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SERETIDE EVOHALER 25/125 mcg

Prescription Only
Drug type: Therapeutic
ATC code: R03AK06
Dosage form: AEROSOL, SPRAY
Route of administration: RESPIRATORY (INHALATION)
Active ingredient: SALMETEROL; FLUTICASONE PROPIONATE; FLUTICASONE PROPIONATE; SALMETEROL

Indications

Pharmaceutical form: Inhalation aerosol.

Asthma

Seretide is indicated in the regular treatment of asthma where use of a combination product (long-acting-beta2-agonist and inhaled corticosteroid) is appropriate:

  • Patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting-beta2-agonist

    or

  • Patients already adequately controlled on both inhaled corticosteroids and long-acting-beta2-agonist

Note: Seretide 25/50 mcg strength is not appropriate in adults with severe asthma.

Contraindications

Seretide is contraindicated in patients with a history of hypersensitivity to any of the ingredients.

Dosage and Administration

Seretide Evohaler is for oral inhalation only.

Patients should be made aware that Seretide Evohaler must be used regularly for optimum benefit, even when asymptomatic. Patients should be regularly reassessed by a doctor, so that the strength of Seretide they are receiving remains optimal and is only changed on medical advice. The dose should be titrated to the lowest dose at which effective control of symptoms is maintained.

Patients should be given the strength of Seretide containing the appropriate fluticasone propionate dosage for the severity of their disease.

Recommended Doses:

Asthma

Adults and adolescents 12 years and older:

  • Two inhalations of 25 mcg salmeterol and 50 mcg fluticasone propionate twice daily.

    or

  • Two inhalations of 25 mcg salmeterol and 125 mcg fluticasone propionate twice daily.

    or

  • Two inhalations of 25 mcg salmeterol and 250 mcg fluticasone propionate twice daily.

Children 4 years and older:

  • Two inhalations of 25 mcg salmeterol and 50 mcg fluticasone propionate twice daily.

There are no data available for use of Seretide in children aged under 4 years.

Special patient groups:

There is no need to adjust the dose in elderly patients or in those with renal or hepatic impairment.

Registrant
GLAXOSMITHKLINE PTE LTD
Approval Date
2001-05-24
Approval Number
SIN11530P
Manufacturer
GLAXO WELLCOME PRODUCTION Glaxo Wellcome S.A.
Licence Holder
GLAXOSMITHKLINE PTE LTD