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cyclosporine ophthalmic

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Brand names: Restasis, Cequa

Immunosuppressant (Ophthalmic) Rx

VEVYE eye drops contain cyclosporine. They help treat the signs and symptoms of dry eye disease.

Drug Pricing (NADAC)

Brand Price

$9.38/unit

Generic Available

No

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

What it does

VEVYE treats dry eye disease.

Common side effects

Irritation where the drop is applied

Key warnings

To avoid injury or contamination, do not touch your eye or other surfaces with the bottle tip.

How It Works

VEVYE contains cyclosporine, which is a type of medicine that lowers your body's immune response in the eye. It reduces inflammation. This helps your eyes make more tears.

How to Take It

Wash your hands before using VEVYE. Put one drop in each eye twice a day, about 12 hours apart. Gently pull down your lower eyelid and let one drop fall into your eye. If you use other eye drops, wait 15 minutes between them.

Pregnancy & Breastfeeding

It is not known if VEVYE can harm an unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant. It is also not known if VEVYE passes into breast milk, so talk to your doctor if you are breastfeeding.

Missed Dose

If you miss a dose of VEVYE, use it as soon as you remember. Then, continue with your regular schedule.

Storage

Store VEVYE at room temperature (59°F to 77°F). Do not freeze or refrigerate.

Serious Warnings

To avoid injury or contamination, do not touch your eye or other surfaces with the bottle tip. Do not use VEVYE while wearing contact lenses. If you wear contacts, take them out before using the drops. You can put them back in 15 minutes after using the drops.

Common Questions

What is the strength of VEVYE?
VEVYE contains 0.1% cyclosporine.
How often should I use VEVYE?
Use one drop in each eye twice a day.
Can I use VEVYE with my contact lenses?
No, remove your contact lenses before using VEVYE. You can put them back in 15 minutes after using the drops.
What should I do if the bottle tip touches my eye?
Try to avoid touching your eye with the bottle tip to prevent injury or contamination.
How should I store VEVYE?
Store VEVYE at room temperature, away from heat and light.
What if I accidentally swallow VEVYE?
VEVYE is for eye use only. If swallowed, contact your doctor or poison control center.
Can I use VEVYE if I am pregnant?
Talk to your doctor if you are pregnant or planning to become pregnant before using VEVYE.
Can I use VEVYE if I am breastfeeding?
Talk to your doctor if you are breastfeeding before using VEVYE.
What should I do if I experience blurry vision after using VEVYE?
Temporary blurry vision is a less common side effect. If it persists or worsens, contact your doctor.
How long can I use VEVYE after opening the bottle?
You can use VEVYE until the expiration date on the bottle, even after opening it.
What are the common side effects of cyclosporine ophthalmic?
The most commonly reported side effects of cyclosporine ophthalmic include Irritation where the drop is applied. Always consult your healthcare provider about potential side effects.
What drug class is cyclosporine ophthalmic?
cyclosporine ophthalmic belongs to the Immunosuppressant (Ophthalmic) drug class. It requires a prescription (Rx). VEVYE treats dry eye disease.
Is cyclosporine ophthalmic safe during pregnancy?
It is not known if VEVYE can harm an unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

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Medication Guides

Related Health & Safety Data

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What the FDA Data Shows for cyclosporine ophthalmic

The FDA label for cyclosporine ophthalmic (sold under brand names such as Restasis, Cequa) classifies it as a prescription-only medication in the Immunosuppressant (Ophthalmic) class. VEVYE treats dry eye disease. Official labeling lists 1 commonly reported side effect, including Irritation where the drop is applied.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. Voluntary reports accumulate over the lifetime of a drug and reflect wide-ranging clinical use. Interaction data is drawn directly from FDA-approved prescribing information. NADAC pricing from CMS.

Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: November 14, 2025

All federal data sources used on this page