HIVID
General description
Hivid is the brand name for zalcitabine, formerly called ddC,
produced by Roche Laboratories. It is a synthetic pyrimidine
nucleoside analogue active against HIV infection. Hivid is
available in tablet form.
Mechanism
Zalcitabine is enzymatically converted to an active form
which inhibits HIV reverse transcriptase activity in two ways. It
competes for utilization of a natureal substrate and it
incorporates itself into viral DNA, terminating viral DNA chain
growth. This drug also inhibits DNA polymerase activity in its
active form.
Indications
Hivid is indicated to be used in combination with other
antiretroviral agents to treat HIV infection.
Usage/Dosage
The general recommendation is one 0.750 mg tablet every 8 hours. For
patients with creatine clearance 10 to 40 mL/min, a reduced dosage of
0.750 mg every twelve hours is recommended, and for a creating clearance
of less than 10 mL/min, 0.750 mg every 24 hours is recommended. This drug
is to be used in combination with other treatment.
Precautions
Patients with lowered CD4 cell counts appear to have higher
rates of incidence of adverse effects. Patients should be
informed that Hivid is not a cure for HIV infection and that they may
continue to acquire illnesses associated with HIV infection and
are still able to transmit HIV to other people. Use of Hivid
concomitantly with drugs associated with peripheral neuopathy is
not recommended. These include chloramphenicol, cisplatin,
dapsone, disulfiram, ethionamide, glutethimide, gold,
hydralazine, iodoquinol, isoniazid, metronidazole,
nitrofurantoin, phenytoin, ribavirin, and vincristine. Hivid has
been shown to be teratogenic in mice in a lab setting.
Contraindications
Hivid is contraindicated for any patients with a hypersensitivity to
any of the drug components. It should not be used with
didanosine.
Potential Adverse Effects
The major adverse toxic effect of hivid has been peripheral neuropathy
characterized by numbness, nurning dysthesia, and sharp pain. Other more
rare effects are pancreatitis, hepatic toxicity, oral and esophageal
ulcers, heart failure, and anaphylactoid reaction. These other effects,
however, occur very rarely.