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Xalatan

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Xalatan 0.005% (Latanoprost) is an ophthalmic solution used to treat high pressure inside the eye, including conditions like glaucoma. It works by increasing the natural drainage of fluid from the eye. Lowering this pressure is essential for preventing vision loss and maintaining ocular health in adults.


Ingredient
Category
Availability
In Stock
Delivery Time
Airmail (14-21 days) | EMS trackable (5-9 days)
Product is shipped in a fully discreet envelope with no content disclosure, including all required documentation inside

Product Sheet

Active Ingredient(s)
Latanoprost
Reference Brand
Xalatan
Manufacturer
Pfizer
Product Form
Eye drops
Regulatory Classification
Rx
Primary Category
Eye Care
Product Category
Antiglaucoma Preparations, Prostaglandin Analogues
Pharmacological Class
Prostaglandin F2-alpha Analogue
Clinical Indications
Manufacturer Description
Medicated eye drops used daily to lower high pressure in the eye and prevent vision loss from glaucoma.
Mechanism of Action
Latanoprost works by increasing the natural drainage of fluid from inside the eye into the bloodstream. This lowers the pressure within the eye, preventing damage to the optic nerve.
Route of Administration
Topical (Eye)
Onset Time
3-4 hours
Duration
24 hours
Contraindications
Hypersensitivity to latanoprost, Active eye inflammation
Severe Adverse Events
Severe eye pain, Swelling of the eyelid, Systemic allergic reaction
Common Side Effects
Mild eye irritation, Eyelash growth, Slight redness
Uncommon Side Effects
Change in eye colour (browning), Blurred vision, Dry eyes
Drug Interactions
Other eye drops containing prostaglandins, Thimerosal eye drops
Pregnancy Safety Warnings
Use only if benefits outweigh risks.
Age Restrictions
Safe for children if prescribed
Storage Guidelines
Store in fridge before opening; room temperature after opening.
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Xalatan FAQ

Can Xalatan 0.005% be used in both eyes at the same time?

Yes. The standard regimen is one drop in each affected eye once nightly. If only one eye requires treatment, the drop can be limited to that eye alone.

What should I do if I experience a change in iris colour?

Iris colour change is a known, usually permanent effect of latanoprost. It does not affect vision, but you should discuss any concerns with your ophthalmologist, especially if the change is unexpected or pronounced.

Are there any special considerations for patients who wear contact lenses?

Remove contact lenses before instilling the drop, wait at least 15 minutes, and then re-insert them. Some patients prefer to wear lenses after dosing to minimise irritation.

How long does a 2.5 ml bottle typically last?

A single 2.5 ml bottle supplies approximately 50 drops (about 0.05 ml per drop). At one drop per eye per night, the bottle will last roughly 3-4 weeks.

Is Xalatan 0.005% safe for use after eye surgery?

It is generally safe after uncomplicated cataract surgery, but the operating surgeon may advise temporary discontinuation to reduce the risk of postoperative inflammation.

Can other eye-drop medications be taken on the same day?

Yes, but the timing should be separated by at least 5 minutes. Use the “blink-and-wait” technique: apply the first drop, close the eye gently, then wait before instilling another medication.

Does Xalatan interact with systemic medications for hypertension?

Latanoprost’s systemic absorption is minimal, and no clinically significant interaction with oral antihypertensive drugs has been reported.

Why is the medication administered in the evening rather than the morning?

Evening dosing aligns with the natural circadian rise in IOP that occurs overnight, providing better IOP control during the early morning hours when pressure peaks.

What packaging differences exist for Xalatan in other countries?

In the United States, Xalatan is supplied in a 3 ml bottle with the same concentration. The UK version is a 2.5 ml bottle, but the dosing instructions remain identical.

Can Xalatan be used by patients with a history of uveitis?

Active uveitis is a contraindication because prostaglandin analogues may exacerbate intra-ocular inflammation. Once inflammation resolves, an ophthalmologist may reassess suitability.

What is Xalatan 0.005%?

Xalatan 0.005% is a brand-name ophthalmic solution that contains latanoprost as its active ingredient. Latanoprost belongs to the prostaglandin-analog class of eye-care medications and is approved in the United Kingdom by the Medicines and Healthcare products Regulatory Agency (MHRA) for the reduction of intra-ocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. The product is supplied in single-use 2.5 ml bottles of sterile eye-drop solution.

How Xalatan 0.5% Works in the Body

Latanoprost is a synthetic analogue of prostaglandin F₂α. After instillation into the conjunctival sac, the drug penetrates the cornea and is hydrolyzed to its active acid form. The active metabolite binds to prostaglandin-F (FP) receptors in the ciliary body and trabecular meshwork, leading to:

  • Increased outflow of aqueous humour through the uveoscleral pathway
  • Modest enhancement of conventional outflow via the trabecular meshwork

These actions lower the pressure inside the eye, which helps prevent optic-nerve damage associated with glaucoma. The therapeutic effect typically begins within 12 hours of the first dose and reaches a plateau after about four to six weeks of consistent nightly use. Because the drug acts locally, systemic exposure is minimal.

Conditions Treated by Xalatan 0.005%

Xalatan 0.005% is approved in the UK for the following indications:

  • Primary open-angle glaucoma (POAG) - a chronic optic-nerve disease characterised by progressive visual field loss.
  • Ocular hypertension - elevated IOP without detectable optic-nerve damage.

Both conditions are managed by maintaining IOP at a level that reduces the risk of visual field deterioration. Xalatan is often prescribed as first-line therapy, especially when a once-daily dosing schedule is preferred.

Off-Label and Investigational Applications

Current peer-reviewed literature does not provide robust evidence for approved off-label uses of latanoprost in the UK. While some small studies have explored its role in secondary glaucoma types (e.g., pseudoexfoliative glaucoma), these applications remain investigational and should only be considered under specialist supervision.

Who Should Not Use Xalatan 0.005%?

Absolute Contraindications

  • Known hypersensitivity to latanoprost, any excipients in the formulation, or other prostaglandin analogues.
  • Active intra-ocular inflammation or infection (e.g., uveitis, bacterial keratitis) in the eye to be treated.

Relative Contraindications

  • Pregnancy - limited human data; prostaglandin analogues are classified as pregnancy category C in the UK.
  • Breast-feeding - caution is advised because the drug may be secreted in milk.
  • Severe ocular surface disease - patients with compromised corneal integrity may experience heightened irritation.

Special Populations

  • Elderly patients - may be more susceptible to eyelash changes and iris pigmentation; routine monitoring is recommended.
  • Pediatric patients - latanoprost is not licensed for use in children under 12 years of age in the UK.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Eyelash changes - increased length, thickness, or darkness (usually reported in > 10 % of users).
  • Iris pigmentation - gradual darkening of the iris, more noticeable in lighter-coloured eyes.
  • Hyperemia - mild redness of the conjunctiva.
  • Eye irritation - transient burning or stinging upon instillation.

These effects are generally mild, reversible on discontinuation (except iris colour change, which may be permanent), and do not require medical intervention.

Serious Adverse Events

  • Anterior uveitis - inflammation of the uveal tract; requires immediate ophthalmic evaluation.
  • Severe ocular allergy - erythema, swelling, or pain persisting beyond 48 hours.
  • Rapid IOP increase - paradoxical pressure rise is rare but warrants urgent assessment.

Drug Interactions

  • Cycloplegic agents (e.g., atropine) may lessen the IOP-lowering effect of latanoprost.
  • Non-steroidal anti-inflammatory eye drops - concurrent use is generally safe, but clinicians may monitor for additive ocular irritation.
  • Systemic prostaglandin inhibitors - no clinically significant interaction has been demonstrated, but patients should disclose all medications.

Food and Lifestyle Interactions

  • Alcohol - no direct interaction, but excessive consumption can impair adherence to a nightly dosing schedule.
  • Driving or operating machinery - latanoprost does not affect visual acuity or cognition; patients may continue normal activities.

Note: Patients should inform their ophthalmologist of all prescription drugs, over-the-counter products, herbal supplements, and vitamins before starting Xalatan 0.005%.

How to Take Xalatan 0.005%

  • Standard dosing - one drop (approximately 0.05 ml) in each affected eye once daily in the evening.
  • Administration technique -
  • Wash hands thoroughly.
  • Tilt the head back and pull down the lower eyelid to create a small pocket.
  • Hold the bottle inverted, avoid touching the tip to any surface, and squeeze gently to release a single drop.
  • Close the eye gently for a few minutes; gently press the inner canthus to limit systemic absorption.
  • Missed dose - If a dose is forgotten, instil it as soon as remembered unless it is close to the next scheduled dose; do not double-dose.
  • Overdose - Excessive instillation may cause ocular irritation, hyperemia, or transient blurred vision. If severe symptoms develop, seek ophthalmic care promptly.
  • Discontinuation - Sudden cessation can lead to rebound IOP elevation. Any change in therapy should be guided by an eye-care professional, often with a tapering plan or substitution.

Monitoring and Follow-Up

  • Baseline assessment - measurement of IOP, visual field testing, and optic-nerve imaging before initiating therapy.
  • Follow-up visits - typically at 4-6 weeks after starting treatment, then every 3-6 months to confirm target IOP and monitor for side effects.
  • Laboratory testing - not required for latanoprost, but clinicians may assess renal or hepatic function if systemic comorbidities exist.

Storage and Handling

  • Store the bottle at room temperature (15 °C-30 °C), protected from direct sunlight and moisture.
  • Keep the container tightly closed when not in use.
  • Do not freeze the solution; a frozen bottle should be discarded.
  • Expiry - use the medication before the printed expiry date; discard any remaining solution after that time.
  • Disposal - empty bottles can be recycled according to local council guidelines; do not flush the solution down the drain.

Medication-Specific Glossary

Prostaglandin F₂α analogue
A synthetic compound that mimics the action of the naturally occurring prostaglandin F₂α, used to increase aqueous-humour outflow in glaucoma therapy.
Uveoscleral pathway
A secondary drainage route for aqueous humour that passes through the ciliary body’s extracellular matrix, accounting for much of the IOP-lowering effect of prostaglandin analogues.
Intra-ocular pressure (IOP)
The fluid pressure inside the eye; elevated IOP is a major risk factor for optic-nerve damage in glaucoma.
Iridial pigmentation
Darkening of the coloured part of the eye (iris) that can occur with prolonged exposure to prostaglandin analogues.

Medical Disclaimer

This article provides educational information about Xalatan 0.005% and is not a substitute for professional medical advice. Treatment decisions, including the use of any medication for unapproved indications, must be made under the guidance of a qualified healthcare provider. The content is intended for informational purposes and does not constitute medical recommendations. Always consult a physician before starting, stopping, or changing any medication regimen.

Information for Xalatan is sourced from established medical standards and updated frequently. It is provided for general guidance and should be confirmed with a healthcare professional before use.
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