Product image of Ophtesia (Oxybuprocaine Hydrochloride) supplied by GNH India

Ophtesia

Active Ingredient:
Oxybuprocaine Hydrochloride
Origin:
EU

Ophtesia (Oxybuprocaine Hydrochloride)

Oxybuprocaine hydrochloride, the active ingredient in Ophtesia, is a local anesthetic presented as a ophthalmic solution for topical eye use. It provides rapid surface anesthesia for diagnostic and minor therapeutic procedures on the ocular surface.

GNH India supplies Ophtesia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Agepha Pharma S.R.O

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Indications & Clinical Uses

Ophtesia is a topical ocular anesthetic used in procedures that involve the surface of the eye. It is employed in the following clinical situations:

  • Corneal abrasion assessment: facilitates painless examination of the cornea.
  • Intra‑ocular pressure measurement: enables comfortable tonometry.
  • Minor ocular surgery: provides short‑lasting anesthesia for procedures such as foreign‑body removal.
  • Diagnostic fluorescein staining: reduces discomfort during dye application.
  • Phototherapeutic keratectomy (PTK) preparation: aids in patient comfort during pre‑treatment assessment.

How It Works

  • Oxybuprocaine hydrochloride blocks voltage‑gated sodium channels on peripheral sensory nerve endings in the cornea and conjunctiva. By inhibiting sodium influx, it prevents the generation and propagation of action potentials, producing a reversible loss of sensation in the ocular surface tissues.

Side Effects

Adverse reactions to Ophtesia are generally mild and transient, but clinicians should be aware of both common and rare events.

Common Side Effects

  • Burning sensation: mild, transient irritation at the application site.
  • Stinging or itching.
  • Redness of the eye.
  • Tearing (epiphora).
  • Blurred vision: temporary loss of visual clarity.
  • Conjunctival hyperemia.

Serious or Rare Side Effects

  • Allergic contact dermatitis: localized swelling and rash.
  • Corneal epithelial toxicity: persistent epithelial defects.
  • Persistent corneal haze.
  • Severe ocular inflammation.
  • Vision loss: rare but reported in cases of overdose or misuse.
  • Anaphylaxis: extremely rare systemic reaction.

Precautions & Warnings

When using Ophtesia, health professionals should consider several safety measures to minimise risk.

  • Patient history: review for known hypersensitivity to ester‑type anesthetics.
  • Application frequency: limit to the minimum number of doses required for the procedure.
  • Contact lens wearers: advise removal of lenses before administration.
  • Pediatric use: exercise caution and adjust technique for children.
  • Concomitant ocular drugs: assess potential additive irritation.
  • Store at room temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Oxybuprocaine hydrochloride may interact with other ophthalmic agents, altering efficacy or safety.

Major Interactions (Avoid)

  • Combined use with other topical anesthetics: risk of cumulative toxicity.
  • Concurrent administration with cytotoxic ophthalmic chemotherapy agents: may increase corneal toxicity.

Moderate Interactions (Monitor Closely)

  • Use with preservative‑containing eye drops: potential for increased irritation.
  • Co‑administration with anti‑inflammatory eye drops: monitor for additive effects on corneal healing.
  • Interaction with systemic antihistamines: may modestly prolong anesthetic effect.
  • Use with ocular lubricants containing benzalkonium chloride: watch for enhanced epithelial disruption.

Frequently Asked Questions

Ophtesia is an ophthalmic solution containing oxybuprocaine hydrochloride that provides short‑acting surface anesthesia for eye examinations, tonometry, fluorescein staining and minor ocular procedures such as foreign‑body removal.

Oxybuprocaine blocks voltage‑gated sodium channels on sensory nerves of the cornea and conjunctiva, preventing nerve impulse generation and producing reversible loss of sensation on the ocular surface.

The prescribed dose of Ophtesia is determined by the treating clinician based on the specific procedure and patient needs; typical regimens involve one to two drops applied to the conjunctival sac immediately before the intervention.

Safety data for oxybuprocaine in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by the prescribing healthcare professional.

To order Ophtesia, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Ophtesia (oxy­buprocaine) is an ester‑type anesthetic offering rapid onset and short duration, similar to proparacaine but with a slightly longer anesthetic window. It is preferred for procedures requiring brief, reliable surface numbness and has a comparable safety profile when used as directed.

Ophtesia should be stored at room temperature, protected from light and moisture, and kept in its original container until use. Unopened vials remain stable for the shelf‑life indicated by the manufacturer.

Ophtesia is applied topically to the eye as one or two drops into the conjunctival sac. The eye should be gently closed for a few seconds to allow even distribution before the intended diagnostic or therapeutic procedure.

Serious risks, though rare, include allergic reactions such as contact dermatitis, corneal epithelial toxicity, persistent haze, and in extreme cases, vision loss. Immediate medical attention is required if severe irritation, swelling or visual changes occur.

Patients with known hypersensitivity to oxybuprocaine, other ester‑type anesthetics, or any component of the formulation should avoid Ophtesi a. Additionally, individuals with active corneal disease or severe ocular surface inflammation should not receive this medication without specialist evaluation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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