Antivirals Flashcards
Simeprevir
Hepatitis C; inhibits viral protease NS3/4A
Oseltamivir
Influenza A+B; neuroaminidase inhibitor (must be given early); resistance prevalent
Peramivir
Influenza A+B; neuroaminidase inhibitor; IV
Grasoprevir
Hepatitis C; inhibits viral protease NS3/4A
Emtricitabine (FTC)
HIV; NRTI/nuc, dC analog, chain terminator
Etravirine
HIV; NNRTI/non-nuc, non-competitive inhibitor of RT; rash and hepatotoxicity
Elvitegravir
HIV; Integrase inhibitors
Lamivudine
HIV; NRTI/nuc, dC analog, chain terminator
Dolutegravir
HIV; Integrase inhibitors
Enfuviritide (Fuzeon®)
HIV; entry, binds to gp41
Ritonavir
HIV; used as PK booster for proteases, inhibits CYP450
Abacavir
HIV; NRTI/nuc, dG analog, chain terminator
Didanosine
HIV; NRTI/nuc, dA analog, chain terminator
side effects of nucs
mitochondrial toxicity, lipoatrophy, lactic acidosis, hepatic steatosis
Elbasvir
Hepatitis C; inhibits NS5A replication complex
Valganciclovir
Pro-drug of ganciclovir, increased bioavailability
Cidofovir
CMV, adenovirus, acyclovir-resistant HSV; dC analog same mechanism as acyclovir, NEPHROTOXICITY/TUBULAR DAMAGE
Zanamivir
Influenza A+B; neuroaminidase inhibitor; Inhaled
Raltegravir
HIV; Integrase inhibitors
Efavirenz
HIV; NNRTI/non-nuc, non-competitive inhibitor of RT; rash and hepatotoxicity, psych
Cobicistat
HIV; inhibits CYP3A4, reduces metabolism of HIV drugs
Maraviroc
HIV; entry, CCR5 inhibitor, prevents gp120 from binding. resistance via CXCR4
Dacaltasvir
Hepatitis C; inhibits NS5A replication complex
Sofosbuvir
Hepatitis C; viral RNA-directed RNA polymerase inhibitor (NS5B); enzyme inhibitor as triphosphorylated form
SOC for Hep C
Give drug course for 12 weeks, come back after 24 wks
Tenofovir
HIV; NRTI/nuc, dA analog, chain terminator
Valacyclovir
Pro-drug of acyclovir, increased bioavailability
non-nuc resistance by?
single point mutation
Nevirapine
HIV; NNRTI/non-nuc, non-competitive inhibitor of RT; rash and hepatotoxicity, used globally
Stavudine
HIV; NRTI/nuc, dT analog, chain terminator because of absence of 3’OH
Ribavarin
Hepatitis C; adenosine/guanosine analog via carboxamide group- leads to hypermutation of virus
Paritaprevir
Hepatitis C; inhibits viral protease NS3/4A
Ombitasvir
Hepatitis C; inhibits NS5A replication complex
Acyclovir
Herpes simplex, VZV; dG analog- monophosphorylated by viral TK, then converted to triphosphate, chain terminator, CRYSTALLIZES IN URINE
Nelpivarine
HIV; NNRTI/non-nuc, non-competitive inhibitor of RT; rash and hepatotoxicity
Lopinavir
HIV; protease inhibitor, used with Ritonavir, once the most widely used HIV drug, causes insulin resistance
Zidovudine (AZT)
HIV; NRTI/nuc, dT analog, chain terminator because of absence of 3’OH;
side effects of HIV protease inhibitors?
GI upset, metabolic effects, fat redistribution, hyperlipidemia, similar to proteases in RAAS
Ledipasvir
Hepatitis C; inhibits NS5A replication complex
Atazanavir
HIV; protease inhibitor, causes bilirubin and rash
Brancidofovir
Pro-drug of cidofovir; increased bioavailability
Darunavir
HIV; protease inhibitor, used as last-line salvage therapy, when drug resistance develops
Ganciclovir
CMV retinitis in immunocompromised; same mechanism as acyclovir, NEUTROPENIA