The majority of patients rated MIEBO as
COMFORTABLE OR VERY COMFORTABLE
on instillation1*
The MIEBO experience
IN GOBI AND MOJAVE PIVOTAL TRIALS:
IN THE KALAHARI STUDY2:
Most patients (~94%) were considered compliant with dosing throughout the study†
Only ~5% of patients (n = 10) used adjunctive artificial tears/mineral oil, as permitted, after Week 4
The majority of patients2‡:
Were satisfied with MIEBO treatment
-
Found MIEBO comfortable
-
Said MIEBO was easy to administer
SD, standard deviation.
*Questionnaire was given on Day 1 of the GOBI and MOJAVE studies. Mean pooled comfort score was 8.0 for MIEBO and 8.4 for saline (scale of 0-10, 0 = not comfortable and 10 = very comfortable). 81% of patients treated with MIEBO reported a score of 7 or higher.1
†Defined as administration of 80% to 120% of the expected doses.2
‡Mean Visual Analog Scale (VAS) score (SD) was assessed at Week 52. Respondents rated MIEBO with the following scores (scale of 0-10): satisfaction, 8.0 (2.3); comfort, 8.4 (2.1); ease of administration, 8.9 (1.9).2
What to expect
AQUEOUS FORMULATION
Not actual size.
Aqueous formulations have a typical drop size of ~30-50 μL3
MIEBO
Not actual size.
The small drop size (11 μL) means MIEBO may feel different from formulations containing water3
There may be no ocular sensation or blink reflex upon instillation4
Not actual size.
One drop per eye, QID dosing5
Preservative free and provided
in a convenient multidose bottle (1-month supply)3,5
How to use MIEBO
MIEBO should not be administered while wearing contact lenses. Contact lenses should be removed before use and for at least 30 minutes after administration of MIEBO.5
CORRECTLY IDENTIFY MIEBO
Ensure you get the right MIEBO when searching online or in an electronic medical/health record (EMR/EHR) system.
Remember: “i before e, to treat DED.”
Storage
MIEBO should be stored at room temperature: 15-25 °C (59-77 °F). After opening, MIEBO can be used until the expiration date on the bottle.5
QID, 4 times daily.
UP NEXT
Savings &
Resources
INDICATION
MIEBO® (perfluorohexyloctane ophthalmic solution) is indicated for the treatment of the signs and symptoms of dry eye disease.
IMPORTANT SAFETY INFORMATION
- MIEBO should not be administered while wearing contact lenses. Contact lenses should be removed before use and for at least 30 minutes after administration of MIEBO
- Instruct patients to instill one drop of MIEBO into each eye four times daily
- The safety and efficacy in pediatric patients below the age of 18 have not been established
- The most common ocular adverse reaction was blurred vision (1% to 3% of patients reported blurred vision and conjunctival redness)
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
Click here for full Prescribing Information for MIEBO.
References: 1. Data on file. Bausch & Lomb, Inc. 2. Protzko EE, Segal BA, Korenfeld MS, Krösser S, Vittitow JL. Long-term safety and efficacy of perfluorohexyloctane ophthalmic solution for the treatment of patients with dry eye disease: the KALAHARI study. Cornea. 2024;43(9):1100-1107. doi:10.1097/ICO.0000000000003418 3. Sheppard JD, Nichols KK. Dry eye disease associated with meibomian gland dysfunction: focus on tear film characteristics and the therapeutic landscape. Ophthalmol Ther. 2023;12(3):1397-1418. doi:10.1007/s40123-023-00669-1 4. Schmidl D, Bata AM, Szegedi S, et al. Influence of perfluorohexyloctane eye drops on tear film thickness in patients with mild to moderate dry eye disease: a randomized controlled clinical trial. J Ocul Pharmacol Ther. 2020;36(3):154-161. doi:10.1089/jop.2019.0092 5. MIEBO. Prescribing Information. Bausch & Lomb, Inc.
You are now leaving MIEBO-ECP.COM
You are now leaving the MIEBO ECP website and are going to a website that Bausch + Lomb does not operate and to which Bausch + Lomb’s Privacy Policy does not apply.
Bausch + Lomb is not responsible for the content, format, maintenance, or policies of the website you are about to visit and does not endorse or monitor any content on such website.
INDICATION AND IMPORTANT
SAFETY INFORMATION
INDICATION
MIEBO® (perfluorohexyloctane ophthalmic solution) is indicated for the treatment of the signs and symptoms of dry eye disease.
IMPORTANT SAFETY INFORMATION
- MIEBO should not be administered while wearing contact lenses. Contact lenses should be removed before use and for at least 30 minutes after administration of MIEBO
- Instruct patients to instill one drop of MIEBO into each eye four times daily
- The safety and efficacy in pediatric patients below the age of 18 have not been established
- The most common ocular adverse reaction was blurred vision (1% to 3% of patients reported blurred vision and conjunctival redness)
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.
Click here for full prescribing Information for MIEBO.