Active substanceLisinoprilLisinopril
Similar drugsTo uncover
  • Dapril®
    pills inwards 
    Medocemi Co., Ltd.     Cyprus
  • Diropress®
    pills inwards 
    Sandoz d.     Slovenia
  • Diroton®
    pills inwards 
    GEDEON RICHTER, OJSC     Hungary
  • Irumed®
    pills inwards 
  • Lizakard
    pills inwards 
  • Lizigamma®
    pills inwards 
  • Lisinopril
    pills inwards 
  • Lisinopril
    pills inwards 
    MEDISORB, CJSC     Russia
  • Lisinopril
    pills inwards 
    PRANAFARM, LLC     Russia
  • Lisinopril
    pills inwards 
    ZIO-HEALTH, JSC     Russia
  • Lisinopril
    pills inwards 
  • Lisinopril
    pills inwards 
    NIZHFARM, JSC     Russia
  • Lisinopril
    pills inwards 
    ALSI Pharma, ZAO     Russia
  • Lisinopril
    pills inwards 
    VERTEKS, AO     Russia
  • Lisinopril
    pills inwards 
    NIZHFARM, JSC     Russia
  • Lisinopril
    pills inwards 
  • Lisinopril
    pills inwards 
    Alkaloid, JSC     Macedonia
  • Lisinopril
    pills inwards 
  • Lisinopril
    pills inwards 
    OZONE, LLC     Russia
  • Lisinopril Grindeks
    pills inwards 
    GRINDEX, JSC     Latvia
  • Lizinopril Canon
    pills inwards 
  • Lysinopril Organica
    pills inwards 
    ORGANICS, JSC     Russia
  • Lisinopril-OBL
    pills inwards 
  • Lisinopril-Krka
    pills inwards 
  • Lizinopril-SZ
    pills inwards 
    NORTH STAR, CJSC     Russia
  • Lizinopril-Teva
    pills inwards 
  • Lysinate®
    pills inwards 
    Aktavis, AO     Iceland
  • Liziprex®
    pills inwards 
    IRBITSK HFZ, OJSC     Russia
  • Lizonorm
    pills inwards 
    Adifarm, EAD     Bulgaria
  • Lysoryl
    pills inwards 
  • Listril®
    pills inwards 
  • Liten®
    pills inwards 
    Boznalek, AO     Bosnia and Herzegovina
  • Rileys-sanovel
    pills inwards 
  • Dosage form: & nbsppills
    Composition:

    one tablet contains:

    active substance - lisinopril (in the form of lisinopril dihydrate) - 5 mg or 10 mg or 20 mg;

    Excipients: calcium hydrophosphate anhydrous - 40 mg or 50 mg or 100 mg, maiitol - 15 mg or 20 mg or 40 mg, corn starch - 36.06 mg or 34.91 mg or 69.83 mg, talc - 2.5 mg or 3 mg or 6 mg . magnesium stearate - 1 mg or 1.2 mg or 2.4 mg.

    Description:

    Tablets 5 mg: round, flat-cylindrical tablets of white color with a facet and with a risk.

    Tablets 10 mg: round, flat-cylindrical tablets of white color with a bevel. Tablets of 20 mg: round, flat cylindrical tablets of white color with a facet and with a risk.

    Pharmacotherapeutic group:Angiotensin-converting enzyme inhibitor
    ATX: & nbsp

    C.09.A.A.03   Lisinopril

    C.09.A.A   ACE Inhibitors

    Pharmacodynamics:

    The angiotensin-converting enzyme (ACE) inhibitor reduces the formation of angiotensin II from angiotensin I. Reducing angiotensin II leads to a direct reduction in the release of aldosterone. Reduces the degradation of bradykinin and increases the synthesis of prostaglandins. Reduces the overall peripheral vascular resistance, arterial pressure (BP), preload, pressure in the pulmonary capillaries, causes an increase in the minute volume of blood and increased tolerance to stress in patients with chronic heart failure. Expands arteries more than veins. Some effects are explained by the effect on tissue renin-angiotensin systems (RAAS). With prolonged use, the severity of myocardial hypertrophy and the walls of arteries of resistive type decreases. Improves the blood supply of the ischemic myocardium.

    ACE inhibitors prolong life expectancy in patients with chronic heart failure (CHF), slow the progression of left ventricular (LV) dysfunction in patients who underwent myocardial infarction without clinical manifestations of heart failure.

    The beginning of the hypotensive effect is after 1 hour. The maximum effect is determined 6-7 hours after ingestion, duration is 24 hours. In arterial hypertension, the effect is observed in the first days after the start of treatment, stable effect develops after 1-2 months of therapy. With a sharp withdrawal of the drug, there is a pronounced increase in blood pressure.

    Pharmacokinetics:Eating nis affects the absorption of lisinopril. Absorption - 30% (6-60%). Bioavailability - 29%. Poorly binds to blood plasma proteins. In unchanged form enters the systemic circulation. The time to reach the maximum concentration (TCmax) - 6 hours At a dose of 10 mg / day the maximum concentration is 32-38 ng / ml. Virtually does not undergo metabolism, is excreted by the kidneys in an unchanged form. The fraction associated with the ACE is output slowly. The half-life period (T1/2) -12.6 h. Permeability through the blood-brain and placental barrier is low.
    Indications:

    - Arterial hypertension (in monotherapy or in combination with other antihypertensive agents);

    - chronic heart failure (as part of combination therapy for patients taking cardiac glycosides and / or diuretics);

    - early treatment of acute myocardial infarction as part of combination therapy (within the first 24 hours with stable hemodynamic parameters to maintain these parameters and prevention of left ventricular dysfunction and heart failure);

    - Diabetic nephropathy (a decrease in albuminuria in patients with type 1 diabetes mellitus with normal BP, and in patients with type 2 diabetes with hypertension).

    Contraindications:

    - Hypersensitivity to lisinopril and other components of the drug, as well as to other ACE inhibitors;

    - angioedema in the anamnesis, incl. on the foyer of the use of ACE inhibitors;

    - Hereditary edema Quincke or idiopathic angioedema;

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

    - pregnancy (see section "Application during pregnancy and during breast-feeding");

    - the period of breastfeeding (see para.section "Application during pregnancy and during breast-feeding");

    - simultaneous use with aliskiren and aliskirenoderzhaschimi drugs in patients with diabetes mellitus or impaired renal function (glomerular filtration rate (GFR) <60 ml / mip / 1.73 m2) (see the sections "Special instructions" and "Interaction with other medicinal products").

    Carefully:Severe renal dysfunction, bilateral renal artery stenosis or arterial stenosis of a single kidney with progressive azotemia, condition after kidney transplantation, azotemia, hyperkalemia, aortic stenosis / mitral stenosis / hypertrophic obstructive cardiomyopathy, primary hyperaldosteronism, arterial hypotension, cerebrovascular diseases (including cerebral circulatory insufficiency), ischemic heart disease, CHF, autoimmune systemic connective tissue diseases (including scleroderma, syphilis emnaya lupus erythematosus); oppression of bone marrow hematopoiesis; diet with restriction of table salt; hypovolemic conditions (including as a result of diarrhea, vomiting); elderly age,hemodialysis using high-permeability dialysis membranes with high permeability, simultaneous use of potassium-sparing diuretics, potassium preparations, potassium-containing substitutes for dietary salt and lithium, diabetes mellitus, surgical intervention / general anesthesia, desensitization therapy, low density lipoprotein (LDL) apheresis, .
    Pregnancy and lactation:The use of Liziprex® during pregnancy is contraindicated. When diagnosing pregnancy, the drug should be stopped as soon as possible. Admission of ACE inhibitors in the II and III trimesters 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). Data on the negative effects of the drug lisinopril on the fetus in the case of application in the I trimester there. 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. Lisinopril penetrates the placenta.There is no data on the isolation of lisinopril in breast milk. If taking the drug is necessary during lactation, then breastfeeding should be canceled.
    Dosing and Administration:

    Inside, once a day in the morning, regardless of food intake, preferably at the same time.

    With arterial hypertension patients who receive other antihypertensive agents receive 5 mg once a day. In the absence of effect, the dose is increased every 2-3 days by 5 mg to an average therapeutic dose of 20-40 mg / day (increasing the dose above 40 mg / day usually does not lead to a further decrease in blood pressure). The usual daily maintenance dose is 20 mg. The maximum daily dose is 40 mg.

    The full effect usually develops in 2-4 weeks from the start of treatment, which should be taken into account when increasing the dose. With insufficient clinical effect, simultaneous use with other antihypertensive agents is possible.

    If the patient received pre-treatment with diuretics, the use of such drugs should be stopped 2-3 days before the Liziprex® drug is used. If this is not possible, the initial dose of Liziprex® should not exceed 5 mg per day.In this case, after taking the first dose, medical supervision is recommended for several hours (the maximum effect is reached after about 6 hours), since there may be a pronounced decrease in blood pressure.

    In chronic heart failure: the initial dose is 2.5 mg per day (recommended lisinopril in tablets of 2.5 mg), with a gradual increase in 3-5 days to 5-10 mg per day. The maximum daily dose is 20 mg. Acute myocardial infarction (as part of combination therapy): in the first 24 hours - 5 mg, then 5 mg every other day, 10 mg after two days and then but 10 mg once a day. The course of treatment - at least 6 weeks.

    When Renovascular hypertension or other conditions with increased activity of RAAS, it is also advisable to prescribe a low initial dose of 5 mg per day, under enhanced medical supervision (control of blood pressure, kidney function, potassium ion content in the blood serum). The maintenance dose, continuing strict medical control, should be determined depending on the dynamics of blood pressure.

    With renal insufficiency due to the fact that lisinopril the initial dose should be determined depending on the creatinine clearance.Further, the selection of doses should be made depending on individual reactions with regular monitoring of kidney function, potassium, sodium in the blood serum.

    Creatinine clearance ml / min

    Initial dose of mg / day

    30-70

    5-10

    10-30

    5

    (including patients on hemodialysis)

    With persistent arterial hypertension, prolonged maintenance therapy of 10-15 mg / day is shown.

    Diabetic Nephropathy: In patients with type 2 diabetes mellitus, 10 mg of Lizierex® is administered once a day. The dose may, if necessary, be increased to 20 mg once a day in order to achieve diastolic blood pressure values ​​below 75 mmHg. in the "sitting" position. In patients with type 1 diabetes mellitus, the dose is the same, in order to achieve diastolic blood pressure values ​​below 90 mm Hg. in the "sitting" position.

    Side effects:

    The incidence of side effects is characterized as often (≥ 1%), rarely (<1%).

    The most common side effects: dizziness, headache, fatigue, diarrhea, dry cough, nausea.

    From the cardiovascular system: often - marked decrease in blood pressure, orthostatic hypotension; rarely - pain in the chest,tachycardia, bradycardia, aggravation of symptoms of chronic heart failure, violation of atrioventricular conduction, myocardial infarction.

    From the central nervous system: often - paresthesia, lability of mood, confusion, drowsiness, convulsive twitching of the muscles of the limbs and lips, rarely - asthenic syndrome.

    From the hematopoiesis: rarely - leukopenia, neutropenia, agranulocytosis, thrombocytopenia, with long-term treatment - anemia (reduction of hemoglobin, hematocrit, erythropenia).

    From the respiratory system: rarely shortness of breath, bronchospasm.

    From the digestive system: rarely - dryness of the oral mucosa, anorexia, dyspepsia, changes in taste, abdominal pain, pancreatitis, jaundice (genotocellular or cholestatic), hepatitis.

    From the skin: rarely - urticaria, pruritus, increased sweating, alopecia, photosensitivity.

    From the genitourinary system: rarely - renal dysfunction, oliguria, anuria, acute renal failure, uremia, proteinuria, sexual dysfunction.

    Laboratory indicators: often - hyperkalemia, hyponatremia; rarely - hyperbilirubinemia, increased activity of "hepatic" enzymes, hypercreatininaemia, increased concentrations of urea and creatinine.

    Allergic reactions: rarely angioedema, swelling of the face, limbs, lips, tongue, epiglottis and / or larynx, skin rashes, itchy skin, fever, false positive antinuclear antibody test results, increased erythrocyte sedimentation rate (ESR), eosinophilia, leukocytosis. In rare cases, there is an intestinal angioedema.

    Other: rarely - arthralgia / arthritis, vasculitis, myalgia.

    If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.

    Overdose:

    Symptoms (occur when taking a single dose of 50 mg): marked decrease in blood pressure, dryness of the oral mucosa, drowsiness, urinary retention, constipation, anxiety, increased irritability.

    Treatment: there is no specific antidote. Symptomatic therapy. Gastric lavage, application of enterosorbents and laxatives.Intravenous introduction of 0.9% sodium chloride solution was shown. In the case of a sustained bradycardia, the use of an artificial pacemaker is necessary. It is necessary to monitor blood pressure, indicators of water-electrolyte balance. Hemodialysis is effective.

    Interaction:

    With the simultaneous use of the drug with potassium-sparing diuretics (spironolactone and its derivative - eplerenone, triamterene, amiloride), potassium preparations, salt substitutes containing potassium, cyclosporine, increases the risk of hyperkalemia, especially with impaired renal function, so they can only be used together with regular monitoring of serum potassium and night function.

    Simultaneous use with bsta-adrenoblockers, blockers of "slow" calcium channels (BCCC), diuretics, tricyclic antidepressants / yerileptics and other antihypertensive agents increases the severity of antihypertensive action.

    Lizinopril slows down the excretion of lithium preparations. Therefore, when combined, it is necessary to regularly monitor the concentration of lithium in the blood serum.

    Antacids and colestramine reduce the absorption of lisinopril in the gastrointestinal tract.

    Hypoglycemic agents (insulin, hypoglycemic agents for oral administration) The use of ACE inhibitors can enhance the hypoglycemic effect of insulin and hypoglycemic agents for ingestion up to the development of hypoglycemia. As a rule, this is observed in the first weeks of simultaneous therapy and in patients with impaired renal function.

    Non-steroidal anti-inflammatory drugs (NSAIDs) (including selective inhibitors of cyclooxygenase-2 (COX-2)), estrogens, adrenomimetics reduce the antihypertensive effect of lisinopril. Simultaneous use of ACE inhibitors and NSAIDs can lead to impaired renal function, including the development of acute renal failure, and an increase in serum potassium, especially in patients with reduced renal function. Care should be taken when prescribing this combination, especially in elderly patients. Patients should receive an adequate amount of fluid, and it is recommended that the kidney function be carefully monitored, both at the beginning and during the treatment.

    With simultaneous use of ACE inhibitors and preparations of gold intravenously (sodium aurotomy malate) describes a symptom complex, which includes facial flushing, nausea, vomiting and lowering blood pressure.

    Joint application with selective serotonin reuptake inhibitors can lead to pronounced hyponatrism.

    Joint application with allopuripol, procainamide, cytostatics can lead to leukopenia.

    Double blockade of RAAS

    In the literature it was reported that in patients with established atherosclerotic disease, heart failure or diabetes with target organ damage, simultaneous therapy with an ACE inhibitor and angiotensin II receptor antagonists (ARA II) is associated with a higher incidence of arterial hypotension, syncope, hyperkalemia and worsening kidney function (including acute renal failure) compared with the use of only one drug that affects RAAS. Double blockade (for example, with the combination of an ACE inhibitor with APA II) should be limited to individual cases with careful monitoring of kidney function, potassium and blood pressure.

    Simultaneous use is contraindicated (cm.section "Contraindications")

    Aliskiren

    In patients with diabetes mellitus or renal dysfunction (GFR less than 60 mL / min), the risk of hyperkalemia, impaired renal function, and increased incidence of cardiovascular morbidity and mortality increases.

    Estramustine

    Simultaneous application can lead to an increased risk of side effects, such as angioedema.

    Baclofen

    Strengthens the antihypertensive effect of ACE inhibitors. You should carefully monitor blood pressure and, if necessary, dosage of antihypertensive medications.

    Glyptins (linaglyptin, saxagliptin, sitagliptin, vitagliptin)

    Co-administration with ACE inhibitors may increase the risk of developing angioedema due to suppression of dipeptidylpentidase IV (DPP-IV) by glyptin.

    Sympathomimetics

    May weaken the antihypertensive effect of ACE inhibitors.

    Tricyclic antidepressants, antipsychotics (antipsychotics) and means for general anesthesia

    Simultaneous use with ACE inhibitors can lead to an increase in antihypertensive action (see section "Special instructions").

    Special instructions:

    Symptomatic arterial hypotension

    Most often, a marked decrease in blood pressure occurs with a decrease in the volume of circulating blood (BCC), caused by diuretic therapy, a decrease in the amount of salt in the diet, dialysis, diarrhea, or vomiting. In patients with chronic heart failure with or without renal insufficiency, a marked decrease in blood pressure is possible.

    Under the strict supervision of a doctor, Liziprex® should be used for patients with coronary heart disease, cerebrovascular insufficiency, in whom a sharp decrease in blood pressure can lead to myocardial infarction or to a stroke.

    Transient arterial hypotension ns is a contraindication for taking the next dose of the drug. In the case of development of arterial hypotension the patient should be transferred to the "lying" position with raised legs. If necessary, BCC should be filled with intravenous 0.9% sodium chloride solution. Transient arterial hypotension ns is an obstacle for further administration of the drug. After the recovery of bcc and blood pressure, treatment can be continued.

    When using the drug Liziprex ®, in some patients with chronic heart failure, but with normal or low blood pressure. there may be a decrease in blood pressure. which is usually not the reason for discontinuing treatment.

    Prior to drug treatment, if possible, should be to normalize the sodium content and / or make up the bcc carefully control action Lizipreks® starting dose of the drug to the patient.

    In the case of renal artery stenosis (especially when bilateral stenosis or in the presence of artery stenosis single kidney) and circulatory failure due to lack of sodium and / or liquid, use Lizipreks® drug can lead to renal failure, acute renal failure, which is usually irreversible even after the drug is discontinued.

    Hyperkalemia

    Hyperkalemia can develop during treatment with ACE inhibitors, including Liziprex®. Risk factors for hyperkalemia include renal failure, decreased renal function, age over 70 years, diabetes mellitus, certain concomitant conditions (dehydration, acute heart failure, metabolic acidosis), simultaneous intake of potassium-sparing diuretics (such as spironolactone and its derivative, epsilon, triamtrins, amiloride), food additives / potassium preparations or potassium-containing substitutes for edible salt, as well as the use of other drugs that increase the potassium content in the blood (for example, heparin). The use of dietary supplements / potassium preparations, potassium-sparing diuretics, potassium-containing substitutes for edible salt can lead to a significant increase in potassium in the blood, especially in patients with reduced renal function. Hyperkalemia can lead to serious, sometimes fatal heart rhythm disturbances. If simultaneous use of the drug Liziprex® and the above drugs is necessary, treatment should be carried out with caution in the context of regular monitoring of potassium in the blood serum (see section "Interaction with other drugs").

    Mitral stenosis / aortic stenosis / hypertrophic obstructive cardiomyopathy

    Liziprex®, like other ACE inhibitors, should be administered with caution to patients with obstruction of the left ventricular outflow tract (aortic stenosis, hypertrophic obstructive cardiomyopathy), as well as to patients with mitral stenosis.

    With acute myocardial infarction

    The use of standard therapy (thrombolytics, acetylsalicylic acid as an antiaggregant agent, beta-blockers). Liziprks® can be used together with intravenous administration or with the use of therapeutic transdermal systems of nitroglycerin.

    Surgery / general anesthesia

    With extensive surgical interventions, as well as with the use of other drugs that cause a decrease in blood pressure, lisipopril, blocking the formation of angiotensin II, can cause a pronounced unpredictable decrease in blood pressure.

    With the development of arterial hypotension, blood pressure should be maintained by replenishing the BCC. It is necessary to alert the surgeon / anesthesiologist that the patient is taking ACE inhibitors.

    In elderly patients the same dose leads to a higher concentration of lisinopril in the blood, therefore special caution is required when determining the dose.

    Hemodialysis

    In patients under hemodialysis using high-permeability membranes (for example, AN69®), cases of anaphylactic reactions against ACE inhibitor therapy were observed.The use of ACE inhibitors should be avoided when using this type of membrane.

    Neutropy / agranulocytosis / thrombocytopaedy / anemia

    Against the background of taking ACE inhibitors, neutropenia / agranulocytosis, thrombocytopenia and anemia can occur. In patients with normal renal function and in the absence of other aggravating factors, neutropenia develops rarely. With particular caution, Liziprex® should be used in patients with systemic connective tissue diseases, when immunosuppressants, allopurinol or procainamide are used, especially in patients with impaired renal function. Some patients had severe infections, in some cases, resistant to intensive antibiotic therapy. When prescribing Liziprex®, it is recommended that such patients periodically check the white blood cell count. Patients should inform the doctor of any signs of infectious diseases (eg, sore throat, fever).

    Anaphylactoid reactions during apheresis of low density lipoproteins (LDL)

    In rare cases in patients receiving ACE inhibitors, during the procedure of apheresis of LDL with the use of dextran sulfate may develop life threatening anaphylactoid reactions. To prevent anaphylactoid reaction, therapy with an ACE inhibitor should be temporarily discontinued before each apheresis procedure.

    Anaphylactoid reactions during desensitization

    There are some reports of the development of anaphylactoid reactions in patients receiving ACE inhibitors during desensitizing therapy, for example, by the venom of Hymenoptera. ACE inhibitors should be used with caution in patients prone to allergic reactions undergoing desensitization procedures. The use of ACE inhibitors should be avoided for patients receiving immunotherapy with bee venom. However, this reaction can be avoided by the temporary withdrawal of the ACE inhibitor before the desensitization procedure begins.

    Hypersensitivity / angioedema

    When taking ACE inhibitors, including the drug Liziprex®, in rare cases and in any period of therapy, development of angioedema of the face, upper and lower extremities, lips, mucous membranes, tongue, vocal cords and / or larynx can be observed (see section "Side effect").When symptoms appear, taking the drug should be stopped immediately, and the patient should be observed until the signs of edema disappear completely. If the swelling affects only the face and lips, then its manifestations usually pass on their own, although antihistamines can be used to treat the symptoms.

    Angioedema, accompanied by swelling of the larynx, can lead to death. Swelling of the tongue, vocal cords, or larynx can lead to airway obstruction. When these symptoms appear, urgent therapy is required, including subcutaneous injection of epinephrine (adrenaline) and / or providing airway patency. The patient should be under medical supervision until the symptoms disappear completely and persistently.

    Patients with a history of Quinck's edema who are not associated with taking ACE inhibitors may be at increased risk of developing this drug when taking this drug (see "Contraindications").

    In rare cases, angiotoneurotic edema of the intestine develops in the foyer of therapy with ACE inhibitors. In this case, patients have abdominal pain as an isolated symptom or in combination with nausea and vomiting,in some cases without a prior angioedema and at a normal level of C1-esterase. The diagnosis was established using computed tomography of the abdominal region, ultrasound examination or surgical intervention. Symptoms disappeared after discontinuation of ACE inhibitors. Therefore, patients with abdominal pain receiving ACE inhibitors should take into account the possibility of angioedema edema development during differential diagnosis (see section "Side effect").

    Kidney Transplantation

    Data on the use of Liziprex® in patients after kidney transplantation are not available.

    Ethnic differences

    It should be borne in mind that in patients of the Negroid race the risk of angioedema development is higher. Like other ACE inhibitors, Liziprex® is less effective in reducing blood pressure in patients of the Negroid race.

    This effect is probably associated with a marked predominance of low-grade status in patients of the Negroid race with arterial hypertension.

    Impaired liver function

    In rare cases, when taking ACE inhibitors, there was a syndrome of cholestatic jaundice with transition tofulminant liver necrosis, sometimes fatal. The mechanism of development of this syndrome is unclear. If there is jaundice or a significant increase in the activity of "liver" enzymes on the foyer of ACE inhibitors, the drug should be stopped (see the "Side effect" section), the patient should be under appropriate medical supervision.

    Double blockade of RAAS

    Arterial hypotension, fainting, stroke, hyperkalemia and renal dysfunction (including acute renal failure) have been reported in susceptible patients, especially when used with medications that affect this system. Therefore, a double blockade of RAAS due to a combination of an ACE inhibitor with ARA II or aliskiren is not recommended.

    The combination with aliskiren is contraindicated in patients with diabetes mellitus or renal dysfunction (GFR <60 ml / min / 1.73 m2 "Contraindications" and "Interaction with other medicinal products").

    Patients with diabetes mellitus

    When the drug is prescribed for patients with diabetes mellitus, who receive hypoglycemic agents for ingestion or insulin,during the first month of therapy, it is necessary to regularly monitor the concentration of glucose in the blood (see section "Interaction with other medicinal products").

    Effect on the ability to drive transp. cf. and fur:Liziprex® should be used with caution in patients who manage motor vehicles and engage in activities that require increased concentration and speed of response, due to the risk of developing arterial hypotension and dizziness.
    Form release / dosage:Tablets of 5 mg or 10 mg or 20 mg.
    Packaging:

    10 tablets per contour cell pack.

    For 30 tablets in a jar of polymer materials.

    3 contour mesh packages or a can of polymeric materials with the instruction for medical use are placed in a pack of cardboard.

    Storage conditions:

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

    Keep out of the reach of children.

    Shelf life:

    2 years.

    Do not use after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-003008
    Date of registration:01.06.2015
    Expiration Date:01.06.2020
    The owner of the registration certificate:IRBITSK HFZ, OJSC IRBITSK HFZ, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp24.02.2018
    Illustrated instructions
      Instructions
      Up