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Is Latisse the Same as Glaucoma Medicine? A Detailed Comparison

4 min read

Latisse is the only FDA-approved prescription treatment for growing eyelashes longer, fuller, and darker [1.9.4]. But is Latisse the same as glaucoma medicine? The answer lies in a shared active ingredient discovered by accident [1.7.2].

Quick Summary

Latisse and certain glaucoma medications, like Lumigan, share the same active ingredient, bimatoprost. However, they differ in concentration, FDA-approved use, application method, and side effect profiles [1.5.1].

Key Points

  • Shared Ingredient: Latisse and the glaucoma medicine Lumigan both use bimatoprost as the active ingredient [1.2.3].

  • Different Purposes: Latisse is FDA-approved for eyelash growth (hypotrichosis), while Lumigan is approved for lowering eye pressure in glaucoma patients [1.8.3].

  • Varying Concentrations: Latisse has a higher concentration of bimatoprost (0.03%) compared to the more common glaucoma formulation, Lumigan (0.01%) [1.5.3].

  • Distinct Applications: Latisse is applied to the upper eyelid margin, whereas glaucoma medication is instilled directly into the eye as a drop [1.5.1].

  • Side Effect Differences: Direct eye application (glaucoma medicine) carries a higher risk of permanent iris color change, while eyelid application (Latisse) is more associated with reversible skin darkening [1.2.3, 1.6.1].

  • Accidental Discovery: The eyelash-growing effect was a side effect discovered in glaucoma patients, which led to the development of Latisse as a cosmetic product [1.7.2].

  • Not Interchangeable: Due to differences in concentration, application, and potential side effects, the two products should not be used interchangeably [1.5.1].

In This Article

The Surprising Link Between Eyelash Growth and Eye Health

It's a fascinating piece of pharmaceutical history: a medication intended to prevent vision loss from glaucoma led to the creation of a blockbuster cosmetic treatment [1.7.2]. The story of Latisse and its glaucoma medication counterpart, Lumigan, revolves around a single active ingredient: bimatoprost. While they are born from the same molecule, they are not interchangeable products. Understanding their differences in purpose, formulation, and application is crucial for safe and effective use [1.5.1].

What is Bimatoprost and How Does it Work?

Bimatoprost is a synthetic prostaglandin analog, a chemical compound that mimics the effects of natural substances in the body called prostaglandins [1.10.1]. These compounds have hormone-like effects and are involved in various bodily processes [1.3.1]. In the eye, bimatoprost works in two distinct ways depending on its application.

  • For Glaucoma: When used as an eye drop (like in Lumigan), bimatoprost lowers intraocular pressure (IOP) by increasing the drainage of aqueous humor, the fluid inside the eye [1.4.5]. Elevated IOP is a primary risk factor for glaucoma, a condition that can damage the optic nerve and lead to irreversible blindness [1.4.4]. Bimatoprost was first approved by the FDA for this purpose in 2001 under the brand name Lumigan [1.7.1, 1.2.2].
  • For Eyelash Growth: The exact mechanism for eyelash growth is not fully understood, but it's believed that bimatoprost increases the duration of the hair's growth phase (anagen phase) and the number of hairs produced during this phase [1.3.4]. This results in eyelashes that grow longer, thicker, and darker [1.9.4].

A Serendipitous Discovery

During the clinical trials and subsequent use of Lumigan for glaucoma, ophthalmologists and their patients noticed a consistent and surprising side effect: significant eyelash growth [1.7.2, 1.4.2]. The lashes weren't just longer; they were also darker and fuller [1.3.5]. Recognizing the cosmetic potential, the manufacturer, Allergan, conducted new clinical trials to study bimatoprost specifically for treating hypotrichosis, the medical term for having inadequate eyelashes [1.7.3, 1.2.2].

This research led to the FDA's approval of a new product, Latisse, in December 2008 [1.7.3, 1.2.2]. Latisse contains bimatoprost formulated specifically for application to the upper eyelid margin to promote eyelash growth [1.8.2].

Latisse vs. Glaucoma Medication (Lumigan): A Head-to-Head Comparison

While they share an active ingredient, their formulations, intended uses, and FDA approvals are distinct [1.5.1]. Using one in place of the other is not recommended and can lead to improper dosing and increased risk of side effects.

Feature Latisse Glaucoma Medication (e.g., Lumigan)
Primary Use FDA-approved for treating hypotrichosis (inadequate eyelashes) [1.8.3] FDA-approved for reducing elevated intraocular pressure in patients with open-angle glaucoma or ocular hypertension [1.5.2]
Active Ingredient Bimatoprost 0.03% [1.5.3] Bimatoprost 0.01% [1.5.3]
Application Applied topically to the base of the upper eyelashes once daily using a sterile, single-use applicator [1.9.4, 1.5.1]. Not applied directly into the eye. Administered as a single eye drop into the affected eye(s) once daily, typically in the evening [1.5.1, 1.9.3].
Packaging Packaged with multiple sterile applicators designed for eyelid application [1.8.1]. Packaged as a multi-dose eye dropper bottle [1.6.1].
FDA Approval Date December 2008 [1.5.5] March 2001 [1.5.5]

Understanding the Side Effects

Because the application methods and concentrations differ, the side effect profiles for Latisse and Lumigan also vary, though there is some overlap. Correct application is key to minimizing risks [1.2.1].

Common Side Effects of Latisse:

  • Itching and redness of the eyes or eyelids [1.2.3, 1.5.2].
  • Skin hyperpigmentation (darkening of the eyelid skin where the product is applied), which is often reversible after discontinuation [1.2.3, 1.6.1].
  • Dry eyes and eye irritation [1.6.3].

Common Side Effects of Lumigan (Glaucoma Medication):

  • Conjunctival hyperemia (eye redness) [1.5.1].
  • Eyelash growth (which is the intended effect of Latisse) [1.6.2].
  • Itchy or irritated eyes [1.6.2].

More Serious, Potentially Permanent Side Effects: A more significant side effect associated with direct instillation of bimatoprost into the eye is a potential change in iris color [1.6.1]. The medication can increase the brown pigment in the iris, causing light-colored eyes (blue, green, hazel) to become permanently browner. This was noted in glaucoma patients using Lumigan but was not reported in the clinical studies for Latisse, likely because Latisse is applied to the eyelid, exposing the eye to only about 5% of the drug compared to the eye drop method [1.2.3, 1.2.1]. Other rare but serious risks include prostaglandin-associated periorbitopathy (PAP), which can cause a loss of orbital fat around the eye, leading to a sunken appearance [1.10.1, 1.10.3].

Conclusion: Two Medicines, One Molecule

So, is Latisse the same as glaucoma medicine? The answer is both yes and no. They share the same active molecule, bimatoprost, born from a medical treatment for a serious eye disease [1.3.5]. However, they are distinct products tailored for different purposes. Latisse is a higher-concentration cosmetic product designed for eyelash enhancement, while Lumigan is a lower-concentration medical eye drop for managing glaucoma [1.5.1, 1.5.3]. One should never be substituted for the other. If you are interested in using Latisse for eyelash growth, or if you are a glaucoma patient using a prostaglandin analog and have questions, consulting with a healthcare professional or ophthalmologist is essential [1.2.1].


For more information from a highly authoritative source on eye health, visit the American Academy of Ophthalmology. [1.2.5]

Frequently Asked Questions

The active ingredient in both Latisse and the glaucoma medication Lumigan is bimatoprost, which is a prostaglandin analog [1.2.3].

While glaucoma eye drops containing bimatoprost (like Lumigan) can cause eyelash growth as a side effect, they are not formulated or approved for this purpose. Latisse is specifically formulated with a different concentration and an applicator for safe use on the eyelids [1.5.1, 1.5.3]. It's important to use the correct product as prescribed.

Latisse contains a 0.03% concentration of bimatoprost, while the common Lumigan formulation for glaucoma contains 0.01% [1.5.3]. Latisse is applied topically to the skin of the eyelid, whereas Lumigan is dropped directly into the eye, resulting in different delivery and absorption.

Yes, the potential darkening of the iris (the colored part of the eye) to a browner shade is considered a permanent side effect. This is more of a risk when bimatoprost is used directly in the eye for glaucoma [1.2.3, 1.6.1].

Latisse was discovered by accident. Patients using the glaucoma eye drop Lumigan (bimatoprost) reported a side effect of their eyelashes growing longer, thicker, and darker. The drug's manufacturer, Allergan, then studied this effect and developed Latisse as a cosmetic treatment [1.7.2].

If you stop using Latisse, your eyelashes will gradually return to their original state over several weeks or months as your natural lash growth cycle continues [1.2.1].

Yes, Latisse (and its generic version, bimatoprost 0.03% solution) is the only prescription treatment approved by the FDA specifically for hypotrichosis, or inadequate eyelashes, to grow them longer, fuller, and darker [1.9.4, 1.8.5].

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.