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Influenza neuraminidase cleaves terminal sialic acid residues, which is essential for release of virus from infected cells and spread to other cells
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Oseltamivir carboxylate binds the neuraminidase active site, causing a conformational change that inhibits its activity
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This leads to viral aggregation at the cell surface and reduced spread within the respiratory tract
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Active against Influenza A and B (including amantadine-resistant strains)
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Goodman & Gilman's Pharmacological Basis of Therapeutics
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Take with or without food; taking with food reduces GI side effects
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Dose must be adjusted in renal insufficiency (drug is renally excreted)
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Harrison's Principles of Internal Medicine 22E (2025)
Note: Families and caregivers should watch for unusual behavior in pediatric patients and contact a healthcare provider immediately if observed.
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Resistance can develop via mutations in viral neuraminidase or hemagglutinin
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Resistance reported in ~15% of healthy children and ~1% of adults
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More common in immunocompromised persons
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Seasonal influenza A (H1N1) has historically shown high oseltamivir resistance; novel/pandemic H1N1 remains susceptible
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Harrison's Principles of Internal Medicine 22E (2025), Goodman & Gilman's Pharmacological Basis of Therapeutics