LACRYVISC 3 mg/g OPHTHALMIC GEL

2. What you need to know before starting to use Lacryvisc

Do not use Lacryvisc

If you are allergic to carbomer or any of the other components of this medication (listed in section 6).

Warnings and Precautions

Consult your doctor or pharmacist before starting to use Lacryvisc.

Use this gel only in your eye(s).

The tip of the container should not come into contact with any surface, including the eye, as it may cause eye injury and the gel may become contaminated.

It is not recommended to wear contact lenses during treatment with this medication. See section "Lacryvisc contains benzalkonium chloride".

In case of iris inflammation or corneal diseases, you should consult your doctor, who will determine the possibility of using Lacryvisc as treatment.

If you experience eye pain, changes in vision, eye irritation, persistent redness, or if symptoms worsen or persist for more than 3 days, discontinue treatment and consult your doctor.

Children and Adolescents up to 18 years of age

In clinical practice, the safety and efficacy of Lacryvisc have been established in children and adolescents at the recommended dose in adults, but no data from clinical trials are available.

Using Lacryvisc with other medications

Tell your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.

Pregnancy, Breastfeeding, and Fertility

If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.

This medication can be used during pregnancy and breastfeeding.

Driving and Using Machines

You may notice that your vision becomes blurry for a while after applying the medication. If this happens, wait until the symptom disappears and your vision is clear before driving vehicles or using machines.

Lacryvisc contains benzalkonium chloride

This medication contains 0.001 mg of benzalkonium chloride per dose, equivalent to 0.05 mg/g.

Benzalkonium chloride can be absorbed by soft contact lenses, altering their color. Remove contact lenses before using this medication and wait 15 minutes before putting them back.

Benzalkonium chloride can cause eye irritation, especially if you have dry eye or other corneal diseases (the transparent layer on the front of the eye). Consult your doctor if you feel any strange sensation, itching, or pain in the eye after using this medication.

3. How to use Lacryvisc

Follow the administration instructions for the medication indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.

The recommended dose is one drop in the eye(s) 2 to 4 times a day, or whenever you experience eye discomfort associated with dry eye.

In certain cases and according to your doctor's instructions, Lacryvisc may be applied more frequently.

Children and Adolescents up to 18 years of age

In clinical practice, the safety and efficacy of Lacryvisc have been established in children and adolescents at the recommended dose in adults, but no data from clinical trials are available.

Elderly Patients

Lacryvisc can be used in elderly patients (over 65 years), and no dose adjustment is necessary.

Instructions for Use

To correctly administer Lacryvisc, follow the steps described below:

Since this is a sterile medication, it is recommended to follow the instructions below:

• Each patient will use their own container.
• The application of the gel should be done with maximum cleanliness, avoiding as much as possible contact between the tip of the tube and any surface (including the eyelid, fingers, etc.).
• After each application, close the container well.
• Lacryvisc should not be used after 4 weeks from the first opening of the tube and should be discarded even if it has not been fully consumed.

If you need to apply any other eye medication besides Lacryvisc, wait at least 5 minutes between applications. Lacryvisc should be administered last.

If you use more Lacryvisc than you should

Given its exclusive ocular administration, overdose is not expected.

In case of overdose or accidental ingestion, consult your doctor or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.

If you forget to use Lacryvisc

Do not use a double dose to make up for forgotten doses.

If you have any other questions about the use of this medication, ask your doctor or pharmacist.

4. Possible Side Effects

Like all medications, this medication can cause side effects, although not everyone will experience them.

The following reactions may appear in your eyes:

Very Common(may affect more than 1 in 10 people):blurred vision.

Common(may affect up to 1 in 10 people):eye discomfort, eyelid crust, eye irritation.

Uncommon(may affect up to 1 in 100 people):eye swelling, eye pain, eye itching, eye redness, increased tear production.

Or, reactions in other parts of your body:

Uncommon(may affect up to 1 in 100 people):skin inflammation.

Other additional side effects have been observed during post-marketing experience with unknown frequency(cannot be estimated from available data): allergy (hypersensitivity).

Reporting Side Effects

If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: https://www.notificaRAM.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.

5. Storage of Lacryvisc

Keep this medication out of sight and reach of children.

Do not store above 30°C.

Keep the container perfectly closed. The contents of the tube are sterile until first opening.

Do not use this medication after the expiration date shown on the tube and carton after EXP. The expiration date is the last day of the month indicated.

To avoid infections, discard the tube 4 weeks after first opening.

Write the opening date of the tube in the space provided on the carton for this purpose.

Medications should not be disposed of through wastewater or household waste. Deposit the containers and medications you no longer need at the SIGRE collection point in your pharmacy. If in doubt, ask your pharmacist how to dispose of containers and medications you no longer need. This will help protect the environment.

6. Package Contents and Additional Information

Lacryvisc Composition

• The active ingredient is carbomer. Each gram of gel contains 3 mg of carbomer.
• The other ingredients are benzalkonium chloride, sorbitol (E-420), sodium hydroxide, and purified water.

Appearance of the Product and Package Contents

Lacryvisc is a slightly opaque and slightly yellowish liquid eye gel.

The gel is presented in a carton containing a 10 g tube with a plastic dispenser tip and plastic cap.

Marketing Authorization Holder

Alcon Healthcare S.A.

World Trade Center Almeda Park

Plaça de la Pau s/n, Edificio 6, planta 3

08940 - Cornellà de Llobregat (Barcelona)

Spain

Manufacturer

S.A. Alcon-Couvreur N.V.

Rijksweg 14, B-2870 Puurs,

Belgium

or

Alcon Laboratories Belgium

Lichterveld 3

2870 Puurs-Sint-Amands

Belgium

Date of Last Revision of this Package Leaflet:February 2018

Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/