Fluorometholone
Flucon belongs to a group of medicinescalled corticosteroids. Their action is to prevent or reduce inflammation.
with the herpes simplex virus(herpes simplex). The patient should consult their doctor for advice if their condition worsens or does not improve.
The topical administration of corticosteroids may be associated with a decrease in cortisol excretion in the urine as well as a decrease in cortisol levels in the serum. An association between corticosteroids and a decrease in growth rate in children has been observed, especially at high doses and with prolonged treatment.
The patient should discuss the use of Flucon with their doctor or pharmacist before starting treatment.
The safety of using Flucon in children under 3 years of age has not been established, so it is not recommended for this age group.
The patient should tell their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take, including those available without a prescription.
If the patient is using other eye drops or ointments, they should wait at least 5 minutes between administrations of the different medicines. Eye ointments should be used last.
Concurrent topical use of steroids and non-steroidal anti-inflammatory drugs (NSAIDs) may increase the risk of corneal healing problems.
No interaction studies have been conducted.
When using eye drops intended to dilate the pupil (e.g., atropine), which can cause increased intraocular pressure, this effect may be enhanced when Flucon is used at the same time.
Corticosteroid eye medicines can cause increased intraocular pressure, reducing the effectiveness of glaucoma medicines.
Some medicines may enhance the effect of Flucon, and therefore the doctor may decide to monitor the patient's condition closely when taking these medicines (including some medicines used to treat HIV: ritonavir, cobicistat).
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before using this medicine.
Flucon has no influence or negligible influence on the ability to drive and use machines.
For some time after administering Flucon, vision may be blurred. The patient should not drive or operate machines until this symptom subsides .
The medicine contains 0.5 mg of benzalkonium chloride in every 5 milliliters of suspension, which corresponds to 0.1 mg/ml.
Benzalkonium chloride may be absorbed by soft contact lenses and change their color. The patient should remove their contact lenses before administering the eye drops and wait at least 15 minutes before putting them back on.
Benzalkonium chloride may also cause eye irritation, especially in people with dry eye syndrome or corneal disorders (the transparent layer at the front of the eye). If abnormal sensations in the eye, stinging, or eye pain occur after using the medicine, the patient should contact their doctor.
Flucon contains 8.5 mg of sodium dihydrogen phosphate monohydrate and 12.5 mg of disodium phosphate in every 5 milliliters of suspension, which corresponds to 2.8 mg of phosphates/ml.
In patients with severe damage to the transparent, front part of the eye (cornea), phosphates may rarely cause corneal clouding due to calcium deposition during treatment.
This medicine should always be used as directed by the doctor.
In case of doubts, the patient should consult their doctor or pharmacist.
If the protective cap is loosened after removing the tamper-evident seal, it should be discarded before using the medicine.
The usual dose of Flucon is one drop into the eye or eyes, two to four times a day. During the first 24 to 48 hours, the doctor may increase the dosage to one drop every 4 hours. The doctor will inform the patient how long the treatment will last.
The safety of using Flucon in children under 3 years of age has not been established.
The doctor will determine how long to use the medicine.
If the medicine is used in patients with glaucoma, the treatment period should be limited to 2 weeks, unless longer treatment is justified.
Flucon is onlyintended for administration into the eye.
Method of using the eye drops
If the drop does not get into the eye, the patient should try again to administer the drop correctly.
In case of accidental administration of an excessive amount of eye drops, the patient should rinse their eyes with lukewarm water.
The patient should not use the medicine until the next scheduled dose.
If a dose of Flucon is missed, the patient should take the next scheduled dose. However, if it is almost time for the next dose, the missed dose should be skipped, and the patient should return to their regular dosing schedule. The patient should nottake a double dose to make up for the missed dose.
If the patient is using other eye drops or ointments, they should wait at least 5 minutes between administrations of the different medicines. Eye ointments should be used last.
If the patient has any further doubts about using this medicine, they should consult their doctor or pharmacist.
Like all medicines, Flucon can cause side effects, although not everybody gets them.
During treatment with Flucon, the following side effects have been observed with unknown frequency(the frequency of occurrence could not be determined from the available data):
delayed healing of eye injuries (see section 2).
Unless the side effects are severe, the patient can usually continue using the eye drops. If in doubt, the patient should consult their doctor or pharmacist.
If side effects occur, the patient should inform their doctor or pharmacist. This includes any side effects not listed in this leaflet.
If side effects occur, including those not listed in this leaflet, the patient should inform their doctor or pharmacist. Side effects can be reported directly to the Department of Monitoring of Adverse Reactions to Medicinal Products, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, tel.: +48 22 49 21 301, fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl
Reporting side effects will help gather more information on the safety of this medicine.
To prevent infections, the bottle should be discarded 4 weeks after it is first opened. The date of opening the bottle should be written in the space provided below.
Date of first opening: ………………
The medicine should be stored out of sight and reach of children.
Do not store above 25°C. Do not store in the refrigerator.
Store the packaging tightly closed.
Do not use Flucon after the expiry date stated on the packaging. The expiry date refers to the last day of the month.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Flucon is a liquid (white to light brown suspension) in a 5 ml bottle made of low-density polyethylene with a polypropylene cap. The cardboard box contains 1 bottle of 5 ml.
For more detailed information, the patient should contact the marketing authorization holder or parallel importer.
Immedica Pharma AB, Solnavägen 3H, SE-113 63 Stockholm, Sweden
Siegfried El Masnou, S.A., Camil Fabra 58, El Masnou, 08320 Barcelona, Spain
Novartis Pharma GmbH
Roonstrasse 25
90429 Nuremberg
Germany
Novartis Farmacéutica, S.A.
Gran Via de les Corts Catalanes, 764
08013 Barcelona
Spain
S.A. Alcon-Couvreur N.V.
Rijksweg 14
B-2870 Puurs
Belgium
InPharm Sp. z o.o., ul. Strumykowa 28/11, 03-138 Warsaw
InPharm Sp. z o.o. Services sp. k., ul. Chełmżyńska 249, 04-458 Warsaw
Marketing authorization number in Greece, the country of export:87337/01-11-2022
47840/14-10-2008
Parallel import authorization number:229/15
[Information about the trademark]
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