No information
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| Maintenance treatment for asthma |
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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.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
Growth inhibition, Cushing’s syndrome, Cushingoid symptoms, adrenergic suppression; anxiety, sleep disorders and behavioural changes including depression, hyperactivity and irritability.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
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
FDA label warning: elevated mortality in studies when ICS/LABA used in adults.
There is insufficient data known about the use of salmeterol/fluticasone in children aged under 4 years. A combination preparation with LABA and ICS is the medicine in step 3 of the asthma treatment and the use should therefore be prescribed as per the guidelines of the NHG (Dutch College of General Practitioners) and the SKL (Paediatric Pulmonary Disease Section). Do not use as treatment for acute asthma attacks.
Particularly in children up to 16 years of age, the use of fluticasone at a dosage of ≥ 1000 micrograms/day can be high-risk. Systemic effects may occur, especially if high doses are prescribed for longer periods. Possible systemic effects include Cushing’s syndrome, Cushingoid symptoms, adrenal cortex suppression, acute adrenal crisis and growth inhibition in children and adolescents and less often a series of psychological or behavioural effects can occur, such as psychomotor hyperactivity, sleep disorders, anxiety, depression and aggression. It is recommended in children who are given long-term treatment that the growth should be checked regularly. If there is growth retardation, the treatment should be reassessed and the dose should be lowered if possible.
Watch out for dysphonia and candidiasis.
Administration: Seretide dosing aerosol can be administered using the following holding chambers: Volumatic (> 4 years) or AeroChamber Plus.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Alpha- and beta-adrenoreceptor agonists | ||
|---|---|---|
| R03AA01 | ||
| Selective beta-2-adrenoreceptor agonists | ||
|---|---|---|
| R03AC13 | ||
| R03AC02 | ||
| R03AC12 | ||
| R03AC03 | ||
| Adrenergics in combination with corticosteroids or other drugs, excl. anticholinergics | ||
|---|---|---|
| R03AK08 | ||
| R03AK11 | ||
| R03AK10 | ||
| R03AK07 | ||
| Adrenergics in combination with anticholinergics incl. triple combinations with corticosteroids | ||
|---|---|---|
| R03AL01 | ||
| R03AL02 | ||
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