Eysuvis (loteprednol etabonate)
Last reviewed · Source: First Databank (FDB) drug data
Overview
Loteprednol etabonate is a synthetic nonfluorinated corticosteroid.
USES: This medication is used for short-term (up to 2 weeks) treatment to help relieve dry eye disease. Loteprednol belongs to a class of drugs known as corticosteroids. It works by decreasing inflammation (swelling).
Generic name: loteprednol etabonate
Pronunciation: (LOE-te-PRED-nol)
Reference product & biosimilars
No reference, biosimilar or interchangeable associated with this drug.
Today’s intelligence on Eysuvis
Indications
The following indications are listed for Eysuvis:
- Dry Eye
Also known as: Eye Dryness, Xerophthalmia.
Dosing
Safety and efficacy of ophthalmic suspensions containing loteprednol etabonate alone or in fixed combination with tobramycin have not been established in children younger than 18 years of age.
Loteprednol etabonate alone or in fixed combination with tobramycin is applied topically to the eye as an ophthalmic suspension. The suspension should be shaken vigorously prior to use. Care should be taken to avoid contamination of the container.
No dosing information is available for this tab.
No dosing information is available for this tab.
Drug interactions
There is no enhanced messaging for this drug.
There are no contraindication interactions for this drug.
There are no severe interactions for this drug.
There are no moderate interactions for this drug.
Contraindications
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There are no contraindication contraindications for this drug.
There are no severe contraindications for this drug.
There are no moderate contraindications for this drug.
Adverse reactions
There is no enhanced messaging for this drug.
There are no severe adverse reactions for this drug.
There are no less severe adverse reactions for this drug.
Precautions
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No enhanced messaging available.
No enhanced messaging available.
No enhanced messaging available.
No enhanced messaging available.
ICD codes
No ICD codes are available for this drug.
Formulary status
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Last reviewed · Source: First Databank (FDB) drug data
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