


Ask a doctor about a prescription for FLUTOX 10 mg FILM-COATED TABLETS
Leaflet:informationforthepatient
Flutox10mgcoatedtablets
Cloperastine hydrochloride
Readtheentireleafletcarefullybeforetakingthismedication,asitcontainsimportantinformationforyou
Follow the administration instructions for the medication contained in this leaflet or as indicated by your doctor or pharmacist.
Contents of the leaflet
The active ingredient of this medication, cloperastine, is an antitussive that inhibits the cough reflex. Flutox is a medication indicated for the treatment of non-productive forms of cough, such as irritative or nervous cough for adults and adolescents over 12 years old.
You should consult a doctor if it worsens or does not improve after 7 days of treatment.
Do not take Flutox if:
Warnings and precautions
Consult your doctor or pharmacist before starting to take Flutox:
Children
Taking Flutox with other medications
Tell your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication.
Flutox may interact with other medications such as:
Taking Flutox with food, drinks, and alcohol
During treatment with Flutox, do not consume alcohol, as it may increase the effects of alcohol.
Taking this medication with food and drinks does not affect its efficacy.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
It is contraindicated in pregnancy and breastfeeding.
Driving and using machines
Flutox may cause drowsiness at usual doses. If so, avoid driving and operating hazardous machinery.
Flutox contains sucrose
This medication contains sucrose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow the administration instructions for the medication contained in this leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist. The recommended dose is:
Inadultsandadolescentsover12yearsold: 1 tablet 3 times a day
Flutox is contraindicated in children under 12 years old.
How to take:
This medication is taken orally
IfyoutakemoreFlutoxthanyoushould
The symptoms of overdose are: excitement and difficulty breathing.
If you have taken more Flutox than you should, consult your doctor or pharmacist immediately or call the toxicology information service at 91 562 04 20, indicating the medication and the amount taken.
IfyouforgettotakeFlutox
Do not take a double dose to make up for forgotten doses.
This treatment is symptomatic. If you do not have a cough, do not take it, and if it returns, take the medication as indicated in section 3. How to take Flutox.
Like all medications, Flutox may cause side effects, although not everyone may experience them.
The most common side effects, although rare, are: drowsiness and dry mouth.
Possible side effects include:
Uncommon (may affect up to 1 in 1000 patients): drowsiness, dry mouth (at high doses)
Very rare (may affect up to 1 in 10,000 patients): allergic reaction, urticaria.
If you experience side effects, consult your doctor or pharmacist, even if they are not listed in this leaflet.
Do not store above 25°C.
Keep this medication out of sight and reach of children.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and any unused medication at the pharmacy's SIGRE point. If in doubt, ask your pharmacist how to dispose of the packaging and any unused medication. This will help protect the environment.
Composition of Flutox coated tablets
The active ingredient of Flutox is Cloperastine hydrochloride.
The other components (excipients) are: for the core: microcrystalline cellulose; hydrated colloidal silica; talc; magnesium stearate. For the coating: hypromellose; povidone; macrogol 4000, talc, sucrose, magnesium carbonate, titanium dioxide (E-171), and erythrosine (E-127) coloring.
Appearance of the product and package contents
Flutox is presented in the form of round, pink, coated tablets in blisters of 20 coated tablets.
Other presentations
Flutox 3.54 mg / ml syrup
Marketing authorization holder and manufacturer
Marketing authorization holder:
Zambon, S.A.U.
Maresme, 5. Can Bernades-Subirà Industrial Estate
08130 Sta. Perpètua de Mogoda – Barcelona
Manufacturer:
Zambon, S.p.A.
Via della Chimica, 9.
Vicenza, Italy
Date of the last revision of this leaflet: April 2013
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for FLUTOX 10 mg FILM-COATED TABLETS – subject to medical assessment and local rules.