Lysoretic, 10 mg+12, 5 mg tablets 28 pcs
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Lysoretic has an antihypertensive, diuretic effect.
Pharmacodynamics
Lysoretic is a combination of an angiotensin-converting enzyme inhibitor (lisinopril) and a diuretic (hydrochlorthiazide). It has antihypertensive and diuretic effects.
Lisinopril. ACE inhibitor, reduces the formation of angiotensin II from angeotensin I. Reduction of angeotensin II leads to a direct reduction of aldosierone release. Reduces bradykinin degradation and increases prostaglandin synthesis. Reduces total peripheral vascular resistance, blood pressure (BP), preload, pulmonary capillary pressure, causes an increase in the minute blood volume and increases exercise tolerance in patients with heart failure.
Dilates arteries to a greater extent than veins. Some effects are explained by the effect on tissue retin-angiotensin systems. Long-term use reduces myocardial hypertrophy and resistive arterial wall hypertrophy. It improves the blood supply to the ischemic myocardium. ACE inhibitors prolong life expectancy in patients with chronic heart failure, slow the progression of left ventricular dysfunction in patients who have had myocardial infarction without clinical manifestations of heart failure. Onset of action in 1 hour, the maximum effect is determined after 6-7 hours, the duration – 24 hours. In case of arterial hypertension, the effect is noted in the first days after the start of treatment, the stable effect develops after 1-2 months.
Hydrochlorothiazide. Thiazide diuretic, the diuretic effect of which is associated with disruption of reabsorption of sodium, chloride, potassium, magnesium and water ions in the distal nephron; it delays excretion of calcium and uric acid ions. It has antihypertensive properties; hypotensive effect is developed due to dilation of the arterioles.
It has practically no effect on normal blood pressure. Diuretic effect occurs after 1-2 hours, reaches maximum after 4 hours and lasts 6-12 hours.
Antihypertensive effect occurs after 3-4 days, but it may take 3-4 weeks to achieve optimal therapeutic effect. Lisinopril and hydrochlorthiazide, if used simultaneously, have an addetive antihypertensive effect.
Indications
Arterial hypertension (in patients who are indicated for combination therapy).
Composition
Active ingredients:
Lisinopril 10 mg;
Hydrochlorothiazide 12.5 mg;
Associates:
calcium hydrophosphate,
mannitol.
Corn starch,
Pre-salted starch,
Red iron oxide dye,
iron oxide dye yellow,
magnesium stearate,
purified water
How to take, the dosage
Take orally, once daily.
Arterial hypertension
1 tablet Lysoretic 10 mg) 12.5 mg once daily. If necessary, the dose can be increased to Lysoretic 20 mg +12.5 mg daily.
Doses in renal failure
In patients with a creatinine clearance of more than 30 and less than 80 ml/min, the drug can be used only after titrating the dose of individual drug components. The recommended starting dose of lisinopril in uncomplicated renal failure is 5-10 mg.
Pre-treatment with diuretics
Symptomatic hypotension may occur after the initial dose of the drug. These cases occur more frequently in patients who have had fluid and electrolyte loss due to prior diuretic treatment. Therefore, it is necessary to stop taking diuretics 2-3 days before starting treatment with Lysoretic.
Interaction
In concomitant use: with potassium-saving diuretics (spironolactone, triamterene, amiloride), potassium preparations, salt substitutes containing potassium – the risk of hyperkalemia increases, especially in patients with impaired renal function;
with vasodilators, barbiturates, phenothiazines, antidepressants, ethanol – the increase of hypotensive effect;
with non-steroidal anti-inflammatory drugs (indomethacin and others) – the increase of hypotensive effect.
with lithium preparations – slowing down the elimination of lithium from the body (intensification of cardiotoxic and neurotoxic effects of lithium);
with antacids and colestramine – reducing absorption in the gastrointestinal tract. It increases neurotoxicity of salicylates, weakens action of oral hypoglycemic agents, norepinephrine, epinephrine and antipodagric agents, increases effects (including side effects) of cardiac glycosides, effects of peripheral muscle relaxants, reduces excretion of quinidine.
It reduces effect of oral contraceptives.
Contraindications
Side effects
Cardiovascular system: marked decrease of blood pressure, chest pain, rarely – orthostatic hypotension, tachycardia, bradycardia, the appearance of symptoms of heart failure, atrioventricular conduction failure, myocardial infarction.
Gastrointestinal tract: nausea, vomiting, abdominal pain, dry mouth, diarrhea, dyspepsia, anorexia, change in taste, pancreatitis, hepatitis (hepatocellular and cholestatic), jaundice.
Nervous system disorders: mood lability, concentration disorders, paresthesias, increased fatigue, somnolence, convulsive twitching of muscles of extremities and lips, rarely – asthenic syndrome, confusion.
Respiratory system disorders – dyspnea, bronchospasm, apnea.
Skin disorders – urticaria, sweating, hair loss, photosensitization.
Allergic reactions: angioedema of the face, extremities, lips, tongue, epiglottis and/or larynx, skin rash, itching, fever, vasculitis, positive results for antinuclear antibodies, increased CRP, eosinophilia.
Hematopoietic disorders: leukopenia, thrombocytopenia, neutropenia, agranulocytosis, anemia (decrease of hemoglobin, hematocrit, erythrocytopenia). Urogenital system – uremia, oliguria/anuria, renal dysfunction, acute renal failure, decreased potency.
Laboratory measures: hyperkalemia and/or hypokalemia, hyponatremia, hypomagnesemia, hypochloremia, hyperuricemia, hyperglycemia, increased level of urea and creatinine, rarely – increased “liver” transaminases activity, hyperbilibinemia, hypercholesterolemia, hypertriglyceridemia, decreased glucose tolerance.
Other: dry cough, arthralgia/arthritis, myalgia, fetal renal impairment, gout exacerbation.
Overdose
Symptoms: pronounced BP decrease.
Treatment: induce vomiting and/or gastric lavage, symptomatic therapy aimed at correction of dehydration and impaired IBS. In case of arterial hypotension, administer isotonic solution. Monitoring of urea, creatinine and electrolytes in the blood serum, as well as diuresis.
Weight | 0.020 kg |
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Shelf life | 2 years |
Conditions of storage | In a dry, light-protected place at a temperature not exceeding 25 °C. |
Manufacturer | Ipka Laboratories Limited, India |
Medication form | pills |
Brand | Ipka Laboratories Limited |
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