Package Leaflet: Information for the Patient
Olopatadina JUTA 1 mg/ml Eye Drops Solution
Read the entire package leaflet carefully before starting to use this medication, as it contains important information for you.
Contents of the Package Leaflet
This medication is indicated for the treatment of signs and symptoms of seasonal allergic conjunctivitis.
In allergic conjunctivitis, certain elements (called allergens) such as pollen, house dust, or animal hair can cause allergic reactions that lead to itching and redness, as well as inflammation of the surface of your eyes.
This medication works by reducing the intensity of the allergic reaction.
Do not use Olopatadina JUTA
Warnings and Precautions
Consult your doctor or pharmacist before starting to use this medication.
If you wear contact lenses, you must remove thembefore using this medication (see section 3).
Children
Do not use this medication in children under 3 years of age. Do not administer this medication to children under 3 years of age, as there is no data indicating that it is safe and effective in children under 3 years of age.
Using Olopatadina JUTA with other medications
Tell your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.
If you are using another eye drop or ointment, wait at least 5 minutes between applying each medication. Ointments should be applied last.
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.
Do not use this medication if you are breastfeeding; consult your doctor before using this medication.
Driving and Using Machines
You may experience blurred vision immediately after applying this medication. Do not drive or use machines until this effect has disappeared.
Olopatadina JUTA contains benzalkonium chloride
This medication contains less than 23 mg of sodium (1 mmol) per unit volume; it is essentially "sodium-free".
Follow the administration instructions for this medication exactly as indicated by your doctor or pharmacist. If you are unsure, consult your doctor or pharmacist again.
The recommended doseis one drop in one eye or both eyes, twice a day: in the morning and in the evening.
Use this amount unless your doctor gives you other instructions. This medication should only be applied to both eyes if your doctor has indicated it. Follow the treatment for the period of time indicated by your doctor.
Remember that this medication should only be applied to the eyes.
Instructions for the proper use of Olopatadina JUTA:
To facilitate the application of the eye drops, it may be helpful to sit in front of a mirror the first few times, so you can see what you are doing.
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If you use more Olopatadina JUTA than you should
You can rinse your eyes with warm water. Do not apply more drops until the next scheduled application.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone: 915 620 420, indicating the medication and the amount used.
If you forget to use Olopatadina JUTA
Apply one drop as soon as you remember and continue with the next dose of your regular schedule. However, if it is almost time for the next dose, do not apply the missed dose and continue with the next dose of your regular schedule. Do not apply a double dose to make up for missed doses.
If you stop using Olopatadina JUTA
Do not stop using this medication without consulting your doctor first.
If you have any other questions about using this medication, ask your doctor or pharmacist.
Like all medications, this medication can cause side effects, although not everyone will experience them. The side effects that have been observed during the use of this eye drop are:
Common(may affect up to 1 in 10 people):
Uncommon(may affect up to 1 in 100 people):
Frequency not known(cannot be estimated from available data):
In very rare cases, some patients with severe damage to the transparent layer on the front of the eye (the cornea) have developed dark spots on the cornea due to calcium accumulation during treatment.
Reporting Side Effects
If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects not listed in this package leaflet. You can also report them directly through the Spanish Medication Surveillance System for Human Use: www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medication.
Keep this medication out of sight and reach of children.
Do not use this medication after the expiration date shown on the bottle (after EXP). The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
To avoid infections, you must discard the bottle four weeks after first opening it and use a new bottle. Write the opening date on the space provided on the label of each bottle and on the box.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the pharmacy's SIGRE point. If you are unsure, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Olopatadina JUTA is a colorless, transparent solution presented in a package containing a 5 ml bottle or three 5 ml plastic bottles with a screw cap.
Only certain package sizes may be marketed.
Juta Pharma GmbH
Gutenbergstr. 13
24941 Flensburg
Germany
Juta Pharma GmbH
Gutenbergstr. 13
24941 Flensburg
Germany
This medication is authorized in the Member States of the European Economic Area under the following names:
Germany: Olopatadin JUTA 1 mg/ml Augentropfen, Lösung
Denmark: Olopatadin JUTA
United Kingdom: Olopatadine USV 1 mg/ml eye drops, solution
Date of the last revision of this package leaflet: September 2019
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/