Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2023 Publisher: Glaxo Wellcome UK Ltd trading as GlaxoSmithKline UK, 980 Great West Road, Brentford, Middlesex, TW8 9GS
Relenza 5 mg/dose, inhalation powder, pre-dispensed.
Pharmaceutical Form |
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Inhalation powder, pre-dispensed. White to off-white powder. |
Each pre-dispensed quantity of inhalation powder (one blister) contains 5 mg zanamivir. Each delivered inhalation (the amount that leaves the mouthpiece of the Diskhaler) contains 4.0 mg zanamivir.
Excipients with known effect:
Lactose monohydrate (approximately 20 mg, which contains milk protein).
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Zanamivir |
Zanamivir is an inhibitor of influenza virus neuraminidase, an enzyme that releases viral particles from the plasma membrane of infected cells and promotes virus spread in the respiratory tract. The activity of zanamivir is extracellular. It reduces the propagation of both influenza A and B viruses by inhibiting the release of infectious influenza virions from the epithelial cells of the respiratory tract. |
List of Excipients |
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Lactose monohydrate (which contains milk protein) |
Relenza inhalation powder is packed in a circular aluminium foil disk (a Rotadisk) with four regularly distributed blisters. An inspiration driven inhaler made of plastic (a Diskhaler) is used for administration of doses (the contents of 2 blisters constitute a dose) from these foil disks, and is provided in the pack.
The pack contains 1 or 5 foil disks and a Diskhaler.
Glaxo Wellcome UK Ltd trading as GlaxoSmithKline UK, 980 Great West Road, Brentford, Middlesex, TW8 9GS
PL 10949/0327
Date of first authorisation: 24 June 1999
Date of last renewal: 02 October 2008
Drug | Countries | |
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RELENZA | Austria, Brazil, Canada, Ecuador, Estonia, Spain, Finland, Hong Kong, Ireland, Japan, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa |
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