Registration Form Details Agenda

COPD Management and
Treatment Options Including
the Role of Onbrez Breezhaler
and Seebri Breezhaler
Speaker: Dr Andrew Bradbeer
Respiratory & Sleep Physician
Registration Form
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Details
Date:
Thursday 9th October, 2014
Venue:
Café Jas
Address: 37 Roberts Place
Horsham, VIC
Agenda
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7:30pm
Arrivals and Registration
7:45pm
Welcome and Introductions
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8:00pm
Presentation and Dinner
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COPD Management and Treatment Options
Including the Role of Onbrez Breezhaler and
Seebri Breezhaler
Email
9:00pm
Questions and Answers
9:30pm
Close and End of Meeting
Dietary Requirements
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♦ Onbrez Breezhaler is indicated for maintenance bronchodilator treatment of airflow limitation in patients with COPD. ♦ Onbrez Breezhaler should not be
used in asthma due to the absence of long-term outcome data in asthma with Onbrez Breezhaler. Long-acting beta2-adrenergic agonists may increase the
risk of asthma-related serious adverse events, including asthma-related deaths, when used for the treatment of asthma.* A differential diagnosis should be
made to exclude asthma or mixed airways disease before initiating Onbrez.♦ The recommended dose is the inhalation of the content of one 150 microgram
capsule once a day, using the Onbrez Breezhaler inhaler. The dose should only be increased on medical advice. ♦ Onbrez Breezhaler should not be used in
combination with other long-acting β2-agonists such as eformoterol and salmeterol or their combination products.
PBS Information: Restricted Benefit. Chronic Obstructive Pulmonary Disease.
See approved Product Information before prescribing.
Approved Product Information available on request.
ONBREZ BREEZHALER (indacaterol maleate)
Indication: Long-term maintenance bronchodilator treatment of airflow limitation in patients with chronic obstructive pulmonary disease (COPD). Dosage
and administration: Recommended dose: 150µg once daily, using the Breezhaler inhaler. The maximum dose is 300 µg once-daily. Contraindications:
Hypersensitivity to any ingredients, galactose intolerance, severe lactase deficiency or glucose-galactose malabsorption. Precautions: Asthma: Should not
be used in asthma. Long-acting beta2-adrenergic agonists may increase the risk of asthma-related serious adverse events, including asthma-related deaths,
when used for the treatment of asthma* ♦ Hypersensitivity: If hypersensitivity reaction occurs, treatment should be discontinued immediately and alternative
therapy instituted ♦ Corticosteroids: COPD patients being treated with long-term inhaled glucocorticoids therapy should continue this therapy when initiating
indacaterol ♦ If paradoxical bronchospasm occurs, treatment should be discontinued immediately. ♦ In case of deterioration of COPD whilst on treatment, a
re-evaluation of the patient and COPD treatment regimen should be undertaken. The patient’s COPD management plan should make this clear. ♦ Should be
used with caution in patients with cardiovascular disorders (coronary artery disease, acute myocardial infarction, cardiac arrhythmias, hypertension); in
patients with convulsive disorders or thyrotoxicosis; in patients who are unusually responsive to β2-adrenergic agonists; ♦ Cardiovascular effects: like other β
2-adrenergic agonists, indacaterol can produce a clinically significant cardiovascular effect in some patients as measured by increases in pulse rate, blood
pressure, and/or symptoms, ECG changes. In case such effects occur, the drug may need to be discontinued. ♦ β 2-adrenergic agonists may produce
significant hypokalemia. Hypokalemia may be potentiated by hypoxia and concomitant treatment which may increase the susceptibility to cardiac
arrhythmias ♦ Clinically notable changes in blood glucose and/or serum potassium were infrequent ♦ Should not be used in conjunction with other longacting β2-adrenergic agonists or medications containing long-acting β2-adrenergic agonists. ♦ Pregnancy (Category B3): Should be used during pregnancy
only if the expected benefit justifies the potential risk to the fetus. ♦ Use in lactation: Should only be considered if the expected benefit to the woman is
greater than any possible risk to the infant. Interactions: Caution in patients being treated with monoamine oxidase inhibitors, tricyclic antidepressants, or
drugs known to prolong the QT interval ♦ Concomitant administration of other sympathomimetic agents may potentiate the undesirable effects ♦
Concomitant treatment with methylxanthine derivatives, steroids, or non-potassium sparing diuretics may potentiate the possible hypokalaemic effect of β 2adrenergic agonists ♦ Should not be given together with β2 -adrenergic blockers (including eye drops) unless there are compelling reasons for their use. Side
effects: Common (1 to 10%): nasopharyngitis, upper respiratory tract infection, sinusitis, cough, oropharyngeal pain, rhinorrhoea, headache, paresthesia,
muscle spasm, myalgia, peripheral oedema, ischaemic heart disease, musculoskeletal pain, chest pain, diabetes mellitus and hyperglycaemia, dry mouth ♦
Uncommon (0.1 to 1%): atrial fibrillation, chest discomfort, vertigo, paresthesia. (obb060214m.doc)
For most up to date Product Information go to http://www.novartis.com.au/products_healthcare.html
*Please note changes in Product Information
PBS Information: Restricted Benefit. Chronic Obstructive Pulmonary Disease (COPD).
See approved Product Information before prescribing.
Approved Product Information available on request.
SEEBRI BREEZHALER (glycopyrronium bromide)
Indication: Once-daily maintenance bronchodilator treatment to relieve symptoms of patients with chronic obstructive pulmonary disease (COPD). Dosage
and administration: Recommended dose: 50μg once daily using only the Breezhaler inhaler. Do not swallow the capsules.* Contraindications:
Hypersensitivity to any ingredients, galactose intolerance, severe lactase deficiency or glucose-galactose malabsorption. Precautions: Acute use: should not
be used as rescue therapy ♦ Hypersensitivity: if hypersensitivity reaction occurs, SEEBRI BREEZHALER should be discontinued immediately and alternative
therapy instituted.* ♦ Paradoxical bronchospasm: as with other inhalation therapy, administration may result in paradoxical bronchospasm that may be lifethreatening. If paradoxical bronchospasm occurs, SEEBRI BREEZHALER should be discontinued immediately and alternative therapy instituted ♦
Anticholinergic effect: use with caution in patients with narrow-angle glaucoma and urinary retention. Discontinue when signs and symptoms of acute
narrow-angle glaucoma occur. Monitor for signs and symptoms of hyperplasia or bladder-neck obstruction.* ♦ Renal impairment: to be used only if
expected benefit outweighs potential risk in patients with severe renal impairment including end-stage renal disease requiring dialysis. ♦ Pregnancy
(Category B3): Should be used during pregnancy only if the expected benefit justifies the potential risk to the fetus. ♦ Use in lactation: Should only be
considered if the expected benefit to the woman is greater than any possible risk to the infant. Interactions: Co-administration with other inhaled
anticholinergic-containing drugs has not been studied and is therefore not recommended. Side effects: Common (1 to 10%): dry mouth, insomnia,
gastroenteritis ♦ Uncommon (0.1 to 1%): dyspepsia, dental caries, pain in extremity, musculoskeletal chest pain, rash, fatigue, asthenia, sinus congestion,
productive cough, throat irritation, epistaxis, rhinitis, cystitis, hyperglycaemia, urinary retention, dysuria, atrial fibrillation, palpitations, hypoaesthesia. ♦ Not
known: angioedema.* ♦ Other ADRs: nasopharyngitis, vomiting, musculoskeletal pain, neck pain, diabetes mellitus ♦ Elderly patients only: headache,
urinary tract infection. (see260614m.doc) For medical enquiries please contact 1800 671 203 (phone) or [email protected] (email)
Novartis Pharmaceuticals Pty Limited. 54 Waterloo Road, North Ryde NSW 2113. Ph (02) 9805 3555. ® Registered Trademark.
*Please note changes in Product Information
For the most up to date Product Information go to http://www.novartis.com.au/products_healthcare.html
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