Leaflet:information for the user
Read this leaflet carefully before your child starts taking this medicine,because it contains important information.
Montelukast Pensa is a leukotriene receptor antagonist that blocks certain substances called leukotrienes. Leukotrienes produce narrowing and swelling of the airways in the lungs. By blocking leukotrienes, Montelukast Pensa improves asthma symptoms and helps control asthma.
Your child's doctor has prescribed Montelukast Pensa to treat your child's asthma and prevent asthma symptoms during the day and night.
The doctor will determine how to use Montelukast Pensa based on your child's symptoms and the severity of their asthma.
What is asthma?
Asthma is a chronic disease.
Asthma includes:
Asthma symptoms include: Coughing, wheezing, and congestion in the chest.
Do not use Montelukast Pensa:
Warnings and precautions
Consult your child's doctor or pharmacist before starting to use montelukast.
Children
For children aged 2 to 5 years, Montelukast Pensa 4 mg chewable tablets are available.
For children aged 6 to 14 years, Montelukast Pensa 5 mg chewable tablets are available.
Taking Montelukast Pensa with other medications
Inform your child's doctor or pharmacist if your child is taking, has taken recently, or may need to take any other medication.
Some medications may affect the functioning of Montelukast Pensa, or Montelukast Pensa may affect the functioning of other medications being used.
Before taking Montelukast Pensa, inform your doctor if your child is taking the following medications:
Taking Montelukast Pensa with food, drinks, and alcohol
Montelukast Pensa should not be taken with meals; it should be taken at least 1 hour before or 2 hours after eating.
Pregnancy, breastfeeding, and fertility
This subsection is not applicable to Montelukast Pensa 4 mg chewable tablets, as its use is indicated in children aged 2 to 5 years. However, the following information is important for the active ingredient, montelukast.
If you are pregnant or breastfeeding, think you may be pregnant, or intend to become pregnant, consult your doctor or pharmacist before using this medication.
Use during pregnancy
Your doctor will evaluate whether you can take Montelukast Pensa during pregnancy.
Use during breastfeeding
It is unknown whether Montelukast Pensa appears in breast milk. If you are breastfeeding or intend to breastfeed, consult your doctor before taking Montelukast Pensa.
Driving and operating machinery
This subsection is not applicable to Montelukast Pensa 4 mg chewable tablets, as its use is indicated in children aged 2 to 5 years. However, the following information is important for the active ingredient, montelukast.
Montelukast Pensa is not expected to affect your ability to drive a car or operate machinery. However, individual responses to the medication may vary. Certain adverse effects (such as dizziness and somnolence) that have been reported rarely with Montelukast Pensa may affect the patient's ability to drive or operate machinery.
Montelukast Pensa contains aspartame,a source of phenylalanine. This medication may be harmful to individuals with phenylketonuria.
Follow exactly the administration instructions for this medication as indicated by your child's doctor or pharmacist. In case of doubt, consult your child's doctor or pharmacist again.
Use in children aged 2 to 5 years:
A daily chewable tablet of 4 mg should be taken at night. Montelukast Pensa 4 mg chewable tablets should not be taken with meals; it should be taken at least 1 hour before or 2 hours after food.
If your child is taking Montelukast Pensa, make sure they do not take any other product containing the same active ingredient, montelukast.
Use in children:
For children aged 2 to 5 years, Montelukast Pensa 4 mg chewable tablets are available.
For children aged 6 to 14 years, Montelukast Pensa 5 mg chewable tablets are available.
Montelukast Pensa 4 mg chewable tablets are not recommended for children under 2 years of age.
If your child takes more Montelukast Pensa than they should:
Seek help from your child's doctor immediately.
In most cases of overdose, no adverse effects were reported. The symptoms that were most frequently reported in cases of overdose in adults and children were abdominal pain, drowsiness, drowsiness, headache, vomiting, and hyperactivity.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicological Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.
If your child forgets to take Montelukast Pensa:
Try to give Montelukast Pensa as prescribed. However, if your child forgets a dose, limit yourself to resuming the usual regimen of one tablet once a day. Do not give a double dose to compensate for missed doses.
If your child interrupts treatment with Montelukast Pensa:
Montelukast Pensa can only treat your child's asthma if your child continues to take it. It is essential to continue taking Montelukast Pensa for the time prescribed by the doctor. It will help control your child's asthma.
If you have any other doubts about the use of this medication, ask your child's doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
In clinical trials conducted with montelukast 4 mg chewable tablets, the side effects related to the administration of montelukast and reported most frequently (occur in at least 1 in 100 patients and less than 1 in 10 patients treated), were:
Additionally, in clinical trials with montelukast 10 mg film-coated tablets and 5 mg chewable tablets, the following side effects were reported:
These side effects were generally mild and occurred more frequently in patients treated with montelukast than with placebo (a tablet that does not contain a medicine).
The frequency of possible side effects, indicated below, is defined using the following convention:
Furthermore, since the medicine has been marketed, the following side effects have been reported:
In patients with asthma treated with montelukast, very rare cases of a combination of symptoms such as flu-like illness, paresthesia or numbness of arms and legs, worsening of pulmonary symptoms, and/or skin rash (Churg-Strauss syndrome) have been reported. Inform your doctor immediately if you experience one or more of these symptoms.
Reporting of side effects:
If your child experiences any type of side effect, consult a doctor or pharmacist, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through theSistema Español de Farmacovigilancia de medicamentos de Uso Humano:https://www.notificaRAM.es.By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
This medication does not require any special temperature for conservation.
Store in the original packaging to protect it from light and humidity.
Do not use this medication after the expiration date that appears on the packaging. The expiration date is the last day of the month indicated.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Montelukast Pensa
The active ingredient is montelukast. Each chewable tablet contains 4 mg of montelukast (as sodium salt).
The other components are: microcrystalline cellulose, mannitol (E-421), sodium croscarmellose, aspartame (E-951), iron oxide red (E-172), magnesium stearate (E-572), cherry flavor (maltodextrin, modified food starch (corn syrup), artificial flavors, triacetin, benzyl alcohol).
Appearance of the product and content of the container
The 4 mg chewable tablets are pink and biconvex with the code M4 engraved on one face.
The chewable tablets are presented in containers containing blisters of 14, 28, and 98 chewable tablets.
Only some container sizes may be commercially marketed.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Towa Pharmaceutical, S.A.
C/ de Sant Martí, 75-97
08107 Martorelles (Barcelona)
Spain
Responsible for manufacturing
Kymos, S.L.
Ronda de Can Fatjó, 7B (Parque Tecnológico del Vallès)
08290 Cerdanyola del Vallès (Barcelona)
Spain
This medicine is authorized in the member states of the European Economic Area with the following names:
PT:Montelucaste Pensa, 4 mg, chewable tablets
ES:Montelukast Pensa 4 mg chewable tablets EFG
IT:Montelukast Pensa 4 mg chewable tablets
Last review date of this leaflet: August 2019
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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