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zalcitabine

Detailed Prescribing Information

October 2005


 

 

Hivid  = zalcitabine = ddC
Forms Available 0.375 and 0.75 mg tablets
Dosing

Wt. < 60 kg: 0.375 mg po three times a day


Wt. > 60 kg: 0.75 mg po three times a day

Renal dosing1 Ccr
(cc/min)
Dose
(mg)
10-40 0.75 twice a day
<10 0.75 daily
hemodialysis not recommended
Hepatic dosing: unknown but zalcitabine does not undergo significant hepatic metabolism
Food dependence This medication may be taken with or without food.
Adverse Effects Well tolerated in most patients

25% incidence of peripheral neuropathy, oral ulcers, skin rash

<1% incidence of pancreatitis.

Rare lactic acidosis and hepatic steatosis

Peripheral neuropathy - initially involves soles of feet, spreads cephlad, and may initially present as foreign body sensation.
Monitor level of discomfort frequently and stop with any progression from "minimal" or “mild.”

“Coasting effect” =  peripheral neuropathy may continue to worsen for several weeks after discontinuation and then decrease in some cases.

Interactions Increased neurotoxicity of other neuropathic drugs
Suggested lab follow-up Serum lipase testing as indicated
Warning

Avoid use with d4T, ddI due to increased neurotoxicity.

Usage suggestions Zalcitabine has been largely abandoned due to the high incidence of peripheral neuropathy and its relative low potency.

Complete prescribing information

http://www.rocheusa.com/products/hivid/pi.html

 

 

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Quick Menu / Table of Contents
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Drug Summary Investigational Adherence Lab Evaluation Resistance Tests
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Updated 10.25.2005

 


 

1. Renal dosing information from: Ian R. McNicholl & Rudolph A. Rodriguez, MD, Dosing of Antiretroviral Drugs in Renal Insufficiency and Hemodialysis, May 2004
http://hivinsite.ucsf.edu/InSite?page=md-rr-18