BIRESP SPIROMAX budesonide / formoterol (eformoterol) fumarate dihydrate 400 microgram / 12 microgram powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

biresp spiromax budesonide / formoterol (eformoterol) fumarate dihydrate 400 microgram / 12 microgram powder for inhalation dry powder inhaler

teva pharma australia pty ltd - budesonide, quantity: 320 microgram; formoterol fumarate dihydrate, quantity: 9 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - asthma: biresp spiromax is indicated in adults (18 years and older) for the treatment of asthma, to achieve overall asthma control, including the relief of symptoms and the reduction of the risk and exacerbations (see section 4.2 dose and method of administration).,biresp spiromax is not indicated in children and adolescents under the age of 18 years as the 100/6 dose is not available.,chronic obstructive pulmonary disease (copd): biresp spiromax is indicated for the symptomatic treatment of moderate to severe copd (fev1=50% predicted normal) in adults with frequent symptoms despite long-acting bronchodilator use, and/or history of recurrent exacerbations. biresp spiromax is not indicated for the initiation of bronchodilator therapy in copd.

BIRESP SPIROMAX budesonide / formoterol (eformoterol) fumarate dihydrate 200 microgram / 6 microgram powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

biresp spiromax budesonide / formoterol (eformoterol) fumarate dihydrate 200 microgram / 6 microgram powder for inhalation dry powder inhaler

teva pharma australia pty ltd - budesonide, quantity: 160 microgram; formoterol fumarate dihydrate, quantity: 4.5 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - asthma: biresp spiromax is indicated in adults (18 years and older) for the treatment of asthma, to achieve overall asthma control, including the relief of symptoms and the reduction of the risk and exacerbations (see section 4.2 dose and method of administration).,biresp spiromax is not indicated in children and adolescents under the age of 18 years as the 100/6 dose is not available.,chronic obstructive pulmonary disease (copd): biresp spiromax is indicated for the symptomatic treatment of moderate to severe copd (fev1=50% predicted normal) in adults with frequent symptoms despite long-acting bronchodilator use, and/or history of recurrent exacerbations. biresp spiromax is not indicated for the initiation of bronchodilator therapy in copd.

ARNUITY ELLIPTA fluticasone furoate 200 microgram powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

arnuity ellipta fluticasone furoate 200 microgram powder for inhalation dry powder inhaler

glaxosmithkline australia pty ltd - fluticasone furoate, quantity: 200 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - arnuity ellipta is indicated for the maintenance treatment of asthma in patients aged 5 years and over.

ARNUITY ELLIPTA fluticasone furoate 100 microgram powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

arnuity ellipta fluticasone furoate 100 microgram powder for inhalation dry powder inhaler

glaxosmithkline australia pty ltd - fluticasone furoate, quantity: 100 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - arnuity ellipta is indicated for the maintenance treatment of asthma in patients aged 5 years and over.

BRIMICA GENUAIR 340/12 aclidinium bromide and formoterol fumarate dihydrate powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

brimica genuair 340/12 aclidinium bromide and formoterol fumarate dihydrate powder for inhalation dry powder inhaler

a menarini australia pty ltd - aclidinium bromide, quantity: 0.4 mg/actuation; formoterol fumarate dihydrate, quantity: 0.012 mg/actuation - inhalation, powder for - excipient ingredients: lactose monohydrate - brimica genuair 340/12 is indicated as a long-term twice daily maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (copd).

BISOLVON DRY HONEY LIME FLAVOUR dextromethorphan hydrobromide monohydrate 10.5 mg pastille blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

bisolvon dry honey lime flavour dextromethorphan hydrobromide monohydrate 10.5 mg pastille blister pack

sanofi-aventis healthcare pty ltd t/a sanofi consumer healthcare - dextromethorphan hydrobromide monohydrate, quantity: 10.5 mg - pastille - excipient ingredients: menthol; acacia; saccharin sodium; white beeswax; betadex; quinoline yellow; sodium cyclamate; light liquid paraffin; maltitol solution; citric acid; flavour - bisolvon dry pastilles are used for the symptomatic treatment of dry, irritant, unproductive coughs and helps soothe the throat.

SYMBICORT TURBUHALER 400/12 powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

symbicort turbuhaler 400/12 powder for inhalation dry powder inhaler

astrazeneca pty ltd - budesonide, quantity: 320 microgram; formoterol fumarate dihydrate, quantity: 9 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - asthma symbicort turbuhaler is indicated in adults and adolescents (12 years and older), for the treatment of asthma, to achieve overall asthma control, including the relief of symptoms and the reduction of the risk of exacerbations (see section 4.2 dose and method of administration). chronic obstructive pulmonary disease (copd) symbicort is indicated for the symptomatic treatment of moderate to severe copd (fev1 < or = 50% predicted normal) in adults with frequent symptoms despite long-acting bronchodilator use, and/or a history of recurrent exacerbations. symbicort is not indicated for the initiation of bronchodilator therapy in copd.

SYMBICORT TURBUHALER 200/6 powder for inhalation  dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

symbicort turbuhaler 200/6 powder for inhalation dry powder inhaler

astrazeneca pty ltd - budesonide, quantity: 160 microgram; formoterol fumarate dihydrate, quantity: 4.5 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - asthma symbicort turbuhaler is indicated in adults and adolescents (12 years and older), for the treatment of asthma, to achieve overall asthma control, including the relief of symptoms and the reduction of the risk of exacerbations (see section 4.2 dose and method of administration). symbicort is indicated for the symptomatic treatment of moderate to severe copd (fev1 < or = 50% predicted normal) in adults with frequent symptoms despite long-acting bronchodilator use, and/or a history of recurrent exacerbations. symbicort is not indicated for the initiation of bronchodilator therapy in copd.

SYMBICORT TURBUHALER 100/6 powder for inhalation  dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

symbicort turbuhaler 100/6 powder for inhalation dry powder inhaler

astrazeneca pty ltd - budesonide, quantity: 80 microgram; formoterol fumarate dihydrate, quantity: 4.5 microgram - inhalation, powder for - excipient ingredients: lactose monohydrate - asthma symbicort turbuhaler is indicated in adults and adolescents (12 years and older), for the treatment of asthma to achieve overall asthma control, including the relief of symptoms and the reduction of the risk of exacerbations (see section 4.2 dose and method of administration).,chronic obstructive pulmonary disease (copd) symbicort is indicated for the symptomatic treatment of moderate to severe copd (fev1 < or = 50% predicted normal) in adults with frequent symptoms despite long-acting bronchodilator use, and/or a history of recurrent exacerbations. symbicort is not indicated for the initiation of bronchodilator therapy in copd.

OXIS TURBUHALER 6 formoterol (eformoterol) fumarate dihydrate 6 microgram per actuation powder for inhalation dry powder inhaler Australia - English - Department of Health (Therapeutic Goods Administration)

oxis turbuhaler 6 formoterol (eformoterol) fumarate dihydrate 6 microgram per actuation powder for inhalation dry powder inhaler

astrazeneca pty ltd - formoterol fumarate dihydrate, quantity: 4.5 microgram/actuation - inhalation, powder for - excipient ingredients: lactose monohydrate - long-term treatment of reversible airways obstruction in asthma (including nocturnal asthma and exercise induced asthma) in adults and children aged 12 years and over and who are receiving inhaled or oral corticosteroids and who require bronchodilator therapy.,oxis turbuhaler can be used on demand (prn) in asthmatics over the age of 18 years who are receiving inhaled or oral corticosteroids. it should not be used in patients whose asthma can be managed alone by occasional use of short acting inhaled beta-2 agonists.