Package Leaflet: Information for the User
Pred Forte 10 mg/ml Eye Drops Suspension
prednisolone acetate
Read this leaflet carefully before you start using this medicine because it contains important information for you.
-This medicine has been prescribed for you only. Do not give it to others even if they have the same symptoms as you, as it may harm them.
1.What Pred Forte is and what it is used for
2.What you need to know before using Pred Forte
3.How to use Pred Forte
4.Possible side effects
6.Contents of the pack and additional information
Pred Forte is used for the treatment in adults of bulbar conjunctiva inflammation, cornea, and the anterior segment of the eyeball, which responds to steroids.
No use Pred Forte:
Warnings and Precautions
Consult your doctor before starting to use Pred Forte:
Children and Adolescents
This medication is not recommended for children under 18 years of age. There is insufficient information.
Using Pred Forte with Other Medications
Pregnancy, Breastfeeding, and Fertility
If you are pregnant, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication, as steroids may be harmful to the baby.
If you are pregnant, consult your doctor before taking this medication, as it may be harmful to your baby due to its boric acid content (see epigraph Pred Forte contains boric acid for more information).
Do not use Pred Forte while breastfeeding.
Driving and Operating Machines
Pred Forte may cause temporary blurry vision. Do not drive or operate tools or machines until symptoms have resolved.
Pred Forte contains benzalkonium chloride
This medication contains 0.0024 mg of benzalkonium chloride in each drop equivalent to 0.06 mg/ml.
Benzalkonium chloride may be absorbed by soft contact lenses, altering their color. Remove contact lenses before using this medication and wait 15 minutes before reinserting them.
Benzalkonium chloride may cause eye irritation, especially if you have dry eye or other corneal conditions (the transparent layer at the front of the eye). Consult your doctor if you experience unusual sensations, stinging, or eye pain after using this medication.
Pred Forte contains boric acid
At doses equal to or less than the maximum recommended dose (2 drops in each eye 4 times a day), do not administer to children under 12 years of age without consulting your doctor, as this medication contains boron and may affect future fertility. At doses above the maximum recommended dose (2 drops in each eye 4 times a day), do not administer to children under 18 years of age without consulting your doctor.
For information on pregnancy, see epigraph Pregnancy, Breastfeeding, and Fertility.
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
The recommended dose is: one or two drops instilled in the affected eye(s), two to four times a day. If necessary and under medical criteria, the dose frequency may be increased. Maintain therapy during the treatment period established by your doctor.
Administration Method
Do not use the product if the safety seal on the neck of the container is broken before the first use.
1.2.3.4.
To avoid product contamination and eye injuries, avoid letting the dropper tip come into contact with your eye or any other surface.
Close the container tightly after each application.
Wipe away any excess liquid from your cheek with a clean tissue.
Wait at least 5 minutes before using other eye drops.
If you have any other questions about using this product, ask your doctor or pharmacist.
If you use more Pred Forte than you should
In case of need, rinse your eye with plenty of water or saline solution.
Like all medications, this medication may produce adverse effects, although not everyone will experience them.
If you notice any of the following adverse effects, please contact your doctor immediately:
You should also contact your doctor if any of the following adverse effects cause you problems or if their duration is prolonged:
Unknown frequency(frequency cannot be estimated from available data)
*Prolonged use
Reporting Adverse Effects
If you experienceany type of adverse effect, consult your doctor or pharmacist, even if it is apossibleadverse effect not listed in this prospectus.You can also report them directly to the Spanish System for Pharmacovigilance of Medicinal Products for Human Use: https://www.notificaRAM.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD.The expiration date is the last day of the month indicated.Dispose of the packaging 4 weeks after opening.
Do not freeze.
Do not use this medication if you observe a change in color or if cloudiness occurs in its contents.
Medications should not be thrown into the drains or trash. Deposit the packaging and medications you no longer need at the SIGRE collection pointof the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Pred Forte
Appearance of the product and contents of the packaging
Pred Forte is a sterile ophthalmic suspension.
Each package contains 5 ml of suspension and is approximately half full.
Holder of the marketing authorization and manufacturer responsible
Holder of the marketing authorization:
AbbVie Spain, S.L.U.
Avenida de Burgos 91,
28050 Madrid,
Spain
Manufacturer responsible:
Allergan Pharmaceuticals Ireland
Castlebar Road, Co. Mayo
Westport,
Ireland
Date of the last review of this leaflet:
November 2024
The detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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