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Dvatse

Remedies for coughs and colds. Mucolytics. Acetylcysteine.

APPROVED

by the Order of the Ministry of Health of Ukraine

15.06.2020 No. 1394

Marketing Authorization

No. UA/18138/01/01

PACKAGE LEAFLET

for medical use of a medicinal product

Dvatse 200

Qualitative and quantitative composition:

active substance: аcetylcysteine;

1 tablet contains 200 mg of acetylcysteine;

list of excipients: maltodextrin, anhydrous citric acid, sodium bicarbonate, orange flavor, leucine, sodium saccharin.

Pharmaceutical form. Effervescent tablets.

Main physical and chemical properties: white on almost white, round tablets with a flat surface.

Pharmacotherapeutic group. Expectorants, excl. combinations with cough suppressants Mucolytics. Acetylcysteine. ATC code R05C B01.

Pharmacological properties.

Pharmacodynamic properties.

N-acetyl-L-cysteine (AC) has a pronounced mucolytic effect on mucous and mucopurulent secretions due to depolymerization of mucoprotein complexes and nucleic acids, which give viscosity to the hyaline and purulent components of sputum and other secretions. Additional properties: a decrease in induced hyperplasia of mucocytes, an increase in surfactant production due to stimulation of type II pneumocytes, stimulation of the activity of the mucociliary apparatus, improves mucociliary clearance.

AC also has a direct antioxidant effect due to the presence of a nucleophilic free thiol group (SH), which is able to interact directly with the electrophilic groups of oxidative radicals. Interesting fact, that AC prevents inactivation of a-1-antitrypsin, an enzyme that inhibits elastase, by hydrochloric acid (HOCl) – a strong oxidant produced by the myeloperoxidase of active phagocytes.

In addition, the molecular structure of AC allows it to easily penetrate cell membranes. Inside the cell, AC is deacetylate to form L-cysteine, an essential amino acid for glutathione synthesis. In addition, AC, which is a precursor of glutathione, has an indirect antioxidant effect. Glutathione is a highly active tripeptide, distributed in various tissues of animals and essential for maintaining the functional capacity of the cell and its morphological integrity. In fact, it is part of the most important intracellular defense mechanism against oxidative radicals, both exo- and endogenous and some cytotoxic substances, including paracetamol.

Paracetamol has a cytotoxic effect by progressively reducing glutathione content. AC plays a primary role in maintaining adequate levels of glutathione, enhancing cellular defenses. As a result, AC is a specific antidote for paracetamol poisoning.

In patients with chronic obstructive pulmonary disease, intake of 1200 mg of AC per day for 6 weeks led to a significant increase in inspiratory volume and forced vital capacity of the lungs, possibly due to a decrease in air entrapment.

In patients with idiopathic pulmonary fibrosis (IPF), the use of acetylcysteine orally at 600 mg 3 times a day for one year in combination with standard IPF therapy (prednisolone and azathioprine) contributed to the preservation of vital capacity and diffuse lung capacity as measured by the method of a single inhalation of carbon monoxide.

In the form of inhalation therapy for one year, AC contributed to a decrease in the intensity of disease progression in patients with IPF.

When it used in very high doses (up to 3000 mg daily for 4 weeks) in patients with cystic fibrosis AC did not have a significant toxic effect.

The antioxidant efficacy of AC is associated with a marked decrease in sputum elastase activity, which is the most significant indicator of lung function in patients with cystic fibrosis. In addition, against the background of treatment, there was a decrease in the number of neutrophils in the respiratory tract, as well as the number of neutrophils, actively secreting elastase-rich granules.

Pharmacokinetic properties.

Absorption:

In humans, after oral administration, acetylcysteine is completely absorbed. Due to intestinal metabolism and the first-pass effect, the bioavailability of acetylcysteine when administered orally is very low (approximately 10%). No differences were found for different dosage forms. In patients with various respiratory and heart diseases, the maximum concentration of AC in the blood plasma is reached within 1-3 hours after administration and remains high for 24 hours.

Distribution

Acetylcysteine is distributed in the body both unchanged (20%) and in the form of metabolites (active) (80%), while it is mainly found in the liver, kidneys, lungs and bronchial secretions. The volume of distribution of AC is from 0.33 to 0.47 l/kg. Plasma protein binding is approximately 50% from 4 hours after administration and decreases to 20% after 12 hours.

Metabolism and excretion

After oral administration, AC is rapidly and extensively metabolized in the intestinal and hepatic walls. The metabolite formed, cysteine, is considered active. Next, acetylcysteine and cysteine are metabolized in the same way. About 30% of the dose is excreted by the kidneys. Т1/2 of AC is 6.25 hours.

Clinical particulars.

Therapeutic indications.

Treatment of acute and chronic diseases of the bronchopulmonary system, accompanied by increased sputum production.

Paracetamol overdose.

Contraindications.

Hypersensitivity to acetylcysteine or any ingredient of the medicinal product. Gastric or duodenal ulcer in the acute stage, hemoptysis, pulmonary hemorrhage, severe exacerbation of bronchial asthma.

Interaction with other medicinal products and other forms of interaction.

Studies of interaction were conducted only in adults.

The use of antitussives with acetylcysteine can increase sputum congestion due to a decrease in the cough reflex.

Activated carbon reduces the effectiveness of acetylcysteine.

Acetylcysteine is pharmacologically incompatible with antibiotics and proteolytic enzymes. When used concomitantly with antibiotics such as tetracyclines (except doxycycline), ampicillin, amphotericin B, cephalosporins, aminoglycosides, their interaction with the thiol group of acetylcysteine is possible, which leads to a decrease in the activity of both medicinal products. Therefore, the interval between the use of these medicinal products should be at least 2 hours. This does not apply to cefixime and loracarbef.

Concomitant use of nitroglycerin and acetylcysteine, there is evidence of significant hypotension and expansion of the temporal artery due to an increase in the vasodilator and antithrombotic effect of nitroglycerin. If nitroglycerin and acetylcysteine are co-administered, patients should be monitored for hypotension, which can be severe, and should be warned of the possibility of headache. Acetylcysteine can be a donor of cysteine and increase the level of glutathione, which helps to detoxify oxygen free radicals and certain toxic substances in the body. Acetylcysteine reduces the hepatotoxic effect of paracetamol.

It is not recommended to dissolve acetylcysteine in one glass with other medicinal products. There is a synergism of acetylcysteine with bronchodilators.

Upon contact with metals or rubber, sulfides with a characteristic odor are formed, so glassware should be used to dissolve the medicinal product.

Effect on laboratory tests

Acetylcysteine may affect the results of colorimetric quantification of salicylates and the determination of ketone bodies in urine.

Special warnings and precautions for use.

Patients with bronchial asthma should be closely monitored during treatment due to the possible development of bronchospasm. In case of bronchospasm, treatment with acetylcysteine should be stopped immediately.

There are isolated reports of severe skin reactions (Stevens-Johnson and Lyell syndromes) when taking acetylcysteine, so in case of changes in the skin or mucous membranes, you should immediately stop using the medicinal product and consult your doctor regarding its further use.

It is recommended to use the medicinal product with caution in patients with a history of gastric and duodenal ulcers, especially in the case of concomitant use of other medications that irritate the gastric mucosa.

Acetylcysteine should be used with caution in patients with liver or kidney disease to avoid the accumulation of nitrogen-containing substances in the body.

The use of acetylcysteine, mainly at the beginning of treatment, can cause a dilution of bronchial secretions and increase its volume. If the patient is unable to effectively cough up sputum, postural drainage and bronchoaspiration are necessary.

Acetylcysteine affects the metabolism of histamine, so long-term therapy should not be prescribed to patients with histamine intolerance, as this can lead to symptoms of intolerance (headache, vasomotor rhinitis, itching).

Mucolytics can cause bronchial obstruction in children under 2 years of age. Due to the physiological characteristics of the respiratory system in children of this age group, the ability to clear the secretion of the respiratory tract is limited. Therefore, mucolytics should not be used in children under 2 years of age.

A light sulfur smell is not a sign of a change in the properties of the drug, but is specific to the active substance.

Important information about excipients.

This medicinal product contains sodium compounds. Caution should be exercised when administering to patients on a sodium-controlled diet.

Fertility, pregnancy and lactation.

Pregnancy.

There are limited amount of clinical data from the use of acetylcysteine in pregnant women. Animal studies have not shown any direct or indirect negative effects on pregnancy, embryofetal development, childbirth and postnatal development.

Lactation.

There is no information on the excretion of acetylcysteine in breast milk.

The medicinal product should be used during pregnancy or lactation only after a careful assessment of the benefit/risk ratio.

Effects on ability to drive and use machines.

There is no evidence that acetylcysteine affects the ability to drive and use machines.

Posology and method of administration.

Adults

400–600 mg per day, divided into 1–3 doses depending on clinical conditions.

Children

2-6 years: 200-400 mg per day, divided into 1-3 doses;

6-12 years: 400-600 mg per day, divided into 1-3 doses;

at the age of 12 years - doses, as for adults.

Effervescent tablets of 200 mg are dissolved in 1/3 cup of water.

Additional fluid intake enhances the mucolytic effect of the medicinal product.

The duration of treatment is determined by the doctor individually, depending on the nature of the disease (acute or chronic). The medicinal product should not be taken for more than 4-5 days without consulting a doctor.

Paracetamol overdose

In the first 10 hours after taking the toxic substance, acetylcysteine is taken as soon as possible at the rate of 140 mg/kg, then at the rate of 70 mg/kg every 4 hours for 1–3 days.

Acetylcysteine should be taken without delay, immediately after preparation of the solution.

Children.

Medicinal product is used for children over 2 years.

Overdose.

There are no data on cases of overdose with oral acetylcysteine. Volunteers received 11.6 g of acetylcysteine per day for 3 months without any serious side effects.

Acetylcysteine, when used in doses of 500 mg / kg / day, does not cause an overdose.

Symptoms. Overdose can present with gastrointestinal symptoms such as nausea, vomiting, and diarrhea.

Treatment. There is no specific antidote for acetylcysteine poisoning, the therapy is symptomatic.

Undesirable effects.

Adverse events have been ranked under headings of frequency using the following convention: Very common (≥ 1/10); common (≥ 1/100, < 1/10); uncommon (≥ 1/1000, <1/100); rare (≥ 1/10000, <1/1000); very rare (<1/10000), frequency unknown (cannot be calculated according to available data).

Ear and labyrinth disorders: uncommon – tinnitus.

Respiratory, thoracic and mediastinal disorders: rare - dyspnea, bronchospasm (mainly in patients with hyper-reactivity of the bronchial system associated with bronchial asthma); frequency unknown - rhinorrhea.

Gastrointestinal disorders: uncommon - vomiting, diarrhea, stomatitis, abdominal pain, nausea, heartburn; rare - dyspepsia; frequency unknown - bad breath.

Nervous system disorders: uncommon- headache.

Cardiac disorders: uncommon - tachycardia, hypotension.

Vascular disorders: very rare - hemorrhage.

Blood and lymphatic system disorders: frequency unknown - anemia has been reported on cases of bleeding with the use of acetylcysteine, sometimes through hypersensitivity reactions.

Immune system disorders: uncommon - hypersensitivity; rare - anaphylactic shock, anaphylactic/anaphylactoid reactions.

Skin and subcutaneous tissue disorders: uncommon - urticaria, rash, Quincke's edema, pruritus; frequency unknown - exanthema, eczema, angioneurotic edema.

General disorders and administration site conditions: uncommon - hyperthermia; frequency unknown - facial edema.

In very rare cases, in connection with the intake of acetylcysteine, there have been reports of individual severe skin reactions (Stevens-Johnson and Lyell syndromes). In most cases, at least one other medication may be more likely to cause mucocutaneous syndrome. Therefore, if any new changes appear on the skin or mucous membranes, you should consult a doctor and immediately stop taking acetylcysteine.

There have been cases of decreased platelet aggregation, but the clinical significance of this has not been determined.

Reported suspected adverse reactions.

Reporting suspected adverse reactions after registration of a medicinal product is an important procedure. This allows for continued monitoring of the benefit/risk ratio for the respective drug. Healthcare providers should be informed of any suspected adverse reactions through the national alert system.

Shelf life. 3 years.

Special precautions for storage.

Store in the original package, in a tightly closed tube, at a temperature below 25°C. Keep out of the reach of children.

Incompatibilities.

When dissolving acetylcysteine, it is necessary to use glassware, avoid contact with metal and rubber surfaces.

It is not recommended to dissolve acetylcysteine in one glass with other drugs.

Antibiotics and acetylcysteine should not be mixed before administration due to the possibility of in vitro inactivation of antibiotics (preferably β-lactam antibiotics).

Nature and contents of container. 20 tablet in a tube, 1 tube in a pack.

Category of release. Non-prescription medicine.

Manufacturer. E-Pharma Trento S.p.A.

The manufacturer's location and address of the place of business.

Frazione Ravina – via Provina, 2 – 38123 Trento (TN), Italy.

Marketing authorisation holder. PrJSC “Pharmaceutical firm “Darnitsa”.

The marketing authorisation holder’s location and address of the place of business.

13, Boryspilska Street, Kyiv, 02093, Ukraine.

Date of last revision.

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N-acetyl-L-cysteine (AC) has a marked mucolytic effect on mucous and mucopurulent secretions due to depolymerization of mucoprotein complexes and nucleic acids, which give viscosity to hyaline and purulent components of sputum and other secretions. Additional properties: reduction of induced mucocyte hyperplasia, increase of surfactant production due to stimulation of type II pneumocytes, stimulation of activity of mucociliary apparatus, which furthers the improvement of mucociliary clearance. AC also has a direct antioxidant effect due to the presence of a nucleophilic free thiol group (SH), which can directly interact with the electrophilic groups of oxidative radicals. Of particular interest is the fact that AC prevents the inactivation of α-1-antitrypsin – an enzyme that inhibits elastase – by hydrochloric acid (HOCl) - a strong oxidant produced by myeloperoxidase of active phagocytes.

Treatment of acute and chronic diseases of the bronchopulmonary system, accompanied by increased sputum production.

Paracetamol overdose.

Adults

400-600 mg per day, divided into 1-3 administrations depending on clinical conditions.

Children

2-6 years old: 200-400 mg per day, divided into 1-3 administrations;

6-12 years old: 400-600 mg per day, divided into 1-3 administrations;

from the age of 12 years - doses as for adults.

Effervescent tablets 200 mg shall be dissolved in 1/3 glass of water.

Additional fluid intake enhances the mucolytic effect of the medicinal product.

The duration of treatment shall be determined by the doctor on a case by case basis, depending on the nature of the disease (acute or chronic). The drug should not be taken for more than 4-5 days without consulting a doctor.

Specialized edition for medical institutions and doctors.