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Acular LS

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Acular LS

Acular LS

SIDE EFFECTS

The most frequently reported adverse reactions for ACULAR LS™ (ketorolac tromethamine ophthalmic solution) ophthalmic solution occurring in approximately 1 to 5% of the overall study population were conjunctival hyperemia, corneal infiltrates, headache, ocular edema and ocular pain.

The most frequent adverse events reported with the use of ketorolac tromethamine ophthalmic solutions have been transient stinging and burning on instillation. These events were reported by 20% - 40% of patients participating in these other clinical trials.

Other adverse events occurring approximately 1% - 10% of the time during treatment with ketorolac tromethamine ophthalmic solutions included allergic reactions, corneal edema, iritis, ocular inflammation, ocular irritation, ocular pain, superficial keratitis, and superficial ocular infections.

Clinical Practice: The following events have been identified during postmarketing use of ketorolac tromethamine ophthalmic solutions in clinical practice. Because they are reported voluntarily from a population of unknown size, estimates of frequency cannot be made The events, which have been chosen for inclusion due to either their seriousness, frequency of reporting, possible causal connection to topical ketorolac tromethamine ophthalmic solutions or a combination of these factors, include corneal erosion, corneal perforation corneal thinning and epithelial breakdown (see PRECAUTIONS, General).

Read the Acular LS (ketorolac tromethamine ophthalmic solution) Side Effects Center for a complete guide to possible side effects

DRUG INTERACTIONS

No information provided.

Read the Acular LS Drug Interactions Center for a complete guide to possible interactions

Last reviewed on RxList: 2/13/2009
This monograph has been modified to include the generic and brand name in many instances.

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Acular LS - User Reviews

Acular LS User Reviews

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Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


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