Ultibro® Breezhaler®

INHALER TECHNIQUE VIDEO FOR ULTIBRO® BREEZHALER®

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See for yourself how the Ultibro® Breezhaler® device works

See how to administer Ultibro® Breezhaler® correctly.

 

Inhaler Technique for Ultibro Breezhaler

 
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IE402214 | January 2024
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Reporting of side effects
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk profile of the medicinal product. All suspected adverse reactions should be reported to HPRA Pharmacovigilance, website www.hpra.ie. Adverse events can also be reported to Novartis preferably at www.novartis.com/report, by emailing [email protected] or by calling (01) 2080 612.