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EC50 is the pharmacodynamic PD index predicting the inhibition of viral replication by intravenous zanamivir. We conducted dose fractionation studies in the hollow-fiber infection model HFIM system with zanamivir against an oseltamivir-resistant influenza virus. A clinical 2.
Dosing every 8 h Q8h suppressed the viral load better than dosing Q12h or Q24h at the 2. The model explained data at both half-lives and holds promise for optimizing clinical zanamivir dosage regimens. Various isolates obtained from disparate parts of the world were shown to be uniformly resistant to the adamantanes but sensitive to the neuraminidase inhibitors oseltamivir and zanamivir. Over time, resistance to oseltamivir became more prevalent among pandemic H1N1 virus isolates, while most remained susceptible to zanamivir.
The government has proposed the use of intravenous i. To use zanamivir effectively for patients with severe influenza, it is necessary to know the optimal dose and schedule of administration of zanamivir that will inhibit the replication of oseltamivir-sensitive and -resistant influenza viruses.
Therefore, we performed studies using the in vitro hollow-fiber infection model system to predict optimal dosing regimens for zanamivir against an oseltamivir-sensitive and an oseltamivir-resistant virus. Our results demonstrated that zanamivir, at a dose of mg given twice a day Q12h , inhibited the replication of oseltamivir-sensitive and oseltamivir-resistant influenza viruses throughout the course of the experiment. Thus, our findings suggest that intravenous zanamivir, at a dose of mg Q12h, could be used to treat hospitalized patients suffering from serious infections with oseltamivir-sensitive or -resistant influenza viruses.