Inhaled Zanamivir (Relenza) for Anti-Influenza
Drug Stockpiling Available to 50 States, DC, and 8 other Jurisdictions at Subsidized
Cost.
On 20 July the
The overall HHS
goal is to stockpile enough anti-influenza medications (including the oral drug
oseltamivir (“Tamiflu”) and the inhaled drug Zanamivir (“Relenza”)) to
stockpile for 25% of the
On March 29,
2006 the US Food and Drug Administration (FDA)announced approval of inhaled Zanamivir (Relenza) for prophylaxis
(prevention) of influenza A and B for children 5 years of age and older. This
drug had previously been FDA-licensed for treatment of actual influenza
illness.
Due to severe
and sometimes fatal respiratory side effects of the drug in persons with
underlying lung disease, Zanamivir is NOT recommended for treatment or
prophylaxis of seasonal influenza in persons with lung diseases such as asthma
or chronic obstructive pulmonary (lung) disease (COPD).
Of note, influenza
viruses that are resistant to the other neuraminidase inhibitor drug
oseltamivir (“Tamiflu”) are still susceptible to Zanamivir (“Relenza”). This
fact could become important as increasing amounts of “Tamiflu” are used around
the world due to high rates of resistance emerging now among influenza viruses
(such as H3N2, H1N1, and H5N1) to the older anti-flu drugs “amantadine” and “rimantadine”.
Daniel R. Lucey,
MD, MPH
Director, Center
for Biologic Counterterrorism and Emerging Diseases
EROne
Institutes,
Adjunct
Professor of Microbiology and Immunology,
Website: www.BePast.org email: Daniel.R.Lucey@Medstar.net