Zhivaya Kaplya Ekolog (Drops) Instructions for Use

Marketing Authorization Holder

Mercana Service, LLC (Russia)

Manufactured By

Kurortmedservis, LLC (Russia)

Or Manufactured By

PLUTON-PHARM, JSC (Russia)

Dosage Form

Zhivaya Kaplya (Ekolog)

Oral drops: 25 ml, 50 ml, or 100 ml bottle

Dosage Form, Packaging, and Product Composition

Composition: hawthorn tincture, ascorbic acid, citric acid, Glutamic acid, Succinic acid, sodium benzoate, sweetener, glycerin, methylene blue, water.

25 ml – bottles with a dropper or mechanical dispenser.
50 ml – bottles with a dropper or mechanical dispenser.
100 ml – bottles with a dropper or mechanical dispenser.

Properties

Dietary supplement. Contributes to the improvement of the functional state of the cardiovascular system, improvement of microcirculation and blood supply to organs and tissues, resulting in increased oxygenation, nutrition, and elimination of metabolic products.

Contributes to the restoration of the normal form of hemoglobin. Contributes to increasing the resistance of the heart muscle to physical and nervous overload, weather changes, normalizes blood pressure.

Contributes to strengthening the body’s protection from the harmful effects of free radicals, promotes their elimination, helps to cope with aggressive environmental factors, increases the body’s adaptive capabilities.

Has a cytoprotective effect, accelerates reparative processes, has a beneficial effect on hematopoiesis and metabolic processes, reduces the toxic effect of biologically active substances.

Scope of Application

As a means to help improve the functional state of the cardiovascular system, in the complex therapy of patients with diabetes mellitus, metabolic syndrome, thyroid diseases and obesity, as an additional agent in the complex therapy of metabolic disorders.

ICD codes

Dosage Regimen

Orally, 2-3 times/day. The course is 3-4 weeks.

Side Effects

From the cardiovascular system and blood system: agranulocytosis (absence or pronounced decrease of granulocytes in peripheral blood), thrombocytopenia (decrease in platelet count), thrombocytosis (increase in platelet count), hyperprothrombinemia (increase in prothrombin in blood plasma), erythropenia (decrease in red blood cell count), neutrophilic leukocytosis (increase in white blood cell count), leukopenia, anemia (decrease in Hb), increased blood pressure, bradycardia, arrhythmia, angina pectoris.

From the nervous system and sensory organs: headache, agitation, irritability, increased excitability, insomnia, anxiety, weakness, dizziness, respiratory depression, tremor.

From the gastrointestinal tract: nausea, vomiting, diarrhea.

From metabolism: metabolic disorders, inhibition of glycogen synthesis, excessive formation of corticosteroids, sodium and water retention, hypokalemia.

From the genitourinary system: increase or decrease in diuresis, damage to the renal glomerular apparatus, formation of oxalate urinary stones.

Allergic reactions: skin rash, skin hyperemia.

Other: chills, short-term hyperthermia; irritation of the oral mucosa, cracks on the lips.

If any of the listed side effects worsen or other side effects not listed in the description appear, you must immediately inform your doctor.

Contraindications

Hypersensitivity to the product components; severe impairment of liver and kidney function (acute hepatitis, acute pyelonephritis, acute glomerulonephritis, or exacerbation of chronic diseases of these organs), nephrotic syndrome; gastric and duodenal ulcer; glaucoma; tendency to thrombosis; diseases of the hematopoietic system, anemia, leukopenia; diabetes mellitus; arterial hypertension, bradycardia, ventricular tachycardia, heart failure, conduction disorders, ventricular fibrillation, pronounced atherosclerosis, pronounced aortic stenosis, acute myocardial infarction; pheochromocytoma, hyperthyroidism, prostate hyperplasia; increased excitability; violently occurring psychotic reactions; obesity; simultaneous use of tricyclic antidepressants, beta-blockers, MAO inhibitors (including within 14 days after their withdrawal), drugs containing paracetamol; pregnancy; breastfeeding period; children under 18 years of age.

Use During Pregnancy and Lactation

Contraindicated for use during pregnancy and breastfeeding.

Special Instructions

This is not a medicinal product.

Consult your doctor before using the product.

Do not exceed the recommended dose of the product used.

In children, only dietary supplements intended for the corresponding age group should be used.

Products derived from plants, during long-term storage, especially with temperature fluctuations, are prone to cloudiness and sediment formation, which, however, does not affect the action of the product.

Drug Interactions

Simultaneous use of tricyclic antidepressants, beta-blockers, MAO inhibitors (including within 14 days after their withdrawal), drugs containing paracetamol is contraindicated.

Storage Conditions

Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.

Dispensing Status

Over-the-Counter

Important Safety Information

This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.