Product image of Hydrocortisone Pos Ursapharm Benelux (Hydrocortisone Acetate) supplied by GNH India

Hydrocortisone Pos Ursapharm Benelux

Active Ingredient:
Hydrocortisone Acetate
Origin:
EU

Hydrocortisone Pos Ursapharm Benelux (Hydrocortisone Acetate)

Hydrocortisone Pos Ursapharm Benelux is an ocular preparation containing the corticosteroid hydrocortisone acetate. It is supplied in a topical eye formulation intended for local anti‑inflammatory therapy. The product is manufactured for the European Union market and follows the regulatory standards applicable to ophthalmic corticosteroids. It is presented as a sterile solution for instillation into the conjunctival sac, and it is packaged in unit‑dose containers to preserve sterility and dosage accuracy.

Manufacturer / TM Owner

Ursapharm Benelux B.V.

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Indications & Clinical Uses

Hydrocortisone Pos Ursapharm Benelux is used in ophthalmology to manage inflammatory conditions of the eye where a topical corticosteroid is indicated. It may be prescribed by eye care professionals for short‑term treatment to reduce swelling, redness, and discomfort.

  • Mild to moderate anterior uveitis
  • Post‑operative inflammation after cataract or intraocular surgery
  • Allergic conjunctivitis with significant inflammatory component
  • Episcleritis or superficial keratitis with edema
  • Contact lens‑related inflammatory irritation

How It Works

  • Hydrocortisone acetate is a glucocorticoid pro‑drug that, after ocular absorption, is hydrolyzed to active hydrocortisone. The active molecule binds to intracellular glucocorticoid receptors, forming a complex that translocates to the nucleus and modulates gene transcription. This action suppresses the synthesis of pro‑inflammatory cytokines, reduces phospholipase A2 activity, and stabilizes lysosomal membranes, collectively decreasing vascular permeability, edema, and leukocyte migration in ocular tissues.

Side Effects

Adverse reactions to ocular hydrocortisone acetate are generally local and dose‑related, though systemic absorption can occur with extensive use.

Common

  • Transient burning or stinging on instillation
  • Temporary blurred vision that resolves within minutes
  • Mild conjunctival hyperemia
  • Localized itching or dryness
  • Eyelid edema
  • Foreign body sensation

Serious

  • Increased intra‑ocular pressure leading to glaucoma
  • Development of cataract with prolonged therapy
  • Secondary ocular infection due to immunosuppression
  • Corneal ulceration or perforation in susceptible eyes

Precautions & Warnings

When prescribing or using Hydrocortisone Pos Ursapharm Benelux, clinicians and patients should observe several safety considerations to minimize risks.

  • Avoid use in eyes with active viral, fungal, or tubercular infections.
  • Limit duration to the shortest effective period to reduce risk of pressure elevation.
  • Monitor intra‑ocular pressure in patients with a history of glaucoma or steroid response.
  • Use with caution in diabetic patients, as systemic absorption may affect glucose control.
  • Do not apply to the cornea if a corneal ulcer is present.
  • Discontinue if signs of secondary infection appear.
  • Keep the container sealed; discard after the indicated period after opening.

Avoid Interactions

Hydrocortisone acetate can interact with other ophthalmic or systemic agents, potentially altering efficacy or safety.

Avoid

  • Concurrent use of potent topical NSAIDs in the same eye, which may increase corneal toxicity.
  • Systemic corticosteroids, as additive immunosuppression can raise infection risk.
  • Anticholinergic eye drops that may exacerbate dry‑eye symptoms.

Use with caution

  • Beta‑blocker eye drops, because steroid‑induced IOP rise may counteract glaucoma control.
  • Antifungal or antiviral ophthalmic preparations, requiring close monitoring for reduced effectiveness.
  • Systemic cyclosporine or tacrolimus, where combined immunosuppression may increase infection susceptibility.

Frequently Asked Questions

It is typically prescribed for inflammatory eye conditions such as anterior uveitis, post‑operative inflammation, allergic conjunctivitis, episcleritis, and contact lens‑related irritation.

When instilled into the eye, hydrocortisone acetate is converted to active hydrocortisone, which then binds glucocorticoid receptors in ocular tissues to reduce inflammation locally.

Yes, prolonged use of ocular corticosteroids can raise intra‑ocular pressure, so patients at risk for glaucoma should be monitored regularly.

Generally, artificial tears can be used before or after the steroid drops, but they should be spaced at least five minutes apart to avoid dilution.

A mild burning or stinging sensation is common; if it persists or worsens, discontinue use and consult your eye care professional.

Systemic absorption from eye drops is minimal, but in rare cases it may affect blood glucose or cause systemic steroid effects, especially with extensive or prolonged use.

No, corticosteroids can worsen viral infections; they should be avoided until the infection is cleared or under specialist guidance.

Follow the manufacturer’s label; typically, ophthalmic solutions are recommended for use within 30 days after opening to maintain sterility.

In many EU countries the product is available by prescription only, though local regulations may vary.

Seek urgent care if you notice sudden vision loss, severe eye pain, increased redness, signs of infection, or a noticeable rise in intra‑ocular pressure.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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