Influenza is a worldwide public health issue. The virus circulates annually
in winter and can cause significant morbidity in time general population a
nd increased mortality rates in those who are more susceptible to complicat
ions if infected by the virus, especially the elderly. Although antivirals
to treat and prevent influenza have been available in several countries for
up to 30 years, annual influenza vaccination strategies remain the primary
focus in reducing the burden of illness caused by this viral infection. Za
namivir is the first of a new class of compounds to offer significant advan
tages over existing influenza treatments. It is a potent and specific compe
titive inhibitor of both influenza A and B virus neuraminidase. The drug is
administered topically by inhalation directly to the site of virus replica
tion in a dose of 10 mg twice daily for 5 days. In both experimental and na
turally acquired treatment studies, zanamivir has been shown to have effica
cy against both influenza A and B virus and to be well tolerated. Significa
nt treatment benefits resulting in reductions in illness of up to 2.5 days
have been demonstrated in both the general population and in patients consi
dered at high risk. In addition, patients receiving zanamivir have been abl
e to return to normal activities significantly faster.