Montelukast
Milukante is a leukotriene receptor antagonist. It blocks the action of substances called leukotrienes. These substances cause narrowing and swelling of the airways and the occurrence of allergy symptoms. By blocking the action of leukotrienes, Milukante alleviates the symptoms of asthma and helps control asthma, as well as alleviates the symptoms of seasonal allergic rhinitis (also known as hay fever). Milukante is indicated for use in patients over 15 years of age.
Your doctor has prescribed Milukante for the treatment of asthma, to prevent the occurrence of asthma symptoms during the day and night.
Your doctor will determine how to take Milukante, depending on the symptoms and severity of asthma.
Asthma is a chronic disease.
In asthma, there are:
Asthma symptoms include: coughing, wheezing, and a feeling of pressure in the chest.
Seasonal allergies (also known as hay fever or seasonal allergic rhinitis) are allergic reactions often caused by airborne pollen from trees, grasses, and weeds. Typical symptoms of seasonal allergies may include: stuffy nose, runny nose, itchy nose, sneezing, tearing, swelling, redness, and itching of the eyes.
Inform your doctor about any current or past illnesses and allergies.
Discuss the use of Milukante with your doctor or pharmacist before starting treatment.
If you experience any of these symptoms while taking montelukast, consult your doctor.
For children aged 2 to 5 years, Milukante chewable tablets 4 mg are available.
For children aged 6 to 14 years, Milukante chewable tablets 5 mg are available.
Some medicines may affect the action of Milukante or Milukante may affect the action of other medicines you are taking.
Tell your doctor or pharmacist about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take.
Milukante can be taken with other asthma medications.
Before taking Milukante, inform your doctor if you are taking any of the following medicines:
Milukante 10 mg coated tablets can be taken with or without food.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
Women who are pregnant or planning to become pregnant should consult their doctor before taking Milukante. The doctor will assess whether they can take Milukante during this period.
Breastfeeding
It is not known whether Milukante passes into breast milk. If you are breastfeeding or plan to breastfeed, consult your doctor before taking Milukante.
It is unlikely that Milukante will affect your ability to drive or use machines. However, individual responses to the medicine may vary.
Some side effects (such as dizziness and drowsiness), which have been very rarely reported during treatment with Milukante, may affect your ability to drive or use machines.
Milukante 10 mg coated tablets contain lactose. If you have been diagnosed with an intolerance to some sugars, consult your doctor before taking the medicine.
The medicine contains less than 1 mmol (23 mg) of sodium per coated tablet, which is considered "sodium-free".
For patients with asthma or asthma and seasonal allergic rhinitis, take one 10 mg Milukante coated tablet once daily, in the evening.
For patients with seasonal allergic rhinitis, take one 10 mg Milukante coated tablet once daily. The time of administration will be determined by your doctor, according to your individual needs.
The medicine can be taken with or without food.
Make sure that the patient taking Milukante does not take any other medicines containing the same active substance, montelukast.
Seek medical attention immediately.
In most cases of overdose, no side effects have been observed. In cases of overdose in children and adults, the following symptoms have been most commonly reported: abdominal pain, drowsiness, excessive thirst, headache, vomiting, and hyperactivity.
Take Milukante as directed by your doctor. However, if you miss a dose, return to your usual dosing schedule - one tablet once daily.
Do not take a double dose to make up for a missed dose.
Milukante is effective in treating asthma only when taken regularly.
It is essential to continue taking Milukante as long as your doctor has prescribed it.
This will help keep your asthma under control.
If you have any further doubts about taking this medicine, consult your doctor or pharmacist.
Like all medicines, Milukante can cause side effects, although not everybody gets them. If any side effect becomes serious or you notice any side effects not listed in this leaflet, please inform your doctor or pharmacist.
During clinical trials with montelukast in the form of 4 mg chewable tablets, the most common side effects (occurring in at least 1 in 100 but less than 1 in 10 children) considered to be related to montelukast were:
The frequency of possible side effects listed below is presented according to the following convention:
Very common (affecting at least 1 in 10 people)
Common (affecting 1 to 10 people in 100)
Uncommon (affecting 1 to 10 people in 1,000)
Rare (affecting 1 to 10 people in 10,000)
Very rare (affecting less than 1 in 10,000 people)
Additionally, after the medicine was placed on the market, the following side effects were reported:
In patients with asthma treated with montelukast, very rare cases of a syndrome of symptoms such as flu-like symptoms, tingling or numbness in the hands and feet, worsening respiratory symptoms, and (or) rash (Churg-Strauss syndrome) have been reported. If your child experiences any of these symptoms, inform your doctor immediately.
If you experience any side effects, including those not listed in this leaflet, please inform your doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety, 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.
Reporting side effects will help gather more information on the safety of the medicine.
Keep the medicine out of the sight and reach of children.
No special precautions for storage are necessary.
Do not use Milukante after the expiry date stated on the blister pack and outer packaging.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance is montelukast (in the form of montelukast sodium).
One coated tablet contains 10 mg of montelukast in the form of montelukast sodium.
Other ingredients of the medicine:
Tablet core:
microcrystalline cellulose, lactose monohydrate, sodium croscarmellose, disodium edetate, magnesium stearate.
Tablet coating:
hypromellose 6cP, hydroxypropylcellulose, titanium dioxide, yellow iron oxide (E172), red iron oxide (E172).
Milukante 10 mg coated tablets are beige, round, coated tablets.
Milukante is available in aluminum/aluminum blisters containing 28 tablets.
Adamed Pharma S.A.
Pieńków, ul. M. Adamkiewicza 6A
05-152 Czosnów
{Poland}
{Milukante}
Date of last revision of the leaflet:05.2024
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