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Important Safety Information
Latisse® (Bimatoprost 0.03%)
FDA-Approved PrescriptionLatisse (bimatoprost ophthalmic solution 0.03%) is the only FDA-approved prescription treatment for hypotrichosis (inadequate or insufficient eyelashes) to grow longer, fuller, and darker lashes. Applied nightly to the upper lash line.
Emergency: If you experience chest pain, severe shortness of breath, a prolonged painful erection (over 4 hours), or sudden vision/hearing loss — call 911 or go to your nearest emergency room immediately.
Who Should Not Use Latisse® (Bimatoprost 0.03%)
- Individuals with eye infection or inflammation
- Contact lens wearers (remove lenses before application, reinsert after 15 minutes)
- Anyone with glaucoma without provider consultation
- Pregnant or breastfeeding without provider guidance
Warnings & Precautions
Iris Pigmentation
Latisse may permanently darken the iris (colored part of the eye) in some patients. This change may not be noticeable for months or years.
Skin Darkening
Skin pigmentation changes may occur around the treated area. This is usually reversible after stopping treatment.
Eye Pressure
Bimatoprost can affect intraocular pressure. Patients with glaucoma or increased eye pressure should discuss with their ophthalmologist.
Applicator Use
Use only the sterile applicators provided. Never use applicator more than once — using across multiple eyes or sharing increases infection risk.
Common Side Effects
This is not a complete list. Contact your provider if you experience any concerning symptoms.
- Eye itching or redness
- Dry eyes
- Skin darkening at application site
- Iris color change (rare, potentially permanent)
- Eye irritation
Drug Interactions
Always inform your provider of all medications, supplements, and substances you are currently taking.
- Other prostaglandin eye drops (additive effects)
- Intraocular pressure-lowering agents
When to Contact Your Provider
- Eye pain, vision changes, or increased redness
- Signs of eye infection
- Unexpected iris or significant skin color changes
This safety information is provided for general educational purposes only and does not constitute medical advice. It is not a substitute for the full prescribing information, package insert, or guidance from your licensed healthcare provider. Individual responses to medications and supplements vary. MEDVera providers review your complete health profile before recommending or prescribing any treatment.