Buy Careprost
Careprost

35.27
Careprost + Applicators (Bimatoprost) provides a complete solution for eyelash enhancement and ocular pressure management. The active ingredient stimulates the eyelash growth phase for fuller lashes while also treating glaucoma symptoms. This kit ensures hygienic and precise application of the solution, supporting both cosmetic goals and ocular health.


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)
Bimatoprost
Reference Brand
Lumigan
Manufacturer
Sun Pharmaceutical
Product Form
Eye drops solution
Regulatory Classification
Rx
Primary Category
Glaucoma Treatment, Lash Growth
Product Category
Ophthalmologicals, Antiglaucoma preparations, Prostaglandin analogues
Pharmacological Class
Prostamide analogue
Manufacturer Description
A treatment for reducing pressure in the eye or enhancing the appearance of eyelashes.
Mechanism of Action
Bimatoprost mimics natural substances in the body to help drain fluid from the eye. This reduces pressure that can damage vision. It also stimulates the growth of hair follicles on the eyelash line.
Route of Administration
Ophthalmic
Onset Time
Within 4 to 8 hours
Duration
24 hours
Contraindications
Hypersensitivity, Macular oedema, Active eye inflammation
Severe Adverse Events
Vision changes, Inflammation inside the eye, Sensitivity to light
Common Side Effects
Irritated eyes, Red eyes
Uncommon Side Effects
Darkening of the skin around eyes, Eyelashes becoming darker, Eye stinging
Drug Interactions
Vyzulta, Xelpros
Pregnancy Safety Warnings
Use only if essential; safety in pregnancy not fully established.
Age Restrictions
Adults
Storage Guidelines
Store in a cool place, typically between 2°C and 25°C.
Related Products
Lumigan, Latisse, Bimat

Careprost FAQ

Can I use Careprost + Applicators if I wear contact lenses?

Yes, you can wear contacts, but it is advisable to remove them before instilling the drop and wait at least 15 minutes before reinserting to avoid drug residue on the lens surface.

Will my eye colour change permanently?

Prolonged use can cause irreversible darkening of the iris, especially in people with light-coloured eyes. The change usually stabilises after several months of continuous therapy.

Is it safe to use the drops while pregnant?

Bimatoprost is not recommended during pregnancy unless the potential benefit outweighs the risk. Discuss any plans for pregnancy with your ophthalmologist before starting treatment.

How long does a 3 ml bottle typically last?

A single 0.01 % drop contains about 0.05 ml. At one drop per eye per day, a 3 ml bottle provides roughly 30 days of therapy for bilateral use.

What should I do if I experience severe eye pain after a dose?

Severe pain may indicate an adverse reaction such as inflammation or ocular hypotony. Seek urgent ophthalmic assessment; do not continue the medication until cleared by a clinician.

Can I combine Careprost with other glaucoma eye drops?

Combination therapy (e.g., with a beta-blocker or carbonic anhydrase inhibitor) is common and often effective. Your eye-care professional will tailor the regimen and monitor IOP closely.

Why does my eye become red after using the drops?

Conjunctival hyperemia (redness) is a frequent, dose-related side effect caused by vasodilation of ocular blood vessels. It is usually mild and may lessen with continued use.

Is there a risk of systemic side effects from a single eye drop?

Systemic absorption is minimal, but trace amounts can enter the bloodstream. Report any unexpected systemic symptoms (e.g., headaches, respiratory changes) to your doctor.

How should I dispose of the empty bottle and applicator?

Return the empty container to a pharmacy for safe disposal or follow local NHS guidance for pharmaceutical waste. Do not discard it in household recycling bins.

What is Careprost + Applicators?

Careprost + Applicators is a branded ophthalmic preparation that contains bimatoprost as its active ingredient. It is supplied in a 3 ml bottle together with a sterile applicator (dropper) for direct instillation into the eye.

  • Therapeutic class: Eye-care (prostaglandin analogue)
  • Regulatory status in the UK: Prescription-only medicine (POM) authorised by the MHRA for the treatment of elevated intra-ocular pressure associated with open-angle glaucoma and ocular hypertension.

The product’s formulation is a sterile aqueous solution intended for topical ocular use.

How Bimatoprost Works in the Body

Bimatoprost belongs to the prostaglandin-analogue family. After a drop is placed on the eye’s surface, the drug penetrates the cornea and reaches the trabecular meshwork, the primary drainage pathway for aqueous humour.

  • Mechanism: It increases outflow of aqueous humour through the uveoscleral and trabecular pathways, thereby lowering intra-ocular pressure (IOP).
  • Onset and duration: IOP-lowering effects can be observed within 4 hours of a single dose and are sustained for at least 24 hours, supporting once-daily dosing.
  • Metabolism: Bimatoprost is hydrolysed by ocular esterases to the active acid form, which binds to prostaglandin-F (FP) receptors in the eye.

By improving fluid drainage, the medication helps protect the optic nerve from pressure-related damage.

Conditions Treated by Careprost + Applicators

Approved indications (UK, MHRA)

  • Primary open-angle glaucoma - a chronic condition characterised by progressive optic-nerve loss due to elevated IOP.
  • Ocular hypertension - sustained IOP > 21 mmHg without detectable glaucomatous damage.

These indications are based on clinical trial evidence showing that bimatoprost effectively reduces IOP compared with placebo and other prostaglandin analogues.

Evidence-Based Off-Label Uses

Bimatoprost is also employed off-label for enhancement of eyelash growth. This use mirrors the formulation marketed elsewhere as Latisse® (the same active ingredient at the same concentration).

  • Evidence quality: Randomised controlled trials demonstrate increased eyelash length, thickness and darkness after nightly application to the lid margin for at least 12 weeks.
  • Regulatory status: Not approved for cosmetic eyelash enhancement in the UK.
  • Safety disclaimer: Off-label use should be undertaken only under the supervision of a qualified ophthalmologist or dermatologist, with regular monitoring for ocular irritation or pigmentary changes.

Who Should (and Should Not) Use Careprost + Applicators?

Ideal candidates

  • Adults (≥ 18 years) diagnosed with open-angle glaucoma or ocular hypertension.
  • Patients who can reliably instil a single daily drop and attend regular IOP-monitoring appointments.

Absolute contraindications

  • Known hypersensitivity to bimatoprost or any excipients in the solution (e.g., benzalkonium chloride).
  • Active ocular inflammation (e.g., uveitis) or infection in the eye to be treated.

Relative contraindications

  • Pregnancy or lactation: Animal data suggest potential fetal risk; use only if clearly needed and prescribed.
  • Severe ocular surface disease (dry eye, corneal epithelial defects) - may worsen irritation.
  • History of intra-ocular surgery within the past 4 weeks - defer treatment until the eye has healed.

Patients with systemic conditions such as uncontrolled asthma or cardiovascular disease are not automatically excluded, but clinicians should assess individual risk.

Safety Profile: Side Effects and Interactions

Common Side Effects

  • Conjunctival hyperemia (eye redness) - reported in the majority of users; usually mild and transient.
  • Eyelash changes - increased length, thickness, or pigmentation (desired for cosmetic use, but may be unwanted for some).
  • Eye irritation or burning on instillation.

These effects generally diminish with continued use or after adjusting the drop technique.

Serious Adverse Events

  • Iridial pigment darkening - permanent brown-gray coloration of the iris, particularly in patients with lighter eye colour.
  • Periorbital skin darkening - hyperpigmentation of the eyelid skin.
  • Anterior chamber inflammation (uveitis) - rare but requires immediate ophthalmic assessment.

If you experience sudden eye pain, vision loss, or severe redness, seek urgent medical attention.

Drug Interactions

  • Other prostaglandin analogues (e.g., latanoprost, travoprost) - additive IOP-lowering effect may increase risk of ocular hypotony.
  • Beta-blocker eye drops - combined therapy is common and generally safe, but the overall IOP-lowering effect may be greater than expected; clinicians often monitor IOP closely.
  • Systemic carbonic anhydrase inhibitors (e.g., acetazolamide) - additive effect on IOP reduction.

Patients should disclose all ocular and systemic medications, including over-the-counter preparations and herbal supplements, to their prescriber.

Food and Lifestyle Interactions

  • Alcohol: No direct interaction, but excessive consumption may exacerbate dry-eye symptoms.
  • Contact lenses: Remove lenses before instilling the drop; wait at least 15 minutes before reinserting to avoid drug adherence to the lens material.
  • Driving: Bimatoprost does not impair cognition or motor function, but transient blurred vision can occur immediately after dosing; allow a few minutes for the drop to settle.

How to Take Careprost + Applicators

  • Formulation strength: 0.01 % (0.1 mg/mL) bimatoprost solution.
  • Standard dosing: Instil one drop into the affected eye(s) once daily in the evening, preferably at the same time each day.
  • Administration steps
  1. Wash hands thoroughly.
  2. Tilt the head backward and pull down the lower eyelid to form a pocket.
  3. Hold the bottle upside-down without touching the tip to the eye or lashes.
  4. Squeeze gently to deliver a single drop.
  5. Close the eye gently for about one minute; press the inner canthus to minimise systemic absorption.
  • Missed dose: If you remember the missed dose within a few hours, you may administer it. Skip it if it is close to the next scheduled dose; do not double-dose.

  • Overdose: Symptoms may include excessive eye redness, severe ocular pain, or blurred vision. Seek urgent medical care; treatment is supportive.

  • Discontinuation: Do not stop abruptly without consulting your eye-care professional. A gradual taper is unnecessary for bimatoprost, but monitoring of IOP after cessation is essential to detect rebound pressure rise.

Monitoring and Follow-Up

  • Initial assessment: Baseline IOP measurement, visual field testing, and optic-nerve imaging before starting therapy.
  • Follow-up visits: Typically at 4-6 weeks after initiation, then every 3-6 months, or as directed by the ophthalmologist.
  • Laboratory tests: Not routinely required for topical bimatoprost, but serum electrolytes may be monitored if systemic carbonic anhydrase inhibitors are co-prescribed.

Regular follow-up ensures that the target IOP is achieved and that any adverse effects are identified early.

Storage and Handling

  • Store the bottle at room temperature (15-30 °C), protected from direct sunlight and moisture.
  • Keep the dropper tip clean; replace the cap immediately after use.
  • Shelf-life: Use until the expiry date printed on the label; once opened, discard after 30 days if the label indicates a limited in-use period.
  • Disposal: Return unused medication to a pharmacy-based disposal service or follow local NHS guidelines for hazardous waste.

Medication-Specific Glossary

Prostaglandin analogue
A class of compounds that mimic the action of prostaglandin F₂α, increasing aqueous-humour outflow to lower intra-ocular pressure.
Intra-ocular pressure (IOP)
The fluid pressure inside the eye; elevated IOP is a major risk factor for glaucoma.
Trabecular meshwork
A porous tissue at the eye’s drainage angle that regulates outflow of aqueous humour.
Iridial pigment darkening
A permanent change in the colour of the iris caused by increased melanin deposition after prolonged prostaglandin-analogue use.

Medical Disclaimer

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

Information for Careprost 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.
Categories