drug inside, reaching a maximum after 6 hours. The duration of action depends on the dose and is 24 hours. For long-term treatment, the effectiveness does not decrease. With a sharp cessation of the treatment of the "withdrawal" syndrome with a sharp increase in blood pressure does not occur.

    Despite the primary effect, manifested in the effect on the renin-angiotensin-aldosterone system, it is effective in hypertension with low renin activity.

    Lizinopril reduces albuminuria not only due to lower blood pressure, but also as a result of changes in the hemodynamics of the glomerular apparatus and its tissue structure. Does not affect the concentration of glucose in the blood in patients with diabetes mellitus and does not increase the incidence of hypoglycemia.

    Amlodipine - blocker of "slow" calcium channels of the third generation, has antianginal and hypotensive action. Prevents the flow of calcium into the cells of the myocardium and, to a greater extent, into the smooth muscle cells of the vascular wall.Reduces the tone of smooth muscle arterioles, peripheral vascular resistance and, consequently, blood pressure. Has an antianginal effect due to the expansion of arterioles and arteries and a decrease in afterload. Reduces the need for oxygen and energy consumption of the myocardium, because does not cause reflex tachycardia. It is probably due to the expansion of the coronary arteries and arterioles that increases the supply of oxygen to the intact (especially with vasospastic angina) and ischemic areas of the myocardium. With angina pectoris improves the tolerance of exercise, prevents the development of an attack of angina and the formation of an ischemic interval of QT, reducing the frequency of angina attacks and the need for nitroglycerin. Does not affect the conductance and contractility of the myocardium. Has a long, dose-dependent hypotensive effect. Does not reduce the fraction of the ejection of the left ventricle. Reduces left ventricular hypertrophy. Has anti-sclerotic and cardioprotective effects in coronary heart disease. Its use against the background of therapy with digoxin, diuretics and ACE inhibitors does not increase the risk of death in patients with chronic heart failure (III-IV Art. by classification of NYHA).

    Slow absorption, wide distribution in the body and slow excretion provides a long-lasting effect, allowing the drug to be taken once a day. For more than 24 hours, it provides a clinically significant reduction in blood pressure in the "sitting" and "lying" positions. Action develops gradually, 2-4 hours after admission. It inhibits platelet aggregation, strengthens glomerular filtration, has a weak natriuretic effect, with diabetic nephropathy does not increase microalbuminuria.

    Does not have a negative effect on metabolic processes, does not change the concentration of plasma lipids. Can be prescribed to patients with concomitant bronchial asthma, diabetes and gout. The combination of lisinopril with amlodipine in a single medicine can prevent the development of possible undesirable effects caused by one of the active substances. Thus, the blocker of the "slow" calcium channels, directly expanding the arterioles, can lead to a delay in sodium and fluid in the body, and, consequently, can activate the renin-angiotensin-aldosterone system.The ACE inhibitor blocks this process, normalizes the reactions to load with salts.

    Pharmacokinetics:

    Lysinopril, unlike other ACE inhibitors, does not require activation in the liver, unchanged enters the systemic circulation and reaches its maximum concentration in the blood (90 ng / ml) 6 hours after ingestion. Absorption of 30% (6-60%), bioavailability of 29%. Communicates exclusively with ACE, is not metabolized, excreted unchanged in urine, half-life of 12.6 hours. After excretion of most of the free lisinopril, a fraction associated with ACE, providing a long-term therapeutic effect. Penetrates through blood-brain and placental barriers.

    Patients with renal insufficiency are prescribed in smaller doses because of impaired renal excretory function; dialysis.

    After ingestion amlodipine slowly and almost completely (90%) is absorbed from the gastrointestinal tract and reaches a maximum concentration 6-10 hours later. Equilibrium concentration is achieved on the 7-8th day of regular intake. Bioavailability of 64-80%. The distribution volume is approximately 20 l / kg.The connection with blood plasma proteins is 95-98%. Penetrates through the blood-brain barrier. Has the effect of "primary transmission", is extensively metabolized in the liver (90%). Most of it turns into a liver in an inactive metabolite. 10% of amlodipine excreted in the urine in an unmodified form, 60% - as metabolites, 20-25% - in the form of metabolites with bile through the intestine; penetrates into breast milk.

    The total clearance is 500 ml / min. The elimination consists of two phases, the half-life of the final phase is 35-50 h; not dialyziruetsya. The half-life in arterial hypertension - 48 hours in the elderly and 65 hours, with liver failure up to 60 hours.

    In young and elderly patients, the time to reach the maximum plasma concentration is approximately the same. In elderly patients, the clearance of amlodipine is somewhat lower, the elimination half-life and the area under the concentration-time curve (AUC) higher. Dose adjustment for elderly patients is not required.

    The interaction between amlodipine and lisinopril, which is part of the preparation Equator®, is unlikely. AUC, the time of reaching and the value of the maximum concentration, the half-lives do not undergo changes in comparison with the indices of each individual active ingredient.Eating does not affect the absorption of active substances. Long circulation in the body of both active substances makes it possible to take the drug 1 time per day.

    Indications:Essential hypertension (patients who are shown combined therapy).
    Contraindications:

    Hypersensitivity to any of the components of the drug or to other ACE inhibitors and dihydropyridine derivatives; angioedema in history, including those caused by the use of other ACE inhibitors, hereditary, or idiopathic angioedema; hemodynamically significant stenosis of the aorta or mitral valve or hypertrophic obstructive cardiomyopathy; severe arterial hypotension; cardiogenic shock; heart failure after acute myocardial infarction (within the first 28 days); unstable angina (with the exception of Prinzmetal's stenocardia); pregnancy; lactation period; age of 18 years (due to lack of data on the efficacy and safety of the drug in this age group, bilateral stenosis of the renal arteries, stenosis of the artery of a single kidney.

    Carefully:

    Cerebrovascular diseases (including cerebral circulatory insufficiency), coronary heart disease, severe bradycardia, tachycardia, chronic heart failure in the stage of decompensation, mild or moderate degree of arterial hypotension, severe autoimmune diseases (including scleroderma, systemic lupus erythematosus), oppression of bone marrow hematopoiesis, diabetes mellitus, hyperkalemia, condition after kidney transplantation, sodium-restricted diet, advanced age, renal and / or hepatic insufficiency, sinus node weakness syndrome, arterial hypotension.

    Pregnancy and lactation:

    Equator® is not recommended for use throughout the pregnancy period, as the risk of teratogenesis and fetotoxicity (decreased renal function, oligohydramnios, ossification of the skull) and neonatal toxicity (kidney failure, arterial hypotension, hyperkalemia) can not be ruled out. There are no well-controlled clinical studies on the use of Equator® in pregnant women.

    After detection of pregnancy, take Equator® immediately.Patients planning a pregnancy should consult a doctor so that they can recommend drugs with proven safety during pregnancy.

    Equator® is not recommended for use during lactation, because lisinopril can be excreted with human milk. There is no information on the penetration of amlodipine into breast milk.

    Dosing and Administration:

    Inside, regardless of food intake. The recommended dose is one tablet of Equator® daily. The maximum daily dose is one tablet of Equator®.

    Patients with renal insufficiency

    To determine the optimal starting and maintenance dose for patients with renal insufficiency, doses should be titrated and determine individually lisinopril and amlodipine. Equator® is indicated only for those patients in whom the optimal maintenance dose of lisinopril and amlodipine is titrated to 20 and 10 mg, respectively. During treatment with Equator®, it is necessary to monitor the kidney function, the content of potassium and sodium in the blood serum. In the case of impaired renal function, the equator® should be withdrawn and replaced with mono-preparations in adequate doses.

    Patients with hepatic insufficiency

    Excretion of amlodipine may be delayed in patients with impaired hepatic function. Clear recommendations on the dosage regimen in such cases are not established, therefore the preparation Equator® should be administered with caution in patients with hepatic insufficiency.

    Elderly patients (over 65 years of age)

    In clinical studies on the efficacy and safety of amlodipine or lisinopril in elderly patients, no changes were detected. To determine the optimal maintenance dose, it is necessary to determine the dosage regimen individually, using separately lisinopril and amlodipine. Equator® is indicated only for those patients in whom the optimal maintenance dose of lisinopril and amlodipine is titrated to 20 and 10 mg, respectively.

    Side effects:

    Side effects caused by a combination drug do not occur more often than in cases of taking each component separately. Most often: headache (8%), dry cough (5%) and dizziness (3%). Possible: weakness, diarrhea, nausea, vomiting, orthostatic hypotension, skin itching, skin rash, swelling of the ankles, redness of the skin of the face, pain in the breasts, arthralgia (1-3%), frequency of other adverse affects - less than 1%.

    With increased sensitivity, it is possible to develop aNguideurotic edema face, limbs, lips, tongue, epiglottis and larynx (0.1%). In such cases, immediately stop treatment and observe the patient until all symptoms disappear.

    From the laboratory indicators: hyperkalaemia, increased levels of creatinine, urea nitrogen, activity of "hepatic" enzymes and bilirubin of blood, especially in kidney disease, diabetes and renovascular hypertension.

    On the part of the organs of hematopoiesis: leukopenia, neutropenia, agranulocytosis (ACE inhibitor effect), thrombocytopenia, erythrocytopenia, with a prolonged treatment, a slight decrease in hemoglobin and hematocrit concentration is possible.

    From the side of the cardiovascular system: arrhythmias, increased heart rate, tachycardia, probably as a result of excessive blood pressure lowering in patients with a high risk of myocardial infarction, stroke, orthostatic hypotension, vasculitis, development or worsening of heart failure.

    From the side of the digestive tract: bowel dysfunction, dry mouth, abdominal pain, pancreatitis,hepatocellular or cholestatic jaundice, hepatitis, gingival hyperplasia, decreased appetite, nausea, vomiting, constipation, flatulence, dyspepsia, diarrhea, anorexia, thirst, gastritis.

    From the skin: urticaria, increased sweating, alopecia.

    From the genitourinary system: a violation of kidney function, frequent urination, painful urination, nocturia, dysuria, polyuria, oliguria, anuria, acute renal failure, uremia, proteinuria, impotence.

    From the immune system: lupus-like syndrome with the appearance of antinuclear antibodies, increased erythrocyte sedimentation rate (ESR) and arthralgia; myalgia; erythema multiforme; fever.

    From the central and peripheral nervous system: increased drowsiness, muscular fasciculation of the extremities and lips, asthenia, mood lability, confusion, sensation of heat and hot flushes to the skin of the face, increased fatigue, dizziness, headache, fainting, hypesthesia, paresthesia, peripheral neuropathy, insomnia, unusual dreams , nervousness, depression, anxiety, cramps, apathy, agitation, ataxia, amnesia.

    From the musculoskeletal system: muscle cramps, myalgia, back pain, arthrosis, myasthenia gravis.

    From the respiratory system: shortness of breath, rhinitis.

    Other: ringing in the ears, gynecomastia, increase / decrease in body weight, blurred vision, diplopia, disturbance of accommodation, xerophthalmia, conjunctivitis, eye pain, taste perversion, chills, nasal bleeding, dermatitis, parosmiya, dermatoxerasia, violation of skin pigmentation.

    Overdose:

    Symptoms: an overdose can cause excessive peripheral vasodilation with marked decrease in blood pressure, acute circulatory failure, disruption of water and electrolyte balance, renal failure, hyperventilation, tachycardia, bradycardia, dizziness, anxiety and cough.

    Treatment: symptomatic therapy, control of cardiac activity, blood pressure, diuresis and water-electrolyte balance, if necessary - its correction. With a pronounced decrease in blood pressure, the patient is given

    horizontal position with raised legs; with an unsatisfactory therapeutic response to intravenous administration of blood substitutes, it may be necessary to administer a peripheral vasopressor (dopamine) to support blood circulation.Intravenous administration of calcium gluconate can have a positive effect on the reverse development of effects caused by calcium channel blockade. If necessary, intravenous angiotensin injection II.

    Because of the slow absorption of amlodipine in some cases, the stomach is washed, used Activated carbon.

    Lizinopril is excreted by hemodialysis, but a strong bond with blood proteins makes amlodipine dialysis ineffective.

    Interaction:

    Lisinopril

    Substances affecting potassium concentration: potassium-sparing diuretics (for example, spironolactone, amiloride and triamterene), nutritional supplements with potassium, potassium-containing salt substitutes, and other medications that result in increased serum potassium levels (eg, heparin) can lead to hyperkalemia when combined with ACE inhibitors, especially in patients with renal insufficiency and other kidney disease in the anamnesis. When appointing a drug that affects the concentration of potassium, along with lisinopril, you should monitor the potassium concentration in the blood serum.Therefore, co-administration should be carefully justified and carried out with extreme caution and regular monitoring as the level of potassium in the blood serum and renal function. Potassium-sparing diuretics can be taken with Equator® only under medical supervision.

    Diuretics: in the case of diuretic administration to the patient receiving Equator®, the hypotensive effect is usually increased, caution should be taken with Equator® in combination with diuretics. Lisinopril softens the potassium -uretic effect of diuretics.

    Other antihypertensive drugs: simultaneous administration of these drugs can enhance the hypotensive effect of Equator®. Simultaneous reception with nitroglycerin, other nitrates or vasodilators can lead to a greater decrease in blood pressure.

    Tricyclic antidepressants / antipsychotics / general anesthetics / narcotic analgesics: Simultaneous administration with ACE inhibitors may lead to a greater decrease in blood pressure.

    Ethanol strengthens the hypotensive effect.

    Allopurinol, procainamide, cytostatics or immunosuppressants (systemic glucocorticosteroids) may lead to an increased risk of developing leukopenia when used concomitantly with ACE inhibitors.

    Antacids and colestramine with simultaneous administration with ACE inhibitors reduce the bioavailability of the latter.

    Sympathomimetics can reduce the hypotensive effect of ACE inhibitors; it is necessary to carefully monitor the achievement of the desired effect.

    Hypoglycemic drugs: while concomitant administration of ACE inhibitors and hypoglycemic drugs (insulin and hypoglycemic agents for oral administration) may increase the likelihood of reducing blood glucose and the risk of hypoglycemia. This phenomenon is most often observed during the first week of combined treatment and in patients with renal insufficiency.

    Non-steroidal anti-inflammatory drugs (NSAIDs): long-term administration of NSAIDs, including high doses of acetylsalicylic acid, more 3 g / day, can reduce the hypotensive effect of ACE inhibitors. The additive effect of NSAIDs and ACE inhibitors is manifested in an increase in serum potassium levels and can lead to impaired renal function. These effects are usually reversible.It is very rare to develop acute renal failure, especially in elderly patients and patients in a state of dehydration.

    Lithium: the elimination of lithium can be slowed down during simultaneous administration with ACE inhibitors and therefore, the concentration of lithium in serum should be monitored during this period. When combined with lithium preparations, it is possible to intensify the manifestation of their neurotoxicity (nausea, vomiting, diarrhea, ataxia, tremor, tinnitus).

    Preparations of gold: while simultaneous use of ACE inhibitors and gold preparations (sodium aurotomy malate) intravenously, a symptom complex including facial flushing, nausea, vomiting and arterial hypotension is described.

    Amlodipine

    Inhibitor inhibitors CYP3A4: studies among the elderly patients showed that diltiazem inhibits the metabolism of amlodipine, probably through CYP3A4 (plasma concentration increases by almost 50% and the effect of amlodipine increases). It is impossible to exclude the possibility that stronger inhibitors of the isoenzyme SURCA4 (i.e. ketoconazole, itraconazole, ritonavir) may increase the serum amlodipine concentration to a greater extent than diltiazem. Simultaneous use should be carried out with caution.

    Inductors of isoenzyme CYP3A4: simultaneous administration with anti-epidemic agents (for example, carbamazepine, phenobarbital, phenytoin, fosphenytoin, primidon), rifampicin, herbal preparations containing St. John's Wort (Nurepcit perforatum), may lead to a decrease concentration of amlodipine in blood plasma. Clinical control with possible correction of amlodipine dose during treatment with isoenzyme inducers CYP3A4 and after their cancellation. Simultaneous use should be carried out with caution.

    As a monotherapy amlodipine well combined with thiazide and loop diuretics, agents for general anesthesia, beta-blockers, ACE inhibitors, long-acting nitrates, sublingual nitroglycerin, digoxin, warfarin, atorvastatin, sildenafil, antacid drugs (aluminum hydroxide, magnesium hydroxide), simethicone, cimetidine, non-steroidal anti-inflammatory drugs, antibiotics and oral hypoglycemic agents.

    Amlodipine does not significantly affect the pharmacokinetics of ethanol.

    Calcium preparations can reduce the effect of blockers of "slow" calcium channels.

    Amlodipine does not cause significant changes in the pharmacokinetics of cyclosporine.

    It is possible to reduce the hypotensive effect of the Equator with simultaneous administration with estrogenic agents, adrenostimulators.

    Procainamide, quinidine and other drugs that extend the interval QT, can contribute to its considerable elongation.

    Special instructions:

    Arterial hypotension

    A marked decrease in blood pressure with the development of clinical symptoms may be observed in patients with a decrease in the volume of circulating blood and / or sodium content due to diuretics, fluid loss, or for other reasons, for example sweating, prolonged vomiting and / or diarrhea. In case of arterial hypotension, the patient should be laid and compensated for fluid loss (intravenous infusion of 0.9% sodium chloride solution), if necessary. Preferably, the recovery of fluid and / or sodium loss is performed prior to the initiation of Equator® treatment.It is necessary to monitor BP after taking the initial dose.

    Aortic and mitral stenosis

    Like all vasodilators, Equator® should be administered with caution to patients with obstruction of the left ventricular outflow tract and stenosis of the mitral valve.

    Impaired renal function

    In some patients with arterial hypertension without pronounced manifestations of renovascular diseases, an increase in creatinine and urea in the blood serum was observed, in most cases minimal or transitory, more pronounced with concurrent administration of ACE inhibitors and a diuretic. This is most typical for patients with a history of kidney disease.

    To determine the optimal maintenance dose, it is necessary to determine the dosage regimen on an individual basis, using separately lisinopril and amlodipine, with simultaneous monitoring of kidney function. Equator® is indicated only for those patients in whom the optimal maintenance dose of lisinopril and amlodipine is titrated to 20 and 10 mg, respectively.

    In the case of a decrease in renal function, the equator® should be withdrawn and replaced by monotherapy with drugs in adequate doses.In addition, a dose reduction or elimination of diuretics may be required.

    Angioedema

    Angioedema, swelling of the face, extremities, lips, tongue, vocal folds and / or larynx were recorded in patients taking inhibitors ACE, including lisinopril. In these cases, the taking of Equator® should be stopped immediately and the patient should be carefully monitored until the symptoms disappear completely.

    Edema of the face, lips and extremities usually pass independently, however, to reduce the severity of symptoms should use antihistamines.

    Angioedema, accompanied by swelling of the larynx, can lead to death. If you detect edema of the tongue, pharynx or larynx, which are the cause of airway obstruction, emergency measures should be urgently started. The appropriate measures include: subcutaneous injection of 0.3-0.5 mg or slow intravenous administration of 0.1 mg of a 0.1% solution of epinephrine (adrenaline), followed by intravenous administration of glucocorticosteroids and antihistamines and simultaneous monitoring of vital functions.

    Patients taking ACE inhibitors rarely had edema of the gastrointestinal tract. These patients complained of abdominal pain (with or without nausea and vomiting); in some cases, the previous edema was not observed and the activity of C-1 esterase was within normal limits. Angioedema has been diagnosed by computed tomography of the gastrointestinal tract, or after ultrasound, or during surgery, the symptoms disappeared after discontinuation of the ACE inhibitor. Edema of the gastrointestinal wall should be included in the differential diagnosis of abdominal pain in patients taking ACE inhibitors.

    Anaphylactic reactions in patients with hemodialysis

    In patients who underwent hemodialysis through a polyacrylonitrile membrane (for example, AN 69®) and which simultaneously produced ACE inhibitors, cases of anaphylactic shock have been reported, so this combination should be avoided. Patients are recommended to use either another type of dialysis membrane, or another type of antihypertensive drug.

    Anaphylactic reactions in patients during apheresis of low-density lipoproteins (LDL)

    Rarely, life-threatening anaphylactic reactions developed in patients who received ACE inhibitors during low density lipoprotein (LDL) apheresis (LDL) dextrin sulfate. Such reactions were prevented by abolishing the administration of ACE inhibitors prior to each apheresis procedure.

    Desensitization from aspen or bee venom

    Sometimes anaphylactic reactions developed in patients taking ACE inhibitors when desiccating the venom of Hymenoptera (eg, wasps or bees). Such life-threatening situations can be avoided with the timely withdrawal of ACE inhibitors.

    Hepatotoxicity

    In rare cases, the administration of ACE inhibitors was accompanied by a syndrome that began with cholestatic jaundice or hepatitis and developed into fulminant liver necrosis and in several cases resulted in death. The mechanism of this syndrome is unclear. Patients who receive Equator® and who develop jaundice or have an increased activity of "liver" enzymes should cancel Equator® and then monitor their condition.

    Liver failure

    In patients with impaired hepatic function, the half-life of amlodipine is longer. At the moment, recommendations on the dosage regimen have not been developed, in connection with which this medication should be administered with caution, having previously determined the expected benefit and the potential risk of treatment.

    Hematological toxicity

    In rare cases of patients receiving ACE inhibitors, neutropenia, agranulocytosis, thrombocytopenia, and anemia. In patients with normal renal function and in the absence of other aggravating factors, neutropenia is rare. Neutropenia and agranulocytosis are reversible and disappear after the withdrawal of the ACE inhibitor. Equator® should be used with extreme caution in patients with vascular collagen, immunosuppressive therapy, during treatment with allopurinol or procainamide, or a combination of these aggravating factors, especially if there is a previous impairment of renal function. Some of these patients developed serious infectious diseases, which in a few cases did not undergo correction with antibiotic therapy.When assigning the Equator®, it is recommended to periodically check the level of white blood cells in such patients, and also to warn them about the need to report the appearance of the first signs of an infectious disease.

    Cough

    Cough was often recorded during the use of ACE inhibitors. As a rule, cough is unproductive, permanent, and stopped after the drug was discontinued. With a differential diagnosis of cough, one must also consider the cough caused by the use of ACE inhibitors.

    Surgery / general anesthesia

    In patients who undergo extensive surgery or during general anesthesia with drugs leading to hypotension, lisinopril can block the formation of angiotensin II after compensatory release of renin. If the arterial hypotension, probably as a result of the above mechanism, it is possible to correct the increase in the volume of circulating blood.

    Elderly patients

    Older patients with impaired renal function should be corrected for the dose of Equator®.

    Hyperkalemia

    In some patients who received ACE inhibitors, an increase in the serum potassium level was observed.The risk group for the development of hyperkalemia is patients with renal insufficiency, diabetes mellitus, acute heart failure, dehydration, metabolic acidosis or with simultaneous admission potassium-sparing diuretics, food additives with potassium, potassium-containing salt substitutes or any other medical, drugs, leading to an increase in the serum potassium level (for example, heparin). If it is necessary to simultaneously take the above drugs, you need to monitor concentration of potassium in blood serum.

    Patients with low body weight, low growth patients and patients with severe liver dysfunction may need a dose reduction.

    Equator® does not have any adverse effect on the metabolism and lipids of the blood plasma and can be used in the treatment of patients with bronchial asthma, diabetes and gout.

    During treatment, it is necessary to control body weight and monitor the dentist (to prevent soreness, bleeding and gingival hyperplasia).

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

    Equator® can affect the ability to drive vehicles and complex machinery. Predominantly at the beginning of treatment, transient arterial hypotension and dizziness may occur. Therefore, at the beginning of treatment it is recommended to avoid driving vehicles, working with mechanisms and performing other work requiring concentration of attention.

    Form release / dosage:

    Tablets, 10 mg + 20 mg.

    Packaging:

    For 10 tablets in a blister of PVC / PE / PVDC - aluminum foil.

    For 1, 3 and 6 blisters in a cardboard box together with instructions for use.
    Storage conditions:

    Store in a dark place at a temperature of no higher than 25 ° C.

    Keep out of the reach of children!

    Shelf life:

    3 years.

    Do not use after the expiry date shown on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-006141/10
    Date of registration:30.06.2010
    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: & nbsp10.02.2015
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