Erdostein
Erdomed contains the active substance erdosteine, which belongs to a group of mucolytic agents - reducing the viscosity of bronchial secretions and facilitating expectoration. Erdomed is recommended for the treatment of secretolytic therapy in acute and chronic upper respiratory tract diseases, bronchi, and lungs with accompanying abnormal secretion and transport of mucus. It is also used for preventive treatment of seasonal exacerbations of chronic bronchitis.
In case of typical symptoms of hypersensitivity (rash, urticaria), treatment should be stopped immediately. Use with caution in patients with weakened cough reflex or disorders of ciliary clearance (due to the risk of accumulation of large amounts of mucus). The risk of side effects can be reduced by using the smallest effective doses for the shortest possible period. If there is no improvement, the doctor will consider stopping treatment. No dose adjustment is required in adults with chronic obstructive pulmonary disease (COPD).
The medicine should not be given to children under 12 years of age.
Food and drink do not affect the absorption of the medicine.
In patients with severe kidney failure, erdosteine metabolites produced in the liver may accumulate.
No dose adjustment is necessary in patients over 65 years of age.
No interactions have been observed with other medicines used to treat respiratory infections and chronic obstructive pulmonary disease, such as theophylline, smooth muscle relaxants (corticosteroids), erythromycin, amoxicillin, or cotrimoxazole. After administration of erdosteine, an increase in amoxicillin concentration in the respiratory tract has been observed. Combined treatment with cough suppressants (antitussives) may cause accumulation of large amounts of bronchial secretions, which can worsen the patient's condition. To avoid complications, do not routinely combine cough suppressants and secretolytic agents (increasing secretion), especially before bedtime.
Before taking the medicine, consult a doctor. The decision to use the medicine is made by the doctor.
Erdomed does not affect the ability to drive and use machines.
povidone, microcrystalline cellulose, magnesium stearate, gelatin, titanium dioxide (E171), yellow iron oxide (E172), indigotine (E132).
Take this medicine always as directed by your doctor. If you are not sure, consult your doctor or pharmacist. The recommended dose for adults is: 1 capsule of 300 mg twice a day. Do not take the medicine before bedtime.
No cases of overdose have been reported. If you have taken more than the recommended dose, consult a doctor immediately.
Take the prescribed dose as soon as possible and then continue with the previous dosing schedule. If it is time for the next dose, take only one dose and then continue with the recommended dosing schedule. Do not take a double dose to make up for the missed dose. If you have any further questions about taking this medicine, consult a doctor or pharmacist.
Like all medicines, Erdomed can cause side effects, although not everybody gets them.
In some people, other side effects may occur during treatment with Erdomed.
If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel. +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children. Store in a temperature below 25°C. Do not take Erdomed after the expiry date stated on the carton. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance is erdosteine. One capsule contains 300 mg of erdosteine. The other ingredients are: povidone, microcrystalline cellulose, magnesium stearate, gelatin, titanium dioxide (E171), yellow iron oxide (E172), indigotine (E132).
The pack contains 10, 20, or 60 capsules in PVC/PVdC/Aluminum blisters in a cardboard box. Not all pack sizes may be marketed.
Marketing Authorization Holder: Angelini Pharma Polska Sp. z o.o., Aleje Jerozolimskie 181B, 02-222 Warsaw, email: angelini@angelini.pl. Manufacturer: Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.p.A., Via Vecchia del Pinocchio, 22, 60131 Ancona, Italy; Astrea Fontaine, Rue des Prés Potets, 21121 Fontaine-les-Dijon, France.
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