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22 Cards in this Set

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