Acetylcysteine Viatris 600 mg effervescent granules EFG
Spain
Table of Contents
- Patient Information Leaflet
- Introduction
- 1. What Acetilcisteína Viatris is and what it is used for
- 2. What you need to know before taking Acetylcysteine Viatris
- 3. How to take Acetylcysteine Viatris
- 4. Possible adverse effects
- 5. Storage of Acetylcysteine Viatris
- 6. Contents of the pack and other information
Patient Information Leaflet
Introduction
Patient Information Leaflet
Acetylcysteine Viatris 600 mg effervescent granules EFG
Read the entire leaflet carefully before you start taking this medicine, as it contains important information for you.
- Keep this leaflet, as you may need to read it again.
- If you have any questions, consult your doctor or pharmacist.
- This medicine has been prescribed for you only and must not be given to other people, even if they have the same symptoms as you, because it could harm them.
- If you experience any adverse effects, consult your doctor or pharmacist, even if they are adverse effects not listed in this leaflet. See section 4.
Leaflet Contents
- What Acetylcysteine Viatris is and what it is used for
- What you need to know before taking Acetylcysteine Viatris
- How to take Acetylcysteine Viatris
- Possible adverse effects
- How to store Acetylcysteine Viatris
- Contents of the pack and other information
1. What Acetilcisteína Viatris is and what it is used for
Acetylcysteine, the active substance of this medicine, belongs to a group of medicines called mucolytics.
Acetilcisteína Viatris is used to liquefy excessive and/or thick bronchial secretions. It is indicated as supportive treatment in respiratory conditions associated with hypersecretion, excessive or thick mucus, such as:
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Acute and chronic bronchitis (inflammation of the bronchi).
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Chronic Obstructive Pulmonary Disease (COPD).
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Emphysema (inflammation of the lung alveoli, leading to reduced respiratory function).
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Atelectasis (reduction in lung volume) due to mucus obstruction: pulmonary complications of cystic fibrosis and other related conditions.
2. What you need to know before taking Acetylcysteine Viatris
Do not take Acetylcysteine Viatris:
- If you are allergic to acetylcysteine and its derivatives, or to any of the other components of this medicine (listed in section 6).
- Do not administer to children under 2 years of age.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Acetylcysteine Viatris.
- If you have asthma or suffer from a serious respiratory disease, you should consult your doctor before taking this medicine.
- The possible sulfur-like odor (resembling rotten eggs) of the medicine is characteristic of the active substance and does not indicate that the medicine is in poor condition.
- If you experience stomach discomfort while taking the medicine, stop treatment and consult your doctor or pharmacist. Caution is advised in patients with peptic ulcer or history of peptic ulcer.
- During the first few days of treatment, you may notice an increase in mucus and phlegm, which will gradually decrease over the course of treatment.
Children and adolescents
This medicine must not be taken by children under 2 years of age.
Other medicines and Acetylcysteine Viatris
Inform your doctor or pharmacist if you are taking, have recently taken, or might need to take any other medicines.
- Concomitant therapy with nitroglycerin may cause headache, and hypotension—which may be severe—should be monitored.
- Concomitant administration with the antiepileptic carbamazepine may reduce the effectiveness of carbamazepine.
- Do not take together with antitussive medicines (for cough) or those that reduce bronchial secretions (such as antihistamines and anticholinergics), as this may lead to accumulation of liquefied mucus.
- When taking medicines containing minerals such as iron or calcium, or medicines containing antibiotics such as amphotericin B, sodium ampicillin, cephalosporins, lactobionate, erythromycin, and certain tetracyclines, separate their administration from that of Acetylcysteine by at least 2 hours.
Dissolving acetylcysteine with other medicines is not recommended.
Taking Acetylcysteine Viatris with food and drinks
Taking this medicine with food and drinks does not affect its efficacy.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to become pregnant, consult your doctor or pharmacist before using this medicine.
Its use should be avoided during breastfeeding.
Driving and using machines
There is no evidence of effects on the ability to drive or operate machinery.
Acetylcysteine Viatris contains sodium, sulfites, and benzyl alcohol
This medicine contains 157.3 mg of sodium per sachet. This corresponds to 7.87% of the maximum daily intake of 2 g sodium recommended by the WHO for adults.
This medicine contains up to 0.0072 mg of sulfites per sachet. Sulfites may rarely cause severe hypersensitivity reactions and bronchospasm.
This medicine contains 0.014 mg of benzyl alcohol per sachet. Benzyl alcohol may cause allergic reactions.
Benzyl alcohol has been associated with the risk of adverse effects, including respiratory problems (“gasping syndrome”), in children.
This product should not be used for more than one week in children under 3 years of age unless directed by your doctor or pharmacist.
Consult your doctor or pharmacist if you are pregnant or breastfeeding. This is because large amounts of benzyl alcohol may accumulate in your body and cause adverse effects (metabolic acidosis).
Consult your doctor or pharmacist if you have liver or kidney disease. This is because large amounts of benzyl alcohol may accumulate in the body and cause adverse effects (metabolic acidosis).
3. How to take Acetylcysteine Viatris
Follow exactly the instructions given by your doctor or pharmacist for taking this medicine. If in doubt, consult your doctor or pharmacist again.
Remember to take your medicine.
Acetylcysteine Viatris is administered orally. The contents of the sachets must be dissolved in a sufficient amount of water and taken once completely dissolved.
Your doctor will determine the duration of treatment with acetylcysteine.
The recommended dose is:
Adults and children over 7 years of age: 600 mg (1 sachet) per day. Do not exceed the dose of 600 mg (1 sachet) per day.
Use in children
The 600 mg dose is not recommended for children under 7 years of age.
Other formulations are more suitable for this population.
Pulmonary complications of cystic fibrosis:
Other formulations are more suitable for this population.
If you take more Acetylcysteine Viatris than you should
If you take more acetylcysteine than you should, you may experience: nausea, vomiting, heartburn and stomach pain, diarrhoea, or any other adverse effect described in section 4. Possible side effects.
In case of overdose or accidental ingestion, contact your doctor or pharmacist immediately or call the Toxicology Information Service at telephone number: 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take Acetylcysteine Viatris
Do not take a double dose to make up for forgotten doses. Take the missed dose as soon as possible. However, if it is almost time for the next dose, wait and continue with your regular dosing schedule.
If you stop taking Acetylcysteine Viatris
Do not stop treatment prematurely, as otherwise you will not achieve the intended effect.
If you have any further questions about the use of this medicine, ask your doctor or pharmacist.
4. Possible adverse effects
Like all medicines, this medicine can cause adverse effects, although not everyone will experience them.
The following adverse effects may occur:
Uncommon (may affect up to 1 in 100 patients):
Hypersensitivity, headache, tinnitus, tachycardia, vomiting, diarrhoea, stomatitis, abdominal pain, nausea, urticaria, skin rash, angioedema, pruritus, increased body temperature, hypotension.
Rare (may affect up to 1 in 1,000 patients):
Somnolence, bronchospasm, breathing difficulty, gastrointestinal discomfort.
Very rare (may affect up to 1 in 10,000 patients):
Allergic reaction, anaphylactic shock, haemorrhage, severe skin reactions such as Stevens-Johnson syndrome and Lyell's syndrome, sometimes identified with at least the concomitant use of another medicinal product.
Frequency not known (cannot be estimated from available data):
Facial swelling.
If any changes occur in the skin or mucous membranes, administration of acetylcysteine must be stopped immediately and medical advice sought.
Reporting of adverse effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this leaflet. You may also report them directly via the Spanish Pharmacovigilance System for Human Medicinal Products: https://www.notificaram.es. By reporting adverse effects, you can help provide more information on the safety of this medicine.
5. Storage of Acetylcysteine Viatris
Keep this medicine out of the sight and reach of children.
Do not store above 30 °C.
Do not use this medicine after the expiry date stated on the packaging after EXP or CAD. The expiry date refers to the last day of the month indicated.
Medicines must not be disposed of via wastewater or household waste. Dispose of unused medicines and their containers at the SIGRE collection point at your pharmacy. If you are in doubt, ask your pharmacist how to dispose of unused medicines and their containers. This will help protect the environment.
6. Contents of the pack and other information
Composition of Acetylcysteine Viatris
- The active substance is acetylcysteine. Each sachet contains 600 mg of acetylcysteine.
- The other components are mannitol (E-421), sodium saccharin, anhydrous colloidal silica, orange flavor (sulphites, benzyl alcohol, sodium), sodium hydrogen carbonate, citric acid, and maltodextrin.
Appearance of the product and contents of the pack
Acetylcysteine Viatris is supplied in sachets made of paper and aluminum with an inner polyethylene coating. It is available in packs containing 20 sachets.
Marketing Authorization Holder
Viatris Pharmaceuticals, S.L.
C/ General Aranaz, 86
28027 - Madrid
Spain
Manufacturer
Farmasierra Manufacturing, S.L.
Carretera N-1, Km 26,200
28700 - San Sebastián de los Reyes (Madrid)
Spain
Date of the most recent review of this leaflet: October 2023
Detailed information on this medicine is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS) https://www.aemps.gob.es/