| Term 
 
        | If we have a drug that we know attacks early in the viruses life cycle, what does that mean for its administration? |  | Definition 
 
        | We must administer the drug early in the infection |  | 
        |  | 
        
        | Term 
 
        | How do drugs that inhibit viral nucleic acid synthesis work? |  | Definition 
 
        | They act as ANTIMETABOLITES because they are structurally similar to purine and pyrimidine bases |  | 
        |  | 
        
        | Term 
 
        | When are acyclovir and ganciclovir first phosphorylated? |  | Definition 
 
        | They are first phosphorylated by viral kinases |  | 
        |  | 
        
        | Term 
 
        | When are AZT and other nucleoside analogs phosphorylated? |  | Definition 
 
        | First by host cell kinases |  | 
        |  | 
        
        | Term 
 
        | How do drugs that inhibit viral nucleic acid synthesis actually do their job? |  | Definition 
 
        | Phosphorylation converts nucleosides to nucleotide analogs that may inhibit viral DNA polymerases OR act as substrates for viral enzymes- they get INCORPORATED into viral nucleic acids |  | 
        |  | 
        
        | Term 
 
        | In order to do their job, Ganciclovir and Acyclovir require what enzyme?  Are they selectively toxic? |  | Definition 
 
        | They require VIRAL kinases This makes them VERY selectively toxic
 |  | 
        |  | 
        
        | Term 
 
        | What enzyme phosphorylates acyclovir? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What enzyme phosphorylates ganciclovir? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What is acyclovir used to treat and why is it more selectively toxic? |  | Definition 
 
        | Herpes Acyclovir's initial phosphorylation is by VIRAL TK, which is absent in uninfected cells
 |  | 
        |  | 
        
        | Term 
 
        | What is the spectrum of activity of acyclovir? |  | Definition 
 
        | Herpes Simplex Epstein-Barr
 Varicella Zoster
 |  | 
        |  | 
        
        | Term 
 
        | How does resistance to acyclovir develop? |  | Definition 
 
        | In HSV or VZV, via alteration in either: a) Viral Thymidine Kinase (TK)
 or
 b) Viral Polymerase
 |  | 
        |  | 
        
        | Term 
 
        | What ester of acyclovir is a longer acting agent?  How does it work? |  | Definition 
 
        | Valacyclovir Converted to acyclovir when ingested orally- serum levels 3-5 times higher than oral acyclovir
 |  | 
        |  | 
        
        | Term 
 
        | What is valacylcovir used to treat? |  | Definition 
 
        | Recurrent genital herpes or zoster infections |  | 
        |  | 
        
        | Term 
 
        | What are the occasional side effects of valacyclovir? |  | Definition 
 
        | Nausea, diarrhea, and headache |  | 
        |  | 
        
        | Term 
 
        | What is famciclovir used to treat? |  | Definition 
 
        | Acute herpes zoster and for the suppression of recurrent genital herpes |  | 
        |  | 
        
        | Term 
 
        | What drug undergoes first pass metabolism to pencivlovir (PCV) after oral administration? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | Where does famciclovir get converted to pencivlovir? |  | Definition 
 
        | Metabolic steps in intestinal wall and liver |  | 
        |  | 
        
        | Term 
 
        | What are the symptoms of herpes encephalitis? |  | Definition 
 
        | ANY AGE- acute onset of fever, headache, decreased consciousness, and seizures |  | 
        |  | 
        
        | Term 
 
        | Which herpes virus is more common in adults and which is more common in infants? |  | Definition 
 
        | Adults- HSV-1 Infants- HSV-2
 |  | 
        |  | 
        
        | Term 
 
        | What is the most rapid test for HSV encephalitis (only available in some places)? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | According to Caldwell, what do we see in a CSF sample of Herpes Encephalitis? |  | Definition 
 
        | WBC's, elevated protein (this contradicts some other courses) |  | 
        |  | 
        
        | Term 
 
        | What do we give to treat CMV? WHAT DO WE GIVE TO TREAT CMV?
 |  | Definition 
 | 
        |  | 
        
        | Term 
 | Definition 
 
        | A guanosine analog to treat CMV |  | 
        |  | 
        
        | Term 
 
        | How does ganciclovir work? |  | Definition 
 
        | Acts as an antimetabolite which is phosphorylated first by viral kinase to from a nucleotide that inhibits CMV DNA polymerase |  | 
        |  | 
        
        | Term 
 
        | Why is ganciclovir selective? |  | Definition 
 
        | It is phosphorylated FIRST by viral kinase (monophosphorylation) |  | 
        |  | 
        
        | Term 
 
        | What drug is used to treat CMV retinitis in AIDS patients?  What is it? |  | Definition 
 
        | Cidofovir A cytosine analog
 |  | 
        |  | 
        
        | Term 
 
        | Cidofovir has broad spectrum in vitro activity against what viruses? |  | Definition 
 
        | CMV, HSV 1 and 2, VZV, EBV, HHV-6, adenovirus, and HPV |  | 
        |  | 
        
        | Term 
 
        | What drug is given topically for mucocutaneous herpes infections? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | How is Cidofovir cleared, and what does this mean? |  | Definition 
 
        | Cleared by the kidney Nephrotoxicity is the major dose-limiting adverse effect with IV use
 |  | 
        |  | 
        
        | Term 
 
        | How can we limit the nephrotoxicity of cidofovir? |  | Definition 
 
        | Give probenacid along with it |  | 
        |  | 
        
        | Term 
 
        | What are the potential side effects of IV cidofovir? |  | Definition 
 
        | Nephrotoxicity, neutropenia, and peripheral neuropathy |  | 
        |  | 
        
        | Term 
 
        | What drug causes dose dependent proximal tubular cell toxicity (kidney) and what can be done to minimize this? |  | Definition 
 
        | Cidofovir- coadminister with probenacid |  | 
        |  | 
        
        | Term 
 
        | How is cidofovir activated? |  | Definition 
 
        | By intracellular enzymes to form an inhibitor of DNA polymerases |  | 
        |  | 
        
        | Term 
 
        | What drug is 1000-fold more effective against DNA polymerases of viruses such as herpes than it is against the DNA polymerase of the host cell? |  | Definition 
 
        | Cidofovir- thus it is very selectively toxic |  | 
        |  | 
        
        | Term 
 
        | What is foscarnet, and what is it used to treat? |  | Definition 
 
        | Inorganic pyrophosphate compound BROAD SPECTRUM- used to treat HSV, VZV, CMV, EBV, HHV-6, HBV, HIV
 |  | 
        |  | 
        
        | Term 
 
        | What is the mechanism of action of foscarnet? |  | Definition 
 
        | It inhibits viral DNA polymerase, RNA polymerase, or HIV reverse transcriptase directly WITHOUT REQUIRING PHOSPHORYLATION |  | 
        |  | 
        
        | Term 
 
        | What broad-spectrum antiviral does NOT require activation by phosphorylation? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What two antivirals are preferentially phosphorylated by viral-encoded enyzmes? |  | Definition 
 
        | Ganciclovir and Acyclovir |  | 
        |  | 
        
        | Term 
 
        | What is the role of hemagglutin in influenza infection? |  | Definition 
 
        | It binds virus to sialic acid residues on host cells allowing internalization and fusion |  | 
        |  | 
        
        | Term 
 
        | What is the role of neuraminidase in influenza infection? |  | Definition 
 
        | It releases newly synthesized virus by cleaving sialic acid from host cell glycoproteins when budding |  | 
        |  | 
        
        | Term 
 
        | What releases newly synthesized influenza virus by cleaving sialic acid? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What binds to sialic acid allowing internalization and fusion of influenza? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What is the mechanism of action of adamantanes? |  | Definition 
 
        | Inhibit uncoating of influenza virus |  | 
        |  | 
        
        | Term 
 
        | What drugs inhibit uncoating of influenza virus? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What are the symptoms of CNS toxicity of amantidine and rimantadine? |  | Definition 
 
        | Nervousness, anxiety, insomnia, difficulty concentrating, lightheadedness Avoid activities requiring mental alertness
 |  | 
        |  | 
        
        | Term 
 
        | What are the symptoms of GI toxicity of amantadine and rimantadine? |  | Definition 
 
        | Nausea, vomiting, anorexia |  | 
        |  | 
        
        | Term 
 
        | What are the symptoms of amantadine or rimantadine overdose? |  | Definition 
 
        | Mental depression, psychosis, seizures |  | 
        |  | 
        
        | Term 
 
        | When should amantadine be avoided? |  | Definition 
 
        | Untreated angle closure glaucoma Anticholinergic Effects
 |  | 
        |  | 
        
        | Term 
 
        | What drugs should NEVER be given to patients with untreated angle closure glaucoma? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What is the mechanism of action of neuraminidase inhibitors? Can you name 2 of these drugs?
 |  | Definition 
 
        | Inhibit viral cleavage of sialic acid Inhibit the release of newly formed virus
 Zanamivir and Oseltamivir
 |  | 
        |  | 
        
        | Term 
 
        | What class of drugs inhibits viral cleavage of sialic acid? |  | Definition 
 
        | Neuraminidase inhibitors -Zanamivir and Oseltamivir
 |  | 
        |  | 
        
        | Term 
 
        | What are neuraminidase inhibitors used for? |  | Definition 
 
        | Reduce duration of uncomplicated influenza A and B infection symptoms by 1 day if started within 2 days of onset of symptoms |  | 
        |  | 
        
        | Term 
 
        | What drugs can be given to prevent up to 84% of influenza infections? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | What drugs are currently available to treat RSV (respiratory syncytial virus)? |  | Definition 
 
        | RSV Immune Globulin Palivizumab
 Ribavirin
 |  | 
        |  | 
        
        | Term 
 
        | What is the mechanism of action of RSV IgG? |  | Definition 
 
        | Neutralizing and protective IgG antibodies against RSV |  | 
        |  | 
        
        | Term 
 
        | What is the mechanism of action of palivizumab, and what is it used to treat? |  | Definition 
 
        | Treats RSV Binds to fusion protein of RSV
 Prevents infection of host cell, reduces replication of RSV and spread to other cells
 |  | 
        |  | 
        
        | Term 
 
        | Describe the dosing, kinetics, and onset of palivizumab: |  | Definition 
 
        | Given IM monthly- up to 5x during RSV season, 1st dose just before RSV season Half life- 13-27 days
 Onset: within 48 hours
 |  | 
        |  | 
        
        | Term 
 
        | What is ribavarin used to treat, and what is the mechanism of action? |  | Definition 
 
        | Treat RSV Synthetic nucleoside analog (guanosine)
 Inhibits viral nucleic acid synthesis and decreases nucleotide pool
 |  | 
        |  | 
        
        | Term 
 
        | What are the pulmonary toxicities of ribavarin? |  | Definition 
 
        | Deaths due to mechanical ventilator dysfunction- caused by precipitation of ribavarin Worsening of respiratory status
 |  | 
        |  | 
        
        | Term 
 
        | What are the cardiovascular toxicities of ribavarin? |  | Definition 
 
        | Cardiac arrest, hypotension, bradycardia, tachycardia (if heart disease) |  | 
        |  | 
        
        | Term 
 
        | What is the hematological effect of ribavarin? |  | Definition 
 
        | Anemia- reversible upon discontinuation |  | 
        |  | 
        
        | Term 
 
        | What are the adverse effects of ribavarin on health care personal, and why do they happen? |  | Definition 
 
        | Ribavarin disperses in immediate bedside area Headache, conjunctivitis, rhinitis, nausea, rash, dizziness, lacrimation, pharyngitis
 |  | 
        |  | 
        
        | Term 
 
        | Who should never be around ribavarin? |  | Definition 
 
        | Pregnant women or women planning to get pregnant |  | 
        |  | 
        
        | Term 
 
        | What drug is teratogenic and pregnant women should never be exposed to it? |  | Definition 
 | 
        |  | 
        
        | Term 
 
        | FROM NOTES: Name 3 indications for acyclovir: |  | Definition 
 
        | Mucocutaneous herpetic lesions Genital herpes lesions
 Prophylaxis in AIDS and other immunocompromised patients
 |  | 
        |  | 
        
        | Term 
 
        | FROM NOTES: name 2 blood related toxicities of ganciclovir: |  | Definition 
 
        | LEUKOPENIA- low leukocytes THROMBOCYTOPENIA- low platelets
 |  | 
        |  | 
        
        | Term 
 
        | FROM NOTES:  what can be monitored to determine duration of action of foscarnet? |  | Definition 
 
        | Clearance is directly proportionate to CREATININE CLEARANCE -daily creatinine and BUN
 |  | 
        |  | 
        
        | Term 
 
        | FROM NOTES: What is the major toxicity of Zanamivir and what population should never receive it? |  | Definition 
 
        | BRONCHOSPASM Never give to patients with COPD or asthma
 |  | 
        |  |