| Subject: | FDA Issues Safety Information for Relenza |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 12 Oct 2009 - 10:00 am |
| Audience: Infectious disease healthcare professionals, hospital risk managers The Food and Drug Administration (FDA) and GlaxoSmithKline are notifying healthcare professionals of a report of the death of a patient with influenza who received Relenza (zanamivir) Inhalation Powder which was solubilized and administered by mechanical ventilation. Relenza (zanamivir) Inhalation Powder is not intended to be reconstituted in any liquid formulation and is not recommended for use in any nebulizer or... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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