Pharmacokinetics in children
No information
dose recommendation of formulary compared to licensed use (on-label versus off-label)
No information is present at this moment.
Available formulations
No information is present at this moment.
Dosages
| Adjuvant maintenance treatment for asthma in atopic patients |
- Oral
-
6 months
up to
6 years
-
6 years
up to
15 years
-
5
mg/day
in 1
dose
- Directions for administration:
Take in the evening.
-
(Step 1: SABA if necessary) (Step 2: start ICS) Step 3: double the initial dose of ICS, then add LABA and lower the ICS to the smallest effective dose, in any event down to the initial dose LTRA as an alternative to LABA if there are side effects or in children aged < 4-6 years Step 4:if LABA has an effect but not enough to control the asthma: continue LABA and double the ICS dose or add LTRA If LABA has no effect: stop LABA and double the ICS dose or add LTRA Step 5: double the ICS dosage (to 4x the initial dose) and continue LABA and LTRA
SABA = short-acting beta agonist; LABA = long-acting beta agonist; ICS= inhalation corticosteroids; LTRA = leukotriene receptor antagonist
Note: Start the treatment at the step that best suits the clinical assessment of the severity
...read more
-
≥ 15 years
-
10
mg/day
in 1
dose
- Directions for administration:
Take in the evening
(Step 1: SABA if necessary) (Step 2: start ICS) Step 3: double the initial dose of ICS, then add LABA and lower the ICS to the smallest effective dose, in any event down to the initial dose LTRA as an alternative to LABA if there are side effects or in children aged < 4-6 years Step 4:if LABA has an effect but not enough to control the asthma: continue LABA and double the ICS dose or add LTRA If LABA has no effect: stop LABA and double the ICS dose or add LTRA Step 5: double the ICS dosage (to 4x the initial dose) and continue LABA and LTRA
SABA = short-acting beta agonist; LABA = long-acting beta agonist; ICS= inhalation corticosteroids; LTRA = leukotriene receptor antagonist
Note: Start the treatment at the step that best suits the clinical assessment of the severity
|
Renal impaiment in children > 3 months
GFR ≥10 ml/min/1.73m2: Dose adjustment not required.
GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.
The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Side effects in children
In children 6-14 years: Headache
In children 2-6 years: stomach ache, thirst
In children 6 months- 2 years: hyperkinesia, diarrhea, eczematous dermatitis, rash.
Neuropsychiatric side effect like nightmares, aggression and behavioral changes, occur in all paediatric agegroups. Dysphemia has been reported in children, especially in children younger than 5 years of age (CMDh, SmPC).
The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
Contra-indications
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
Warnings & precautions in children
Montelukast granulate can be administered either directly via the mouth or mixed with a spoon into soft food that is cold or at room temperature (for example apple sauce, ice cream, carrots and rice). If mixed with
food montelukast granulate may not be stored for later use. Montelukast granulate is not intended to be administered by dissolution in liquid. But liquids can be drunk after administration. Montelukast granulate can be administered with or without food.
Be aware of neuropsychiatric side effects (in children, especially stuttering, nightmares, aggression and behavioral changes). When these side effects occur, continuation of treatement with montelukast should be reconsidered.
Interactions
The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
OTHER SYSTEMIC DRUGS FOR OBSTRUCTIVE AIRWAY DISEASES
This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.
| Other systemic drugs for obstructive airway diseases |
|
|
|
R03DX09
|
|
|
|
R03DX05
|
|
|
|
R03DX11
|
References
-
MSD BV, SPC Singulair granulaat en tablet (RVG 104604 en 25800), www.cbg-meb.nl, Geraadpleegd 10 juni 2010, http://db.cbg-meb.nl/IB-teksten/h104604.pdf
-
Coordination Group for Mutual Recognition and Decentralised Procedures - Human (CMDh), Montelukast: Scientific conclusions and grounds forthe variation to the terms of the Marketing Authorisation(s) , https://www.ema.europa.eu/en/documents/psusa/montelukast-cmdh-scientific-conclusions-grounds-variation-amendments-product-information-timetable/00002087/201807_en.pdf, 08-05-2019
-
Ratiopharm, SmPC Montelukast-ratiopharm® 4 mg Granulat (80995.00.00), 08/2016
-
Ratiopharm, SmPC Montelukast-ratiopharm® mini 4 mg Kautabletten (70602.00.00), 10/2015
-
Ratiopharm, SmPC Montelukast-ratiopharm® junior 5 mg Kautabletten (70603.00.00), 10/2015
-
Online GL, Montelukast-ratiopharm® 10 mg Filmtabletten | Gelbe Liste, Accessed March 19, 2018
-
Ratiopharm, SmPC Montelukast-ratiopharm® 10 mg Filmtabletten (70604.00.00), 08/2016
-
Online GL, SINGULAIR® 10 mg Filmtabletten | Gelbe Liste, Accessed March 16, 2018
-
MSD, SmPC Singulair® mini 4 mg Granulat, Singulair®mini 4 mg Kautabletten, Singulair junior®5 mg Kautabletten, Singulair® 10 mg Filmtabletten (42011.00.02, 42011.01.00, 42011.00.00, 42011.00.01), 08/2016
-
Coordination Group for Mutual Recognition and Decentralised Procedures - Human (CMDh), Montelukast: Scientific conclusions and grounds forthe variation to the terms of the Marketing Authorisation(s), https://www.ema.europa.eu/en/documents/psusa/montelukast-cmdh-scientific-conclusions-grounds-variation-amendments-product-information-timetable/00002087/201807_en.pdf, 08-05-2019
-
MSD, SmPC Singulair® mini 4 mg Granulat, Singulair®mini 4 mg Kautabletten, Singulair junior®5 mg Kautabletten, Singulair® 10 mg Filmtabletten (42011.00.02, 42011.01.00, 42011.00.00, 42011.00.01), 08/2016
Therapeutic Drug Monitoring
Overdose