Xalatan (Latanoprost)
Pronunciation: luh-TAN-oh-prost.
- Generic name
- latanoprost
- Drug class
- Prostaglandin F2-alpha analogue (ophthalmic)
- Form
- Ophthalmic solution, 50 micrograms/mL (0.005%)
- Route
- Topical ophthalmic (eye drops)
- Legal status
- Prescription-only in all 6 markets reviewed (US, UK, EU, Canada, Australia, New Zealand).
Availability and supply rules vary by country
Trade names by country: United States · United Kingdom · Canada · Australia · New Zealand
Australia: Xalatan (5), Latanoprost Sandoz / Latanoprost CA / APO-Latanoprost (generics) (5) · Full directory
What latanoprost is and how it works
Xalatan (latanoprost) is a prostaglandin eye drop used once daily to lower elevated pressure inside the eye (intraocular pressure, IOP) in open-angle glaucoma and ocular hypertension, by increasing natural fluid outflow from the eye. (2) (7)
Latanoprost is generally well tolerated and has no boxed warning, but it has two real, well-documented effects worth knowing about before starting. First, it can cause a gradual, likely permanent increase in brown pigmentation of the iris (the coloured part of the eye), especially in eyes with mixed colouring -- this is a cosmetic change, not a sign the medicine is harming the eye, but it will not reverse if you stop treatment. Second, prolonged use can cause changes around the eye socket itself (deepening of the upper eyelid crease, slight sinking of the eye, tightened eyelids) from gradual fat loss around the eye -- a real, documented effect of this drug class that is usually reversible if the medicine is stopped. Eyelash growth and periorbital skin darkening can also occur and are usually reversible.
Mechanism of action: how latanoprost works
Latanoprost is a prodrug hydrolysed by corneal esterases to its biologically active acid form, a selective prostaglandin F2-alpha (FP) receptor agonist. It lowers intraocular pressure primarily by increasing uveoscleral outflow of aqueous humour, a distinct mechanism from beta-blockers and other older IOP-lowering classes. (6)
What latanoprost is used for
Open-angle glaucoma
Used once daily to reduce elevated intraocular pressure in adults (including elderly) with open-angle glaucoma, helping to protect the optic nerve from pressure-related damage. (1) (2)
Ocular hypertension
Used to reduce elevated intraocular pressure in people with ocular hypertension (raised eye pressure without diagnosed glaucoma), to reduce the risk of future optic nerve damage. (1) (2)
Paediatric elevated eye pressure and paediatric glaucoma (in markets where authorised)
In the UK/EU, also indicated for reduction of elevated intraocular pressure in paediatric patients with elevated IOP and paediatric glaucoma. (2)
Before taking latanoprost
Do not take / not appropriate for
- Do not use if you have a known hypersensitivity (allergic) reaction to latanoprost, benzalkonium chloride, or any other ingredient in this product. (all countries) (1)
- Avoid use during an active herpes simplex (cold sore virus) eye infection. (all countries) (2)
Tell your clinician about
- Any past episode of iritis or uveitis (inflammation inside the eye), or active eye inflammation.
- If you do not have a natural lens in the treated eye (aphakic) or have an artificial lens with a torn posterior capsule, or any other risk factor for macular oedema (swelling at the back of the eye).
- Any past history of herpes simplex keratitis (cold-sore-virus eye infection).
- Any history of asthma or breathing problems, since asthma flare-ups and breathlessness have been reported.
- If you wear contact lenses -- these should be removed before applying the drops and can be reinserted after 15 minutes.
- Any other eye drops you use, especially another prostaglandin-type eye drop, since using two together is not recommended and can paradoxically raise eye pressure.
- If you are pregnant, planning pregnancy, or breastfeeding.
How to take latanoprost
- Use exactly one drop in the affected eye(s) once daily -- using it more often than once a day can reduce how well it works and may even raise eye pressure instead of lowering it.
- The best effect is usually obtained when the dose is given in the evening.
- If using other eye drops at the same time, space them at least 5 minutes apart.
- Remove contact lenses before applying the drops; they can be put back in after 15 minutes.
- Wash your hands before use and avoid letting the dropper tip touch your eye or any other surface, to reduce the risk of contamination and eye infection.
Procedures and treatment changes
Tell the treating team before surgery, procedures, or any medicine change. Do not alter treatment without the responsible clinician. (1) (2) (3) (4) (5) (6) (7)
Missed dose
If a dose is missed, continue with the next regularly scheduled dose the following day. Do not use an extra drop to make up for a missed dose -- using it more than once daily can reduce its effect or raise eye pressure. Ask your pharmacist or clinician if you are unsure.
Overdose
Ocular overdose (too many drops at once) may cause temporary eye irritation, redness, or watering; rinse the eye with lukewarm water and contact a clinician or pharmacist if irritation persists. If the product is accidentally swallowed, contact a doctor or poison control centre for advice. (1)
Side effects
Side effects and their urgency vary; report severe, persistent, or concerning symptoms.
Increased brown pigmentation of the iris (likely permanent).
What to notice: Increased brown pigmentation of the iris (likely permanent).
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1) (2)
Eye redness (conjunctival hyperaemia), burning, stinging, itching, or a gritty/foreign-body sensation.
What to notice: Eye redness (conjunctival hyperaemia), burning, stinging, itching, or a gritty/foreign-body sensation.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (2)
Blurred vision.
What to notice: Blurred vision.
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Changes to eyelashes -- increased length, thickness, number, or darkening (usually reversible on stopping).
What to notice: Changes to eyelashes -- increased length, thickness, number, or darkening (usually reversible on stopping).
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (2)
Punctate keratitis (small areas of irritation on the clear front surface of the eye).
What to notice: Punctate keratitis (small areas of irritation on the clear front surface of the eye).
What to do: Discuss persistent or troublesome symptoms with the treating clinician or pharmacist. (1)
Serious warnings
Permanent iris pigmentation change — high caution
Symptoms: A gradual increase in brown colouring of the iris (the coloured part of the eye), particularly in eyes with mixed colouring, usually becoming noticeable within the first 8 months but sometimes up to 3 years of treatment.
Action: This is a cosmetic, likely permanent change and does not itself indicate eye damage, but discuss it with your clinician before starting, especially if only one eye will be treated (which can cause a visible colour difference between the two eyes). (2)
Prostaglandin-associated periorbitopathy (periorbital fat atrophy) — high caution
Symptoms: Deepening of the upper eyelid crease, a slightly sunken appearance of the eye, tightened or altered-looking eyelids, developing gradually over weeks to years of use.
Action: Tell your clinician if you notice these changes -- they are a real, documented effect of this class of eye drop (less pronounced with latanoprost than with some related products) and are usually reversible if treatment is stopped, though this should only be decided together with your eye specialist given the importance of controlling eye pressure. (7)
Eye inflammation, swelling at the back of the eye, or infection — high caution
Symptoms: New or worsening eye pain, redness, light sensitivity, or vision changes.
Action: Contact your eye clinician promptly -- latanoprost is used cautiously in people with a history of intraocular inflammation (uveitis/iritis) or macular oedema risk factors, and should be stopped and evaluated if active inflammation, infection, or macular oedema develops. (1) (2)
Asthma or breathing difficulty — high caution
Symptoms: New wheeze, chest tightness, or shortness of breath after starting the drops.
Action: Tell your clinician promptly, particularly if you have a history of asthma -- exacerbation of asthma and breathlessness have been reported after latanoprost use. (2)
Interactions
- Other prostaglandin-type eye drops (prostaglandins, prostaglandin analogues, or prostaglandin derivatives): using two or more together is not recommended, as it has been linked to a paradoxical increase in eye pressure rather than a further decrease. (2)
- Other topical eye drops: if using more than one type, space them at least 5 minutes apart to avoid one washing out the other. (1)
- Thimerosal-containing eye drops: may precipitate (form particles) if physically mixed with latanoprost -- avoid direct mixing. (1)
Pregnancy, breastfeeding, kidney/liver function, age
Pregnancy
Not recommended -- potential for hazardous effects on the course of pregnancy and the fetus, per the UK SmPC reviewed. (1) (2) (3) (4) (5) (6) (7)
Breastfeeding
Latanoprost may pass into breast milk; a decision should be made to discontinue treatment or avoid breastfeeding, in consultation with your clinician. (1) (2) (3) (4) (5) (6) (7)
Children
Used in some markets (UK/EU) for paediatric elevated intraocular pressure and paediatric glaucoma under specialist supervision; not described as authorised for this in all markets reviewed -- check your local product information. (1) (2) (3) (4) (5) (6) (7)
Elderly
No dose adjustment is required based on age alone; used at the standard adult dose in elderly patients per the sources reviewed. (1) (2) (3) (4) (5) (6) (7)
Hepatic_impairment
No specific dose adjustment described in the sources reviewed for this dossier. (1) (2) (3) (4) (5) (6) (7)
Renal_impairment
No specific dose adjustment described in the sources reviewed for this dossier. (1) (2) (3) (4) (5) (6) (7)
Source_ids
Monitoring
Before starting
- Baseline eye examination including iris colour and eyelid/periorbital appearance, for later comparison.
- Review of any history of uveitis/iritis, macular oedema risk factors, herpes keratitis, or asthma.
- Confirm no other prostaglandin-type eye drop is being used concurrently.
During treatment
- Periodic eye pressure checks to confirm the medicine is working as intended.
- Watch for gradual iris colour change, eyelid/periorbital changes, or new eye inflammation, and report these to your eye clinician.
- Report any new asthma symptoms or breathing difficulty.
Storage
Store as directed on the product label (unopened bottles typically require refrigeration; once opened, many latanoprost products can be kept at room temperature for a limited time -- check your specific product's leaflet). Keep out of reach of children, and discard any opened bottle after the period stated on the label.
Professional information
Clinician-facing context only, sourced from the current US FDA/DailyMed prescribing information, UK EMC SmPC, EU EMA national-authorisation documentation, Health Canada's DIN/product database, Australia's TGA ARTG, and New Zealand's Medsafe data sheet reviewed for this dossier; verify against the current full label before prescribing.
United States, United Kingdom, European Union, Canada, Australia, New Zealand
Indication: Open-angle glaucoma / ocular hypertension (and, in the UK/EU, paediatric elevated IOP/glaucoma)
Dose summary: One drop in the affected eye(s) once daily, optimally in the evening; more frequent dosing may reduce efficacy or paradoxically raise IOP.
Renal context: No specific renal dose adjustment described in the sources reviewed. (1) (2)
Hepatic guidance
No specific hepatic-impairment dose adjustment was identified in the sources reviewed for this dossier.
Overdose note
No specific systemic antidote described; ocular overdose is managed by irrigation and symptomatic care; if swallowed, manage supportively and contact poison control. (6)
Frequently asked questions
Is Xalatan (latanoprost) available in the US, UK, EU, Canada, Australia, and New Zealand?
Yes, it is authorised and marketed as both the original brand (Xalatan) and multiple generics in all six of these markets. In the EU it is authorised nationally across member states (monitored via the EMA's own periodic safety update procedure) rather than through one single centralised EMA marketing authorisation. (1) (2) (3) (4) (5) (6)
Will Xalatan permanently change my eye colour?
It can cause a gradual increase in brown pigmentation of the iris, especially in eyes with mixed colouring (such as green-brown, blue-brown, or grey-brown), and this change is considered likely permanent even if you stop the medicine. It is a cosmetic effect, not a sign of eye damage, but it is worth discussing with your eye clinician before starting, particularly if you will only be treating one eye. (2)
Can Xalatan change the appearance around my eyes?
Yes -- with prolonged use, a real, documented effect called prostaglandin-associated periorbitopathy can occur, involving gradual fat loss around the eye that deepens the upper eyelid crease, tightens the eyelids, and can make the eye look slightly more sunken. Latanoprost causes this less often/severely than some related eye drops (such as bimatoprost), but it is a real effect of the same drug class, and it is usually reversible if the medicine is stopped. (7)
Does Xalatan carry a boxed warning?
No. Latanoprost has no boxed warning in any of the six markets reviewed for this page. Its main safety considerations are the pigmentation and periorbital changes described above, plus caution in people with a history of eye inflammation, certain lens conditions, herpes eye infections, or asthma. (1)
What is the mechanism of action of latanoprost?
Latanoprost is a prodrug hydrolysed by corneal esterases to its biologically active acid form, a selective prostaglandin F2-alpha (FP) receptor agonist. It lowers intraocular pressure primarily by increasing uveoscleral outflow of aqueous humour, a distinct mechanism from beta-blockers and other older IOP-lowering classes. (6)
References
- XALATAN (latanoprost ophthalmic solution) 0.005% -- full prescribing informationDailyMed (U.S. National Library of Medicine) / FDA-approved prescribing information · United States · accessed 2026-07-30 · source 1
- Xalatan 50 micrograms/ml eye drops, solution -- Summary of Product Characteristicselectronic medicines compendium (emc), United Kingdom -- Summary of Product Characteristics · United Kingdom · accessed 2026-07-30 · source 2
- Latanoprost -- list of nationally authorised medicinal products (PSUSA/00001832)European Medicines Agency (EMA) -- PSUSA periodic safety update assessment / list of nationally authorised medicinal products · European Union · accessed 2026-07-30 · source 3
- XALATAN (latanoprost) -- DIN 02231493, product monographHealth Canada -- Drug Product Database (DIN) / product monograph · Canada · accessed 2026-07-30 · source 4
- XALATAN latanoprost 50 microgram/mL eye drops -- ARTG entry 58775Therapeutic Goods Administration (TGA), Australia -- Australian Register of Therapeutic Goods (ARTG) · Australia · accessed 2026-07-30 · source 5
- XALATAN Eye Drops (Latanoprost 50 micrograms/mL) -- New Zealand Data SheetMedsafe (New Zealand regulator) -- New Zealand Data Sheet · New Zealand · accessed 2026-07-30 · source 6
- Periorbital muscle/fat atrophy associated with topical prostaglandin analogue therapy (Prostaglandin-Associated Periorbitopathy, PAP)peer-reviewed ophthalmology literature (PMC) · international / clinical literature · accessed 2026-07-30 · source 7
Brand names by country
Single-ingredient latanoprost names are shown separately by country. Product availability, strengths, and supply rules can change; combination products are not included here.
Priority countries
United States
- XELPROS.05 mg/mL · sun pharmaceutical industries, inc.
- XALATAN50 ug/mL · viatris specialty llc
- IYUZEH50 ug/mL · thea pharma inc.
United Kingdom
Canada
- XALATAN
- MED-LATANOPROST
Australia
New Zealand
View brands in additional countries.
European Union
Xalatan / Akistan / national generic brand names (3)