Buy Travoprost
Travoprost

30
Prescription eye drops used daily to prevent vision loss caused by high pressure in the eye.


Ingredient
Availability
In Stock
Delivery
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

Alternative/Local Brand
Travatan
Active Ingredient(s)
Travoprost
Primary Category
Eye Care, Glaucoma Treatment
Therapeutic Class
Ophthalmologicals, Antiglaucoma preparations
Pharmacological Class
Prostaglandin analogue
Indications
Open-angle glaucoma, Ocular hypertension
Contraindications
Hypersensitivity, Active intraocular inflammation
Minor Side Effects
Eye redness, Itchy eyes, Dry eyes
Moderate Side Effects
Increased eyelash growth, Eye pain, Foreign body sensation
Serious Side Effects
Changes in iris colour (permanent), Macular oedema, Uveitis
Dosage Forms
Eye drops
Administration Route
Ophthalmic
Mechanism of Action
It increases the natural drainage of fluid (aqueous humour) from inside the eye, which reduces the pressure within the eyeball.
Prescription Status
Rx
Patient Summary
Prescription eye drops used daily to prevent vision loss caused by high pressure in the eye.
Onset Time
2 hours
Duration
24 hours
Storage Instructions
Store below 25°C; discard 4 weeks after opening
Drug Interactions
Bimatoprost, Latanoprost
Age Restrictions
Adults only
Pregnancy Use
Avoid during pregnancy
Alternative Drugs
Latanoprost, Lumigan

Travoprost: Generic Medication Overview

Travoprost is a prostaglandin analog used in ophthalmic care to lower intra-ocular pressure (IOP) in patients with certain types of glaucoma and ocular hypertension. This article covers Travoprost, available as a generic medication and marketed under brand names such as Travatan and Travatan Z. It is supplied as a sterile ophthalmic solution in a 0.004% concentration, packaged in a single-dose or multi-dose bottle. In Hong Kong, travoprost is a prescription-only product regulated by the Department of Health.

How Travoprost Works in the Body

Travoprost mimics the activity of prostaglandin F₂α, binding to prostanoid FP receptors located on the ciliary muscle and trabecular meshwork of the eye. Activation of these receptors enhances uveoscleral outflow, the alternative pathway by which aqueous humor drains from the anterior chamber. Increased outflow reduces intra-ocular pressure, helping to prevent optic nerve damage associated with glaucoma.

  • Onset of action: Typically within 3-4 hours after a single dose.
  • Peak effect: Around 12 hours post-instillation.
  • Duration: IOP-lowering effect persists for at least 24 hours, supporting once-daily dosing.

Because travoprost is administered topically, systemic absorption is minimal, and the drug’s bioavailability is confined to ocular tissues.

Conditions Treated by Travoprost

Travoprost is approved in Hong Kong for the reduction of elevated intra-ocular pressure in:

  • Primary open-angle glaucoma (POAG)
  • Ocular hypertension

These indications are based on clinical studies demonstrating a sustained IOP reduction of approximately 20-30 % compared with baseline measurements. Travoprost is generally prescribed for adult patients; pediatric use is considered only in specialist settings when benefits outweigh risks.

Evidence-Based Off-Label Uses

No robust peer-reviewed evidence currently supports off-label indications for travoprost. Consequently, this section is omitted.

Who Should Not Use Travoprost?

Absolute Contraindications

  • Known hypersensitivity to travoprost, any prostaglandin analog, or any component of the ophthalmic solution (e.g., benzalkonium chloride).
  • Active ocular infections (e.g., conjunctivitis, keratitis) that could be aggravated by prostaglandin exposure.

Relative Contraindications

  • Inflammatory eye conditions such as uveitis; use only under specialist supervision.
  • Recent ocular surgery (e.g., trabeculectomy) where prostaglandin-induced inflammation may compromise healing.
  • Pregnancy and breastfeeding: safety data are limited; the drug should be used only if clearly needed and after risk-benefit assessment.

Special Populations

  • Elderly: No dosage adjustment required solely based on age, but clinicians should monitor for ocular surface changes.
  • Renal/Hepatic Impairment: Systemic exposure is negligible; no specific adjustments are required.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Conjunctival hyperemia (eye redness) - frequently reported.
  • Eyelash changes (increased length, thickness, or darkening).
  • Periocular skin darkening - mild hyperpigmentation around the treated eye.
  • Transient ocular irritation - stinging or burning sensation upon instillation.

These effects are generally mild and may diminish with continued use.

Serious Adverse Events

  • Anterior uveitis - rare inflammation of the uveal tract; requires immediate ophthalmic evaluation.
  • Corneal edema - uncommon; patients should report persistent visual disturbance.

If any severe ocular pain, vision loss, or sudden swelling occurs, seek urgent medical attention.

Drug Interactions

  • Non-steroidal anti-inflammatory eye drops (e.g., ketorolac): May reduce the IOP-lowering effect of travoprost; consider spacing administration by at least 5 minutes.
  • Topical corticosteroids: Potential to diminish prostaglandin efficacy; monitor IOP closely.

Because systemic absorption is minimal, systemic drug interactions are not a major concern.

Food and Lifestyle Interactions

  • Alcohol: No direct interaction, but excessive intake can affect ocular blood flow; maintain moderate consumption.
  • Driving/Machinery: Travoprost does not impair cognition or motor skills.
  • Sunlight: Prolonged exposure may accentuate peri-ocular pigmentation; advise patients to use sunscreen around the eyes if cosmetically concerned.

How to Take Travoprost

  • Standard dosing: One drop (approximately 0.05 mL) of the 0.004 % solution instilled into the affected eye(s) once daily in the evening.
  • Administration tips: Wash hands, avoid touching the tip of the bottle to the eye or any surface. Gently pull down the lower eyelid to create a small pocket and place the drop without squeezing the bottle.
  • Special populations: No routine dosage changes are required for elderly patients or those with mild renal/hepatic impairment.
  • Missed dose: If a dose is forgotten, apply it as soon as remembered unless the usual dosing time is near; do not double the next dose.
  • Overdose: Excessive application may cause prolonged ocular redness and irritation. If large quantities are applied accidentally, rinse the eye with sterile saline and seek ophthalmic advice.
  • Discontinuation: Travoprost does not require tapering. Stopping treatment may result in a gradual rise in IOP; patients should discuss alternative therapy with their eye-care professional.

Monitoring and Follow-Up

  • Baseline evaluation: Measure intra-ocular pressure, assess optic nerve health (optical coherence tomography or visual field testing).
  • Follow-up schedule: Re-check IOP 4-6 weeks after initiation, then every 3-6 months, or as directed by the treating ophthalmologist.
  • Adverse event monitoring: Observe for signs of inflammation, persistent redness, or pigment changes; report concerns promptly.

Storage and Handling

  • Store the bottle at room temperature (15-30 °C).
  • Protect from direct sunlight and freezing temperatures.
  • Keep the container tightly closed when not in use.
  • Discard any solution that has changed color or become cloudy.
  • Do not use the product beyond the expiration date indicated on the label.
  • Keep out of reach of children and pets.

Medication-Specific Glossary

Prostaglandin F₂α analog
A class of compounds that imitate the natural prostaglandin F₂α molecule, promoting increased outflow of aqueous humor through the uveoscleral pathway.
Intra-ocular pressure (IOP)
The fluid pressure inside the eye; elevated IOP is a primary risk factor for optic nerve damage in glaucoma.
Uveoscleral outflow
One of the two main drainage routes for aqueous humor, involving passage through the ciliary muscle and surrounding tissues.
Hyperemia
Redness of the eye caused by increased blood flow in the conjunctival vessels.
Periocular hyperpigmentation
Darkening of the skin around the eye, a reversible side effect observed with prolonged prostaglandin analog use.

Medical Disclaimer

This article provides educational information about travoprost and is not a substitute for professional medical advice. Treatment decisions, including use 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.

Travoprost FAQ

Can travoprost be used for both eyes at the same time?

Yes. Travoprost can be administered to each affected eye once daily. Apply one drop to one eye, wait a few minutes, then apply a drop to the other eye to avoid cross-contamination.

What should I do if I experience persistent eye redness after starting travoprost?

Persistent conjunctival hyperemia may be managed with artificial tears or a mild anti-inflammatory eye drop, but you should contact your ophthalmologist to confirm that the reaction is not due to an underlying condition.

How does travoprost compare with latanoprost in terms of efficacy?

Both travoprost and latanoprost are prostaglandin analogs that lower IOP by enhancing uveoscleral outflow. Clinical trials have shown comparable IOP reductions, though individual response can vary; your eye-care professional will select the most appropriate agent for you.

Is there any concern about using travoprost with contact lenses?

Travoprost is generally safe with contact lenses, but the drop may cause temporary blurry vision. It is advisable to insert lenses after the medication has been absorbed, or remove lenses before dosing and re-insert them later.

Can travoprost cause changes in eyelash growth?

Yes. A common side effect is increased eyelash length, thickness, or darkness. This effect is usually mild and reversible after discontinuation of the medication.

Will travoprost affect my ability to drive or operate machinery?

Travoprost does not impair cognitive function or motor skills. However, if you experience significant visual disturbances, you should refrain from driving until the issue resolves.

Are there any special considerations for patients with dry eye syndrome?

Travoprost may cause transient ocular irritation. Patients with dry eye may benefit from preservative-free artificial tears, used at a different time than the prostaglandin drop.

How long does a bottle of travoprost typically last?

A standard 5 mL bottle contains approximately 100 drops. At one drop per eye daily, a single bottle can last up to 100 days, though usage frequency should be confirmed with your ophthalmologist.

Is travoprost safe for use during pregnancy?

Safety data in pregnancy are limited. Travoprost should be used only if the potential benefit justifies the potential risk to the fetus, after discussion with a qualified healthcare provider.

What are the disposal guidelines for unused travoprost solution?

Unused or expired travoprost should be placed in a sealed container and disposed of according to local pharmacy or hazardous waste collection programs to prevent accidental exposure.

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