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Summary of Antiviral Drugs

This document summarizes key antiviral drugs, their mechanisms of action, uses, forms, adverse effects, and resistance characteristics. It includes nucleoside and non-nucleoside reverse transcriptase inhibitors for HIV, as well as protease inhibitors, viral neuraminidase inhibitors, and antimyxovirus and antiherpetic drugs. Common adverse effects include peripheral neuropathy, hematotoxicity, and nephrotoxicity. Resistance can develop due to mutations in viral genes encoding for targets like reverse transcriptase and viral polymerases. Combination therapy is often used to combat resistance.
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0% found this document useful (0 votes)
197 views2 pages

Summary of Antiviral Drugs

This document summarizes key antiviral drugs, their mechanisms of action, uses, forms, adverse effects, and resistance characteristics. It includes nucleoside and non-nucleoside reverse transcriptase inhibitors for HIV, as well as protease inhibitors, viral neuraminidase inhibitors, and antimyxovirus and antiherpetic drugs. Common adverse effects include peripheral neuropathy, hematotoxicity, and nephrotoxicity. Resistance can develop due to mutations in viral genes encoding for targets like reverse transcriptase and viral polymerases. Combination therapy is often used to combat resistance.
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Drug MOA Uses Forms AE Resistance Other Characteristics

ANTIHERPETICS
(Aint For Valentines, Goes Forever)
Acyclovir(Zovirax) HSV, VZV IV IV form: Crystalluria, Due to Thymidine kinase
Oral Neurotoxic changes in converts it to
Topical DNA acyclovir mono-
(-) DNA Polymerase then acyclovir
Polymerase→ triphosphate
DNA chain (active form)
Famciclovir & Valacyclovir termination HSV, VZV More expensive
*against strains than acyclovir
resistant to acyclovir
but NOT to TK strains
Ganciclovir (-) DNA HSV, VZV, CMV Retinal Dose-limiting Due to
Polymerase→ (prophylaxis + tx) implant HEMATOTOXOCITY (↓WBC, changes in
Ganulocyte(granulocyte) DOES NOT *CMV Retinitis IV plt) DNA
– WBC, thus CAUSE DNA Oral Mucositis, fever, rash, Polymerase
hematotoxicity chain Crystalluria, Seizures
termination
Foscarnet (-) DNA and RNA HSV, VZV, CMV IV Dose-limiting Common: Seizures
Polymerases→ NEPHROTOXICITY with ATN as AE
foscar
NEThrotoxicity DNA chain *identical to (acute tubular necrosis),
termination Ganciclovir, but > electrolyte imbalance, ↓Ca =
activity versus tremors and Seizures
acyclovir-resistant
strains of HSV

ANTIMYXOVIRUS
(viral nucleic acid synthesis inhibitors)

Ribavirin (-)viral RNA Aerosol HEMATOTOXIC, upper airway Teratogenic, CI to


Polymerase and RSV (respiratory Topical irritation preggy
end capping of syncytial virus)- CROUP,
viral RNA Infuenza A & B, Lassa
fever (Lassa virus of
arenaviridae),
hantavirus, adjuncts to
IFN-α in Hepatitis C

MINA, J.A
Made for Section 2B 2012
Drug MOA Uses Forms AE Resistance Other Characteristics

ANTI-RETROVIRUS
Nucleoside Reverse Transcriptase Inhibitors (NRTIs)
 Components of the most combination drug regimens used in HIV infection
 Use 2 NRTIs + PI (protease inhibitor)
 Used in HAART (highly active antiretroviral therapy)
*peripheral neuropathy- most common SE
Zidovudine/ZDV HIV-1, HIV-2, HTLV-1 Oral Dose-limiting HEMATOTOXICITY (PMN, Hematotoxic→ needs
(Azidothhmidine/ AZT) RBC, Plt), HA, asthenia, myalgia, blood transfusion
myopathy, peripheral neuropathy,
lactic acidosis
Didanosine/ddI HIV-1, HIV-2 Pancreatitis (major, dose-limiting),
(-) peripheral neuropathy, hyperuricemia,
liver, dysfunction
Mutation
Zalcitabine/ddC
Reverse HIV-1, HIV-2, HBV Peripheral neuropathy (major, dose-
limiting), GI distress, pancreatitis, in the
“Salisi (Zalci) gang will
Stab You (Stavu) causing
neutropenia, rash genes that peripheral neuropathy;
Stavudine/d4T Transcrip HIV-1, HIV-2 Peripheral neuropathy (major, dose- Salisi (Zalci) gang will
limiting), myelosuppression < ZDV codes RT also eat your Lomi
Lamivudine/3TC tase (RT) HIV-1, HIV-2, HBV LEAST TOXIC of NRTIs, but some GI (Lami) infected with
Hepa B”
effects and neutropenia

*Peripheral neuropathy
= Zalci + Stavu
*Hepa B = Zalci + Lami
Non-nucleoside RTIs (Non-NRTIs)
 Resistance emerges if used individually, thus used in combination with HAART
 “add-on” (the mistress, kabit, other woman, paramour)
 Additive/ synergistic against HIV
Protease Inhibitors
Indinavir (indi na virgin) Nephrolithiasis, GI distress, plt, (-) P450
Ritonavir (-) HIV GI distress, asthenia, paresthesia, (-
HIV-1, HIV-2
aspartate *In combination with 2 NRTIs
)P450
Saquinavir [Least toxic, very low oral
protease bioavailability]
Viral Neuraminidase Inhibitors
Oseltamivir Oral Nausea, vomiting Given in patients with
TUMMY FLU (i.e during
influenza A and B outbreak of H1N1)
Zanamivir (-) neuraminidase of Aerosol Nasal and throat irritation
*prophylaxis, ↓duration of
influenza A and B
flu symptoms by 2-3 days

NOTES:
>HEMATOTOXIC – Ganciclovir (WBC,plt), Ribavirin, ZDV/AZT (PMN, RBC, Plt),
>Crystalluria – Acyclovir, Ganciclovir

MINA, J.A
Made for Section 2B 2012

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