ACETYLCYSTEINE FARMASIERRA 600 mg EFFERVSCENT POWDER
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Introduction
Package Leaflet: Information for the User
Acetilcisteína Farmasierra 600 mg Effervescent Powder EFG
Read this package leaflet carefully before starting to take this medicine, as it contains important information for you.
- Keep this package leaflet, as you may need to read it again.
- If you have any further questions, ask your doctor, pharmacist, or nurse.
- This medicine has been prescribed for you only. Do not give it to others, as it may harm them, even if their symptoms are the same as yours.
- If you experience any side effects, consult your doctor, pharmacist, or nurse, even if they are not listed in this package leaflet. See section 4.
Contents of the Package Leaflet:
- What Acetilcisteína Farmasierra is and what it is used for.
- What you need to know before taking Acetilcisteína Farmasierra.
- How to take Acetilcisteína Farmasierra.
- Possible side effects.
- Storage of Acetilcisteína Farmasierra.
- Contents of the pack and further information.
1. What Acetilcisteína Farmasierra is and what it is used for
Acetilcisteína, the active substance of this medicine, belongs to a group of medicines called mucolytics and is used to thin out excessive and/or thick bronchial secretions.
This medicine is indicated to facilitate the elimination of excess mucus and phlegm in respiratory processes that involve excessive or thick mucous secretion, such as: acute and chronic bronchitis, Chronic Obstructive Pulmonary Disease (COPD), emphysema, pulmonary complications of fibrosis, and other related pathologies.
2. What you need to know before taking Acetilcisteína Farmasierra
Do not take Acetilcisteína Farmasierra
- If you are allergic to acetilcisteína or any of the other components of this medicine (listed in section 6).
- In children under 2 years of age.
Warnings and Precautions
Consult your doctor or pharmacist before starting to take acetilcisteína.
If you are asthmatic or have a severe respiratory disease, you should consult your doctor before taking this medicine.
The possible sulfurous odor (like rotten eggs) of the medicine is characteristic of the active substance, but it does not indicate that the medicine is in poor condition.
If you experience stomach discomfort when taking the medicine, you should stop treatment and consult your doctor or pharmacist. Caution is recommended 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 that will decrease throughout the treatment.
It should be administered with caution in long-term treatment in patients with histamine intolerance.
Children and Adolescents
It is contraindicated in children under 2 years of age.
Other Medicines and Acetilcisteína Farmasierra
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicine.
Concomitant therapy with nitroglycerin may cause headache and hypotension should be monitored, which can be severe.
Concomitant administration with the antiepileptic carbamazepine may decrease the efficacy of carbamazepine.
Do not take it together with antitussive medicines (for cough) or those that decrease bronchial secretions (such as antihistamines and anticholinergics), as it may cause an accumulation of thinned mucus.
When taking any medicine that contains minerals such as iron or calcium, or any medicine with antibiotics (such as amphotericin B, ampicillin sodium, cephalosporins, lactobionate, erythromycin, and some tetracyclines), you should separate the intake of acetilcisteína from the intake of these medicines by at least 2 hours.
It is not recommended to dissolve acetilcisteína with other medicines.
Taking Acetilcisteína Farmasierra with Food and Drinks
Taking food and drinks does not affect the efficacy of this medicine.
Pregnancy, Breastfeeding, and Fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan 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 and use machines.
Warning on Excipients
This medicine contains 156 mg of sodium per sachet, equivalent to 7.8% of the maximum daily intake of 2 g of sodium recommended by the WHO for an adult.
3. How to Take Acetilcisteína Farmasierra
Follow exactly the administration instructions of this medicine indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended daily dose for adults and children over 7 years is 600 mg of acetilcisteína, 1 sachet of Acetilcisteína Farmasierra 600 mg 1 time a day (600 mg of acetilcisteína 1 time a day).
The dose of 600 mg can be administered in three doses of 200 mg each, for which acetilcisteína 200 mg will be used.
For its administration, reconstitute the effervescent powder in water until a pleasant-tasting solution is obtained, which is drunk directly from the glass.
Use in Children and Adolescents
Children between 2 and 7 years
The dose of 600 mg is not recommended.
There are other formulations more suitable for administering to this population.
It is contraindicated in children under 2 years of age.
If You Take More Acetilcisteína Farmasierra Than You Should
If you take more acetilcisteína than you should, you may notice: nausea, vomiting, burning, and stomach pain, diarrhea, or any other adverse effect described in section 4. Possible side effects.
In case of overdose or accidental ingestion, consult your doctor or pharmacist or call the Toxicology Information Service, phone 915 620 420, indicating the medicine and the amount taken.
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
If You Forget to Take Acetilcisteína Farmasierra
Do not take a double dose to make up for the forgotten dose.
If You Stop Taking Acetilcisteína Farmasierra
If you have any other questions about the use of this medicine, ask your doctor or pharmacist.
4. Possible Side Effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects may occur:
Uncommon (may affect up to 1 in 100 people): hypersensitivity, headache, tinnitus, tachycardia, vomiting, diarrhea, stomatitis, abdominal pain, nausea, urticaria, skin rash, angioedema, pruritus, increased body temperature, hypotension.
Rare (may affect up to 1 in 1,000 people): somnolence, bronchospasm, respiratory distress, gastrointestinal disorders.
Very rare (may affect up to 1 in 10,000 people): allergic reactions, anaphylactic shock, hemorrhage, severe skin reactions such as Stevens-Johnson syndrome and Lyell syndrome, sometimes identified with the concomitant use of another drug.
Frequency not known (cannot be estimated from the available data): facial swelling.
If any alteration in the skin or mucous membranes occurs, the administration of acetilcisteína should be interrupted immediately and medical assistance should be sought.
Reporting of Side Effects:
If you experience any type of side effect, consult your doctor or pharmacist, even if it is not listed in this package leaflet. You can also report them directly through the Spanish Medicines and Healthcare Products Agency (AEMPS) website: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
5. Storage of Acetilcisteína Farmasierra
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 CAD. The expiry date is the last day of the month indicated.
Medicines should not be disposed of via wastewater or household waste. Return the packaging and any unused medicine to a pharmacy for proper disposal. Ask your pharmacist how to dispose of the packaging and any unused medicine. This will help protect the environment.
6. Contents of the Pack and Further Information
Composition of Acetilcisteína Farmasierra
The active substance is acetilcisteína. Each sachet contains 600 mg of acetilcisteína.
The other components (excipients) are: mannitol, colloidal anhydrous silica, sodium saccharin, orange flavor, citric acid, sodium bicarbonate, and maltodextrin.
Appearance of the Product and Contents of the Pack
Acetilcisteína Farmasierra 600 mg is presented in paper and aluminum sachets with an internal polyethylene coating.
Each pack contains 20 sachets of white effervescent powder with a slight sulfurous odor.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Farmasierra Laboratorios S. L.
Carretera de Irún km 26,200
28709 – San Sebastián de los Reyes
Madrid
Spain
Phone: 916 570 659
Fax: 916 570 820
e-mail: [email protected]
Manufacturer
Farmasierra Manufacturing S. L.
Carretera de Irún km 26,200.
28709 – San Sebastián de los Reyes.
Madrid.
Spain
Date of the Last Revision of this Package Leaflet: April 2022
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) (http://www.aemps.gob.es).
- Country of registration
- Active substance
- Prescription requiredYes
- Manufacturer
- This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
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