SYMBICORT

Nazione: Indonesia

Lingua: indonesiano

Fonte: Badan Pengawas Obat dan Makanan RI - Indonesian Food and Drug Supervisory Agency

Scheda tecnica Scheda tecnica (SPC)
01-01-2020

Principio attivo:

BUDESONIDE; FORMOTEROL FUMARATE

Commercializzato da:

ASTRAZENECA INDONESIA - Indonesia

INN (Nome Internazionale):

BUDESONIDE; FORMOTEROL FUMARATE

Dosaggio:

160/4.5/DOSIS

Forma farmaceutica:

SERBUK INHALER

Confezione:

DUS,1 TURBUHALER @ 120 DOSIS

Prodotto da:

ASTRAZENECA Pharmaceuticals - Sweden

Data dell'autorizzazione:

2017-01-31

Scheda tecnica

                                SYMBICORT
® TURBUHALER
® 160/4.5 MCG/DOSE
_budesonide/formoterol _
Inhalation Powder
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each delivered dose (the dose that leaves the mouthpiece) contains
budesonide 160
micrograms/inhalation and formoterol fumarate dihydrate 4.5
micrograms/inhalation.
SYMBICORT Turbuhaler 160/4.5 micrograms/inhalation delivers the same
amount of
budesonide and formoterol as the corresponding Turbuhaler
monoproducts, i.e. budesonide
200 micrograms/inhalation (metered dose) and formoterol 6
micrograms/inhalation (metered
dose) alternatively labelled as 4.5 micrograms/inhalation (delivered
dose).
Excipient: Lactose monohydrate 730 micrograms per dose.
PHARMACEUTICAL FORM
Inhalation powder. White powder
THERAPEUTIC INDICATION
ASTHMA
Symbicort is indicated in adults and adolescents (aged 12 years and
older) for the treatment
of asthma to relieve symptoms and the reduction of the risk of
exacerbations, where the use
of inhaled corticosteroids is appropriate.
CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)
Symptomatic treatment of patients with severe COPD (FEV1 <50%
predicted normal) and a
history of repeated exacerbations, who have significant symptoms
despite regular therapy
with long-acting bronchodilators.
POSOLOGY AND METHOD OF ADMINISTRATION
ASTHMA
SYMBICORT is not intended for the initial management of asthma. The
dosage of the
components of SYMBICORT is individual and should be adjusted to
severity of the disease.
This should be considered not only when treatment with combination
products is initiated but
also when the maintenance dose is adjusted. If an individual patient
should require a
combination of doses other than those available in the combination
inhaler, appropriate
doses of beta-agonist and/or corticosteroids by individual inhalers
should be prescribed.
The dose should be titrated to the lowest dose at which effective
control of symptoms is
maintained. Patients should be regularly reassessed by their
prescriber/health care provider,
so that the dosage of SYMBICORT remains optimal
                                
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