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Montelukast Paediatric 5mg chewable tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
5 mg
Contains active substance:
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Patient leaflet - Montelukast paediatric 5 mg chewable tablets

1. What Montelukast is and what it is used for

The full name of this medicine is Montelukast Paediatric 5mg chewable tablets (referred to as Montelukast in the rest of this leaflet).

Montelukast Paediatric 5mg chewable tablets contains the active substance montelukast.

Montelukast is a leukotriene receptor antagonist that blocks substances called leukotrienes. Leukotrienes cause narrowing and swelling of airways in the lungs. By blocking leukotrienes, Montelukast improve asthma symptoms and helps control asthma.

Your or your child’s doctor has prescribed Montelukast to treat asthma, preventing your or your child’s asthma symptoms during the day and night.

  • Montelukast is used for the treatment of patients who are not adequately controlled on their medication and need additional therapy.
  • Montelukast may also be used as an alternative treatment to inhaled corticosteroids for 6 to 14 year old patients who have not recently taken oral corticosteroids for their asthma and have shown that they are unable to use inhaled corticosteroids.
  • Montelukast also helps prevent the narrowing of airways triggered by exercise.

Your or your child’s doctor will determine how Montelukast should be used depending on the symptoms and severity of your or your child’s asthma.

What is asthma?

Asthma is a long-term disease. Asthma includes:

  • difficulty breathing because of narrowed airways. This narrowing of airways worsens and improves in response to various conditions.
  • sensitive airways that react to many things, such as cigarette smoke, pollen, • cold air, or exercise.
  • swelling (inflammation) in the lining of the airways. Symptoms of asthma include: Coughing, wheezing, and chest tightness.

2. What you need to know before you take Montelukast

Tell your doctor about any medical problems or allergies you or your child has now or has had.

Do not take Montelukast

  • If you are or your child is allergic to montelukast or any of the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your or your child’s doctor, pharmacist or nurse before taking or giving him/her Montelukast:

  • If you or your child’s asthma or breathing gets worse, tell your doctor immediately. • It is not meant to treat acute asthma attacks. If an attack occurs, follow the instructions your doctor has given you for your child.

Always have your inhaled rescue medicine for asthma attacks with you.

  • It is important that you or your child takes all asthma medications prescribed • by your or your child’s doctor. Montelukast should not be used instead

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of other asthma medications your child’s doctor has prescribed for your child. • If you or your child is on anti-asthma medicines, be aware that if you or he/she develops a combination of symptoms such as flu-like illness, pins and needles or numbness of arms or legs, worsening of pulmonary (lung) symptoms, and/or rash, you should consult your doctor or your child’s doctor.

  • You or your child should not take acetylsalicylic acid (aspirin) or anti-inflammatory
  • medicines (also known as non-steroidal anti-inflammatory drugs or NSAIDs) if they make your or his/her asthma worse.

Various neuropsychiatric events (for example behaviour and mood-related changes, depression and suicidality) have been reported in patients of all ages treated with montelukast (see section 4). There have also been reports of these symptoms continuing after treatment is stopped. If you develop such symptoms while taking montelukast or if these symptoms do not resolve after montelukast is stopped, you should contact your prescriber.

Children and adolescents

Do not give this medicine to children less than 2 years of age.

There are different form(s) of this medicine available for paediatric patients under 18 years of age based on age range.

Other medicines and Montelukast

Tell your or your child’s doctor or pharmacist if you or your child are taking, have recently taken or might take other medicines including those obtaining without a prescription.

Some medicines may affect how Montelukast works, or Montelukast may affect how other medicines work.

It is especially important to tell your or your child’s doctor if you or your child are taking the following medicines before starting Montelukast:

  • phenobarbital (used for treatment of epilepsy)
  • phenytoin (used for treatment of epilepsy)
  • rifampicin (used to treat tuberculosis and some other infections)
  • gemfibrozil (used for treatment of high lipid levels in plasma)

Montelukast with food, drink and alcohol

Montelukast Paediatric 5mg chewable tablets should not be taken immediately with food; it should be taken at least 1 hour before or 2 hours after food. (See also section 3. How to take Montelukast)

Pregnancy, breast-feeding and fertility

Pregnancy

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have baby, ask your doctor or pharmacist for advice before taking Montelukast. Your doctor will assess whether you can take montelukast during this time.

Breast-feeding

It is not known if Montelukast appears in breast milk. You should consult your doctor before taking Montelukast if you are breastfeeding or intend to breast-feed.

Driving and using machines

Montelukast is not expected to affect your ability to drive a car or operate machinery. However, individual responses to medication may vary. Certain side effects (such as dizziness and drowsiness) that have been reported very rarely with montelukast may affect some patient’s ability to drive or operate machinery.

Montelukast contains Aspartame

Montelukast chewable tablets contain aspartame, a source of phenylalanine. May be harmful for people with phenylketonuria. If you or your child have phenylketonuria (a rare hereditary disorder of the metabolism) you should take into account that each Montelukast Paediatric 5mg chewable tablets contains phenylalanine (equivalent to 0.674mg phenylalanine per 5mg chewable tablets).

Information on sodium content:

This medicine contains less than 1 mmol sodium (23 mg) per tablet, that is to say essentially ‘sodium-free’.

3. How to take Montelukast

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

  • Your child should take only one tablet of Montelukast once a day as prescribed by your doctor.
  • It should be taken even when your child has no symptoms or if he/she has an acute • asthma attack.

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  • To be taken by mouth. The tablets are to be chewed before swallowing. If swallowed it should be taken with a sufficient amount of fluid (e.g. with a glass of water).

Use in children 6 to 14 years of age

One Montelukast Paediatric 5mg chewable tablet daily, to be taken in the evening. Montelukast Paediatric 5mg chewable tablets should not be taken at the same time as food; it should be taken at least 1 hour before or 2 hours after food.

The tablets are to be chewed before swallowing. If you or your child is taking Montelukast, be sure that you or he/she does not take any other products that contain the same active ingredient, montelukast.

If you or your child takes more Montelukast than you or he/she should

Contact your child’s doctor immediately for advice.

There were no side effects reported in the majority of overdose reports. The most frequently occurring symptoms reported with overdose in adults and children included abdominal pain, sleepiness, thirst, headache, vomiting, and hyperactivity.

If you forget to take or give Montelukast to your child

Try to take Montelukast as prescribed. However, if you or your child misses a dose, just resume the usual schedule of one tablet once daily.

Do not take a double dose to make up for a forgotten dose.

If you or your child stop taking Montelukast

Montelukast can treat your or your child’s asthma only if you or he/she continues taking it.

It is important to continue taking Montelukast for as long as your doctor prescribes. It will help control your or your child’s asthma.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist, or nurse.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

In clinical studies with Montelukast Paediatric 5mg chewable tablets, the most commonly reported side effects (occurring in more than 1 in 10 people) thought to be related to Montelukast were:

  • headache

Additionally, the following side effect was reported in clinical studies with montelukast 10mg film-coated tablets

  • abdominal pain

These were usually mild and occurred at a greater frequency in patients treated with Montelukast than placebo (a pill containing no medication).

Serious side effects

Talk with your doctor immediately if you notice any of the following side effects, which may be serious, and for which you may need urgent medical treatment.

Uncommon: the following may affect up to 1 in 100 people

  • allergic reactions including swelling of the face, lips, tongue, and/or throat which may cause difficulty in breathing or swallowing
  • behaviour and mood related changes: agitation including aggressive behaviour or hostility, depression
  • seizure

Rare: the following may affect up to 1 in 1,000 people

  • increased bleeding tendency
  • tremor
  • palpitations

Very rare: the following may affect up to 1 in 10,000 people

  • combination of symptoms such as flu-like illness, pins and needles or numbness ofarms and legs, worsening of pulmonary symptoms and/or rash (Churg-Strauss syndrome) (see Section 2)
  • low blood platelet count
  • behaviour and mood related changes: hallucinations, disorientation, suicidal thoughts and actions
  • swelling (inflammation) of the lungs • severe skin reactions (erythema multiforme) that may occur without warning
  • inflammation of the liver (hepatitis)

Additionally, while the medicine has been on the market, the following side effects have been reported:

Very common (may affect more than 1 in 10 people)

  • upper respiratory infection

Common (may affect more than 1 in 10 people)

  • diarrhoea, nausea, vomiting
  • fever
  • rash
  • elevated liver enzyme

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Uncommon (may affect up to 1 in 100 people)

  • behaviour and mood related changes such as dream abnormalities, including nightmares, trouble sleeping, sleep walking, irritability, feeling anxious, restlessness
  • dizziness, drowsiness, pins and needles numbness
  • nosebleed
  • dry mouth, indigestion
  • bruising, itching, hives
  • joint or muscle pain, muscle cramps • weakness/tiredness, feeling unwell, swelling
  • bedwetting in children

Rare (may affect up to 1 in 1000 people)

  • behaviour and mood related changes: disturbance in attention, memory impairment, uncontrolled muscle movements

Very rare (may affect up to 1 in 10,000 people)

  • tender red lumps under the skin, most commonly on your shins (erythema nodosum)
  • behaviour and mood related changes: obsessive-compulsive symptoms, stuttering

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellowcard Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Montelukast

  • Keep this medicine out of the sight and reach of children.
  • Do not use this medicine after the expiry date which is stated on the carton and blister (EXP). The expiry date refers to the last day of that month.
  • Store below 250C. Store in the original package in order to protect from light and moisture.
  • Do not throw away any medicines via waste water or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help to protect the environment.

6. Contents of the pack and other

information

What Montelukast contains

  • The active substance is montelukast. Each tablet contains 5.2mg montelukast sodium, which corresponds to 5mg montelukast.
  • The other ingredients are: Mannitol (E421), microcrystalline cellulose, red ferric oxide (E172), croscarmellose sodium, cherry flavour, aspartame (E951), and magnesium stearate, hydroxypropyl cellulose (E463).

What Montelukast look like and contents of the pack

Chewable tablets

Montelukast chewable tablets are Pink coloured, round, bi-convex, diameter 9.6mm, tablets, debossed with ‘BL 5’ on one side and plain on other side.

Blister pack: Aluminium/Aluminium Blister

Pack size: 28, 30 tablets.

Not all pack sizes may be marketed.

Marketing Authorisation Holder and Manufacturer:

Bristol Laboratories Limited

Unit 3, Canalside, Northbridge Road, Berkhamsted, Hertfordshire, HP4 1EG, United Kingdom.

Telephone: 0044(0)1442200922 Email: info@bristol-labs.co.uk

Manufacturer:

Bristol Laboratories Limited

Laporte Way Luton, Bedfordshire LU4 8WL, United Kingdom

Montelukast Paediatric 5mg chewable Tablets; PL 17907/0476

This leaflet was last revised in May 2026

To request a copy of this leaflet in Braille, large print or audio, please contact the licence holder at the address (telephone or email) above.

V15 15-05-26 D0

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About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 17907/0476

Last revision stated in the text: May 2026 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Facts about Montelukast paediatric 5 mg chewable tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Montelukast
Strength 5 mg
Pharmaceutical form Chewable tablet
Chewable tablet
Pink coloured, round, bi-convex, diameter 9.6 mm, tablets debossed with ‘BL 5’ on one side and plain on other side
How is it taken Oral
Excipients Mannitol (E421), Microcrystalline cellulose (E460), Croscarmellose sodium (E468), Iron Oxide Red (E172), Hydroxy propyl Cellulose (E463), Cherry flavour (Cherry 501027 AP0551) {which consist of: Corn maltodextrin, Natural flavour, Nature identical flavourings} Aspartame (E951), Magnesium stearate (E572)
Pack sizes 28 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 2 years
Storage Store below 25°C. Store in the original package in order to protect from light and moisture.
Drug group (ATC) Leukotriene receptor antagonist
  1. R Respiratory system drugs
    1. R03 Drugs for obstructive airway diseases
      1. R03D Other systemic drugs for obstructive airway diseases
        1. R03DC Leukotriene receptor antagonists for obstructive airway diseases
          1. R03DC03 montelukast
Marketing authorisation PL 17907/0476 (first authorised 24 December 2024)
Marketing authorisation holder Bristol Laboratories Limited
Codes GTIN 5060013945359 · BNF 03030200

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.1.0 of 12 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.