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Pronunciation |
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(vye
DARE a
been) |
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U.S. Brand
Names |
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Vira-A®
Ophthalmic |
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Generic
Available |
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No |
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Synonyms |
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Adenine Arabinoside; Ara-A; Arabinofuranosyladenine; Vidarabine
Monohydrate |
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Pharmacological Index |
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Antiviral Agent, Ophthalmic |
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Use |
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Treatment of acute keratoconjunctivitis and epithelial keratitis due to
herpes simplex virus type 1 and 2; superficial keratitis caused by herpes
simplex virus |
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Pregnancy Risk
Factor |
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C |
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Contraindications |
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Hypersensitivity to vidarabine or any component; sterile trophic
ulcers |
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Warnings/Precautions |
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Not effective against RNA virus, adenoviral ocular infections, bacterial
fungal or chlamydial infections of the cornea, or trophic ulcers; temporary
visual haze may be produced; neoplasia has occurred with I.M. vidarabine-treated
animals; although in vitro studies have been inconclusive, they have
shown mutagenesis |
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Adverse
Reactions |
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Percentage unknown: Burning eyes, lacrimation, keratitis, photophobia,
foreign body sensation, uveitis |
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Overdosage/Toxicology |
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No untoward effects anticipated with ingestion |
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Drug
Interactions |
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Allopurinol (may increase vidarabine levels) |
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Mechanism of
Action |
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Inhibits viral DNA synthesis by blocking DNA polymerase |
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Usual Dosage |
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Children and Adults: Ophthalmic: Keratoconjunctivitis: Instill
1/2
" of ointment in lower conjunctival sac 5 times/day every 3 hours while awake
until complete re-epithelialization has occurred, then twice daily for an
additional 7 days |
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Administration |
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Administer by I.V. infusion over 12 to 24 hours; vidarabine must be filtered
with a 0.45 micron or smaller pore size inline filter; administer at a final
concentration not to exceed 0.45 mg/mL to prevent precipitation. However,
concentrations up to 0.7 mg/mL have been administered to fluid-restricted
patients. |
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Mental Health: Effects
on Mental Status |
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None reported |
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Mental Health:
Effects on Psychiatric
Treatment |
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None reported |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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For ophthalmic use only. Store in refrigerator. Apply prescribed amount as
often as directed. Wash hands before using and do not let tip of applicator
touch eye or contaminate tip of applicator. Tilt head back and look upward.
Gently pull down lower lid and put drop(s) in inner corner of eye. Close eye and
roll eyeball in all directions. Do not blink for
1/2
minute. Apply gentle pressure to inner corner of eye for 30 seconds. Wipe away
excess from skin around eye. Do not use any other eye preparation for at least
10 minutes. Do not touch tip of applicator to eye or contaminate tip of
applicator. Do not share medication with anyone else. May cause sensitivity to
bright light (dark glasses may help); temporary stinging or blurred vision may
occur. Inform prescriber if you experience eye pain, redness, burning, watering,
dryness, double vision, puffiness around eye, vision disturbances, or other
adverse eye response; worsening of condition or lack of improvement within 7-14
days. Pregnancy/breast-feeding precautions: Inform prescriber if you are
pregnant. Consult prescriber if breast-feeding. |
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Dosage Forms |
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Ointment, ophthalmic, as monohydrate: 3% [30 mg/mL = 28 mg/mL base] (3.5
g) |
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References |
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"Drugs for Non-HIV Viral Infections," Med Lett Drugs Ther, 1994,
36(919):27.
Whitley R, Arvin A, Prober C, et al,
"A Controlled Trial Comparing Vidarabine With Acyclovir in Neonatal Herpes Simplex Virus Infection. Infectious Diseases Collaborative Antiviral Study Group,"
N Engl J Med, 1991, 324(7):444-9.
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