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22 Cards in this Set
- Front
- Back
NRTI prototype and MOA
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zidovudine; activated by cell enzymes, competitively inhibit HIV-1 RT and incorporate into viral DNA chain causing termination
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NNRTI prototype and MOA
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delavirdine; binds HIV-1 RT to inhibit RNA/DNA dep DNA polymerase binding
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Protease inhibitor prototype and MOA
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indinavir; prevents cleavage of Gag-Pol polypeptide resulting in production of immature, noninfectious viral particles
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Fusion inhibitor prototype and MOA
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enfuvirtide; binds gp41 subunit to prevent conformational change needed to fuse with cell mem
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Integrase inhibitor prototype and MOA
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raltegravir; binds integrase to inhibit strand transfer which interferes with HIV DNA integration into host cell chromosome
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Drug used to tx HBV and HCV
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interferon alfa
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DOC for influenza A
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Amantadine
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DOC for RSV
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Ribavirin
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DOC for CMV retinitis
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Ganciclovir
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SE for ganciclovir
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Neutro, leuko and thrombocytopenia
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Anti-viral agents associated with Stephen Johnson syndrome
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Nevirapine, amprenavir
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HIV antiviral class known to have severe drug interactions by causing inhibition of metabolism
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Protease inhibitors
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Antivirals that are teratogens
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Delavirdine, efavirenz, and ribavirin
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Antivirals associated with neutropenia
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Ganciclovir, zidovudine, saquinavir, and interferon
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HIV med used to reduce transmission during birth
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AZT (zidovudine)
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MOA and use of adefovir dipivoxil
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activated by phosphorylation, competitively inhibits HBV DNA polymerase and incorporates into viral DNA causing chain termination; tx of HBV
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MOA and use of entecavir
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competitively inhibits all 3 functions of HBV DNA polymerase; tx HBV
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Indications (2) for lamivudine
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HIV, HBV
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Indications (2) for tenofovir
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HIV, HBV
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Drug used to tx HCV and MOA
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ribavirin; interferes with synthesis of guanosine triphosphate, inhibits capping of mRNA and inhibits viral RNA-dep polymerase of certain viruses
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anti-influenza agents active only against type A; MOA
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amantadine and rimantadine; blocks M2 proton ion channel of virus to inhibit uncoating
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anti-influenza agents active against type A and B; MOA
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oseltamivir and zanamivir; reversibly interacts with neuraminidase to inhibit activity to interfere with progeny release, destroys receptors recognized by viral hemagglutinin
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