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Antivirals for Pandemic Influenza
Author(s) -
Frederick G. Hayden
Publication year - 1997
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/514177
Subject(s) - rimantadine , amantadine , neuraminidase inhibitor , zanamivir , pandemic , neuraminidase , medicine , intensive care medicine , drug , virology , chemoprophylaxis , drug resistance , adverse effect , orthomyxoviridae , oseltamivir , influenza a virus , antiviral drug , virus , immunology , pharmacology , biology , covid-19 , microbiology and biotechnology , infectious disease (medical specialty) , disease
Amantadine and rimantadine share features that would make them useful agents in responding to pandemic influenza. These include an antiviral spectrum encompassing influenza A viruses, favorable pharmacokinetics, a potential for stockpiling supplies, and documented prophylactic and therapeutic effectiveness in pandemic influenza. However, current production capability is insufficient to provide adequate drug for mass chemoprophylaxis in the event of vaccine unavailability. The risk of adverse drug effects, particularly central nervous system side effects, which occur more often with amantadine than rimantadine, and potential drug interactions are additional concerns. Short-course treatment of ill persons would provide symptom benefit, but convincing evidence that early antiviral treatment reduces bacterial and other influenza complications is currently lacking. Drug-resistant viruses emerge during therapy, appear to be fully pathogenic, and are transmissible to close contacts. Influenza neuraminidase inhibitors are promising investigational agents, but remaining issues include prophylactic efficacy, cost, efficient administration, and resistance emergence.

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