Medical Editor: John P. Cunha, DO, FACOEP
- irritation of the eyes for 1 to 2 minutes
- temporary blurred vision when you apply this medication
Other side effects of FML forte include sensitivity to light.
The dose of FML Forte is one drop instilled into the conjunctival sac two to four times daily. Do not discontinue treatment prematurely. FML Forte may interact with oral steroid medications such as prednisone, methylprednisolone, hydrocortisone, and others. Other drugs may interact with FML Forte ophthalmic. Tell your doctor all prescription and over-the-counter medications and supplements you use. During pregnancy, FML Forte should be used only when prescribed. It is not known if the medication in this product passes into breast milk. Consult your doctor before breastfeeding.
Our FML Forte (fluorometholone ophthalmic suspension 0.25%) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Stop using this medication and call your doctor at once if you have any of these serious side effects:
- pain behind your eyes, sudden vision changes, severe headache;
- sudden eye irritation;
- blurred vision, tunnel vision, eye pain, or seeing halos around lights; or
- signs of new eye infection, such as swelling, draining, or crusting of your eyes.
Less serious side effects may include:
- increased sensitivity to light; or
- mild stinging, burning, itching, or irritation in your eyes.
This is not a complete list of side effects and others may occur. Tell your doctor about any unusual or bothersome side effect. You may report side effects to FDA at 1-800-FDA-1088.
Read the entire detailed patient monograph for Fluorometholone Forte (Fluorometholone Ophthalmic Suspension 0.25%)
Adverse reactions include, in decreasing order of frequency, elevation of intraocular pressure (IOP) with possible development of glaucoma and infrequent optic nerve damage, posterior subcapsular cataract formation, and delayed wound healing.
Corticosteroid-containing preparations have also been reported to cause acute anterior uveitis and perforation of the globe. Keratitis, conjunctivitis, corneal ulcers, mydriasis, conjunctival hyperemia, loss of accommodation and ptosis have occasionally been reported following local use of corticosteroids.
The development of secondary ocular infection (bacterial, fungal and viral) has occurred. Fungal and viral infections of the cornea are particularly prone to develop coincidentally with long-term applications of steroids. The possibility of fungal invasion should be considered in any persistent corneal ulceration where steroid treatment has been used. (see WARNINGS).
Other adverse events reported with the use of FML FORTE® (fluorometholone ophthalmic suspension 0.25%) include transient burning and stinging upon instillation, ocular irritation, taste perversion and visual disturbance (blurry vision).
Read the entire FDA prescribing information for Fluorometholone Forte (Fluorometholone Ophthalmic Suspension 0.25%)
© Fluorometholone Forte Patient Information is supplied by Cerner Multum, Inc. and Fluorometholone Forte Consumer information is supplied by First Databank, Inc., used under license and subject to their respective copyrights.