Instructions Cardiolin drops for oral use bottle 50 ml
Composition
active ingredient: tincture of medicinal plant raw materials: adonidus vernalis (Herba adonidus vernalis), common juniper fruit (Fructus juniperi communis), arnica flowers (Arnicae flos), peppermint leaves (Menthae piperitae folium);
1 bottle of drops contains tinctures of medicinal plant raw materials (1:12.5): adonidus vernalis (Herba adonidus vernalis), juniper fruit (Fructus juniperi communis), arnica flowers (Arnicae flos), peppermint leaves (Menthae piperitae folium) (extractant – 40% ethanol) – 30 ml or 50 ml;
1 ml of the drug contains 0.35 ml of ethanol.
Dosage form
Drops for oral use.
Main physicochemical properties: clear light brown liquid with a pleasant odor.
Pharmacotherapeutic group
Combined cardiological drugs. ATX code C01E X.
Pharmacological properties
Pharmacodynamics.
In functional heart disorders, the drug has a cardioprotective and antioxidant effect.
Cardiolin is a combined preparation containing an extract of medicinal plants: adenium vernum herb, which has a mild diuretic, sedative effect and antiarrhythmic properties; juniper berries, which have a diuretic effect; arnica flowers, which have cardioprotective activity; mint leaves, which exhibit moderate antispasmodic, sedative, choleretic activity.
The drug has a positive effect on metabolism in the myocardium and liver, in particular, it inhibits lipid peroxidation processes, increases the activity of antioxidant enzymes, the energy balance of cells, stimulates the synthesis of adenyl nucleotides, glycogenolysis, and increases the activity of a number of Krebs cycle enzymes.
The drug has a mild sedative effect, reduces the manifestations of diencephalic disorders, improves the tolerance of physical exertion, and helps increase performance.
Indication
In the complex treatment of neurocirculatory dystonia, cardiac neuroses, ischemic heart disease (angina pectoris I–II FC).
Contraindication
Depression, history of alcoholism, simultaneous use of drugs containing alcohol, gastric and duodenal ulcers, liver cirrhosis, taking neuroleptics and tranquilizers, hypersensitivity to the components of the drug, severe bradycardia, atrioventricular block, glycoside intoxication, WPW syndrome, severe kidney disease.
Interaction with other medicinal products and other types of interactions
Concomitant use with cardiac glycosides is undesirable, as the drug contains adenium herb and possible manifestations of toxicity.
Since the drug Cardiolin contains 40% ethyl alcohol and adenium herb, potentiation of the effects of hypnotics, tranquilizers, sedatives, neuroleptics is possible, and the drug can also enhance the cardiotonic effect and toxicity of cardiac glycosides.
When used simultaneously with class IA antiarrhythmics (quinidine, procainamide, disopyramide), calcium preparations, laxatives, and glucocorticosteroids, their effect and toxicity are enhanced.
Application features
During treatment with the drug, you should refrain from drinking alcoholic beverages.
Patients with gastroesophageal reflux should not use the drug, as heartburn may worsen.
Patients with gallstone disease and other diseases of the biliary tract should use the drug with caution.
Use during pregnancy or breastfeeding.
Use is contraindicated.
The ability to influence the reaction speed when driving vehicles or other mechanisms.
During the period of use of the drug, it is forbidden to drive a car and work with potentially dangerous mechanisms.
Method of administration and doses
Adults take 20–30 drops orally 2–3 times a day 30 minutes before or 1 hour after meals. The drug can be diluted with water in a ratio of 1:3 or 1:5.
The duration of the treatment course is determined by the doctor individually; the average duration is 20–30 days.
Children.
There is no experience in children.
Overdose
With a significant increase in the dose, drowsiness, dyspeptic disorders, and allergic reactions are possible, requiring discontinuation of the drug and symptomatic therapy.
Side effects
Cardiolin may cause hypersensitivity reactions, dyspeptic disorders, nausea, vomiting, abdominal pain, constipation, diarrhea, drowsiness, increased diuresis, sweating, chills.
Expiration date
2 years.
Do not use the drug after the expiration date indicated on the package.
Storage conditions
Store in original packaging at a temperature not exceeding 25 °C. Keep out of reach of children. Sedimentation may occur during storage.
Packaging
30 ml or 50 ml in a bottle. 1 bottle in a cardboard pack.
Vacation category
Without a prescription.
Producer
PrJSC "Biolik".
Address
Ukraine, 02660, Kyiv, Starosilska St., Building 1 U.
Applicant
LLC "Ukrainian Pharmaceutical Company".
