Dextromethorphan hydrobromide
This medicine should always be taken exactly as described in this patient leaflet or as directed by a doctor or pharmacist.
Acodin is available in tablet form and contains the active substance dextromethorphan. Dextromethorphan has an antitussive effect; it suppresses the cough reflex by acting directly on the central nervous system. At therapeutic doses, it does not have a suppressive effect on respiratory function and the action of the bronchial mucosa (structure responsible for transporting secreted mucus). Acodin is used for periodic suppression of non-productive cough (so-called dry cough, not associated with the accumulation of secretions in the airways) of various origins:
This medicine should always be taken in accordance with the doctor's instructions and the indications contained in this patient leaflet. Do not exceed the recommended dose and duration of treatment. Cases of abuse of this medicine have been reported, including by children and adolescents. Taking this medicine can lead to dependence. Therefore, treatment should be short-term.
Before taking Acodin, the patient should talk to their doctor, pharmacist, or nurse:
Dextromethorphan, the active substance of Acodin, has addictive properties. The recommended treatment time should not be exceeded, as tolerance to dextromethorphan may develop, as well as psychological and physical dependence. The recommended dose and treatment time should not be exceeded. Particular caution is recommended when using this product in adolescents and young adults, as well as in individuals with a history of abuse of medicinal products or psychoactive substances. The medicine suppresses cough but does not eliminate its cause. If the cough does not subside within 3 days or recurs despite taking the medicine, or if the disease is accompanied by fever, headache, or rash, the patient should contact their doctor. The medicine should not be taken by patients with respiratory diseases associated with increased mucus production, such as bronchitis, bronchiectasis, or cystic fibrosis. Dextromethorphan enhances the inhibitory effect of alcohol on the central nervous system (see "Acodin with food, drink, and alcohol").
The patient should tell their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take. Acodin should not be taken simultaneously with the following medicines:
Concomitant administration of these medicines may cause symptoms from the central nervous system (dizziness, excitement, significant increase in body temperature, nausea, muscle tremors, increased blood pressure). Concomitant use of Acodin and medicines that inhibit the CYP2D6 enzyme, which is responsible for the metabolism of dextromethorphan, may increase the concentration of dextromethorphan. These medicines include fluoxetine, paroxetine, quinidine, and terbinafine, amiodarone, flecainide, propafenone, sertraline, bupropion, methadone, cinacalcet, haloperidol, perphenazine, and thioridazine. As a result, symptoms of overdose have been observed. Concomitant use of Acodin and expectorant medicines in patients with existing lung disease, such as cystic fibrosis and bronchiectasis, in whom there is excessive mucus production, may lead to increased mucus accumulation.
Food does not affect the absorption of the medicine from the gastrointestinal tract. The medicine can be taken with or without food. The patient should not drink alcoholic beverages while taking dextromethorphan. Dextromethorphan enhances the effect of alcohol on the central nervous system.
Acodin in tablet form is not intended for use in children under 12 years of age. The medicine can be used in adolescents over 12 years of age.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before taking this medicine. High doses of dextromethorphan may cause respiratory depression in newborns, even if taken for a short time. The use of Acodin during pregnancy should always be under medical supervision. Acodin is contraindicated during breastfeeding, as it cannot be excluded that respiratory depression may occur in infants.
Acodin, even if taken as directed, may cause mild drowsiness or dizziness and alter reaction time to the extent that the ability to drive vehicles or operate machinery is impaired. This risk increases if the medicine is taken in combination with alcohol. When taken in doses higher than recommended, it has a suppressive effect on the central nervous system.
Each tablet contains 10 mg of lactose. If the patient has previously been diagnosed with intolerance to some sugars, they should consult their doctor before taking the medicine.
This medicine should always be taken in accordance with the doctor's or pharmacist's instructions. In case of doubt, the patient should consult their doctor or pharmacist. The medicine is taken orally. Adults and adolescents over 12 years of age: 15 mg (1 tablet) every 4 hours or 30 mg (2 tablets) every 6-8 hours. Adults and adolescents over 12 years of age:do not exceed the daily dose of 120 mg of dextromethorphan (8 tablets). The maximum treatment duration should not exceed 3 days. If after 3 days there is no improvement or the patient feels worse, they should contact their doctor. Acodin can be taken with or without food. If the patient feels that the effect of Acodin is too strong or too weak, they should consult their doctor.
In case of taking a higher dose of the medicine than recommended, the patient should immediately consult their doctor or pharmacist. If the patient takes a higher dose of Acodin than recommended, the following symptoms may occur: nausea and vomiting, involuntary muscle contractions, excitement, confusion, drowsiness, impaired consciousness, involuntary rapid eye movements, cardiac disorders (rapid heartbeat), coordination disorders, psychosis with visual hallucinations, and increased excitability. Other symptoms of a large overdose may include: coma, severe respiratory disorders, and convulsions. In case of any of the above symptoms, the patient should immediately consult their doctor or go to the hospital.
In case of missing a dose, the patient should take it as soon as possible, unless it is close to the time of the next dose. The patient should not take a double dose to make up for the missed dose. In case of any further doubts about the use of this medicine, the patient should consult their doctor or pharmacist.
Like all medicines, Acodin can cause side effects, although not everybody gets them. After the medicine was placed on the market, the following side effects were reported:
Very common(more than 1 in 10 patients):
Common(less than 1 in 10 patients):
Very rare(less than 1 in 10,000 patients):
Frequency not known(frequency cannot be estimated from the available data):
If any side effects occur, including those not listed in the leaflet, the patient should inform their doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the 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. Side effects can also be reported to the marketing authorization holder. By reporting side effects, more information can be collected on the safety of the medicine.
Store the medicine at a temperature below 25°C. Store the medicine out of sight and reach of children. Do not use this medicine after the expiry date stated on the carton. The expiry date refers to the last day of the month. Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The package contains 10, 20, or 30 tablets.
Marketing authorization holder: STADA Arzneimittel AG, Stadastrasse 2-18, 61118 Bad Vilbel, Germany. Manufacturer: Opella Healthcare Poland Sp. z o.o., Branch in Rzeszów, ul. Lubelska 52, 35-233 Rzeszów.
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