Lisinopril-Teva, tablets 20 mg 30 pcs

Pharmacotherapeutic group: angiotensin-converting enzyme inhibitor
ATX code: C09AA03

Pharmacological properties

Pharmacodynamics. Angiotensin-converting enzyme (ACE) inhibitor, reduces the formation of angiotensin II from angiotensin I. Decreased angiotensin II leads to a direct reduction in aldosterone release. Reduces bradykinin degradation and increases prostaglandin synthesis. Reduces total peripheral vascular resistance (TPR), blood pressure (BP), preload, pulmonary capillary pressure, causes an increase in the minute blood volume and increases myocardial tolerance to exercise in patients with chronic heart failure. Dilates arteries more than veins. Some effects are attributed to effects on the renin-angiotensin-aldosterone system (RAAS). Long-term use reduces myocardial hypertrophy and resistive arterial wall hypertrophy. It improves the blood supply to the ischemic myocardium.

The ACE inhibitors prolong life expectancy in patients with chronic heart failure (CHF), slow the progression of left ventricular dysfunction in patients who have had acute myocardial infarction without clinical manifestations of heart failure. Onset of action of the drug is within 1 hour, the maximum antihypertensive effect is achieved after 6-7 hours and is maintained for 24 hours. The duration of the effect also depends on the dose taken. In arterial hypertension, the effect is noted in the first days after the start of treatment, a stable effect develops after 1-2 months of therapy. No pronounced increase in BP was observed when lisinopril was abruptly withdrawn.

Lisinopril reduces albuminuria. It does not affect blood glucose concentration in diabetic patients and does not lead to increased incidence of hypoglycemia.

Pharmacokinetics

Intake. After oral administration, lisinopril is absorbed from the gastrointestinal tract (GIT) by an average of 25%, but absorption can vary from 6 to 60%. The bioavailability is 29%. Maximum plasma concentration (Cmax) is reached after 7 h. Food intake does not affect absorption of lisinopril.

Distribution. Lisinopril binds insignificantly to plasma proteins. Permeability through the blood-brain barrier and the placental barrier is low.

Metabolism. Lisinopril is not biotransformed in the body.

Elimation. It is excreted unchanged by the kidneys. The elimination half-life (T1/2) is 12.6 hours. Lisinopril clearance is 50 ml/min. Decrease in serum concentration of lisinopril occurs in two phases. The bulk of lisinopril is excreted during the initial alpha phase (effective T1/2- 12 h), followed by the terminal distant beta phase (about 30 h).

Pharmacokinetics in selected patient groups

In patients with CHF the absorption and clearance of lisinopril are reduced and the bioavailability is 16%.

In patients with renal insufficiency (creatinine clearance (CK) less than 30 ml/min), lisinopril concentrations are several times higher than plasma concentrations in
healthy volunteers, with increased time to reach Cmax in plasma and increased T1/2.

In elderly patients the plasma concentrations of the drug and the area under the curve “concentration-time” are twice as high as in younger patients.

In patients with cirrhosis the bioavailability of lisinopril is reduced by 30% and clearance by 50% compared to patients with normal liver function.

Indications

Arterial hypertension (in monotherapy or in combination with other antihypertensive drugs).
Chronic heart failure (as part of combination therapy).
Early treatment of acute myocardial infarction (in the first 24 hours with stable hemodynamic parameters to maintain these parameters and prevent left ventricular dysfunction and heart failure).
Diabetic nephropathy (decreased albuminuria in patients with type 1 diabetes mellitus with normal blood pressure, and in patients with type 2 diabetes mellitus with arterial hypertension).

Pharmacological effect

Pharmacotherapeutic group: angiotensin-converting enzyme inhibitor
ATX code: C09AA03

Pharmacological properties

Pharmacodynamics. An angiotensin-converting enzyme (ACE) inhibitor, reduces the formation of angiotensin II from angiotensin I. A decrease in angiotensin II leads to a direct decrease in the release of aldosterone. Reduces the degradation of bradykinin and increases the synthesis of prostaglandins. Reduces total peripheral vascular resistance (TPVR), blood pressure (BP), preload, pressure in the pulmonary capillaries, causes an increase in minute blood volume and an increase in myocardial load tolerance in patients with chronic heart failure. Dilates arteries more than veins. Some effects have been attributed to effects on the renin-angiotensin-aldosterone system (RAAS). With long-term use, hypertrophy of the myocardium and the walls of resistive arteries decreases. Improves blood supply to ischemic myocardium.

ACE inhibitors extend life expectancy in patients with chronic heart failure (CHF) and slow the progression of left ventricular dysfunction in patients who have suffered acute myocardial infarction without clinical manifestations of heart failure. The onset of action of the drug is after 1 hour, the maximum antihypertensive effect is achieved after 6-7 hours and lasts for 24 hours. The duration of the effect also depends on the size of the dose taken. In case of arterial hypertension, the effect is observed in the first days after the start of treatment, a stable effect develops after 1-2 months. therapy. When lisinopril was abruptly discontinued, no significant increase in blood pressure was observed.

Lisinopril reduces albuminuria. Does not affect the concentration of glucose in the blood in patients with diabetes and does not lead to an increase in cases of hypoglycemia.

Pharmacokinetics

Suction. After oral administration, lisinopril is absorbed from the gastrointestinal tract (GIT) by an average of 25%, but absorption can vary from 6 to 60%. Bioavailability is 29%. The maximum concentration in blood plasma (Cmax) is reached after 7 hours. Food intake does not affect the absorption of lisinopril.

Distribution. Lisinopril is slightly bound to plasma proteins. Permeability through the blood-brain and placental barrier is low.

Metabolism. Lisinopril is not biotransformed in the body.

Excretion. It is excreted unchanged by the kidneys. The half-life (T1/2) is 12.6 hours. The clearance of lisinopril is 50 ml/min. The decrease in serum concentration of lisinopril occurs in two phases. The bulk of lisinopril is eliminated during the initial alpha phase (effective T1/2—12 hours), followed by the terminal late beta phase (about 30 hours).

Pharmacokinetics in selected patient groups

In patients with CHF, absorption and clearance of lisinopril are reduced, bioavailability is 16%.

In patients with renal failure (creatinine clearance (CC) less than 30 ml/min), the concentration of lisinopril is several times higher than the concentration in the blood plasma of
healthy volunteers, and there is an increase in the time to reach Cmax in the blood plasma and an increase in T1/2.

In elderly patients, the concentration of the drug in the blood plasma and the area under the concentration-time curve are 2 times greater than in young patients.

In patients with liver cirrhosis, the bioavailability of lisinopril is reduced by 30% and clearance by 50% compared to patients with normal liver function.

Special instructions

Most often, a pronounced decrease in blood pressure occurs when there is a decrease in blood volume caused by diuretic therapy, a decrease in the content of sodium chloride in food, dialysis, diarrhea or vomiting. Under the supervision of a physician, it is recommended to use the drug Lisinopril-Teva in patients with coronary artery disease, cerebrovascular insufficiency, in whom a sharp decrease in blood pressure can lead to myocardial infarction or stroke. The use of the drug Lisinopril-Teva can lead to impaired renal function, acute renal failure, which is usually irreversible even after discontinuation of the drug.

Transient arterial hypotension is not a contraindication for further use of the drug.

In case of renal artery stenosis (especially with bilateral stenosis or in the presence of stenosis of the artery of a single kidney), as well as with peripheral circulatory failure resulting from hyponatremia and hypovolemia, the use of the drug Lisinopril-Teva can lead to impaired renal function, acute renal failure, which is usually irreversible after discontinuation of the drug.

The drug Lisinopril-Teva can be used simultaneously with standard therapy for acute myocardial infarction (thrombolytics, acetylsalicylic acid as an antiplatelet agent, beta-blockers).

The drug Lisinopril-Teva can be used simultaneously with intravenous administration of nitroglycerin or with the use of therapeutic transdermal nitroglycerin systems.

The use of Lisinopril-Teva is not recommended in patients who have suffered acute myocardial infarction if systolic blood pressure does not exceed 100 mmHg. Art. During surgical interventions, as well as when using other drugs that cause a decrease in blood pressure, lisinopril, by blocking the formation of angiotensin II, can cause a pronounced, unpredictable decrease in blood pressure. Before surgery (including dental surgery), the surgeon/anesthesiologist should be informed about the use of an ACE inhibitor.

In elderly patients, the use of standard doses leads to higher concentrations of the drug in the blood, so special care is required when determining the dose, despite the fact that no differences in the antihypertensive effect of Lisinopril-Teva were found in elderly and young patients.
Since the potential risk of agranulocytosis cannot be excluded, periodic monitoring of peripheral blood is required.

Angioedema of the face, extremities, lips, tongue, epiglottis and/or larynx, which may occur during any period of treatment, has rarely been reported in patients taking an ACE inhibitor, including lisinopril. In this case, treatment with the drug should be stopped as soon as possible, and the patient should be monitored until symptoms completely regress. Angioedema with laryngeal edema can be fatal. Swelling of the tongue, epiglottis or larynx can cause airway obstruction, so appropriate therapy (0.3-0.5 ml of 1:1000 epinephrine (adrenaline) solution subcutaneously) and/or measures to ensure airway patency should be immediately carried out. In cases where the swelling is localized only on the face and lips, the condition most often goes away without treatment, but the use of antihistamines is possible. ACE inhibitors are more likely to cause the development of angioedema in patients of the Black race than in representatives of other races. The risk of developing angioedema is increased in patients who have a history of angioedema not associated with previous treatment with ACE inhibitors.

In extremely rare cases, patients taking ACE inhibitors during desensitization to hymenoptera venom may develop life-threatening anaphylactoid reactions. This can be avoided by temporarily stopping ACE inhibitor treatment before each Hymenoptera desensitization procedure. Anaphylactoid reactions have also been observed in patients on hemodialysis using high-flow dialysis membranes (AN69®) who are also taking ACE inhibitors. In such cases, the use of a different type of dialysis membrane or another antihypertensive agent should be considered. In patients receiving oral hypoglycemic agents and insulin, blood glucose should be regularly monitored during the first month of ACE inhibitor therapy.

Very rarely, when using ACE inhibitors, a syndrome was observed that began with cholestatic jaundice and progressed to fulminant liver necrosis, sometimes with death. The mechanism of development of this syndrome is unknown. If jaundice appears during the use of the drug Lisinopril-Teva or a marked increase in the activity of “liver” transaminases, the drug is discontinued and the patient’s condition is monitored.

Cough has been reported when using ACE inhibitors. The cough is dry and prolonged, which disappears after stopping treatment with an ACE inhibitor. In the differential diagnosis of cough, cough caused by the use of an ACE inhibitor must also be taken into account.

Impact on the ability to drive vehicles and machinery

Caution should be exercised when taking Lisinopril-Teva due to the possible development of arterial hypotension, dizziness and drowsiness, which may affect the ability to drive vehicles and work with potentially dangerous mechanisms.

Active ingredient

Lisinopril

Composition

1 tablet contains:

active substance: lisinopril dihydrate (lisinopril) – 21.84 mg (20.00 mg);

excipients: pregelatinized starch 12.00 mg, corn starch 40.00 mg, calcium hydrogen phosphate (anhydrous) 73.96 mg, mannitol 70.00 mg, magnesium stearate 2.20 mg.

Pregnancy

The use of Lisinopril-Teva during pregnancy is contraindicated. If pregnancy is diagnosed, the drug should be stopped as soon as possible. Taking ACE inhibitors in the second and third trimesters of pregnancy has an adverse effect on the fetus (a marked decrease in blood pressure, renal failure, hyperkalemia, hypoplasia of the skull bones, and intrauterine death are possible).

There is no data on the negative effect of the drug on the fetus when used in the first trimester.

For newborns and infants who have been exposed in utero to ACE inhibitors, it is recommended to conduct careful monitoring for timely detection of a pronounced decrease in blood pressure, oliguria, and hyperkalemia. There is no data on the penetration of lisinopril into breast milk. If it is necessary to use the drug Lisinopril-Teva during lactation, breastfeeding should be discontinued.

Contraindications

Hypersensitivity to lisinopril, other components of the drug or other ACE inhibitors; history of angioedema (including from the use of other ACE inhibitors); hereditary angioedema and/or idiopathic angioedema; age under 18 years (efficacy and safety have not been established); pregnancy and breastfeeding period.

With caution:
Bilateral renal artery stenosis or stenosis of the artery of a single kidney with progressive azotemia; condition after kidney transplantation; renal failure; hemodialysis using high-flow dialysis membranes (AN69®); azotemia; hyperkalemia; aortic stenosis; hypertrophic obstructive cardiomyopathy; primary hyperaldosteronism; arterial hypotension; cerebrovascular diseases (including cerebrovascular insufficiency); coronary heart disease (CHD); coronary insufficiency; autoimmune connective tissue diseases (including scleroderma, systemic lupus erythematosus); inhibition of bone marrow hematopoiesis; conditions accompanied by a decrease in circulating blood volume (CBV) (including as a result of diarrhea, vomiting); use in patients on a salt-restricted diet; in elderly patients; simultaneous use with potassium drugs, diuretics, other antihypertensive drugs, non-steroidal anti-inflammatory drugs (NSAIDs), lithium drugs, antacids, cholestyramine, ethanol, insulin, other hypoglycemic drugs, allopurinol, procainamide, gold drugs, neuroleptics, tricyclic antidepressants, barbiturates, beta-blockers, blockers slow calcium channels.

Side Effects

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

The incidence of side effects is classified according to the recommendations of the World Health Organization: very often – at least 10%; often – at least 1%, but less than 10%; infrequently – not less than 0.1%, but less than 1%; rarely – not less than 0.01%, but less than 0.1%; very rarely – less than 0.01%.

From the cardiovascular system: often – marked decrease in blood pressure, orthostatic hypotension; uncommon – acute myocardial infarction, tachycardia, palpitations; Raynaud’s syndrome; rarely – bradycardia, tachycardia, worsening symptoms of CHF, impaired atrioventricular conduction, chest pain.

From the central nervous system: often – dizziness, headache; uncommon – mood lability, paresthesia, sleep disturbances, stroke; rarely – confusion, asthenic syndrome, convulsive twitching of the muscles of the limbs and lips, drowsiness.

From the hematopoietic and lymphatic systems: rarely – decrease in hemoglobin, hematocrit; very rarely – leukopenia, neutropenia, agranulocytosis, thrombocytopenia, eosinophilia, erythropenia, hemolytic anemia, lymphadenopathy, autoimmune diseases, bone marrow suppression.

From the respiratory system: often – cough, infrequently – rhinitis, very rarely – sinusitis, bronchospasm, allergic alveolitis/eosinophilic pneumonia, shortness of breath.

From the digestive system: often – diarrhea, vomiting; uncommon – dyspepsia, taste changes, abdominal pain; rarely – dryness of the oral mucosa; very rarely – pancreatitis, jaundice (hepatocellular or cholestatic), hepatitis, liver failure, intestinal edema, anorexia.

From the skin: infrequently – itching, rash; rarely – angioedema of the face, limbs, lips, tongue, larynx, urticaria, alopecia, psoriasis; very rarely – increased sweating, vasculitis, pemphigus, photosensitivity, toxic epidermal necrolysis (Lyell’s syndrome), erythema multiforme, Stevens-Johnson syndrome.

From the urinary system: often – impaired renal function; uncommon – uremia, acute renal failure; very rarely – anuria, oliguria, proteinuria.

From the reproductive system: infrequently – impotence, rarely – gynecomastia.

Metabolism: very rarely – hypoglycemia.

From laboratory parameters: infrequently – increased concentration of urea in the blood, hypercreatininemia, hyperkalemia, increased activity of “liver” transaminases, rarely – hyperbilirubinemia, hyponatremia, increased erythrocyte sedimentation rate, false positive test results for antinuclear antibodies.

From the musculoskeletal system: rarely – arthralgia/arthritis, myalgia.

Other: rarely – when used simultaneously with gold preparations intravenously, a symptom complex has been described, including facial flushing, nausea, vomiting and decreased blood pressure (see section “Interaction with other drugs”).

Interaction

Lisinopril should be used with caution simultaneously with potassium-sparing diuretics (spironolactone, triamterene, amiloride, eplerenone), potassium supplements, salt substitutes containing potassium, cyclosporine – the risk of hyperkalemia increases, especially with impaired renal function. Therefore, these combinations should be used only on the basis of an individual physician’s decision with regular monitoring of serum potassium levels and renal function.

When used simultaneously with diuretics and other antihypertensive drugs, the antihypertensive effect of lisinopril is enhanced.

When used simultaneously with NSAIDs (including selective cyclooxygenase-2 (COX-2) inhibitors), acetylsalicylic acid at a dose of more than 3 g/day, estrogens, and sympathomimetics, the antihypertensive effect of lisinopril is reduced. NSAIDs, including COX-2, and ACE inhibitors increase serum potassium and may impair renal function. This effect is usually reversible. Lisinopril slows down the elimination of lithium preparations, therefore, with simultaneous use, there is a reversible increase in its concentration in the blood plasma, which may increase the likelihood of adverse events, so the concentration of lithium in the blood serum should be regularly monitored.

When used simultaneously with antacids and cholestyramine, the absorption of lisinopril from the gastrointestinal tract is reduced. Ethanol enhances the effect of lisinopril.

When used simultaneously with insulin and oral hypoglycemic agents, the risk of developing hypoglycemia increases.

When lisinopril is used simultaneously with vasodilators, barbiturates, antipsychotics (neuroleptics), tricyclic antidepressants, slow calcium channel blockers, beta blockers, the antihypertensive effect may be enhanced.

With the simultaneous use of ACE inhibitors and intravenous gold preparations (sodium aurothiamalate), a symptom complex has been described, including facial flushing, nausea, vomiting and decreased blood pressure.

Combined use with allopurinol, procainamide, and cytostatics can lead to leukopenia.

Overdose

Symptoms: marked decrease in blood pressure, dryness of the oral mucosa, water-electrolyte imbalance, renal failure, increased breathing, tachycardia, palpitations, bradycardia, dizziness, anxiety, increased irritability, cough, drowsiness, urinary retention, constipation, collapse, hyperventilation.

Treatment: there is no specific antidote. Gastric lavage, use of enterosorbents and laxatives. Intravenous administration of 0.9% sodium chloride solution is indicated. In case of treatment-resistant bradycardia, it is necessary to use an artificial pacemaker. Monitoring of blood pressure and water and electrolyte balance is necessary. Hemodialysis is effective.

Storage conditions

Store at a temperature not exceeding 25 °C. Keep out of the reach of children!

Shelf life

2 years. Do not use after expiration date.

Manufacturer

Teva LLC (Russia), Russia