RESOURCES DESIGNED
TO HELP PATIENTS

: 9.1 IOP reduction vyzulta product box

90-day supply to be prescribed as 3 bottles of 2.5 mL solution each.

90-day supply copay offer only applies if each of the three 2.5 mL bottles is covered by the patient’s commercial insurance.

EXPLORE THE OFFER

MORE COVERAGE OPTIONS FOR
YOUR ELIGIBLE* VYZULTA PATIENTS

Savings offer applies for a 1-, 2-, or 3-month supply of VYZULTA for first Rx and eligible refills.

Exclusively at Walgreens and other participating independent pharmacies. At non-participating pharmacies, eligible commercial patients may pay as little as a $35 copay.

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ON PATIENT SAVINGS

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Discounted pricing is available for eligible uninsured patients.* Ask a VYZULTA representative for more information about additional savings options.

*Terms, conditions, and limitations apply. See eligibility criteria and terms and conditions at www.BauschAccessProgram.com.

EASY ACCESS FOR MILLIONS OF PATIENTS WITH
COMMERCIAL INSURANCE AND MEDICARE PART D

UNRESTRICTED ACCESS FOR

75million
21million

NO STEP EDITS OR PRIOR AUTHORIZATIONS‡

†MMIT data, March 2021.

‡A PA may be required for some claims. To date, the majority of prior authorizations submitted for VYZULTA through PARx have been approved.

Visit parxsolutions.com or call (866) 725-7279. Source: PARx Solutions, January 2021.

 

ACCESS SUPPORT RESOURCES

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NEED TO REQUEST A TIER EXCEPTION?

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WRITING A LETTER OF MEDICAL NECESSITY?

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SUPPORT THROUGH PARx CALL (866) 725-7279 OR VISIT ONLINE

Eye care professionals talk about why getting patients access to VYZULTA is worth it.

CONVENIENT ONCE-NIGHTLY DOSING1

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One drop in the conjunctival sac of the affected eye(s) once nightly1

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Administer other topical ophthalmic intraocular pressure drugs at least 5 minutes apart1

 

 

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Can be stored at room temperature for up to 8 weeks once opened1

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Remove contact lenses prior to administration. Lenses may be reinserted 15 minutes after administration1

GET A COPY OF THE VYZULTA
PATIENT ADHERENCE FLASH CARD.

Help to reinforce with your patients
the importance of taking VYZULTA
every day as directed


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INDICATION

VYZULTA® (latanoprostene bunod ophthalmic solution), 0.024% is indicated for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

IMPORTANT SAFETY INFORMATION

  • Increased pigmentation of the iris and periorbital tissue (eyelid) can occur. Iris pigmentation is likely to be permanent
  • Gradual changes to eyelashes, including increased length, increased thickness, and number of eyelashes, may occur. These changes are usually reversible upon treatment discontinuation
  • Use with caution in patients with a history of intraocular inflammation (iritis/uveitis). VYZULTA should generally not be used in patients with active intraocular inflammation
  • Macular edema, including cystoid macular edema, has been reported during treatment with prostaglandin analogs. Use with caution in aphakic patients, in pseudophakic patients with a torn posterior lens capsule, or in patients with known risk factors for macular edema
  • There have been reports of bacterial keratitis associated with the use of multiple-dose containers of topical ophthalmic products that were inadvertently contaminated by patients
  • Contact lenses should be removed prior to the administration of VYZULTA and may be reinserted 15 minutes after administration
  • Most common ocular adverse reactions with incidence ≥2% are conjunctival hyperemia (6%), eye irritation (4%), eye pain (3%), and instillation site pain (2%)
PLEASE SEE FULL PRESCRIBING INFORMATION >

Reference: 1. VYZULTA Prescribing Information. Bausch & Lomb Incorporated.

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INDICATION

VYZULTA® (latanoprostene bunod ophthalmic solution), 0.024% is indicated for the reduction of intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension.

IMPORTANT SAFETY INFORMATION 
  • Increased pigmentation of the iris and periorbital tissue (eyelid) can occur. Iris pigmentation is likely to be permanent