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Vidarabine
Pronunciation
U.S. Brand Names
Generic Available
Synonyms
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Mechanism of Action
Usual Dosage
Administration
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Patient Information
Dosage Forms
References

Pronunciation
(vye DARE a been)

U.S. Brand Names
Vira-A® Ophthalmic

Generic Available

No


Synonyms
Adenine Arabinoside; Ara-A; Arabinofuranosyladenine; Vidarabine Monohydrate

Pharmacological Index

Antiviral Agent, Ophthalmic


Use

Treatment of acute keratoconjunctivitis and epithelial keratitis due to herpes simplex virus type 1 and 2; superficial keratitis caused by herpes simplex virus


Pregnancy Risk Factor

C


Contraindications

Hypersensitivity to vidarabine or any component; sterile trophic ulcers


Warnings/Precautions

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


Adverse Reactions

Percentage unknown: Burning eyes, lacrimation, keratitis, photophobia, foreign body sensation, uveitis


Overdosage/Toxicology

No untoward effects anticipated with ingestion


Drug Interactions

Allopurinol (may increase vidarabine levels)


Mechanism of Action

Inhibits viral DNA synthesis by blocking DNA polymerase


Usual Dosage

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


Administration

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.


Mental Health: Effects on Mental Status

None reported


Mental Health: Effects on Psychiatric Treatment

None reported


Dental Health: Local Anesthetic/Vasoconstrictor Precautions

No information available to require special precautions


Dental Health: Effects on Dental Treatment

No effects or complications reported


Patient Information

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.


Dosage Forms

Ointment, ophthalmic, as monohydrate: 3% [30 mg/mL = 28 mg/mL base] (3.5 g)


References

"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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